SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6157685 | snp | A/C/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105247606 | TAGAGGGGTCTGCCC[A/C/G]CAGGGACAGTGCAGT | 71816 |
rs6159285 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Rnf180 | Mm_Celera | 13:105247865 | AATGAGTTGTTTGGA[C/T]GGATGTCACTACTCA | 71816 |
rs6277139 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnf180 | Mm_Celera | 13:105266733 | AGCATAACAGGTCAT[C/T]TCCTTGCCAATAGGG | 71816 |
rs6277538 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105266757 | AATAGGGAACTTACA[C/T]GCTAGACAAGGCTAT | 71816 |
rs6317918 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105159170 | ATATGGAGCTTCTTT[A/G]TATTTTTCTATGGTG | 71816 |
rs6317964 | snp | A/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105159195 | ATGGTGAGGAGATTT[A/T]AATACAAATNATCAG | 71816 |
rs6317978 | snp | G/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105159205 | GATTTNAATACAAAT[G/T]ATCAGATAGCTTCCA | 71816 |
rs6318471 | snp | G/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105159300 | CACACATATACGAGT[G/T]GGTTCTNGAGGACTA | 71816 |
rs6318487 | snp | G/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105159307 | ATACGAGTNGGTTCT[G/T]GAGGACTAGNTTAAT | 71816 |
rs6318501 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105159317 | GTTCTNGAGGACTAG[C/T]TTAATATGACTGAAA | 71816 |
rs6318551 | snp | G/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105159345 | AAAACCTTGTCAGTT[G/T]GACACTATTAAGGTG | 71816 |
rs6318996 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105159366 | TATTAAGGTGGAACA[C/T]TATAAAGGANACTAT | 71816 |
rs6319015 | snp | A/C | 0.42 | 0.183303 | intron-variant | Rnf180 | Mm_Celera | 13:105159376 | GAACANTATAAAGGA[A/C]ACTATTGCCTAGAAA | 71816 |
rs6384347 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105245911 | CAATCGACCAGTCAC[A/G]GGTGGGAGGAGCCAC | 71816 |
rs6385443 | snp | A/C | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105246075 | CTTGCCAGTTTTCTA[A/C]GTTAGGCTGAGAAGA | 71816 |
rs6385500 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105246109 | GCCTAGCTTCTGTTC[C/T]CCACCTACTTCTTCT | 71816 |
rs6385575 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnf180 | Mm_Celera | 13:105246148 | GCTTCCTGACACTTC[C/T]GGCTTTTCCTTCTTT | 71816 |
rs6399070 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Rnf180 | Mm_Celera | 13:105246269 | ATTGTCCTCAGGCTT[A/G]TAGAGAAATGCACAA | 71816 |
rs6399103 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105246294 | GCACAAATGAACATA[C/T]NTCAACANGTGTGAA | 71816 |
rs6399104 | snp | A/C | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105246295 | CACAAATGAACATAN[A/C]TCAACANGTGTGAAG | 71816 |
rs6399118 | snp | A/C | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105246302 | GAACATANNTCAACA[A/C]GTGTGAAGAAGACGC | 71816 |
rs6399222 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105246352 | GACTTACTGAAAATT[A/G]GCTGTANTCTCTCTT | 71816 |
rs6399606 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105246359 | TGAAAATTNGCTGTA[A/G]TCTCTCTTTGCTACT | 71816 |
rs6408929 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105164450 | ataataaaCCAAACT[A/G]CAGAACTTCNGGTGA | 71816 |
rs6409358 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105164460 | AAACTNCAGAACTTC[C/T]GGTGAGAATTTACTT | 71816 |
rs6410441 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105164664 | TATGACCCAGGAAAA[C/T]GTAGGCATTTATAGC | 71816 |
rs6411078 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105164796 | GCTCTTTACTGAAAT[A/G]GATCAATTTCAGAAA | 71816 |
rs6411162 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105164836 | GAGTGACAAAGCAAG[C/T]TTAGAATATACATAT | 71816 |
rs29226507 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rnf180 | Mm_Celera | 13:105153431 | ATATTTGCTGTTCCC[A/G]TTCTCCACTGCCTTT | 71816 |
rs29226789 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105170810 | TTTGACCCAGAATTG[C/T]TCCTGTCTAAAAGAA | 71816 |
rs29228793 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Rnf180 | GRCm38.p3 | 13:105215074 | GCAGGGAGTTCCACT[G/T]GGGCATCTTCTTTTG | 71816 |
rs29228966 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Rnf180 | GRCm38.p3 | 13:105216934 | ATCCCAGAGAGTTGA[A/T]GGCTAGTGTTGGCTA | 71816 |
rs29229081 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105166545 | TCAACCATACAAACT[C/G]TGCATGCATATGTCC | 71816 |
rs29232988 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105200867 | AAGGTGAGTGCCCTT[C/G]CATTTGGAGCACAGA | 71816 |
rs29234261 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Rnf180 | Mm_Celera | 13:105195529 | GGTTGCTTAAACGAT[A/G]CAATAGAATTTTAAC | 71816 |
rs29234297 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105197866 | TACATGTCTGTATGT[A/G]TATATGTCACATGTG | 71816 |
rs29235514 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105208204 | TCCACATTTCCTCCC[A/G]TGAGTATTTTGAAAA | 71816 |
rs29237487 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Rnf180 | Mm_Celera | 13:105206293 | ATTATAAAAAGAACA[C/T]TGCAAAATGCCAGAG | 71816 |
rs29239788 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105223111 | TCTCAGGAGTGCTAT[C/G]CCCTGCTTCTGAATT | 71816 |
rs29240512 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105218927 | AACAACAGACAAGCC[A/G/T]ACAAGCTGTGCAATA | 71816 |
rs29240801 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105207743 | AAACTAGGGCATTGA[A/G]CCTTCACAGAACCAA | 71816 |
rs29242011 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105182822 | TCAGTGAGGATTGCA[C/T]TGCTTCACCTGACAC | 71816 |
rs29242499 | snp | A/G/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | GRCm38.p3 | 13:105216266 | GGGGCCTTTTCTTTC[A/G/T]GAATATATTTATATA | 71816 |
rs29244507 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105174570 | TATAACAAAATATAA[A/C]ATACACACCCCCCCC | 71816 |
rs29244590 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105221282 | AAGATTTTCAATGGT[C/T]TTGACGTTCTTTTTA | 71816 |
rs29245540 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Rnf180 | Mm_Celera | 13:105206554 | CTTCAAAAGGGCTAA[A/T]GGTAGATGCCCTAAG | 71816 |
rs29245684 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105220113 | AAATAAACATCATTA[G/T]TGGGCACTGATCTAA | 71816 |
rs29246961 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105190019 | AAAGAGGTTCCAGAA[A/T]GTCATCTGCACTCTA | 71816 |
rs29247620 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105182019 | CAGAATGTTGCCATG[A/G]CATCAGTCTCTCTTC | 71816 |
rs29250703 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rnf180 | Mm_Celera | 13:105177598 | AGGATGTTTGTAAAA[A/G]GATCCTCACTTTGTT | 71816 |
rs29493555 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105182823 | CAGTGAGGATTGCAT[G/T]GCTTCACCTGACACT | 71816 |
rs29493595 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Rnf180 | GRCm38.p3 | 13:105215106 | TTTCCTCTAGTCTTC[A/G]CAAAATGACCTTTGG | 71816 |
rs29493636 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105195168 | AGGTTTGGCCTCCAT[C/T]GACTCCTGTGTTTGA | 71816 |
rs29493827 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105170328 | CATTATTGAAGGGTG[C/T]TATTATCCTATAGAT | 71816 |
rs29494191 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105183126 | TGAACCTCATTATTC[A/G]TTGGTCCTGAGTAAT | 71816 |
rs29495487 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105203621 | CCTAACTAGACTGCC[C/T]TGTCTGGCTTCAGTG | 71816 |
rs29496553 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf180 | Mm_Celera | 13:105194535 | AATTTTAGAATTTAA[A/G]GATTCACTTAGATGG | 71816 |
rs29496835 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105206060 | TACTTTGTTTTATGC[C/T]TAAAGGTTGCCATAC | 71816 |
rs29508685 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105182945 | GTTGCAGTACCAAGA[C/T]CTGGTGGTTTGTGCT | 71816 |
rs29509285 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105208203 | CTCCACATTTCCTCC[C/T]ATGAGTATTTTGAAA | 71816 |
rs29509713 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105206494 | CTTTCATCTTTATCT[A/T]GTTACCAGATCTCAG | 71816 |
rs29510863 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Rnf180 | GRCm38.p3 | 13:105204278 | CAACCTCAGCCTATT[C/G]TGTCAGGCTCTGCCT | 71816 |
rs29514175 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Rnf180 | GRCm38.p3 | 13:105182321 | CCAGGTGATCCACTG[A/C]AAACACTTAGCTCAA | 71816 |
rs29514595 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Rnf180 | Mm_Celera | 13:105217459 | TTGTTACACTAGTAC[A/G]TTTATTTGGTCTCTA | 71816 |
rs29515950 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105144911 | AGTTCACAACTTGTG[A/G]GCTGTGCCCCCTTGG | 71816 |
rs29517474 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105181803 | CTGTTTCTGTAACAC[A/G]TTCCAAGTGATATAA | 71816 |
rs29526561 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105190249 | ACATACATTATACAT[A/G]ATTTTATATATACAT | 71816 |
rs29528340 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rnf180 | GRCm38.p3 | 13:105204446 | TGTATACGTCTCCAT[A/G]CATGCCCCAGTCCAC | 71816 |
rs29528985 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105170761 | GATGGGACATTAAGT[A/G]GAGGAATAGGGCTGC | 71816 |
rs29530190 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105211130 | AAATATAAGATATAT[A/G]AAGATCTTATACTTT | 71816 |
rs29533954 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Rnf180 | GRCm38.p3 | 13:105208259 | TCTGATGTATTGTCA[C/T]TTTCTAATGCTTTCC | 71816 |
rs29534475 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105222205 | CTGTGCAGGTGAGGT[A/G]CAGGGCCTGCTCCTA | 71816 |
rs29534818 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105251436 | ATACTATTTTATTTA[A/G]TACTACTGAGAGGAA | 71816 |
rs29546049 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105172000 | TGGTTCCTATGGGCT[A/C]ATATATTTGAGTACT | 71816 |
rs29546929 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105200892 | CACAGATGCTCAGAA[C/T]TAAGAATTCATCTTG | 71816 |
rs29551192 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105171737 | GATGGCCCCGGATGT[G/T]TACTTCCTATTACAA | 71816 |
rs29573910 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105197901 | TGTGCCCAAGTGGGC[A/G]AGAAGGTGCTAGATC | 71816 |
rs29584878 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Rnf180 | GRCm38.p3 | 13:105208216 | CCCATGAGTATTTTG[A/G]AAAGCTTTTAAGGCC | 71816 |
rs29589036 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105219839 | TGCCCATTTGGGGAC[A/G]AGCTACGGTGGAAGC | 71816 |
rs29590016 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105221324 | TTTAATACCAGTGTG[C/G]GCATATGCGAGTGGG | 71816 |
rs29620659 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Rnf180 | Mm_Celera | 13:105190050 | GTGTCCATTATTGGG[A/G]CTGTGGGCTAAATTA | 71816 |
rs29638873 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105185302 | AGTCTACCTCTTACC[A/G]TGATATATTAATCAA | 71816 |
rs29639669 | snp | A/C/T | 0.426035 | 0.177515 | intron-variant | Rnf180 | GRCm38.p3 | 13:105214492 | GAAGTGTCAGAAGTG[A/C/T]GTGCTGCCTAGCACT | 71816 |
rs29665165 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105191546 | GGCTACATAGCTCAA[A/G]CTGGTCTTGACTTGC | 71816 |
rs29676236 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf180 | GRCm38.p3 | 13:105187223 | AGAAAGTGTATCATA[C/T]CATGCGACCCAGAAA | 71816 |
rs29679204 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105198270 | ACAATATACTCAAGG[A/G]AAGTAAAGGATGGGA | 71816 |
rs29682018 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105172089 | AGGTGGGGGGGGGGG[C/T]GCTTTGAGATTTCAA | 71816 |
rs29710382 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105182516 | ATGAGATCAGTGAGT[A/G]AGATTTGAAAGGACT | 71816 |
rs29734770 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rnf180 | Mm_Celera | 13:105206373 | AAAAACGACGACCTT[A/G]AGTAAACAGTTCCTG | 71816 |
rs29755934 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105190413 | CTGTCCTCAAACTCA[C/T]AGAGATGCACCTGTT | 71816 |
rs29757792 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105172119 | AAAGCCCATACCATT[C/T]TCAGTTAGCTCTCTT | 71816 |
rs29763642 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105172087 | GGAGGTGGGGGGGGG[G/T]GTGCTTTGAGATTTC | 71816 |
rs29777384 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105170766 | GACATTAAGTAGAGG[A/G]ATAGGGCTGCCATCC | 71816 |
rs29779487 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105190530 | AGTGTTTAAGCCTGG[A/G]TTGCACATGTGTATG | 71816 |
rs29781053 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105207969 | TAACTCCTCCATTAG[A/G]AACCCCATGCTCAGT | 71816 |
rs29783619 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105148844 | AGTATATGTACTAAA[C/T]TGTAATTTGGGAGAT | 71816 |
rs29834280 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105214048 | CTTCGTAATTTTGCT[C/T]CTGTCATGAACTGTA | 71816 |
rs29853132 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105203042 | TCCTGACAAACCATG[C/T]TCACATGCAATTGTG | 71816 |
rs29856291 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnf180 | Mm_Celera | 13:105190125 | AACTCTAAAATAAGT[C/T]CTTCATTATTCCTGT | 71816 |
rs29864903 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Rnf180 | Mm_Celera | 13:105293552 | TACATCAGGCAAGTT[C/T]TAATACCAGCTTCCA | 71816 |
rs29871246 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | GRCm38.p3 | 13:105220719 | ACAATTTTCTCCTTT[C/T]CTGCCTTTTATCTCC | 71816 |
rs29895543 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105184880 | TTCTCATATATATAT[A/G]TATATATATATATAT | 71816 |
rs29903598 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105202939 | TGGTGAGTTTTCATA[A/G]TGCCAGAATGTACTG | 71816 |
rs29913824 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105222319 | AGGGCAGCATCTCTC[C/T]CTCACCCATGTAACC | 71816 |
rs29918722 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105221326 | TAATACCAGTGTGCG[C/T]ATATGCGAGTGGGAA | 71816 |
rs29926948 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105226876 | GAAAGAGAATTTAGT[A/G]TACTGGGTTATTATT | 71816 |
rs29927642 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105191173 | GCTTGGTGCTAGCCC[A/G]TATATGATTCTTGGA | 71816 |
rs29948039 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Rnf180 | GRCm38.p3 | 13:105214967 | CTGGAAGCTGTCATG[C/T]GGTTTCCTTGTTGGC | 71816 |
rs29960112 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf180 | Mm_Celera | 13:105182625 | GAAATTAACTACCGA[A/G]CCCTCTATTACACAT | 71816 |
rs29962425 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105183085 | TTGAATTTTCACTTT[C/T]CTTTTAGGCATGGGG | 71816 |
rs29964281 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105221584 | CACATCATGCACCCC[A/G]GCCCACTCATCTCTC | 71816 |
rs29967062 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105186211 | CTTAGGAAGGACTCA[A/C]TGATGTGACTCGGCT | 71816 |
rs29975637 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105182040 | GTCTCTCTTCCTTCT[C/T]GCACTGTACCTGGAA | 71816 |
rs29995750 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105195892 | TTCCAGTATAGCCAG[A/G]GCTACACAGAGAAAC | 71816 |
rs29996322 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Rnf180 | Mm_Celera | 13:105185225 | GTCATGTTAGCTTTT[G/T]GATAGTTTCCCCAGT | 71816 |
rs29997718 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Rnf180 | GRCm38.p3 | 13:105191073 | TGGTGTATTATGTGC[A/G]TGATGTGGGGACATG | 71816 |
rs30001939 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105203200 | GGTCACAGGCCCTAG[A/G]GGACATGCTACTATT | 71816 |
rs30004186 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105185486 | AAACTCTTGTCATAA[A/G]GAGTGGTAGTAGGCT | 71816 |
rs30008365 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105227636 | CTTGGTGGCAACCAA[C/T]ATCTCTCTAAAAGGA | 71816 |
rs30024234 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Rnf180 | GRCm38.p3 | 13:105204486 | GGTTCCCAACCTGGC[G/T]GCATTGCCTGCTTCT | 71816 |
rs30064100 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105182940 | CTTGTGTTGCAGTAC[C/T]AAGACCTGGTGGTTT | 71816 |
rs30070344 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105199288 | CTGTGCTCAGTCCGA[G/T]GGTTGGCTGTGAGTA | 71816 |
rs30072505 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105206043 | TCTACATATGGGGGG[A/G]ATACTTTGTTTTATG | 71816 |
