SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3654286 | snp | A/C/T | 0.5 | 0 | intron-variant | Fam188b | GRCm38.p3 | 6:55220620 | CAAATATGCTATCAA[A/C/T]GAAAGCTAGACTCCC | 330323 |
rs3655446 | snp | C/G | 0.5 | 0 | intron-variant | Fam188b | Mm_Celera | 6:55220741 | TAAGTAGTGTGATGC[C/G]TCAAGTCCTTTGGAA | 330323 |
rs3673621 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fam188b | Mm_Celera | 6:55310920 | CCTACCTTGAGGGTA[A/G]CTTCTTGCCTGAGAT | 330323 |
rs3695233 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fam188b | Mm_Celera | 6:55238851 | AATCATGACATTCCA[C/T]TCCCTGGCCCCCAAA | 330323 |
rs3723803 | snp | A/G | 0.5 | 0 | intron-variant | Fam188b | Mm_Celera | 6:55217040 | AGCCTAAGTCTCTTG[A/G]CAATCCGTTTTTGGT | 330323 |
rs3723892 | snp | A/G | 0.5 | 0 | intron-variant | Fam188b | Mm_Celera | 6:55217086 | CCTTTATTCTCTTGG[A/G]CACAAGTTTAGCATA | 330323 |
rs3724456 | snp | A/G | 0.5 | 0 | intron-variant | Fam188b | Mm_Celera | 6:55217131 | TTCATTTTCCTTAGT[A/G]CGTTGTTTCTTCAGA | 330323 |
rs3726706 | snp | A/G | 0.5 | 0 | intron-variant | Fam188b | Mm_Celera | 6:55220362 | GTAACTGCTTTGTAT[A/G]TAGTTTTGCAAATCT | 330323 |
rs6307503 | snp | G/T | 0.5 | 0 | intron-variant | Fam188b | Mm_Celera | 6:55241296 | TTTTACTGTTGAGGT[G/T]AAAAGAGAATGTGTT | 330323 |
rs13478767 | snp | A/G | 0.437396 | 0.165477 | missense, nc-transcript-variant | Fam188b | Mm_Celera | 6:55224284 | GCCCACTGGGGTACA[A/G]CCACACAGAGGGGAA | 330323 |
rs29870271 | snp | A/C | 0.32 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55219964 | GTTCCCAGCGACCAA[A/C]TTGGATTGCTCATAA | 330323 |
rs29871331 | snp | C/G | 0.5 | 0 | intron-variant | Fam188b | Mm_Celera | 6:55214760 | CTCAAGGCCATGTCT[C/G]GACACAGCTCAGCAG | 330323 |
rs29872369 | snp | G/T | 0.188366 | 0.242283 | intron-variant | Fam188b | Mm_Celera | 6:55277992 | TGGTCTTGCTGGCTG[G/T]AGAGTGAGCCTTTTC | 330323 |
rs29876783 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fam188b | Mm_Celera | 6:55281777 | AGGGAAGGGGAGACA[A/G]AGGGAGAGCTCCCTA | 330323 |
rs29877336 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55295694 | TTGGGGGCCTTGTGA[C/T]GTGTGTGGTCAGTGG | 330323 |
rs29886265 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55280342 | GGTCCTAGAATAGCT[A/G]TCTGTCACTTGTGCC | 330323 |
rs29919673 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Fam188b | Mm_Celera | 6:55222366 | GAAATGCTTAGAGAT[A/T]CTGAAGTCCGGACCA | 330323 |
rs29920455 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55289125 | GTTTTGGCCTTGGTC[A/G]AGAAGTAGAGACATA | 330323 |
rs29920850 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Fam188b | Mm_Celera | 6:55315230 | CAAAAAAATTACATT[A/C]TTACAGATACTGAAT | 330323 |
rs29922494 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55259012 | CAGTGTGTTCTTCTT[C/T]CTTTGTGCCCTTATT | 330323 |
rs29923864 | snp | C/T | 0.32 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55282166 | CTGGGCTGTCACACT[C/T]GCTTTCCTTGCCTGG | 330323 |
rs29926549 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55207746 | CTCCAACTCTTGAAT[G/T]CCAGCTAGGTGTCCC | 330323 |
rs29935536 | snp | C/T | 0.32 | 0.24 | intron-variant | Fam188b | GRCm38.p3 | 6:55220148 | CTGTACTTGTGTGCA[C/T]AACTCATATTCACAT | 330323 |
rs29937075 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55232955 | ACACTAGGTGGCAGT[A/G]TAACTTTGCCCATCT | 330323 |
rs29965307 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Fam188b | Mm_Celera | 6:55222955 | CACAGGATTACTGAA[C/G]AATCCTCATTCAAAA | 330323 |
