SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6186876 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Abl1 | Mm_Celera | 2:31700205 | GATCTTTGGCTTTTA[A/G]AACGTTCTATTTTCC | 11350 |
rs6187891 | snp | A/G | 0.5 | 0 | intron-variant | Abl1 | Mm_Celera | 2:31700346 | cttgggaggcagggg[A/G]caggcggagttctga | 11350 |
rs6188950 | snp | C/T | 0.5 | 0 | intron-variant | Abl1 | Mm_Celera | 2:31772444 | gaagtcagtattctg[C/T]tagcagccttcagat | 11350 |
rs6189023 | snp | A/G | 0.5 | 0 | intron-variant | Abl1 | Mm_Celera | 2:31772490 | tgaacatgtaagccc[A/G]cctcagttaaatgtt | 11350 |
rs6202722 | snp | A/G | 0.5 | 0 | intron-variant | Abl1 | Mm_Celera | 2:31772751 | gaactgtgtaggacc[A/G]ctggcccaggagctt | 11350 |
rs13460304 | snp | C/G | | | utr-variant-3-prime, intron-variant | Abl1 | Mm_Celera | 2:31803256 | AGCGACCTTGAATAG[C/G]CAGACACCGCCATCC | 11350 |
rs13460305 | snp | A/C | | | utr-variant-3-prime, intron-variant | Abl1 | Mm_Celera | 2:31803091 | TCCACTGCAGGTGTG[A/C]TGTGCTGGCCCCAGG | 11350 |
rs13460306 | snp | A/G | | | synonymous-codon, intron-variant | Abl1 | Mm_Celera | 2:31801461 | CACCCCCTCCACAGC[A/G]CCAGCTCCTTCACCC | 11350 |
rs13460307 | snp | C/T | | | utr-variant-3-prime, intron-variant | Abl1 | Mm_Celera | 2:31803261 | CCTTGAATAGCCAGA[C/T]ACCGCCATCCCCTGA | 11350 |
rs27176868 | snp | A/C/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Abl1 | GRCm38.p3 | 2:31802013 | AGGAGCTTTAAAGAG[A/C/T]GACAAGCAGAGCCTG | 11350 |
rs27176869 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon, intron-variant | Abl1 | Mm_Celera | 2:31801410 | AAAGCCCCAGTCGAC[A/G]GCTAAGCCTCCAGGG | 11350 |
rs27176870 | snp | C/T | 0.231111 | 0.249285 | missense, intron-variant | Abl1 | Mm_Celera | 2:31801304 | CAAAGACAAAATGCA[C/T]GAGTCTGGCTATGGA | 11350 |
rs27176871 | snp | A/G | 0.142012 | 0.225474 | missense, intron-variant | Abl1 | Mm_Celera | 2:31801030 | CACAAGGAAGAGGCC[A/G]CCAAGGGCAGTGCCT | 11350 |
rs27176872 | snp | A/G | 0.260355 | 0.249785 | synonymous-codon, intron-variant | Abl1 | Mm_Celera | 2:31800927 | AGGCTTCAAAGACAC[A/G]GAATCCAGCCCTGGC | 11350 |
rs27176873 | snp | A/C | 0.244898 | 0.249948 | synonymous-codon, intron-variant | Abl1 | Mm_Celera | 2:31800660 | GAGCTCCAGTAAGCG[A/C]TTCCTGCGTTCTTGT | 11350 |
rs27176874 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, intron-variant | Abl1 | Mm_Celera | 2:31800258 | TCCTCGGAAAGAGCG[C/T]GGGCCCCCAGACGGC | 11350 |
rs27176875 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31800071 | TGTCTTCTGCCCTCC[A/G]GTGGCACTGAGCTCC | 11350 |
rs27176876 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31799532 | AGTCTTAGGACAGAT[A/G]TACAGTCTACCTCAG | 11350 |
rs27176877 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31799495 | ATCCTCTGCTCACCT[C/T]GTTCTGATGCTCATC | 11350 |
rs27176878 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31799386 | TTACTGACGCTCTGG[A/G]TAGTCATCTCCTGGT | 11350 |
rs27176879 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31799098 | GAGACGCTACCTCAG[A/G]CAAGCTTGGAAGGAA | 11350 |
rs27176880 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Abl1 | Mm_Celera | 2:31799053 | AAATTTAGGGGCCAG[C/T]TAGCATGACATACAC | 11350 |
rs27176881 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31798891 | ACAGGTGCCAAAGGA[A/G]CTTGTTTGGAAGGTT | 11350 |
