SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs31092840 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Rnf40 | Mm_Celera | 7:127600506 | ATGCAGGTCCTTAGC[C/T]TGGCTTCTGCTGTCC | 233900 |
rs31379148 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf40 | Mm_Celera | 7:127593254 | CTTCCGAGTGCTGGG[A/T]TTAAAGGCGTGCGCC | 233900 |
rs31548369 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf40 | Mm_Celera | 7:127595369 | GAGCGGTGGCTCAGT[A/G]GTTCAGAGCACTGAC | 233900 |
rs31578896 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Rnf40 | Mm_Celera | 7:127593513 | TTCTGGTAGCAAGTC[C/G]TGTGCGTTAGAGCAG | 233900 |
rs31580908 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rnf40 | Mm_Celera | 7:127597565 | TGGGCTTTTGGATAT[A/G]GTAACTTGTGATTGG | 233900 |
rs31735087 | snp | C/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587329 | CCTGGGCCTTGGCAT[C/T]GGTGTGCACAGTGCT | 233900 |
rs32157466 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf40 | Mm_Celera | 7:127595329 | TTGTCCCCTATCCAC[C/T]TCCCTCTCCGCCTCC | 233900 |
rs32254618 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf40 | Mm_Celera | 7:127594390 | AGCCAGGGTTTCTGT[A/G]TCTAGCCCTGGCTGT | 233900 |
rs32404784 | snp | C/G | 0.33241 | 0.236027 | upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588670 | TGGGACTAAAAGACT[C/G]GAGAGGAGGAACCAA | 233900 |
rs32437835 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Rnf40 | Mm_Celera | 7:127593600 | ACAAGAAAGAGCTTG[C/G]TTTAAACACCTTCAG | 233900 |
rs33154106 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127592057 | TGAGAAGCCCAGGCC[C/T]GTGGGCGCTGCCCTT | 233900 |
rs33154109 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf40 | GRCm38.p3 | 7:127592124 | AATGTGTGTGAAATC[A/C]CTTTGTGTTTTGCCT | 233900 |
rs33154112 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf40 | Mm_Celera | 7:127592288 | AGCTTCAAATCAAAC[A/G]TTTTCTTACTAAACT | 233900 |
rs33154133 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127586709 | TGCCTCTGCAGCCCT[A/G]AACACAAGCCTCTTC | 233900 |
rs33154936 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127586922 | ACAAATCACTGGTGG[C/T]TCATACAACTTCCCC | 233900 |
rs33154941 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587623 | GACAGATTATGGGAC[A/G]AATAGATACGACAGT | 233900 |
rs33154965 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127592327 | TTCTCTTATGAGGGA[A/G]TAATAAAGATTCCGT | 233900 |
rs33154967 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf40 | Mm_Celera | 7:127592404 | TTAGTTGGTAGTTAC[A/G]TTGGTAGTTACGTTG | 233900 |
rs33154970 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf40 | Mm_Celera | 7:127593013 | GGAAATGAGACTAGA[C/T]CTTTAGACTTGAGAC | 233900 |
rs33154973 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127593487 | GTTGGGGTTTTTTCC[C/T]ATGCACCTGGTTCTG | 233900 |
rs33155819 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf40 | Mm_Celera | 7:127593711 | CCAGTCAAAGTCTAC[A/G]TTTTCTCTTAAGAGA | 233900 |
rs33155822 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127593775 | CGTTGTCTGCTGCAG[A/G]TGCAAGCCGCAGCTC | 233900 |
rs33155834 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587684 | ATTTCTAGCAGGTCT[A/G]AGTGTGCTATAATTT | 233900 |
rs33155837 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587773 | CCTATTTACAATCAA[A/G]GCAACTCCAGGAAAT | 233900 |
rs33155840 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587822 | GTAATGACTGGCGGC[A/G]CCTTTTTTGGGAAAC | 233900 |
rs33155843 | snp | A/G | 0.231111 | 0.249285 | missense, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587996 | CGTCCACCGAGCTGG[A/G]ACTCCTGTCCAGTTC | 233900 |
rs33156696 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588020 | CCAGTTCCTCCTGCA[A/G]TTTGGGAGATTGTTC | 233900 |
rs33156699 | snp | C/T | 0.124444 | 0.216185 | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588185 | TCCTGCCCCTTCTAG[C/T]GTTTCTTCAGAGGCG | 233900 |
rs33156702 | snp | G/T | 0.124444 | 0.216185 | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588301 | AGCCCACGCCAATCA[G/T]TGAAAAGATAGAGCG | 233900 |
rs33156924 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127593832 | GTTATTCCTGTTAGG[C/T]TTTGATCATGTCAAC | 233900 |
rs33156927 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127593911 | GATGGCATATGTGTA[A/T]TCATGCTATGTATGT | 233900 |
rs33156930 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127594267 | ATCACCATGCTTAGA[G/T]TAGTTATCTGTCTTA | 233900 |
rs33156933 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127594342 | ATGAGAAAATGAAAT[A/G]ACCAGTGCTGGCTTT | 233900 |
