SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3685176 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Abl2 | Mm_Celera | 1:156599799 | GCCATCAGGTGTTTG[C/T]CAAAAAGAAAGTGGT | 11352 |
rs3705667 | snp | A/G | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156600846 | CTGGGTTAATCCCTA[A/G]GACCATATAAACTGG | 11352 |
rs3710643 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | Abl2 | Mm_Celera | 1:156645874 | TCCTAACCTGGGAGC[A/T]CACAAACATCCTCTA | 11352 |
rs3710691 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Abl2 | Mm_Celera | 1:156645894 | AACATCCTCTAGAGA[C/T]TTTTAAAGGAAAACT | 11352 |
rs3711214 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Abl2 | Mm_Celera | 1:156645940 | CTTTGATGGAATCCC[C/T]GGTGGGATGAGAGAC | 11352 |
rs3711833 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | Abl2 | Mm_Celera | 1:156646042 | GAGGAGACGGGAGAG[G/T]ACTGTTGTCACTAGT | 11352 |
rs6185284 | snp | C/T | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156603533 | tcttgccactatagt[C/T]ttcgtcttttcaaag | 11352 |
rs6269987 | snp | C/G | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156587486 | GCCAACCAGTGACTG[C/G]GCAAGCTGAGATCCA | 11352 |
rs6334707 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Abl2 | Mm_Celera | 1:156636635 | GAACCAAGGATAGAT[C/T]GGTCTAGCACTATGA | 11352 |
rs6334835 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Abl2 | Mm_Celera | 1:156636711 | TCTCATAGTTCCTGT[A/G]CATGCTGTAACTCTG | 11352 |
rs6355411 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156598305 | AAAAAATCTCAGCTA[C/T]CTTCTCTGCCTGCAT | 11352 |
rs6355429 | snp | C/T | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156598323 | TCTCTGCCTGCATGC[C/T]ACCATGCTTCCTGCC | 11352 |
rs6356411 | snp | G/T | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156598527 | ATTGTCTCAGAAACT[G/T]ACTGCTGAATAAGCT | 11352 |
rs13476194 | snp | A/G | 0.49426 | 0.0532631 | utr-variant-3-prime | Abl2 | Mm_Celera | 1:156649115 | CCTGCACTTCTTCTC[A/G]TTTGCAATCTGATTC | 11352 |
rs30464767 | snp | A/T | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156633501 | AGGGCTTATGTTGCT[A/T]ACCTGTGAAATCTAG | 11352 |
rs30466582 | snp | A/G | 0.375 | 0.216506 | missense | Abl2 | Mm_Celera | 1:156642255 | GCAGCTCCAGGCCCA[A/G]TGCCCAGTAGTGGGA | 11352 |
rs30467430 | snp | A/T | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156612321 | TATTTTCCTTTAGCA[A/T]TTCTTCTAGAGCCAG | 11352 |
rs30468510 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156637940 | CAACTTAAGCACCTA[A/G]CAAGCTTTTATTTAT | 11352 |
rs30473047 | snp | A/T | 0.625 | 0.125 | intron-variant | Abl2 | GRCm38.p3 | 1:156594653 | GATTGGCTTTTTTTT[A/T]AATCAGTTTTTACAT | 11352 |
rs30495830 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Abl2 | Mm_Celera | 1:156596717 | CTCAGGACACATAAC[C/G]TGCCCTGGGCTCTGC | 11352 |
rs30513957 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Abl2 | Mm_Celera | 1:156575968 | GGCCTTGTGCTTGAG[C/T]CTGTCTTCTGTGTCA | 11352 |
rs30513963 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Abl2 | Mm_Celera | 1:156622218 | AAGCCCAGGAAATAA[C/T]AGCACCTATGCCAAC | 11352 |
rs30551337 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | Abl2 | Mm_Celera | 1:156649154 | CTATCAGTGGAACTG[C/G]CCGACTTTGTGTTTG | 11352 |
rs30568418 | snp | A/G | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156617655 | TGTGTTGATTATATA[A/G]TAAATATATTACCTA | 11352 |
rs30590318 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156592474 | CAAGAGGTTTTTAAA[A/C]TGTTTTAACCTACAT | 11352 |
