| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs6569 | snp | G/T | 0.499673 | 0.0127754 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933271 | TAGAGGTGCTGCAGC[G/T]GCTCCTGCTCTCTGA | 10422 |
| rs14254 | snp | A/G | | | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933281 | CCTGGACTGTTAGAG[A/G]TGCTGCAGCGGCTCC | 10422 |
| rs872373 | snp | A/G | 0.336017 | 0.234736 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942379 | TTTAGGTTAGGCACA[A/G]TGGCTCATGCCTGTA | 10422 |
| rs915236 | snp | A/G | 0.40595 | 0.195396 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948678 | CAGTGGCAGGGGAGC[A/G]GGGCAGACACAGCCA | 10422 |
| rs1044191 | snp | A/G | 0 | 0 | missense | UBAC1 | GRCh38.p7 | 9:135945173 | CGCCTCTTCCTGGCC[A/G]AGCTCCCCCAGAGGC | 10422 |
| rs1044193 | snp | A/G | 0.166632 | 0.23569 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939721 | GGGGTTCGACGAGAA[A/G]GAGGTGATAGATGCC | 10422 |
| rs1044239 | snp | A/C | | | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933074 | TTGCTTGGAGAGTCC[A/C]CTTGTTATTTGACGG | 10422 |
| rs1810986 | snp | C/T | 0.28052 | 0.24813 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934477 | GAGACAGGGTTTTAC[C/T]GTATTAGCCAGGATG | 10422 |
| rs2297688 | snp | C/G | 0.324145 | 0.238752 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948231 | GGGGCTCAGCTGCAG[C/G]CTGGGTGGTTCTTCT | 10422 |
| rs2297689 | snp | A/G | 0.396546 | 0.202545 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948042 | CTCCAGGCTCCCCCA[A/G]CTCATCAAGGAGTTT | 10422 |
| rs2297690 | snp | C/T | 0.312837 | 0.241974 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946459 | CTCAACTCTCAGAAT[C/T]AAGAGTTCTAGGACA | 10422 |
| rs2297691 | snp | A/G | 0.335101 | 0.23507 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946112 | GCAACTCCTGTTGAT[A/G]TGCCTGAGGGCGGGC | 10422 |
| rs2297692 | snp | C/T | 0.309894 | 0.242719 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944849 | TGGCGAGCCTGGGGG[C/T]GGTGGGCCTGGGGAC | 10422 |
| rs4301514 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935294 | AACATTCAACAAAGG[A/C]AGATGTGCCTAATAT | 10422 |
| rs4351484 | snp | A/G | 0.335559 | 0.234904 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935542 | cataactacccatga[A/G]gatgacttgagccca | 10422 |
| rs4355852 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935739 | ataaccaaaaggaat[A/G]caagtggccaggcgc | 10422 |
| rs4841900 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941676 | ACACCTGGCAGTCCC[C/T]GCCCTCCCTCCCAGC | 10422 |
| rs4841901 | snp | A/T | 0.406296 | 0.19512 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959686 | CCCAGAGAAGTTTTT[A/T]AAAATACACACAACT | 10422 |
| rs4841902 | snp | A/C | 0.498964 | 0.02274 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960280 | GAACTAGTTCCAAAA[A/C]TCAGCAACCTAAGGA | 10422 |
| rs4842054 | snp | A/G | 0.316243 | 0.241064 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941361 | CAGTGAGCCAAGATC[A/G]CACCACTGTACTCCA | 10422 |
| rs4842055 | snp | G/T | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945413 | AGGTGCGACGGAAGC[G/T]CTGGTCCTTGCCTCA | 10422 |
| rs6537919 | snp | A/G | 0.336702 | 0.234484 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954000 | AAAAATTAGCCAGGC[A/G]TGGTGGCGCATGCCT | 10422 |
| rs6537920 | snp | A/G | 0.49907 | 0.0215454 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958455 | ACCACGGTGATCCCA[A/G]TTTGCACAAAACAGA | 10422 |
| rs6537921 | snp | C/T | 0.386504 | 0.209444 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961478 | GGGGCGCGCTGTGGC[C/T]ACCGCAAAGGAAGTG | 10422 |
| rs6537922 | snp | C/T | 0.0275645 | 0.114116 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961540 | GCTGTAGTTCTCTGG[C/T]AGCTTCGTTCCTCCC | 10422 |
| rs6537923 | snp | C/G | 0.0689305 | 0.172377 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961559 | TTCGTTCCTCCCCGA[C/G]CTGCAGGCGGTTCCC | 10422 |
| rs7024472 | snp | A/G | 0.0707826 | 0.174302 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962538 | TAAGGCACAGTTCCC[A/G]TTCTCAGAGGTTAGC | 10422 |
| rs7026477 | snp | C/T | 0.336702 | 0.234484 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950137 | cctgaacacagccct[C/T]cggcaccctgatttc | 10422 |
| rs7028495 | snp | C/T | 0.0114815 | 0.0748929 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946294 | CTTAAACAATTCCAC[C/T]GCATCTGGGTTCAGC | 10422 |
| rs7029100 | snp | A/G | 0.397271 | 0.202018 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956424 | ACACGGGGGCTAGGC[A/G]CGTCGGCTCACCATT | 10422 |
| rs7029359 | snp | A/C | 0.397452 | 0.201886 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955935 | TCACTAAGTAACAGC[A/C]ATGCTGCATCCCGAG | 10422 |
| rs7030007 | snp | A/C | 0.396546 | 0.202545 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956394 | CTGGCTTGCGGGAGT[A/C]CTGCTTTCCTTTGAA | 10422 |
| rs7848205 | snp | A/G | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954157 | AAAAAAAAAAAAAAA[A/G]AAGAAGAGCAGGGCT | 10422 |
| rs7860947 | snp | C/G | 0.499137 | 0.0207489 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957463 | AAACCCACAGTCCAC[C/G]TGTCACCAGCACACC | 10422 |
| rs7868264 | snp | A/G | 0.396182 | 0.202807 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958764 | TGACTAACGCATTCT[A/G]GCCCTGCCTGCAGAA | 10422 |
| rs7870592 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947307 | CCGAGGCTGGAGTAC[A/G]ATGATGCAATCTCGG | 10422 |
| rs7871519 | snp | C/G | 0.396727 | 0.202413 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947343 | TGCAACCTCCGCCTC[C/G]CGGGTTCAAGTGATT | 10422 |
| rs10116480 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944609 | GCCTGAGCGGCCCCT[C/T]GCTCATGGACACCCC | 10422 |
| rs10119464 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952778 | gggaatatttgcatt[C/T]caaataatcaactca | 10422 |
| rs10122454 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944602 | GCTGGCAGCCTGAGC[A/G]GCCCCTCGCTCATGG | 10422 |
| rs10448315 | snp | G/T | 0.286042 | 0.247388 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961917 | AGATCAGAGAGTCAC[G/T]GTTCCTGCGAAGCCT | 10422 |
| rs10553564 | in-del | -/CTCA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939504 | CACAGCCCACACTCA[-/CTCA]GCCCACACTCACTCA | 10422 |
| rs10690817 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958050 | CAGGTATAATTTTCT[-/T]TTTTTTTTTTTTTTG | 10422 |
| rs10735241 | snp | C/G | 0.084364 | 0.187256 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949143 | TTATGAGCCAGGACA[C/G]ACGGCCCACGGAGGA | 10422 |
| rs10745377 | snp | A/C | 0.404559 | 0.196498 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935900 | GCACGGTGGCGGGCA[A/C]CTGTAGTCCCAGCTA | 10422 |
| rs10745378 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937626 | AATGAGAGATTGTTT[A/G]AGGAGACACAAATAC | 10422 |
| rs10776856 | snp | C/T | 0.496263 | 0.0430645 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945267 | TGCAAGGCAAGAGAC[C/T]CTTTCCAACATCCCC | 10422 |
| rs10858184 | snp | C/T | 0.280256 | 0.248162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937118 | GCTCCAGAGACACTT[C/T]CAGCCTGCTCGGGTG | 10422 |
| rs10858185 | snp | A/G | 0.28052 | 0.24813 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937699 | GGCGACGGCCACACC[A/G]GAGGGAGGGATGAGG | 10422 |
| rs10858186 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948905 | TGAAACCCCATCTCT[A/C]CTAAAAAGACAAAAA | 10422 |
| rs10858187 | snp | A/G | 0.499563 | 0.0147699 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956777 | ACTCAGAGCTTGGAC[A/G]GAGAGAAGGCTGACT | 10422 |
| rs10858188 | snp | A/C | 0.301177 | 0.244706 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960141 | GAGTCGCCACTAGAA[A/C]ATTGCAGCCTCCTTC | 10422 |
| rs10858189 | snp | C/G | 0.28052 | 0.24813 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960239 | AGGCTTCTTAGCTGA[C/G]CTTACTGAGTCCTTT | 10422 |
| rs10858190 | snp | C/T | 0.279461 | 0.248258 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960381 | GGACTTCTCTCTTGA[C/T]CAATTTTACCTCTGC | 10422 |
| rs10858191 | snp | C/T | 0.284209 | 0.247648 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962454 | TAGTTCAGGTTAGAC[C/T]TGACACATTGACTGA | 10422 |
| rs11103230 | snp | A/C | 0.278664 | 0.248351 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932692 | CGGTCATGTTTTTTA[A/C]AATGAAAAAAAAGGA | 10422 |
| rs11103231 | snp | C/G | 0 | 0 | missense | UBAC1 | GRCh38.p7 | 9:135933496 | GCTGTTCAGTGGGTT[C/G]TCCAGCATGTCTTCA | 10422 |
| rs11103232 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937249 | gagttcgagaccagc[C/T]tggcaaacatggtga | 10422 |
| rs11103233 | snp | C/T | 0.499968 | 0.00399348 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937863 | CATCGAAGACCCTGA[C/T]GAGTAGTAAGAGCAA | 10422 |
| rs11103234 | snp | A/G | 0.280256 | 0.248162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938586 | AGTCCGCTTTTCTCT[A/G]CAGACCCTGGTGTCG | 10422 |
| rs11103235 | snp | A/C | 0.334871 | 0.235153 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942816 | ATGTCTACACACAGA[A/C]AGAACGTGCGCCTTG | 10422 |
| rs11103237 | snp | C/T | 0.279195 | 0.248289 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953079 | AGGCGGACAGCAGCG[C/T]GGGAGTGAACCGTCA | 10422 |
| rs11103238 | snp | A/C | 0.366266 | 0.221319 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960368 | GACCCTACTCCTGGG[A/C]CTTCTCTCTTGACCA | 10422 |
| rs11405597 | in-del | -/C | 0.336017 | 0.234736 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932735 | GGTAGGCGGAGGCAG[-/C]CCGTGCTTGGGCTCA | 10422 |
| rs11435128 | in-del | -/A | 0.499451 | 0.0165644 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940280 | TTAGAAAAAAAAAAA[-/A]TCCTAGGGCCGGGCG | 10422 |
| rs11542895 | snp | G/T | 0.00873346 | 0.0655016 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933361 | TCGGGCCGCACCAGG[G/T]GGCTGCTGTGGCCTG | 10422 |
| rs11791688 | snp | C/T | 0.00975586 | 0.0691575 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938720 | CCTGTGGTCCTGTTA[C/T]GGGCAGTCAGCAGTG | 10422 |
| rs12115351 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952476 | CGCCACTTGCAGAAC[A/G]CATCTTCCTCTGCTC | 10422 |
| rs12345224 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945381 | GTGACCCTTATAACA[A/T]GAACCTGAATGAACA | 10422 |
| rs12352445 | snp | C/T | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934706 | CTCAGAAAGAACAAA[C/T]TATAAGGTGCGAAAC | 10422 |
| rs12380316 | snp | C/T | 0.298905 | 0.24517 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959133 | ATCATGATGGCCATG[C/T]ACATCGCACCGAGTG | 10422 |
| rs12380331 | snp | C/G | 0.299411 | 0.245069 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959229 | ATATTTTTGTCTATT[C/G]CATTAACCCACAAGT | 10422 |
| rs12552793 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959415 | gagtcttgctctgtc[A/G]ccaggctggagtgca | 10422 |
| rs12554408 | snp | C/G | 0.281313 | 0.248031 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944520 | GGGGAGATGAGGCGC[C/G]GGCGAGGAAGGTCCA | 10422 |
| rs28757690 | snp | A/C/G | 0.0149611 | 0.0851875 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945157 | TGCTGTGGCCCCCTC[A/C/G]GCCTCTGGGGGAGCT | 10422 |
| rs34017249 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935801 | GAGGCCGAGACGGGC[-/T]GGATCACGAGGTCAG | 10422 |
| rs34065736 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950270 | TGTGTGGCGATTTGT[C/T]AGGTGGCAACGGAAA | 10422 |
| rs34292104 | in-del | -/T | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959393 | GGGTTTTTTGTCTGG[-/T]TTTTTTTTTTTTTTT | 10422 |
| rs34386340 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947166 | CCTGCCCTGCCTGCT[-/G]GCGGCGTCCACGTGA | 10422 |
| rs34581200 | in-del | -/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947746 | CCCCCCCACAGCAAT[-/C]CCCCCACACGGGGAC | 10422 |
| rs34640525 | in-del | -/A | 0.0685596 | 0.171987 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960591 | TCAAAGATGCTGCTG[-/A]AAAAAAACCTCACCC | 10422 |
| rs34729162 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935894 | GCCGGGCACGGTGGC[-/T]GGGCACCTGTAGTCC | 10422 |
| rs34773979 | in-del | -/CAG | 0.300421 | 0.244863 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959333 | GGCTCAGGGAGGACA[-/CAG]CAGCACCTCAGAGAA | 10422 |
| rs34795677 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957330 | TGGCTCTGCTCCCTG[-/A]AAATACTGGGGGTGC | 10422 |
| rs34895090 | in-del | -/C | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961823 | GCTGTGATATTTCTT[-/C]TTGCACTGCACTGCT | 10422 |
| rs35005080 | snp | C/T | 0.0413956 | 0.137783 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938235 | ACCTAGCAATGTTTT[C/T]GGGTTGGTCAGGCCC | 10422 |
| rs35360444 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942060 | GGAGGGAATGGCAAT[-/G]GGGGAAGATCTTAGG | 10422 |
| rs35492042 | in-del | -/AC | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959330 | ACTGGCTCAGGGAGG[-/AC]ACACAGCACCTCAGA | 10422 |
| rs35653463 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942650 | GAGTGAAACTGTCTC[-/A]AAAAAAAAAAAAAAA | 10422 |
| rs35679979 | snp | A/G | 0.301429 | 0.244653 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960943 | GGACCCCAGGTCGGG[A/G]CGGTTCGGGGACTGA | 10422 |
| rs35719015 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942122 | GCATCCATATTTAAC[-/A]AAAAGGCTTAAGATG | 10422 |
| rs35803292 | in-del | -/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955221 | CCTGTGGGTGGACCA[-/C]CCCCCTCCTGGCTCC | 10422 |
| rs35897611 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947237 | ACCCAAAATAACTCA[C/T]GGGTTCAGATTTGTG | 10422 |
| rs35925532 | snp | C/T | 0.395087 | 0.203592 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939515 | CTCACTCAGCCCACA[C/T]TCACTCATCACAGCC | 10422 |
| rs36016562 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947172 | CTGCCTGCTGCGGCG[-/T]TCCACGTGAGCACTG | 10422 |
| rs36068848 | snp | C/T | 0.00103819 | 0.02276 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938262 | GCCCAGCTGCACCAC[C/T]GGGTTATCCAGGATG | 10422 |
| rs55907616 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937302 | AAAAATTAGCCAGGC[A/G]TGGTAGTGCACGCCT | 10422 |
| rs55984832 | snp | C/T | 0.00790225 | 0.0623593 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947778 | CCATGCACCCGCCGC[C/T]GCTCTGGGCTGACAC | 10422 |
| rs56142900 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957791 | TTTTTTTTTTTTTTT[-/T]AAAGACAGGGTCTCA | 10422 |
| rs57527185 | in-del | -/A | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937441 | AAAAAAAAAAAAAAA[-/A]TCAGGAGTGGCACCA | 10422 |
| rs59299034 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944221 | CGGGGGTTACACTGC[A/G]GGACATGGTGGGGCA | 10422 |
| rs61532150 | snp | A/G | 0.316485 | 0.240998 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935793 | GCACTTTGGGAGGCC[A/G]AGACGGGCGGATCAC | 10422 |
| rs62582964 | snp | A/G | 0.316485 | 0.240998 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937342 | GGTACTCAGGAGGCT[A/G]AGGCAGGAGAATTGC | 10422 |
| rs62582965 | snp | A/G | 0.381891 | 0.212379 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939290 | AAAACCTAGAATTCC[A/G]TATTTTTAAATTTTT | 10422 |
| rs62582974 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959165 | GTTAAAGTAAATGCC[A/G]TGCCAACGCAGGGGA | 10422 |
| rs62582975 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959174 | AATGCCGTGCCAACG[A/C]AGGGGACATCCCATG | 10422 |
| rs62585226 | snp | C/T | 0.320335 | 0.239902 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934254 | CCAGTAGCCCATGGC[C/T]GAGCACAGAGCTCAG | 10422 |
| rs62585227 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934654 | AGCAGAGTGAGACTC[C/T]GTCTCAAAAAATAAA | 10422 |
| rs66767056 | in-del | -/CTC | 0 | 0 | cds-indel | UBAC1 | GRCh38.p7 | 9:135945100 | CTCATCTCTGGCCTC[-/CTC]ATCGGTGGCGCTGGC | 10422 |
| rs71384033 | in-del | -/G | 0.261884 | 0.249717 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938813 | GGCACGGGGGATGGT[-/G]TGGGGGGGGGATGTG | 10422 |
| rs71384034 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939210 | AAAAAAAAAAAAAAA[-/A]TGAACAAATTACCCA | 10422 |
| rs71384035 | in-del | -/A | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942651 | AAAAAAAAAAAAAAA[-/A]GAGAAACTTTTACAT | 10422 |
| rs71483264 | snp | C/G | 0.298905 | 0.24517 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961379 | GGGGCGCGCCGTCGC[C/G]GCCGCACCGGAAGTG | 10422 |
| rs71507091 | in-del | -/C | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937512 | CCTGGGTTCCCAGTG[-/C]CCTTCCATCAAGAAA | 10422 |