rs33157467 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB, utr-variant-5-prime | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588731 | CGCCACATCCGGAGC[C/G]GCTCTGACGCCTGCG | 233900 |
rs33157470 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, utr-variant-5-prime | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588931 | TTTCTGCAGGTGACG[A/G]AAGTGCCGCCTCCAC | 233900 |
rs33157472 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, synonymous-codon | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589008 | CGCTATGTCTGGCCT[C/T]AGCAACAAGCGCGCC | 233900 |
rs33157616 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Rnf40 | Mm_Celera | 7:127594615 | CCTGCAGAGTGATGA[A/G]TTGGGGCTGCAGAAG | 233900 |
rs33157619 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rnf40 | Mm_Celera | 7:127594666 | CCAGCTGGAAGACAC[C/T]CTGGCCCAGGTACGC | 233900 |
rs33157622 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127594806 | CAACTCACCCATGGC[A/G]CTTAGCTAGATGCAA | 233900 |
rs33158225 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127600032 | AGGGATGTGACTTTA[A/G]GGCTGAGTCCACGGG | 233900 |
rs33158228 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127600055 | TCCACGGGACAGTAT[A/G]CATGTTAGAGGAGTT | 233900 |
rs33158233 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf40 | Mm_Celera | 7:127600637 | ACAAGGTGGGACGAG[G/T]CTGGTGACAGTGGGG | 233900 |
rs33158495 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, synonymous-codon | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589116 | CATTCGTCTCGGCGG[C/T]ATTTCTTCCACGGTT | 233900 |
rs33158498 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589164 | GTCACATTTGGCCTG[C/T]GCCCAAAGTGTTTGG | 233900 |
rs33158501 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589442 | CCCCTTTCAGTCTAA[C/T]CCTTGTCCTATTGTG | 233900 |
rs33158515 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127594858 | CTCAGAGCCTCAGGC[C/T]GCCACAGGAGACAGG | 233900 |
rs33158518 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf40 | Mm_Celera | 7:127595802 | GTGGAGTTGGTGAGC[C/T]GAAGGAGACAGCTCA | 233900 |
rs33158521 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Rnf40 | Mm_Celera | 7:127596219 | GGCTGGAGCCACCTC[G/T]GCTACTTCTTCCATA | 233900 |
rs33159106 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf40 | GRCm38.p3 | 7:127600900 | GCAGACCCAAAGCTC[A/C]AAGAATGGAGGTGAG | 233900 |
rs33159109 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127601088 | GGGTAGGACTTTACA[C/T]GAGCTGCACACACAC | 233900 |
rs33159112 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127601700 | TGGGTAGAACAAGGG[C/T]GGTCAGAGCTCCCGG | 233900 |
rs33159344 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Rnf40 | Mm_Celera | 7:127596348 | CAAGCGAGAACTTCG[A/G]GAACGGGAAGGGCCT | 233900 |
rs33159347 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127596737 | CCGAGCCTTGAGCCA[A/G]CAAGGTCACTTGTTT | 233900 |
rs33159350 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127597027 | TTAAGTGCCATCAGC[A/G]TGTGGCGTTTTGGTC | 233900 |
rs33159353 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Rnf40 | Mm_Celera | 7:127597209 | AAACGGGCGGCTACT[C/T]CAGCAGTTACGGGAA | 233900 |
rs33159374 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, synonymous-codon | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589617 | GAGAGAATTGAGAAA[C/T]TGGAGAAGAGGCAGG | 233900 |
rs33159377 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589729 | AAGCCCTGAGGCATT[C/T]CTAACCTCTTGTTCT | 233900 |
rs33159379 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB, missense | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589871 | GATGTGATCCCTCGA[A/C]CAGACCCAGGGACAT | 233900 |
rs33159382 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589919 | ACCAGGGCCCTGGGG[A/C]GCTTATGTTCTCAGA | 233900 |
rs33159865 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127602082 | AATGACAAGTGACCA[C/G]TTGGGGATTTTGCCC | 233900 |
rs33159868 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127602324 | AAAACTTGGCTCTGA[C/G]CCTGTATCCTCGTTC | 233900 |
rs33159870 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Rnf40 | Mm_Celera | 7:127602373 | CCTTCAGAAGTTATG[G/T]TCAGAATTAGAGGCC | 233900 |
rs33159873 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127602379 | GAAGTTATGTTCAGA[A/G]TTAGAGGCCTCAACC | 233900 |
rs33160186 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127597372 | TGTGGTGCTTGTGGA[C/T]GAGGCTGAAGAGGCT | 233900 |
rs33160189 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rnf40 | Mm_Celera | 7:127597521 | TCTGCGCAGCCAGGC[C/T]CTGGAGCTTAATAAG | 233900 |
rs33160295 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590001 | ACTTGGGAAGCAGAA[C/G]TTGCTGTCCTGGAAC | 233900 |
