| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs13465784 | snp | A/G | 0.484429 | 0.0868505 | synonymous-codon, nc-transcript-variant | Anapc5 | GRCm38.p3 | 5:122799405 | GCTGAATGCGGGTGT[A/G]CAGCAGAACAATACT | 59008 |
| rs13465785 | snp | A/G | | | synonymous-codon, missense, nc-transcript-variant | Anapc5 | GRCm38.p3 | 5:122791880 | GGCACACAAGCTACT[A/G]CAGAAGTTGCTGACG | 59008 |
| rs13465786 | snp | C/T | | | missense, nc-transcript-variant | Anapc5 | Mm_Celera | 5:122799376 | CTGAGTCCTTTGCCG[C/T]CGCTCTCTGCCATCT | 59008 |
| rs13465788 | snp | C/T | | | synonymous-codon, missense, nc-transcript-variant | Anapc5 | Mm_Celera | 5:122791733 | CTATCGGTGGCAGAG[C/T]TGTACTGGCGATCTT | 59008 |
| rs29509503 | snp | G/T | 0.46875 | 0.121031 | intron-variant | Anapc5 | GRCm38.p3 | 5:122811948 | CACTAATAATTGTTG[G/T]TGCCTTTACTCCTAA | 59008 |
| rs29511267 | snp | G/T | 0.375 | 0.216506 | intron-variant | Anapc5 | GRCm38.p3 | 5:122803324 | TTGGTTTTGGTTTTG[G/T]TTTTGTTTTTTTGAG | 59008 |
| rs29525224 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Anapc5 | Mm_Celera | 5:122805954 | GTCTTGAGCTTGCAC[C/T]TGTCCTCTTACCTCC | 59008 |
| rs29525692 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Anapc5 | Mm_Celera | 5:122794664 | TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGCAG | 59008 |
| rs29525740 | snp | A/T | 0.375 | 0.216506 | intron-variant | Anapc5 | GRCm38.p3 | 5:122811330 | AATGTTCCAGGCCTG[A/T]CAGACCTATACAGTA | 59008 |
| rs29528375 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, missense, nc-transcript-variant | Anapc5 | GRCm38.p3 | 5:122791865 | TAGCTTCTGACAGTA[C/T]GTCAGCAACTTCTGT | 59008 |
| rs29528784 | snp | C/T | 0.456747 | 0.140554 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | Anapc5, LOC105246784 | GRCm38.p3 | 5:122787991 | TAGTTCTTGGCTTCA[C/T]TGAGGTTCTGAATGG | 59008 |
| rs29531070 | snp | G/T | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122801309 | TCCAGAGAATGGGCG[G/T]AAGAGATCTTATGGT | 59008 |
| rs29545273 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Anapc5 | GRCm38.p3 | 5:122814404 | AAATGACATGCAGGC[A/G]AGGACCCACAGCCAT | 59008 |
| rs29550012 | snp | A/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Anapc5, LOC105246784 | Mm_Celera | 5:122787023 | ACGCTTTTTTTTTTT[A/T]AATGCAGTTTTGTGG | 59008 |
| rs29562395 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Anapc5 | Mm_Celera | 5:122809125 | TCTCAATACAGTTGG[C/T]TGCAAGCCACCATGT | 59008 |
| rs29630278 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Anapc5 | GRCm38.p3 | 5:122813394 | GGAGGCTGGTTCTCT[C/T]GTCCCACCATGCGAG | 59008 |
| rs29630761 | snp | G/T | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122797420 | GCTTACATACAGAAT[G/T]GTGCTGAAATTTCTT | 59008 |
| rs29632334 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Anapc5 | GRCm38.p3 | 5:122802528 | CCTCTCTATACTTGG[C/T]AACTGTTTGCTACAC | 59008 |
| rs29676154 | snp | A/G | 0.5 | 0 | intron-variant | Anapc5 | Mm_Celera | 5:122795587 | ACAAAAGCACGCACA[A/G]CTACTTGTAATCCTT | 59008 |
| rs29677204 | snp | G/T | 0.5 | 0 | intron-variant | Anapc5 | Mm_Celera | 5:122809639 | CCCCTGGCTGACCCC[G/T]ATATATAGACCAAGC | 59008 |
| rs29677319 | snp | A/T | 0.48 | 0.0979796 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Anapc5, LOC105246784 | Mm_Celera | 5:122787705 | TCAACCCAGAAAAAT[A/T]AAAAAAAACCCACTT | 59008 |
| rs29726776 | snp | A/G | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122788528 | CTGTACACACGCATG[A/G]CCTGTGCCCATTGCC | 59008 |
| rs29779301 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Anapc5 | GRCm38.p3 | 5:122812923 | CTTGTCTGTCACCCT[A/T]GCTCCAGGGGATCCA | 59008 |
| rs29780285 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Anapc5 | Mm_Celera | 5:122814823 | TGAGCTCCAGGACAG[C/T]CAGAGCTATAAAGAG | 59008 |
