| 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 |
| rs212985802 | snp | A/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594531 | TTTTTTTATAAGCAA[A/T]AAATCAGGTCTTCCG | 233900 |
| rs213112787 | snp | C/T | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127602517 | GAAGGATGCCGTGCT[C/T]ACCAAGTGCTTCCAC | 233900 |
| rs213193024 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590144 | AACATGGGTTTTTTG[-/TT]TTTTTTTTTTTTTTT | 233900 |
| rs213668865 | in-del | -/GCACT | | | intron-variant | Rnf40 | Mm_Celera | 7:127599221 | CTGGGTCAGTCTCTA[-/GCACT]GCATAAACTGGGCAC | 233900 |
| rs213703007 | in-del | -/TG | | | intron-variant | Rnf40 | Mm_Celera | 7:127595502 | TGGTGCATAGAAATC[-/TG]TAAGTAAAACACCGT | 233900 |
| rs213780913 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589942 | TTCTCAGAAAGGTTT[G/T]GAGGAGGAGGTGACT | 233900 |
| rs213898528 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127600216 | CTCCACTGCAGGCAG[G/T]CAGGCAGGATGTTCA | 233900 |
| rs213921840 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127592063 | GCCCAGGCCCGTGGG[C/T]GCTGCCCTTCCCTGA | 233900 |
| rs214033940 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127599272 | CTGGGAACTTAGTAC[C/T]TGCAAGGTCAACAGG | 233900 |
| rs214571753 | in-del | -/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127596542 | CTCCTCCTGCTAAGA[-/C]CCCCTCCTGTACCTT | 233900 |
| rs214997122 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127595725 | ACAGTGTTCTTACCT[A/G]CCGAGCCGTTTCTCC | 233900 |
| rs215004972 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127596800 | TTCCTTCCCGTGGAT[C/G]CAGGTGGATGAGCTT | 233900 |
| rs215226951 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127601622 | TTAAGTGAAGCCTGG[G/T]GAGTGGGGAAAGCCT | 233900 |
| rs215403047 | in-del | -/TT | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603196 | TCTGATTCAGGGGCA[-/TT]TTTTTTTTTAGCCAG | 233900 |
| rs215468241 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591035 | CTCCTCCCTAGTGTC[C/T]ATTTTCTTGGCTGAA | 233900 |
| rs215777692 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588854 | GCGGGGTCCGGGAGA[C/T]ATGTCCAGGGGGACG | 233900 |
| rs215942528 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127600064 | CAGTATACATGTTAG[A/G]GGAGTTGATGGCAAC | 233900 |
| rs215991201 | in-del | -/TG | | | intron-variant | Rnf40 | Mm_Celera | 7:127592111 | GATGCTGTATTTCAA[-/TG]TGTGTGAAATCCCTT | 233900 |
| rs216701110 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594063 | CTATGAACCTCCCAG[C/T]AATGGTTGGAAACCA | 233900 |
| rs216781152 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127597021 | TCCCTGTTAAGTGCC[A/G]TCAGCGTGTGGCGTT | 233900 |
| rs216807554 | snp | A/G | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603011 | CTGACCAGGGACCTG[A/G]GCTTCACATTGGGTC | 233900 |
| rs217025231 | snp | G/T | | | upstream-variant-2KB, synonymous-codon | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589834 | GACAGAGGTGCCTGG[G/T]TGCCAAGAGGGCCTG | 233900 |
| rs217076898 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590003 | TTGGGAAGCAGAAGT[G/T]GCTGTCCTGGAACTC | 233900 |
| rs217098182 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599127 | GGTGCTGAGAGCCCT[A/G]ATATTTAATTCAAGC | 233900 |
| rs217110471 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127590866 | CTAGAGAGACGGCTG[G/T]AGGAGCTGTTGATGC | 233900 |
| rs217136077 | in-del | -/TTTGTGGGAGT | | | intron-variant | Rnf40 | Mm_Celera | 7:127602177 | CACTTTCGAGTTTTG[-/TTTGTGGGAGT]TTTGTTTGTTTGTTT | 233900 |
| rs217196625 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598215 | AGAGAGGGTAAGCTG[C/G]CGTGTCAGTGCTGGG | 233900 |
| rs217277824 | in-del | -/AAA | | | intron-variant | Rnf40 | Mm_Celera | 7:127598619 | ATAAAAAAAGAACTT[-/AAA]AATCATTGGGTAGTT | 233900 |
| rs217677075 | snp | A/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127593299 | TTCTATTTTTCTTCC[A/T]CTGTTTTTGTAAGAC | 233900 |
| rs217708359 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594011 | AGTGCCCTCTGAGGC[C/T]GGAAAACAGCATCCA | 233900 |
| rs217874281 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594975 | TTTGTTTTACAAAGA[C/T]TTATTGTGTAATCCT | 233900 |
| rs218180641 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597124 | TCCTCCCTCCCCACT[C/T]GCAGGAGGAGGAGGC | 233900 |
| rs218203680 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588245 | GGCGTCTTCCCAACT[A/T]GTCTCCCCGGTGACC | 233900 |
| rs218210744 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127597608 | CTCCGTCTCTGCTTG[A/G]CAATGTTACCACAGA | 233900 |
| rs218383581 | snp | A/G | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127594657 | AGAAGTTATCCAGCT[A/G]GAAGACACCCTGGCC | 233900 |
| rs218522332 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127600843 | GGGATGGGATGGAGG[A/G]TTGTGTGGCAACAGG | 233900 |
| rs218558647 | snp | A/C | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127592862 | CCGCATGCTGCAGGC[A/C]CAGTTCTCCCTGCTC | 233900 |
| rs218559731 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127601713 | GGTGGTCAGAGCTCC[C/T]GGTCTCTGGAGCACT | 233900 |
| rs218575307 | in-del | -/TCAGATGCT | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589330 | GTCCTGTGTGATGTG[-/TCAGATGCT]TCTGAGTTGGAAACA | 233900 |
| rs218669393 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598965 | TCCGATACCCTCAAA[C/G]TGCAGTTATGATGGC | 233900 |
| rs218881938 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587262 | TCTTGAAAACCCCCC[-/CA]AAAAAACAACTTTGA | 233900 |
| rs219209923 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127597032 | TGCCATCAGCGTGTG[A/G]CGTTTTGGTCTGAGT | 233900 |
| rs219313180 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127600460 | AGGTGCGTCCTCGGG[C/T]GGGGAGGGCTGGTTG | 233900 |
| rs219511318 | in-del | -/A | | | intron-variant | Rnf40 | Mm_Celera | 7:127592537 | GCTGGACGACTGGGG[-/A]AAAATACTGCCCATC | 233900 |
| rs219607055 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127597877 | CTTAGTTTTGAAATA[C/G]GGTCTGTCGATGAAC | 233900 |
| rs219632848 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601556 | CTTGCCATGAGAAGG[A/G]ACAGGGGACATTCTT | 233900 |
