| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs13467550 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Ncf1 | GRCm38.p3 | 5:134221810 | TCCGCGACCCAGCTC[A/G]GACCTCATCCTGCAC | 17969 |
| rs29545717 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134229858 | GGGCTGGAGAGCTGG[C/T]GCAGTGCTTAAGAGC | 17969 |
| rs45648740 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134231575 | CTGAGCTGACTAGAC[A/G]GATTTCCTGGGAGGA | 17969 |
| rs45993438 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ncf1 | Mm_Celera | 5:134227057 | CACTGTCTGTCTGTG[C/G]GGCAGTCCCTCACCC | 17969 |
| rs46074477 | snp | C/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134226472 | CCCATAGCCCCTCCT[C/T]CTCAGTGTTCTGTCC | 17969 |
| rs46106847 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134220083 | TACATAGTGAAACCT[A/G]TTTCCCAAGAAGAAA | 17969 |
| rs46239548 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134227295 | CTCAGCGGCTCGTTG[C/T]CCATCAAACCACCTG | 17969 |
| rs46363190 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Ncf1 | GRCm38.p3 | 5:134229541 | GAAGCCCAGCAGGGC[A/G]ATATGGCGAATGAAG | 17969 |
| rs46701729 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf1 | Mm_Celera | 5:134227096 | CTTGGGGCTCCCTCA[C/T]GCCCTGTGCATTCTG | 17969 |
| rs47071363 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Ncf1 | Mm_Celera | 5:134219797 | GACATCTAATCAGGA[C/T]TTCACTTTAGGAACC | 17969 |
| rs47076105 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Ncf1 | GRCm38.p3 | 5:134221517 | TTCTGCAAACTTGGT[C/T]GAGACTACAGCAGCA | 17969 |
| rs47090648 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134229712 | CTTTCACTTTCTGAG[A/G]ATTTTTGAGCTTCAA | 17969 |
| rs47391243 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134222135 | GGCTAAGGCGCTTCC[G/T]AGAACGCTGGTGGAT | 17969 |
| rs47690220 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134227475 | TGGGATGACTCTGTT[C/T]TCTGTGTGGATCTCG | 17969 |
| rs47771542 | snp | C/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134226530 | GTCCTGTTCACAGTA[C/T]CTGTGTTCCCCCGCC | 17969 |
| rs47849877 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ncf1 | Mm_Celera | 5:134222861 | AGGGGACCTTCATAG[A/T]GTCTCACCCTTGAGG | 17969 |
| rs47902802 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Ncf1 | Mm_Celera | 5:134219828 | AAACAACAAAACTAG[A/G]AATGGTAAACACTAG | 17969 |
| rs47951025 | snp | G/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134226427 | GGACTATGCTGGTGA[G/T]GACAGCCCCAATCTC | 17969 |
| rs47956911 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Ncf1 | GRCm38.p3 | 5:134221489 | TCCTAGGGCGTTCCT[A/G]AGGCACTTGGCTTTC | 17969 |
| rs47959088 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Ncf1 | GRCm38.p3 | 5:134221648 | TTTGCTGTAGAGTCT[A/C]AGTCCATTTCAAACC | 17969 |
| rs48358892 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Ncf1 | GRCm38.p3 | 5:134226622 | TTTGGGCACCAGGTA[C/T]GTCTCAGGCTTCTTC | 17969 |
| rs48625031 | snp | C/T | 0.32 | 0.24 | intron-variant | Ncf1 | Mm_Celera | 5:134228708 | GGCTGCCATGCAGGG[C/T]CACTCCTGGAGCTGA | 17969 |
| rs48727295 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf1 | Mm_Celera | 5:134223215 | AATAGACCATCATTT[C/T]CCTTCTCGTCTGCTC | 17969 |
| rs49077502 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134222124 | ATAGGTGTCCTGGCT[A/G]AGGCGCTTCCGAGAA | 17969 |
| rs49094833 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ncf1 | Mm_Celera | 5:134222997 | TCTGGGCAAGGGAAG[A/G]AAGCAGATGTGTACA | 17969 |