rs29966402 | snp | C/G | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55258718 | CCATATGTGTTATGG[C/G]ATCCTGCTTCCTAGA | 330323 |
rs29970249 | snp | A/G | 0.32 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55282215 | GTCCAGAAAACCCTG[A/G]CAGAGCCTCTCCTTC | 330323 |
rs29973655 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55298262 | AGAATGGCCGTGTGG[A/G]TCATATTAACATGCT | 330323 |
rs29974950 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Fam188b | Mm_Celera | 6:55230905 | CAAAACCAGTCTGTG[C/T]GCCCGATCTCGTGCT | 330323 |
rs29982954 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fam188b | Mm_Celera | 6:55257147 | AAAGGAAGTAAAGGA[C/T]GGGAAGAGAAGCGCT | 330323 |
rs30018113 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55298317 | ACTCACAGTCTTCTG[C/T]CCCAGCTGGGAAACC | 330323 |
rs30020408 | snp | C/T | 0.32 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55224951 | TCGCTGGATGCTGGT[C/T]CCTTTCTCTTCTCTT | 330323 |
rs30021767 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55223046 | TAAAATTGCTTCCAC[A/G]GATGACTCTGCTGTA | 330323 |
rs30025031 | snp | A/G | 0.32 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55210623 | TGTCCTGTGATGGGG[A/G]TGAAGCAGCTGTTGT | 330323 |
rs30032062 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fam188b | Mm_Celera | 6:55230461 | TCTACAGAGAATGGA[C/T]GCTTAATGATAGCAT | 330323 |
rs30068134 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55284090 | CAGCCAGGCGGGGTG[A/T]CTGAGATGCAAAATA | 330323 |
rs30079345 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fam188b | GRCm38.p3 | 6:55211678 | TCTCTCTCTCTCTCT[A/C]TCTCTATATATATAT | 330323 |
rs30080744 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Fam188b | Mm_Celera | 6:55204181 | TAGGAATCTGTGCTT[C/T]CACATGATGTCATAT | 330323 |
rs30108452 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Fam188b | Mm_Celera | 6:55277383 | TATGAATCATTTATT[A/T]ATGTAAGTAGATGGT | 330323 |
rs30112767 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fam188b | GRCm38.p3 | 6:55211682 | TCTCTCTCTCTCTCT[A/C]TATATATATATATAT | 330323 |
rs30113566 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Fam188b | Mm_Celera | 6:55202813 | CCTGGTGCCACCTTG[A/T]TCACCAGCTTGCAGG | 330323 |
rs30117868 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fam188b | Mm_Celera | 6:55281796 | GAGAGCTCCCTAGGA[C/T]AACTACAAGGTGGTA | 330323 |
rs30118368 | snp | C/T | 0.32 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55206508 | TGCTACTTGTCTTTG[C/T]CATCCATGGTCAGGC | 330323 |
rs30120329 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55207707 | CAACACCAAATACAC[A/G]TTTTTCCTCTCTCCC | 330323 |
rs30120407 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB | Fam188b | Mm_Celera | 6:55202342 | CTCAGGACACCAAAG[C/T]GGACCATGAAGTCTC | 330323 |
rs30120408 | snp | A/T | 0.277778 | 0.248452 | upstream-variant-2KB | Fam188b | Mm_Celera | 6:55203160 | GACTTTAAGAACCAC[A/T]GGGTAGGGCGTGTTT | 330323 |
rs30120409 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fam188b | Mm_Celera | 6:55203767 | AGCCCTCCCTAATGC[A/G]AGGGCACGTCCACAA | 330323 |
rs30120410 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fam188b | GRCm38.p3 | 6:55204164 | GGCTGAGGACTATAC[A/G]CTAGGGATCTGTGCT | 330323 |
rs30120412 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fam188b | Mm_Celera | 6:55204170 | GGACTATACACTAGG[A/G]ATCTGTGCTTTCACA | 330323 |
rs30120693 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fam188b | Mm_Celera | 6:55251946 | TCTGCATGATGTCTG[G/T]CTGTGCGTTGGTTCC | 330323 |