| rs219639242 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127598429 | GGCTTGCACAGTGGC[C/T]CAGCTGGGCAAAGAC | 233900 |
| rs219861307 | snp | C/T | | | downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603691 | CATTTGAGAAACCAG[C/T]CCAGCCCACCCTACA | 233900 |
| rs219934131 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601896 | CTCCAAATAGGCCAA[A/G]CAGTGCTCACCCAAG | 233900 |
| rs220254689 | snp | C/T | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603396 | TTCCAGGTAGAAGAG[C/T]TTTGCCCGTGCTCCA | 233900 |
| rs220283889 | snp | C/T | | | missense | Rnf40 | Mm_Celera | 7:127596194 | ACTGCAAGAAGGAGA[C/T]GGCTTTATTGGCTGG | 233900 |
| rs221853384 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127593752 | GGGCACGGGAAGCCC[C/T]CAGGGCTCGTTGTCT | 233900 |
| rs222164410 | in-del | -/CA | | | intron-variant | Rnf40 | Mm_Celera | 7:127601095 | ACTTTACATGAGCTG[-/CA]CACACACACCTTACC | 233900 |
| rs222167750 | in-del | -/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127593479 | GTGGCTCTGTTGGGG[-/T]TTTTTCCTATGCACC | 233900 |
| rs222240529 | snp | A/G | | | missense, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587917 | TCAGCCACTTCCACA[A/G]GGCTACTAGTGGCTT | 233900 |
| rs222448087 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591102 | ATAAGCAGTTGGTGA[A/G]ATAGCTGGTGCATAA | 233900 |
| rs222496263 | snp | C/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589163 | AGTCACATTTGGCCT[C/G]CGCCCAAAGTGTTTG | 233900 |
| rs222969245 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590308 | TTCAAGACAGGGTTT[C/T]TCTGTGTAATGTTGG | 233900 |
| rs223152523 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594278 | TAGAGTAGTTATCTG[C/T]CTTAGGATCATTTAC | 233900 |
| rs223495682 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590393 | GGATTAAAGGTGTGC[A/G]CCACCACCACCCGGC | 233900 |
| rs223496850 | in-del | -/A | | | downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603615 | CCGTCCATTTGGTCT[-/A]AACCTGAGTCTCTGC | 233900 |
| rs223524640 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591182 | GGGACTCCAGGATCA[A/G]CTAGTTCTTCCTTGG | 233900 |
| rs223748503 | in-del | -/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127601528 | ACTGGACTCTGGCTG[-/C]CCATTGAGGGCTCTT | 233900 |
| rs223818230 | in-del | -/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127592533 | GCGTGCTGGACGACT[-/G]GGGGAAAATACTGCC | 233900 |
| rs223855066 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127595339 | TCCACCTCCCTCTCC[A/G]CCTCCCACTGGCTAG | 233900 |
| rs223865489 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127592242 | CTTGCCTTCTAAGTG[A/G]TGAAACTCTAGGCTT | 233900 |
| rs223906290 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127596691 | GGCTGAGGTAGGGGC[A/G]GCTAGAGCCGAGAGT | 233900 |
| rs224010483 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601995 | CACCAGGGGTGGGTC[A/G]GACTGACTGTGCAGA | 233900 |
| rs224012903 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127593271 | TAAAGGCGTGCGCCA[C/T]CACGCCCGGCTTTTC | 233900 |
| rs224052651 | in-del | -/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594515 | TTCCTGGCAGCTTTA[-/T]TTTTTTTATAAGCAA | 233900 |
| rs224189460 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591699 | GAGAGTGGATGGGAC[A/C]AAATTGAGTACTTGG | 233900 |
| rs224249421 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127592456 | GCAGGGCTGACCTCC[C/T]ATTCCCCCAAGAGCC | 233900 |
| rs224327663 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598878 | GGAACTCACTGGGTA[A/G]ACCAAGCTGGCTTCT | 233900 |
| rs224388953 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599941 | CTGCTAGAATATCAA[A/G]TACACACCACTGTAC | 233900 |
| rs224398518 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591493 | TTTGGGTTTGCTATC[C/T]GAGGACCTCAGGAAA | 233900 |
| rs224459518 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127600653 | CTGGTGACAGTGGGG[C/T]GTAGTCTCCGGAGCT | 233900 |
| rs224624797 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595991 | AGGGAGTTTCCAGGG[G/T]GAAGTCTTAGCTCGA | 233900 |
| rs224756141 | in-del | -/AGCACCGAGCACTCTTAATC | | | intron-variant | Rnf40 | Mm_Celera | 7:127598253 | TTGGGTCTCTGCAAG[-/AGCACCGAGCACTCTTAATC]AGAGAGTGTCTCTCC | 233900 |
| rs224941723 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595047 | AACAGAGTAAGGCAT[C/T]TCTGCTGTTCCCGAG | 233900 |
| rs225199527 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601308 | GAGCTGCGGGGCTCA[A/G]GGATGGGTCACAGAA | 233900 |
| rs225213089 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589219 | ATACACAAACCGGGT[A/G]GTGAGGGTGGGTGTG | 233900 |
| rs225479015 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127598301 | TTGTTAACTGTCCCA[C/T]CATTGAGGAAGCTCA | 233900 |
| rs225596471 | snp | C/T | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127602930 | AGAAGACAGATACAT[C/T]CTTACCCCTAGAAGG | 233900 |
| rs225950572 | snp | A/G | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127596836 | CCGCATCCGAGAGCT[A/G]GAAGAACGAGACCGA | 233900 |
| rs225986840 | snp | C/T | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127597242 | GGATGACGCCAACTT[C/T]AAGCTCATGTCGGAG | 233900 |
| rs226196178 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127601767 | ATTGATTAGCTATCC[C/T]CCCATTGGCCTTCTC | 233900 |
| rs226345475 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127600151 | GGAGCTGTGTCAGGA[A/G]TGAGGATGCGTAGGA | 233900 |
| rs226382766 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601193 | AGCGGCTGCAGAAGG[C/G]GGGGGGGGTTGTTAG | 233900 |
| rs226826110 | in-del | -/ATAAA | | | intron-variant | Rnf40 | Mm_Celera | 7:127599561 | AAAACACCTATACAC[-/ATAAA]ATAAAAAATAAAAGT | 233900 |
| rs226961780 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127598562 | GTTTATATACCTCCC[A/C]CCACCACCACCAAAA | 233900 |
| rs227217265 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599385 | TGCAGAGAGGATTAA[A/G]ATGGAGGATTGACAG | 233900 |
| rs227899095 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587016 | AGGAACCTTTAGCAA[A/G]TCATTTCACTGTCAA | 233900 |
