SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6254703 | snp | C/T | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326232 | TATATAATATATATG[C/T]GCTAAAATATANTCT | 13728 |
rs6254727 | snp | C/T | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326244 | ATGNGCTAAAATATA[C/T]TCTACCCTATAGATA | 13728 |
rs6255265 | snp | C/T | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326325 | TGGCAATCCTGTTGC[C/T]TAACCACCCAAAGGC | 13728 |
rs6255856 | snp | A/T | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326442 | ATGCGCTTTAAAAAT[A/T]TTTTTAAAAAtcatt | 13728 |
rs6268681 | snp | A/G | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326510 | cagacaaggccagac[A/G]cgtnggatccctaga | 13728 |
rs6268690 | snp | A/T | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326514 | caaggccagacncgt[A/T]ggatccctagaagct | 13728 |
rs6268759 | snp | C/G | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326564 | gagtgagctgacggc[C/G]ctggaacttantctg | 13728 |
rs6268772 | snp | C/G | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326575 | cggcnctggaactta[C/G]tctgcagcttaatcc | 13728 |
rs6269660 | snp | A/G | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326710 | ccatacccagCAAAG[A/G]GACCTTTATTAAAGA | 13728 |
rs6270172 | snp | G/T | 0.5 | 0 | intron-variant | Mark2 | Mm_Celera | 19:7326812 | CCTGTGGAAACCATG[G/T]AGCTGAAAGGACCGC | 13728 |
rs13471369 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Mark2 | GRCm38.p3 | 19:7276563 | CTCTCCCCACTTCTT[C/T]CCCCCTTCAAGCGAC | 13728 |
rs13471370 | snp | A/G | | | synonymous-codon | Mark2 | GRCm38.p3 | 19:7283458 | CTCTGCCAACCCCAA[A/G]CAACGACGCTCCAGT | 13728 |
rs13471371 | snp | C/T | | | synonymous-codon | Mark2 | GRCm38.p3 | 19:7283449 | CCCCAAGCAACGACG[C/T]TCCAGTGACCAGGGT | 13728 |
rs30351432 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mark2 | GRCm38.p3 | 19:7326999 | CCAGCACCAGGGTGG[G/T]AGAGGCAGATGGATC | 13728 |
rs30358446 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mark2 | GRCm38.p3 | 19:7313795 | GGTTTATTTCAGTTT[A/T]TATCTCCAGGTCACA | 13728 |
rs30397377 | snp | A/G | 0.18 | 0.24 | intron-variant | Mark2 | Mm_Celera | 19:7322737 | TTGTACCTCATGAGT[A/G]TACTTGAACTGGCAT | 13728 |
rs30424204 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mark2 | GRCm38.p3 | 19:7311116 | TCAAACCAGGAGAAG[C/T]GAGAAAGTCAAGAGT | 13728 |
rs30450054 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mark2 | GRCm38.p3 | 19:7289931 | TAGCAATGCTATAGA[C/T]GTGTTTCTGCAGAGA | 13728 |
rs30494818 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Mark2 | GRCm38.p3 | 19:7342370 | TAAAGCCTGGGACAG[A/G]CACCAGGTCGGACAG | 13728 |
rs30508032 | snp | A/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Mark2 | GRCm38.p3 | 19:7292672 | CCTCCCCTCTGCCTC[A/T]GCTGCTAAGTGGGCG | 13728 |
rs30517760 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mark2 | GRCm38.p3 | 19:7338740 | GCACCTGGAAGGGTG[C/T]GCACCTAGCTTTTCC | 13728 |
rs30521294 | snp | C/T | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Mark2, LOC102639888 | GRCm38.p3 | 19:7295119 | GCAAAGTACAGAGAC[C/T]GGGATGAGCCAGGCC | 13728 |
rs30564311 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mark2, LOC102639888 | GRCm38.p3 | 19:7303077 | CTCATCCTAAGTTCC[C/T]TTCTAGGAGCTGGGG | 13728 |
rs30567385 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mark2 | Mm_Celera | 19:7321989 | TCTCAAACTACAGCC[A/G]CAGAGGATCAGATAC | 13728 |
rs30615505 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mark2 | GRCm38.p3 | 19:7312803 | GGCATGTGTGCTCTC[C/T]GACACATAAAAAATA | 13728 |