rs30073144 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Rnf180 | Mm_Celera | 13:105293899 | AAAGTCTGCACAGTC[C/T]CGACTCTGGGCTGCA | 71816 |
rs30079042 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105210989 | ACCTACAACAACCCA[C/G]ACGTCACCATTTAAC | 71816 |
rs30081406 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105216425 | GAGAAGAGAGGAAAG[A/T]TGAGGGGGGAAAACA | 71816 |
rs30092203 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105170630 | GGAAGATAGGAATGG[C/T]GGGACCCTCTAGAGA | 71816 |
rs30094073 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105204253 | CAAAAAACAACACTC[C/T]TTCATACTTCAACCT | 71816 |
rs45634188 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105278842 | GGGTAGTCCTTTGAA[A/C]AGTTTTGAACAATTT | 71816 |
rs45638259 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Rnf180 | Mm_Celera | 13:105206800 | GGCCTGGGAAGAGAT[A/G]GCCCAGCCAAGTGAT | 71816 |
rs45646360 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105169307 | GCAGGGTCAACCTGA[G/T]TTCATGATCCTCGGA | 71816 |
rs45646554 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105251549 | AGATATTTCATTCTC[G/T]TGATACAACTATCAA | 71816 |
rs45650947 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf180 | Mm_Celera | 13:105178286 | ATTATAGAACTTTAC[C/T]GAAAAGTGACAAACT | 71816 |
rs45672461 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Rnf180 | Mm_Celera | 13:105296479 | TGAAATAACATGCAT[C/T]GAAGAAACCCAAATG | 71816 |
rs45690154 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105279664 | TCTCAACCCGGTCTT[A/C]GCAATACAACTTGAG | 71816 |
rs45725160 | snp | C/T | 0.277778 | 0.248452 | upstream-variant-2KB | Rnf180 | GRCm38.p3 | 13:105296740 | GTTAAAGGACACCGA[C/T]GGTCACATCCCAAAC | 71816 |
rs45729725 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Rnf180 | Mm_Celera | 13:105205910 | GTATCGTACCAAGAG[C/G]CTCAGGTATATTGGC | 71816 |
rs45730205 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105283128 | GCTATGCCCCACCCC[A/C]TAAGTGTCCACTATC | 71816 |
rs45736677 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105259376 | TAGTAACCATTTCAC[C/G]CACAGATCACAGGTC | 71816 |
rs45775413 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105174340 | TACTACATAAAACAA[A/T]TTTAAAATTTAAATA | 71816 |
rs45781143 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105271448 | ATGAGTGTAAGCTGT[A/T]GCATTCTGCGGGATC | 71816 |
rs45786016 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | GRCm38.p3 | 13:105208657 | TAAATGTGGGATCAA[A/G]GACAGTTTAGTCTAA | 71816 |
rs45792245 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105146778 | TAGTTGGTTAGAAGC[A/T]AAAAGGGAATATATT | 71816 |
rs45801671 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105150549 | CTCAAACTTTCACTT[C/T]GATAGAGGCAGCAAG | 71816 |
rs45803255 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105192335 | TTCATGTGGACTCTG[A/G]CATTGCTGAAGCTCT | 71816 |
rs45806721 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105205021 | CAACCTTATTACATT[G/T]TTCTTAACTTTATTT | 71816 |
rs45818730 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Rnf180 | Mm_Celera | 13:105204679 | AATTTCTGTAATAAC[C/G]TTCTGAATCATTGGT | 71816 |
rs45831519 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105184489 | TAGGCTAGATGGGAA[A/C]GGGCTCTAACTATTT | 71816 |
rs45841305 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105186128 | GACAACTCACTTTTG[C/T]CCTGGCATGCATTTG | 71816 |
rs45853578 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105235034 | TCACTCCTAACAAGC[A/G]AATCATCCTGTCTTT | 71816 |
rs45854744 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105209136 | AGGGACTCTCGGATA[A/T]CCCTAAGCATGAGAT | 71816 |
rs45864283 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105198419 | AGGCTCAAGAGAAAC[G/T]GCTATTTAAAGCATA | 71816 |
rs45892961 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105231000 | AATCTTAAATGGCAA[C/T]ATTTTTCACTTTATT | 71816 |
rs45894039 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105243679 | TCAGGAAATGCTGAT[A/G]ACATCGCTCCCACCA | 71816 |
rs45898426 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105279506 | AGCAGGAAGCCATAA[A/C]ACACTGCATGCTTGG | 71816 |
rs45917000 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105206680 | CAGAATTTAAAATAC[C/T]TCCCATAAAGTAGAA | 71816 |
rs45922897 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105252643 | TGACTCTGACTTTCT[A/T]TGGATCCTACTGTCA | 71816 |
rs45924529 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105248742 | AACCCTACTTACTCT[A/G]TCTGAAGCACTCAGC | 71816 |
rs45929171 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105252730 | GGAGTGAACACAATC[C/T]GACATGCTGACAACC | 71816 |
rs45945647 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105249125 | AAATGTCAGTCTCAA[C/T]ACTCAGTCAAGTTAT | 71816 |
rs45968675 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105256718 | GTCAATGAAGGTAGT[A/G]TTTCCCATAAAGAGG | 71816 |
rs45968723 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105198478 | GTTTTTAGGGATAAA[C/G]AGAAAGGACAGAGAA | 71816 |
rs45972834 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105242122 | AGTGAAGCCATATAT[A/G]AAGAGTTAGAATGGA | 71816 |
rs45973456 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105146313 | AAGAACGAGCAACAC[C/T]TTATATTCTAACCTG | 71816 |
rs45983437 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105252249 | TGGAACCAAGAAGCT[C/T]ACCTTCTGCAGCAAG | 71816 |
rs45987854 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105193308 | AGGTACATCAAATTT[A/G]CCACATGTGGGTTGC | 71816 |
rs46048691 | snp | C/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105226123 | TATACTGAGGCAAGG[C/G]AACTGTCATTTTGAA | 71816 |
rs46057642 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105277931 | GAGCTCCTCACATTC[A/C]CTTTATCTCTTCATG | 71816 |
rs46077720 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105186761 | TTAAGTGCCTTCTTC[C/T]ACAACAACTAAATAT | 71816 |
rs46101172 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105231292 | AGGCCTTAAAAGAAC[A/G]GAGAAATCCAATGAA | 71816 |
rs46103632 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105161879 | TATTAAATAAATCCA[C/G]TACAACGGGCTTGCT | 71816 |
rs46117280 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105147917 | CCATAAGTCAGTTGC[A/C]CTGTGGAATCAAAGG | 71816 |
rs46125956 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105281092 | TGAAGTCAGTCTTAA[C/T]GGTTCTTGGATATTC | 71816 |
rs46127673 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105268966 | AGTCGTCTGGGCAGG[C/T]GTCAGAATGTAGGGG | 71816 |
rs46128625 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105267054 | TTCTCCTTTGGATGG[A/G]ACTTAATTTTTTAAA | 71816 |
rs46139802 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105271536 | GAATTCCAACTTAGG[C/T]CATGGACAGGTCCTG | 71816 |
rs46143183 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rnf180 | Mm_Celera | 13:105220463 | CACTGAATAGTATGT[A/G]TAGCCAACCTGTCTA | 71816 |
rs46143775 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105186357 | AGCAGACAACTGGTT[C/T]TCATACTCAATCGAT | 71816 |
rs46156187 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf180 | Mm_Celera | 13:105189497 | ACAGCATATGGAAGT[C/T]ATCTTAAATATAGCT | 71816 |
rs46157055 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105193077 | CTGTCCCAAAGGCTC[C/G]TGTAATCCAGTGTGC | 71816 |
rs46163526 | snp | A/G | 0.42 | 0.183303 | intron-variant | Rnf180 | Mm_Celera | 13:105144834 | ACATGATGAATGCTA[A/G]AAGTACACTTTTTCT | 71816 |
rs46181970 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105193415 | AGAAAAAAATGTGAT[C/T]GGTTTAAGCGAGGAA | 71816 |
rs46182866 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf180 | GRCm38.p3 | 13:105214590 | CAATATGAAGCCTAG[A/G]GTTTTGCTGTCCAAG | 71816 |
rs46198444 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105221149 | AGAACAGACATGAGG[C/T]TGACCTCTGACCTCT | 71816 |
rs46202692 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105285013 | TCCCTATCCCTTGAC[A/C]AATAGGTACAATACA | 71816 |
rs46208774 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105192334 | TTTCATGTGGACTCT[C/G]ACATTGCTGAAGCTC | 71816 |
rs46219211 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105266141 | TTACTTTTAAATTAA[C/G]CAAAACAACAGACTA | 71816 |
rs46223475 | snp | C/G/T | 0.42 | 0.183303 | intron-variant | Rnf180 | Mm_Celera | 13:105237935 | TCATCTGAGAGGAAA[C/G/T]CAAGAATGTCTTTCC | 71816 |
rs46229828 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105252731 | GAGTGAACACAATCT[C/G]ACATGCTGACAACCA | 71816 |
rs46243789 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105231637 | CACAATCATTCATCA[A/G]TTTCTATCCTTTGAC | 71816 |
rs46276620 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rnf180 | Mm_Celera | 13:105158164 | CAGTTAGTTTATCAG[C/T]ATCCAACTGGTATCA | 71816 |
rs46277100 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105205295 | CAGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 71816 |
rs46283039 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf180 | Mm_Celera | 13:105162770 | TATGTTATTCCATAT[C/T]AGTGGAGAAGTGATG | 71816 |
rs46283615 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105142220 | CAAGTCTAAGGTATT[A/C]AGCCTGCAGAATTTG | 71816 |
rs46291694 | snp | C/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105193642 | GCAGACAGGTGTGTA[C/T]CGCGTGGCAGAGCTG | 71816 |
rs46300909 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105217042 | GTGTACCAGCTCAGG[A/G]CGACATGCACAATAA | 71816 |
rs46321644 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105245621 | AATGTATTACAATAG[G/T]GCATATTTGTGTAAT | 71816 |
rs46345966 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rnf180 | Mm_Celera | 13:105284055 | ACAAGTAAATACCAT[C/T]AAGATGCACAGATTA | 71816 |
rs46349009 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Rnf180 | Mm_Celera | 13:105205890 | CACAAAGATTGAGAT[A/G]TCAAGTATCGTACCA | 71816 |
rs46351258 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105215676 | TCTATCAGCATCATT[C/G]AATTTAGGATTAAGA | 71816 |
rs46359707 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105243970 | TTATTCCTGGGCATC[C/T]ATTCAGCTGTCTCCA | 71816 |
rs46360785 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf180 | GRCm38.p3 | 13:105283653 | CAACTTAAAGAAGGA[C/T]GCAGTGTTCAGTGTG | 71816 |
rs46381257 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105271461 | GTAGCATTCTGCGGG[A/G]TCCCAAACTGATGCT | 71816 |
rs46383114 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105169110 | GTAATGGTGCCTGAG[C/T]TACTGTTGGGACGAG | 71816 |
rs46416884 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105205854 | TGTACAACTGGAGCC[A/G]GCTGTAAAGTGGGCT | 71816 |
rs46419412 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105249117 | TCTGCTACAAATGTC[A/G]GTCTCAACACTCAGT | 71816 |
rs46429899 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105278803 | GGAAGGATGAGACAC[C/T]GAAGTCTAACTTATT | 71816 |
rs46431267 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rnf180 | Mm_Celera | 13:105228487 | GCTAAAAAAATTTCC[C/T]GAACATCTTCCATTG | 71816 |
rs46436729 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105235212 | CTTCTCTATCAGCAT[A/G]TGGCACTTTTCTACT | 71816 |
rs46458196 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105267599 | GTCACACCCTACCAG[A/T]GACTTCTCATCTATG | 71816 |
rs46495857 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf180 | Mm_Celera | 13:105153874 | CATTTAGGAGTGGAC[A/G]TACAAATTTCTCATA | 71816 |
rs46499982 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105252947 | CAGCCCATGTTAAAT[C/T]CCCCAAGATGGTAAC | 71816 |
rs46501146 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105205165 | TAAATCCACATTGGG[C/T]TGCAGGCTCCTGAGG | 71816 |
rs46502107 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105248180 | CTCTGTTAGTCGCTA[C/T]ACTGACAGGTAGCAC | 71816 |
rs46506258 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Rnf180 | GRCm38.p3 | 13:105205034 | TTTTTCTTAACTTTA[C/T]TTAGCAAAGCATAAA | 71816 |
rs46507159 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105254318 | AGAGGACATTACTGC[A/G]TAGGTGAAAACTTAG | 71816 |
rs46527017 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105258638 | CCATTATAACACCAA[A/G]ATATTTAAGAAGTTT | 71816 |
rs46530376 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105205337 | TCCAGGACAGCCAAG[A/G]CTACACAGAGAAACC | 71816 |
rs46537451 | snp | C/T | 0.244898 | 0.249948 | downstream-variant-500B, intron-variant | Rnf180 | Mm_Celera | 13:105147459 | TGAGTTCTGCTTAGC[C/T]TACCTCTAAAATATT | 71816 |
rs46537804 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105189107 | CTACCAACATCCTGA[C/T]ACTTAGAAAGCACTA | 71816 |
rs46540966 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Rnf180 | GRCm38.p3 | 13:105145437 | TACTTCTTTCTCTGA[C/T]TAATATTGAGTACAG | 71816 |
rs46548509 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105274916 | TCATTAAGAATAAAT[A/G]TGTGCAAATCTATAG | 71816 |
rs46556373 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105249595 | TTTCTTGCTAAACTG[A/G]TTGCAAAGCGCTTAC | 71816 |
rs46568965 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105228788 | TTTCTTCCTCACTTA[A/C]CAAAAATATATAATA | 71816 |
rs46586660 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105186036 | AAGCAGGTTCAGGAA[C/T]AGAAGTATCGATACA | 71816 |
rs46611059 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105252119 | CCAGAAAGAGTGGAC[A/G]AGCAGGTGAGTGTAA | 71816 |
rs46614133 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105224880 | TTTAATATTTAAAAT[A/G]AGTCGACAGTTCTTA | 71816 |
rs46629891 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105230748 | CACTGAAGTAGAATG[C/T]CCTTAGAGATGACCT | 71816 |
rs46639308 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105245946 | CAGAATGGGGACTCA[C/T]CATAAACCCTGCTAA | 71816 |
rs46644246 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105160389 | CATCTAGATGTATCC[A/G]TGGCGCAGAGCAGGA | 71816 |
rs46650798 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105186370 | TTCTCATACTCAATC[G/T]ATAAGGTACTCTAAA | 71816 |
rs46668077 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105231227 | TTGCCCATGTCTTCA[C/T]AACGATGGACAACAC | 71816 |
rs46670976 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105186135 | CACTTTTGTCCTGGC[A/C]TGCATTTGAGAGAAA | 71816 |
rs46677354 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105235471 | TTAATTCTCTGGAGT[A/G]TCACTTTTTATTTCC | 71816 |
rs46680531 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105279071 | CTGCTATAGTGGCTG[A/G]CGCTTCCTGAATGTT | 71816 |
rs46693884 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105158065 | TTTGAAAATGAATGG[A/G]AGTAACAGGGATAGA | 71816 |
rs46710405 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | GRCm38.p3 | 13:105193613 | ACATGGACGAGACTG[A/G]ACAGGAAGTGGCTGC | 71816 |
rs46710609 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105216139 | ATATAACCAGCTTCA[A/C]TGAATTTTTAAAGGC | 71816 |
rs46728527 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105145146 | ACTAGGGTGATTGCT[G/T]TATAGGATTTGGATA | 71816 |
rs46730787 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105224320 | CGTCATGACATGTGC[A/G]GCTTCCTGTCATATG | 71816 |
rs46730799 | snp | C/G | 0.336735 | 0.234472 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105147510 | AGCAGTTAACAGTAC[C/G]GTCAATTTTATATTA | 71816 |
rs46792778 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Rnf180 | Mm_Celera | 13:105183265 | CCATTTTGTATTTAT[G/T]TAAGAACCATTGTCC | 71816 |
rs46794718 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105259378 | GTAACCATTTCACGC[A/T]CAGATCACAGGTCAG | 71816 |
rs46809165 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rnf180 | Mm_Celera | 13:105158734 | GAATGAAGCTGTTGC[C/T]GATTAGAGTAGCTGT | 71816 |
rs46850070 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105248711 | CCTATAATTATGCTA[C/T]GTAACTGACGAAGGA | 71816 |
rs46852209 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | GRCm38.p3 | 13:105208721 | AAGTGAAAGGTCAGT[C/T]AAGTGCCAAACAATC | 71816 |
rs46861618 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105248135 | TGCCTGTCTGCTGCG[C/T]AGTCTACCAGTGACG | 71816 |
rs46875354 | snp | A/G | 0.42 | 0.183303 | intron-variant | Rnf180 | Mm_Celera | 13:105240904 | CTTACAAAGGATGAA[A/G]TCTCATCGTTTTTAA | 71816 |
