SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3022801 | snp | A/G | 0.33099 | 0.236518 | intron-variant | Satb2 | Mm_Celera | 1:56835144 | GCCATTTGGACACTG[A/G]CTCCTTTTTGTTAAT | 212712 |
rs3089908 | snp | A/G | 0.287335 | 0.247197 | intron-variant | Satb2 | Mm_Celera | 1:56835113 | CATCTTTTTGTTTAC[A/G]CCATCTCTCCAGGAG | 212712 |
rs3653534 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Satb2 | GRCm38.p3 | 1:56809453 | CTCTTAGCACATACA[A/G]CTGTAGGAAGGGGAT | 212712 |
rs3664259 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56814006 | ATACCAAACACTTCA[C/T]AGGACAAGGCACACA | 212712 |
rs6152247 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Satb2 | Mm_Celera | 1:56888858 | GCAAGAAGCCTCTAT[C/T]AAATGAAAAGAACCA | 212712 |
rs6152302 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Satb2 | Mm_Celera | 1:56888888 | AGCTAGGCTCAACAC[A/T]TCTGTTTNCTGAGGG | 212712 |
rs6152314 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56888896 | TCAACACNTCTGTTT[C/T]CTGAGGGTAGAAAGT | 212712 |
rs6154767 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876148 | GTTTNTGCCTATTTA[C/T]TTCATGTTTGTCTTA | 212712 |
rs6154863 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56882762 | ctctctctctctctt[C/T]ctctctctctctctc | 212712 |
rs6155380 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56882840 | ctctctctcCTTACA[A/T]CTAATGATGCCCACA | 212712 |
rs6155498 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Satb2 | Mm_Celera | 1:56882901 | AAAGTAAATTCAGCA[C/T]ATGATGAAAAAAAAT | 212712 |
rs6155864 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Satb2 | Mm_Celera | 1:56876315 | AAAACACTCAGGAGC[C/T]ANTGAAACACAAATG | 212712 |
rs6155865 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876317 | AACACTCAGGAGCNA[C/T]TGAAACACAAATGCT | 212712 |
rs6156443 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56876433 | GGGTAAAGTGGCTGC[A/G]AAGTCCCAGGCATGA | 212712 |
rs6156494 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56876462 | GATCAGACTTAAGGC[C/T]TTTGTGTCTCCTTCC | 212712 |
rs6156557 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876504 | TCCTCACTCCCACAG[G/T]CCCCAGGAAAGCATG | 212712 |
rs6157102 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876602 | GAGAAGAACTGCAGA[G/T]CAGGGGCCAGTNCAA | 212712 |
rs6157480 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876614 | AGANCAGGGGCCAGT[A/G]CAAGAGAACATCGTT | 212712 |
rs6157538 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56876650 | GTGTTACAGCCCGTG[C/T]CTGCAGAAGCCTTAC | 212712 |
rs6164778 | snp | A/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56928700 | TTGCCAAAGCCACTG[A/T]CCTCAGTCTGGCCTT | 212712 |
rs6164900 | snp | A/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56928771 | ATTAGCCACAGATGA[A/T]TAATAACCGATTCCC | 212712 |
rs6236725 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56964701 | GCGTGGGTGGGTGAG[C/T]Gcacatacacacaca | 212712 |
rs6237814 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56964903 | TCTGTTTAATGTGTA[C/T]GTTCCATTGCATATA | 212712 |
rs6238252 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56926440 | TGTCCTGTTTACTGT[A/C]TTTCAAACAATGTTT | 212712 |
rs6238391 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56965030 | AGGACATGTTAGACG[A/G]GTAGATGACCCCCAA | 212712 |
rs6238718 | snp | C/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926505 | tgtgtgtgtgtgtgt[C/G]tgtgtgtgtgCGCGC | 212712 |
rs6238815 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926561 | ATGTGCACATGGGTA[C/T]AGGTACCTATGGAGG | 212712 |
rs6238902 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56965125 | GGATGGGTAGGGAAG[C/T]CTTCCCTCTGCAACC | 212712 |
rs6239296 | snp | A/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926629 | ACCCAAATTTGGACT[A/T]CGANTACCTNCCAGG | 212712 |
rs6239309 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926633 | AAATTTGGACTNCGA[A/G]TACCTNCCAGGTGTT | 212712 |
rs6239311 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926639 | GGACTNCGANTACCT[G/T]CCAGGTGTTAATAAC | 212712 |
rs6239337 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56965160 | GTCCTTCCTATCAGC[A/G]TATGCTCCAACTGCC | 212712 |
rs6326859 | snp | A/T | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56904525 | ATCAAAAGGTTTGTA[A/T]NCAGTGCTAAGCATC | 212712 |