| rs228367490 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127591876 | CTCCAGGTCTGCCTC[A/G]GACTTTCCTGAGGGC | 233900 |
| rs228385951 | in-del | -/AGTGAGC | | | intron-variant | Rnf40 | Mm_Celera | 7:127596010 | TCTTAGCTCGACCTT[-/AGTGAGC]AGTGAGCAGTTCATC | 233900 |
| rs228419154 | snp | A/G | | | missense | Rnf40 | Mm_Celera | 7:127592945 | TGCTGGCCTCCAAGA[A/G]CTCCCACTTGAGACA | 233900 |
| rs229072153 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597345 | CTTAAGTCCCAGGTA[C/T]GGCAGCTGCAGTGTG | 233900 |
| rs229415955 | snp | A/C | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589730 | AGCCCTGAGGCATTC[A/C]TAACCTCTTGTTCTT | 233900 |
| rs229818202 | in-del | -/A | | | intron-variant | Rnf40 | Mm_Celera | 7:127601680 | GGAGCCAAGCCAGGG[-/A]AACCTGGGTAGAACA | 233900 |
| rs229999884 | in-del | -/G | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603161 | ACCCTATTCAGGTCA[-/G]GGACACTGCCACCTC | 233900 |
| rs230006036 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588549 | CCGAACAGCAGCAAA[A/G]GCTCCACCCCTCCAT | 233900 |
| rs230013426 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127594599 | GTCTTTCATACCCAA[A/C]CCTGCAGAGTGATGA | 233900 |
| rs230099944 | in-del | -/GC | | | intron-variant | Rnf40 | Mm_Celera | 7:127593928 | ATGCTATGTATGTGT[-/GC]ATGGCGTAGCATTTT | 233900 |
| rs230163092 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594219 | CAAGATCCACAAGCT[A/G]TTGCTTCCTGAGTGC | 233900 |
| rs230302232 | snp | A/C | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589304 | TACTTATGCGCACAT[A/C]TGTTCCCGTAAGTCC | 233900 |
| rs230388928 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598159 | GTCAGGTGCCCCCAG[A/G]GGCCAGAAAATAGTG | 233900 |
| rs230532915 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127597561 | AGGCTGGGCTTTTGG[A/C]TATGGTAACTTGTGA | 233900 |
| rs230747246 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127593241 | TGCCTGCCTCTGCCT[C/T]CCGAGTGCTGGGTTT | 233900 |
| rs230867603 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127593784 | CTGCAGGTGCAAGCC[A/G]CAGCTCTGCCCAGTG | 233900 |
| rs230899862 | in-del | -/A | | | intron-variant | Rnf40 | Mm_Celera | 7:127601745 | GGTGGAGAAGGTGGC[-/A]AGAGTCATTGATTAG | 233900 |
| rs230946120 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127592222 | CTGAGACTGATCCTG[C/G]CATACTTGCCTTCTA | 233900 |
| rs230981107 | in-del | -/AC | | | intron-variant | Rnf40 | Mm_Celera | 7:127598577 | CCCACCACCACCAAA[-/AC]ACACACTGAATGAAG | 233900 |
| rs231099031 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599288 | TGCAAGGTCAACAGG[A/G]AGTTCAAGGTCACCC | 233900 |
| rs231141682 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595190 | ACCCCTGCACATGGG[G/T]AACAGAGGCAGGGAG | 233900 |
| rs231166441 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127600220 | ACTGCAGGCAGGCAG[G/T]CAGGATGTTCAACAG | 233900 |
| rs231169290 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591106 | GCAGTTGGTGAGATA[C/G]CTGGTGCATAACACT | 233900 |
| rs231498160 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589849 | GTGCCAAGAGGGCCT[A/G]ACCCGTGATGTGATC | 233900 |
| rs231502652 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595727 | AGTGTTCTTACCTAC[C/T]GAGCCGTTTCTCCAG | 233900 |
| rs231646431 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127598018 | GTGACAGGGTTAGGA[C/T]TCAGGCCCACGTCGC | 233900 |
| rs231653755 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594448 | GGCCTTGAACTCAGA[A/G]ATCTCCCTGCCTTTA | 233900 |
| rs231723276 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594926 | AGCTGGGCAGGCATC[A/G]CCAGACTGAGCTACT | 233900 |
| rs231924614 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127598695 | GGATTCAGGTCCACG[C/T]GCTTGAAAGGTAAGC | 233900 |
| rs232162783 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127602387 | GTTCAGAATTAGAGG[C/G]CTCAACCATTTGGTG | 233900 |
| rs232164436 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594392 | CCAGGGTTTCTGTGT[C/G]TAGCCCTGGCTGTCC | 233900 |
| rs232304711 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601680 | GGGAGCCAAGCCAGG[A/G]AACCTGGGTAGAACA | 233900 |
| rs232345012 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590482 | GTGGCCTTTCATTCT[G/T]ATGAGGATTCTCTGT | 233900 |
| rs232406771 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127596751 | AACAAGGTCACTTGT[C/T]TTTATTCTCACTGTA | 233900 |
| rs232648796 | in-del | -/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595454 | GGATCCAGCACCCTC[-/T]TCTGGCCTTTGAGTA | 233900 |
| rs232923909 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127599089 | CCAACTTGAGCTCTT[G/T]ATCCTCTTGCCTCAG | 233900 |
| rs233083918 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127600946 | AAAGGCCGCAGGTGG[A/G]GAGTGAAGGCTGAAC | 233900 |
| rs233307268 | in-del | -/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599017 | AGGAGCTGAAACTAA[-/G]TCCTCTGCCAGACCT | 233900 |
| rs233326233 | snp | A/G | | | downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603752 | GACATGTTTACAAAG[A/G]GCCCCACCCCGCCGC | 233900 |
| rs233549714 | snp | A/G | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127597194 | AGACATGCAGGAGCA[A/G]AACGGGCGGCTACTT | 233900 |
| rs233603792 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588478 | CTCCGCGGAGGCCAG[A/G]AGAGGATGACGGATC | 233900 |
| rs233610927 | in-del | -/CTGTGGTACC | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587356 | GCTCCATCATTGCAG[-/CTGTGGTACC]CTGTGTACATTCCTG | 233900 |
| rs233625872 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127600033 | GGGATGTGACTTTAA[A/G]GCTGAGTCCACGGGA | 233900 |
| rs233958906 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127590907 | ACAGCCCTTCAGCAG[A/G]AGGGCTCTCTGGAAC | 233900 |
| rs234103636 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590084 | TCCCGAGTGCTGGGA[C/T]TAAAGGCGTGTGCCA | 233900 |
| rs234215801 | snp | A/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127599166 | AATGGACTGGAGATG[A/T]AGCTCAGTCAGTAGG | 233900 |
| rs234356857 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127594031 | AACAGCATCCAGGGA[A/C]CTGGAGTTGCAGATG | 233900 |
| rs234496195 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127602336 | TGAGCCTGTATCCTC[A/G]TTCATGCAGTGCTGG | 233900 |