| rs29780932 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Anapc5 | GRCm38.p3 | 5:122807415 | GCCTGAAATTAAAAC[A/G]ACAGCACATTAGAAT | 59008 |
| rs29813176 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Anapc5 | GRCm38.p3 | 5:122799300 | TTCCTCCGCAGTGCT[A/G]CCATAGCAACAGAGC | 59008 |
| rs33033998 | snp | C/T | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122813195 | ATAACTGTGAAATCC[C/T]GAGAGTTACTATGGG | 59008 |
| rs33035472 | snp | A/G | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122789822 | TATGATCTTAGATGT[A/G]ACAACCACTTCTTTG | 59008 |
| rs33078956 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Anapc5 | GRCm38.p3 | 5:122804271 | TTAAGACCAGGCTGG[A/G]CTACATGAAACTGTT | 59008 |
| rs33098171 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Anapc5 | GRCm38.p3 | 5:122807707 | GAGTCCTCTGCACTC[C/T]CCCTTCCTACAGCAC | 59008 |
| rs33099834 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, missense, nc-transcript-variant | Anapc5 | GRCm38.p3 | 5:122791852 | TTTCTGTGTTCTTTA[A/G]CTTCTGACAGTACGT | 59008 |
| rs33099903 | snp | C/T | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122813465 | CCTTTACACACTGAG[C/T]CACCTTGTCTGCACC | 59008 |
| rs33117385 | snp | A/G | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122789666 | TACACACACACACAC[A/G]CACACGCACACGCAC | 59008 |
| rs33222184 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Anapc5 | GRCm38.p3 | 5:122812117 | TTCCCCCATGTTGTC[C/G]TTTGCCTTGTAATTA | 59008 |
| rs33238470 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Anapc5 | Mm_Celera | 5:122795190 | AAAGAAAGAAAAAAA[A/G]AGAAGCAGCAGCCAA | 59008 |
| rs33247762 | snp | C/T | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122798574 | AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCCG | 59008 |
| rs33296033 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Anapc5 | Mm_Celera | 5:122809064 | TTATTTAATGTGTAT[A/G]AGCACACTTTCGCTG | 59008 |
| rs33301785 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Anapc5 | GRCm38.p3 | 5:122807251 | CTGATACACTGAACA[G/T]CACCGTCCCTTCCTT | 59008 |
| rs33302228 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Anapc5 | GRCm38.p3 | 5:122791989 | TCTGCAAGCCTTTCA[A/G]CTGTAGCCATTTGGG | 59008 |
| rs33326194 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Anapc5 | Mm_Celera | 5:122792619 | GGTGGCTCACAACCA[C/T]CTGTAATGAGATCTG | 59008 |
| rs33362623 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Anapc5 | GRCm38.p3 | 5:122797063 | TTGAGTCTTAGAAGG[A/G]AATAGTACAGGAGGA | 59008 |
| rs33385378 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Anapc5 | Mm_Celera | 5:122814723 | TTCAAGGCAGCTGGG[C/T]GTGGTGGTGCACGCC | 59008 |
| rs33429601 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Anapc5 | Mm_Celera | 5:122810989 | ACCATGTTTCAATTC[C/T]CAGTGCCCACAAGGC | 59008 |
| rs33446998 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | Anapc5, LOC105246784 | Mm_Celera | 5:122788197 | TCTCACTTTTTTTTT[G/T]TTTTTAAAAATTAAA | 59008 |
| rs33558481 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Anapc5 | GRCm38.p3 | 5:122816068 | TTGCCTGTTCTGCAA[C/T]TGGAGTTGCAGAACA | 59008 |
| rs33619280 | snp | A/C/G | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122812526 | AGCTCTGGCTAACCT[A/C/G]GAACTGCCTGCTTCT | 59008 |
| rs33719862 | snp | C/T | 0.5 | 0 | intron-variant | Anapc5 | Mm_Celera | 5:122809896 | CCATCTCTCCAACCC[C/T]GCTAACTCATTTTTT | 59008 |
| rs33724261 | snp | A/C | 0.5 | 0 | intron-variant | Anapc5 | Mm_Celera | 5:122812226 | TCATAAAGGCTCCCC[A/C]ACCCAGAGGCAGTTA | 59008 |
| rs33730925 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Anapc5 | GRCm38.p3 | 5:122801461 | CTGAAGTAACAACTC[A/C]GCCTCTTCCTGTCAT | 59008 |