| rs71508828 | snp | A/G | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944581 | GCAGACTGTGCCATG[A/G]AGGCGGCTGGCAGCC | 10422 |
| rs72771952 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935629 | AGATCAAGACCCTGT[A/C]TCCATAAAAAGAAGG | 10422 |
| rs72771956 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937983 | GTTTTCTGAGGCCTA[C/T]GTCAGGGTCATCGCG | 10422 |
| rs72771957 | snp | A/C | 0.0652674 | 0.168445 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946047 | CCTCAGGTTCAGGGG[A/C]CTTATCTGAGCACAA | 10422 |
| rs73668047 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944689 | AGAGGCTGCCGAACA[A/G]GGGGGGCTTGTGGAT | 10422 |
| rs73668048 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952462 | TGTGGGGTAGGACAC[A/G]CCACTTGCAGAACGC | 10422 |
| rs73668049 | snp | G/T | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959372 | AGGGTTTTTTGTCTG[G/T]TTTTTTTTTTTTTTT | 10422 |
| rs73668050 | snp | A/G | 0.0792508 | 0.182605 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962826 | CGACTGTTAGAGACC[A/G]CAGTGGAGGTGGTGG | 10422 |
| rs74312190 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958382 | CATTAACTACCTGTT[A/G]TACAAGACAGGTTCC | 10422 |
| rs74338681 | snp | C/G | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957815 | GGTCTCATTCTGTCA[C/G]CCAGGCTGGAGTGCA | 10422 |
| rs74600155 | in-del | -/AAGAA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954155 | AAAAAAAAAAAAAAA[-/AAGAA]GAAGAGCAGGGCTTC | 10422 |
| rs74667710 | snp | C/G | 0.0450349 | 0.143141 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135961058 | CTTGAGCTTCTCCAC[C/G]GAGGTGTCCTCGGTG | 10422 |
| rs74925685 | snp | A/C/T | 0.0263992 | 0.111815 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963291 | CTGGGGGCATTCACA[A/C/T]GGAGGTGGCCTGGAG | 10422 |
| rs75276844 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949987 | GTAGGAATGCAGGCC[A/G]CGCCCAGGCCCTGAG | 10422 |
| rs75415013 | snp | A/G | 0.0116769 | 0.0755123 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947942 | AAGTCTGAGGTGAAC[A/G]TAAGAGCAGCAAAAA | 10422 |
| rs75535862 | snp | A/C | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949060 | GTGAGACACCATCTC[A/C]AAAAAAAAAAAAAAG | 10422 |
| rs75861826 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956429 | GGGGCTAGGCGCGTC[A/G]GCTCACCATTTTGTG | 10422 |
| rs75946163 | snp | C/T | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943955 | GAAGGGAACAACACA[C/T]ACTGGGGCCTGTCAT | 10422 |
| rs76146588 | snp | C/G | 0.306927 | 0.243432 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960968 | GACTGAGGCGGGGTC[C/G]GCAGTCGGAGGGGTC | 10422 |
| rs76206796 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942054 | GATGACGGGAGGGAA[C/T]GGCAATGGGGAAGAT | 10422 |
| rs77244768 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959083 | TATCTGTGGATCAAA[C/T]AGCTCTCATTTCCTA | 10422 |
| rs77523095 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944670 | CAGGGCCCCCACCCC[A/G]CAGAGAGGCTGCCGA | 10422 |
| rs77609618 | snp | C/T | 0.0298908 | 0.118541 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961949 | GGTTTGCGGGGCACC[C/T]AGAGGGGAGGGAAGC | 10422 |
| rs77898087 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938067 | TAGCGGGACTACACC[C/T]GCAGGATGCCAACCT | 10422 |
| rs78114871 | snp | A/C | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949061 | TGAGACACCATCTCA[A/C]AAAAAAAAAAAAAGG | 10422 |
| rs78737831 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939855 | TCCCCGCACCCTAGC[A/G]GAGGGTGCTCCCAAC | 10422 |
| rs79085806 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957434 | CCAAAATAATTCTCA[C/T]ACTGATTCCCAAAAA | 10422 |
| rs79117952 | snp | C/G/T | 0.0240643 | 0.107019 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962588 | TCTCTGCCTCCTGCC[C/G/T]GCAGGCTTTTATTCT | 10422 |
| rs79351196 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957500 | AACACGGAAGCACTA[A/G]GACGACCGTGTCACT | 10422 |
| rs79935052 | snp | A/T | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939210 | TGACTCCAAAAAAAT[A/T]AAAAAAAAAAAAAAA | 10422 |
| rs79996973 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957475 | CACGTGTCACCAGCA[C/T]ACCAGGAACAACACG | 10422 |
| rs80024626 | snp | A/C/T | 0.0103365 | 0.0712171 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945406 | TGAACACAGGTGCGA[A/C/T]GGAAGCGCTGGTCCT | 10422 |
| rs111251848 | snp | A/G | 0.000435993 | 0.0147583 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135947822 | GTTGGTCTGGACCGC[A/G]GCCCGGTCCATGTTG | 10422 |
| rs111300483 | snp | C/T | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953118 | GTGTCCCTACCCTCC[C/T]CTCTGTCTCAGAAAA | 10422 |
| rs111332254 | snp | C/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961502 | GGAAGTGCGTCACGG[C/G]GCGCGCCCGGAGCAT | 10422 |
| rs111412357 | snp | A/G | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944752 | TTTTCAAAAGGTGAC[A/G]AATGTGGCAACACAG | 10422 |
| rs111467194 | snp | C/T | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955989 | CATGACTGCTCTCGG[C/T]GTGGCCCAGCTCACG | 10422 |
| rs111539413 | snp | C/G | | | splice-acceptor-variant | UBAC1 | GRCh38.p7 | 9:135955416 | GCTCCCATGAGCACA[C/G]TGGGGAAAAATAGAA | 10422 |
| rs111639696 | snp | C/T | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955816 | TTTTCCACAGACGCA[C/T]GAAAGGGGCCAGAAA | 10422 |
| rs111779991 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947136 | CAGCCGTCCTCCCAC[C/T]CCGGCACAGCACGTG | 10422 |
| rs111948954 | snp | C/T | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947344 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 10422 |
| rs111961408 | in-del | -/CACT | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939569 | ACTCACCACAGCCCA[-/CACT]CACTCACCACAGCCC | 10422 |
| rs112107476 | snp | A/G | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939986 | GTAGTTAGCAGAGCC[A/G]GGGGGCAGTGCAGCT | 10422 |
| rs112161627 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953307 | TATAATTCTTTTTTT[C/T]TTAAGTTTGTATTTA | 10422 |
| rs112188768 | snp | A/G | 0.0253472 | 0.109686 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933353 | GCCCGGTCTCGGGCC[A/G]CACCAGGGGGCTGCT | 10422 |
| rs112298604 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933170 | CTCCACTTCCCAGTG[C/T]GACAACCACTTTTTT | 10422 |
| rs112483965 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956802 | CTGACTATTTTCTTG[C/G]TCTTACAGATCCCCT | 10422 |
| rs112505519 | snp | C/G | 0.00312736 | 0.0394195 | missense | UBAC1 | GRCh38.p7 | 9:135938274 | CACCGGGTTATCCAG[C/G]ATGGCCTGAAAGAGA | 10422 |
| rs112538743 | snp | A/G | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952311 | CTGCTCTTTCTCTGG[A/G]GTGAACACTCTCCTT | 10422 |
| rs112614991 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950021 | AGCCCCCAGCTGGCC[A/G]CCAGCAAGAAAATGG | 10422 |
| rs112988243 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958606 | GAAGGAAAAAATCAT[C/G]CCGGCGTCAGCACGC | 10422 |
| rs113297107 | snp | C/T | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936616 | TTCTCTGCCTCAGCT[C/T]CAGAGTAGCTGGGAT | 10422 |
| rs113392598 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952276 | CTACCAGGCATGGGC[C/T]TAGCCCAAAAGAGTT | 10422 |
| rs113430958 | snp | A/C | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948274 | ACGAACTCATCTCTG[A/C]TCCTTCTGGAAGCTC | 10422 |
| rs113480786 | snp | A/G | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936861 | AGGACATCAAAACAC[A/G]GGATTCTGCCCATCA | 10422 |
| rs113632428 | snp | A/G | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944797 | CCTGGATTCAAGCCA[A/G]GATAACTTACAGGTG | 10422 |
| rs113800964 | snp | A/G | 0.0162345 | 0.0886209 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135947798 | TGGGCTGACACTCAC[A/G]TCTCTCATGTTGGTC | 10422 |
| rs113829236 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934742 | TTTCACACACAGGGC[A/G]GGGAACTTAATTTCC | 10422 |
| rs113865015 | snp | C/T | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954117 | GCACTCCAGCCTGGG[C/T]AACAGAGCAAGACTT | 10422 |
| rs113903506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950571 | GTGTAAGAAGGATAG[A/T]TAATCTTAATCTATT | 10422 |
| rs113953180 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938518 | ACCGTGAAGACAAAC[C/G]CAGTCTGGATTCACT | 10422 |
| rs113967206 | snp | C/T | 0.5 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958402 | AGACAGGTTCCTCTG[C/T]CCCCTTCTCCACTCC | 10422 |
| rs114140947 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937301 | GAAAAATTAGCCAGG[A/C]GTGGTAGTGCACGCC | 10422 |
| rs114141783 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946101 | GAGCTCCACCTGCCC[A/G]CCCTCAGGCACATCA | 10422 |
| rs114216175 | snp | A/G | 0.00534853 | 0.0514359 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939727 | TATCACCTCTTTCTC[A/G]TCGAACCCCATCTCC | 10422 |
| rs114233726 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939963 | GCCGAGGAAGTGCAG[A/G]GATGACTGTAGTTAG | 10422 |
| rs114280388 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948115 | TCTGCTCTGACGTAA[A/G]TAAGAGTGAAGCGGT | 10422 |
| rs114307634 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952978 | CTTATTCTGTGTGGT[A/G]GTTGGTTACCCACTT | 10422 |
| rs114323834 | snp | A/G | 0.030665 | 0.119967 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935559 | ATGACTTGAGCCCAG[A/G]AGGTCAAGGCTGCAG | 10422 |
| rs114495738 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937529 | CTTCCATCAAGAAAA[C/T]ACTCCACAACCCCCA | 10422 |
| rs114514136 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963245 | GGCCAGGAAGGTGTT[A/G]GGTAGTTTTGGACAC | 10422 |
| rs114925381 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940007 | CAGTGCAGCTCCCAG[G/T]CTTGTCTTCAGGGAG | 10422 |
| rs115013139 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934907 | TTTTTTTGAGACAGC[A/G]ACTTGCTTTGTTGCC | 10422 |
| rs115103279 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947033 | CACAGAACTCTCTGG[A/G]AGACACCCCAAGAGG | 10422 |
| rs115120233 | snp | C/T | 0.0052818 | 0.0511175 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933378 | GCTGCTGTGGCCTGA[C/T]AGCCGAGTGGAACAA | 10422 |
| rs115273557 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940051 | CAGGTAGAAACGCAT[C/T]GCTTATGTGGACACG | 10422 |
| rs115400874 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949102 | AGCAGCACAAAGTGA[A/G]GAGTCAGCAGGGAAG | 10422 |
| rs115447551 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957507 | AAGCACTAGGACGAC[C/T]GTGTCACTCTGCTTC | 10422 |
| rs115575748 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950389 | ATGCGCAGGCCAGAG[C/G]GATCTGGAGGGAGGG | 10422 |
| rs115765694 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939406 | CACCACGCCCGGGGC[A/G]CTCACGAGTGAGGCT | 10422 |
| rs115984036 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950799 | TAAAAATAACAAGAG[C/T]TATGAGTGGTTGGGC | 10422 |
| rs116104525 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957575 | AGCCCCAACCAAGGC[C/T]GCTGGAGTAGGGAGG | 10422 |
| rs116225985 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943734 | ATAAGAAAAGAAACC[A/G]GATAGACTGAATAAA | 10422 |
| rs116227373 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948928 | GACAAAAATAAGCCC[A/G]GTGTCCTGGTGCACA | 10422 |
| rs116315060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945360 | TGACTTCTCCAGCAT[C/T]AGCTGGTGACCCTTA | 10422 |
| rs116458245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935466 | GCCTGAGCAAAAAAA[C/T]GAGACCCCATCTCAA | 10422 |
| rs116658139 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960129 | ACTTATCACATGGAG[G/T]CGCCACTAGAAAATT | 10422 |
| rs116715104 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956575 | AGCACCATACAGCCC[A/G]ACACACGACAGCACA | 10422 |
| rs116740657 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962366 | CTGCAAGCCCCCTTG[A/G]CAGTGGTCTCTGTAC | 10422 |
| rs116768611 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937515 | TGGGTTCCCAGTGCC[C/T]TCCATCAAGAAAATA | 10422 |
| rs116796992 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959172 | TAAATGCCGTGCCAA[A/C]GCAGGGGACATCCCA | 10422 |
| rs116914235 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939397 | CACGGCCTCCACCAC[A/G]CCCGGGGCGCTCACG | 10422 |
| rs117060097 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960148 | CACTAGAAAATTGCA[A/G]CCTCCTTCAACCTAA | 10422 |
| rs117235396 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952903 | ATGCTGAGGCTGTGC[A/G]GTGTGAGGTGGGGCT | 10422 |
| rs117238994 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939161 | GAGTGTGATCACACC[A/G]CTGCACTCCAGCCTG | 10422 |
| rs117271674 | snp | A/C/G | 0.0185938 | 0.0946107 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957926 | ATTACAGGAGTCCGC[A/C/G]ACCATGCCAGGCTAT | 10422 |
| rs117534714 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942312 | ACAAGCACAACGAGA[C/T]AAACTTCCTGCTAAA | 10422 |
| rs117753465 | snp | C/T | 0.0644444 | 0.167538 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957943 | CCATGCCAGGCTATT[C/T]TTTTACATTTTTAGT | 10422 |
| rs117980673 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957695 | AGGACCCATCTTCAT[A/G]CGATCTAGGAAATGG | 10422 |
| rs118034043 | snp | C/T | 0.000824104 | 0.0202823 | missense | UBAC1 | GRCh38.p7 | 9:135947862 | AGGTTGGCGGTGGCC[C/T]GCAGTATGGCCTCTT | 10422 |
| rs118079164 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956057 | GTGGACCAATGGGCA[C/T]GCAGTCACCAGGGCC | 10422 |
| rs137956961 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933842 | CTTCCCCAACAACTC[C/T]ACTTCCAATCCCACC | 10422 |
| rs137958401 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947548 | CCAAACTCAGGGCCG[A/G]ATTGACGTTTTCCCA | 10422 |
| rs138168681 | in-del | -/G | | | frameshift-variant | UBAC1 | GRCh38.p7 | 9:135945122 | GTGGCGCTGGCTCCC[-/G]CGGCAGCCTCGGAGG | 10422 |
| rs138172100 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944429 | AGATCTGCCATCTGA[A/G]CATGTCGGAGACAGA | 10422 |
| rs138500609 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957532 | TGCTTCTTTGTTCTC[A/C/G]GCAGAAGCTGGGGTA | 10422 |
| rs138561011 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954533 | TGCATGGCCCTAGCT[C/G]AGGTACAAGCTCCCA | 10422 |
| rs138622094 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951060 | GTGAGATCGTACCAC[A/G]CACTCCAGCCTGGTG | 10422 |
| rs138689234 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959753 | GCCCACGGAGTTACC[A/G]GCGCTGGAGCTTAGT | 10422 |
| rs138844665 | snp | A/C/G | 5.15206e-05 | 0.00507524 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939795 | TAGCTCGCTGGGGGC[A/C/G]GCAGGAGGCCGAGGA | 10422 |
| rs138871017 | snp | C/T | 0.0015485 | 0.0277822 | missense | UBAC1 | GRCh38.p7 | 9:135945111 | CCTCCTCATCGGTGG[C/T]GCTGGCTCCCGCGGC | 10422 |
| rs138882581 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934531 | TGGGCGTGGTGGCAG[G/T]CGCCTATAATCCCAG | 10422 |
| rs138890376 | in-del | -/CCCCC | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942612 | GCCATGATTGTGCCA[-/CCCCC]CCGCCACTCCAGCCT | 10422 |
| rs138949354 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947492 | TTCTGACCTCAGGTG[A/G]TCCACCCGCTTCGGG | 10422 |
| rs139053905 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942045 | ACACAGAGAGATGAC[A/G]GGAGGGAATGGCAAT | 10422 |
| rs139089543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946820 | CAGGCAGGAGGAGCC[A/G]TGGGATGGACCGGAG | 10422 |
| rs139209042 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963260 | GGGTAGTTTTGGACA[C/T]GGGGACCTGGATGTG | 10422 |
| rs139214439 | snp | C/T | 3.3413e-05 | 0.00408722 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945897 | CACGCACTGGTTCAG[C/T]TGAAGGGCCTTGGTG | 10422 |
| rs139297035 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957306 | CCTCAAGTGCCTCTG[C/G]ATTTGACAATGGCTC | 10422 |
| rs139362045 | snp | A/T | 0.0170251 | 0.090679 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932769 | CCTGTGTCCCAGGAA[A/T]ACGGGCTCAGCTCCA | 10422 |
| rs139386456 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952623 | GAATGTAAACACCAA[C/T]GACATCCAGTTCTGT | 10422 |
| rs139530690 | snp | G/T | 0.000131848 | 0.00811828 | missense | UBAC1 | GRCh38.p7 | 9:135945108 | TGGCCTCCTCATCGG[G/T]GGCGCTGGCTCCCGC | 10422 |
| rs139791104 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940684 | TTTTGGGGAAGGACA[C/T]ACATTTTCTGGACAC | 10422 |
| rs139792544 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958009 | TTTCATGAATGTTTA[C/T]GACACACCAAAAACT | 10422 |