rs46883948 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105285419 | CCTGTGCCTCTGTAC[C/T]CTCTCCTGATTCTCT | 71816 |
rs46885454 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Rnf180 | GRCm38.p3 | 13:105205601 | CAGTCAGAGCACTCT[C/G]TATGGAGCTTTCAGG | 71816 |
rs46895861 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105205263 | TTTAATCCTAGTACT[C/T]GGGAGGCAGAGGAAG | 71816 |
rs46919663 | snp | A/G/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105227383 | TCCCAATGGCGTAAA[A/G/T]TAAGTTCCTTTTGTT | 71816 |
rs46946478 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105217841 | AGTGCATATTTGTTT[C/T]CCATGAAAAAGGACT | 71816 |
rs46948042 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105175654 | TGGCCAATTGCGCCC[A/T]TGATGAAAATTCCAA | 71816 |
rs46949060 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105168599 | AGTCCACTGCCAGGA[A/G]CATCCCTTCAGTCAA | 71816 |
rs46960296 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rnf180 | GRCm38.p3 | 13:105249752 | CTGGGAGAGGTGCTC[C/T]TCTTGGTCCGAGGCC | 71816 |
rs46976134 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105165703 | TTGGACTCTTGTTTA[C/T]GCTACTGGAGACGTG | 71816 |
rs46977696 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105197190 | TCACCTTGTACCCAA[C/T]CTCTTTCTCACCAAG | 71816 |
rs47013454 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105257804 | CCAGGCTAATGGGTT[C/T]CAAGCTAAAACCATG | 71816 |
rs47056511 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105144767 | ATGATCTGTTAAAAA[C/G]TTACCACAATATGCT | 71816 |
rs47087643 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rnf180 | Mm_Celera | 13:105155192 | CATGGAGCATCTCCA[G/T]CTGTGGCTCGATTAG | 71816 |
rs47088162 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105141715 | GAGCAGCGTGCAGAG[C/T]GTTGGTTCTCCGTGA | 71816 |
rs47124853 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105153453 | ACTGCCTTTTCACAT[G/T]GTTTTCCGATGGGTT | 71816 |
rs47141873 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105284641 | ATGTTATCTTCAATA[C/T]GATTAACAGTTTTTA | 71816 |
rs47150070 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105194952 | ACAGAGAGCAGTAAA[A/G]GGAAGATAGGAAGCA | 71816 |
rs47157145 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105281185 | CCATATTCCCACAGA[A/G]CTCCTATCCCATACC | 71816 |
rs47157624 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105240809 | ACAACAAATGTCCCC[A/G]CAAAACTGGAGAACC | 71816 |
rs47169726 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rnf180 | Mm_Celera | 13:105158783 | CAGTTAGAAGCCAAA[C/G]CACACTGCAAGTCTC | 71816 |
rs47174679 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105269669 | TATTTCACAGTCTCT[C/T]TTCTAGGAAGCCTTC | 71816 |
rs47204945 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105150990 | GTGGCCATATATGGG[C/G]AGTTCTGCAATGCTC | 71816 |
rs47205069 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105241835 | TGCTGTTCTTGTGTT[A/G]CCTTCGCATGTGAGA | 71816 |
rs47208208 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105187613 | AATACAGCTTGAGAT[A/G]CCTATCAAATATTAA | 71816 |
rs47212654 | snp | A/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105224952 | ATACTGGAATACTTA[A/T]ATAGCGTATGGACCT | 71816 |
rs47216565 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rnf180 | Mm_Celera | 13:105141486 | AGACCCATTTAAAAC[G/T]CTTCCAAATTGCTGT | 71816 |
rs47222213 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105268416 | AGTACCATCCCAGCA[C/T]CAACAAATTGACCCA | 71816 |
rs47236203 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105268841 | GAAAGTTGCCTCTCA[G/T]ATTTGTGCAGAGATG | 71816 |
rs47236819 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105178670 | AATAAGGACAAAGGT[C/T]AAACAACTGACGCTA | 71816 |
rs47246509 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf180 | Mm_Celera | 13:105161274 | TGATAATGAGTAGAA[A/C]AAAAAGCATAAGAAA | 71816 |
rs47264920 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, intron-variant | Rnf180 | Mm_Celera | 13:105147151 | ATTCACTTATCTACT[C/T]TTTTTTGATGTGTAT | 71816 |
rs47265215 | snp | C/T | 0.124444 | 0.216185 | missense | Rnf180 | GRCm38.p3 | 13:105249829 | GGCTGTTAGCGTTAG[C/T]GTGATCCGAGTAGAC | 71816 |
rs47277960 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105170963 | ACAGACAGAAACCTA[A/G]CATGGCTGCCTCTGA | 71816 |
rs47281896 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105136022 | CAAATAATTTCTACT[C/T]TCCTTCAAATTCATT | 71816 |
rs47286792 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105196405 | AAGTTTCTGAGAACA[A/G]AGATGATACTGGCTG | 71816 |
rs47303276 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105190972 | TGACCAATAATCATA[C/T]GAAATTTAACTAAGG | 71816 |
rs47315487 | snp | C/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105187717 | CACAAGTCTGGCTGC[C/T]AGCACTCACAGCAGG | 71816 |
rs47318784 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105186510 | CTAGATTAACTGCAG[C/T]GTTCCCTATGAATTC | 71816 |
rs47350119 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105209545 | GATAAGGACTTGGAT[A/T]CCATGACCCCAGGAA | 71816 |
rs47365184 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rnf180 | GRCm38.p3 | 13:105207178 | ACAAAAACAGACAAT[C/T]GATCATGCTAACTCC | 71816 |
rs47380145 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105283693 | AATGCTTCAGATTTC[A/G]TACAACAAACCTTTG | 71816 |
rs47382133 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Rnf180 | Mm_Celera | 13:105185555 | GATTTTCAAACTGAG[A/T]ATTAAACATGTTACA | 71816 |
rs47403328 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105234736 | ATGGGGCAGCAGGCA[C/T]GACAACTACTCAACT | 71816 |
rs47410506 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105283725 | TGACTACAGCCATAA[C/T]TTCTGACCCAGCACT | 71816 |
rs47426686 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf180 | Mm_Celera | 13:105144116 | CATTGAATTGAAACT[A/G]TTATTAGCTTTGTGT | 71816 |
rs47445794 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105192241 | TTCACTGTGGGGATG[A/G]GAGCACAGCACTGTT | 71816 |
rs47456341 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105186788 | ATATTTCTTCATGGA[A/G]GATGTCATTTGCAAC | 71816 |
rs47470252 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105252196 | AGGAAGAGAAGCCCA[C/T]GTGACTGGGTTGAAG | 71816 |
rs47483001 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105251601 | GGTGCAAAGGACATA[C/T]GACCTAGCAAAGAGT | 71816 |
rs47491823 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105158224 | CTCTTGAAATCCTTA[A/G]GAATAGTCAAAGGAA | 71816 |
rs47520952 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105186222 | CTCACTGATGTGACT[C/T]GGCTACTGTTGGTCT | 71816 |
rs47522935 | snp | C/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105225364 | ACATGTCCCCAGCTG[C/T]GCTGCCCATCTTAGA | 71816 |
rs47527120 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Rnf180 | Mm_Celera | 13:105130109 | ATTAGAATAATAATC[C/T]ACACCACTTTTGTAT | 71816 |
rs47530643 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rnf180 | Mm_Celera | 13:105130982 | AGAATACATAGTGCT[C/T]GACTAAACATCTTAG | 71816 |
rs47532797 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105198843 | CACAGTCTGCATTTA[A/G]TATACACTCCAGAAG | 71816 |
rs47534062 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105231241 | ATAACGATGGACAAC[A/G]CAATTTTTCTCGCAC | 71816 |
rs47544084 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105254126 | CTTATCTCAACAGAG[C/T]TTGAAAACAGTTTCA | 71816 |
rs47544185 | snp | C/G | 0.142012 | 0.225474 | missense | Rnf180 | Mm_Celera | 13:105181543 | TTCGTAGGCAGGGCT[C/G]GCAGAAGATGTGGTG | 71816 |
rs47546927 | snp | C/T | 0.152778 | 0.230321 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105148007 | GAGCTCTGAAAGGAG[C/T]AATCATCTTTATGTG | 71816 |
rs47552982 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105210535 | TGTGAAGCCCTTTTC[A/G]GCCGACTGTCCTCTA | 71816 |
rs47564877 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105196796 | TGTATACAGCAATGA[A/G]CATGCCATTTTAGGG | 71816 |
rs47566765 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105237262 | CTTTTTAACATTTTC[C/T]GCAGCAAACATCAAA | 71816 |
rs47596365 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105183014 | ATGTTTACTTTCCAT[A/G]GTCATTCTCATTTCA | 71816 |
rs47609478 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105186445 | TGTACAACTGTCCAA[C/T]GCGTCAGTGCAGAAT | 71816 |
rs47609785 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105192827 | ATAATAAAGTCAGGA[A/G]TGGTCTAGCGGCTAA | 71816 |
rs47646245 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105235059 | GTCTTTGAAGCTAGA[C/T]GGTGGAAGACCATCT | 71816 |
rs47652728 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105199391 | AATCCAGACACTATT[A/G]CTGATGCCAAGAAGT | 71816 |
rs47657115 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105230250 | ATGTGGAGCTGTTGC[C/T]TAATAACACAGACTG | 71816 |
rs47662229 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rnf180 | GRCm38.p3 | 13:105235124 | AAGGCTGTTCTATCT[C/T]CATGGGAACATCTCT | 71816 |
rs47706680 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105183144 | GGTCCTGAGTAATGT[A/G]TTATACATGGTTTTC | 71816 |
rs47708765 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105280868 | TTTACATTGGCATTC[A/G]CTAAGTCAAAGATAT | 71816 |
rs47724667 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105131850 | GCAGGGCAGCAGACA[C/T]ACTTGGATCAGTGAC | 71816 |
rs47726177 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Rnf180 | Mm_Celera | 13:105181821 | CCAAGTGATATAAGC[G/T]TAATCTGTTAAAGTG | 71816 |
rs47731246 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105185697 | CTATAGCTTATGGAA[A/T]GGCAGCATGGATGGG | 71816 |
rs47746274 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105178778 | TGAATGACAAAGGGG[C/T]AAGATTGCTATCCAC | 71816 |
rs47752281 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105186161 | AGAAACTGTCACCTC[C/G]GATAAACTGGGAGTC | 71816 |
rs47762667 | snp | C/G | 0.18 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105153843 | CTCAAGGCTTGCTTG[C/G]TTGACTGGAGTTACA | 71816 |
rs47767687 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105134892 | CATGGGTCAAGTAAC[A/T]AACATTGCTAGTATG | 71816 |
rs47770037 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105199374 | TGATGCCAAGAAGTG[C/T]TTGCTGACAGGAGCC | 71816 |
rs47776991 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105251657 | CCATTCTGTTGGAGG[C/T]CCTTAGAAATTAACA | 71816 |
rs47782474 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105280955 | AACAATTCTAGGCAC[A/T]GGACCTGCAGTGACT | 71816 |
rs47790893 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Rnf180 | Mm_Celera | 13:105193424 | TGTGATCGGTTTAAG[C/T]GAGGAATACATAAAT | 71816 |
rs47841121 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105255533 | CCAACACCTGAATGA[C/T]GGCTTAGAACTGTCT | 71816 |
rs47842856 | snp | C/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105225193 | AGAGTCAATCAGACA[C/T]GGTGCAGGTTGAAGG | 71816 |
rs47848464 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105141951 | CCTGGAATAATGCTC[A/T]GAAGGAGACATGCCC | 71816 |
rs47849619 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105168670 | GTGCCTCCTCTGTGC[A/C]ATTCACACTCTTGAA | 71816 |
rs47857790 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Rnf180 | GRCm38.p3 | 13:105249632 | CTGTAGCCATCGTTC[G/T]CGCCTCTGCTGCCTT | 71816 |
rs47865606 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf180 | Mm_Celera | 13:105144690 | GGGAGTAATATAATT[C/T]TCATTCCACTAGGTA | 71816 |
rs47868384 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105234115 | CTAAAACAAAGAAAT[A/C]ATTTAAAAAGGGAAT | 71816 |
rs47886941 | snp | A/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105193592 | GCAGAACACAGGACA[A/T]GAAAGACATGGACGA | 71816 |
rs47896202 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105153358 | CAATATTTTTGTACC[C/T]TTCTATTTAAATAGT | 71816 |
rs47911420 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105234594 | GTTTTCAATTTACTT[A/T]GCCCAGATTTCTCAG | 71816 |
rs47911819 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105234691 | GTCAGAACTACTGCA[C/T]GATCCGATCCATGCG | 71816 |
rs47915123 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105184753 | GGGATTAAAGGCATG[C/T]GTCACCACTGCCCGG | 71816 |
rs47919323 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Rnf180 | Mm_Celera | 13:105183041 | TTCATAAAAGAACAC[A/T]GCTGAGTTTGAGCTA | 71816 |
rs47923969 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105284590 | AATATTTACTTCCAG[C/T]CTGAATATCTTTAAA | 71816 |
rs47943422 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105252799 | TGTCCTGAAGTCATC[C/G]AAGTTGAGAAAGAGA | 71816 |
rs47980454 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105185800 | ACTACTCCAAGAAAA[A/G]TGAGCAAAGATAAGG | 71816 |
rs47993532 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Rnf180 | GRCm38.p3 | 13:105173473 | AAAGCAATGGAAATT[A/C]ACAAGCTGTTACCAA | 71816 |
rs48059911 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105180875 | ATGCTTATGCTCCCA[C/T]GAAAGGAGGAGTAAC | 71816 |
rs48062520 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105171294 | ACAGTTGATACGAGG[C/T]CCCCAACACATATAC | 71816 |
rs48064317 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105270771 | ATGAAAAGTTTCAAG[C/T]TTTCGCCCTCTGAAG | 71816 |
rs48068046 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105188399 | CTTACAGGCTTCTTC[C/T]CTTGCCTTAGGCCTT | 71816 |
rs48075314 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105146944 | CATTTTTAGAGAATG[C/T]TTTTCTTTTCAGAAT | 71816 |
rs48080121 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105248003 | TCTTGCTAGTATCTG[C/T]CTTTCTGTTTGAATC | 71816 |
rs48091273 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105280570 | TGGGAATGGCCTATA[C/T]CCATAAGGTCATTAT | 71816 |
rs48096059 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Rnf180 | GRCm38.p3 | 13:105208759 | GAACTTACACAGCCT[A/G]AGTCAGAGACAGGTC | 71816 |
rs48102532 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime, intron-variant | Rnf180 | GRCm38.p3 | 13:105148202 | ACAGACAGCACTTCA[C/T]GGACTTCCTCCCTAT | 71816 |
rs48104318 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105152953 | CCAGGCTCCCAGTCT[C/T]CTTAATCGATCCTGC | 71816 |
rs48111631 | snp | C/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105160946 | AATATTTGTGGAAAG[C/T]GAGTTACCGCTTCAA | 71816 |
rs48117899 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Rnf180 | GRCm38.p3 | 13:105209566 | ACCCCAGGAAATGCT[C/T]ACAGAGCTCAGGAGA | 71816 |
rs48126372 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105282878 | TGAAAGGATACATTT[G/T]CCAAGTTCCACACCT | 71816 |
rs48131045 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105235442 | ATGTCAGATAGTGCT[C/G]TTTTTAATTCCTTTT | 71816 |
rs48149146 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf180 | Mm_Celera | 13:105238389 | CTGGCACGATAATAA[C/T]AAAGATATAATCAAG | 71816 |
rs48156560 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105234802 | AGAGCCACTTGTCAA[C/T]GAACAGCAGAGTAAT | 71816 |
rs48171498 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105184466 | TTGAGACTTATGAAA[A/G]CTTGTCCTAGGCTAG | 71816 |
rs48176451 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105192777 | ATATTTCACAGGAAA[A/G]CCAGCCTAACTCAAA | 71816 |
rs48200145 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105231271 | CATTATCACGTGTGA[A/G]AAATCAGGCCTTAAA | 71816 |
rs48200336 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105280312 | TACAAGCACTATGAT[A/G]TATTTGTAGGCGTTA | 71816 |
rs48204448 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105254431 | GTAGAAACTGGCTCA[C/T]TGATTCCTTTTCTTG | 71816 |
rs48209805 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105188808 | TGCTATGGTAAGACA[C/T]TGGTAGATCTCTACC | 71816 |
rs48218085 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105185976 | TTGTGGGTAGCCACC[A/G]GGAAGCAGGAGCAGT | 71816 |
rs48222862 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf180 | Mm_Celera | 13:105204639 | ATGTCTTTTTCCTGG[C/T]TATTCTCTCAAACTT | 71816 |
rs48223562 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105213944 | CTATTTTTCTAGAAC[C/T]GCGGCTCTCAACCTT | 71816 |
rs48228472 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105279783 | GGACAAATAAGTCCC[C/T]GTGAAAGAAACATTA | 71816 |