rs27176882 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31798341 | ATGATTCTGATAGGC[C/G]TTCATAAGAGGCATT | 11350 |
rs27176883 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31797986 | ACTAAACAACATGGA[A/C]CCATCAGAGCAGCCC | 11350 |
rs27176884 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Abl1 | Mm_Celera | 2:31797841 | CAGGGAGGAAGATTC[A/G]CTCCTGCCCAGGGGA | 11350 |
rs27176885 | snp | A/C | 0.32 | 0.24 | intron-variant | Abl1 | Mm_Celera | 2:31797515 | AGAATCCCTTTCAGT[A/C]TGGCACCTTTGCTGA | 11350 |
rs27176886 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31796965 | TGACATGGGTCTTCT[C/T]CATCCAGGTTGGCAG | 11350 |
rs27176887 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31796912 | CTGGTGCTTGGGAAT[A/G]GCTAGTCTGGTTTGT | 11350 |
rs27176888 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31796862 | GTCACGGCATCAGCT[A/G]TCAGCAGGCTTGGAA | 11350 |
rs27176889 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Abl1 | Mm_Celera | 2:31796719 | GAAGTTTGGAGAAAC[A/G]TTTATAGATGCAATT | 11350 |
rs27176890 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31796320 | ACAGATGGTTGTCGC[A/G]GTTTACACTCCAGCA | 11350 |
rs27176891 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Abl1 | Mm_Celera | 2:31796037 | GTAAGGCAGAGAGGC[A/G]CACTTTCCCTTGTTG | 11350 |
rs27176892 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Abl1 | Mm_Celera | 2:31795398 | TCATATTATCATTCC[C/T]TCATCATTTTCTTCT | 11350 |
rs27176893 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31793573 | CTCACTAGCAGCTCT[A/G]TCACGTGATCAGTCT | 11350 |
rs27176894 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31793511 | GAAGGTTGGGAAACC[A/G]CTGCACCAGAGGGCT | 11350 |
rs27176895 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31793396 | CCCTTTGGCAACCTT[C/T]TATCTCCAAAAATAT | 11350 |
rs27176896 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Abl1 | Mm_Celera | 2:31793283 | TTTTCTTTCATTAAG[A/T]ACATTAGCAGAGGCG | 11350 |
rs27176897 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31793244 | CACAGTCAGACCCGG[A/G]TAGCTCCTGACACTT | 11350 |
rs27176898 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31793135 | ATAAACTCTGTCACC[A/G]TTCCTTTAGACTTTC | 11350 |
rs27176899 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31792540 | TCTGGTTCATTTCTG[A/G]CTTAGTTTAAACTCC | 11350 |
rs27176900 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Abl1 | Mm_Celera | 2:31792536 | TCTTTCTGGTTCATT[C/T]CTGGCTTAGTTTAAA | 11350 |
rs27176901 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31791751 | GATCAAGCTGTATCA[C/T]GCAGTCGTTGCCCTG | 11350 |
rs27176902 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31791545 | CTTTTTCTGCTCCAC[A/G]AGAGCCCAATCCAAA | 11350 |
rs27176903 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31791330 | TGCTTTGCTGGTGGA[A/G]GTGGCTTCCTAGCAG | 11350 |
rs27176904 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31791065 | AAAGGCCTTCTTCCT[G/T]ATAGTCTTGGTTCCC | 11350 |
rs27176905 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31790899 | CTCAGCCCCAGCCTT[A/G]GTCCTGGCAGACACA | 11350 |
rs27176906 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Abl1 | Mm_Celera | 2:31790771 | GGTGAGCGCCGTGGT[A/G]CTGCTCTACATGGCC | 11350 |
rs27176907 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Abl1 | Mm_Celera | 2:31790684 | TACCCGGGAACCACC[A/G]TTCTACATAATCACT | 11350 |