| rs139894232 | in-del | -/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954719 | CTCAGAGGTCAAAAC[-/C]TGAGATGCAGCTCAT | 10422 |
| rs139960127 | in-del | -/TGAAACCTA | 0.021333 | 0.101051 | cds-indel | UBAC1 | GRCh38.p7 | 9:135933047 | ACATTAACTCTGGGT[-/TGAAACCTA]CCTCCGTCAAATAAC | 10422 |
| rs139971113 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958538 | GGAGTGCACACCCAG[C/G]AGCACAGCAGGGAGA | 10422 |
| rs139972573 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956024 | AACAGCCATGCTGCA[C/T]CCCTGGGCGGCTTGA | 10422 |
| rs139985754 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953068 | CACGCAGGTGAAGGC[A/G]GACAGCAGCGCGGGA | 10422 |
| rs139999560 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955602 | CATCATAGCACCAGT[A/G]AGCTGATCCCCAGCC | 10422 |
| rs140179403 | snp | A/G | 0.0432022 | 0.14048 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945859 | GCCCCAGGTGTCTCC[A/G]GCAAGGGAAGGAGGT | 10422 |
| rs140205081 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933744 | ATGCACTCAATTCTG[C/G]CAGGTGGGCAGTGTG | 10422 |
| rs140354891 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941738 | GGGAGAGGGGCCTTG[C/T]GCTCACGGGCTGCAG | 10422 |
| rs140356695 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958855 | TATGTCGGCTCTTGC[A/G]GTGTGAAAATCCCCT | 10422 |
| rs140388230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953380 | GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACTGC | 10422 |
| rs140422188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938506 | GGAAGGGACTCTACC[A/G]TGAAGACAAACGCAG | 10422 |
| rs140571151 | snp | A/G/T | 1.6651e-05 | 0.00288535 | missense, synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945987 | CTCATCCTCGTCCTC[A/G/T]TCCAGCATTGCTGCA | 10422 |
| rs140612025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937285 | GTCTCTACTAAAATA[C/T]GAAAAATTAGCCAGG | 10422 |
| rs140620854 | snp | C/T | 8.27602e-05 | 0.0064322 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938325 | CTTGTCCAGCTCCTC[C/T]GGAGAGGGCTTCCGG | 10422 |
| rs140777739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959203 | TGTCGATGCAGTGTG[C/G]GGTCCACAGGATATT | 10422 |
| rs140894564 | in-del | -/GATA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950570 | CAGCTGTGTAAGAAG[-/GATA]GATAATCTTAATCTA | 10422 |
| rs140946801 | in-del | -/CCT | 0.357563 | 0.225677 | cds-indel | UBAC1 | GRCh38.p7 | 9:135945096 | TCAGCTCATCTCTGG[-/CCT]CCTCATCGGTGGCGC | 10422 |
| rs140986243 | in-del | -/T | 0.277867 | 0.248442 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960698 | TTCCCGATCTGCCCC[-/T]ACCTCCCTGCGTGGC | 10422 |
| rs140989702 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949821 | CAGGTTACATCACGC[A/C/G]GCACAGCCGACTGTG | 10422 |
| rs141027492 | in-del | -/CA | 0.316726 | 0.240931 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939482 | CTCACAGCCCACACT[-/CA]CTCACCACAGCCCAC | 10422 |
| rs141125062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956621 | GCACAGCACAGCACC[A/G]CACACCACACCAAAC | 10422 |
| rs141238198 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947500 | TCAGGTGATCCACCC[A/G]CTTCGGGTTCAGAAT | 10422 |
| rs141333725 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939163 | GTGTGATCACACCGC[A/T]GCACTCCAGCCTGGG | 10422 |
| rs141385784 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937803 | AGTTACATCATCATA[C/T]ACACTTTTGTATGTA | 10422 |
| rs141436718 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942308 | GGAGACAAGCACAAC[A/G]AGACAAACTTCCTGC | 10422 |
| rs141493529 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961800 | GAATTTTAAATTGCC[G/T]ACATGGCTGCTGTGA | 10422 |
| rs141495107 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952537 | GCAGCCAGTAAACAA[A/C]ACACTGCACGGTGTT | 10422 |
| rs141514246 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950789 | AGAGAATTGTTAAAA[A/G]TAACAAGAGTTATGA | 10422 |
| rs141643021 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954939 | ATAAGCAATTACATG[A/G]ATGTGTGTGTCTAAC | 10422 |
| rs141825787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944047 | GGTGATGGGCTGACA[C/T]GTGCAGCAAACCACC | 10422 |
| rs141840977 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959858 | ATACCGGCCCTTGAA[A/C]GCAGGAGGCTCAGCC | 10422 |
| rs141880303 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957577 | CCCCAACCAAGGCCG[C/G]TGGAGTAGGGAGGCC | 10422 |
| rs141920852 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937481 | GAGTGGCACCACATG[C/T]AGACAACCCAACGAG | 10422 |
| rs141973137 | snp | C/G | 1.65438e-05 | 0.00287605 | missense | UBAC1 | GRCh38.p7 | 9:135939711 | TCACTCTGAGGGCAT[C/G]TATCACCTCTTTCTC | 10422 |
| rs141991641 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936564 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAACCT | 10422 |
| rs142001879 | snp | A/G | 0.0183209 | 0.0939404 | missense | UBAC1 | GRCh38.p7 | 9:135955409 | CTTCTAAGCTCCCAT[A/G]AGCACACTGGGGAAA | 10422 |
| rs142043344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939823 | GGAACCAGTGACCTG[C/T]GTGCAGAGGGGCCCG | 10422 |
| rs142082711 | snp | A/G | 3.37849e-05 | 0.00410991 | missense | UBAC1 | GRCh38.p7 | 9:135945218 | TCTTCTGCGTGTTCA[A/G]TTAGCCACTCCATGG | 10422 |
| rs142139721 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941949 | ACCAAAGGCTAGGAG[G/T]ACTGATGGGCTGGCC | 10422 |
| rs142176550 | snp | A/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933258 | ATAAGCAATAAGATC[A/T]GAGAGCAGGAGCAGC | 10422 |
| rs142239379 | snp | A/G | 1.6507e-05 | 0.00287284 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135933441 | TTCTAGAGATCTGCA[A/G]CATGACAGGCCCCGT | 10422 |
| rs142283539 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956484 | CGTGTGATGAAGACT[A/G]AGGTCGGCACATGTG | 10422 |
| rs142439879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951742 | TTGAACCTGGAAGGC[A/G]GAGGTTGCAGTGAGC | 10422 |
| rs142487389 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945822 | GAGGACGTCACCCAC[A/G]GTGGGAGCCCCACAA | 10422 |
| rs142629108 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958999 | TATATATCAGGAGTA[C/T]AATAATTAGCATTGC | 10422 |
| rs142632320 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934137 | CCAGGATCGATGGCT[C/G]CATGCTGACCTGACA | 10422 |
| rs142837939 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937303 | AAAATTAGCCAGGCG[C/T]GGTAGTGCACGCCTG | 10422 |
| rs142858133 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935672 | TGACACGCATAGACA[A/G]TATGTAAAAGAAGAA | 10422 |
| rs142902317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949682 | GACCAAGGGACAGAT[C/G]GAGAAGAACAAGACA | 10422 |
| rs143031188 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957228 | TGGCCAGGCTGAGGG[G/T]ATGTTGGGGGGACGC | 10422 |
| rs143168319 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955947 | AGCCATGCTGCATCC[C/T]GAGATTGGGATAAGA | 10422 |
| rs143326917 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956678 | CTCCCCAGCCGGAAT[C/T]GTGGGGTGAGAGGAG | 10422 |
| rs143360355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957489 | ACACCAGGAACAACA[C/T]GGAAGCACTAGGACG | 10422 |
| rs143445227 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954985 | CAACATCACCACAAC[A/G]AAGGTGAAACCTGCA | 10422 |
| rs143463883 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962711 | TTGCCTCTCACAGGT[A/G]GGAGCCTCTGCTACT | 10422 |
| rs143528687 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958608 | AGGAAAAAATCATGC[C/T]GGCGTCAGCACGCAC | 10422 |
| rs143549320 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951394 | ACTCGGGAGGCTGAG[A/G]CAGGAGGACTGCTTG | 10422 |
| rs143729310 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943423 | TACCATCTCATGCCA[A/G]TCAGAATGATGATTA | 10422 |
| rs143735714 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944456 | CAGACAGAAACCTCC[A/C]AGGAGGAAGTAAAAC | 10422 |
| rs143836098 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938988 | CAAAGCAGGAGGATC[A/G]ATTGAAGCCAGGAGT | 10422 |
| rs143880729 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948503 | GGGACAAGGAGCGAG[A/C]CTCAGGAGCTAGCGC | 10422 |
| rs143940407 | snp | A/C | 0.00321842 | 0.0399856 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945871 | TCCGGCAAGGGAAGG[A/C]GGTGGCCCCCCACGC | 10422 |
| rs144081763 | snp | C/T | 1.66114e-05 | 0.00288192 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945936 | CTCCGGAAAGCCCAT[C/T]TCCGTGAGCTGCCGC | 10422 |
| rs144137856 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935951 | GAATGGCGTGAACCC[A/G]GTAGGCGGAGCTTGC | 10422 |
| rs144170530 | snp | A/C/T | 0.0253062 | 0.110099 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932771 | TGTGTCCCAGGAATA[A/C/T]GGGCTCAGCTCCAGT | 10422 |
| rs144479483 | snp | A/G | 0.00140928 | 0.0265076 | missense | UBAC1 | GRCh38.p7 | 9:135945188 | TGGCCAGGAAGAGGC[A/G]TGTCTATGGTCGGGT | 10422 |
| rs144639770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940143 | GTCTCGGCAGCCACC[A/G]CAGGTTTACCCCAGA | 10422 |
| rs144680335 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958446 | CTAGAGGCCACCACG[G/T]TGATCCCAATTTGCA | 10422 |
| rs144700638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952118 | GGCAGGCCCAGATCT[C/G]TCCGCTGCAGATGGG | 10422 |
| rs144701328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952880 | TGCGTTTGGATTTTC[C/T]GATGGGGATGCTGAG | 10422 |
| rs144764635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949857 | AGAGTATGATCCTTG[C/G]TGGGCCTCAACTAAT | 10422 |
| rs144794237 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954431 | CCTGGGTGACTGAGC[A/G]ACACCCTGTCTCAAA | 10422 |
| rs144794687 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935110 | CTATGTTACCCAGGC[C/T]GGTCTCGAACTCCTG | 10422 |
| rs144989065 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953606 | TACAGGCGCGAGCCA[C/G]TGTACCCAGCCTGTA | 10422 |
| rs145083507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942913 | AAATAGACTAGAAAA[A/G]CATTTGTCTCAATGG | 10422 |
| rs145115840 | snp | C/T | 0.0279056 | 0.114778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939794 | TTAGCTCGCTGGGGG[C/T]GGCAGGAGGCCGAGG | 10422 |
| rs145180067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956164 | ACCACAGCCACCTCC[A/G]AGCAGCGCTCACGGG | 10422 |
| rs145229604 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946587 | GGAAAGGGACAGGAA[C/T]GCCTGGTGACGGTCA | 10422 |
| rs145323411 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953198 | ACTGACACGGATTAA[A/C]CAGGCTCTGCCGGGA | 10422 |
| rs145463679 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938829 | GGGGGGGGGATGTGG[A/G]CCACCACAGGGACCT | 10422 |
| rs145491392 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956058 | TGGACCAATGGGCAC[A/G]CAGTCACCAGGGCCC | 10422 |
| rs145541224 | snp | C/G | 0.0012698 | 0.0251652 | missense | UBAC1 | GRCh38.p7 | 9:135938237 | CTAGCAATGTTTTCG[C/G]GTTGGTCAGGCCCAG | 10422 |
| rs145565363 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936134 | TTGCATGGACAGTGG[C/T]GCCATCACTGCACTC | 10422 |
| rs145619460 | snp | A/G | 0.000165505 | 0.00909534 | missense | UBAC1 | GRCh38.p7 | 9:135938326 | TTGTCCAGCTCCTCC[A/G]GAGAGGGCTTCCGGT | 10422 |
| rs145692785 | snp | A/G | 0.000412647 | 0.014358 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946270 | GGGTTGACTCATACC[A/G]TTCGCCTTCTTAAAC | 10422 |
| rs145794081 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936582 | CTCACTGCAACCTCC[A/G]CCCCCCAGGTTTAAG | 10422 |
| rs145849093 | in-del | -/G | 0.0341408 | 0.126114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948305 | CTGAAGGGCAGTCAT[-/G]GCAGTAGAAACTCAC | 10422 |
| rs145936595 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948410 | GATGGAGGGATCAGC[A/G]GAGCTACAAAGGCTC | 10422 |
| rs145940630 | snp | C/T | 0.000601877 | 0.0173371 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945854 | ACCAGGCCCCAGGTG[C/T]CTCCGGCAAGGGAAG | 10422 |
| rs146063353 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932678 | TCATTTTAAGACACC[A/G]GTCATGTTTTTTAAA | 10422 |
| rs146099279 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937318 | TGGTAGTGCACGCCT[A/G]TAATCCCAGGTACTC | 10422 |
| rs146185875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952589 | GACGGTGCAGACCAT[A/G]AATCAATAACGTGTG | 10422 |
| rs146264890 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962793 | ATGGGGCATTTTTAA[C/T]GCAGGAAGCAGAAGT | 10422 |
| rs146278201 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946693 | CTGAAGACCCTCTCT[C/G]GCTTCACTGAAGAAA | 10422 |
| rs146299420 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962066 | CTGAACCTTCTACAT[C/T]ATCTGTACACTTCCT | 10422 |
| rs146481625 | snp | A/G | 0.00874735 | 0.0655527 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932911 | AGCCGCGGGGATGTG[A/G]CCTCTCGGGGACGCA | 10422 |
| rs146489932 | snp | A/G | 1.66062e-05 | 0.00288146 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945969 | GGCAGCCTCGTCCAC[A/G]CGCTCATCCTCGTCC | 10422 |
| rs146624935 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942211 | AGTGCGAAGTCCAAC[C/T]TCAGAGCACAAGGGA | 10422 |
| rs146721970 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958612 | AAAAATCATGCCGGC[A/G]TCAGCACGCACTGGG | 10422 |
| rs146740352 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956697 | GGGTGAGAGGAGAGG[A/G]GCTGCACTTCTGTGT | 10422 |
| rs146809302 | snp | C/G/T | 0.000561408 | 0.0167465 | missense | UBAC1 | GRCh38.p7 | 9:135938312 | CGGGGTCGATGCCCT[C/G/T]GTCCAGCTCCTCCGG | 10422 |
| rs146841803 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946139 | TTGCCGGTGAGGCAG[A/G]CCCCAGGCCCTCATC | 10422 |
| rs146861167 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943142 | AGAAGACAGTTGGCC[A/G]GGCGCAGTGTCTCAC | 10422 |
| rs146918249 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933812 | GTCTGGCAGCCGCCA[A/G]GGCTCAAAAATCATC | 10422 |
| rs147039807 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950832 | GGCATGGTGGTTCAC[C/G]CCTGTAATCCCAACA | 10422 |
| rs147121393 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959925 | AGTTATTCACAGCCA[C/G]TGCGTTCCAGAAGGG | 10422 |
| rs147165858 | snp | A/G | 0.000155988 | 0.00883003 | missense | UBAC1 | GRCh38.p7 | 9:135961071 | ACCGAGGTGTCCTCG[A/G]TGGCCTCCTCCAGCC | 10422 |
| rs147192491 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944539 | GAGGAAGGTCCACAC[A/G]CACAGGCGCAGGGAC | 10422 |
| rs147195871 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941384 | GTACTCCAGCCTGGG[C/T]GACACAGTGAGACTC | 10422 |
| rs147510380 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955955 | TGCATCCCGAGATTG[G/T]GATAAGAGGGGCACT | 10422 |
| rs147518190 | snp | A/G/T | 0.000675581 | 0.0183685 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945106 | TCTGGCCTCCTCATC[A/G/T]GTGGCGCTGGCTCCC | 10422 |
| rs147558894 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936535 | GAGTCTTGCTCTGAC[A/G]CCCAGGCTAGAGTGC | 10422 |
| rs147568418 | snp | A/G | 0.000148492 | 0.00861532 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135933430 | TGTCTGGAAGATTCT[A/G]GAGATCTGCAGCATG | 10422 |
| rs147581386 | snp | A/G | 0.00281284 | 0.0373966 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938358 | CCCCAGCAGCCACTC[A/G]CACTGCAAAGCCAAG | 10422 |
| rs147992760 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955223 | CTGTGGGTGGACCAC[C/T]CCCTCCTGGCTCCAG | 10422 |
| rs148044627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951667 | TACAAAAGATTAGCC[A/G]GGCGTGGTGGCACGC | 10422 |
| rs148081438 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943635 | GAATAGAAATCATTC[G/T]GTTATAAAGATATGT | 10422 |
| rs148103016 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935598 | GATTGTACCACTGCA[C/T]TCCAGCCTGGGTGAC | 10422 |
| rs148313214 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961596 | GGCACTCACCACGTG[A/G]GACCTCATGGGTTCT | 10422 |
| rs148367988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936852 | ACACACTGAAGGACA[C/T]CAAAACACGGGATTC | 10422 |
| rs148503318 | in-del | -/TT | 0.403334 | 0.197456 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959373 | GGGTTTTTTGTCTGG[-/TT]TTTTTTTTTTTTTTT | 10422 |
| rs148589969 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949241 | GCCAGATCAAAGAGG[C/T]TACAGAATGCTTAGA | 10422 |
| rs148678099 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937757 | AAAGCTGAATAGTAG[A/G]TACATGGCTATTAGT | 10422 |
| rs148724299 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956337 | GGCCAGCATCCTCTC[C/T]GCAAAACAGCACACA | 10422 |