rs30590341 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Abl2 | Mm_Celera | 1:156578036 | TTGCTATGATAAGTC[A/G]TAGCTCTCCACCTCT | 11352 |
rs30597149 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Abl2 | Mm_Celera | 1:156605734 | CCTGTCTGCACTGCA[C/T]GGCGTAACAGTTGCA | 11352 |
rs30598322 | snp | G/T | 0.375 | 0.216506 | intron-variant | Abl2 | Mm_Celera | 1:156618130 | CATGCCGGGGACTTT[G/T]GTTGGTTGGTTGGTT | 11352 |
rs30604424 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime | Abl2 | Mm_Celera | 1:156643999 | CAGTCATGGAAGCTA[A/T]TAGAGTAACATGGGA | 11352 |
rs30612619 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156563392 | TGGAATTTTTCTCTT[C/T]TGTATCTGTAGTGCA | 11352 |
rs30618479 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Abl2 | Mm_Celera | 1:156580401 | GTAGACTATTCCAGG[C/T]AACTTTTCAGATTTT | 11352 |
rs30639749 | snp | C/T | 0.5 | 0 | intron-variant | Abl2 | GRCm38.p3 | 1:156572576 | AAACAAACAAAAAAA[C/T]CCCCCAGTCTGACAA | 11352 |
rs30643677 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156560191 | ATAGACAAGGTTATA[A/G]TAATTAACAAATAAT | 11352 |
rs30688466 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156565809 | GTTTATATCCTCCAC[A/G]TGTTCTTTATCTGTA | 11352 |
rs30698560 | snp | C/T | 0.375 | 0.216506 | intron-variant | Abl2 | Mm_Celera | 1:156634462 | TCAAGGATATCATCT[C/T]GTCTTACCTTGTCCT | 11352 |
rs30700683 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156630522 | ATGCCCTTTTTAGTA[A/G]AAGTAGAAATGACAA | 11352 |
rs30701390 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Abl2 | Mm_Celera | 1:156577652 | CCTTAGTTGGACCCC[C/T]TCCCCAAAAGAAGTC | 11352 |
rs30754695 | snp | A/G | 0.375 | 0.216506 | intron-variant | Abl2 | Mm_Celera | 1:156603172 | TCATTTAAAAATTTT[A/G]CTGTAGAATTTTTTA | 11352 |
rs30755943 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Abl2 | Mm_Celera | 1:156558029 | TTAAAGATTCATTTA[C/T]TTATTATATGTTAGT | 11352 |
rs30757302 | snp | A/C | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156598770 | TCTGACTCGTTCTTT[A/C]AAATCTTTCTCTGAT | 11352 |
rs30759102 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Abl2 | Mm_Celera | 1:156623448 | TTTTGTCTGCAATTC[C/T]AGCATTTTGAAATAC | 11352 |
rs30802177 | snp | G/T | 0.375 | 0.216506 | intron-variant | Abl2 | Mm_Celera | 1:156618121 | CATGTGCCACATGCC[G/T]GGGACTTTGGTTGGT | 11352 |
rs30803412 | snp | A/C | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156634301 | CTGTGACTGTGTCAG[A/C]CTTCTTATGTCACAT | 11352 |
rs30851566 | snp | A/G | 0.375 | 0.216506 | intron-variant | Abl2 | Mm_Celera | 1:156634483 | ACCTTGTCCTGCATC[A/G]TTACCTTTGTCCTAT | 11352 |
rs30852463 | snp | C/T | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156570858 | GCTGGAGTCAGAACT[C/T]GGGTCTTCATGCTTG | 11352 |
rs30859304 | snp | C/T | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156563064 | TGTGTGACTTGCTAG[C/T]TTCTAGTTGATGGTT | 11352 |
rs30859428 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156589244 | AAGTACATTAAAAAA[A/T]TTTTTTAGGTACATT | 11352 |
rs30896707 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156620341 | CACAGGGGAACTGCT[A/G]AGTGTTGAAAAGTGA | 11352 |
rs30898022 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156568269 | AATGCAGCAAGGCCC[A/G]TCCAGAACCAGGAAG | 11352 |
rs30909609 | snp | C/T | 0.375 | 0.216506 | intron-variant | Abl2 | Mm_Celera | 1:156594723 | TCATCTCACAAATTT[C/T]ATGTATACAGTTTTG | 11352 |
rs30917108 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156634655 | CCATGAGTTTGAGAC[C/G]TGCCTGAACAGTATG | 11352 |