| rs49259387 | snp | G/T | 0.32 | 0.24 | intron-variant | Ncf1 | Mm_Celera | 5:134224037 | CGCTGGGCTTAGTTG[G/T]TTTTGCCTAAGCTGT | 17969 |
| rs49357613 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134226380 | AGTGTATGGAGCCAA[A/G]GATAACTTTGAACTC | 17969 |
| rs49378175 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ncf1 | Mm_Celera | 5:134222634 | ACCTACCCAGCCAGA[A/C]ACCTCCTCAGACCTC | 17969 |
| rs49543340 | snp | A/G | 0.32 | 0.24 | intron-variant | Ncf1 | Mm_Celera | 5:134227383 | GTGGAAAGGGGTTTT[A/G]GAGAGCAGAGGAGGA | 17969 |
| rs49740481 | snp | A/G/T | | | intron-variant | Ncf1 | GRCm38.p3 | 5:134226793 | GAGTGGGGACACAGA[A/G/T]TGTCTTACAAATGAG | 17969 |
| rs49838666 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134226637 | TGTCTCAGGCTTCTT[C/G]GCCCTGGAGAAAGAA | 17969 |
| rs49990456 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Ncf1 | Mm_Celera | 5:134228561 | GATAGAGTCTAGATA[A/T]ATGGGCAGATATTCC | 17969 |
| rs50000260 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ncf1 | Mm_Celera | 5:134225388 | AGAAGAAAGTGAGGG[C/T]GGCGACTGGCTGCCT | 17969 |
| rs50081479 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134225694 | CTCGCTCTTCTCCAC[A/G]ACGTCCACCACGTCT | 17969 |
| rs50141827 | snp | A/G | 0.32 | 0.24 | intron-variant | Ncf1 | Mm_Celera | 5:134221946 | TCTAGTCCTGATCCC[A/G]TCCCTAGGTCTCGTC | 17969 |
| rs50224638 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134226559 | CCCCTGGGTTCCCCC[A/G]CCCCTGGGCACCTCT | 17969 |
| rs50344573 | snp | C/T | 0.32 | 0.24 | intron-variant | Ncf1 | Mm_Celera | 5:134222521 | CCCCCCACGCATCTT[C/T]GGGCACCTCACTGGG | 17969 |
| rs50439098 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134226656 | CTGGAGAAAGAACAG[A/G]CCAGAAGGGAGGGTT | 17969 |
| rs50497756 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ncf1 | Mm_Celera | 5:134228176 | GGGCATTAGAGCCGA[A/G]AGGGGCACTCAGCAC | 17969 |
| rs50570722 | snp | A/T | 0.336735 | 0.234472 | synonymous-codon, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134226628 | CACCAGGTATGTCTC[A/T]GGCTTCTTCGCCCTG | 17969 |
| rs50621785 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134226432 | ATGCTGGTGATGACA[A/G]CCCCAATCTCCAAGG | 17969 |
| rs50684862 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ncf1 | Mm_Celera | 5:134226891 | GGGAGATGGCAAAGC[C/T]AGCCTTCTATGCCAG | 17969 |
| rs50710684 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134227277 | GAGAGTGCCCTGGCG[A/G]CTCTCAGCGGCTCGT | 17969 |
| rs50754189 | snp | A/C | 0.32 | 0.24 | intron-variant | Ncf1 | Mm_Celera | 5:134222287 | GGGTACGGAGAAACT[A/C]GGACACCCTGAGATC | 17969 |
| rs50820916 | snp | A/C | | | intron-variant | Ncf1 | Mm_Celera | 5:134226683 | GGTTTCAGGTTACAC[A/C]GGCAGGAGGACTTTC | 17969 |
| rs50831937 | snp | A/C | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Ncf1 | GRCm38.p3 | 5:134227265 | GAAGTATTCAGTGAG[A/C]GTGCCCTGGCGACTC | 17969 |
| rs50850542 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf1 | Mm_Celera | 5:134226697 | CCGGCAGGAGGACTT[C/T]CCAAGAGAAAAAGGA | 17969 |
| rs51100936 | snp | A/T | 0.244898 | 0.249948 | missense, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134222050 | GTGCCATCCGTGCTC[A/T]GCGGCCCGGGTCGCC | 17969 |
| rs51378600 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134226777 | CCTGGGAGTGGAGGC[A/G]GAGTGGGGACACAGA | 17969 |
| rs51552710 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ncf1 | Mm_Celera | 5:134222234 | TCCCGGGGCACGGGT[A/G]GACACCCCTGTCATC | 17969 |