| rs148780120 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952806 | TCAAAAAGCACCAAC[A/G]AGCACTTCCATTAAG | 10422 |
| rs148849276 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936162 | CTCTAGCCTGGGTGA[A/C]AGAGAAAGAGCCTAT | 10422 |
| rs148952304 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943313 | GTAGTCCCAGCTACT[C/T]AGGAGGCTGAGGCAG | 10422 |
| rs149006722 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938880 | GCCCAGCTGGCACAC[A/G]GGCACAGGACGGGAA | 10422 |
| rs149026295 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957195 | ACGGCTTCAGGGGCT[C/G]ACTCCTTCACACAAA | 10422 |
| rs149093025 | snp | A/G | 0.00517822 | 0.0506191 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932941 | ACGGGTTTCTTGTGC[A/G]GCACCAAGAAAAGAC | 10422 |
| rs149136617 | snp | C/T | 0.00342124 | 0.0412184 | missense | UBAC1 | GRCh38.p7 | 9:135946332 | GCTTCTGCGCCACCT[C/T]GATGAGAGACACCAG | 10422 |
| rs149265068 | snp | C/T | 0.000906611 | 0.0212717 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945121 | GGTGGCGCTGGCTCC[C/T]GCGGCAGCCTCGGAG | 10422 |
| rs149400108 | snp | A/G | 0.000234145 | 0.0108175 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939754 | CTCCATCAGGGAAAT[A/G]ACGGCCTAGAGGACA | 10422 |
| rs149496082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948166 | GCAAGGGTCACAGAA[C/T]GACAACCACACAGGG | 10422 |
| rs149533843 | snp | A/G | 1.64947e-05 | 0.00287177 | UBAC1 | 9 | allele_origin=G(germline)/A(somatic) | 9:135945124 | GGCGCTGGCTCCCGC[A/G]GCAGCCTCGGAGGCA | 10422 |
| rs149605506 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960297 | CAGCAACCTAAGGAA[C/G]TAAATACACAGGAGT | 10422 |
| rs149653472 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952650 | CTGTTTTGCAAGAAA[C/T]AGACAAGACAGGCAG | 10422 |
| rs149656592 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938682 | GGGAAGGTGATTAAC[A/G]AATGTACCAAGTGCC | 10422 |
| rs149707881 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936083 | GGTCTTGTCTATAAT[A/G]TGGAGGTGGGCAAGT | 10422 |
| rs149761532 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958276 | ATGGTCTCGATCTCC[A/T]GACCTTGTGATCTGC | 10422 |
| rs150041834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946558 | GCCTCCCTGCAGGTG[A/G]GACTGAAGCCAGTGG | 10422 |
| rs150197332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944326 | ACTCCATGGAAAACA[C/T]GAGCTCCGCAGGTGA | 10422 |
| rs150333448 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957106 | ACACACTTCACCTCT[C/G]AACACTGGCATTTTC | 10422 |
| rs150385089 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953553 | TTGATCTCTTGACCT[C/T]GTGATCCACCCGCCT | 10422 |
| rs150401622 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939967 | AGGAAGTGCAGGGAT[G/T]ACTGTAGTTAGCAGA | 10422 |
| rs150633521 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957951 | GGCTATTTTTTTACA[C/T]TTTTAGTACAGAAGG | 10422 |
| rs150700674 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955509 | ACACCAGGAATTTAC[A/T]GGGTTTTCTTATGAG | 10422 |
| rs150773520 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947546 | TGCCAAACTCAGGGC[C/T]GGATTGACGTTTTCC | 10422 |
| rs150946293 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959164 | AGTTAAAGTAAATGC[C/T]GTGCCAACGCAGGGG | 10422 |
| rs151001239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956511 | TGTGCCTGCATGTTC[A/G]TGCCCAAGTCGGTCC | 10422 |
| rs151048239 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953335 | TTATTTATTTAATTT[C/T]GAGATGGAGTCTTAC | 10422 |
| rs151083447 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939065 | TAATTAGCCGGGCAT[A/G]GTGGTGCATGCCTGT | 10422 |
| rs151091472 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949765 | GGCAGTTGCCCGTGC[A/G]TGGCTGCACAGCATG | 10422 |
| rs151141109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942025 | TTCTACGGAATGTTG[C/T]TCTGACACAGAGAGA | 10422 |
| rs151159711 | snp | A/G | 0.0445534 | 0.142449 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933392 | ATAGCCGAGTGGAAC[A/G]ACGCCACCTACGTGC | 10422 |
| rs151217888 | snp | A/G | 1.67683e-05 | 0.00289549 | missense | UBAC1 | GRCh38.p7 | 9:135945890 | GGCCCCCCACGCACT[A/G]GTTCAGCTGAAGGGC | 10422 |
| rs180703097 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935417 | CTAGAAGGCAGAGGT[C/G]GGGGGAGCGCTTGAA | 10422 |
| rs180730950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952907 | TGAGGCTGTGCGGTG[G/T]GAGGTGGGGCTTGTC | 10422 |
| rs180739738 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944112 | ATCCTGCATATGTAT[A/C]CCAGAACTTAACATT | 10422 |
| rs180753808 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961721 | AATATTTTGTATCTA[C/T]TGAGTTAAGAAAAAT | 10422 |
| rs180902530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949709 | GACACCTGGTCCTGC[A/G]GCAGGCAGAACTCGA | 10422 |
| rs181060548 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940406 | AACACGGTGAAACCC[C/G]GTCTCTACTAAAAAT | 10422 |
| rs181076192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957270 | AGACACACTCCTGCC[A/G]TTTACAACAGGGCAG | 10422 |
| rs181143102 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958220 | CCCGGCTAATTTTTC[C/T]GTATTTTTAGTAAAG | 10422 |
| rs181149960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941093 | ATGCTGGCTAGAGCT[A/C]AACTGTGTGCATGAT | 10422 |
| rs181222638 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948826 | TGTAATCCCAGCACT[A/T]TGGGAGGCCAAGGTG | 10422 |
| rs181505581 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950054 | CGGAACTGGACTCTG[A/C]CAACCGCCGGAAGAC | 10422 |
| rs181524613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957504 | CGGAAGCACTAGGAC[A/G]ACCGTGTCACTCTGC | 10422 |
| rs181562003 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960685 | TCCAGGCCTCAGTTT[A/C]CCGATCTGCCCCTAC | 10422 |
| rs181644674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940646 | ACAAAACTTAAGCTA[C/T]AACTGAACATATGCT | 10422 |
| rs181714513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943720 | TCAAATGCCCACGGA[G/T]AAGAAAAGAAACCGG | 10422 |
| rs181725025 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937145 | GGTGGCAAAGGCCCT[C/T]CCAACATCCAGGAAC | 10422 |
| rs181876280 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936957 | GCATCCAGGAGGTGA[A/G]GACCTTTCTGAATGA | 10422 |
| rs181887684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953960 | CCTGGCCAACACGGT[G/T]AAACCCCATCTCTAC | 10422 |
| rs181939743 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954795 | TGGTCATCTCAGCGG[A/G]TATCTGTTAGCAATA | 10422 |
| rs182111774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955532 | CTTATGAGCTAAGAA[A/G]TTACACCATGGATGA | 10422 |
| rs182117274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937905 | ACACCTTGTCCTCCC[A/G]TGAGTTCCTAAGCTG | 10422 |
| rs182224439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934199 | AGGTCTACAGGCTCC[A/G]GGGACAGTGCTCACT | 10422 |
| rs182228866 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958557 | ACAGCAGGGAGAAGC[C/T]GACATCATTCCCCTC | 10422 |
| rs182235202 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950853 | AATCCCAACACTTGG[C/G]AGACCAAGGTGAACA | 10422 |
| rs182589923 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941611 | ATAGGAAGTACTGTC[A/G]CTCATTTCTACCTCA | 10422 |
| rs182666438 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942402 | TGCCTGTAATTCCAG[C/T]GCTTTGGGAGGCCAA | 10422 |
| rs182677775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959214 | TGTGGGGTCCACAGG[A/T]TATTTTTGTCTATTC | 10422 |
| rs182935387 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933007 | AAAAGTCATCTGTGA[A/G]TGACTAGTTAAATTA | 10422 |
| rs182969330 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950404 | GGATCTGGAGGGAGG[G/T]AACACCCCAGTGACC | 10422 |
| rs183060128 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945668 | GGATTCACCTTGAGT[A/T]CTCATACAACGGCCC | 10422 |
| rs183073432 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963319 | GAGGCAGCTGGACCT[A/G]CAGGACTGAAGTTGA | 10422 |
| rs183225493 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955679 | CTACTGACAATTCGC[A/G]GCCACCAGAATTGCT | 10422 |
| rs183393251 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946597 | AGGAACGCCTGGTGA[C/T]GGTCACTCAGTGCTG | 10422 |
| rs183825299 | snp | C/G/T | 4.96482e-05 | 0.00498217 | missense | UBAC1 | GRCh38.p7 | 9:135945041 | ACCCGAGCATCAGCC[C/G/T]GAAACTCCCTTTTCC | 10422 |
| rs183864876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953037 | GGCTGCTTGAAAAGA[A/G]GAGGGAACAGGAGCA | 10422 |
| rs183874627 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935756 | AAGTGGCCAGGCGCA[A/G]TAGCTCAAGCCTGTA | 10422 |
| rs183993824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958783 | CTGCCTGCAGAACCA[C/T]GCTGGGATGTGGTGG | 10422 |
| rs184008858 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962361 | CCCCACTGCAAGCCC[A/C]CTTGGCAGTGGTCTC | 10422 |
| rs184022184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938146 | CTCCGTATCGCCTCC[A/G]CAGCACCTATTTGTC | 10422 |
| rs184162397 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942212 | GTGCGAAGTCCAACC[G/T]CAGAGCACAAGGGAC | 10422 |
| rs184286384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957181 | TGAAAAAGGGATTGA[C/T]GGCTTCAGGGGCTCA | 10422 |
| rs184292193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940153 | CCACCGCAGGTTTAC[C/G]CCAGAGGGCCTTGTT | 10422 |
| rs184393232 | snp | A/G | 0.000628876 | 0.0177212 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947779 | CATGCACCCGCCGCC[A/G]CTCTGGGCTGACACT | 10422 |
| rs184400976 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942826 | ACAGACAGAACGTGC[A/G]CCTTGGGCCCATGGG | 10422 |
| rs184540153 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959557 | TTTTTTGTATTTTAG[G/T]TGAGACGGGGTTTCA | 10422 |
| rs184556018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952025 | AGTCTGAACACCAAC[A/G]GTCAAACTGTAATCT | 10422 |
| rs184702375 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947408 | AGGTGCCTGCCACTA[C/T]GCCCGGCTAATTTTT | 10422 |
| rs184801968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951078 | CTCCAGCCTGGTGTG[C/T]ACTGCCTGGCTTGTG | 10422 |
| rs184808306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934716 | ACAAACTATAAGGTG[C/T]GAAACAGCTGTTTCA | 10422 |
| rs184877659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935281 | AAAAACAGTTTACAA[C/T]ATTCAACAAAGGAAG | 10422 |
| rs185210399 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938879 | AGCCCAGCTGGCACA[C/T]GGGCACAGGACGGGA | 10422 |
| rs185286594 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943723 | AATGCCCACGGATAA[C/G]AAAAGAAACCGGATA | 10422 |
| rs185300585 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960818 | AAAGGCCAGGCCCGG[A/G]ACGAGCGTCCAGAGG | 10422 |
| rs185336885 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956490 | ATGAAGACTGAGGTC[G/T]GCACATGTGCCTGCA | 10422 |
| rs185384914 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957389 | AGTTCATTTGTCAAG[G/T]TCAGAATACAGACTA | 10422 |
| rs185489117 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940420 | CCGTCTCTACTAAAA[A/C]TACAAAAAAATTAGC | 10422 |
| rs185639208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941181 | GAGGCCGGGGTGGGA[A/G]GATCACTTGAGGTCA | 10422 |
| rs185654695 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958337 | CAGGCATGAGCCACC[A/G]TGCTCAGCCAGGTAT | 10422 |
| rs185692786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960019 | CGAAAGTACTGTATG[C/T]GAGCAGCTACTATGG | 10422 |
| rs185834057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943299 | GTGGGTGTGTGCCTG[C/T]AGTCCCAGCTACTCA | 10422 |
| rs185991125 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961899 | TCTTTCTAATTCACA[C/T]GCAGATCAGAGAGTC | 10422 |
| rs185996161 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950236 | AGCTACAAGCGGAGT[A/G]CTGTTTTAAGCAGCT | 10422 |
| rs186041703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944389 | ACGATCAGTGCCACA[A/C]GAGACGACAGCATGC | 10422 |
| rs186194415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955057 | AAGCAAAATTCACAT[C/T]TGGCTTCTCAAATGC | 10422 |
| rs186299838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949851 | GGGGAAAGAGTATGA[A/T]CCTTGGTGGGCCTCA | 10422 |
| rs186328152 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937373 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGGGC | 10422 |
| rs186576305 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953999 | CAAAAATTAGCCAGG[C/T]GTGGTGGCGCATGCC | 10422 |
| rs186582582 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955571 | AATTCCCACTAATGG[C/T]AGATGCCAAATGAAG | 10422 |
| rs186584105 | snp | A/G | 4.96249e-05 | 0.00498096 | missense | UBAC1 | GRCh38.p7 | 9:135945042 | CCCGAGCATCAGCCC[A/G]AAACTCCCTTTTCCT | 10422 |
| rs186589583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938055 | CCCACAGTGACGTAG[C/T]GGGACTACACCCGCA | 10422 |
| rs186724123 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949082 | AAAAAAAAGGAACAA[C/T]AGAAAGCAGCACAAA | 10422 |
| rs186869831 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940714 | CAATTCATGTAACAA[A/G]ATAATACATCCTCTA | 10422 |
| rs186876435 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933053 | ACTCTGGGTTGAAAC[C/T]TACCTCCGTCAAATA | 10422 |
| rs187030792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946198 | GTCAGTGGTCAGTGC[A/G]TGGAGCTGCAGACGC | 10422 |
| rs187043423 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958607 | AAGGAAAAAATCATG[C/G]CGGCGTCAGCACGCA | 10422 |
| rs187057645 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958191 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 10422 |
| rs187181343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942519 | AAAAATTAGCCCTGT[A/G]TGGTGGTGCGTGCCT | 10422 |
| rs187190850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959402 | TTTTTTTGAGACGGA[G/T]TCTTGCTCTGTCGCC | 10422 |
| rs187221073 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941671 | AGGCAACACCTGGCA[A/G]TCCCTGCCCTCCCTC | 10422 |
| rs187379195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937055 | TACAGGCGGCCAATA[C/T]GCTTCTGAAAGAAGG | 10422 |
| rs187422116 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962568 | CAATCTAACCGGGGA[A/G]GCTGTCTCTGCCTCC | 10422 |
| rs187463633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942222 | CAACCTCAGAGCACA[A/G]GGGACCCAGCTGGAG | 10422 |
| rs187555369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946598 | GGAACGCCTGGTGAC[A/G]GTCACTCAGTGCTGG | 10422 |
| rs187616396 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951023 | GGATCACTTAAGCCC[A/G]GGAGGCAGAGGCTGC | 10422 |
| rs187623839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934212 | CCAGGGACAGTGCTC[A/G]CTACAGAATTCACAG | 10422 |
| rs187863983 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956679 | TCCCCAGCCGGAATC[A/G]TGGGGTGAGAGGAGA | 10422 |
| rs188127683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939361 | GCCACATAGCCGGCT[A/G]CATGTGAAAGTAGGC | 10422 |
| rs188154523 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933830 | CTCAAAAATCATCTT[C/T]CCCAACAACTCCACT | 10422 |
| rs188244004 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940332 | CACCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 10422 |
| rs188258917 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957192 | TTGACGGCTTCAGGG[A/G]CTCACTCCTTCACAC | 10422 |
| rs188337874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951138 | TTTGTAGAGACAGGG[C/T]TTCATCATGCTGCCC | 10422 |
| rs188385072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953106 | GTCACGCAGGATGTG[C/T]CCCTACCCTCCTCTC | 10422 |
| rs188392865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936860 | AAGGACATCAAAACA[C/T]GGGATTCTGCCCATC | 10422 |
| rs188436580 | snp | C/T | 0.000399281 | 0.0141238 | missense | UBAC1 | GRCh38.p7 | 9:135947812 | CGTCTCTCATGTTGG[C/T]CTGGACCGCGGCCCG | 10422 |
| rs188459246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950671 | TCTAACCCTCAAGGG[A/C]GGAGAGAGGGAGGTA | 10422 |
| rs188585867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944012 | GAAAAATAGCTAGTG[A/C]ATGCTGGGCTTCATA | 10422 |
| rs188588751 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958798 | CGCTGGGATGTGGTG[A/G]TGGGGAACCTTTCTG | 10422 |
| rs188601794 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960876 | GCAAACGGGCAGGAG[A/G]CGCTGCCTCCACCCC | 10422 |
| rs188911036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943661 | TATGTGCACACGTAT[A/G]TTCACTGCAGCACTA | 10422 |