| rs235119501 | snp | C/G | | | upstream-variant-2KB, synonymous-codon | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589113 | ACCCATTCGTCTCGG[C/G]GGCATTTCTTCCACG | 233900 |
| rs235134563 | in-del | -/TG | | | intron-variant | Rnf40 | Mm_Celera | 7:127593923 | TATTCATGCTATGTA[-/TG]TGTGTATGGCGTAGC | 233900 |
| rs235139700 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127597964 | GCCTGTCTCCACTGG[A/G]CTACAGGTGTGCGCT | 233900 |
| rs235783477 | snp | A/C | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127592910 | AGTGAAGACCCAGCT[A/C]GATGAGGCCCGGGGG | 233900 |
| rs235797762 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127599971 | CCTGCTTCAAACACT[G/T]TGATGAAGGAAACTA | 233900 |
| rs235835636 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127600899 | GGCAGACCCAAAGCT[C/T]CAAGAATGGAGGTGA | 233900 |
| rs235853751 | in-del | -/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127600290 | GTCCTCTCCTTCCCG[-/T]TCCCGCCCACCTCAG | 233900 |
| rs236022322 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127593715 | TCAAAGTCTACGTTT[C/T]CTCTTAAGAGAAGCA | 233900 |
| rs236117809 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601715 | TGGTCAGAGCTCCCG[A/G]TCTCTGGAGCACTGT | 233900 |
| rs236209081 | in-del | -/CC | | | intron-variant | Rnf40 | Mm_Celera | 7:127601249 | CTATACATAGCTAAG[-/CC]CTACACACCTGAGAC | 233900 |
| rs236219778 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587394 | CTCCCTTCTCACACC[A/G]CCACTTTACACTGAG | 233900 |
| rs236373770 | snp | A/G | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127596890 | TGAAGATGCCCTGCG[A/G]CGGATCCGGCAGGCA | 233900 |
| rs236444737 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127597034 | CCATCAGCGTGTGGC[A/G]TTTTGGTCTGAGTGT | 233900 |
| rs236801510 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127591895 | TTTCCTGAGGGCAGG[C/T]ATCTTCATCAGAGTC | 233900 |
| rs236918028 | in-del | -/GGAGAGCTCTGAGTGTGAGGCCAGCCT | | | intron-variant | Rnf40 | Mm_Celera | 7:127595202 | GGGGAACAGAGGCAG[-/GGAGAGCTCTGAGTGTGAGGCCAGCCT]GGTCTACAGAGTGAG | 233900 |
| rs236937270 | in-del | -/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598915 | TACCACAAGCTTCAA[-/G]CTTTCCTGATGCACT | 233900 |
| rs237228912 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589953 | GTTTTGAGGAGGAGG[C/T]GACTTTGATGTGGGG | 233900 |
| rs237404941 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127594073 | CCCAGTAATGGTTGG[A/C]AACCAAACTCGTGTC | 233900 |
| rs238179370 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127598460 | AATTGCCTCTAAACC[C/T]GATGACCCAAGTTCT | 233900 |
| rs238241699 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127597905 | AACTTGGCGCTCTCC[A/G]TTTTAGATAGGCAGG | 233900 |
| rs238271827 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127598372 | AGCTGGGCTTTGAAT[A/C]CATGCCTTGTTCCCA | 233900 |
| rs238305229 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599836 | TATGTCGTCCTCCTG[A/G]CTGTTATGGAGTTTG | 233900 |
| rs238315017 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587132 | GCCAGGTAGTGGTGG[-/T]TACACTCACTGTACC | 233900 |
| rs238335324 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587330 | CTGGGCCTTGGCATC[A/G]GTGTGCACAGTGCTC | 233900 |
| rs238432441 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590320 | TTTCTCTGTGTAATG[C/T]TGGCTGACTTGGAAC | 233900 |
| rs238540512 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127600722 | AGCCACGTGGCAGAG[A/G]AGAGATTACACCTGG | 233900 |
| rs238577117 | snp | C/T | | | downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603630 | TAACCTGAGTCTCTG[C/T]GCTACACCTCACAAG | 233900 |
| rs238636223 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601971 | GGACAGTCCACAGCA[A/G]GGCCTTGGCACCAGG | 233900 |
| rs238717010 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603571 | CTAATTGTTATGAAT[-/A]AAATACCCAACCCTA | 233900 |
| rs238806988 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591036 | TCCTCCCTAGTGTCC[A/G]TTTTCTTGGCTGAAT | 233900 |
| rs238821516 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594316 | CTTTTTTTTTTTTTT[C/T]CTGGAGAAACATGAG | 233900 |
| rs239020902 | in-del | -/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127591933 | TGGCATTGCTGCACA[-/T]TTTTTTTTCATTCCT | 233900 |
| rs239853649 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601589 | TCCTTAGAAGTCTCA[A/G]CTTTTAAGTGACAGG | 233900 |
| rs239893465 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127593390 | ATTTCTTTAATACTC[C/G]GATGCAAATACACAG | 233900 |
| rs239915000 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597387 | CGAGGCTGAAGAGGC[C/T]GCCCCTGGTACTGAG | 233900 |
| rs239960535 | snp | C/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588912 | CCACAGCTCAGCTCT[C/G]TGTTTTCTGCAGGTG | 233900 |
| rs240597600 | snp | C/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589193 | GGAATCTTGTGTGTG[C/G]TCGTGTGTATATACA | 233900 |
| rs240926144 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594268 | TCACCATGCTTAGAG[G/T]AGTTATCTGTCTTAG | 233900 |
| rs241019597 | snp | C/T | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603018 | GGGACCTGGGCTTCA[C/T]ATTGGGTCCTGGCCC | 233900 |
| rs241239312 | in-del | -/C | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588474 | AGGGCTCCGCGGAGG[-/C]CAGGAGAGGATGACG | 233900 |
| rs241331647 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595604 | TATGTCTGTGCATCT[C/T]AGGAATGTGTGCCTG | 233900 |
| rs241334729 | in-del | -/AA | | | intron-variant | Rnf40 | Mm_Celera | 7:127601631 | GCCTGGTGAGTGGGG[-/AA]AGCCTTGATGGGAGG | 233900 |
| rs241645393 | in-del | -/T | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603117 | GTACCCTGGTGTAGC[-/T]TTTGTGTTGAAGACA | 233900 |
| rs241788139 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598228 | TGGCGTGTCAGTGCT[A/G]GGAACCAAACTTGGG | 233900 |
| rs241857413 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588333 | ATGCGTAACGAGTTG[C/T]ACGTGCCTCTTAGAA | 233900 |
| rs242001982 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598212 | TGTAGAGAGGGTAAG[C/G]TGGCGTGTCAGTGCT | 233900 |