| rs51580169 | snp | A/C | 0.32 | 0.24 | intron-variant | Ncf1 | Mm_Celera | 5:134222329 | CTCAGCAAGTGGGTT[A/C]AGAGGGACTCGCACC | 17969 |
| rs51741177 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134231526 | GAAGAGACAAAAAGC[C/T]GCGGTCAGCAGGCCT | 17969 |
| rs52024618 | snp | A/T | 0.132653 | 0.220748 | utr-variant-3-prime, intron-variant, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134221672 | TCAAACCTTAAGGCA[A/T]GGGAGGAGTCTCTAA | 17969 |
| rs212106905 | snp | G/T | | | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134230580 | TCCGACCTGAGCAAG[G/T]GGAGGTCCTAAATTC | 17969 |
| rs212330081 | snp | C/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134225009 | CCTCCAGGAAGCCCT[C/T]CTTCCCAGCCTTTGT | 17969 |
| rs212492949 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134224198 | CCATCCTGGGCGGGC[A/G]GTCCCGGATTGTATA | 17969 |
| rs212718100 | snp | A/G | | | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134231274 | AGTTTTAAGTTAGCA[A/G]TAGACCCTGTCTCAG | 17969 |
| rs212737980 | snp | A/C | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | Ncf1 | Mm_Celera | 5:134221186 | GCCCGGTTGCATGCT[A/C]GTCAAGCTCTACCAA | 17969 |
| rs212798759 | snp | C/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134227702 | GTAATGAGTTTGAAG[C/T]CAGTCTTAGATACAT | 17969 |
| rs212896730 | snp | C/T | | | utr-variant-3-prime, intron-variant | Ncf1 | Mm_Celera | 5:134220477 | ACCAGCCTAGGATGG[C/T]ACCACCAGCCCAGGA | 17969 |
| rs213047618 | snp | C/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134226131 | TGAACTCAGGACTTT[C/T]GGAAGAGCAGTCGGT | 17969 |
| rs213085843 | snp | G/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134226672 | CCAGAAGGGAGGGTT[G/T]CAGGTTACACCGGCA | 17969 |
| rs213276656 | snp | A/C | | | intron-variant | Ncf1 | Mm_Celera | 5:134228332 | GATTGTCTCCAGGGG[A/C]GGGATGGAGGACATG | 17969 |
| rs213735994 | in-del | -/TGTGTG | | | intron-variant | Ncf1 | Mm_Celera | 5:134227847 | CCCACCCACCCCCTT[-/TGTGTG]TGTGTGTGTGTGTGT | 17969 |
| rs213919607 | snp | G/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134222245 | GGGTGGACACCCCTG[G/T]CATCCTAAGCCTGGC | 17969 |
| rs214105410 | snp | C/T | | | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134229895 | TGCTCTTCCAGAGGT[C/T]CTCAGTTCAATTCCC | 17969 |
| rs214530021 | snp | A/C | | | upstream-variant-2KB | Ncf1 | GRCm38.p3 | 5:134230519 | AATCTTTGGGCGGAG[A/C]AAGCAGGGACTGATG | 17969 |
| rs214630989 | snp | G/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134226999 | GCCTCATGGTGACAT[G/T]GACCTGTGTAGATGC | 17969 |
| rs215166292 | in-del | -/CGAG | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134221516 | TTCTGCAAACTTGGT[-/CGAG]TGAGACTACAGCAGC | 17969 |
| rs215234024 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134225962 | ATGATGGCGGATGAG[A/G]TTAGCATGCCCCCAG | 17969 |
| rs215258708 | snp | C/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134228490 | GTCCCAGGTAAACAG[C/T]TTACAAGTGCTGGGC | 17969 |
| rs215300751 | snp | A/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | Ncf1 | Mm_Celera | 5:134221290 | CCCGATGTTGTGGGG[A/T]CCCCCAGTCATAAAA | 17969 |
| rs215825199 | in-del | -/CC | | | intron-variant | Ncf1 | Mm_Celera | 5:134225844 | CAGCAGGGAGGGCAG[-/CC]CCCCCCCCCCGTGGG | 17969 |
| rs215927946 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134227923 | GTCCCTGTCTCCTTC[A/G]TTTGTTTATTTTGAG | 17969 |
| rs215963948 | in-del | -/TGTGTG | | | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134230879 | AAGCTCAGAATCCTC[-/TGTGTG]TGTGTGTTTGTGTGT | 17969 |