| rs33742313 | snp | C/T | 0.5 | 0 | intron-variant | Anapc5 | GRCm38.p3 | 5:122793252 | CCACCTGCCTCTGCC[C/T]CCCAAGTGCTGGGAT | 59008 |
| rs33757574 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Anapc5 | GRCm38.p3 | 5:122807829 | ATTGCTAGTTCACAT[A/G]GATAGAATCAACAAT | 59008 |
| rs36255718 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Anapc5 | Mm_Celera | 5:122788662 | ATGCAGGAGAGAGTG[C/G]CCATTTGTAGCATGG | 59008 |
| rs36276131 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Anapc5 | Mm_Celera | 5:122816625 | AAAAGAACTTCCCTA[G/T]AGAAAGCTAAAAATA | 59008 |
| rs36287896 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Anapc5 | Mm_Celera | 5:122801439 | CCTTAGCACGGCTTC[C/T]GTGTCACTGAAGTAA | 59008 |
| rs36338186 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Anapc5 | Mm_Celera | 5:122817649 | ACCCATGCCTCCCAG[C/T]CAATCTGAAGCCACA | 59008 |
| rs36362619 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Anapc5 | Mm_Celera | 5:122807206 | CTTGCCAACGTGATT[C/G]CTGTTAGAACCTAAA | 59008 |
| rs36366355 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Anapc5 | Mm_Celera | 5:122805610 | TCACTACCTCCAAAC[A/G]TCCTTTGGGGAACCC | 59008 |
| rs36394642 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Anapc5 | Mm_Celera | 5:122805302 | TTAGCAGCCACTTGT[C/G]CAGCCAAGCCAAACC | 59008 |
| rs36440468 | snp | A/G | 0.197531 | 0.244432 | upstream-variant-2KB | Anapc5 | Mm_Celera | 5:122822337 | TTTGTAAGGACAAGA[A/G]CCCATGTTTTTCTTC | 59008 |
| rs36477321 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Anapc5 | Mm_Celera | 5:122818406 | ATAACCAACTGATGT[C/T]GACTAACATAAAAAT | 59008 |
| rs36478944 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Anapc5 | Mm_Celera | 5:122818616 | GTCCGCAGGACTGTG[A/G]AAAGAGCTGAGCGAC | 59008 |
| rs36481454 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Anapc5 | GRCm38.p3 | 5:122818133 | AGTGCTCTTCCCGCA[C/T]GCTCTCCCTCCATTC | 59008 |
| rs36482168 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Anapc5 | Mm_Celera | 5:122818261 | TAGTCAAAAGCTGAG[A/G]TGTAATTATGTTATC | 59008 |
| rs36503917 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Anapc5 | Mm_Celera | 5:122791599 | CGGGGGGGACCCACA[C/T]TGGCTTACCTGGGCA | 59008 |
| rs36545130 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Anapc5 | Mm_Celera | 5:122809447 | TCTCTGACTTTCTGA[A/G]ACAAAACAAGGTTTC | 59008 |
| rs36551913 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Anapc5 | Mm_Celera | 5:122819915 | ACAGGATTTATAGGA[C/T]AAGGCTCTCTTTCCT | 59008 |
| rs36572955 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Anapc5 | Mm_Celera | 5:122809413 | TCCAATTCTTCTGCT[C/T]GCTCACTGTTTGTGT | 59008 |
| rs36618530 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Anapc5 | Mm_Celera | 5:122819022 | CACACCCTGCACATT[C/T]CATAGTCCTGAATTA | 59008 |
| rs36625913 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Anapc5 | Mm_Celera | 5:122807469 | TGACTAATCTTGCCC[A/G]ACTGCAGCCTCATCA | 59008 |
| rs36635822 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Anapc5 | Mm_Celera | 5:122819553 | TCATCTTAGACTTAA[C/T]TGCTCCCCACTCCTT | 59008 |
| rs36637300 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Anapc5 | Mm_Celera | 5:122808311 | AATTTTGGACTTAAA[A/T]ATTAAAATCTGTGAG | 59008 |
| rs36640594 | snp | A/G | 0.375 | 0.216506 | intron-variant | Anapc5 | Mm_Celera | 5:122800773 | TATGACCTGACCTCA[A/G]CCCTGACCCATGAGA | 59008 |
| rs36644712 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Anapc5 | Mm_Celera | 5:122815354 | TCTGTAGCCTGTATC[A/G]CAGTCTCAGTTTCAT | 59008 |
| rs36693849 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Anapc5 | Mm_Celera | 5:122801334 | TATGGTCTATGGTCA[A/C]GGATTCAGCAGAGGC | 59008 |
| rs36702788 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Anapc5 | Mm_Celera | 5:122819951 | ACTCTTAACAGGCAA[C/T]GCTGAGCCCGTCTCC | 59008 |