| rs188922476 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960184 | GCCAAGCCCTCAGAT[C/G]ATGTCAGGTATAGAC | 10422 |
| rs189063766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955760 | CCATTGTTTCCTGAT[A/G]ACCTAAAGATCTACC | 10422 |
| rs189155406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949549 | GTGCAGGGAGGAGCG[C/G]CTCAGAGCTGCCTCA | 10422 |
| rs189341876 | snp | C/T | 0.000179575 | 0.00947393 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947772 | GGGACCCCATGCACC[C/T]GCCGCCGCTCTGGGC | 10422 |
| rs189533374 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958405 | CAGGTTCCTCTGCCC[C/T]CTTCTCCACTCCAGG | 10422 |
| rs189585998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935383 | AGGCACAATGGCTCT[C/T]GCCTACAATCCCAGC | 10422 |
| rs189706359 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941334 | TCGCTTGAACCTGGG[A/G]AGTGGAGGTTGCAGT | 10422 |
| rs189857337 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938068 | AGCGGGACTACACCC[A/G]CAGGATGCCAACCTG | 10422 |
| rs189872602 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955662 | CTCTGATATACCACA[A/C]CCTACTGACAATTCG | 10422 |
| rs189874379 | snp | A/C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952801 | TCAACTCAAAAAGCA[A/C/T]CAACGAGCACTTCCA | 10422 |
| rs190100499 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958193 | CTGGGACTACAGGTG[A/C]CCGCCACCACGCCCG | 10422 |
| rs190153155 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937428 | CCTGGGTGACAAGGC[A/G]AGACTCTGTCTCAAA | 10422 |
| rs190279603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959949 | AGAAGGGGGCTTGCC[A/C]AGCTTGCCTCTGACA | 10422 |
| rs190414073 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940523 | AGGCGGAGCTTGCAG[A/T]GAGCCAAGATCGCGC | 10422 |
| rs190448614 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945465 | AGAATCAGAAGCCCA[C/T]GTCTAAGGAGAGGCA | 10422 |
| rs190466321 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962918 | GGGGGAAGCTAGAGG[A/G]CTTGGAGGAGCCGGG | 10422 |
| rs190511292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942917 | AGACTAGAAAAGCAT[C/T]TGTCTCAATGGGATC | 10422 |
| rs190605003 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950742 | GGTCATTCAAGGAAT[A/G]ATAATATACACATAT | 10422 |
| rs190619878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940773 | AGGGGTCCATTTTGA[A/C]AAAATATAAATAAGT | 10422 |
| rs190680833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957462 | AAAACCCACAGTCCA[C/T]GTGTCACCAGCACAC | 10422 |
| rs190905489 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962143 | AGAACTCCCAGCCTC[A/G]ATATCAGATCACCCT | 10422 |
| rs191163361 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944485 | ACCCGAATCAAAGAA[C/T]AGGAGAGAGAAGGAA | 10422 |
| rs191256647 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942713 | CAAGAAAGGGATATC[C/T]ACAAGTGAGAAACCC | 10422 |
| rs191273138 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959501 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 10422 |
| rs191488267 | snp | C/T | 0.0144648 | 0.0838045 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955255 | GCCCCCAGCAGTGCA[C/T]GATGCCTGCTGCCAA | 10422 |
| rs191574649 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954748 | ATCCTCGGCCCACGA[C/T]GGTGCCCATCCCCCA | 10422 |
| rs191690770 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956894 | CTAAACCCGGTAGCA[A/G]GCTCAGCCTGTGGGT | 10422 |
| rs191703190 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939969 | GAAGTGCAGGGATGA[C/G]TGTAGTTAGCAGAGC | 10422 |
| rs191819752 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937109 | GCCATCGCAGCTCCA[A/G]AGACACTTCCAGCCT | 10422 |
| rs192015062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942087 | TAGGAAAACGAGCAC[A/G]TTAAGATTGTTAAGA | 10422 |
| rs192033725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950288 | GTGGCAACGGAAAAC[C/T]TGCATAGACTTAGCA | 10422 |
| rs192314237 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942387 | AGGCACAATGGCTCA[C/T]GCCTGTAATTCCAGC | 10422 |
| rs192324777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959131 | GTATCATGATGGCCA[C/T]GCACATCGCACCGAG | 10422 |
| rs192379140 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958733 | TTCAAATACACAACT[C/T]GAGGGTTCTCTTTTC | 10422 |
| rs192518200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933873 | CCGAGAAGGTCAGCA[A/G]ATGCAGAAAGGACAC | 10422 |
| rs192592347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951052 | GCAGTGAGGTGAGAT[C/T]GTACCACACACTCCA | 10422 |
| rs192603554 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934445 | GCAGGCGGATCATGA[A/G]GTCAGGAGATCGAGA | 10422 |
| rs192800106 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947122 | ATGAAGTTGGAAGCC[A/G]GCCGTCCTCCCACCC | 10422 |
| rs192820937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956025 | ACAGCCATGCTGCAC[A/C]CCTGGGCGGCTTGAA | 10422 |
| rs192986148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934929 | TTTGTTGCCCAGGCT[A/G]GAGTGCAGTGGAGTG | 10422 |
| rs193019476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938490 | CAGGGCTGATCTCCC[G/T]GGAAGGGACTCTACC | 10422 |
| rs193064663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943222 | GTCAGGAGTTTGAGA[C/T]GAGCCTGGCCAACAT | 10422 |
| rs193200738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951797 | CTTGGGTAACAAAAG[C/T]GAAACTCTGTCTCAA | 10422 |
| rs193232048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959951 | AAGGGGGCTTGCCAA[C/G]CTTGCCTCTGACAGT | 10422 |
| rs199527336 | snp | C/T | 6.93013e-05 | 0.00588607 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939805 | GGGGCGGCAGGAGGC[C/T]GAGGAACCAGTGACC | 10422 |
| rs199555001 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934017 | AAATGAAAACTTGGG[-/T]TTTTAACAGCTTTAC | 10422 |
| rs199588175 | snp | C/G/T | 8.9074e-05 | 0.00667308 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953660 | AACCAAGGTCCCCAA[C/G/T]TGCAAACTTTGAAAT | 10422 |
| rs199742576 | in-del | -/AAAAAAC | 0.0279526 | 0.114869 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939274 | TAAGGCACCCTTTTA[-/AAAAAAC]AAAACCTAGAATTCC | 10422 |
| rs199930583 | snp | C/T | 3.3211e-05 | 0.00407485 | missense | UBAC1 | GRCh38.p7 | 9:135945933 | GTTCTCCGGAAAGCC[C/T]ATCTCCGTGAGCTGC | 10422 |
| rs200015238 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954157 | AAAAAAAAAAAAAAA[-/G]AAGAAGAGCAGGGCT | 10422 |
| rs200087166 | snp | A/T | 1.69338e-05 | 0.00290974 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946420 | ATGTCCACCAAACCT[A/T]CTTGGATCTATGACT | 10422 |
| rs200156859 | snp | A/C/T | 0.00399 | 0.0445204 | missense | UBAC1 | GRCh38.p7 | 9:135938311 | TCGGGGTCGATGCCC[A/C/T]TGTCCAGCTCCTCCG | 10422 |
| rs200169387 | snp | A/C | | | missense | UBAC1 | GRCh38.p7 | 9:135945100 | CTCATCTCTGGCCTC[A/C]TCATCGGTGGCGCTG | 10422 |
| rs200284234 | snp | A/G | 3.49406e-05 | 0.0041796 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938410 | GCCTTCAGTGCCTCC[A/G]CAAGACGCCACCAGC | 10422 |
| rs200423294 | snp | A/C/T | 6.59896e-05 | 0.00574378 | missense | UBAC1 | GRCh38.p7 | 9:135938297 | GAAAGAGAGGACTGT[A/C/T]GGGGTCGATGCCCTT | 10422 |
| rs200472058 | snp | C/T | 9.97672e-05 | 0.00706213 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945939 | CGGAAAGCCCATCTC[C/T]GTGAGCTGCCGCAGG | 10422 |
| rs200558202 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956036 | GCACCCCTGGGCGGC[C/T]TGAAGGTGGACCAAT | 10422 |
| rs200601924 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937309 | AGCCAGGCGTGGTAG[-/T]GCACGCCTGTAATCC | 10422 |
| rs200690398 | snp | C/G/T | 0.000113776 | 0.00754165 | missense | UBAC1 | GRCh38.p7 | 9:135961080 | TCCTCGGTGGCCTCC[C/G/T]CCAGCCACTCGGCGC | 10422 |
| rs200719236 | snp | A/G | | | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961200 | GCGCCCGCCACCCGG[A/G]CCCCTGAAGGTCACC | 10422 |
| rs200830896 | snp | A/C/G | 3.66322e-05 | 0.00427961 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945851 | AAAACCAGGCCCCAG[A/C/G]TGTCTCCGGCAAGGG | 10422 |
| rs201008912 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940346 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 10422 |
| rs201047343 | in-del | -/TAAT | 0.0178098 | 0.0926698 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951842 | TAATAAAAATAATAA[-/TAAT]TAATTCATAAAAATA | 10422 |
| rs201066242 | snp | A/C/G | 0.000428831 | 0.014637 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947773 | GGACCCCATGCACCC[A/C/G]CCGCCGCTCTGGGCT | 10422 |
| rs201105140 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953584 | CGGCCTCCCAAAGTG[A/C]TGGGATTACAGGCGC | 10422 |
| rs201115937 | snp | A/C/G | 0.000131865 | 0.00811895 | missense | UBAC1 | GRCh38.p7 | 9:135946356 | ACACCAGTATCTTCC[A/C/G]GAGTTCTGTCTGGAA | 10422 |
| rs201221202 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953300 | ACTTCTTTATAATTC[-/T]TTTTTTTTTAAGTTT | 10422 |
| rs201327657 | snp | C/G | 6.71558e-05 | 0.00579425 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939670 | CCACAGCCCAACACT[C/G]ACCGCGGCATTCTGC | 10422 |
| rs201358352 | snp | A/G | 0.000381806 | 0.0138115 | missense | UBAC1 | GRCh38.p7 | 9:135961092 | TCCTCCAGCCACTCG[A/G]CGCCGTCGGACGCGC | 10422 |
| rs201427853 | snp | C/G | 1.65545e-05 | 0.00287697 | missense | UBAC1 | GRCh38.p7 | 9:135945176 | TCTGGGGGAGCTTGG[C/G]CAGGAAGAGGCGTGT | 10422 |
| rs201456643 | snp | A/G/T | 0.000164916 | 0.00907914 | missense | UBAC1 | GRCh38.p7 | 9:135945122 | GTGGCGCTGGCTCCC[A/G/T]CGGCAGCCTCGGAGG | 10422 |
| rs201493161 | snp | A/G | 0.000446441 | 0.0149339 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955256 | CCCCCAGCAGTGCAC[A/G]ATGCCTGCTGCCAAC | 10422 |
| rs201652411 | snp | C/T | 0.000739003 | 0.0192082 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947755 | CAGCAATCCCCCACA[C/T]GGGGACCCCATGCAC | 10422 |
| rs201754078 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940280 | TCAGATTTTATCTTA[A/G]AAAAAAAAAAATCCT | 10422 |
| rs201970345 | snp | C/G | 0.00299544 | 0.0385843 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933376 | GGGCTGCTGTGGCCT[C/G]ATAGCCGAGTGGAAC | 10422 |
| rs201993005 | snp | A/G | 0.000466846 | 0.015271 | missense | UBAC1 | GRCh38.p7 | 9:135953730 | GTGGTGATGGAGCAC[A/G]CTTTTTTATCAATAA | 10422 |
| rs202057983 | snp | C/T | 0.00204562 | 0.0319159 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946029 | GGGCCATGAGGGCTC[C/T]AGCCTCAGGTTCAGG | 10422 |
| rs202121996 | snp | C/G | 0.000360438 | 0.0134197 | missense | UBAC1 | GRCh38.p7 | 9:135938348 | GCTTCCGGTCCCCCA[C/G]CAGCCACTCGCACTG | 10422 |
| rs202151720 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936500 | CTTTTTTTTTTTTTT[-/T]GAGGTGGAGTCTTGC | 10422 |
| rs202168038 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953975 | GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 10422 |
| rs202233594 | in-del | -/AG | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959337 | CAGGGAGGACACAGC[-/AG]CACCTCAGAGAAGTT | 10422 |
| rs367633101 | snp | C/G/T | 0.000454522 | 0.0150685 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946009 | ATTGCTGCAGGGAGA[C/G/T]GACAGGGCCATGAGG | 10422 |
| rs367669989 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948051 | GATGAGCTGGGGGAG[C/G]CTGGAGAGTTCTGTG | 10422 |
| rs367824586 | snp | A/G | 0.00107515 | 0.0231607 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939786 | CACAGCCGTTAGCTC[A/G]CTGGGGGCGGCAGGA | 10422 |
| rs367867455 | in-del | -/GCA | | | cds-indel | UBAC1 | GRCh38.p7 | 9:135961351 | CTCGCTCCCGCCGCC[-/GCA]GCAGCCGCCGGGGGC | 10422 |
| rs367872540 | snp | C/T | 9.96545e-05 | 0.00705814 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933352 | TGCCCGGTCTCGGGC[C/T]GCACCAGGGGGCTGC | 10422 |
| rs368026740 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135933647 | GCCACACAGAGCTCA[C/G]TGCTAAGTGTGCACT | 10422 |
| rs368040154 | snp | A/C | 3.37353e-05 | 0.00410689 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938384 | CCAAGAGCACCAATA[A/C]CACTGTTAGCGCCTT | 10422 |
| rs368066357 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938018 | AGACAGTCACACCAC[G/T]ATCAGAACCTGACCT | 10422 |
| rs368093917 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936624 | CTCAGCTCCAGAGTA[C/G]CTGGGATTACAGGTG | 10422 |
| rs368151652 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940340 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGCAGGCG | 10422 |
| rs368235716 | snp | A/G | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932798 | CAGTCCCTTAAACCC[A/G]ATACAACACGAGGCT | 10422 |
| rs368257809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959674 | TACCGTGCCCGGCCC[A/G]GAGAAGTTTTTTAAA | 10422 |
| rs368270149 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946379 | GTCTGGAACTGTGGT[A/G]AAAAAAAAGGAGATC | 10422 |
| rs368286865 | snp | C/T | 8.72045e-05 | 0.00660262 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955289 | GCCCGCCCACAGCAG[C/T]CTTACCTTGGTCCTG | 10422 |
| rs368393437 | in-del | -/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961567 | CCCCGAGCTGCAGGC[-/G]GGTTCCCACCCGGGG | 10422 |
| rs368440666 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956586 | GCCCGACACACGACA[A/G]CACAGCACAGCACAC | 10422 |
| rs368680920 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938056 | CCACAGTGACGTAGC[A/G]GGACTACACCCGCAG | 10422 |
| rs368772191 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949034 | CCGCACTCAAGCCTG[G/T]GTGAGTGACAGTGAG | 10422 |
| rs368779034 | snp | C/T | 8.78125e-05 | 0.0066256 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955283 | CAACCCGCCCGCCCA[C/T]AGCAGCCTTACCTTG | 10422 |
| rs368954201 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | UBAC1 | GRCh38.p7 | 9:135946305 | CCACTGCATCTGGGT[C/T]CAGCGCTAACAGCTT | 10422 |
| rs369147042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957290 | CAACAGGGCAGAGAA[C/G]CCTCAAGTGCCTCTG | 10422 |
| rs369234684 | snp | A/G | 4.94711e-05 | 0.00497324 | missense | UBAC1 | GRCh38.p7 | 9:135945060 | ACTCCCTTTTCCTCC[A/G]GATCTTCTTGAAGAT | 10422 |
| rs369326093 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955948 | GCCATGCTGCATCCC[A/G]AGATTGGGATAAGAG | 10422 |
| rs369446496 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950226 | CAGAACTGCGAGCTA[C/T]AAGCGGAGTGCTGTT | 10422 |
| rs369500378 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949700 | GAAGAACAAGACACC[C/T]GGTCCTGCGGCAGGC | 10422 |
| rs369625764 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935015 | CCCCTGAGTAGCAGG[A/G]ACTACAGGTACGTGT | 10422 |
| rs369649922 | snp | A/G | 9.98685e-05 | 0.00706571 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946225 | ACGCTCCCCAAGGCC[A/G]GCAGTGAACCGCCCT | 10422 |
| rs369824185 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939098 | TCCCAGCTACTCAGG[A/T]GGCTGAGGCAGGAGG | 10422 |
| rs369929265 | snp | A/G | 3.30126e-05 | 0.00406266 | missense | UBAC1 | GRCh38.p7 | 9:135933404 | AACAACGCCACCTAC[A/G]TGCGATTTAGTGTCT | 10422 |
| rs369937474 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933559 | GCCCACGCCCCCACT[C/T]AGCCCACAGGCACAG | 10422 |
| rs370086939 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946932 | GGTGCGGACACCACA[C/T]TAGAGAAATACCTCT | 10422 |
| rs370109086 | snp | C/T | 0.000121579 | 0.00779583 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953767 | ATCTAGAAAAAACAA[C/T]ACGTATATCCAACAC | 10422 |
| rs370399626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936773 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 10422 |
| rs370456490 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958083 | ACGGAGTCTCTCTCC[A/G]TCGCCCAGGCTGGAG | 10422 |
| rs370619971 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953151 | CAGAGGCAGGTTTTC[C/T]GTGCTGGTCCCGTGA | 10422 |
| rs370621094 | snp | C/G/T | 0.000116231 | 0.00762264 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945924 | GGTGGCTCTGTTCTC[C/G/T]GGAAAGCCCATCTCC | 10422 |
| rs370804233 | snp | A/G | 0.000153988 | 0.00877327 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135961139 | CACCTTGCCCGCGAA[A/G]ATCTTCTCCTCCTGC | 10422 |
| rs370823986 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947978 | TGACAACTGAATCAG[C/T]GGAGCTCTGCCCAAG | 10422 |
| rs370906682 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952298 | AAAAGAGTTTGACCT[C/G]CTCTTTCTCTGGGGT | 10422 |
| rs371048180 | snp | C/T | 3.30109e-05 | 0.00406256 | missense | UBAC1 | GRCh38.p7 | 9:135938303 | GAGGACTGTCGGGGT[C/T]GATGCCCTTGTCCAG | 10422 |