| rs242035590 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127598952 | CCAGAAGAGGGTATC[A/C]GATACCCTCAAACTG | 233900 |
| rs242113581 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591445 | GTTGGAGGTAGGAGT[C/T]GGGCTTTGGGTGCGG | 233900 |
| rs242176016 | snp | C/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590448 | TTCTGGGACTTGGTA[C/G]AGGTTGATGGTCCCT | 233900 |
| rs242231573 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127600481 | GGGCTGGTTGGCCGG[C/T]ATGGGAGACATGCAG | 233900 |
| rs242263339 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127590849 | GTTCCTGAAGTGGGG[C/G]TCTAGAGAGACGGCT | 233900 |
| rs242290556 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591723 | TACTTGGGGCCCCGG[G/T]TTCTGCCCTTTGCAT | 233900 |
| rs242498450 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127595029 | TCTGGGGTTTTGCCA[A/G]TAAACAGAGTAAGGC | 233900 |
| rs242559921 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594388 | TGAGCCAGGGTTTCT[C/G]TGTCTAGCCCTGGCT | 233900 |
| rs242835155 | in-del | -/TC | | | intron-variant | Rnf40 | Mm_Celera | 7:127598837 | TGTGTATAAACAAGG[-/TC]TCTCTATTTCACTCT | 233900 |
| rs243091276 | in-del | -/A | | | intron-variant | Rnf40 | Mm_Celera | 7:127593006 | AGGGCTGGAAATGAG[-/A]ACTAGATCTTTAGAC | 233900 |
| rs243412837 | in-del | -/CAGC | | | intron-variant | Rnf40 | Mm_Celera | 7:127591845 | GCAGAAGGTAAGCAG[-/CAGC]CCTCCTCCCCCTCCC | 233900 |
| rs243734270 | in-del | -/CCAAGA | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127586788 | CTTGTGTCTCCCCTC[-/CCAAGA]GTTCAGTCTCGCCCA | 233900 |
| rs243814075 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127593278 | GTGCGCCATCACGCC[C/T]GGCTTTTCTATTTTT | 233900 |
| rs244146038 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594497 | CAGAGGCCTATACCA[C/T]CCTTCCTGGCAGCTT | 233900 |
| rs244184215 | snp | C/T | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127596869 | AGAAAGCAAGAAGAT[C/T]GCGGATGAAGATGCC | 233900 |
| rs244357732 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127592469 | CCTATTCCCCCAAGA[C/G]CCCTTAGAAAACGCA | 233900 |
| rs244412896 | snp | A/G | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127597254 | CTTCAAGCTCATGTC[A/G]GAGCGGATCAAGGCC | 233900 |
| rs244455011 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588558 | AGCAAAGGCTCCACC[C/T]CTCCATCTCCTAGTG | 233900 |
| rs244522128 | snp | A/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127598102 | CTCAACAATAATCCT[A/T]CCAAGGTTTTTTCTA | 233900 |
| rs244554835 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127598704 | TCCACGCGCTTGAAA[G/T]GTAAGCACTCCATCA | 233900 |
| rs244765765 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601221 | TAGAGCATTGCAGTC[A/G]CTGAGGCAGAAACTA | 233900 |
| rs244774835 | snp | C/T | | | missense, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587987 | TGGCCGAGCCGTCCA[C/T]CGAGCTGGGACTCCT | 233900 |
| rs244891906 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595107 | AAGGAAAAGGTAAAA[C/T]GTGAGAGAGTGAAAA | 233900 |
| rs245183874 | in-del | -/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127597069 | TGTTTCTTTGGAGTT[-/C]CCCGGCACCCATCTT | 233900 |
| rs245416217 | snp | A/G | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127597206 | GCAAAACGGGCGGCT[A/G]CTTCAGCAGTTACGG | 233900 |
| rs245576082 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590234 | TTCATAATCCCAGCC[C/T]TCTGAAAAGTAGAAG | 233900 |
| rs245645416 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127593805 | CTGCCCAGTGATGCA[A/G]ACGAGTTCTAGGTTA | 233900 |
| rs245768537 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588480 | CCGCGGAGGCCAGGA[A/G]AGGATGACGGATCCT | 233900 |
| rs245983648 | in-del | -/A | | | intron-variant | Rnf40 | Mm_Celera | 7:127593416 | CACAGCGTGCAATGC[-/A]AAGCCCGCTGAGTGG | 233900 |
| rs246002620 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127600205 | GGCAGGGTCAGCTCC[A/C]CTGCAGGCAGGCAGG | 233900 |
| rs246365667 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601820 | GGCTTTCCAGTGTGC[A/G]TGGCCCTGTCCTGAG | 233900 |
| rs246419685 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127593754 | GCACGGGAAGCCCCC[A/G]GGGCTCGTTGTCTGC | 233900 |
| rs246703313 | in-del | -/TTTTTA | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603206 | GGCATTTTTTTTTTT[-/TTTTTA]AGCCAGACTCTTTCC | 233900 |
| rs247056210 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591518 | AGGAAACAGGCCACT[G/T]TCCACTGCCCCTAGT | 233900 |
| rs247090981 | in-del | -/TTT | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603195 | TCTGATTCAGGGGCA[-/TTT]TTTTTTTTTTTAGCC | 233900 |
| rs247443979 | in-del | -/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127600230 | GGCAGGCAGGATGTT[-/C]AACAGAAGCATCAAT | 233900 |
| rs247547924 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595362 | CTGGCTAGAGCGGTG[G/T]CTCAGTAGTTCAGAG | 233900 |
| rs247552915 | snp | A/G | | | missense | Rnf40 | Mm_Celera | 7:127596151 | CCAGGGAAGGAAGAT[A/G]GTGGGCCAGGCCCTG | 233900 |
| rs247641344 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127599641 | CTATTGGAATATTCT[C/T]TTATGGTGAGTTTAT | 233900 |
| rs247795980 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127586876 | GTGCATAGAATGGAT[A/G]TCCAGGTATTTCCTG | 233900 |
| rs247871077 | in-del | -/TAC | | | cds-indel | Rnf40 | Mm_Celera | 7:127596171 | GCCAGGCCCTGGAGG[-/TAC]CCCTGACTGCAAGAA | 233900 |
| rs247899096 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589971 | CTTTGATGTGGGGCT[A/G]CCGAAATGCCCGGCA | 233900 |
| rs248103539 | snp | C/T | | | downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603709 | AGCCCACCCTACAAC[C/T]ACTTGGGTTAGCAGC | 233900 |
| rs248162525 | snp | C/T | | | upstream-variant-2KB, synonymous-codon | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589780 | AACTGTAGAAGCCCT[C/T]CTCCAGTGCTACGAG | 233900 |
| rs248367862 | in-del | -/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127601081 | AAACCTGGGTAGGAC[-/T]TTTACATGAGCTGCA | 233900 |
| rs248370823 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597811 | CCACAAGGGTGGGGA[C/T]GAAGGACGGGATTGT | 233900 |