rs30918987 | snp | C/G | 0.444444 | 0.157135 | intron-variant, missense | Abl2 | Mm_Celera | 1:156616040 | GATGCCTCGGAGTTC[C/G]CTGTGGCCCACGTGA | 11352 |
rs30999523 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Abl2 | Mm_Celera | 1:156600659 | TGAGTACTTGGTATA[C/T]TGAGCCTAACTGATC | 11352 |
rs31000062 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156623254 | CACTTGCTATTCTAT[C/T]CCTGCAGAGGACCCT | 11352 |
rs31003942 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Abl2 | Mm_Celera | 1:156579630 | ATAGTGAGACTCAAA[A/G]TCAGATAATGAGAGC | 11352 |
rs31058174 | snp | C/T | 0.375 | 0.216506 | intron-variant | Abl2 | Mm_Celera | 1:156622016 | CATTACACAACAGTG[C/T]ATCACATGTGCTTTA | 11352 |
rs31060687 | snp | C/T | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156618698 | CCATGGGCACCCATA[C/T]GTGAGTGCAGAAATG | 11352 |
rs31061119 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Abl2 | Mm_Celera | 1:156594124 | TCCATTAGGCCAATT[C/T]TTTTTTCTAGTTATT | 11352 |
rs31076284 | snp | C/T | 0.33241 | 0.236027 | upstream-variant-2KB | Abl2 | Mm_Celera | 1:156556444 | CTTTTACAACAAATA[C/T]GCTTTTCCTCCTGCC | 11352 |
rs31105154 | snp | C/T | 0.32 | 0.24 | intron-variant | Abl2 | Mm_Celera | 1:156567994 | TTGATTATTTCTCTG[C/T]TTTCCTTTTCTCTCA | 11352 |
rs31132480 | snp | A/G | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156622175 | TTTGACTACAGTATT[A/G]CAGTTTCAACAAGTC | 11352 |
rs31159286 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Abl2 | Mm_Celera | 1:156644433 | AACTATTTTAAGTCG[A/C]ATTTGGCATCCTTAA | 11352 |
rs31173489 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Abl2 | Mm_Celera | 1:156580486 | GCATGGCAAACATGT[A/G]GTGGTAAGAAGACAG | 11352 |
rs31197955 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156589243 | TAAGTACATTAAAAA[A/T]ATTTTTTAGGTACAT | 11352 |
rs31240183 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156627730 | GTGAAGAAACAGGTA[A/T]TTTTCACTCCTGGCT | 11352 |
rs31240277 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156618209 | GGGGGGGGGGGCAGC[A/G]GCTGTTGTTGTTCTG | 11352 |
rs31268684 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Abl2 | Mm_Celera | 1:156617620 | CATTTATTAAATTTT[G/T]AAGAAGAGTTTTTTG | 11352 |
rs31268685 | snp | C/T | 0.32 | 0.24 | intron-variant | Abl2 | Mm_Celera | 1:156616627 | TAGCCTCTTAGAGCA[C/T]ATACAAAGTAGAATA | 11352 |
rs31268686 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Abl2 | Mm_Celera | 1:156616137 | CCTGTAGTCTCCACT[G/T]GGCTCAGTGAGGATT | 11352 |
rs31268687 | snp | G/T | 0.32 | 0.24 | intron-variant | Abl2 | Mm_Celera | 1:156616125 | GGGTTATCTGCTCCT[G/T]TAGTCTCCACTGGGC | 11352 |
rs31268688 | snp | A/C | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Abl2 | Mm_Celera | 1:156615872 | GTCCCACGTGTATGG[A/C]TTGCTGGCCAGAGTG | 11352 |
rs31268689 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime | Abl2 | Mm_Celera | 1:156615685 | AGTTTCTATGCTTAC[C/T]GACCCTAGCTGATTG | 11352 |
rs31268690 | snp | C/G | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Abl2 | Mm_Celera | 1:156614461 | CTTTCTGCTTCAGCG[C/G]TTTTGCCTCTCAGGA | 11352 |
rs31268691 | snp | A/G | 0.473373 | 0.11227 | intron-variant, upstream-variant-2KB | Abl2 | Mm_Celera | 1:156614419 | GCCTCAGGCGTCCTC[A/G]GCAGTGACCACACAC | 11352 |
rs31268692 | snp | A/T | 0.473373 | 0.11227 | intron-variant, upstream-variant-2KB | Abl2 | Mm_Celera | 1:156614388 | AGCTGTAAATCCTTC[A/T]GTGCTTGCTCTGGCA | 11352 |