rs48258648 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105254498 | CTAATGGCTGCAGTA[C/T]TGTACAGTGGGAACA | 71816 |
rs48260294 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105149176 | GTCTATGCCAACCCT[A/G]CTGCCCTGCACGAAC | 71816 |
rs48271852 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105267767 | TGCTGAAGGCCTCCA[C/T]GGTCTTTGCCCTGCA | 71816 |
rs48290262 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105226279 | CAATATCCATGTTTG[C/T]ATTGTGGTACCCTCT | 71816 |
rs48306824 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105280536 | TGCCTCCTGGACAGA[A/T]CGCCATGCACAAGTC | 71816 |
rs48309212 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf180 | Mm_Celera | 13:105220284 | GTAATTGCTCTAAAA[C/T]GCAGCAAGCCTAGGT | 71816 |
rs48350972 | snp | G/T | 0.42 | 0.183303 | intron-variant | Rnf180 | Mm_Celera | 13:105285335 | TCAAAATAATAATAA[G/T]AATAAGGTCTCTTTA | 71816 |
rs48357695 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105177898 | CAGTGGATCCAGAAG[C/T]ACCCGGTCAACCATC | 71816 |
rs48363300 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105147633 | TACAATAAATCCCTT[A/G]CTAATAAAAACTGTT | 71816 |
rs48366631 | snp | A/C/T | 0.486111 | 0.0821678 | intron-variant | Rnf180 | GRCm38.p3 | 13:105217431 | CCAAAGACAGACACA[A/C/T]ACAAGGAAGCTTTTG | 71816 |
rs48368613 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105174611 | CTGTGGAGTGCATTC[C/T]ATGTTGTCAGCTACT | 71816 |
rs48375149 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105188027 | TTCAAATAAAGTCAG[C/T]GGGAGATAATCCCCA | 71816 |
rs48382843 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105214453 | GTCAGTGGCACAGAC[A/C]AGTTGTGGCCACTGT | 71816 |
rs48390914 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105216941 | AGAGTTGAAGGCTAG[C/T]GTTGGCTACAAAGCA | 71816 |
rs48392123 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105251962 | TGAGAAGATGGACAG[C/T]GGTTGCCAGTTGCTA | 71816 |
rs48402990 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105280371 | TTGTATGATTGGCAG[A/G]TCTCCCTGAAATGAG | 71816 |
rs48408503 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105231540 | TTGGTACGGCAATTG[C/T]TTATTGGCCTCAGTG | 71816 |
rs48470760 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105182962 | TGGTGGTTTGTGCTG[A/C]AATAACACCATGGTA | 71816 |
rs48483713 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105196126 | TCCAATGGCTGTCTT[A/G]TGGTTTTGCCAATCT | 71816 |
rs48485186 | snp | A/C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105206679 | ACAGAATTTAAAATA[A/C/T]CTCCCATAAAGTAGA | 71816 |
rs48493823 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105239881 | ATAAAAAGTTTGATG[C/T]TCGACCTGAAACATT | 71816 |
rs48494697 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Rnf180 | Mm_Celera | 13:105158211 | TCTCTGGAACTGGCT[C/T]TTGAAATCCTTAGGA | 71816 |
rs48508391 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105206632 | GTCTGTCCTTTATAA[A/T]CTTGATTATTGACAT | 71816 |
rs48509976 | snp | G/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105225353 | CAAAATGTTATACAT[G/T]TCCCCAGCTGCGCTG | 71816 |
rs48518193 | snp | C/G | 0.244898 | 0.249948 | missense | Rnf180 | Mm_Celera | 13:105270930 | TGAGTCTCAAGAGGA[C/G]TCATGAAGCAACCAG | 71816 |
rs48523327 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf180 | Mm_Celera | 13:105228252 | ATAAATGTTGGAGAA[A/C]TATTTAGTAATGGAC | 71816 |
rs48531473 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105280116 | CCATCTCTATCTTTC[A/G]TTGTTGCGTTTTGAG | 71816 |
rs48546532 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Rnf180 | Mm_Celera | 13:105245646 | TGTAATGAAGGAGAA[G/T]TTTTCATCTTTGAGC | 71816 |
rs48546945 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Rnf180 | GRCm38.p3 | 13:105250274 | TTCTGTAAGTCTTCC[A/G]AGGCCGTTACTGTTT | 71816 |
rs48547769 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | GRCm38.p3 | 13:105210345 | CACAAATGAAGCCAT[A/C/T]GCAAATAAAAGAGGC | 71816 |
rs48574742 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105242017 | CACACTACCTGAATG[C/T]AACCAGTCTTCCTAA | 71816 |
rs48591006 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105193719 | CTCAGAAGAGAACGG[C/T]GATGCTGTGCTATGT | 71816 |
rs48594753 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105215395 | TTCAGGTGTTCATAA[A/G]GTATGTAGCCATGCT | 71816 |
rs48597142 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105134679 | TCACACTCATAATCA[C/T]CCAAAGGCACCAAGA | 71816 |
rs48611183 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105191214 | TTTATGGTTTAATCC[C/T]GTCTTTGTCTCTTAA | 71816 |
rs48623942 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105188991 | GCTGAGGCATCATGA[G/T]TAGACAGTAAGGGTT | 71816 |
rs48628610 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105216391 | GCTCCTGGCTGACAA[A/T]GTGCAGAGATTGCTG | 71816 |
rs48660522 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105205619 | TGGAGCTTTCAGGAA[A/G]TGCTAAAGAGTGTGA | 71816 |
rs48707353 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105207502 | GAAGGGAAGATTGTG[A/T]GATATCTTTACATGA | 71816 |
rs48708050 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105245691 | CTATAAGCAAATAAC[A/G]GTTGACAGAGTAGGC | 71816 |
rs48742342 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105283938 | TTTCAGGGCAAACCC[C/T]GAGAATGGCAATTAT | 71816 |
rs48749043 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105268090 | TCTTGGAAACTTCAC[A/C]AAGATCATTCTTCTG | 71816 |
rs48749770 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105189214 | AACATGTGTGATCAG[A/G]CAAGTTATTTGACCA | 71816 |
rs48759060 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105134885 | TTAAGTGCATGGGTC[A/G]AGTAACTAACATTGC | 71816 |
rs48762776 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf180 | Mm_Celera | 13:105178094 | AATTTATTCACTAAG[C/T]AATTCCTAACACTAA | 71816 |
rs48779325 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105171289 | CACACACAGTTGATA[C/T]GAGGTCCCCAACACA | 71816 |
rs48789616 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105205018 | GCACAACCTTATTAC[A/G]TTTTTCTTAACTTTA | 71816 |
rs48801859 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf180 | Mm_Celera | 13:105269255 | ATTATTTACTCGTTA[C/T]TTCTAAATATTTTTC | 71816 |
rs48809876 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf180 | Mm_Celera | 13:105160566 | AGAGGGGACAACGTT[C/T]CTTGCAAGGGGTGCA | 71816 |
rs48820621 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105247960 | ATGATTTGTCAAACT[C/G]TGCCATTATTTTATC | 71816 |
rs48828173 | snp | C/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105205116 | ATAGTGTTCCCCTAA[C/T]TCACCTTTCTAACAA | 71816 |
rs48841974 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105240947 | TACAATACACCCTTC[C/T]ATAGTGTACTCCAGG | 71816 |
rs48845348 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105235184 | GGTAGAGTTTCTGGA[A/T]AACTTGCTGTTGCTT | 71816 |
rs48845958 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105225651 | ATTTTAAGACCTGCC[A/G]TGTGTGTGTGTGTTA | 71816 |
rs48866151 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105283451 | CTAAATCTCTAAAAC[A/G]AAGCACTATTCTGCA | 71816 |
rs48936125 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105231489 | ACAGCTGTACCTGGG[A/G]CACAAAGAGATTTAG | 71816 |
rs48980473 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105239914 | ATTCAGATTCTACAC[A/T]ACCTCTCTTGTGTGC | 71816 |
rs48989688 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105145121 | CACTGATAGAGTGAG[A/G]TTAGTGTTAACTAGG | 71816 |
rs48993941 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105222716 | CTCCTGTTCTCATGA[A/G]CTTAGGGCTAGCTCT | 71816 |
rs48998620 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf180 | Mm_Celera | 13:105162832 | TTATCAAAACTCATA[A/G]AAAACTGGATTCCTA | 71816 |
rs49000224 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105282794 | CACTGCAGCTTGGGC[A/C]GGTGAGTCTTGAAAG | 71816 |
rs49001279 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105235153 | CTTCCTTAGGCAAGC[C/T]ATCACCAATGATCTT | 71816 |
rs49021082 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105285175 | GGCAGTGCTGGGAGT[A/C]CTACACACTCTTGGG | 71816 |
rs49030129 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rnf180 | Mm_Celera | 13:105146856 | TTTTGAATTCTAAAC[C/T]AATAGGAAATATTCA | 71816 |
rs49041786 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105193568 | AGTTACAGGGCATCG[A/T]GAAGGCAAGCAGAAC | 71816 |
rs49061715 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Rnf180 | Mm_Celera | 13:105228118 | GACCTGTGCAACCTT[C/T]TGAATCCAGTTGACA | 71816 |
rs49068213 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105214675 | GGCGATGGATATCTG[C/G]CTGGCCCTGGGTACC | 71816 |
rs49095045 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105234064 | ATTCCTGAACAGGGC[A/G]GTGTTACTGATAATG | 71816 |
rs49105044 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105212407 | ATCTGGTGGGAATGA[A/G]GTTCAGGTCGAATTT | 71816 |
rs49113056 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105178413 | GAAGTGAGATCATGG[C/T]TCCTGACACAGTAGC | 71816 |
rs49114656 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105214918 | AAAGGCCAGTTTGCA[C/G]AGTTTCCAGCACATC | 71816 |
rs49119301 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105205415 | AAAAACCTTCAGGGA[G/T]CCCAAGCAGAAACCC | 71816 |
rs49134695 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105196115 | AGGGCATTGGTTCCA[A/C]TGGCTGTCTTGTGGT | 71816 |
rs49136216 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105153022 | ATCCATGACAGGCAG[A/C]AAAAGATTCGAATTG | 71816 |
rs49152432 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf180 | Mm_Celera | 13:105228514 | ATTGCAAACTGTAGA[C/T]TTTTTTTTTACTTGT | 71816 |
rs49157732 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105267625 | CTATGACACAGATCG[A/G]ACTGTTTAGTTTGAG | 71816 |
rs49165077 | snp | A/C/G | 0.297521 | 0.245442 | intron-variant | Rnf180 | GRCm38.p3 | 13:105224326 | GACATGTGCGGCTTC[A/C/G]TGTCATATGCTCACA | 71816 |
rs49196652 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105285144 | AGATGATCTGCTCAA[A/G]GCCATTGTTAACAGT | 71816 |
rs49206435 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105281010 | AAAGTGTCTAAATCC[G/T]GAATTACAGAGACCT | 71816 |
rs49210948 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Rnf180 | Mm_Celera | 13:105149674 | TAAGTAACAAAAGAA[A/T]AGAAACATAATCAGA | 71816 |
rs49211934 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105228956 | GAACAATTCAGACAA[A/G]TAAGCATGAGAGGAA | 71816 |
rs49214205 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105277322 | AAGGCTGGACATAAC[C/T]CTTCTAGGAGTACAT | 71816 |
rs49217940 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105268824 | AGAGGATGCTGTTGT[A/G]TGAAAGTTGCCTCTC | 71816 |
rs49229218 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105282691 | CATGAACTTGATACT[C/T]TCATGGATTTCCTAC | 71816 |
rs49234446 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105176463 | TCTGGATAAGATTGG[A/G]TATTTATAACTGCCA | 71816 |
rs49241734 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105282676 | ATGAGAAAAAAATTA[C/T]ATGAACTTGATACTT | 71816 |
rs49258130 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105237995 | ATGGAGAAACTCCTA[A/T]GGTACTGAGCTTATT | 71816 |
rs49263538 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105217540 | AACTGGTACCATTTT[A/G]TAGAAAGCAGGGTCT | 71816 |
rs49287999 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105220137 | GATCTAACAACTCTG[G/T]GTTGGGTCCACTAAG | 71816 |
rs49289857 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105280056 | CAGCAACTTAGAAAG[C/T]CAAATGGTTATGGGA | 71816 |
rs49290269 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105186552 | CAGTGAGAACCAAAC[A/G]TGTGTCTTCATATAT | 71816 |
rs49305658 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105189003 | TGAGTAGACAGTAAG[A/G]GTTGCTTAGTCAGCA | 71816 |
rs49311054 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105230588 | TTTAAACACTTGAGC[C/T]GGTTATCAAAGATAT | 71816 |
rs49324412 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Rnf180 | Mm_Celera | 13:105243642 | GCACAGCAGACATCG[A/C]ATGCTGTCCCTCCAG | 71816 |
rs49347653 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105153293 | TTGCATGTATGTTGC[A/G]TTTATGTCTGTGCGC | 71816 |
rs49367307 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105225244 | ATATTCAACTGTGTG[A/G]CAGTGCTAAATACAT | 71816 |
rs49386053 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105230524 | AAAATGTGTTCAGAT[A/G]CTAGAAGCTTCCATT | 71816 |
rs49398018 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105234668 | CCTCTTTTCAATAAC[A/G]TTTGAAAGTCAGAAC | 71816 |
rs49433149 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rnf180 | Mm_Celera | 13:105220956 | GTGCAGGCTTTGGGA[C/T]AGCTCTATGAGCACA | 71816 |
rs49452189 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Rnf180 | Mm_Celera | 13:105262017 | ACGCTCACCAATGGA[C/T]AGGTCATTGAAACAG | 71816 |
rs49453641 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Rnf180 | Mm_Celera | 13:105206767 | TTAATATTAGTGAAG[C/T]CATTAAGAATATGTG | 71816 |
rs49488192 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105258227 | ATCTCAGAAAGGTGT[A/T]TCCCAGAACATGGGT | 71816 |
rs49501120 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105186879 | CACAAACCTCCTCTT[C/T]CACAAAATGAACCAA | 71816 |
rs49550109 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105192694 | TGAAAATGGTGGCTG[C/T]CTCTGTGTTCCACAT | 71816 |
rs49560889 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105189114 | CATCCTGACACTTAG[A/C]AAGCACTAGAAACGT | 71816 |
rs49562169 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105209596 | AGTGGCTCCGGGCCA[C/T]GGAGTGGACCAAGAA | 71816 |
rs49565084 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105205413 | CCAAAAACCTTCAGG[A/G]ATCCCAAGCAGAAAC | 71816 |
rs49578889 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105270804 | TACCAGATCTTAAAA[A/G]GTATTTGTCATATGC | 71816 |
rs49594486 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105142260 | ATAGAAGTTAAAATG[G/T]GATTACTTATCGCTC | 71816 |
rs49598935 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105145912 | AGCCCAAGGTCTCAT[C/T]TCATTTTACACCAAA | 71816 |
rs49617747 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105146707 | ATATAAGTTATTAGG[A/G]TGGTGAATTAACTTG | 71816 |
rs49646950 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105268660 | TGCTGAAAAAGGCAG[C/G]CATGACATCTAGGAT | 71816 |
rs49647882 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105179843 | GGGAGGACCTCATGG[C/T]GAATGTTAACCTGTA | 71816 |
rs49653749 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105248110 | TTCTGCTTACCATAT[A/C]CTCGGCACGTGCCTG | 71816 |
rs49661685 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105152697 | TGAGGCAGGTAAGCT[A/C]AGATAATCTTTTTGA | 71816 |
rs49669926 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105283018 | ACTATATTTTGTAGG[C/G]AAAGTATGGTGTACA | 71816 |
rs49690181 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105216376 | TGTGGAACTCTGTTT[A/G]CTCCTGGCTGACAAA | 71816 |
rs49690211 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105268591 | GACGATGGGGCCCAG[A/G]ATGCCTATTGGTTCA | 71816 |
rs49692857 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105186046 | AGGAACAGAAGTATC[A/G]ATACAACACAGTCTA | 71816 |
rs49697186 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105204219 | TCTCTGCCCTTGCCT[C/T]TTGTCATCACTTAAA | 71816 |
rs49700271 | snp | A/C | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105193057 | ATTAGGAAGATTGAG[A/C]ACTGCTGTCCCAAAG | 71816 |
rs49704962 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Rnf180 | Mm_Celera | 13:105130188 | AACAATTGTGCTGGC[A/G]TTTTGGCAATTTACA | 71816 |
rs49708615 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105150203 | AACATGGAAGCTGGC[A/G]ATTTTCCACCCCAGC | 71816 |
rs49721784 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105193051 | TATAACATTAGGAAG[A/G]TTGAGAACTGCTGTC | 71816 |
rs49721956 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105190511 | TATTGAGAAAAGTAG[A/G]AGCAGTGTTTAAGCC | 71816 |
rs49733460 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105277857 | ATCAAATGCAGTATC[C/T]GATCTTAAGAAACTC | 71816 |