rs30121864 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Fam188b | Mm_Celera | 6:55204310 | TGTGTGTGTGTGTGT[G/T]TTTGCATGGAACAAA | 330323 |
rs30121866 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Fam188b | Mm_Celera | 6:55204329 | GCATGGAACAAAGGA[A/C]AAGGATTTGAGGTCA | 330323 |
rs30121868 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fam188b | Mm_Celera | 6:55204393 | GAAATGTAAGTTTGA[C/T]GTTACTACCTCATCT | 330323 |
rs30121869 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fam188b | Mm_Celera | 6:55204414 | TACCTCATCTTCTCT[C/T]TAACGGGAACTTTTA | 330323 |
rs30121870 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fam188b | Mm_Celera | 6:55204591 | AGCATGCACAGTTGT[A/G]ATTACTTTCGTCACT | 330323 |
rs30121871 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Fam188b | Mm_Celera | 6:55205023 | TTGGATGATCCGTGT[C/T]GTCATGCCCTGAGAG | 330323 |
rs30121873 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Fam188b | Mm_Celera | 6:55206725 | TGCTCTGCAATGGGC[G/T]TGGCTCTCTTGTCTT | 330323 |
rs30122895 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Fam188b | Mm_Celera | 6:55206970 | TCCCATCTCCGGCTT[C/T]CCATACATTCTCCCT | 330323 |
rs30122897 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Fam188b | Mm_Celera | 6:55207405 | GTTCCGGCCATTTCT[C/T]CTCCTCCTCACACTG | 330323 |
rs30122900 | snp | C/T | 0.197531 | 0.244432 | synonymous-codon, nc-transcript-variant | Fam188b | Mm_Celera | 6:55216669 | CACTCAGAGACCACA[C/T]TGGTGAATATATACG | 330323 |
rs30122902 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fam188b | GRCm38.p3 | 6:55216788 | TGCCTACACCAGCCC[A/G]GCCAGGCAAGGCTCC | 330323 |
rs30123724 | snp | A/T | 0.18 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55277152 | GATCAGTTTGATGAC[A/T]TTAGCATAGTGCTTA | 330323 |
rs30123974 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | GRCm38.p3 | 6:55216832 | GGCCCTGTTTTTCCT[C/T]ACTTCTTGCTCTTCC | 330323 |
rs30123976 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | GRCm38.p3 | 6:55216841 | TTTCCTCACTTCTTG[C/T]TCTTCCTCCCTCCCT | 330323 |
rs30123978 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55217499 | GTTGGCATCAGCTTG[C/T]ATCCCTAATCAGACT | 330323 |
rs30123980 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fam188b | Mm_Celera | 6:55217530 | TGCACTTCCTCTCTC[C/T]TTTCCCTGATCCATA | 330323 |
rs30123982 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55217772 | GGGAGATTCAGCCCC[A/G]TCGAGACATGGCTGG | 330323 |
rs30124844 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55218112 | TGCTGCTTCCGTTCC[A/G/T]TACCTCTCCCAACTG | 330323 |
rs30124846 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55218191 | TATTATTTGGAGGCT[A/C]TGTTTAAATGGAAGT | 330323 |
rs30124848 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55218218 | AAGTGTTACATTTCT[A/G]CAGGCATGACAGTCT | 330323 |
rs30124850 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fam188b | Mm_Celera | 6:55218522 | GCAGTGAGAGATGTG[C/T]GTTGGGCACTGCTGG | 330323 |
rs30124852 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55218657 | ACCTGAGTTAGTGAA[A/G]TGAATGCTTTGATTT | 330323 |
rs30125794 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55218934 | TTAGGTACGAGGGTA[C/T]AGCAGATGAGAGGAC | 330323 |
rs30125796 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55218989 | ACAAATGGGGAAATA[C/T]CAGAAACATGAGTGG | 330323 |
rs30125798 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Fam188b | Mm_Celera | 6:55219120 | TTCTCACCCTTGTCG[A/C]GTTAGGACAAAGAGG | 330323 |