rs31268693 | snp | A/G | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Abl2 | Mm_Celera | 1:156613059 | AACGATTTCACTTAT[A/G]TATGTGGTTAGGAGT | 11352 |
rs31269324 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156574660 | AAAGGGTGAGGATTT[C/T]AGTACAACCACCATT | 11352 |
rs31269325 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Abl2 | GRCm38.p3 | 1:156573822 | TGATGTGTGTGTCCA[A/C/G]TGAATGTGTGGAGTT | 11352 |
rs31269326 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Abl2 | Mm_Celera | 1:156573729 | ATATACACCGTTTTT[C/T]GATTTATCTCCTACC | 11352 |
rs31269327 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl2 | Mm_Celera | 1:156573295 | ACTGCTGAAGGGCTT[A/G]GTATTTCTTTTAAGC | 11352 |
rs31269328 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Abl2 | Mm_Celera | 1:156573268 | TAAAATATTCTTTTG[G/T]CATTTATTCCTACTG | 11352 |
rs31269329 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Abl2 | Mm_Celera | 1:156573214 | TTTGGCTTGTCTGTA[A/G]GGTTTAATGGTTGCT | 11352 |
rs31269330 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Abl2 | Mm_Celera | 1:156573058 | TGGAGTGGGCAGGCA[A/G]AGCCTGGTGCAAGCC | 11352 |
rs31269331 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Abl2 | Mm_Celera | 1:156572986 | AAATGGAGAGCCAGT[A/G]GAGCTAAGCGCAAAG | 11352 |
rs31269332 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Abl2 | Mm_Celera | 1:156570616 | TGTTGTTTGCTTTTG[C/T]GTGCATTTGTCTAGT | 11352 |
rs31269333 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Abl2 | Mm_Celera | 1:156570313 | AGTATCAGGAGATAA[C/T]GTTTCTTTTAAACAA | 11352 |
rs31269524 | snp | A/T | 0.5 | 0 | intron-variant | Abl2 | Mm_Celera | 1:156610532 | CACATTTAATATCAG[A/T]CTTTACTTTGAGGAA | 11352 |
rs31269525 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Abl2 | Mm_Celera | 1:156610392 | CTTACTGACTTGTGT[C/T]CTGTTTTCAGACCTG | 11352 |
rs31269526 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Abl2 | Mm_Celera | 1:156610352 | GTACCTGAAAACTGT[A/G]ACTACTGGAAAAATG | 11352 |
rs31269527 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Abl2 | Mm_Celera | 1:156609777 | ACATTTTTATATGAG[C/T]AGGGTGAGTTTCCAT | 11352 |
rs31269528 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Abl2 | Mm_Celera | 1:156608972 | GTTTTAGATTAGGCG[A/G]CTGGTCAGCAAGCCA | 11352 |
rs31269529 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Abl2 | Mm_Celera | 1:156608629 | ATTTGTTCTCTTTTT[A/T]AAATCCCTGTATGGT | 11352 |
rs31269530 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Abl2 | Mm_Celera | 1:156608533 | CCCAAATACCTTATC[A/G]ACAGTTGGGTTCGAG | 11352 |
rs31269531 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Abl2 | Mm_Celera | 1:156606508 | AATTGAGTGTGCTTG[C/T]TACTCAGCTATACCT | 11352 |
rs31269532 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Abl2 | Mm_Celera | 1:156606433 | GGAATGTAAGAATCC[A/G]TCTACCTAGTAAAAA | 11352 |
rs31269533 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Abl2 | Mm_Celera | 1:156606303 | TTGTTGAGCCATCTG[C/T]TGATGTGGAAAATTT | 11352 |
rs31270204 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Abl2 | Mm_Celera | 1:156570138 | TTTTGCTTGTTGTTC[C/T]AAAGCCTTTATCATA | 11352 |
rs31270205 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Abl2 | Mm_Celera | 1:156569867 | TTAGAGATTGTTTCC[A/G]GCCATTGGCTTGACT | 11352 |
rs31270206 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Abl2 | Mm_Celera | 1:156564347 | GCCCATGTGGTAAAC[G/T]CACCACCTGCACATA | 11352 |
rs31270207 | snp | G/T | 0.408163 | 0.193609 | upstream-variant-2KB | Abl2 | Mm_Celera | 1:156557910 | CAAGGTCAAAGTGAT[G/T]TATCTTTTCCTTGCC | 11352 |