rs27176908 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31789582 | TATCTGACCTGTGAG[A/G]CACTCTGGAAAGTGG | 11350 |
rs27176909 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31789451 | ACAGATGGTTCTCTG[A/C]GTGCTCAGAGAGCTG | 11350 |
rs27176910 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31789391 | ACAGCCCTTCAGACT[C/T]AGCCTGGAAAGGGTC | 11350 |
rs27176911 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31789320 | TGCTTCCTGCTTGTG[A/G]GAGTTGATTCAAAGC | 11350 |
rs27176912 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31789058 | CATGTTTGGTGATAA[C/G]ACGTCATCACGCTGG | 11350 |
rs27176913 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31789027 | GTAGACAGCATCTCC[A/G]TAGTCTTTTAGAACC | 11350 |
rs27176914 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31788979 | CAGCCGCATGCTGTG[A/G]TACATGAGAGCAGCC | 11350 |
rs27176915 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31788957 | CCTCCGCACAGCTGG[A/G]CAGCAGCAGCCGCAT | 11350 |
rs27176916 | snp | A/G | 0.32 | 0.24 | intron-variant | Abl1 | Mm_Celera | 2:31788773 | AGCAGTTGTGTCAAA[A/G]CCAGTTGTATTGTGC | 11350 |
rs27176917 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31788637 | ATAATTCTGCCTTGA[A/G]ATCATTGGTCTTCTG | 11350 |
rs27176918 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Abl1 | Mm_Celera | 2:31788537 | ACAGACATGCAGATA[G/T]ACAGGAAGGAATGAT | 11350 |
rs27176919 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Abl1 | Mm_Celera | 2:31787926 | AAAAATAAGCAGAGG[A/G]ACCTCAGGACCTCAC | 11350 |
rs27176920 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31787899 | ATGTCTTCAGAAGGA[C/T]GCCATGAGTTAAAAA | 11350 |
rs27176921 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Abl1 | Mm_Celera | 2:31787849 | GTTTCTTCCACCTGA[A/G]CCTTCACAGTTCTGT | 11350 |
rs27176922 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Abl1 | Mm_Celera | 2:31787800 | GACAAGCATAAGCAC[A/G]AGGACTAAGGAGAGA | 11350 |
rs27176923 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Abl1 | Mm_Celera | 2:31787766 | CCCCGTGAAGGGAGC[A/G]GTTGAGCCTTCTTTT | 11350 |
rs27176924 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31786897 | TAAACATAAGCCTCA[A/G]TTCTGCCCCTTAGGA | 11350 |
rs27176925 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Abl1 | Mm_Celera | 2:31786864 | CTTTACAGTCTTACC[C/T]CTCAGACCCCATGAA | 11350 |
rs27176926 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31786741 | CGTGGTACTGAGAGA[C/T]GCGCGAGCACTAAGG | 11350 |
rs27176927 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31786654 | AACTTACAGAAATGG[C/T]CAGTTGCTGAGTTAG | 11350 |
rs27176928 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31786591 | TTCTCAGTGAGAGGC[A/G]TAAAGGATTTTGGCT | 11350 |
rs27176929 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31786012 | TACAAACACAGCCAG[A/G]CTTTGGAAAGCATTG | 11350 |
rs27176930 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31785850 | GAGAGACACTAGGAA[A/G]CCCTAACTGAGGAGG | 11350 |
rs27176931 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31785711 | ACAGACATGGACAAA[A/T]CCCTGATGATGGCAG | 11350 |
rs27176932 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31785534 | CATATTGAGCATTTT[C/T]CTTCCTTTGGCTCCG | 11350 |