| rs371051323 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962512 | AAAAAACTTTACTGC[A/G]CAGAGATGAATAAGG | 10422 |
| rs371273147 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135951285 | TTTGTAGTATTATTC[A/G]ACCTTTTAAAAACAT | 10422 |
| rs371290638 | snp | A/G | 1.67818e-05 | 0.00289665 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938377 | TGCAAAGCCAAGAGC[A/G]CCAATACCACTGTTA | 10422 |
| rs371325023 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936104 | GTGGGCAAGTGTGTG[C/T]GCTGGGGGCAGATCT | 10422 |
| rs371460236 | snp | C/T | 3.39928e-05 | 0.00412253 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938394 | CAATACCACTGTTAG[C/T]GCCTTCAGTGCCTCC | 10422 |
| rs371494523 | in-del | -/GCA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959338 | AGGGAGGACACAGCA[-/GCA]CCTCAGAGAAGTTTC | 10422 |
| rs371504023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944301 | GATGTCTACAGCCTG[A/G]CCACATGGAACTCCA | 10422 |
| rs371902214 | snp | C/T | 3.38702e-05 | 0.00411509 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946017 | AGGGAGACGACAGGG[C/T]CATGAGGGCTCCAGC | 10422 |
| rs371978443 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935003 | TCCCACCTCAGTCCC[-/CT]GAGTAGCAGGGACTA | 10422 |
| rs372032137 | snp | C/T | 1.6676e-05 | 0.00288751 | missense | UBAC1 | GRCh38.p7 | 9:135955336 | ATGGTCCTGGCATCA[C/T]TCAGCACCCTCTCTG | 10422 |
| rs372102711 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950999 | TTTACTCCTGGGGCT[A/G]AGGGAGAAGGATCAC | 10422 |
| rs372118064 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941162 | TGTAATCCCAGCACT[G/T]TGGGAGGCCGGGGTG | 10422 |
| rs372147173 | snp | A/C/T | 6.96506e-05 | 0.00590096 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955427 | CACACTGGGGAAAAA[A/C/T]AGAAATTTCAAGGTA | 10422 |
| rs372236413 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937128 | CACTTCCAGCCTGCT[C/T]GGGTGGCAAAGGCCC | 10422 |
| rs372262824 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939897 | CGCTGTCCGTCCACG[C/T]TCTTTCCTCACAGCT | 10422 |
| rs372402422 | snp | A/G | 4.9445e-05 | 0.00497193 | missense | UBAC1 | GRCh38.p7 | 9:135945080 | TTCTTGAAGATTTCC[A/G]TCAGCTCATCTCTGG | 10422 |
| rs372524004 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959357 | CTCAGAGAAGTTTCT[A/G]GGGTTTTTTGTCTGG | 10422 |
| rs372577322 | snp | G/T | 0.000882003 | 0.0209815 | missense | UBAC1 | GRCh38.p7 | 9:135938340 | CGGAGAGGGCTTCCG[G/T]TCCCCCAGCAGCCAC | 10422 |
| rs372606046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937620 | GCAGCAAATGAGAGA[C/T]TGTTTAAGGAGACAC | 10422 |
| rs372814288 | snp | C/T | 1.68972e-05 | 0.0029066 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938186 | AACCAGCCAGCCTCC[C/T]CGACCCGAGACTTAG | 10422 |
| rs372826512 | snp | C/T | 1.65899e-05 | 0.00288005 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946240 | GGCAGTGAACCGCCC[C/T]GGAATGCAGCATCGG | 10422 |
| rs372895433 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935030 | GACTACAGGTACGTG[A/T]GCCACCACTCCTGGC | 10422 |
| rs373083888 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943370 | AAGGCTCAACATCAC[A/T]GATCATTAGAGAAAT | 10422 |
| rs373115143 | snp | A/C | 0.000132946 | 0.008152 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946390 | TGGTGAAAAAAAAGG[A/C]GATCAATTCTCTAAA | 10422 |
| rs373225127 | in-del | -/CA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939469 | ACCACAGCCCACACT[-/CA]CAGCCCACACTCACT | 10422 |
| rs373267083 | snp | C/G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946197 | GGTCAGTGGTCAGTG[C/G/T]GTGGAGCTGCAGACG | 10422 |
| rs373296398 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938822 | GGATGGTGGGGGGGG[-/G]ATGTGGGCCACCACA | 10422 |
| rs373362222 | snp | A/G | 4.94825e-05 | 0.00497381 | missense | UBAC1 | GRCh38.p7 | 9:135945125 | GCGCTGGCTCCCGCG[A/G]CAGCCTCGGAGGCAG | 10422 |
| rs373387378 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950008 | AGGCCCTGAGAGCAG[A/C]CCCCAGCTGGCCGCC | 10422 |
| rs373424571 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935752 | ATGCAAGTGGCCAGG[C/T]GCAGTAGCTCAAGCC | 10422 |
| rs373436022 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950552 | TTCCAGGAAAAATAC[A/G]GCTGTGTAAGAAGGA | 10422 |
| rs373448901 | in-del | -/AC | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939483 | TCACAGCCCACACTC[-/AC]TCACCACAGCCCACA | 10422 |
| rs373488037 | snp | C/T | 0.000677306 | 0.0183901 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961163 | CTCCTGCACGAACAT[C/T]CCGCCGCCGCCGCAG | 10422 |
| rs373516461 | snp | A/T | 0.000153988 | 0.00877328 | missense | UBAC1 | GRCh38.p7 | 9:135933506 | GGGTTCTCCAGCATG[A/T]CTTCAAATGCTGCAG | 10422 |
| rs373531170 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952662 | AAATAGACAAGACAG[A/G]CAGAACTCAGCCTCT | 10422 |
| rs373653564 | snp | C/T | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961980 | CGCCCTTGGTGCAGG[C/T]GATGCCAGGCAGACT | 10422 |
| rs373683287 | snp | A/G | 5.10843e-05 | 0.00505366 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945007 | GCGACTCTGCCTGGC[A/G]ACAGGTCTAGTAACA | 10422 |
| rs373720003 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962783 | CAGTCCTGGAATGGG[A/G]CATTTTTAACGCAGG | 10422 |
| rs373751922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953403 | CTCACTGCAACCTCT[G/T]CCTCCCGGGTTCAAG | 10422 |
| rs373770754 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936867 | TCAAAACACGGGATT[A/C]TGCCCATCAGTGTGA | 10422 |
| rs373786482 | snp | G/T | 1.64928e-05 | 0.00287161 | missense | UBAC1 | GRCh38.p7 | 9:135938291 | TGGCCTGAAAGAGAG[G/T]ACTGTCGGGGTCGAT | 10422 |
| rs373881678 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939524 | CCCACACTCACTCAT[C/T]ACAGCCCCCACTCAC | 10422 |
| rs373928981 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938381 | AAGCCAAGAGCACCA[A/G]TACCACTGTTAGCGC | 10422 |
| rs374201390 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940554 | ACTGCACTGCAGCCT[-/T]GGGCGACAGAGCGAG | 10422 |
| rs374260888 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936536 | AGTCTTGCTCTGACG[A/C]CCAGGCTAGAGTGCA | 10422 |
| rs374340521 | snp | A/G | 8.70557e-05 | 0.00659699 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953770 | TAGAAAAAACAACAC[A/G]TATATCCAACACACT | 10422 |
| rs374366523 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135951681 | CGGGCGTGGTGGCAC[A/G]CACTTGTAACCCCAG | 10422 |
| rs374563252 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933300 | TAACAGTCCAGGGCT[C/G]AGGCGCTGAAGGTGA | 10422 |
| rs374623417 | snp | C/G | 1.71287e-05 | 0.00292644 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947789 | CCGCCGCTCTGGGCT[C/G]ACACTCACGTCTCTC | 10422 |
| rs374638887 | snp | C/G | 1.74573e-05 | 0.00295438 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955288 | CGCCCGCCCACAGCA[C/G]CCTTACCTTGGTCCT | 10422 |
| rs374666650 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935653 | AAGAAGGAAAACAAA[C/T]AGATGACACGCATAG | 10422 |
| rs374694285 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934349 | GTTCTGATTAAAAGT[C/G]TCCAAAAACCACTTT | 10422 |
| rs374856305 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958843 | AGTCCTGAAATGTAT[A/G]TCGGCTCTTGCGGTG | 10422 |
| rs374885055 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945014 | TGCCTGGCGACAGGT[C/T]TAGTAACACATACCC | 10422 |
| rs375089690 | snp | A/G | 3.32491e-05 | 0.00407719 | missense | UBAC1 | GRCh38.p7 | 9:135945940 | GGAAAGCCCATCTCC[A/G]TGAGCTGCCGCAGGG | 10422 |
| rs375145585 | snp | A/G | 6.6143e-05 | 0.0057504 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946254 | ACACCAGTATCTTC[A/G] | 10422 |
| rs375169633 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949395 | CCAGAACTCAAACAT[C/G]TGAATCTCCAGAGTC | 10422 |
| rs375182519 | snp | C/T | 0.000449637 | 0.0149872 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946224 | GACGCTCCCCAAGGC[C/T]GGCAGTGAACCGCCC | 10422 |
| rs375188942 | snp | A/G | 0.00303228 | 0.0388194 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953636 | AATTCTTAAATGTAG[A/G]CTTCTACCAACCAAG | 10422 |
| rs375195058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939975 | CAGGGATGACTGTAG[A/T]TAGCAGAGCCGGGGG | 10422 |
| rs375283401 | in-del | -/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957772 | TTTTATGAACTCCTT[-/C]TTTTTTTTTTTTTTT | 10422 |
| rs375525870 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945503 | CCAGAGATATCTGCT[A/G]AGGGCTTAGATAGGG | 10422 |
| rs375652793 | snp | A/G | 4.95184e-05 | 0.00497562 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938304 | AGGACTGTCGGGGTC[A/G]ATGCCCTTGTCCAGC | 10422 |
| rs375665911 | snp | A/G | 0.000461513 | 0.0151837 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945112 | CTCCTCATCGGTGGC[A/G]CTGGCTCCCGCGGCA | 10422 |
| rs375717980 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939579 | GCCCACACTCACTCA[C/T]CACAGCCCACACTCA | 10422 |
| rs375766890 | snp | G/T | 0.000305582 | 0.0123571 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946021 | AGACGACAGGGCCAT[G/T]AGGGCTCCAGCCTCA | 10422 |
| rs376038470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944240 | CATGGTGGGGCAGGG[A/G]CCCCACTCATCACCA | 10422 |
| rs376045224 | snp | A/C | | | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961353 | CGCTCCCGCCGCCGC[A/C]GCAGCCGCCGGGGGC | 10422 |
| rs376048507 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943392 | TAGAGAAATGCAAAT[A/C]AAAACCACAATGAGA | 10422 |
| rs376076369 | snp | A/G | 8.4386e-05 | 0.00649507 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938188 | CCAGCCAGCCTCCCC[A/G]ACCCGAGACTTAGCA | 10422 |
| rs376268840 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942473 | TGGGCAACACAGGGA[C/G]ATCCCTATCTGTACA | 10422 |
| rs376285654 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933363 | GGGCCGCACCAGGGG[A/G]CTGCTGTGGCCTGAT | 10422 |
| rs376602524 | snp | A/C/G | 3.37588e-05 | 0.00410834 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939661 | ACTCACTCACCACAG[A/C/G]CCAACACTCACCGCG | 10422 |
| rs376632652 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937154 | GGCCCTCCCAACATC[C/T]AGGAACTCAGCTCCT | 10422 |
| rs376666512 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939499 | CTCACCACAGCCCAC[A/G]CTCACTCAGCCCACA | 10422 |
| rs376726563 | snp | C/G | 1.67211e-05 | 0.00289142 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933557 | GTGCCCACGCCCCCA[C/G]TCAGCCCACAGGCAC | 10422 |
| rs376756872 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936068 | AGTTAAAACAATGAA[C/G]GTCTTGTCTATAATA | 10422 |
| rs376784312 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960848 | GTGTGGGATCCGAAA[C/G]GGGGAGAGTCGGGCA | 10422 |
| rs376802397 | snp | A/G | 0.000241796 | 0.0109927 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939800 | CGCTGGGGGCGGCAG[A/G]AGGCCGAGGAACCAG | 10422 |
| rs376816656 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958030 | ACCAAAAACTCTACT[A/G]CACCACAGGTATAAT | 10422 |
| rs376925493 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960140 | GGAGTCGCCACTAGA[A/C]AATTGCAGCCTCCTT | 10422 |
| rs376932033 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941219 | GAGACCAGCCTGGCC[A/C]ACATGGGAAAACCCC | 10422 |
| rs377025666 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956723 | TGTGTTTCACAAAAT[A/T]CCCACAGTTTCCATA | 10422 |
| rs377028883 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946776 | CATGGCTGCCACACA[C/G]CGTCTGCGGCGGCCA | 10422 |
| rs377195572 | snp | C/T | 0.000297275 | 0.0121881 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933394 | AGCCGAGTGGAACAA[C/T]GCCACCTACGTGCGA | 10422 |
| rs377262960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953080 | GGCGGACAGCAGCGC[A/G]GGAGTGAACCGTCAC | 10422 |
| rs377336441 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950688 | GAGAGAGGGAGGTAC[C/T]ATAGCCTCTTCATTA | 10422 |
| rs377363568 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951982 | TGTATGGTCAGACCC[C/T]GCTGTTTATATTAGT | 10422 |
| rs377384644 | snp | A/G | 0.000155988 | 0.00883003 | missense | UBAC1 | GRCh38.p7 | 9:135961104 | TCGGCGCCGTCGGAC[A/G]CGCAGATGTGCAGCC | 10422 |
| rs377390960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937240 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCAA | 10422 |
| rs377450515 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940355 | GAGGCCGAGGCAGGC[A/G]GATCACCAGGTCAGG | 10422 |
| rs377564954 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957234 | GGCTGAGGGGATGTT[-/G]GGGGGACGCAGCTAC | 10422 |
| rs377578052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958474 | GCACAAAACAGAAAA[A/G]GGAAAGGCAAAAGCA | 10422 |
| rs377643807 | snp | C/T | 0.000185894 | 0.00963911 | missense | UBAC1 | GRCh38.p7 | 9:135947803 | TGACACTCACGTCTC[C/T]CATGTTGGTCTGGAC | 10422 |
| rs377654494 | snp | A/G | 0.000268348 | 0.0115802 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961181 | GCCGCCGCCGCAGGG[A/G]CCTGCGCCCGCCACC | 10422 |
| rs386416444 | in-del | -/C | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932736 | GTAGGCGGAGGCAGC[-/C]CGTGCTTGGGCTCAG | 10422 |
| rs386416445 | in-del | -/C | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932737 | TAGGCGGAGGCAGCC[-/C]GTGCTTGGGCTCAGG | 10422 |
| rs386739520 | multinucleotide-polymorphism | AAA/TAC | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932769 | CCTGTGTCCCAGGAA[AAA/TAC]GGGCTCAGCTCCAGT | 10422 |
| rs386739521 | multinucleotide-polymorphism | CC/GT | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947343 | TGCAACCTCCGCCTC[CC/GT]GGGTTCAAGTGATTC | 10422 |
| rs397936183 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940291 | TTAGAAAAAAAAAAA[-/A]TCCTAGGGCCGGGCG | 10422 |
| rs397951716 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937461 | AAAAAAAAAAAAAAA[-/A]TCAGGAGTGGCACCA | 10422 |
| rs398012569 | in-del | -/A | 0 | 0 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939225 | AAAAAAAAAAAAAAA[-/A]TGAACAAATTACCCA | 10422 |
| rs527348170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958154 | CAGGTTCACACCATT[C/G]TCCTGTCTCAGCCTC | 10422 |
| rs527398018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957565 | GCAGCAAAAAAGCCC[A/C]AACCAAGGCCGCTGG | 10422 |
| rs527521959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941650 | AATGATGCCCCAGTA[C/G]TCCCAAGGCAACACC | 10422 |
| rs527535345 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940047 | GTGACAGGTAGAAAC[A/G]CATCGCTTATGTGGA | 10422 |
| rs527548496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941732 | GGCAATGGGAGAGGG[A/G]CCTTGCGCTCACGGG | 10422 |
| rs527599277 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963303 | ACACGGAGGTGGCCT[A/G]GAGGCAGCTGGACCT | 10422 |
| rs527624065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946807 | TCACTGTCCTCCCCA[A/G]GCAGGAGGAGCCGTG | 10422 |
| rs527702438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942237 | AGGGACCCAGCTGGA[A/G]AGTGACTGCTCCACT | 10422 |
| rs527770019 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932863 | TGCTGCGGTGGCCCC[A/G]GTGCCCGCCCCGGGT | 10422 |
| rs527957426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953821 | AAAATGGCATAAAGG[A/G]TGCTGGATGCCCTGA | 10422 |
| rs528089267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944970 | GCTTCCTTTCCATGG[C/T]GCCACCTCAAGGGAA | 10422 |
| rs528098597 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938891 | ACACGGGCACAGGAC[A/G]GGAATCATTCTTGAG | 10422 |
| rs528178959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934948 | TGCAGTGGAGTGATC[A/G]TGGCTCACTGCAGCC | 10422 |
| rs528189371 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944917 | TCTCTCTCCTGGGAC[A/G]GGAGCCAGCTCAGCC | 10422 |
| rs528227015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940202 | TTAGGGAAAGGCCAC[A/G]TCAGTAAGTGCAATC | 10422 |
| rs528236182 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958445 | GCTAGAGGCCACCAC[A/G]GTGATCCCAATTTGC | 10422 |
| rs528238931 | snp | C/T | 1.66161e-05 | 0.00288232 | missense | UBAC1 | GRCh38.p7 | 9:135938338 | TCCGGAGAGGGCTTC[C/T]GGTCCCCCAGCAGCC | 10422 |
| rs528377061 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962179 | TCTGGTCAGGTTCCT[C/T]GTCCCCCAGGTGCTG | 10422 |
| rs528390335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956103 | CACCCGGGCAGGGAA[C/T]GGGAGGCAACACATG | 10422 |
| rs528549715 | snp | C/G | 4.9812e-05 | 0.00499034 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945951 | CTCCGTGAGCTGCCG[C/G]AGGGCAGCCTCGTCC | 10422 |