rs30125800 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Fam188b | Mm_Celera | 6:55219439 | CTTGAGTAGTTAACG[A/C]CAGGAGAGTGCTGTG | 330323 |
rs30125802 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55219619 | TCCTGCACTCTGGTT[G/T]GAAGCCGGTGTGAAG | 330323 |
rs30126664 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fam188b | Mm_Celera | 6:55219629 | TGGTTGGAAGCCGGT[G/T]TGAAGATTGTACTAT | 330323 |
rs30126666 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55220125 | GGCGCCTGACTCCTT[C/T]TTCAGGCCTGTACTT | 330323 |
rs30126670 | snp | A/G | 0.32 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55221120 | GTTGCACACGCCGTA[A/G]CCGCTGTCCTTCCTA | 330323 |
rs30126672 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55221333 | TTAGATTCCTGTGCA[C/T]GGCCAGCCGTGTTCC | 330323 |
rs30126673 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55221355 | CCGTGTTCCTGCCGC[C/T]GCTGTGCACCTTAAA | 330323 |
rs30127635 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55221416 | TTCTGCTGTCTGTCA[A/G]TTGCCTGTCACTCTA | 330323 |
rs30127637 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55221498 | TGTGGGTCCGAGAGT[C/T]TTACAGCTTCTGTGT | 330323 |
rs30127639 | snp | C/T | 0.32 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55221525 | GTGTGTTCAGACTCT[C/T]GTGAAGTCCCTTTGT | 330323 |
rs30127641 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fam188b | Mm_Celera | 6:55221720 | TCAAAGAGTATTACC[C/T]CTGAGATCTCAACTT | 330323 |
rs30127643 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55221730 | TTACCTCTGAGATCT[C/T]AACTTTCTTCTTCTG | 330323 |
rs30127674 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188b | Mm_Celera | 6:55232526 | AATGATTGCCTTCTA[C/T]CCTCAGTCTGTCTGT | 330323 |
rs30127676 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fam188b | Mm_Celera | 6:55232637 | CTGGGCTTTGTGTGA[A/G]CAGGGATGCAGGAAA | 330323 |
rs30127678 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fam188b | Mm_Celera | 6:55232835 | CTAAAACAGCTCCTT[C/T]AGACTCTCAGGCCCC | 330323 |
rs30127680 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fam188b | Mm_Celera | 6:55232880 | TCCAGGCCAGTGGTT[G/T]CTGCTTCAGGAGACC | 330323 |
rs30127682 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fam188b | Mm_Celera | 6:55232921 | GACTCTGGTAGAGCT[A/T]TCAGGTTCCATAGAA | 330323 |
rs30128324 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188b | Mm_Celera | 6:55233163 | TGGGACAGAGGGACT[C/T]CTGCCAGCTGAGGTT | 330323 |
rs30128326 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188b | Mm_Celera | 6:55233531 | GTGACCTTGTGCATG[C/T]ACTCCTATCCTAGCC | 330323 |
rs30128328 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fam188b | Mm_Celera | 6:55233910 | CTGATGGAAGGAGGC[A/C]GCTGAGCTCAGAGAT | 330323 |
rs30128330 | snp | A/C | 0.32 | 0.24 | intron-variant | Fam188b | Mm_Celera | 6:55233999 | TTTCTGATTCTGAGA[A/C]TCCAGTCTTCTGGGC | 330323 |
rs30128332 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Fam188b | Mm_Celera | 6:55234006 | TTCTGAGAATCCAGT[C/T]TTCTGGGCTCCAAGA | 330323 |
rs30128615 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fam188b | Mm_Celera | 6:55221745 | CAACTTTCTTCTTCT[A/G]GGCCCTACCATGTCA | 330323 |
rs30128617 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Fam188b | Mm_Celera | 6:55221772 | GTCACTTTAATGACA[C/G]CAAGCTCACACATTC | 330323 |
rs30128619 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fam188b | Mm_Celera | 6:55221876 | CCCACTTTGAGAACC[A/T]GTGGTTTAGTGGGTG | 330323 |