rs49735252 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105271336 | CTGTGAACCAGAATT[C/T]CTTAGACTTCCATAG | 71816 |
rs49741819 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105217087 | GAAGAACCTCATGTT[A/T]GTCTATTATAAACAA | 71816 |
rs49757870 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Rnf180 | Mm_Celera | 13:105180734 | TTAGCTCATGGCACT[C/G]TGGCCAGGATCTGCT | 71816 |
rs49761116 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105284439 | CCTCTTGTATAAAAT[A/T]TAAATCTCACATAAA | 71816 |
rs49771851 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105286305 | TAAAGTGTTCAGGAC[A/G]CCATTCTTAAGATTG | 71816 |
rs49780952 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105217581 | TGGTGTGTTGGTATA[C/T]TGATGGTTAATGTGG | 71816 |
rs49784585 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105205294 | GCAGATTTCTGAGTT[A/C]AAGGCCAGCCTGGTC | 71816 |
rs49804471 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105192464 | CATTTATTCTAAGGA[A/G]ATTCACAACTCCTTG | 71816 |
rs49821589 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105207628 | CCTTTCCTAGTTTCC[C/T]CTCCGGAAAGCCTCT | 71816 |
rs49827941 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105206470 | TGACAGATGAATTAT[C/T]CTTTAGGCCTTTCAT | 71816 |
rs49845690 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105192979 | TGAAATGGCAACAAA[A/G]ATAATTTTATGGTTG | 71816 |
rs49861310 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105146006 | GGTCATCATAACCTT[C/T]AGTAAATTATTCACC | 71816 |
rs49872477 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105258287 | ATGCTCAAGCTTTGA[C/T]TTACCTCTTCCTCAT | 71816 |
rs49897340 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105188206 | GCTTCTGATTACTAG[A/G]TAGGTAAGAGGTCTC | 71816 |
rs49904376 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105188303 | CCAGAAAACACTGAT[A/G]CAGCCCCTCCTAAGT | 71816 |
rs49905499 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105215691 | GAATTTAGGATTAAG[A/C]TTTTCGATAGCCATG | 71816 |
rs49914300 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Rnf180 | GRCm38.p3 | 13:105208741 | GCCAAACAATCAAGG[A/T]AGGAACTTACACAGC | 71816 |
rs49919057 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105280325 | ATGTATTTGTAGGCG[C/T]TATTCTGTAGGTTAC | 71816 |
rs49936240 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105208423 | TGAGCAAATCTGATA[A/C]GATACAGAAACTCTA | 71816 |
rs49952095 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105210076 | GGGTCATGCTGGTGC[A/G]TCTCACAATGGACTA | 71816 |
rs49970199 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105213076 | CCCAATGCTCCTTAA[A/T]TTGATGGCCTCTTTC | 71816 |
rs49976826 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105178941 | AGACAAGAGTTTAAC[A/T]GCTACCTCTGCTTCT | 71816 |
rs49978315 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105238918 | ATCCTGATAGAAGCC[A/G]ATCCTGTGAGTACAC | 71816 |
rs50024726 | snp | C/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105225250 | AACTGTGTGACAGTG[C/G]TAAATACATGTAAGA | 71816 |
rs50035867 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105230329 | AGTGTTAAAATGAGA[A/C]GAGTCCTATGCACTA | 71816 |
rs50039465 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105271155 | TCTTGTACTGTGGTG[C/T]GAGATGCCGAGCTCC | 71816 |
rs50046779 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105228855 | ACACAATGACTTACT[G/T]TTATATATACAGGAG | 71816 |
rs50052293 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105285169 | AACAGTGGCAGTGCT[A/G]GGAGTCCTACACACT | 71816 |
rs50072150 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105198018 | GCATCCGGTCAAGGT[G/T]CACCTGCAGCCTCTC | 71816 |
rs50087559 | snp | C/T | 0.396694 | 0.202437 | downstream-variant-500B, intron-variant | Rnf180 | Mm_Celera | 13:105147069 | GAGCCCTGAGGGCCT[C/T]ACATAGAGCTATCAG | 71816 |
rs50099674 | snp | A/C | 0.142012 | 0.225474 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105148079 | CTTTCCTTGACACGC[A/C]TGTCACTTATTTTGG | 71816 |
rs50135159 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105179877 | ACTTTGAGGACTGCA[C/T]GGCTTATATCAACCT | 71816 |
rs50136677 | snp | G/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105133079 | CTGTTTGTGTCAAGC[G/T]ATGGACTTATTTGTA | 71816 |
rs50166380 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Rnf180 | Mm_Celera | 13:105250367 | CTTATCACAACCTGA[C/T]GGGACTCCGGGATGT | 71816 |
rs50180376 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105284692 | TATGTATGATATTCT[C/T]CATTCTAATATCTAT | 71816 |
rs50199822 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105186520 | TGCAGTGTTCCCTAT[C/G]AATTCTTGGGTAAAG | 71816 |
rs50210385 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105285948 | ATAGTCCTCCTCACT[C/T]GTGTGCTTTAGAGGA | 71816 |
rs50217632 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105209464 | TCATCTCAGTGGTCC[G/T]TGGGATGCTTGGTGC | 71816 |
rs50249962 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Rnf180 | Mm_Celera | 13:105245422 | TAGACACTTTAACAA[G/T]CAAGGAAGAGTTCTG | 71816 |
rs50256855 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105240586 | GTCTTAAGTTACTTG[A/G]CTTTCTTCTCACACC | 71816 |
rs50259963 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf180 | Mm_Celera | 13:105134711 | AAAGTCCCAGAGTTT[C/T]TATCACCTTTCACAG | 71816 |
rs50263671 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rnf180 | Mm_Celera | 13:105160122 | AGAGACAAAGTAAAG[A/G]CATGATAACTCAGTA | 71816 |
rs50301552 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Rnf180 | GRCm38.p3 | 13:105214880 | AACTTGAAGACACAT[A/G]AGCACTGCAATGAGC | 71816 |
rs50309899 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105192963 | ACAAAAATCACAGTT[A/G]TGAAATGGCAACAAA | 71816 |
rs50346134 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105254279 | AGCCTTGAAACAGGG[A/G]CAGTGAAATGCATGA | 71816 |
rs50355048 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105214915 | TAAAAAGGCCAGTTT[A/G]CACAGTTTCCAGCAC | 71816 |
rs50370911 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf180 | Mm_Celera | 13:105181218 | GAGACATAACAGCAG[C/T]TGTCTAGGTGCTTAG | 71816 |
rs50372002 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105248941 | AGGTAATCTTCAAAA[A/G]GAGTTTATACTAGCT | 71816 |
rs50373442 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105241788 | GAGGCAAAAGCGAGG[C/G]TCCTGGCATGTTGGC | 71816 |
rs50373714 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105235095 | TGAAAGCCTTAGATG[A/G]CAATTTCTAACAGAA | 71816 |
rs50386611 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105186928 | ACACTCTGAAATGAG[C/T]GATTGGTGGTCCACC | 71816 |
rs50395057 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105171367 | AACCCTCGAGAAACT[C/T]GAGGCCCTAGGGAGT | 71816 |
rs50402021 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105281270 | ATTCACAACTTTAGC[A/G]AGTGTGGTGCTTTGA | 71816 |
rs50424466 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105216990 | AGGCAGCTTTGTCAC[A/C]GTTCTATTGGGAAAT | 71816 |
rs50434798 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105277122 | ATGGTGTACATATGT[C/T]CATCCTTTGACCTGT | 71816 |
rs50438298 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105271816 | ATCTATAAAGCCATC[A/G]CAGTACTTTTAAGAA | 71816 |
rs50452928 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105238930 | GCCAATCCTGTGAGT[A/C]CACTAAGTGGCAGTG | 71816 |
rs50456038 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105281105 | AACGGTTCTTGGATA[G/T]TCACAGTCAAACTGT | 71816 |
rs50469318 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105185627 | GATGTTTATGCACAC[A/G]CTCTTAAGGGAGTTG | 71816 |
rs50471566 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105141992 | GTGGGATGGGCCAGG[C/T]GAAGGACAAACCCCG | 71816 |
rs50480337 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105187553 | TTTCAGGTTTCACAA[C/T]GATCTCCAAAGAACA | 71816 |
rs50495396 | snp | A/C | 0.260355 | 0.249785 | synonymous-codon | Rnf180 | GRCm38.p3 | 13:105181640 | CTCCTCTGGGAACTC[A/C]GTTTCCTCATCTGTA | 71816 |
rs50498354 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105168736 | GTCCTCCAGGGCTAC[C/T]GATTTTAATTTGCAT | 71816 |
rs50512865 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105252871 | CTGGTATCTTCCTTA[A/C]GCAGAAAAGGAACAC | 71816 |
rs50518729 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rnf180 | GRCm38.p3 | 13:105204528 | AGACAGCACCCTAGA[C/T]GGATCTATCAACCCC | 71816 |
rs50521974 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf180 | Mm_Celera | 13:105158751 | ATTAGAGTAGCTGTA[A/G]AGGCAACTGTACCTT | 71816 |
rs50537555 | snp | A/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105279506 | GCAGGAAGCCATAAA[A/T]CACTGCATGCTTGGG | 71816 |
rs50562334 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105237184 | GACCTCCAAGTTGAG[A/G]TCACCCAGCTGGAGC | 71816 |
rs50573973 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105196805 | CAATGAGCATGCCAT[C/T]TTAGGGATACCATGA | 71816 |
rs50576973 | snp | A/T | 0.124444 | 0.216185 | downstream-variant-500B | Rnf180 | Mm_Celera | 13:105130289 | TATCAGGTTACAGCA[A/T]GACAGGCAGAAAGGG | 71816 |
rs50579288 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105186307 | ATGAAAGGAGGAAGG[C/G]GACATTTGGAAATTC | 71816 |
rs50580815 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105257694 | CTGATCCAGTCTCAA[A/G]GATTCAACAACTGAC | 71816 |
rs50592906 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105249431 | AGAAGCAGTGCTTAT[A/C]CATATACACAGTGCT | 71816 |
rs50610109 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105218088 | CCGCAATCAATAAAA[C/T]AGCTTTTAACTCAAT | 71816 |
rs50612041 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105275237 | TCTTCTCTATTGCTC[A/G]TTGCCCAATTTTTAA | 71816 |
rs50656751 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rnf180 | GRCm38.p3 | 13:105205003 | TGAGTAACTTAAAAT[A/G]CACAACCTTATTACA | 71816 |
rs50691829 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105279647 | CTTAACATTATCTCA[G/T]TTCTCAACCCGGTCT | 71816 |
rs50693065 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105184766 | TGCGTCACCACTGCC[C/G]GGCAGAGTCGACAGT | 71816 |
rs50696891 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105270050 | AATCAATTAGTGATG[A/G]AAAGGTACCACCACC | 71816 |
rs50702663 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105193559 | ATCAAGGGAAGTTAC[A/G]GGGCATCGAGAAGGC | 71816 |
rs50716179 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105222655 | CGCAGCTCCTGAAAT[A/G]TGCTAGTCGATTGCC | 71816 |
rs50721292 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | GRCm38.p3 | 13:105181047 | TAATTAACAACATCA[C/T]GTAACAGTGCCAAAC | 71816 |
rs50727446 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105274682 | TGTCCTCTTGACTTG[C/T]AGTGACATACAAATA | 71816 |
rs50730980 | snp | A/C | 0.231111 | 0.249285 | downstream-variant-500B | Rnf180 | Mm_Celera | 13:105130413 | ATCCCGATATTGTCC[A/C]CGTCTCCTGCTCACG | 71816 |
rs50739179 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105184156 | ACACCTTCCAGACTG[C/T]TTTCCCATGATCTGT | 71816 |
rs50752253 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105280615 | ATGCCAGCCCATGCT[C/T]GTGCTCTTGAACCCT | 71816 |
rs50753513 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105231253 | AACACAATTTTTCTC[G/T]CACATTATCACGTGT | 71816 |
rs50753654 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105188683 | TCCATCAGGCTCCTC[C/T]TATCTTGTCCCTCTG | 71816 |
rs50754166 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105185939 | CAGCAGAGGACAATA[A/C]GTAACCGAAGAAAGA | 71816 |
rs50767514 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105280584 | ACCCATAAGGTCATT[A/T]TGTAAAATTAGTAAG | 71816 |
rs50822351 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105150116 | GAGATTAAGACTTCT[A/G]TCTCATGTGAGTTGA | 71816 |
rs50826518 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105231151 | TGAGGATTGAACCAA[A/G]ACCTAGAGGGAGTAG | 71816 |
rs50831967 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Rnf180 | Mm_Celera | 13:105146464 | TGGTGAACAGTGATG[A/C]ATAAGCAGAGCTCTG | 71816 |
rs50833477 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105234524 | GCTTTTACTTCCTCG[A/C]ATGAATCACACAATG | 71816 |
rs50838003 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105283029 | TAGGGAAAGTATGGT[A/G]TACAAATTATGAGCA | 71816 |
rs50838781 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105237242 | GTGTGGGAAGATTGC[C/T]GGTCCTTTTTAACAT | 71816 |
rs50843589 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105210242 | AAGACAAACACCAAA[C/G]CAAACTAACAAACCA | 71816 |
rs50849626 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105271701 | TCATTTAATTCTGAT[C/T]ATGGTAGTGCATTAT | 71816 |
rs50850441 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105220954 | AGGTGCAGGCTTTGG[A/G]ACAGCTCTATGAGCA | 71816 |
rs50899747 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105230467 | GCTGTGATGATGTCA[C/T]ATCTTCCCAAACGTC | 71816 |
rs50947590 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105257843 | TAAGCCCTGTAGGTT[C/T]TTTCAGATATCTTAA | 71816 |
rs50949509 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105145257 | ACTTTTGAAATATGG[A/G]CCATTGAATTTAGGG | 71816 |
rs50958462 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105279142 | TCAAATGCTGAACAC[A/G]TCAATGGCACAATAC | 71816 |
rs50973329 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105205227 | AAAACTTCAGGAAGC[C/T]GGGCAGTGGTGGCGC | 71816 |
rs50995587 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105185269 | CTCTGGTTTTAACAT[C/T]CATGCTTTTCCTTAG | 71816 |
rs51008837 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | GRCm38.p3 | 13:105193965 | ATAGTAAATTTTGCT[A/G]TGGATAGGGACACAT | 71816 |
rs51016966 | snp | A/G | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105138834 | ATGTATTTCAACCAT[A/G]CTGTATTAAAGTATA | 71816 |
rs51018433 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105266524 | GATGAAGACTATTTT[C/T]AGGAGGTAAAGTCAA | 71816 |
rs51021926 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105215242 | CATAGCTGGATATTT[C/T]CCTTAGCAATTTCAC | 71816 |
rs51034947 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Rnf180 | Mm_Celera | 13:105167223 | AACTGAAGTAGAGGT[C/T]TGAGACTGCCTTACA | 71816 |
rs51038158 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Rnf180 | Mm_Celera | 13:105183090 | TTTTCACTTTTCTTT[G/T]AGGCATGGGGACATT | 71816 |
rs51047258 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105210549 | CGGCCGACTGTCCTC[G/T]ACTGTCCTCTCAGAT | 71816 |
rs51056620 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105217729 | TTGGCAGACACCTGC[A/G]CATGGGTGAACAGTG | 71816 |
rs51075671 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105195543 | TACAATAGAATTTTA[A/C]CTGAGTTATTTTTAT | 71816 |
rs51104987 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105181251 | GGATCCGAGTGCAGA[A/G]CTAGAGGTCAGCAGG | 71816 |
rs51112419 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105278765 | AAAATGAGATGGCTT[C/T]TGGCCAATAACTTAT | 71816 |
rs51127054 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105185093 | AAGCACAGAGATGAG[A/G]ACTCACATGGTGGGA | 71816 |
rs51131406 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105204384 | GACCCAGTCACCTGA[A/G]AGATTTCTCCAAATT | 71816 |
rs51134451 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | GRCm38.p3 | 13:105218449 | TACATGGCCAAGGAA[C/T]CACCTGCTAGACATA | 71816 |
rs51143474 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105284092 | AATAAAGGAAGAGAG[A/C]GCCCTGGGAGCTAAA | 71816 |
rs51167945 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105282918 | TTATCCATTTCAGCT[G/T]CTGTTACTTTCTGGT | 71816 |
rs51190296 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105237891 | AACCATAATAGAACC[C/T]GAACAATCTATGTCC | 71816 |
rs51216470 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105205256 | GCAAGCCTTTAATCC[C/T]AGTACTTGGGAGGCA | 71816 |
rs51216812 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105196888 | TCCAGGTAGGGAACA[A/G]CACACTGCACATGAT | 71816 |
rs51223703 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105279991 | TCTTTAAAACTAAGA[C/T]TGAAATCAAGTGAGG | 71816 |
rs51238043 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105248581 | ACAGGATCCAACACC[A/G]TGGGGAATGATACAA | 71816 |