rs30618567 | snp | A/G | 0.5 | 0 | intron-variant | Mark2, LOC102639888 | GRCm38.p3 | 19:7303344 | GCATGGCTGGGGCTT[A/G]CAGTGAAATAGGAGA | 13728 |
rs30640834 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mark2 | GRCm38.p3 | 19:7319700 | AATATTAGTTTAAAA[A/G]CGTTTGCTTGGCCAG | 13728 |
rs30693897 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mark2 | GRCm38.p3 | 19:7285310 | CTCTGCCTCCCAAGT[A/G]CTAGGATTAAAGGTG | 13728 |
rs30740124 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB, nc-transcript-variant | Mark2, LOC102639888 | Mm_Celera | 19:7297253 | CACCCCCCCCCCCAC[A/C]CACACACACACAGGC | 13728 |
rs30750394 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mark2 | GRCm38.p3 | 19:7294492 | CCCAGACTTTCAGAC[C/T]GGGAGCTTATGGTGC | 13728 |
rs30787944 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Mark2 | GRCm38.p3 | 19:7291613 | ACAGTAGAATAAGAA[C/T]TCGTCATATGGAAGG | 13728 |
rs30799559 | snp | A/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Mark2 | GRCm38.p3 | 19:7278817 | GGGACGAGAAGGAGA[A/G]AGCAGCAGCAGCAGC | 13728 |
rs30850968 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mark2 | GRCm38.p3 | 19:7288556 | AAAAAAAAAAAAAAA[A/G]CAAAGGCTCTTGGCC | 13728 |
rs30858454 | snp | C/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Mark2, LOC102639888 | GRCm38.p3 | 19:7295986 | GTCCACCTTAAGCAC[C/G]AAACAACAAAATTGC | 13728 |
rs30863954 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mark2 | GRCm38.p3 | 19:7294471 | ATCTTCCACCTACTG[A/G]ACCCACCCAGACTTT | 13728 |
rs30893114 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB, nc-transcript-variant | Mark2, LOC102639888 | Mm_Celera | 19:7297251 | CTCACCCCCCCCCCC[A/C]CACACACACACACAG | 13728 |
rs30903447 | snp | C/T | 0.32 | 0.24 | intron-variant | Mark2 | GRCm38.p3 | 19:7294914 | TCATAGCCAATGTCT[C/T]TTCGACATCCAGATG | 13728 |
rs30913192 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Mark2 | GRCm38.p3 | 19:7290889 | GTGCAGGGGCAGACT[C/T]CAAAGCAGACTGGCA | 13728 |
rs30928772 | snp | G/T | 0.32 | 0.24 | intron-variant | Mark2 | GRCm38.p3 | 19:7308085 | GTACAGAGCAGTGAA[G/T]CGGGCAAGCTGAGTC | 13728 |
rs30994589 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB | Mark2 | GRCm38.p3 | 19:7342288 | GCACACCCGCCCATC[A/T]TGCGACTATCTTGGC | 13728 |
rs31002763 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Mark2 | GRCm38.p3 | 19:7310432 | CAGGGTGAATAGAGT[A/C]CGCGCTCAAGCTTTC | 13728 |
rs31077411 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mark2 | GRCm38.p3 | 19:7288883 | TAGATACATGGTGAG[C/T]TCAAGAGTAGCCTGG | 13728 |
rs31099051 | snp | C/T | 0.32 | 0.24 | intron-variant | Mark2 | GRCm38.p3 | 19:7310712 | CATCTGCCCCATCCG[C/T]AAACTCCCTGCTCCT | 13728 |
rs31167723 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Mark2 | GRCm38.p3 | 19:7319044 | ACTTCTAGAACTGAT[A/G]TAAAAGTCATGGACT | 13728 |
rs31180855 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mark2 | GRCm38.p3 | 19:7310434 | GGGTGAATAGAGTAC[A/G]CGCTCAAGCTTTCTA | 13728 |
rs31245089 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Mark2 | GRCm38.p3 | 19:7289271 | TATCAATTCTGATTC[G/T]GGGAACAGCGCCCTC | 13728 |
rs31284976 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mark2 | GRCm38.p3 | 19:7313215 | ACTGACTGCTCTTCC[A/G]AAGGTCCTGAGTTCA | 13728 |
rs36250391 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Mark2 | Mm_Celera | 19:7283214 | GGGACGGCTATGGGG[C/T]GATGTAAAATGGGTA | 13728 |
rs36251478 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mark2 | Mm_Celera | 19:7315411 | CTACTCAAGACCGCT[G/T]ACTACCAATCGAGAA | 13728 |