| rs216151192 | snp | A/G | | | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134231163 | GCTGTAGTTAAAGGC[A/G]TGTGCCACCACTGCC | 17969 |
| rs216185585 | snp | A/C | | | synonymous-codon, nc-transcript-variant | Ncf1 | Mm_Celera | 5:134222064 | CAGCGGCCCGGGTCG[A/C]CCCGGGCGTCTGCGC | 17969 |
| rs216297590 | snp | A/T | | | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134230542 | GACTGATGGAGAGAG[A/T]AGAGTTATCTGAAGT | 17969 |
| rs216378779 | in-del | -/TG | | | intron-variant | Ncf1 | Mm_Celera | 5:134224479 | ACATGCATACACACA[-/TG]CAAGTACACACAAGT | 17969 |
| rs216533512 | snp | C/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134227632 | ATGGGACGTGGGGTG[C/T]ACACACTCAGGAATT | 17969 |
| rs216729284 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134226067 | ACTCCAGAAGAGGGG[A/G]TCAGATCGTGTTAGG | 17969 |
| rs216869597 | snp | C/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134225399 | AGGGTGGCGACTGGC[C/T]GCCTTCCTCCTCCAC | 17969 |
| rs217043221 | snp | A/C | | | intron-variant | Ncf1 | Mm_Celera | 5:134223265 | TTGATTGCAGAAGGT[A/C]CTGGAGATGAAACTC | 17969 |
| rs217237924 | snp | A/G | | | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134229844 | CCCCAACAAACATGG[A/G]GCTGGAGAGCTGGTG | 17969 |
| rs217488756 | snp | A/C | | | intron-variant | Ncf1 | Mm_Celera | 5:134224171 | AGAGGCCTCAGCCCA[A/C]TGTGGGCACTGCCAT | 17969 |
| rs217609879 | in-del | -/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134222830 | CAGTCAGTCACGGGG[-/T]GGGGGTGCACAGAGC | 17969 |
| rs217856196 | snp | A/G | | | utr-variant-3-prime, intron-variant | Ncf1 | Mm_Celera | 5:134220430 | TGCTCCCCATCGCTT[A/G]CTCAGCCTGCCTTCT | 17969 |
| rs217993355 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134222423 | TGCGTGGGGGTCAAG[A/G]ATCCTCCCAGGCCTG | 17969 |
| rs218002368 | snp | A/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134225461 | CACCAATGTCCCCAA[A/T]CTCTACACTCAGATC | 17969 |
| rs218098818 | snp | C/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134229066 | TTCTCCCTCCCCCCA[C/T]ATCCTTCCCTGGTCC | 17969 |
| rs218130973 | snp | A/G | | | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134230139 | ATACAGAGAAACCCT[A/G]TCTCAGGAAAAAAAA | 17969 |
| rs218159969 | snp | A/G | | | intron-variant | Ncf1 | Mm_Celera | 5:134224591 | ACAGGATGTCACTAC[A/G]TTGCCCAGACTGGGA | 17969 |
| rs218283927 | snp | A/G | | | synonymous-codon, nc-transcript-variant, intron-variant | Ncf1 | Mm_Celera | 5:134223485 | CTCTTCAACAGCAGC[A/G]TACGCTTTGATGGTT | 17969 |
| rs218382332 | snp | A/G | | | downstream-variant-500B | Ncf1 | Mm_Celera | 5:134219623 | TAGTAAGCAAGGACT[A/G]AGACCAGCTGGTGAG | 17969 |
| rs218430853 | in-del | -/CGCCCCTTGGA | | | intron-variant | Ncf1 | Mm_Celera | 5:134221966 | AGGTCTCGTCCCGCC[-/CGCCCCTTGGA]CCTGGAACCCTAAGA | 17969 |
| rs218457566 | snp | G/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134226485 | CTCCTCAGTGTTCTG[G/T]CCCCACAACCCCACA | 17969 |
| rs219071419 | in-del | -/TGTTTCCTCAATCGAGGTTCCCTCTCTTAGA | | | utr-variant-3-prime, intron-variant | Ncf1 | Mm_Celera | 5:134220734 | TCTTAACCACTGAGG[lengthTooLong]TGACACCAGCTCGTG | 17969 |
| rs219088788 | in-del | -/A | | | upstream-variant-2KB | Ncf1 | Mm_Celera | 5:134230147 | AAACCCTATCTCAGG[-/A]AAAAAAAAAAAGCCT | 17969 |
| rs219104074 | in-del | -/GC | | | intron-variant | Ncf1 | Mm_Celera | 5:134227566 | GGGCTCCGTGGCACA[-/GC]GATTGCCTAGTATGC | 17969 |
| rs219852751 | in-del | -/T | | | intron-variant | Ncf1 | Mm_Celera | 5:134224730 | AGTCTTTTTCTTTTC[-/T]TTTTTTTTTTTCGAG | 17969 |