rs51240149 | snp | A/T | 0.5 | 0 | intron-variant | Rnf180 | Mm_Celera | 13:105139135 | TGTATTTAAAGTTAG[A/T]ATGTATTATAAATGG | 71816 |
rs51269496 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105214767 | ACAACGCAGATGTCA[G/T]CTTTCTCCATACCAC | 71816 |
rs51280190 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105225629 | TTTTGTTAGCGGTTG[A/T]AATGTAATTTTAAGA | 71816 |
rs51280560 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Rnf180 | Mm_Celera | 13:105241059 | CAAACTAGGACTTCA[C/T]ACAAACAGAACCGAG | 71816 |
rs51285551 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | Mm_Celera | 13:105186686 | AATAGATCAAAAAGC[A/T]AAGATTAGACAGAAT | 71816 |
rs51292192 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105285086 | TAGCAGGGCCTTAGC[G/T]GGCTGTGCAGGGATG | 71816 |
rs51307138 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Rnf180 | Mm_Celera | 13:105205726 | AAAATGTCAAGAATT[A/G]TAATTTACCTTAAAG | 71816 |
rs51319064 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf180 | GRCm38.p3 | 13:105193164 | ACCCTGGGACCTCAG[C/T]GAGGGATCCTGAAAA | 71816 |
rs51338296 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105174273 | TTGGTATGATGATAT[G/T]TTAACCCTTTAGTTA | 71816 |
rs51340817 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105188652 | TTCTCAGCACAAGTG[A/G]TGGATCTGGAGCATC | 71816 |
rs51352767 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105196048 | TCATTTCTGGAGTGT[A/G]TGAAGAGCAATGTAA | 71816 |
rs51365526 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf180 | Mm_Celera | 13:105145399 | TAATGTCTTTCTTCC[C/T]GGAGAAACAGAAATT | 71816 |
rs51365594 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105187096 | ATGAGTCAGAGAAAG[A/C]CCCAGGATACTTGTG | 71816 |
rs51366100 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105252886 | CGCAGAAAAGGAACA[C/T]CCTGACCTGTGAGCA | 71816 |
rs51366528 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf180 | Mm_Celera | 13:105144878 | CGAAGTAGGAATTAT[G/T]AAGTCATTTAGTGCA | 71816 |
rs51377705 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105250827 | TATCTGAACAACCAA[A/G]AATTCCTAAAGAAAG | 71816 |
rs51383591 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105239041 | AAAGCAATCATCAGG[C/T]CATCAAACAAGGAAG | 71816 |
rs51420359 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf180 | Mm_Celera | 13:105188611 | GGTAAACCATGTAGC[A/G]TTTTATTTTCCAAGT | 71816 |
rs51426575 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105205373 | TCAAAACAACCAACC[C/T]CCCCCCGAAAAAAAA | 71816 |
rs51464198 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105215795 | CGTTCTGCCCTTTAT[C/T]CTGCTCATTTCACAT | 71816 |
rs51465986 | snp | C/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105225272 | CATGTAAGATGGAAA[C/T]TAAGAATTACAAAAG | 71816 |
rs51478890 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105186405 | TTAAGAAACAGAGAT[C/T]ACCTGGAGTCAAAGA | 71816 |
rs51491040 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105267273 | GACTATCAGTTAGCA[A/T]TGTTATTTGTTTTCA | 71816 |
rs51491145 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105207142 | TATTTAAAATGCGCT[C/G]AATTTATTAAACAGA | 71816 |
rs51517209 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Rnf180 | Mm_Celera | 13:105164553 | GTGACAAGCCAGGGT[G/T]TCCACATAGGGAGGA | 71816 |
rs51575684 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105184209 | CAGGAATCCTGAACT[C/T]TCAGAGCCCTGAAGC | 71816 |
rs51579784 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105252155 | AGAACCAGAATTCCT[C/T]GTTGTGTTTTGAAAC | 71816 |
rs51593244 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105217957 | CATTCATTACCACTA[C/G]TATATCTTTAGGAGA | 71816 |
rs51596587 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105284161 | ACAAGACATTATATC[C/T]ATCTTGACACGGGCA | 71816 |
rs51597386 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105274088 | TAAAGATCTATAATA[C/T]GCAAGTAGAAAGGAT | 71816 |
rs51602189 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Rnf180 | Mm_Celera | 13:105171697 | CAAGCTTGGCGATAA[C/T]TGTCTTTGCCAGATG | 71816 |
rs51606543 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Rnf180 | Mm_Celera | 13:105243188 | CAGTGGTCTGAAAGG[A/C]TAAAAGAGAAACCTT | 71816 |
rs51606992 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf180 | Mm_Celera | 13:105241868 | AGTGCATGACAACTT[C/T]CATCCCAGCAGAGAC | 71816 |
rs51609276 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf180 | GRCm38.p3 | 13:105240445 | TGAAGCTATTGGCTG[C/T]CATGATGGAAACTGA | 71816 |
rs51609603 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105278924 | GGCTTAAGCAAGTCA[A/G]GGAACTATGTGACTA | 71816 |
rs51612385 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Rnf180 | Mm_Celera | 13:105130427 | CCCGTCTCCTGCTCA[C/T]GTTGTTATGGTTATA | 71816 |
rs51623295 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf180 | Mm_Celera | 13:105241562 | AGAGTTTCAGCCCTC[C/T]ATATAGCAACTCAGA | 71816 |
rs51626500 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rnf180 | Mm_Celera | 13:105153307 | CGTTTATGTCTGTGC[A/G]CACATGCACATATTT | 71816 |
rs51646685 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf180 | Mm_Celera | 13:105217507 | GTACAGTTTTCCTAT[A/G]TATGTCATACTCTAC | 71816 |
rs51646871 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105218411 | TGATCAGGAACAGTA[C/G]GAAACAAAGTAGCCA | 71816 |
rs51654098 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105215780 | ATTAGATACTGAGGA[C/T]GTTCTGCCCTTTATT | 71816 |
rs51669582 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105285064 | AGGCAGAAGGAACAG[C/T]AGTGTATAGCAGGGC | 71816 |
rs51687269 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105193540 | GGGATTTCTGCAACC[A/G]TTCATCAAGGGAAGT | 71816 |
rs51700820 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105192789 | AAAGCCAGCCTAACT[A/C]AAAAAATAAATGTTG | 71816 |
rs51710785 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105280739 | TAGATAGAACTGGGG[A/G]CAACTTCTTAGCTAT | 71816 |
rs51719997 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105266708 | CAGGGGAACTAAAAG[C/T]CTTTCTAACAGCATA | 71816 |
rs51721568 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105282838 | TTCAAACCAGGTGAC[A/T]CTTTGAGGGATTGTA | 71816 |
rs51743362 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105135021 | GGCATCCTCGGCTGA[A/G]TTGAGTGCTGTGATA | 71816 |
rs51774410 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105280023 | GAACTTGGTAAATAT[A/G]TGAAAAAAGTTAAAG | 71816 |
rs51783637 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105234946 | CTACAAGCAAATTAA[A/G]CCTCACTTGACGTGA | 71816 |
rs51800996 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105177903 | GATCCAGAAGTACCC[A/G]GTCAACCATCATCAG | 71816 |
rs51810724 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105258558 | GACAGTTCAGGCATT[A/G]TAAGCTGCCTTCCTC | 71816 |
rs51820463 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105274653 | TACTCAGGTTCCTCT[C/T]AGATAGTCGCCCATG | 71816 |
rs51841571 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf180 | GRCm38.p3 | 13:105160427 | CAGGGAAATCGGCTG[C/T]AGTCCAGTAGGGGAG | 71816 |
rs51843072 | snp | C/T | 0.396694 | 0.202437 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105147817 | ATGCTTTCATACTAC[C/T]CTATAAAATTTAATA | 71816 |
rs51846718 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf180 | Mm_Celera | 13:105242153 | AGCGTAAGGCAGTAT[A/G]TCCCGGAGTCTGAAG | 71816 |
rs51854685 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105284766 | CACTGAATTTGATGG[C/G]TCTCTTTTCCCCCAT | 71816 |
rs51863880 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Rnf180 | Mm_Celera | 13:105189672 | AGTTCTAACATATGC[C/T]AGTTTCCATAAGAGC | 71816 |
rs51866966 | snp | A/C | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105185595 | TAAATGTAATAACTC[A/C]ACAGAAAGTAGATGG | 71816 |
rs51873450 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105274420 | ACTGAAACCATCAAT[A/G]ATAAGGACTATGATA | 71816 |
rs51892267 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105234763 | AACTTTTACTGTATT[C/T]TTCCACCAGGGCTCA | 71816 |
rs51914917 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105188894 | AAGGAACGCCTACAT[C/T]GTGCTATTTTCAGAA | 71816 |
rs51921940 | snp | A/C/T | 0.396694 | 0.202437 | intron-variant | Rnf180 | GRCm38.p3 | 13:105175862 | GATTAGTATAGAAAA[A/C/T]CTTGGCTTTAGCAAA | 71816 |
rs51923394 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Rnf180 | GRCm38.p3 | 13:105210365 | ATAAAAGAGGCAGAG[A/G]CACAGGACTCCTACA | 71816 |
rs51923583 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf180 | Mm_Celera | 13:105159794 | TCTTTCTAAACCAAA[A/T]TCAGAAATGAAGCTG | 71816 |
rs51939257 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf180 | Mm_Celera | 13:105240537 | ATGACAAACACGTGC[A/G]AGAGGAGCAGCTCCT | 71816 |
rs51942510 | snp | C/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105192836 | TCAGGAATGGTCTAG[C/G]GGCTAATCACAGTCT | 71816 |
rs51992651 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105249088 | CAAGGAGTTCAAACT[C/G]TAAAGAATCCAGCTC | 71816 |
rs51999604 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105279543 | AGAGAATGAAAGGAC[C/T]ACTGGCAGGCAAGCC | 71816 |
rs52003206 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105235324 | CCTTACTTCTCGAGC[C/T]TTTACATGAGAGATG | 71816 |
rs52008800 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Rnf180 | Mm_Celera | 13:105153064 | TAGAAAAGCTTATTT[A/C]GCCTCACAGAGGCCA | 71816 |
rs52044612 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105283740 | TTTCTGACCCAGCAC[C/T]TACGAGCTTGCACAT | 71816 |
rs52103112 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105281645 | GCCTTCCCTGTCATG[C/T]CTTCCCTGCCTTGTC | 71816 |
rs52117430 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105281701 | GTCTTCCCTGCCATG[C/T]CTTCCCTGTCTTGTC | 71816 |
rs52177653 | snp | A/G | 0.336735 | 0.234472 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105148594 | GGAAATGGGACCAGA[A/G]TTATTACATACACAT | 71816 |
rs52197956 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105189860 | CTCTCTCTCTCTCTC[A/T]CTCACTCACACACAC | 71816 |
rs52236072 | snp | A/C | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105166401 | GAAAGAAAGAAAGAA[A/C]GAACGAAGGAAGAAG | 71816 |
rs52264067 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105171561 | TAATAAGTAGTAGTA[A/G]TAGTAGTTTATTTAT | 71816 |
rs52271692 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105171138 | GGAAGAAGAGGAGGA[A/G]GAAGAAGAGGAGGAG | 71816 |
rs52293851 | snp | C/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105218177 | ACACACACACACACA[C/G]AGAGAGAGAGAGAGA | 71816 |
rs52320819 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105189870 | CTCTCACTCACTCAC[A/T]CACACACACACACAC | 71816 |
rs52332361 | snp | A/C/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105218197 | AGAGAGAGAGAGAGA[A/C/G]AGAGAGAGAGAGAGA | 71816 |
rs52357590 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105171587 | TTTATTGTGTGTGTT[G/T]CAGAGGGGTCCATGC | 71816 |
rs52374393 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105171470 | AATGGGATGAGGAAC[A/T]CTCAGAGGGCAGACT | 71816 |
rs52495956 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105281612 | GCCATGCCTTCCCTG[C/T]CTTGTCTTCCCTGCC | 71816 |
rs52580562 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105205356 | CACAGAGAAACCCTG[C/T]CTCAAAACAACCAAC | 71816 |
rs52592924 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf180 | Mm_Celera | 13:105251848 | TGATGATATATTTGC[A/G]TGTCCCTGTATGCAC | 71816 |
rs52592988 | snp | A/T | 0.260355 | 0.249785 | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105148781 | CATTGCTGGTAGTAA[A/T]AAGCAGTCCTCAAAT | 71816 |
rs52593228 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105190175 | CCTAATCCATATTCT[A/G]TTTGGTAATGCTTGC | 71816 |
rs52596962 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rnf180 | Mm_Celera | 13:105174462 | AATAGAAACCCAGTA[A/G]AACAAAACCTTCTTC | 71816 |
rs52602191 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105207290 | TTTTACTAGTTATCT[C/T]AATTTTACTTCTTTT | 71816 |
rs52615948 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105272191 | AAATTGGGTGAGTAT[A/G]GAAGTGGGAAGGATC | 71816 |
rs52619767 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105194172 | GACAGCCCATGGATG[A/G]CCATGAAGAGGCCAG | 71816 |
rs52623539 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105184975 | ATTTACTTCATTTCC[C/T]AAGATGTCTTTTGTA | 71816 |
rs52627041 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105258492 | AATTTGTATGCCTAT[A/C]TTATCTGCCTTTTCT | 71816 |
rs52636159 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105189942 | AGCTCTCATTTCTGT[A/G]TGTAAACAAGTGAGA | 71816 |
rs52642208 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf180 | Mm_Celera | 13:105269270 | TTTCTAAATATTTTT[C/T]TGTTTCTCCAGTAGC | 71816 |
rs52649591 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf180 | Mm_Celera | 13:105218142 | TTGCCTTATAGACCA[C/T]TCCATTCTTGATTTG | 71816 |
rs52652985 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105258536 | TTGATGTTGAACGTC[G/T]TGCAATGACAGTTCA | 71816 |
rs52655017 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf180 | Mm_Celera | 13:105258354 | TCTCTGTGCCTCGAG[G/T]TTAAGAATCCCGAAA | 71816 |
rs107681401 | snp | C/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105220245 | CAGAAAGCTTGTCTC[C/T]GTATCTATACCATGC | 71816 |
rs107858467 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105139007 | TATCAACTCAAGATA[A/C]TGTCTATGTGTATTT | 71816 |
rs107906808 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105171401 | GAGGTCTGATAGGGT[A/G]GGGGTGGGGGTGGGG | 71816 |
rs107962814 | snp | A/G | | | downstream-variant-500B, intron-variant | Rnf180 | Mm_Celera | 13:105147397 | GATAGAATAGTAAAT[A/G]AATATTTTCAAATTA | 71816 |
rs108062120 | snp | A/G | | | downstream-variant-500B, intron-variant | Rnf180 | Mm_Celera | 13:105147323 | AGAAAAATTAACAAA[A/G]GAAAATATGTCTTAA | 71816 |
rs108158435 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105146834 | ATTTTCTGGTACTAG[C/T]TAAGTATTTTGAATT | 71816 |
rs108295933 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105146510 | CCAGTTGTTTTCCAG[G/T]CTTTTTGTCAGCTAG | 71816 |
rs108438151 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105146821 | GATGTATGCAGTGAT[C/T]TTCTGGTACTAGTTA | 71816 |
rs108493865 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105145952 | GTTGTGAATTAGTTT[A/C]CCAGGAAATACCCAT | 71816 |
rs108678659 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105205318 | CCTGGTCTACAGAGT[A/G]AGTTCCAGGACAGCC | 71816 |
rs108736326 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105204044 | TTCCTTCCTCCCAAG[A/G]GACTGCTCCCACAGC | 71816 |
rs211710604 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105212484 | GGCTATTCAGTGCTG[C/T]CTCTCTGTTGTTATG | 71816 |
rs211711251 | in-del | -/GTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | Rnf180 | Mm_Celera | 13:105243308 | CAAAGAATTAACAAA[-/GTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 71816 |
rs211747463 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105213198 | GTTTATATAAGACTC[C/T]AGAGCTCACTACTTT | 71816 |
rs211765932 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105259767 | ACAAATGAAAGGATG[A/G]ATGAAGTATGGAGGC | 71816 |
rs211776157 | in-del | -/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Rnf180 | Mm_Celera | 13:105292382 | ACAGGATTCTTAAGC[-/T]TTTTTTTTGGAGGGC | 71816 |
rs211780520 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105206205 | GTTTTTCACTTCAAA[A/C]TTTAATTTTAGAGTT | 71816 |
rs211783253 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105166700 | ATGATAAGTGGTATG[C/T]AGAGGCCTCAGGAGT | 71816 |
rs211820582 | snp | A/G | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105167032 | ATTTCATACACAGGT[A/G]CACACATGTGCCCCC | 71816 |
rs211828339 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105251513 | TTACTTTAAATGTGT[C/G]TATGTATGGTGGATG | 71816 |
rs211859490 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105160757 | CTAGATTTCAAGATG[C/T]TCTATCACTAGTAAA | 71816 |
rs211886912 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105152766 | CTTCATAGGCTGTAT[A/C]ACATTTCCTATAGAA | 71816 |