rs6326861 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56904526 | TCAAAAGGTTTGTAN[G/T]CAGTGCTAAGCATCC | 212712 |
rs6336903 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56917322 | TTAAAATATAATACA[C/T]AGGCCAGGCACACAT | 212712 |
rs6337424 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56917367 | AGTCCTGGTCCAGTG[A/G]CTCAATTTTGTTACA | 212712 |
rs6337500 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56917400 | ATAATACATATGCTT[A/G]TTTTGAACATAAAAA | 212712 |
rs6338592 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56917576 | AGACTGAATGTCTAC[G/T]AACCAACAAGCNAAG | 212712 |
rs6338623 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56917588 | TACNAACCAACAAGC[A/G]AAGGTATAATTAAAA | 212712 |
rs6341554 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Satb2 | Mm_Celera | 1:56904968 | AAAATGAGACATTAG[C/T]TTTAATATCCAAAGG | 212712 |
rs6374058 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56958086 | TTGGCTTATAAGCAT[A/C]GGTGCAGGCTTGTGG | 212712 |
rs6375223 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56958319 | GGGGGCTTTCCTAAG[C/T]GGTGCTATCAGAGAA | 212712 |
rs6375686 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Satb2 | Mm_Celera | 1:56958381 | ATGGAAAGGAATTGT[C/G]TCTCTCAACCTTGCT | 212712 |
rs6403535 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926881 | TAAGTGTGCACGACG[A/C]ATGATAACTCACAGG | 212712 |
rs6404090 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926992 | AGAAAGCCACCCATC[C/T]GCCTGTCAGCGGGCA | 212712 |
rs6404717 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56927130 | ATAGAGGAAGCAGCC[A/G]AACCATTTATCCNGA | 212712 |
rs6404740 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56927143 | CCNAACCATTTATCC[A/G]GAAAAGACTGTTTTA | 212712 |
rs6411272 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Satb2 | Mm_Celera | 1:56888425 | TGTAACAGAATCACA[G/T]AGCTTATGTTTAGGA | 212712 |
rs6411341 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56953810 | CTCGCACTATCTGTC[A/G]CCTAAGATTCCAGAA | 212712 |
rs6411834 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Satb2 | Mm_Celera | 1:56888532 | ACATATTTAAGGATG[A/G]AGCCTGCATTTTGTT | 212712 |
rs6411879 | snp | A/C | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56888552 | TGCATTTTGTTTAGG[A/C]CATCGGTAAGCTGGC | 212712 |
rs6412419 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Satb2 | Mm_Celera | 1:56888622 | TGTATGCTGGTGACT[C/G]CATGACTTGACCAGG | 212712 |
rs6413099 | snp | A/G | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56888769 | CATGGTCACCAGCAA[A/G]TGTTAGAAAGCAAAC | 212712 |
rs32742539 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56901669 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 212712 |
rs32778009 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Satb2 | Mm_Celera | 1:56799388 | TAACCGCATTTAGAT[A/G]GGCATTTTAATATCC | 212712 |
rs36242908 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Satb2 | GRCm38.p3 | 1:56955876 | GGAAAGAGACAGACA[C/T]GTGGATTCACGAGCT | 212712 |
rs36246795 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56836405 | GGGATCACACTGTCC[A/T]TGGGAGAACTGCTAA | 212712 |
rs36252917 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56934019 | ACCTCAAGATGTCCA[G/T]GCAGAGGCAGCACCG | 212712 |
rs36254185 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56869719 | TCTTTAAGCTCCACC[C/T]TGCTGTGTTGCTGAA | 212712 |
rs36254371 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56836241 | AAATCAAAACCAAGA[G/T]AAGCTTGATGCAATA | 212712 |
rs36260345 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56939895 | CTTAGAGCTGGAAAA[C/T]GATGGCGTCCAAACA | 212712 |
rs36260772 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56881437 | GGCACATAAATGCTT[A/G]GAATACCAGCCTATG | 212712 |
rs36264461 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Satb2 | GRCm38.p3 | 1:56915862 | CTCAGTCCATGGCAC[C/T]TGCTAAGAGTTGCTG | 212712 |
rs36266348 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56903908 | GTTATCTGCAAACAT[C/T]CAGAAAATGCCTGGT | 212712 |
rs36266711 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56812000 | ACTGTGTGTCTGAGG[C/G]CTGTGTAGGATATGG | 212712 |
rs36269229 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56854261 | TGCCTCATTGTAGGG[A/T]ACAGAACATTTTCCA | 212712 |