rs36255805 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mark2 | Mm_Celera | 19:7316433 | TAGATAAACCATATA[A/C]GCTCATGTTCACTAT | 13728 |
rs36269808 | snp | C/T | 0.32 | 0.24 | intron-variant | Mark2 | Mm_Celera | 19:7324734 | TAGAGAACAGTCTTA[C/T]ACGAAATTGTGTAGA | 13728 |
rs36272479 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mark2 | Mm_Celera | 19:7287540 | CTCTTAAAGAAACCA[A/G]GCTGAAACCCATGGA | 13728 |
rs36274120 | snp | A/C | 0.32 | 0.24 | intron-variant | Mark2 | Mm_Celera | 19:7320599 | ACACTTCTGTCTGGA[A/C]CTGGAACGCTCTCCA | 13728 |
rs36284526 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7326188 | GGTCTTTCTAAGTTT[A/G]AGTTGACTCAAAAAT | 13728 |
rs36287199 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Mark2 | Mm_Celera | 19:7305223 | CAGACTGCACCACAG[C/T]TCCTCAGGCACAGTG | 13728 |
rs36295856 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mark2 | Mm_Celera | 19:7306785 | AGAGGACATATGGCA[A/G]GTGTATACTTAAAGG | 13728 |
rs36307220 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mark2 | Mm_Celera | 19:7331298 | TAACAAGAATATGCC[C/T]TTGAGGGCTGGAGAA | 13728 |
rs36313097 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7310633 | AGGATTGAAAACACT[A/G]AAATGAAACATCAAT | 13728 |
rs36317444 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Mark2, LOC102639888 | Mm_Celera | 19:7296005 | CAACAAAATTGCTAT[C/G]ATCTATCTGCACTTG | 13728 |
rs36320353 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Mark2 | Mm_Celera | 19:7289843 | GAGATCCAGGGGTAG[G/T]CTCTGCTTCTTTAAC | 13728 |
rs36320495 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7319212 | AAGACTTGCTGAATG[A/G]TGGGAAAACCAACTA | 13728 |
rs36336660 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mark2 | Mm_Celera | 19:7327912 | AGATATCTTTTTTCT[C/T]CCAATATTTTTAAAC | 13728 |
rs36352586 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7325672 | GTCCTCATTTGACTC[C/T]TCTGATTGGCCTCAG | 13728 |
rs36355994 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Mark2 | Mm_Celera | 19:7289203 | ACCCTTCAGGGATAA[C/T]ACAATTTGTAAACAC | 13728 |
rs36368171 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7317130 | CTGAAACAATTGAGG[A/C]TATATTGCTTGGGTT | 13728 |
rs36373805 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mark2 | Mm_Celera | 19:7286716 | TTTTGAAGTATCATG[C/T]AAACAAGCAGAGGAT | 13728 |
rs36374906 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Mark2 | Mm_Celera | 19:7287008 | AGACCTACCGCCACT[A/G]GCATACTCCATGACA | 13728 |
rs36384455 | snp | A/C | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Mark2 | Mm_Celera | 19:7291281 | CAGTGAGATTGGAAA[A/C]CCACGAAGACAGTCT | 13728 |
rs36386825 | snp | A/G | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime | Mark2 | Mm_Celera | 19:7279442 | CCAAGGGACCCTAAT[A/G]TCCCTGTAGTACCTC | 13728 |
rs36412901 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mark2 | Mm_Celera | 19:7284290 | ACCCAACCTTTCTCC[A/G]GACTCCTGCTCATCC | 13728 |
rs36433884 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7316110 | ATCACTGAGGACACC[C/T]GAAGACACCTGTGCA | 13728 |
rs36439120 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Mark2 | Mm_Celera | 19:7294798 | TGTCCTTGGTCCCAG[C/G]TGGACTCCCACTACG | 13728 |
rs36446528 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Mark2 | Mm_Celera | 19:7306320 | AACCAGCTACCTACA[C/G]CAAACACTACTCAGC | 13728 |
rs36447159 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7329207 | GGAAACTAAGATTCA[C/T]TCTCTAAAGGCTCTA | 13728 |
rs36455533 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mark2 | Mm_Celera | 19:7283411 | ATAAAGGTGTCCCTG[A/G]CTTGAGATTCCCAAG | 13728 |