| rs248422904 | snp | A/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589244 | GGTGTGCCAACGGCG[A/T]GAATGTGATCAGAGA | 233900 |
| rs248539026 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127593980 | GCATGTTCATCTGTG[C/T]AGCACTTACATGCTC | 233900 |
| rs248573406 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601018 | TGGGCAAGCAGAGTA[A/G]AGAAGCCTTTTTATT | 233900 |
| rs248630448 | in-del | -/TTGGTAGTTACA | | | intron-variant | Rnf40 | Mm_Celera | 7:127592393 | TACGTTGGTAGTTAG[-/TTGGTAGTTACA]TTGGTAGTTACGTTG | 233900 |
| rs248715270 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127596723 | CTTCCCAGGCACTTC[C/T]GAGCCTTGAGCCAAC | 233900 |
| rs248883260 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127593077 | CTGAGAGTCCCTTGG[A/G]CATAGATTGTTCCTT | 233900 |
| rs249186517 | snp | A/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597116 | CCTTTCCATCCTCCC[A/T]CCCCACTTGCAGGAG | 233900 |
| rs249292556 | in-del | -/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601191 | AGAGCGGCTGCAGAA[-/G]GGGGGGGGGGTTGTT | 233900 |
| rs249361796 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601441 | AGGTGATGAGAACTC[A/G]GTGCCTCTGGGACCT | 233900 |
| rs249583658 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127600769 | TAAAGTAATTCTGCC[A/G]TCTCAGTGATGAGTC | 233900 |
| rs249624796 | snp | A/G | | | downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603819 | TTGGCCGAATGGATA[A/G]CAGCCTTTGTGGGTT | 233900 |
| rs249676704 | in-del | -/C | | | downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603617 | GTCCATTTGGTCTAA[-/C]CCTGAGTCTCTGCGC | 233900 |
| rs249692910 | in-del | -/A | | | intron-variant | Rnf40 | Mm_Celera | 7:127598667 | TTTTTTTTTTTTTTT[-/A]CTGTGGGTTCTGGGA | 233900 |
| rs249704393 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599364 | AGACCTTGTCTTAAA[A/G]GGAGATGCAGAGAGG | 233900 |
| rs249758936 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127593609 | AGCTTGCTTTAAACA[C/T]CTTCAGTGCCTCTCC | 233900 |
| rs249801441 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127594208 | CAAGATATTCACAAG[A/C]TCCACAAGCTATTGC | 233900 |
| rs249886164 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127592223 | TGAGACTGATCCTGC[C/T]ATACTTGCCTTCTAA | 233900 |
| rs249958857 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591144 | GAAACTCCAGGATCA[A/G]CTAGTTCTTCCTTGG | 233900 |
| rs250041274 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587333 | GGCCTTGGCATCGGT[A/G]TGCACAGTGCTCCAT | 233900 |
| rs250085703 | snp | G/T | | | downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603690 | ACATTTGAGAAACCA[G/T]CCCAGCCCACCCTAC | 233900 |
| rs250138205 | in-del | -/TT | | | intron-variant | Rnf40 | Mm_Celera | 7:127596047 | CTGCTTTTCTCTCTC[-/TT]TAACAGCTCCGGGCA | 233900 |
| rs250296166 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595755 | CAGCCTCTGAGGCTT[C/T]GTCTGCTTCTCTGTG | 233900 |
| rs250341450 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598586 | ACCAAAACACACACT[A/G]AATGAAGTCATTTTA | 233900 |
| rs250358286 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594974 | ATTTGTTTTACAAAG[A/G]CTTATTGTGTAATCC | 233900 |
| rs251121641 | in-del | -/GGGGT | | | intron-variant | Rnf40 | Mm_Celera | 7:127601200 | CAGAAGGGGGGGGGG[-/GGGGT]GTTGTTAGAGCATTG | 233900 |
| rs251226924 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597413 | CTGAGGCTTCCCTCC[G/T]CAGGTGGATGCCCAG | 233900 |
| rs251430127 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590484 | GGCCTTTCATTCTGA[C/T]GAGGATTCTCTGTCC | 233900 |
| rs251722487 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590099 | TTAAAGGCGTGTGCC[A/G]CCACGCCCATCGTGA | 233900 |
| rs251864450 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597125 | CCTCCCTCCCCACTT[G/T]CAGGAGGAGGAGGCG | 233900 |
| rs251960105 | in-del | -/GGAA | | | intron-variant | Rnf40 | Mm_Celera | 7:127593891 | ATATTTTAGGACTTG[-/GGAA]GGATGGCATATGTGT | 233900 |
| rs252305501 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599204 | CAGAGCCTGCATCAA[A/G]CTCTGGGTCAGTCTC | 233900 |
| rs252364147 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598374 | CTGGGCTTTGAATAC[A/G]TGCCTTGTTCCCAAG | 233900 |
| rs252423197 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595606 | TGTCTGTGCATCTCA[G/T]GAATGTGTGCCTGGT | 233900 |
| rs252758352 | snp | C/T | | | utr-variant-3-prime | Rnf40 | Mm_Celera | 7:127603033 | CATTGGGTCCTGGCC[C/T]GAGGAGCCTTGCTTC | 233900 |
| rs252836250 | snp | A/C | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589213 | GTGTATATACACAAA[A/C]CGGGTGGTGAGGGTG | 233900 |
| rs252853313 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127591880 | AGGTCTGCCTCGGAC[G/T]TTCCTGAGGGCAGGC | 233900 |
| rs253021831 | in-del | -/GT | | | intron-variant | Rnf40 | Mm_Celera | 7:127599566 | ACCTATACACATAAA[-/GT]AAATAAAAGTTATTA | 233900 |
| rs253103240 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127593731 | CTCTTAAGAGAAGCA[A/G]TGAGAGGGCACGGGA | 233900 |
| rs253228849 | snp | A/G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127602013 | CTGACTGTGCAGATA[A/G/T]CATGCTTCTCACAGT | 233900 |
| rs253248929 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587075 | TGTAGATTTAGCAGA[-/TT]TTTTTTTTTTATTTA | 233900 |
| rs253318105 | in-del | -/TCCCTTAG | | | intron-variant | Rnf40 | Mm_Celera | 7:127596995 | TCTGAATGCGGGGAT[-/TCCCTTAG]CCCTCCCTGTTAAGT | 233900 |
| rs253318107 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594258 | AAGGCACACATCACC[A/G]TGCTTAGAGTAGTTA | 233900 |
| rs253497452 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127602367 | TTCCCACCTTCAGAA[A/G]TTATGTTCAGAATTA | 233900 |
| rs253527910 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594042 | GGGAACTGGAGTTGC[A/G]GATGGCTATGAACCT | 233900 |
| rs253664804 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | GRCm38.p3 | 7:127587988 | GGCCGAGCCGTCCAC[C/T]GAGCTGGGACTCCTG | 233900 |
| rs253841921 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597976 | TGGGCTACAGGTGTG[C/T]GCTACCGTGCCTCGG | 233900 |