| rs528638089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945526 | AGATAGGGACCACAG[A/G]GGGAACTGCCCCCGG | 10422 |
| rs528736844 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935161 | CTCAACCTCCCAAAG[G/T]GCTACAATTACAGGC | 10422 |
| rs528738168 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956032 | TGCTGCACCCCTGGG[A/C]GGCTTGAAGGTGGAC | 10422 |
| rs528753343 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135933616 | CTAATGAAGAGGGTG[C/T]GTCTCCAATACAAAG | 10422 |
| rs528767066 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936439 | ACTTTTAACATTTTT[C/G]GAAAAAAAAATAAAA | 10422 |
| rs528829443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935942 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGTAGGC | 10422 |
| rs528844138 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947139 | CCGTCCTCCCACCCC[A/G]GCACAGCACGTGCCT | 10422 |
| rs528870202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953254 | ACTGTAAATGGCGAA[C/T]GCGTGGGTTGGTGAA | 10422 |
| rs528986474 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938541 | GATTCACTGCCGTGC[A/G]TGTCAGACCAGGCCA | 10422 |
| rs529019470 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947398 | CTGGGATTACAGGTG[C/G/T]CTGCCACTACGCCCG | 10422 |
| rs529099564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943164 | GTGTCTCACACCTGT[A/T]ATCCCAGCACTTTGG | 10422 |
| rs529138056 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933314 | TGAGGCGCTGAAGGT[C/G]AGTTTCCAGGTGAGG | 10422 |
| rs529273598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933774 | GCCTGTGCGTGCTCA[C/T]GGCACCCCCACTCTC | 10422 |
| rs529315575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955014 | CAGAACCCCTGGAGT[A/C]TCTGGCTTTGCTCTG | 10422 |
| rs529423046 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955485 | ATATAGGACCTGGCA[A/T]CCCAAGCTACACCAG | 10422 |
| rs529426913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948260 | CCGAGGCCAAAACCA[C/T]GAACTCATCTCTGCT | 10422 |
| rs529544943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944436 | CCATCTGAGCATGTC[A/G]GAGACAGACAGAAAC | 10422 |
| rs529574680 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950715 | ATTAAGAAGTCAATA[A/G]AGACTAAAGTTGGTC | 10422 |
| rs529674762 | snp | C/G | | | missense | UBAC1 | GRCh38.p7 | 9:135945164 | GCCCCCTCGGCCTCT[C/G]GGGGAGCTTGGCCAG | 10422 |
| rs529756734 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963041 | GCAGGGCATCCTTGC[A/G]GGGGAGCAATGCGGA | 10422 |
| rs529818300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951252 | ACCCAGCCAAGACTG[C/T]TAATTTTTATTAAAA | 10422 |
| rs529898756 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946318 | GTTCAGCGCTAACAG[C/T]TTCTGCGCCACCTCG | 10422 |
| rs529911590 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935634 | AAGACCCTGTCTCCA[C/T]AAAAAGAAGGAAAAC | 10422 |
| rs529923665 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952680 | GAACTCAGCCTCTCT[C/T]AGCATTAACAGTGCA | 10422 |
| rs530024475 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938045 | ACCTGCGGGCCCCAC[A/G]GTGACGTAGCGGGAC | 10422 |
| rs530053685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941107 | TAAACTGTGTGCATG[A/T]TCAGGTCAAAAGTCC | 10422 |
| rs530073163 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936870 | AAACACGGGATTCTG[A/C]CCATCAGTGTGAGGA | 10422 |
| rs530120149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946658 | AACCGTCGGCCCAGC[A/T]GGCGCAGGTGCAGGG | 10422 |
| rs530268027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936729 | TGAACTCCTGACCTC[A/G]TGATCCACCTGCCTC | 10422 |
| rs530318155 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950068 | GCCAACCGCCGGAAG[-/AC]CTCAGAAGCAGAATC | 10422 |
| rs530380678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958753 | GTTCTCTTTTCTGAC[C/T]AACGCATTCTGGCCC | 10422 |
| rs530411083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948592 | CAGAGAGCTGGGCTT[C/G]AGACCCCGGGCCAGG | 10422 |
| rs530418770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958240 | TTTTAGTAAAGATGG[A/G]GTTTCACTGTGTTAG | 10422 |
| rs530456254 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932772 | GTGTCCCAGGAATAC[A/G]GGCTCAGCTCCAGTC | 10422 |
| rs530504719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943958 | GGGAACATCACACAC[C/T]GGGGCCCATCAGGGG | 10422 |
| rs530567884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944393 | TCAGTGCCACACGAG[A/G]CGACAGCATGCAGAT | 10422 |
| rs530649465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938416 | AGTGCCTCCGCAAGA[C/T]GCCACCAGCAGCAGG | 10422 |
| rs530657427 | in-del | -/A | 0.305685 | 0.24372 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940580 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10422 |
| rs530791813 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961548 | TCTCTGGTAGCTTCG[G/T]TCCTCCCCGAGCTGC | 10422 |
| rs530827999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960919 | CCTGGGAGCTGCGGA[A/C]TGGGCGGCGGACCCC | 10422 |
| rs530866979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934865 | GATTATTTATCTGAG[A/G]AAGGACTTTCCTTTT | 10422 |
| rs530994623 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954860 | CTTCCACAATTAAAG[C/G]CATTATTTGAATGAC | 10422 |
| rs531036309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956426 | ACGGGGGCTAGGCGC[A/G]TCGGCTCACCATTTT | 10422 |
| rs531045859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949683 | ACCAAGGGACAGATC[A/G]AGAAGAACAAGACAC | 10422 |
| rs531071830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940263 | GTGAAAAAAGGTTTT[A/G]TTCAGATTTTATCTT | 10422 |
| rs531072199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935502 | ACAAAAAAAATAGCT[A/G]GGCATGGTCGTGCAT | 10422 |
| rs531135662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939883 | AACAGCACTGAGGAC[A/G]CTGTCCGTCCACGTT | 10422 |
| rs531182001 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942792 | GCTGCCCTGGGAGGG[C/T]GGGGTCTGATGTCTA | 10422 |
| rs531279623 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946827 | GAGGAGCCGTGGGAT[G/T]GACCGGAGATGCCCT | 10422 |
| rs531387778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941771 | CGTCGGGCCCTGCCA[A/G]CTCTGCCCCCGGACA | 10422 |
| rs531409362 | snp | A/C/G | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953214 | CAGGCTCTGCCGGGA[A/C/G]AGAGAACCCCTTATA | 10422 |
| rs531461134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943026 | ATCTATTCACCTGAC[A/G]AAGGTCTAATATCCA | 10422 |
| rs531546768 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942369 | CAAAAATGCTTTTAG[A/G]TTAGGCACAATGGCT | 10422 |
| rs531600118 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937996 | TATGTCAGGGTCATC[A/G]CGCAGGAGACAGTCA | 10422 |
| rs531612816 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932893 | TCAGAGCAGCCGGCA[C/T]GGAGCCGCGGGGATG | 10422 |
| rs531821727 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959589 | CATGTTGGCCAAGAT[A/G]GCCTCAATCTCCTGA | 10422 |
| rs531874041 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933277 | AGCAGGAGCAGCTGC[A/G]GCACCTCTAACAGTC | 10422 |
| rs531987551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939838 | CGTGCAGAGGGGCCC[A/G]CTCCCCGCACCCTAG | 10422 |
| rs532007486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948196 | GACCGTGGCAGGGCT[A/G]GGGCAAGGGAGGCGA | 10422 |
| rs532014324 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937940 | CGCAGTCTCCACCCC[A/G]CTGGCCCTCGGAAAG | 10422 |
| rs532276738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951117 | CCTAACTAACTTTTT[A/G]TATTTTTTGTAGAGA | 10422 |
| rs532312519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956962 | CACCCCAGGACAGGC[C/T]GTCCTCGGACGTCTC | 10422 |
| rs532335093 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956601 | GCACAGCACAGCACA[C/G]CACCGCACAGCACAG | 10422 |
| rs532494813 | in-del | -/CA | 0.00557542 | 0.0525036 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960062 | TTTATCCTTAGAGAC[-/CA]CACTCAGCTCAAGTG | 10422 |
| rs532592473 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938095 | CCTGCATGGCAGGAC[A/G]TGCTGCCAGCGCACG | 10422 |
| rs532601411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936581 | GCTCACTGCAACCTC[C/T]GCCCCCCAGGTTTAA | 10422 |
| rs532606346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935968 | TAGGCGGAGCTTGCA[A/G]TGAGCTGAGATCGTG | 10422 |
| rs532610084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941017 | GTCTGGACTGCACCA[C/T]CAGATGCTTCCAAGA | 10422 |
| rs532699238 | snp | C/T | 0.000778371 | 0.0197124 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946245 | TGAACCGCCCTGGAA[C/T]GCAGCATCGGGGTTG | 10422 |
| rs532757969 | snp | C/T | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961504 | AAGTGCGTCACGGGG[C/T]GCGCCCGGAGCATGC | 10422 |
| rs532856441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938083 | GCAGGATGCCAACCT[A/G]CATGGCAGGACGTGC | 10422 |
| rs533014693 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943809 | AAAGGAACGAGATCA[C/T]GTCCTTTGCAGGGTC | 10422 |
| rs533034390 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944524 | AGATGAGGCGCGGGC[A/G]AGGAAGGTCCACACA | 10422 |
| rs533050243 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936321 | GAATAAAAATAAACT[C/T]ACAAAAGACCATTCT | 10422 |
| rs533058428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934303 | CTGTTCATGATTGGA[A/C]AATCCCCAGGCCTTA | 10422 |
| rs533131036 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937881 | GTAGTAAGAGCAAAA[A/G]CCCAAACCACACCTT | 10422 |
| rs533158130 | snp | A/G | 0.000221546 | 0.0105225 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938395 | AATACCACTGTTAGC[A/G]CCTTCAGTGCCTCCG | 10422 |
| rs533240168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955968 | TGGGATAAGAGGGGC[A/G]CTTAGCATGACTGCT | 10422 |
| rs533344589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949651 | TCCTGGCACCCGAGG[A/C]AGTCAGGCTCCACCA | 10422 |
| rs533360627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960841 | TCCAGAGGTGTGGGA[G/T]CCGAAAGGGGGAGAG | 10422 |
| rs533437467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948962 | GTAATCCCAGCTACC[C/T]GGGAGGCTGAGGCAG | 10422 |
| rs533474125 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955564 | ATTAAAGAATTCCCA[C/T]TAATGGTAGATGCCA | 10422 |
| rs533612676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946111 | TGCCCGCCCTCAGGC[A/G]CATCAACAGGAGTTG | 10422 |
| rs533822156 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947310 | AGGCTGGAGTACGAT[C/G]ATGCAATCTCGGCTT | 10422 |
| rs534054179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957924 | GGATTACAGGAGTCC[A/G]CGACCATGCCAGGCT | 10422 |
| rs534062965 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936815 | GTTTTCTTTAAAGGT[A/T]CACATCTTAAAAAAA | 10422 |
| rs534153280 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942718 | AAGGGATATCCACAA[C/G]TGAGAAACCCAAGAA | 10422 |
| rs534160502 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952522 | ACATGAGCTTCTAGG[C/G]CAGCCAGTAAACAAC | 10422 |
| rs534400277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953005 | ACTTTCCTCCGTTTT[C/T]CTGTCAGGACTGACT | 10422 |
| rs534463943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947410 | GTGCCTGCCACTACG[C/T]CCGGCTAATTTTTGG | 10422 |
| rs534502841 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947079 | AAACAGGGCTTATAG[C/G]AGTGCCCTTAGGTTG | 10422 |
| rs534544006 | snp | C/G/T | 7.24034e-05 | 0.00601635 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960993 | GGGGTCCGGAGCGGG[C/G/T]GTTGGGGGCAGGGGA | 10422 |
| rs534610563 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933975 | TCAAAAAACCAGCAC[A/G]TTAAAAATGCAACAC | 10422 |
| rs534737056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960511 | AAGCAGCCGGCTCTG[A/C]GGGAAAGGGGAAGAG | 10422 |
| rs534800004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948353 | GAGAGGAACAGAACC[A/G]GAAGAGTGACAGCAC | 10422 |
| rs534839504 | snp | A/G | 1.67136e-05 | 0.00289076 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939676 | CCCAACACTCACCGC[A/G]GCATTCTGCTGGTTG | 10422 |
| rs534921370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949157 | AGACGGCCCACGGAG[A/G]AACACACCAGAACAC | 10422 |
| rs535011949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939157 | CAGTGAGTGTGATCA[C/T]ACCGCTGCACTCCAG | 10422 |
| rs535048223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951099 | CTGGCTTGTGCCAAC[A/G]AGCCTAACTAACTTT | 10422 |
| rs535197909 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940472 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10422 |
| rs535278551 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937582 | AGGCCTGCTTAAAAC[A/T]TGATTCTACTTACAC | 10422 |
| rs535278634 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932677 | CTCATTTTAAGACAC[C/T]GGTCATGTTTTTTAA | 10422 |
| rs535406007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946877 | CAGGGCCTAGAGGTC[A/G]GGCGTCAGCTGTCCC | 10422 |
| rs535407140 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932918 | GGGATGTGGCCTCTC[A/G]GGGACGCACGGGTTT | 10422 |
| rs535447942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953409 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGAGATTC | 10422 |
| rs535473522 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959711 | ACAACTAGACAAGCA[A/C]CACCACCTGGCTCAA | 10422 |
| rs535522892 | snp | A/G | 0.000503592 | 0.0158601 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135947855 | GGAGGGCAGGTTGGC[A/G]GTGGCCCGCAGTATG | 10422 |
| rs535560978 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954087 | GAGGTTGCACTGAGC[A/C]AAGATTGCACCACTG | 10422 |
| rs535576233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941902 | TCTCGATCCCTACTG[C/G]ACGACTGCCTGATCT | 10422 |
| rs535745772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938485 | GCCCCCAGGGCTGAT[A/C]TCCCTGGAAGGGACT | 10422 |
| rs535871570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959119 | TTTCATAAAAGAGTA[C/T]CATGATGGCCATGCA | 10422 |
| rs536037742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945798 | ATTCAGTCAAAGAGT[C/T]TAGGGTAGGAGGACG | 10422 |
| rs536069109 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955224 | TGTGGGTGGACCACC[C/G]CCTCCTGGCTCCAGC | 10422 |
| rs536077317 | snp | A/G | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932566 | GAAGGGGAGGGGGCT[A/G]GTTCAGAAGAGAAGT | 10422 |
| rs536127245 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933576 | GCCCACAGGCACAGG[C/G]GTGACTTTCCTCTTC | 10422 |
| rs536168478 | snp | C/T | 5.08177e-05 | 0.00504046 | missense | UBAC1 | GRCh38.p7 | 9:135947875 | CCCGCAGTATGGCCT[C/T]TTTATCTGGAGCTTT | 10422 |
| rs536195850 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949237 | TACAGCCAGATCAAA[G/T]AGGCTACAGAATGCT | 10422 |
| rs536236870 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962506 | CATTTAAAAAAACTT[C/T]ACTGCGCAGAGATGA | 10422 |
| rs536297616 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935571 | CAGGAGGTCAAGGCT[C/G]CAGTAAGCTGTGATT | 10422 |
| rs536335093 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944046 | AGGTGATGGGCTGAC[A/G]CGTGCAGCAAACCAC | 10422 |
| rs536347829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949832 | ACGCGGCACAGCCGA[C/T]TGTGGGGAAAGAGTA | 10422 |
| rs536361340 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963361 | TGGGCTGGAGACAAA[C/T]ACTGGGCAGCCGGCC | 10422 |
| rs536370944 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934102 | ACTGTGAAGGAGCAC[A/G]CGTTCTGCCAGCCCC | 10422 |
| rs536511744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946472 | TTGATTCTGAGAGTT[A/G]AGATGACATTGCTTT | 10422 |
| rs536586411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946046 | GCCTCAGGTTCAGGG[C/G]CCTTATCTGAGCACA | 10422 |
| rs536589713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940052 | AGGTAGAAACGCATC[A/G]CTTATGTGGACACGA | 10422 |
| rs536656437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936048 | AAAAAAAAAAGAGGA[A/G]TACAAGTTAAAACAA | 10422 |
| rs536833476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957746 | GCGGGTACTCTCTTC[C/T]AGTCTGGCAATTTTA | 10422 |
| rs536908128 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942925 | AAAGCATTTGTCTCA[A/G]TGGGATCTAACTAAA | 10422 |
| rs536910306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952940 | GAGTGCTCCCTCACC[A/G]GCCACTCTCTGCATG | 10422 |
| rs536950593 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952442 | GGCACGGGCTCAGGC[C/G]CTGCTGTGGGGTAGG | 10422 |