| rs36717351 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Anapc5 | Mm_Celera | 5:122807806 | TCATCTCCTGTCCTG[G/T]CCTGCACATTGCTAG | 59008 |
| rs36728422 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Anapc5 | Mm_Celera | 5:122802243 | AGAACCATCAAAGGC[A/G]TCATAACAATGGCAA | 59008 |
| rs36731486 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Anapc5 | Mm_Celera | 5:122808123 | AAAAAGTAGGACAAG[C/T]GGTAGGAATGATGTT | 59008 |
| rs36731768 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Anapc5 | Mm_Celera | 5:122819147 | TCCTCAAGAGTATCA[C/T]ACATTGCTAACTTAA | 59008 |
| rs36749984 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Anapc5 | Mm_Celera | 5:122788949 | CACCACAGGAAGAGA[A/G]AACTAGACAGTTAAA | 59008 |
| rs36770097 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Anapc5 | Mm_Celera | 5:122800249 | CAGAGGAGAGATCAC[A/C]CAGCGGTTGGTTAAA | 59008 |
| rs36800486 | snp | G/T | 0.32 | 0.24 | intron-variant | Anapc5 | Mm_Celera | 5:122817694 | AGTTGTAACCTGTGA[G/T]CCAACCTCCGGAATC | 59008 |
| rs36805757 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Anapc5 | Mm_Celera | 5:122791057 | GCTCAATGGATCAGT[G/T]TGGAGTTTGCCACAC | 59008 |
| rs36820613 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Anapc5 | Mm_Celera | 5:122804439 | GTGCAGAGTCAGGAG[C/T]ACACTGCTCAAACAA | 59008 |
| rs36835068 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Anapc5 | Mm_Celera | 5:122819720 | TAAGGTTAGAGATAA[C/T]GGGCAAAGAGCTTCG | 59008 |
| rs36903383 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Anapc5 | Mm_Celera | 5:122804798 | TGTCCAACACTACGG[A/G]GCTACGAATGTAACT | 59008 |
| rs36921875 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Anapc5 | Mm_Celera | 5:122816444 | CTAATACTAATCTGC[A/G]AAAAAAAGAAATTCT | 59008 |
| rs36927978 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Anapc5 | Mm_Celera | 5:122818994 | GGGATGCATGGTTTA[A/G]GAAGGCTCGCTGCAC | 59008 |
| rs36929238 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Anapc5 | Mm_Celera | 5:122815919 | ACACCAAGAGTTTCC[C/T]TAGATGAAAGGAGGC | 59008 |
| rs36934839 | snp | C/T | 0.375 | 0.216506 | intron-variant | Anapc5 | Mm_Celera | 5:122807009 | TACTGAATTTAAAAA[C/T]TTGTTTGAAAACATT | 59008 |
| rs36953125 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Anapc5 | Mm_Celera | 5:122812473 | GGGCAATTCATTTAG[A/G]CTAGGTTAATTTAGT | 59008 |
| rs36956839 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Anapc5 | Mm_Celera | 5:122814297 | GAAATAAGTAAGTGC[A/G]TAACTGCAAAAAGAA | 59008 |
| rs36975297 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Anapc5 | Mm_Celera | 5:122819258 | TGGGGGAAGAATACA[C/T]GAACCTAACTTCTAA | 59008 |
| rs36993985 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Anapc5 | Mm_Celera | 5:122806730 | CCTCCCAAACTGAGG[C/T]ATTAAGGAACACTGA | 59008 |
| rs37102211 | snp | C/G | 0.142012 | 0.225474 | upstream-variant-2KB | Anapc5 | Mm_Celera | 5:122821363 | ACCAGAAGGAAGACT[C/G]ACAGCCAATCAAAAC | 59008 |
| rs37124610 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Anapc5 | Mm_Celera | 5:122804413 | TCTCCATCACCTCCT[A/G]TTTTTCTCACGTGCA | 59008 |
| rs37178832 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Anapc5 | Mm_Celera | 5:122818530 | CTAAAGCTTAAGAGC[A/G]GTCTCCACTCACCTC | 59008 |
| rs37256857 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Anapc5 | Mm_Celera | 5:122804113 | GGCTTCGGAAGGAAG[A/G]GTTAGAGAGAACCCT | 59008 |
| rs37316765 | snp | A/G | 0.32 | 0.24 | intron-variant | Anapc5 | Mm_Celera | 5:122817526 | CCCAGAAGTGTAGAA[A/G]ATCATCTGACAGAAA | 59008 |
| rs37333100 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Anapc5 | Mm_Celera | 5:122807824 | TGCACATTGCTAGTT[C/T]ACATGGATAGAATCA | 59008 |