| rs254260449 | in-del | -/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127599969 | TACCTGCTTCAAACA[-/C]TTTGATGAAGGAAAC | 233900 |
| rs254850000 | snp | A/G | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127596637 | ACCCAAGGAGCAGCG[A/G]GACAAGGTGCAGCTC | 233900 |
| rs254917501 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127592001 | TGCTAGGAGCTAGGC[A/G]GGCTGAAGAGGACGA | 233900 |
| rs254924523 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127595333 | CCCCTATCCACCTCC[A/C]TCTCCGCCTCCCACT | 233900 |
| rs255218186 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127599852 | CTGTTATGGAGTTTG[C/T]TGCGTAGACAAGTTT | 233900 |
| rs255402196 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127598739 | AGCTAATCTCTTCAG[C/T]CTGTAATTGTTTTCT | 233900 |
| rs256094320 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589710 | GCGAGCGTCCTACTG[A/G]GAGAAGCCCTGAGGC | 233900 |
| rs256094648 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598542 | ACTTCCACAGGTGTG[C/G]CATGGTTTATATACC | 233900 |
| rs256130101 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590388 | TGCTGGGATTAAAGG[C/T]GTGCGCCACCACCAC | 233900 |
| rs256151505 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597951 | ATCCCTGGGCTCTGC[C/T]TGTCTCCACTGGGCT | 233900 |
| rs256193532 | in-del | -/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127601574 | GGGGACATTCTTCTT[-/C]CCTTAGAAGTCTCAG | 233900 |
| rs256484584 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594334 | GGAGAAACATGAGAA[A/G]ATGAAATAACCAGTG | 233900 |
| rs256541755 | in-del | -/G | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590143 | AAACATGGGTTTTTT[-/G]TTTTTTTTTTTTTTT | 233900 |
| rs256603910 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601979 | CACAGCAGGGCCTTG[C/G]CACCAGGGGTGGGTC | 233900 |
| rs257394579 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127587090 | ATTTTTTTTTTATTT[A/G]TAAACCCACTGATTA | 233900 |
| rs257488295 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127596763 | TGTTTTTATTCTCAC[G/T]GTATGGACCAACGTT | 233900 |
| rs257592884 | snp | A/T | | | missense | Rnf40 | Mm_Celera | 7:127596181 | GGAGGTACCCCTGAC[A/T]GCAAGAAGGAGATGG | 233900 |
| rs257819995 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601300 | CTAAGGTGGAGCTGC[A/G]GGGCTCAGGGATGGG | 233900 |
| rs257912090 | in-del | -/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127598760 | TTGTTTTCTTGCTCA[-/C]CCCCCCCCCCTTTTT | 233900 |
| rs257931674 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127599095 | TGAGCTCTTGATCCT[C/T]TTGCCTCAGGCTCCC | 233900 |
| rs257969267 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127590994 | GGCTTTTTGAGGCAA[G/T]GGGTTTTTTCCTCCT | 233900 |
| rs258163752 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591037 | CCTCCCTAGTGTCCA[C/T]TTTCTTGGCTGAATG | 233900 |
| rs258395086 | snp | A/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127601606 | TTTTAAGTGACAGGC[A/C]TTAAGTGAAGCCTGG | 233900 |
| rs258419753 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597830 | GGACGGGATTGTCAT[C/T]GGGATGTCCCCCTTT | 233900 |
| rs258523884 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594270 | ACCATGCTTAGAGTA[G/T]TTATCTGTCTTAGGA | 233900 |
| rs258662201 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594412 | CCTGGCTGTCCTGGA[A/G]CTCACTCTGTAGACC | 233900 |
| rs259211527 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597359 | ACGGCAGCTGCAGTG[C/T]GGTGCTTGTGGACGA | 233900 |
| rs259322240 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588445 | TGTGCGCACATATGT[A/G]CAGGATGTTCGGGAG | 233900 |
| rs259728693 | in-del | -/ATGG | | | intron-variant | Rnf40 | Mm_Celera | 7:127593673 | AAACCCTTTCTGGTA[-/ATGG]TTTTACAGTTAACCT | 233900 |
| rs259728853 | snp | C/T | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127592929 | GAGGCCCGGGGGTTG[C/T]TGCTGGCCTCCAAGA | 233900 |
| rs259798937 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591771 | TCTGCAGCTCAACTC[C/T]GGCTACTATGTGTCT | 233900 |
| rs260208715 | snp | A/G | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127596914 | GCAGGCAGAAGAGCA[A/G]ATTGAACACTTGCAA | 233900 |
| rs260269759 | in-del | -/GG | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127590134 | CTGTCTTAAAAACAT[-/GG]GTTTTTTGTTTTTTT | 233900 |
| rs260508992 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598279 | TCTCCAGCCCAGCCA[A/G]AAGGATTTGTTAACT | 233900 |
| rs260784996 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601724 | CTCCCGGTCTCTGGA[C/G]CACTGTGGTGGAGAA | 233900 |
| rs261158835 | snp | A/C | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127600374 | GCAGACTCGACTTCG[A/C]GAGATCCAGCCCTGC | 233900 |
| rs262089486 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127592753 | GGACTAACCTCAGAT[C/T]GATCCTGCTGCTAAC | 233900 |
| rs262260946 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597028 | TAAGTGCCATCAGCG[C/T]GTGGCGTTTTGGTCT | 233900 |
| rs262315888 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591583 | GACCAAGGTCCTAGA[A/G]ATGGAGACCACAGTG | 233900 |
| rs262852443 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127594784 | GGGCCTCAGAGGGGT[A/G]CTGGACCAACTCACC | 233900 |
| rs262944453 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127589273 | GAACAACTTTACGGA[G/T]TCCCTTCTGGCCTTT | 233900 |
| rs263001408 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601061 | GAGCATACGATGCTT[A/G]GGAGTAAACCTGGGT | 233900 |
| rs263020904 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127593213 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCTGC | 233900 |
| rs263277128 | in-del | -/C | | | intron-variant | Rnf40 | Mm_Celera | 7:127592785 | AACCCTTCTGGACAT[-/C]TTCACCGCCAGGTGG | 233900 |
| rs263299866 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127594438 | AGACCAGGCTGGCCT[C/T]GAACTCAGAGATCTC | 233900 |
| rs263432297 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127599762 | ATGCACTTGTCCATC[A/G]TTTATCTCTTTTCTG | 233900 |
| rs263518231 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127598681 | TACTGTGGGTTCTGG[A/G]ATTCAGGTCCACGCG | 233900 |
| rs263638543 | snp | C/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127595823 | AGACAGCTCAGCACA[C/G]TCACTTGCTGACCTT | 233900 |