rs36269637 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56828772 | CTCTTAAGTCCAATG[C/G]CCTGGCATGTGCTCA | 212712 |
rs36269733 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56933264 | GGAGTTAACAAGTCA[C/T]GTGGTGCGATTCTTA | 212712 |
rs36269740 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56876179 | AACTGACTGAACACC[A/G]CTGTTTCGCCTATAA | 212712 |
rs36273503 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56812589 | AACGAGCTGTCAGTC[C/T]AGGAGCATTCTTTTT | 212712 |
rs36273696 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Satb2 | Mm_Celera | 1:56882628 | CCATGGAAAAAGTGA[C/T]CACTGTTCACTTAAC | 212712 |
rs36273806 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56801234 | ATAGATAAATATAAA[C/T]GTAATCCTACAATTC | 212712 |
rs36274161 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Satb2 | GRCm38.p3 | 1:56909793 | CATGTGCGTGCACCC[A/G]TAAATAGATGCAGAA | 212712 |
rs36276263 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56830212 | GTAAGCACTGTGGTT[C/T]AGCCTCCCTGAATAA | 212712 |
rs36279138 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56915805 | GGAAAGCCTTTGGCT[A/G]TAACCCTAAGAGCAA | 212712 |
rs36280067 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56814460 | GGAATCTTGAACCAA[A/G]AAAGAATCTACAAAA | 212712 |
rs36280661 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56900164 | GACTCCATAGCTGTG[A/G]GGCAAAATTCAGAGG | 212712 |
rs36280769 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56943515 | GACTCTACATCTGCT[A/G]AGGTTCATCCCTGTT | 212712 |
rs36283732 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56894664 | CTATATATTAATATG[C/T]AATGCCTGACAATCA | 212712 |
rs36286174 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56959773 | AGAGAAGGTGGTTGC[A/G]TGAAAGAAATACCAC | 212712 |
rs36288113 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56818685 | ATAGATGAAGCAAAC[C/T]AAGGTGTGAGTGTAT | 212712 |
rs36288364 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56802546 | TTATAAACTACTTCA[A/G]TCAGCCTTGGTTTTC | 212712 |
rs36291231 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56854513 | ATGAGCTTTGCAGAC[C/T]ATTGCTAGGACCAGC | 212712 |
rs36294685 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56837403 | TATGTTAGGTGTAGA[G/T]GTGTCTGATGTACCT | 212712 |
rs36295390 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56949827 | TGAGACGACTCAAAC[A/G]TTAGGCAAAGGAGAT | 212712 |
rs36295725 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56803971 | TAAGGTGCAGCACCA[A/T]GTTCCTGTGATTTTC | 212712 |
rs36300180 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56905713 | CCTCTCAACTCACCA[A/G]TCTGGGAGCCTAGAA | 212712 |
rs36302941 | snp | A/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56886382 | GATCCAATATTTATC[A/T]AAAATTCAAAGGGCT | 212712 |
rs36303111 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56880994 | TTCCAGGCTCCTGGT[A/G]CCTATGGTCTGTTGC | 212712 |
rs36305174 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | GRCm38.p3 | 1:56837072 | AGGAAGGAGACCGCT[A/G]GAGGAGGTGACAGTT | 212712 |
rs36309515 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56939783 | CTGTGGGCTTTCAAC[A/G]CGACAATCATTTTCC | 212712 |
rs36311999 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56910492 | CCCTCTCAAATTATC[C/T]CAGAGACCCTCTGCA | 212712 |
rs36313415 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Satb2 | GRCm38.p3 | 1:56842965 | TTATCCCAGCAGCCT[C/T]GACTCTTCACTTCCC | 212712 |
rs36314309 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56945990 | AGAGTATTTAACCTT[C/T]TAATCATCAGAATGG | 212712 |
rs36314601 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56956101 | GGACCACGGCCTACA[C/T]TGCAGCAAAACGCCT | 212712 |
rs36316567 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56886022 | TTTATTTCTTTTACT[C/T]CATCAATTCTGTTAT | 212712 |
rs36322383 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56934419 | ATATGTGAGACGTTA[C/T]AGCAGCTTTTATTGG | 212712 |
rs36327710 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56955555 | ATAACAAAGAATGAG[C/T]GACACCAGGGACCGC | 212712 |
rs36328370 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56811296 | TGCACACCACTATCA[C/T]TGTTATCATGTCTTC | 212712 |
rs36330619 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56816252 | GGCCCGCCAAAATTC[A/G]CACCACTGGATAGCA | 212712 |