rs36488138 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mark2 | Mm_Celera | 19:7314205 | TTAAAAAGTCAGAGC[C/T]AGAAACTGTAGCTCA | 13728 |
rs36497060 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Mark2, LOC102639888 | Mm_Celera | 19:7299517 | CTGCTGGGTAGTGGG[A/T]GACTGCCACTGAAGT | 13728 |
rs36498294 | snp | C/G | 0.18 | 0.24 | upstream-variant-2KB | Mark2 | Mm_Celera | 19:7343782 | GTCAATCTCTAGAAC[C/G]AAAAATAAAATAAAA | 13728 |
rs36511286 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Mark2 | Mm_Celera | 19:7292299 | AGAAGCCCTTGCACA[C/T]GGACAACCGTGAAGG | 13728 |
rs36518977 | snp | A/G | 0.35503 | 0.226867 | upstream-variant-2KB | Mark2 | Mm_Celera | 19:7343727 | GGGTTGTAGGATAGT[A/G]GGAGAGCTTTAACTC | 13728 |
rs36535283 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Mark2 | Mm_Celera | 19:7282102 | CAGGGAGAGCTAAGG[A/T]AAAGCCATTGTAAGT | 13728 |
rs36536739 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Mark2 | Mm_Celera | 19:7343419 | ATGACTTTTAAAATA[G/T]TCTACAATGTTTAAG | 13728 |
rs36538117 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Mark2, LOC102639888 | Mm_Celera | 19:7298480 | CAAGAGAATATCCAC[A/G]CTTATCACAGTACTG | 13728 |
rs36543777 | snp | A/C | 0.42 | 0.183303 | intron-variant | Mark2 | Mm_Celera | 19:7294863 | GGCTGGTGAGGCCAA[A/C]GATCTTTTGGTATCT | 13728 |
rs36563851 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mark2 | Mm_Celera | 19:7283418 | TGTCCCTGACTTGAG[A/G]TTCCCAAGAGCACAT | 13728 |
rs36566156 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mark2, LOC102639888 | Mm_Celera | 19:7298327 | CTCTGCCTAACTGTA[C/T]ATAAGAAGTGGCACG | 13728 |
rs36572475 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mark2 | Mm_Celera | 19:7293181 | CTGGGCTCACTGTTA[C/T]ACCTCAGGCAGTAGC | 13728 |
rs36593092 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7316212 | CAGCGGGATCAGAAA[A/G]TCAATGAACTTCAAA | 13728 |
rs36618507 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7283340 | CCATGGCCATGCTAT[G/T]ACGAAGGAGATAAAC | 13728 |
rs36661279 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Mark2 | Mm_Celera | 19:7291467 | AAGCCACAATAGTTA[C/G]ATACAAAGTGCATAG | 13728 |
rs36672486 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7316510 | TTTAGAAGGGCCACA[C/T]GCACTGTAGCAGAGA | 13728 |
rs36696848 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Mark2, LOC102639888 | Mm_Celera | 19:7303125 | TCAGTGGTGTACTGG[C/T]TCTACCATGAGCCTA | 13728 |
rs36701137 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Mark2 | Mm_Celera | 19:7290917 | GCAGGAAATACAAGG[A/G]ATCATAAGGCAGGGG | 13728 |
rs36707664 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7316624 | AAGGGCTAGCAGGAT[A/G]CCCAGAGATCAACTC | 13728 |
rs36723685 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Mark2 | Mm_Celera | 19:7314258 | TGTACTTGGGCTCTG[C/T]CCCAGATCCAATAAA | 13728 |
rs36727871 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Mark2, LOC102639888 | Mm_Celera | 19:7295705 | TCGGAAGGACAACCA[A/G]CAAACCTTGCCCAGT | 13728 |
rs36744260 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mark2 | Mm_Celera | 19:7284134 | GCCTCCTGTAAATCA[A/G]ATACGCACAGAAACC | 13728 |
rs36764087 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mark2 | Mm_Celera | 19:7307810 | GAGAAGCCTGGTTAA[A/G]GGGCATTGTACTACA | 13728 |
rs36774048 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mark2 | Mm_Celera | 19:7316536 | AGAGACCAGCTTCAG[G/T]AGACAAACATGAATC | 13728 |
rs36776889 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mark2 | Mm_Celera | 19:7316886 | AAGGCCACTGTGCCA[C/T]AGACCAAGGCATTTA | 13728 |