rs33160298 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590190 | TCTTTTTTAATGGAA[A/T]GAACAAAGTTTTAGA | 233900 |
rs33160301 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590248 | CTTCTGAAAAGTAGA[A/G]GCAGAAGTCTTTCTG | 233900 |
rs33160716 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127602426 | CTGGAGTCTGGGGAC[A/G]GTCAGACTTGCTCCA | 233900 |
rs33160719 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127602860 | GCCTCGGGGACTCCC[A/G]GGTACACAGCATCCT | 233900 |
rs33160722 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127602875 | AGGTACACAGCATCC[C/T]ACTGTAACCTTGGAA | 233900 |
rs33160934 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127597614 | CTCTGCTTGGCAATG[C/T]TACCACAGATGGCCC | 233900 |
rs33160937 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127597678 | CTCAGGACTGTTACC[A/G]TATGTGCTGTGTGTC | 233900 |
rs33160940 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf40 | Mm_Celera | 7:127598117 | ACCAAGGTTTTTTCT[A/T]AGGATTGGTTTTGTT | 233900 |
rs33160943 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf40 | Mm_Celera | 7:127599732 | CCTTCTCACCAGTAA[C/T]CCACAAAGAAAAGAA | 233900 |
rs33161034 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590481 | TGTGGCCTTTCATTC[C/T]GATGAGGATTCTCTG | 233900 |
rs33161037 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127590637 | ATTCTCCAAGGCTGC[A/C]GTGTCTCGGGTGGTC | 233900 |
rs33161040 | snp | A/C | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127590814 | GGGACAACTTAGTTC[A/C]GACGGGGATTTCAGC | 233900 |
rs33161043 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591481 | ACTTGGGCAGGGTTT[A/G]GGTTTGCTATCCGAG | 233900 |
rs33161595 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603074 | CCCCAGGCCTGGGCA[A/G]GGATTTGGCCTTCCA | 233900 |
rs33161598 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603146 | CACTCTTGGGTGTGC[A/G]CCCTATTCAGGTCAG | 233900 |
rs33161601 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603258 | GTCCACTTTACCCTT[C/T]CTCACGCATCCTGGT | 233900 |
rs33161826 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf40 | Mm_Celera | 7:127599748 | CCACAAAGAAAAGAA[C/T]GCACTTGTCCATCGT | 233900 |
rs33161956 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf40 | Mm_Celera | 7:127591886 | GCCTCGGACTTTCCT[A/G]AGGGCAGGCATCTTC | 233900 |
rs33161959 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf40 | Mm_Celera | 7:127591918 | TCAGAGTCCGTTTCC[A/T]GGCATTGCTGCACAT | 233900 |
rs33162494 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant, downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603986 | TTCATTGTAGCTTGG[A/G]CCATTAGCTGGACCC | 233900 |
rs33162497 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant, downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127604060 | AGAGTGGTGTTGGTG[A/G]CTCTCCCGGTGGCGC | 233900 |
rs33162500 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant, downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127604074 | GGCTCTCCCGGTGGC[A/G]CTTTTACGGATTAGC | 233900 |
rs33162503 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant, downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127604092 | TTTACGGATTAGCTA[C/T]GTGGCCTGCGCTAAG | 233900 |
rs48992499 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127598671 | TTTTTTTTTTTACTG[G/T]GGGTTCTGGGATTCA | 233900 |
rs108823720 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599786 | TTTTCTGCCTCCCCC[A/G]CCCCCTTTTGGTTTG | 233900 |
rs211920463 | snp | G/T | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127596872 | AAGCAAGAAGATTGC[G/T]GATGAAGATGCCCTG | 233900 |
rs211958508 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587338 | TGGCATCGGTGTGCA[A/C]AGTGCTCCATCATTG | 233900 |
rs211965292 | snp | C/T | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127597278 | CAAGGCCAACCAGAT[C/T]CACAAGCTGCTCCGA | 233900 |
rs211973817 | in-del | -/GTTGGTAGTTA | | | intron-variant | Rnf40 | Mm_Celera | 7:127592381 | ATAGACAGTGCTTAC[-/GTTGGTAGTTA]GTTGGTAGTTACATT | 233900 |
rs212091756 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595784 | TGGGCACTGACTCCG[C/T]CTGTGGAGTTGGTGA | 233900 |
rs212195678 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588560 | CAAAGGCTCCACCCC[C/T]CCATCTCCTAGTGCA | 233900 |
rs212689492 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127593263 | GCTGGGTTTAAAGGC[A/G]TGCGCCATCACGCCC | 233900 |
rs212946048 | snp | C/T | | | intron-variant, nc-transcript-variant, downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127604081 | CCGGTGGCGCTTTTA[C/T]GGATTAGCTACGTGG | 233900 |
rs212947911 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594215 | TTCACAAGATCCACA[A/G]GCTATTGCTTCCTGA | 233900 |