| rs263673426 | in-del | -/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127595988 | TAGAGGGAGTTTCCA[-/G]GGGGAAGTCTTAGCT | 233900 |
| rs263868194 | snp | G/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127595043 | AATAAACAGAGTAAG[G/T]CATCTCTGCTGTTCC | 233900 |
| rs263920785 | snp | C/T | | | intron-variant | Rnf40 | Mm_Celera | 7:127597641 | GCCCAGAGTGAAGCT[C/T]GGCTCTGCTCCTGGC | 233900 |
| rs264190382 | snp | A/G | | | synonymous-codon | Rnf40 | Mm_Celera | 7:127597149 | GGAGGCGTTGCTGTC[A/G]GAGATGGATGTAACA | 233900 |
| rs264532368 | in-del | -/TGTGTC | | | intron-variant | Rnf40 | Mm_Celera | 7:127598813 | AGATTTGAACTTGTG[-/TGTGTC]TGTGTCTGTGTGTAT | 233900 |
| rs265313071 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | Mm_Celera | 7:127588535 | GTGTACCGAGTACCC[C/G]GAACAGCAGCAAAGG | 233900 |
| rs265420819 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127601842 | TGTCCTGAGAGATGG[A/G]GAAACAGTAATTTGG | 233900 |
| rs265580301 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127595146 | ATAAAAATGCATCAG[A/G]AAACCTAGCATGATG | 233900 |
| rs265678235 | snp | A/G | | | intron-variant | Rnf40 | Mm_Celera | 7:127597980 | CTACAGGTGTGCGCT[A/G]CCGTGCCTCGGTATT | 233900 |
| rs265730778 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf40 | Mm_Celera | 7:127591459 | TTGGGCTTTGGGTGC[A/G]GTTAGAACTTGGGCA | 233900 |
| rs265844551 | in-del | -/TT | | | intron-variant | Rnf40 | Mm_Celera | 7:127593129 | ATATATCTATTTTTC[-/TT]TTTTTTTTTTTTTTA | 233900 |
| rs266221760 | snp | A/G | | | downstream-variant-500B | Rnf40, 1700120K04Rik | Mm_Celera | 7:127603740 | AATATATCTACAGAC[A/G]TGTTTACAAAGGGCC | 233900 |
| rs578389136 | snp | A/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127601566 | GAAGGAACAGGGGAC[A/G]TTCTTCTTCCTTAGA | 233900 |
| rs578577637 | snp | A/G | | | utr-variant-3-prime | Rnf40 | GRCm38.p3 | 7:127603172 | GTCAGGGACACTGCC[A/G]CCTCATGGTCTGATT | 233900 |
| rs578803251 | snp | A/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127593407 | ATGCAAATACACAGC[A/G]TGCAATGCAAAGCCC | 233900 |
| rs578911004 | snp | C/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127591854 | TAAGCAGCCTCCTCC[C/T]CCTCCCCTCCAGGTC | 233900 |
| rs579343845 | snp | C/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127599205 | AGAGCCTGCATCAAG[C/G]TCTGGGTCAGTCTCT | 233900 |
| rs580056776 | snp | C/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127593905 | GGGAAGGATGGCATA[C/T]GTGTATTCATGCTAT | 233900 |
| rs580447662 | snp | A/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127595185 | CTATAACCCCTGCAC[A/G]TGGGGAACAGAGGCA | 233900 |
| rs580632577 | snp | C/G | | | downstream-variant-500B | Rnf40, 1700120K04Rik | GRCm38.p3 | 7:127603623 | TTTGGTCTAACCTGA[C/G]TCTCTGCGCTACACC | 233900 |
| rs580845947 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | GRCm38.p3 | 7:127590143 | AAACATGGGTTTTTT[G/T]TTTTTTTTTTTTTTT | 233900 |
| rs581095579 | snp | G/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127595516 | TCTAAGTAAAACACC[G/T]TACAAACAAAGTGAA | 233900 |
| rs581252849 | snp | A/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127598926 | TTCAACTTTCCTGAT[A/G]CACTCAGAAGCCAGA | 233900 |
| rs581606356 | snp | A/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127600243 | TTCAACAGAAGCATC[A/G]ATGGACTGTGGTTCC | 233900 |
| rs581740107 | snp | C/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127591864 | CCTCCCCCTCCCCTC[C/T]AGGTCTGCCTCGGAC | 233900 |
| rs582003850 | snp | C/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127593470 | AGAAAGGAGGTGGCT[C/T]TGTTGGGGTTTTTTC | 233900 |
| rs582022999 | snp | C/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127592792 | TCTGGACATTTCACC[C/G]CCAGGTGGCCCTGCG | 233900 |
| rs582309432 | snp | G/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127601666 | AGGGAAGGAAGGAAG[G/T]GAGCCAAGCCAGGGA | 233900 |
| rs582415522 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | Rnf40, 1700120K04Rik | GRCm38.p3 | 7:127603602 | GGCTGCAGAGAAGCC[C/G]GTCCATTTGGTCTAA | 233900 |
| rs583190423 | snp | A/C | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127596978 | CCTGTGGTCTCCTTG[A/C]TTCTGAATGCGGGGA | 233900 |
| rs583200878 | snp | C/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127595240 | GCCTGGTCTACAGAG[C/T]GAGTTCCAGGTCAAC | 233900 |
| rs583542276 | snp | C/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127593917 | ATATGTGTATTCATG[C/T]TATGTATGTGTATGG | 233900 |
| rs584852310 | snp | G/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127591867 | CCCCCTCCCCTCCAG[G/T]TCTGCCTCGGACTTT | 233900 |
| rs584945824 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf40 | GRCm38.p3 | 7:127591175 | TTATCCAGGGACTCC[A/G]GGATCAACTAGTTCT | 233900 |
| rs585437734 | snp | C/T | | | utr-variant-3-prime | Rnf40 | GRCm38.p3 | 7:127603106 | TGGAGTTTCCTGTAC[C/T]CTGGTGTAGCTTTTG | 233900 |
| rs585458461 | snp | A/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127593158 | TTAATGGTTTTTCGA[A/G]ACAGGGTTTCTCTGT | 233900 |
| rs585992668 | snp | A/G | | | downstream-variant-500B | Rnf40, 1700120K04Rik | GRCm38.p3 | 7:127603621 | CATTTGGTCTAACCT[A/G]AGTCTCTGCGCTACA | 233900 |
| rs586165926 | snp | C/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127593493 | GTTTTTTCCTATGCA[C/T]CTGGTTCTGGTAGCA | 233900 |
| rs586388811 | snp | A/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127593929 | ATGCTATGTATGTGT[A/G]TGGCGTAGCATTTTT | 233900 |
| rs586606759 | snp | A/G | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127595440 | CCCATAATTCCCAGG[A/G]ATCCAGCACCCTCTT | 233900 |
| rs586753255 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccdc189, Rnf40, Gm166 | GRCm38.p3 | 7:127587249 | AAGGAGAAACAATGT[C/T]TTGAAAACCCCCCAA | 233900 |
| rs587002966 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ccdc189, Rnf40, Gm166 | GRCm38.p3 | 7:127590137 | TCTTAAAAACATGGG[G/T]TTTTTGTTTTTTTTT | 233900 |
| rs587333825 | snp | G/T | | | intron-variant | Rnf40 | GRCm38.p3 | 7:127596987 | TCCTTGCTTCTGAAT[G/T]CGGGGATTCCCTTAG | 233900 |