rs27176933 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31785405 | CGTCCAATACATCTG[A/T]CAGCCCCGGCTCTGC | 11350 |
rs27176934 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31785391 | TGTCTCAGCTCAGCC[A/G]TCCAATACATCTGTC | 11350 |
rs27176935 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31785277 | ATGATCCGAGCTTGT[C/T]CCTGTGATGAGAGTG | 11350 |
rs27176936 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31785219 | TCCACTGTTGACCCA[C/T]GTGTCGTGTTTGCAG | 11350 |
rs27176937 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31785157 | AGAAGCAAGTCCTGC[G/T]TGTCACTAGGCTGTG | 11350 |
rs27176938 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Abl1 | Mm_Celera | 2:31784971 | TCAAAGCCTGCCTTC[C/T]GTTCTTGTTGGGTGA | 11350 |
rs27176939 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31784856 | CTGTGTGAGGCTGAG[C/T]GTCTTCCATCTGTGG | 11350 |
rs27176940 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31784444 | TCTAAACAGTGTGTA[A/G]AGCCTTTCTTTCCCC | 11350 |
rs27176941 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31784053 | CTCCACCCTGGTGGT[A/G]GCCTCATACTGGACA | 11350 |
rs27176942 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31784006 | CTGCAAGGTGCTGAC[A/C]GAAACGTGGCTGGGT | 11350 |
rs27176943 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31783538 | AGGCCATGCATACCG[A/G]CCGTCAGACAGCGGT | 11350 |
rs27176944 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31783448 | GCAGGAGAACTCTGG[A/G]CTCCCAGGAAGGCCT | 11350 |
rs27176945 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31783419 | CCCTTTGTAACCCCC[C/T]CTTGTACTCTGGAGC | 11350 |
rs27176946 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31783334 | AGCAGTGGATTAGTG[G/T]AGTAGTCAGTCAGCT | 11350 |
rs27176947 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31783306 | GCAGCGTGGTACAGG[C/T]CCTTGGCCCAGGAGC | 11350 |
rs27176948 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Abl1 | Mm_Celera | 2:31782969 | AGCCTGGAGGGTTCT[A/G]TGCTCAGAGGCAGCT | 11350 |
rs27176949 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31782891 | GTCCTAGTCTAACTT[A/C]CTGTGGCTCCAGAAC | 11350 |
rs27176950 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Abl1 | Mm_Celera | 2:31782675 | GCCGGCTGTAATATT[G/T]AATGATGCCATGTAA | 11350 |
rs27176951 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31782040 | TGGGTGACTCTGCCT[C/T]TCTTGCCTTTCGTTC | 11350 |
rs27176952 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31782004 | GTGCTTTTCTGAGGC[A/C]GTTTGGGCAGGGCTT | 11350 |
rs27176953 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31781955 | GGATCTCTGTTCTGT[A/C]CTCATGACTCCCGTT | 11350 |
rs27176954 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31781833 | TAAGAGAACATTTAA[A/G]AACAGTGGGAGGCAC | 11350 |
rs27176955 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Abl1 | Mm_Celera | 2:31781662 | CTATCTGTAGAGAGT[A/T]TATACAAGGAAGCTG | 11350 |
rs27176956 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Abl1 | Mm_Celera | 2:31780429 | CTTAGAGAAGTCTGT[A/G]TACCCACTTTCAGGT | 11350 |
rs27176957 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Abl1 | Mm_Celera | 2:31779922 | CTAGCTCAGTCTGCC[C/T]ACTGCTGCCAGCTCC | 11350 |
rs27176958 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Abl1 | Mm_Celera | 2:31779661 | CAGATACTGTGGCTG[C/T]GTTCTATGTACACAC | 11350 |