rs211897824 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105242871 | TGCCTGTACTTCTGG[G/T]TATGGTTGGGACCTC | 71816 |
rs211900591 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105236116 | CCAAAGGAATCCTAA[A/G]TAGAAAGAACTATGC | 71816 |
rs211963048 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105194258 | CAGTGGAGCTGGGAC[A/G]TACCTTCTTAGGTCA | 71816 |
rs211974747 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105153232 | CCTCTCCCTGGGGAG[C/G]GGGGGGTGGGGGGGG | 71816 |
rs211976809 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105200270 | GCTTTCAGGTGTGCT[C/G]TTAAGCTGCTAATGT | 71816 |
rs211990634 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105290927 | TTCTAGTTTCCCTGA[C/T]TCTGTGGCCAAAATT | 71816 |
rs212004684 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105195181 | ATTGACTCCTGTGTT[A/T]GAATATGCTTGGCCC | 71816 |
rs212004792 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105186972 | AGAGGAACTGGTATG[C/T]TTTCATATTCAGAGA | 71816 |
rs212011225 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105135459 | CTACACTGGGGCATC[A/G]AGCATTCCCTGGACC | 71816 |
rs212016941 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105236550 | GACAGGATTACTTTA[C/T]TTTAAAATATTTGTG | 71816 |
rs212017301 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105229155 | AAAGAGAATAGATAT[C/T]GTGGGTGGACTGGGG | 71816 |
rs212027964 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105144954 | AGCCTTTCACCGGCA[C/T]TGCCTAAGACCATCA | 71816 |
rs212059463 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105230179 | ACATAGTTACTGGGG[A/G]GTGGGTGGGGAGCTG | 71816 |
rs212059878 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105290484 | TCTGGGAGGCCAAAA[A/C]CTGGAGCTGACATTA | 71816 |
rs212071949 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105224322 | TCATGACATGTGCGG[C/T]TTCCTGTCATATGCT | 71816 |
rs212087626 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105282736 | TCTTAGACTGTATCA[G/T]CTTCAGCTGAAGTTG | 71816 |
rs212145409 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105146274 | AGACATATATGTCTT[-/A]TTTAAAATTCCTTAT | 71816 |
rs212147436 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105187614 | ATACAGCTTGAGATA[C/T]CTATCAAATATTAAA | 71816 |
rs212151896 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105281364 | GTAAGGCTGTGGAAA[A/C]TTTAAGAGGTGATCC | 71816 |
rs212159679 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105145780 | CTCCAAATGGTGCCA[C/T]TCAATAGCCCAAGAA | 71816 |
rs212171187 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105174938 | ATGGCAAAGATCACT[A/G]TGATTTGAACAATAT | 71816 |
rs212187610 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105136020 | CTCAAATAATTTCTA[C/T]TTTCCTTCAAATTCA | 71816 |
rs212188623 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105219606 | ATAACCATTATGAAT[A/G]TATTTTATTGCTACG | 71816 |
rs212193237 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105270823 | TTTGTCATATGCTCG[A/G]GTGTGGCAGAGTAGG | 71816 |
rs212206429 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105260889 | GAGATTGACACAACT[A/G]TCAAAGAAAATTCAA | 71816 |
rs212206469 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105271595 | TGGGATGACCTCAAG[A/G]GTGGGTTTTGTGAGA | 71816 |
rs212232660 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105224014 | ACAAAATAAACCAAA[A/G]ACCGTAGACAGAAAC | 71816 |
rs212268826 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105167877 | TTTAGAAAGAGAAGC[A/G]TCTGCACTGGGAGTC | 71816 |
rs212272689 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105214556 | TGGAGGTATGAGCTG[A/G]GAACCAAGTTTGATG | 71816 |
rs212273310 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105262698 | CCAAGAGGCAGTATC[C/T]AAATCAATAAAATTA | 71816 |
rs212305016 | in-del | -/AAT | | | intron-variant | Rnf180 | Mm_Celera | 13:105285324 | TGTTCTTTGTATCAA[-/AAT]AATAATAATAATAAG | 71816 |
rs212312209 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105214996 | GCTGGGGAGGTATCC[A/G]TGGTTTCCCTGGTTG | 71816 |
rs212312608 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105207671 | TTCTCCCTGCTTCTA[C/T]GAGGGTGTTCTCCTA | 71816 |
rs212322822 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105180424 | AGAGACTGTTAAAAT[G/T]ACTTATTTTAGAATA | 71816 |
rs212343672 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105253589 | AAACTGAACCCTCTG[A/G]GGCATTAAGGCAACT | 71816 |
rs212350560 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105208241 | AAGGCCCATCATGTA[C/G]CCTCTGATGTATTGT | 71816 |
rs212359259 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105160054 | ATCTTAGTAAAGAAC[-/A]AAAAGAAAAATAAGT | 71816 |
rs212376215 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105155026 | TGTGAACACCTGCAT[A/G]TGTGTGTGTATCATA | 71816 |
rs212383915 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105245231 | GCAACACCCTCTTCT[A/G]GCCTCTGTGAGTACC | 71816 |
rs212403637 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105161440 | ATGACTGAGGCCTCA[C/T]CTGCCAACAGCTGTC | 71816 |
rs212405072 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105168162 | TGCGTCTCCATCAAC[C/T]GCCTACCTTTATCTT | 71816 |
rs212442882 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105162276 | TATGTATATATGCAT[G/T]TATTCTTGTATGTAT | 71816 |
rs212443141 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105202314 | TGAAAATAATCATTC[C/T]GAGTAAGGAAATATA | 71816 |
rs212468084 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105237272 | TTTTCTGCAGCAAAC[A/G]TCAAATGAGATTGCA | 71816 |
rs212471563 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105175401 | TTTCCTGTTATCACA[A/G]AGACACTTGCTCAAC | 71816 |
rs212479327 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105253014 | AGGTCTAAAGTAGCC[A/G]TACAGGATGTGATAA | 71816 |
rs212482073 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105195916 | GAGAAACTCTGTCTC[A/G]AAAAACCAAAAAAAA | 71816 |
rs212502847 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105219984 | GTGTGAATTACAACA[A/G]TCTGAGGCCCGGCCT | 71816 |
rs212502994 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105174321 | GACTTTGCTTAATGA[C/T]TTTTACTACATAAAA | 71816 |
rs212542285 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105146716 | ATTAGGGTGGTGAAT[A/T]AACTTGCCCCAGGAT | 71816 |
rs212553236 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Rnf180 | Mm_Celera | 13:105292053 | CAGGCGGGTGGGATG[C/G]AGGGGAAAGGGAAAC | 71816 |
rs212566783 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Rnf180 | Mm_Celera | 13:105292555 | GGGCGCCTTACACAC[C/T]GGCACATCCTCCAGC | 71816 |
rs212567870 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105284498 | ACCCATCTTTAATAG[A/C]TATTACTCTTCCATT | 71816 |
rs212573330 | in-del | -/AAAAAA | | | intron-variant | Rnf180 | Mm_Celera | 13:105203821 | AGTAAAAAATAAATT[-/AAAAAA]AAAAAAAAAAAGAAC | 71816 |
rs212580727 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105188253 | GAAAGAAACCCTACT[C/T]AGTACCATCTCTGAC | 71816 |
rs212613840 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105139281 | CTCTGTCTTCCTGCT[G/T]TGCACATTCTATCAC | 71816 |
rs212644286 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105231718 | GTTAACGCAGACTTT[A/G]GACCAAACCACTCAG | 71816 |
rs212649791 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105138415 | TCCTCATAGCATGTA[A/C]GTTTGATTTATTTTA | 71816 |
rs212674192 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105220839 | AGCCAGGTAAGACAA[C/T]TTATTCTTTCAAGTG | 71816 |
rs212677816 | in-del | -/TTTT | | | intron-variant | Rnf180 | Mm_Celera | 13:105273380 | CCTTGTCTTTCTGTA[-/TTTT]TTTTTTTTTATTATT | 71816 |
rs212682092 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105273152 | ACCAAGTCAACTAAG[C/T]GGGTCTTAATTGGGC | 71816 |
rs212735658 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105132170 | TAGGGGACTGAATGG[C/T]GGAGAAAAATATAAT | 71816 |
rs212740787 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105177101 | CAGACAGAAACAGGA[G/T]AATTGAGAAATATTT | 71816 |
rs212755687 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105245825 | TTAGCTATGATTAAT[A/G]CAGAACTCTTGCCAC | 71816 |
rs212777825 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105168768 | ATTTCCCAATAACTC[A/G]AGTATCTGATAGGTG | 71816 |
rs212785133 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105265523 | TTCATGTTAGTCAAC[C/T]TTACAATATTTACTA | 71816 |
rs212797644 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105266100 | CATTGACATTTTTTC[C/T]AACTCTCACAGAAGC | 71816 |
rs212797754 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105183489 | ATCTGTCTTTTTTTA[A/T]AAATCCCAGCCCACT | 71816 |
rs212807620 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105277243 | TTTTATTTATTTATT[-/A]TTTTTTTTACTGGCT | 71816 |
rs212829403 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105202807 | GCTATTGTTGCCAAT[A/G]TTCTTTGTTACCCTC | 71816 |
rs212856054 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105255534 | CAACACCTGAATGAT[A/G]GCTTAGAACTGTCTG | 71816 |
rs212866414 | in-del | -/AGACAA | | | intron-variant | Rnf180 | Mm_Celera | 13:105218159 | CATTCTTGATTTGGC[-/AGACAA]ACACACACACACACA | 71816 |
rs212876647 | in-del | -/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105235280 | TTAAGATGTATGAAT[-/C]CTAAAAAGAAAAAAA | 71816 |
rs212879296 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105196551 | GGCAAATCTAATACT[A/C]GTAAGTCATTTTGAT | 71816 |
rs212894971 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105216108 | TCCTGAGTGCTGGGA[A/T]TAAACATATACACCA | 71816 |
rs212911375 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105203438 | GTCAACTAACCTGGG[A/C]CCCAGTGTGGGGGTG | 71816 |
rs212912167 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105155768 | ACTCTGCCTTCTGAG[A/C]AGGCTTCTAGAGCTG | 71816 |
rs212931541 | in-del | -/GTATTAA | | | intron-variant | Rnf180 | Mm_Celera | 13:105170271 | TAATAGTATTTAAAT[-/GTATTAA]GCCTTACCTTACATT | 71816 |
rs212932863 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105209384 | TAGGATGACCTTAGA[A/C]TTCTGATCCTCCTAC | 71816 |
rs212946214 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105203222 | CTACTATTATTCTGC[-/A]AAAAAGAATATAATG | 71816 |
rs212953813 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105246823 | GTAGAGAAATCATGG[C/T]TCATTTACAGAATGG | 71816 |
rs212971470 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105209888 | TCAAGTGTAAGGTCG[C/T]CTTATGATGGTGTGC | 71816 |
rs212984581 | snp | C/T | | | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105148482 | GTTCCATCCCATGCC[C/T]ATGTGGATGTTCCTG | 71816 |
rs212990091 | in-del | -/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105221526 | CCTGAGACAGATTAA[-/T]TTTTTTCCAAATTTT | 71816 |
rs212990397 | snp | A/G | | | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105147511 | GCAGTTAACAGTACC[A/G]TCAATTTTATATTAC | 71816 |
rs212993776 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105163875 | TCTTTTTATCTGCAC[G/T]TCACCTTAAATATTT | 71816 |
rs212994426 | snp | A/C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105239172 | CCTGTGCCACACACT[A/C/T]GGTCGAGTCAGCTTG | 71816 |
rs212995717 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105256066 | GGTGTTTCATACTGT[A/G]GTACAAAACAGAACC | 71816 |
rs213031026 | in-del | -/TTAC | | | intron-variant | Rnf180 | Mm_Celera | 13:105168286 | TTTATGTTTGACCTA[-/TTAC]TTACTGCCTTATGCT | 71816 |
rs213034670 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105157369 | GACATTGCTTATTGG[C/T]ATCAACAGTTATGTT | 71816 |
rs213057818 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105197807 | ATAAAAGAGCAGGAA[A/C]ATATTTTTAAAGATC | 71816 |
rs213059211 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105225720 | GTGTGTGTGTGTGTC[C/T]GTCAGTCAGTCTGTA | 71816 |
rs213072746 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105285133 | GAGGAGGGAGCAGAT[A/G]ATCTGCTCAAGGCCA | 71816 |
rs213074277 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105158133 | ACTCATTTACCACTT[C/G]CAGGCCTCACACGGA | 71816 |
rs213131142 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105233728 | CAAGAACGATTCCCA[A/G]CACCCATGCTGAATG | 71816 |
rs213150273 | snp | A/G | | | upstream-variant-2KB | Rnf180 | Mm_Celera | 13:105294946 | GGAGCAATTAAAACG[A/G]CTGATCAAAAGATTG | 71816 |
rs213164513 | snp | C/T | | | upstream-variant-2KB | Rnf180 | Mm_Celera | 13:105295662 | GGGTAGAGAAGGGGA[C/T]CCCAGAGTCGGGGAG | 71816 |
rs213166452 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105191325 | AGCTGTCTTTAGACA[C/T]ACCAGAAGAGGGCAT | 71816 |
rs213174462 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105142995 | AGAATTTCAATTCCC[C/T]CTTGCCAGGATTTCT | 71816 |
rs213176572 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105277318 | TTCAAAGGCTGGACA[C/T]AACCCTTCTAGGAGT | 71816 |
rs213181290 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105190779 | AATGCCGATGCTAGC[A/G]ACTGAACTCAGGTCC | 71816 |
rs213191053 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105177575 | TATGGACCTCAAGTC[C/T]ATTAGTCAGGATGTT | 71816 |
rs213212568 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105184240 | TGGAGTTCTAGGCAG[A/T]AGAAGTCACCTGATG | 71816 |
rs213220337 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105286850 | TTAAACCGCCTGCAT[A/G]ATCATCAGAAAATCC | 71816 |
rs213225699 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105150147 | CTTCCTTTATGGCTG[G/T]TTTGGTTTGGTAAGC | 71816 |
rs213227788 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105133133 | GACCAGTTAAAGGGA[A/G]AACAGTGTATGCTTT | 71816 |
rs213249401 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105169243 | TCTCCACTGTAAGAA[A/G]CAGTCGTCTGAGTCC | 71816 |
rs213252346 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105226541 | TAATAAAAATAAAAT[A/T]AAATTAAAAAAAAGA | 71816 |
rs213255897 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105234355 | AAGCAAGTCCTTAGC[A/T]GCTGAACCTTCACCA | 71816 |
rs213263864 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105221963 | TCCTGCAAACAGGGC[C/T]AGCTTTACCCTGCTG | 71816 |
rs213293455 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105227034 | TGACTATATGTATAT[A/G]CATTTATATTCCCAA | 71816 |
rs213321171 | in-del | -/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105286533 | TTCTACTTTAACTTA[-/G]GAAAAAGTCAGTCGG | 71816 |
rs213338014 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105201555 | ATAGGCATCAAGACC[A/C]ACAATTAATAAATGG | 71816 |
rs213361365 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105202177 | AGCTAGGAAGTAGAA[A/G]CAGCCTACATATCTA | 71816 |
rs213373319 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105195329 | TCAGAATAAGATATA[A/G]AACCCTTAGCTCCTT | 71816 |
rs213377853 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105236713 | GGCTTTAAATAGCCA[C/T]AGGCAGTTATGATAT | 71816 |
rs213381864 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105245191 | ATGTAGCACACATCT[A/G]CATCAAACTCTAGCT | 71816 |
rs213397021 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105195889 | GAGTTCCAGTATAGC[C/T]AGGGCTACACAGAGA | 71816 |
rs213408167 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105154271 | GCAGGGTTTTTTGAT[A/T]TTTTTTGTTTGTTGT | 71816 |
rs213443909 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105247612 | GGTCTGCCCGCAGGG[A/T]CAGTGCAGTCCCTAC | 71816 |
rs213447750 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105145874 | AATTTTAAGTTTATT[A/G]GTGAAATTGTGACAG | 71816 |
rs213492513 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105239768 | TTTTGAGGCAGCACC[C/T]GGTCCCCACCTTCTT | 71816 |
rs213507582 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105231210 | CCAGAGACATGCACC[A/G]TTTGCCCATGTCTTC | 71816 |
rs213516050 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105204217 | TCTCTCTGCCCTTGC[C/T]TTTTGTCATCACTTA | 71816 |
rs213523022 | snp | C/T | | | intron-variant, synonymous-codon, utr-variant-5-prime | Rnf180 | Mm_Celera | 13:105291881 | CGTGGGGGGTGGGGC[C/T]GCCAGAGAAGATGCA | 71816 |
rs213530933 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105283656 | CTTAAAGAAGGACGC[A/C]GTGTTCAGTGTGGAG | 71816 |
rs213531434 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105139207 | CCTACTGTGTTCCTC[A/G]CCCTGTGCCCCAGGT | 71816 |