| rs537003638 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956582 | TACAGCCCGACACAC[A/G]ACAGCACAGCACAGC | 10422 |
| rs537063370 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953357 | GAGTCTTACTCTGTC[A/G]CCAGGCTGGAGTGCA | 10422 |
| rs537122757 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939100 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGGAT | 10422 |
| rs537170518 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135951671 | AAAGATTAGCCGGGC[A/G]TGGTGGCACGCACTT | 10422 |
| rs537174908 | snp | A/G | 1.6516e-05 | 0.00287362 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933395 | GCCGAGTGGAACAAC[A/G]CCACCTACGTGCGAT | 10422 |
| rs537184309 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938523 | GAAGACAAACGCAGT[A/C]TGGATTCACTGCCGT | 10422 |
| rs537259141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934643 | CCAGCCTGGGCAGCA[C/G]AGTGAGACTCCGTCT | 10422 |
| rs537287338 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948447 | AGAGCAGAGCATGGA[C/T]GCAAGACCATTCCAG | 10422 |
| rs537307098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955616 | TGAGCTGATCCCCAG[A/C]CCATGGAGTACTCCT | 10422 |
| rs537314128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948423 | GCGGAGCTACAAAGG[C/T]TCAGGCCAAGAGCAG | 10422 |
| rs537346361 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955184 | CTCGTTTTTGTGCTC[A/G]TGTCCAGCTCAGAAC | 10422 |
| rs537374615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935117 | ACCCAGGCTGGTCTC[A/G]AACTCCTGAGCTCAA | 10422 |
| rs537442720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946129 | TCAACAGGAGTTGCC[A/G]GTGAGGCAGGCCCCA | 10422 |
| rs537479243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951670 | AAAAGATTAGCCGGG[C/T]GTGGTGGCACGCACT | 10422 |
| rs537494168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933904 | ACACAGACACTGTTG[A/C]AAAGTTAACAACAAA | 10422 |
| rs537521285 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941307 | GCTACTCGGGAGCCT[A/G]AGGCAGGAGAATCGC | 10422 |
| rs537558908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940685 | TTTGGGGAAGGACAT[A/T]CATTTTCTGGACACA | 10422 |
| rs537639885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936873 | CACGGGATTCTGCCC[A/T]TCAGTGTGAGGAAAT | 10422 |
| rs537775102 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935883 | TACAAAAAATTAGCC[A/G]GGCACGGTGGCGGGC | 10422 |
| rs537800814 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957634 | GCTCCTCCCCAGAAG[-/A]GTAGTGACTTCGTTT | 10422 |
| rs537847883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952396 | CAGCAGAGGAAAGTG[A/G]CTGCCCTTCTAGCTG | 10422 |
| rs537954789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953078 | AAGGCGGACAGCAGC[A/G]CGGGAGTGAACCGTC | 10422 |
| rs537956171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946430 | AACCTACTTGGATCT[A/G]TGACTTGCTCCCCTG | 10422 |
| rs537971468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958961 | ACATCCCAAATGATA[C/T]ATCTCAACACCAAAT | 10422 |
| rs538008721 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935452 | GGAGTTCAAGACTAG[C/T]CTGAGCAAAAAAACG | 10422 |
| rs538070364 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962229 | CTTCAGCAAGAACCC[C/T]GTCAGGTCGGTTTAG | 10422 |
| rs538081065 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939311 | TTAAATTTTTATACT[G/T]TTTGAGCCATCTATC | 10422 |
| rs538208249 | snp | A/G | 0.000964219 | 0.0219358 | intron-variant | UBAC1 | GRCh38.p7 | 9:135961017 | CAGGGGAGGGGGCCC[A/G]GCCTTACGTGCTTGA | 10422 |
| rs538324727 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949512 | AAGGTTCTACAAGGA[A/G]CAGAGGAAGGGGAGG | 10422 |
| rs538412690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952992 | TGGTTGGTTACCCAC[C/T]TTCCTCCGTTTTTCT | 10422 |
| rs538492842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956176 | TCCGAGCAGCGCTCA[C/T]GGGGGACCTGGGAAG | 10422 |
| rs538501858 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934453 | ATCATGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 10422 |
| rs538550864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942810 | GGTCTGATGTCTACA[C/G]ACAGACAGAACGTGC | 10422 |
| rs538646751 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948597 | AGCTGGGCTTGAGAC[A/C]CCGGGCCAGGAGCCC | 10422 |
| rs538750818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955720 | AGAAAGATCTGGAAA[A/G]TAATTTTAAATGAAA | 10422 |
| rs538786376 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935663 | ACAAATAGATGACAC[A/G]CATAGACAGTATGTA | 10422 |
| rs538861284 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949456 | CCTGCAGCAGAGACA[C/G]CATGGAATATTCCAG | 10422 |
| rs538905901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945652 | GTCCCTGCTACGAAC[A/G]GGATTCACCTTGAGT | 10422 |
| rs538943662 | snp | C/T | 0.000498902 | 0.0157861 | missense | UBAC1 | GRCh38.p7 | 9:135945195 | GAAGAGGCGTGTCTA[C/T]GGTCGGGTCTTCTGC | 10422 |
| rs539182337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956778 | CTCAGAGCTTGGACG[C/G]AGAGAAGGCTGACTA | 10422 |
| rs539261928 | snp | C/T | 6.63956e-05 | 0.00576137 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933356 | CGGTCTCGGGCCGCA[C/T]CAGGGGGCTGCTGTG | 10422 |
| rs539445674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955092 | TGCTTGTTCAATTTC[A/G]ATTTCTGCTGTTTTT | 10422 |
| rs539488070 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932957 | GCACCAAGAAAAGAC[A/G]AAGACAGGAAATAGG | 10422 |
| rs539517907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944192 | CTGTGCAGGGAAGAC[A/C]TGAGCTGCGAAGCCG | 10422 |
| rs539550756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937628 | TGAGAGATTGTTTAA[A/G]GAGACACAAATACGG | 10422 |
| rs539713020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934617 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 10422 |
| rs539853605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954369 | AGGACTGCTTGAGCC[C/G]AGGAGGTCAAGGCAA | 10422 |
| rs539874309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949961 | CTCTGAAGGAGGAGG[A/C]GGCTGTGCGGGTAGG | 10422 |
| rs539905017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935440 | CGCTTGAAGCCAGGA[A/G]TTCAAGACTAGCCTG | 10422 |
| rs539970515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939819 | CCGAGGAACCAGTGA[A/C]CTGCGTGCAGAGGGG | 10422 |
| rs540006395 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941686 | GTCCCTGCCCTCCCT[C/T]CCAGCCCATGGGGGC | 10422 |
| rs540106539 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959034 | GAACTGGCTGCCTAA[A/C]TGACCCTCCGTGCTC | 10422 |
| rs540137409 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962878 | AGGAGAAAGGGGAGG[A/G]ACACCAAGGTGGTGA | 10422 |
| rs540154855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934140 | GGATCGATGGCTCCA[C/T]GCTGACCTGACACAC | 10422 |
| rs540233231 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962149 | CCCAGCCTCAATATC[A/G]GATCACCCTGGACGT | 10422 |
| rs540321728 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935943 | AGGCAGGAGAATGGC[A/G]TGAACCCGGTAGGCG | 10422 |
| rs540335702 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934986 | CCCAGACTCAATGAT[C/T]CTCCCACCTCAGTCC | 10422 |
| rs540335753 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957011 | CTGCTGGCAGCTCAC[-/T]TTTCCACCACCCTTT | 10422 |
| rs540365934 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935675 | CACGCATAGACAGTA[G/T]GTAAAAGAAGAAATG | 10422 |
| rs540465994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940971 | ACTTCATGCAGCACT[A/G]CACCCCGCGGACGGT | 10422 |
| rs540492534 | in-del | -/T | 0.49089 | 0.0668743 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957773 | TTTATGAACTCCTTC[-/T]TTTTTTTTTTTTTTT | 10422 |
| rs540530141 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939431 | GAGGCTCCCAGCACT[C/T]GCCCAGCCTGACACA | 10422 |
| rs540811911 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934705 | ACTCAGAAAGAACAA[A/T]CTATAAGGTGCGAAA | 10422 |
| rs540826567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946569 | GGTGGGACTGAAGCC[A/C]GTGGAAAGGGACAGG | 10422 |
| rs540875988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937062 | GGCCAATACGCTTCT[A/G]AAAGAAGGCCAGCCT | 10422 |
| rs540925421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938600 | TGCAGACCCTGGTGT[C/T]GCAGGGATCACTGAC | 10422 |
| rs540936859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941508 | AACTCTGGAAGAACC[C/T]ACCGCACAATATTTT | 10422 |
| rs541022081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934255 | CAGTAGCCCATGGCT[A/G]AGCACAGAGCTCAGA | 10422 |
| rs541147536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954608 | CACAGCACGGCCCCA[A/G]TAATTGTGCAAAGAA | 10422 |
| rs541150905 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953421 | TCCCGGGTTCAAGAG[A/G]TTCTCCTGCCTCAGC | 10422 |
| rs541213459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943802 | GCCATAAAAAGGAAC[A/G]AGATCACGTCCTTTG | 10422 |
| rs541259811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948099 | AGACGTGTCCTCAGC[A/G]TCTGCTCTGACGTAA | 10422 |
| rs541307547 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961413 | CACGGGCGCGTCTGG[C/T]GCATGCCGGGAGATG | 10422 |
| rs541347687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949604 | CTCCACAGCTGCTGC[A/G]CTGGAATACGAGGCC | 10422 |
| rs541421046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936328 | AATAAACTCACAAAA[C/G]ACCATTCTCAAGTTT | 10422 |
| rs541442700 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947254 | GTTCAGATTTGTGTG[-/T]TTTTTTTTTTTCTTG | 10422 |
| rs541578158 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958115 | GCAGTGGCTTGATCT[C/T]GGCTCACTGCAAGTC | 10422 |
| rs541738706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952723 | TCATCTGAAATGCCC[A/G]GGACCAGAACTGTTT | 10422 |
| rs541814442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947197 | GCACTGCAAACACTT[C/T]TCTTTTTTAACTTAG | 10422 |
| rs541849233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953091 | GCGCGGGAGTGAACC[A/G]TCACGCAGGATGTGT | 10422 |
| rs541926012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942822 | ACACACAGACAGAAC[A/G]TGCGCCTTGGGCCCA | 10422 |
| rs542181275 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962936 | TGGAGGAGCCGGGTC[A/G]GAGCATTAAGACGTT | 10422 |
| rs542181840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947149 | ACCCCGGCACAGCAC[A/G]TGCCTGCCCTGCCTG | 10422 |
| rs542249827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949548 | GGTGCAGGGAGGAGC[A/G]GCTCAGAGCTGCCTC | 10422 |
| rs542301262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937390 | AGGTTGCAGTGGGCC[A/G]AGATCATGCCATTGC | 10422 |
| rs542360196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944825 | GTGTGCTCAGAAACT[C/T]GGGCCACGGTCCCCA | 10422 |
| rs542476588 | snp | C/T | 0.000129294 | 0.0080393 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945290 | ACATCCCCAGACTAA[C/T]GGACCAGGGCCTTCG | 10422 |
| rs542574497 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933144 | GAGGAGCACTGGAGA[C/T]GAGGCCATCACTCCA | 10422 |
| rs542617901 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937641 | AAGGAGACACAAATA[C/T]GGCAAAACTCTACCG | 10422 |
| rs542636108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948599 | CTGGGCTTGAGACCC[C/T]GGGCCAGGAGCCCTA | 10422 |
| rs542704342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939325 | TGTTTGAGCCATCTA[C/T]CCAATTGTCTCACTT | 10422 |
| rs542955553 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940318 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10422 |
| rs542960730 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962811 | AGGAAGCAGAAGTAC[C/T]GACTGTTAGAGACCG | 10422 |
| rs542978287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935420 | GAAGGCAGAGGTGGG[A/G]GGAGCGCTTGAAGCC | 10422 |
| rs543159295 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950237 | GCTACAAGCGGAGTG[A/C]TGTTTTAAGCAGCTA | 10422 |
| rs543161224 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956886 | GGCACTTTCTAAACC[C/T]GGTAGCAGGCTCAGC | 10422 |
| rs543166086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953216 | GGCTCTGCCGGGAGA[A/G]AGAACCCCTTATAAC | 10422 |
| rs543210147 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956011 | CAGCTCACGAAGCAA[C/G]AGCCATGCTGCACCC | 10422 |
| rs543272497 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940798 | ATAAGTAAGATGAAG[C/G]CTTCATCAAAATTTC | 10422 |
| rs543310068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946165 | TCATCAGCGCTTCCA[C/T]AAAGCACTGAGGTTC | 10422 |
| rs543317049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943759 | AATAAAGAAAATGTG[A/G]GATATATACACCATG | 10422 |
| rs543366257 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936012 | GCCTGGGTGACAGAG[C/T]GAGATTCCATCTCAA | 10422 |
| rs543393646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958696 | GCAGGATGACATCCA[C/G]GGACCGGCTTCCAGA | 10422 |
| rs543565129 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960620 | CCCAACAGCAAAAAG[A/G]TACAACTGCCGGAAA | 10422 |
| rs543594006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947738 | CCGCAGGAACCCCCC[C/T]ACAGCAATCCCCCAC | 10422 |
| rs543654800 | snp | A/G | | | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961210 | CCCGGGCCCCTGAAG[A/G]TCACCGGGAAGGCGG | 10422 |
| rs543668232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953600 | TGGGATTACAGGCGC[A/G]AGCCACTGTACCCAG | 10422 |
| rs543703310 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943046 | TCTAATATCCAGAAT[C/T]TACATGGAATAAACA | 10422 |
| rs543711746 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944527 | TGAGGCGCGGGCGAG[G/T]AAGGTCCACACACAC | 10422 |
| rs543842464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939876 | TGCTCCCAACAGCAC[C/T]GAGGACGCTGTCCGT | 10422 |
| rs543984530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935843 | CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC | 10422 |
| rs544045141 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962980 | CTAACGGTGTGACCA[C/G]GTGGCAGAATGAATG | 10422 |
| rs544164192 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957508 | AGCACTAGGACGACC[A/G]TGTCACTCTGCTTCT | 10422 |
| rs544220284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934621 | GCCGAGATTGCGCCA[C/G]TGCACTCCAGCCTGG | 10422 |
| rs544225353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957957 | TTTTTTACATTTTTA[C/G]TACAGAAGGGGTATT | 10422 |
| rs544247051 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936186 | AGCCTATTTCTATTA[C/G]GAAAAAAAAAAGAAA | 10422 |
| rs544307912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952092 | ACAGGCCTGACTCAG[C/G]GACAGGCGGAGGCAG | 10422 |
| rs544323211 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955812 | TCTTTTTTCCACAGA[C/T]GCATGAAAGGGGCCA | 10422 |
| rs544333783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959796 | GTTGTTCAGACGGCA[A/G]AATCATGCAGACTGG | 10422 |
| rs544497447 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940821 | AAAATTTCAAGGGCC[C/T]CTCCTAATCCCTGAA | 10422 |
| rs544558782 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937767 | AGTAGATACATGGCT[A/G]TTAGTTTTATTCTTC | 10422 |
| rs544580166 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936687 | TTTAGTAAAGACAGC[A/G]TTTCACCATCTTGGC | 10422 |
| rs544653192 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960556 | CTCTTCATGAAGGAG[C/T]CTACGTTAATTCTCA | 10422 |
| rs544801357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948568 | CCATCCAGTCCTGCC[C/G]GCAACTCCCAGAGAG | 10422 |
| rs544819868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937093 | TCAAGATCAGGGCAC[A/G]GCCATCGCAGCTCCA | 10422 |
| rs544876936 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937907 | ACCTTGTCCTCCCGT[A/G]AGTTCCTAAGCTGCT | 10422 |
| rs544920436 | snp | G/T | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932848 | ACAAGGCCTCCCACA[G/T]GCTGCGGTGGCCCCG | 10422 |
| rs544927794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934790 | CAGCAAAATAAATTC[G/T]GGAAGGATGAAAGAG | 10422 |
| rs545021662 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952659 | AAGAAATAGACAAGA[C/T]AGGCAGAACTCAGCC | 10422 |
| rs545036258 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954823 | ATACTTCCAGGATTT[C/T]CAAAACAGCTTACTT | 10422 |
| rs545200172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938818 | CGGGGGATGGTGGGG[G/T]GGGGATGTGGGCCAC | 10422 |
| rs545259629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944362 | CAGCACAATGTCACA[C/T]ACCCCAAGGAAACGA | 10422 |