rs213540855 | snp | A/C/T | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105284383 | TAGAAGTTGAGAAAA[A/C/T]GTCTCATATGAATAT | 71816 |
rs213541140 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105272181 | ATTGAACATAAAATT[A/G]GGTGAGTATAGAAGT | 71816 |
rs213547680 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105224828 | AGAGTCGAGGTGGCA[A/G]AGACTCAGGTGAATC | 71816 |
rs213561585 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105138354 | AAAGAAAATACTAAA[A/T]AAAGAATTTCAGTCT | 71816 |
rs213572294 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105198154 | ATAAGTGGATATTAG[G/T]CAAAAAGTGTGGTAC | 71816 |
rs213588760 | in-del | -/TCTA | | | intron-variant | Rnf180 | Mm_Celera | 13:105140060 | GTCAGACAAGGTTTC[-/TCTA]TCTATCGTTGTGTGT | 71816 |
rs213592856 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105175584 | AATTATATTTATTTT[A/G]GATTACCAAATCTTT | 71816 |
rs213595618 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105237730 | TGTTTCTATAACGAC[-/A]ATCACTCATGGTGGG | 71816 |
rs213597779 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105273063 | GTGCTCCAGTCAGGG[A/T]GGGGCAAGGTGTCTC | 71816 |
rs213607622 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105188133 | TATCTTAAGCTCATA[G/T]TTTTTGAGATGAAGT | 71816 |
rs213631825 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105176776 | GACAAATGGACACAG[C/T]CAAATAGTCTCCCTG | 71816 |
rs213643124 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105149573 | ATTTTACATCAGCAA[C/T]AGAAATCTAAGATGG | 71816 |
rs213680622 | in-del | -/ACGT | | | intron-variant | Rnf180 | Mm_Celera | 13:105289918 | TGGGCTGTGGCAAAA[-/ACGT]ACCTGCTATCCATGT | 71816 |
rs213685938 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105215695 | TTAGGATTAAGATTT[G/T]CGATAGCCATGCATG | 71816 |
rs213721926 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105216056 | GCTATGTAGATCAGG[A/C]TGGCCTTGAACTTGC | 71816 |
rs213767094 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105162138 | TCTAACTGATTACAG[A/G]AAGATTATAGGAAGA | 71816 |
rs213773196 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105266057 | TCTAGGACCATGCAC[C/T]GCATCTCCCACCTGA | 71816 |
rs213782285 | in-del | -/AGG | | | intron-variant | Rnf180 | Mm_Celera | 13:105144023 | CCTCTTAATTTACTC[-/AGG]AGTCCTTAAATTGTG | 71816 |
rs213801145 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105208211 | TTCCTCCCATGAGTA[G/T]TTTGAAAAGCTTTTA | 71816 |
rs213804333 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105169158 | AAATGCCAGCACTTC[A/C]CTCTCAGACTCCATT | 71816 |
rs213816316 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105246511 | AGTACACACAGTATT[A/G]GAGTGACCGAAACAC | 71816 |
rs213847127 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105265234 | AATAAGAACGAGGAC[A/G]TACTGCATTTTGCAG | 71816 |
rs213870251 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105208646 | ATGCTAACTCCTAAA[C/T]GTGGGATCAAAGACA | 71816 |
rs213939866 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105197447 | CCATTGAAAGCAATG[C/T]TCCCAGACAAAAGCT | 71816 |
rs213945274 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105155015 | GGGTGCGTGTGTGTG[A/C]ACACCTGCATATGTG | 71816 |
rs213968505 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105197995 | GTCTTTTGGAACCAA[A/T]GCCAACAGCATCCGG | 71816 |
rs213969300 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105140177 | CGTGTTCCCACTAGA[A/G]CAGAGAGAAGGTTTG | 71816 |
rs213969322 | snp | C/T | | | missense, intron-variant | Rnf180 | Mm_Celera | 13:105149455 | GCCTCGTATCTCATT[C/T]CTGTATCCAAGATCC | 71816 |
rs213973582 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105239434 | AATCCAGCAGGACTG[C/G]AGAAAGGAAGTTACC | 71816 |
rs213986412 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105163441 | AGAGTTTTCAAAGTC[A/G]TCATCAGCATATAGT | 71816 |
rs214000144 | in-del | -/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105209956 | GGAGAGGGGAGATTC[-/T]TTACTTGATACCTAC | 71816 |
rs214000368 | in-del | -/A | | | upstream-variant-2KB | Rnf180 | Mm_Celera | 13:105295543 | ATAGATCATTTTAAC[-/A]AAAATGATCCTCAAC | 71816 |
rs214002014 | snp | C/T | | | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105148301 | ATGCAGCCATGAACT[C/T]AGAGCAGCAGGCTGC | 71816 |
rs214006831 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105233574 | AAATTAGGATCCTCT[G/T]TAAGAGCAGCGAGTG | 71816 |
rs214032139 | in-del | -/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105168939 | CCCCCTACCAAGTTC[-/T]AAAATGTTGATGTAG | 71816 |
rs214046951 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Rnf180 | Mm_Celera | 13:105292512 | TACAGTACCACAGAA[A/G]ATGACAAACACAAGC | 71816 |
rs214047382 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105156675 | TGGCACTGAGAATGA[C/T]GGCTTTACATCCTTG | 71816 |
rs214078696 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105188560 | GTCCCAAGGAATGGA[A/T]AACACACAGTATGTA | 71816 |
rs214082620 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105202961 | AATGTACTGTGTATG[C/T]CTCCAGAGGAGAAAA | 71816 |
rs214089079 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105190566 | ATACATGTGTGTATG[C/T]GCATGAGTGTGGAGG | 71816 |
rs214124985 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105277264 | TTTACTGGCTCACAC[A/C]GTTCTAGGGTATACT | 71816 |
rs214127375 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105182913 | TCCTTATAGATTTCC[C/T]AGTCTATGGTACTTG | 71816 |
rs214134941 | in-del | -/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105180311 | TATTTCATTGACATA[-/T]TTTTTAAGATTTTAT | 71816 |
rs214135246 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105266629 | ATAACGAAGGCCACG[A/G]TTCTGTACTCTAAGC | 71816 |
rs214146246 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rnf180 | Mm_Celera | 13:105293670 | TAACCTGCCCACACC[A/G]TACTCCTTTGAAGTT | 71816 |
rs214157815 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105225105 | GTGAAGATCCACAGA[C/T]CTAAAGCCTGACTGG | 71816 |
rs214173475 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105221930 | CTCTTCTGCCTTCAG[G/T]GGTGGCTCCCCAGCA | 71816 |
rs214208322 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105216446 | GGGGAAAACACGGGT[A/G]GAACGCTGTCAGTGT | 71816 |
rs214226005 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105285331 | TGTATCAAAATAATA[A/T]TAATAATAAGGTCTC | 71816 |
rs214230099 | in-del | -/TT | | | intron-variant | Rnf180 | Mm_Celera | 13:105172133 | TCTCAGTTAGCTCTC[-/TT]TGCCTTTTTCTCCAG | 71816 |
rs214236520 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105233089 | TACAGCCCTCCCACA[A/C]CTGTTCTCTCCCAGA | 71816 |
rs214264512 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105267257 | ACAAACTCTGTCACA[A/G]GACTATCAGTTAGCA | 71816 |
rs214281260 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105225918 | CCTGAAGCTAGAGCT[A/C]ACGGATTTGTTAGCC | 71816 |
rs214298117 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105143796 | TGCATTTCTTTACTT[-/A]AAGTGTCTTCCCATG | 71816 |
rs214355096 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105165185 | CATTACAGAGAATTC[A/T]CCTGCTGGGTTCTGC | 71816 |
rs214363085 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105255466 | AAAGAACACAAGTTT[C/T]TTTATTTTATATGCT | 71816 |
rs214371298 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105152817 | CTCAGACATCACTTT[-/A]AAAGAAAAGACAACC | 71816 |
rs214376181 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105240928 | TTTTTAATCATCAAG[A/G]GATTACAATACACCC | 71816 |
rs214385361 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105183825 | TCTGCTTTTATTTGA[A/G]CCAGTACTTGCCTTC | 71816 |
rs214415519 | in-del | -/TG | | | intron-variant | Rnf180 | Mm_Celera | 13:105237061 | TGGGTGGATGGTCAT[-/TG]TGTGTGTGTGTGTGG | 71816 |
rs214425312 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105132349 | ACACCTTGAGAGAGG[A/G]AAGATCAATTGAGAA | 71816 |
rs214425984 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105163832 | TTTTAGGAACTCCAC[C/T]GCCAATCTCTTTATT | 71816 |
rs214433618 | in-del | -/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105240761 | AACCCAAGGAAACTC[-/T]TTTTTTTTTCTTTTT | 71816 |
rs214437647 | in-del | -/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105215480 | AACCCACAGTAGGCC[-/G]TTTGCCTGCTGGAGA | 71816 |
rs214452976 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105209145 | CGGATAACCCTAAGC[A/C]TGAGATGACTATTTA | 71816 |
rs214462891 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105198909 | ACTGTGGAGAGGGGA[A/G]ACTGAGCCAGGAAAC | 71816 |
rs214467179 | snp | A/G | | | upstream-variant-2KB | Rnf180 | GRCm38.p3 | 13:105295866 | CCTCCCCTGTTTCTC[A/G]TGGCTTAACAGGTAT | 71816 |
rs214469994 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105157281 | ACGTCTCCTTCACTG[A/C]TTCAGTAGGGCTGTC | 71816 |
rs214479941 | snp | A/T | | | upstream-variant-2KB | Rnf180 | Mm_Celera | 13:105296625 | ATTGAAATTGATTGA[A/T]CTGATGAATATTTCA | 71816 |
rs214509177 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105203400 | TTTAGAACATTCAAG[G/T]ATATCACAAGAAGAA | 71816 |
rs214510040 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105178704 | AAAAGAAAACCAACC[C/T]AACCCAAAATCTAGA | 71816 |
rs214519025 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105256208 | GGAAATATGTACATT[A/G]CTGTGAATCAACTGG | 71816 |
rs214527137 | in-del | -/C/GC | | | intron-variant | Rnf180 | GRCm38.p3 | 13:105237097 | GGGGGGTGCGGGGGG[-/C/GC]GGGGCAGGGTAGACT | 71816 |
rs214534522 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105222391 | AACAAGCTCAACTAG[A/G]ACCCCACCATCAGGG | 71816 |
rs214536356 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105143688 | ATGTTTTGAGTCTCT[A/G]TCTCTCCCACCAATG | 71816 |
rs214537590 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105192480 | ATTCACAACTCCTTG[C/T]GTCTTGCTGTGAAAT | 71816 |
rs214544041 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105235036 | ACTCCTAACAAGCAA[A/G]TCATCCTGTCTTTGA | 71816 |
rs214572514 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105143267 | ATATTTTCTTATATT[G/T]CCCTTATTATTTTCT | 71816 |
rs214595305 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | Rnf180 | Mm_Celera | 13:105294703 | TCTAAAGGTGGAACC[A/T]CCACTACCTGGGTTC | 71816 |
rs214620676 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105267307 | AATATTTAAAGAGTT[-/A]ACATGTTTAAAATCC | 71816 |
rs214633776 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105205425 | AGGGATCCCAAGCAG[-/A]AACCCTCCCTGCGCC | 71816 |
rs214657713 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105134900 | AAGTAACTAACATTG[C/T]TAGTATGTATTGCAC | 71816 |
rs214673209 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105185625 | GTGATGTTTATGCAC[A/C]CGCTCTTAAGGGAGT | 71816 |
rs214692401 | in-del | -/TACCCCCTG | | | intron-variant | Rnf180 | Mm_Celera | 13:105177502 | TACTGACTCTGTAAT[-/TACCCCCTG]TAATACCCGGGATAT | 71816 |
rs214694444 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105134570 | AGCCTGTGGGCCTTA[G/T]CACGAGATAAGAGAA | 71816 |
rs214699283 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105267976 | ATGTTAAATATTAAA[G/T]CAGAAATTTAAATTC | 71816 |
rs214705454 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105226405 | TTGGACTTGAAAACT[G/T]TATATGCCCCAGTAC | 71816 |
rs214713003 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105268722 | CCAGACCCTGAAAAG[A/G]GCACTGTTGATTAGT | 71816 |
rs214731638 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105172619 | TGTGGAGCAGAGACT[A/G]AAGGAAAGGCCATCC | 71816 |
rs214731808 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105286102 | AGCAAAGCTGCCAGC[A/G]CCTGCTCTTGGCCTT | 71816 |
rs214738675 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105249032 | TAAATTTTATTATTT[A/G]CTTTCATACACAGAA | 71816 |
rs214750221 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105133077 | TGCTGTTTGTGTCAA[A/G]CTATGGACTTATTTG | 71816 |
rs214764865 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105217776 | TGACGAAGGCATTCT[C/G]TTACGGTGGGCAAAC | 71816 |
rs214772083 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105258547 | CGTCTTGCAATGACA[A/G]TTCAGGCATTATAAG | 71816 |
rs214796160 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105184206 | GACCAGGAATCCTGA[A/C]CTTTCAGAGCCCTGA | 71816 |
rs214805717 | snp | G/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105218446 | CAGTACATGGCCAAG[G/T]AACCACCTGCTAGAC | 71816 |
rs214830033 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105205264 | TTAATCCTAGTACTT[A/G]GGAGGCAGAGGAAGG | 71816 |
rs214868670 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105199327 | CATATTGGTCAGAAT[A/C]TGGCAGAGTCTTTCA | 71816 |
rs214872280 | in-del | -/CGGCCGCG | | | upstream-variant-2KB, intron-variant | Rnf180 | GRCm38.p3 | 13:105294126 | AGCCCCCGGTCACGC[-/CGGCCGCG]CGGCCGCCCAGGCCC | 71816 |
rs214875467 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rnf180 | Mm_Celera | 13:105293138 | CTAAGTAACTCTTTG[A/G]CCTAGTGACTCACTT | 71816 |
rs214887236 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105285145 | GATGATCTGCTCAAG[A/G]CCATTGTTAACAGTG | 71816 |
rs214906006 | in-del | -/CT | | | intron-variant | Rnf180 | Mm_Celera | 13:105201869 | CTCCAATCAGAATGG[-/CT]CCCCCTAAAAAACCC | 71816 |
rs214920491 | snp | C/T | | | utr-variant-3-prime, intron-variant | Rnf180 | Mm_Celera | 13:105148213 | TTCACGGACTTCCTC[C/T]CTATTGTCTGTCTCA | 71816 |
rs214922580 | in-del | -/AATT | | | intron-variant | Rnf180 | Mm_Celera | 13:105134343 | AATAACCAGTAAAAA[-/AATT]AAATAAAAGAAAAAA | 71816 |
rs214945965 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105183773 | GGCTGGTATTTTCCC[A/T]TTTAAACAAAAGCAT | 71816 |
rs214949566 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105285908 | TTATCAGCACCCCAT[A/C]CCTGCAGCAGAAGCT | 71816 |
rs214958847 | in-del | -/A | | | intron-variant | Rnf180 | Mm_Celera | 13:105256782 | GGGGACCTGCAGTCC[-/A]GTTCTCCTCCTTTTC | 71816 |
rs214960274 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105151996 | TTCCAAACGCTGACA[C/T]CATTGCATACACTAG | 71816 |
rs214964249 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105225760 | ATGCTTGTCTGTCTG[C/T]GCGTGTATGATATGA | 71816 |
rs214977488 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105177596 | TCAGGATGTTTGTAA[A/G]AAGATCCTCACTTTG | 71816 |
rs214998499 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105221356 | AAGTACTTGAGAAAA[C/T]GGTTCTTCTGTTAGT | 71816 |
rs215000438 | snp | A/C | | | intron-variant | Rnf180 | Mm_Celera | 13:105226361 | GTATTAGAAATTCCT[A/C]GTCGGCCATCACTGC | 71816 |
rs215020420 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105228101 | ACCAATACTGATGTC[C/T]TGACCTGTGCAACCT | 71816 |
rs215020700 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105256789 | CTGCAGTCCGTTCTC[C/T]TCCTTTTCAAATGAG | 71816 |
rs215037602 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105221846 | AAGAAAATGTTGGGG[C/T]GAGCCAATTCAAAAG | 71816 |
rs215047749 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105288960 | AGACTGAATCAAGAG[A/G]GAGGATTTCTGGTTC | 71816 |
rs215051062 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105277244 | TTTATTTATTTATTA[A/T]TTTTTTTACTGGCTC | 71816 |
rs215067813 | snp | A/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105248441 | CATTGTTTTGAAGAT[A/T]TTCTTTCTGAAGAAT | 71816 |
rs215105232 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105178125 | GTCAGATGACAGAAA[C/G]AGAAGAATGCGAGAC | 71816 |
rs215123467 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105256130 | AGCTATTAACAAACC[C/T]ATGAACTGGGCTTTG | 71816 |
rs215137754 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105158975 | AATCTAACACCTTCA[C/G]AACAACTGATCACCA | 71816 |
rs215155790 | snp | C/T | | | intron-variant | Rnf180 | Mm_Celera | 13:105179695 | ATCAACCTGTAGTTA[C/T]TGGGAGGACCCCACA | 71816 |
rs215161686 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105247786 | CCAGGGCGTGGCTCC[A/G]AGCCAGGGAAGTCAC | 71816 |
rs215172743 | snp | C/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105204724 | TCGTGATCTCTGTGG[C/G]GGTCAACTGACCTTT | 71816 |
rs215180004 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105223381 | ACAGCAGCCACATCT[A/G]CAAACTCTAGGGACA | 71816 |
rs215198994 | snp | A/G | | | intron-variant | Rnf180 | Mm_Celera | 13:105173638 | TGTCAACAAGGTAGA[A/G]AAAGCTCGGTCTGTT | 71816 |