SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6165633 | snp | G/T | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62914784 | AACATTTGTAAAATT[G/T]TTTAAGTCTGTAAGA | 56469 |
rs6174220 | snp | A/G | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62948536 | AGTTTCAAGTCTGGG[A/G]TGCATGAGACCTTAT | 56469 |
rs6182689 | snp | A/G | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62922176 | CAAAGATCTTTCCAG[A/G]GTTGCATACAGGCTC | 56469 |
rs6182824 | snp | G/T | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62922249 | TTTTGATATGGCCCC[G/T]GAAACATCTTGCTGG | 56469 |
rs6183992 | snp | A/G | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62922446 | CACACAAAAACATTA[A/G]TTTTTACATTAAATG | 56469 |
rs6185002 | snp | C/T | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62922576 | ggttaagaacactgg[C/T]tcctattccaacaga | 56469 |
rs6317485 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Pias1, Gm35574 | Mm_Celera | 9:62978901 | TTGTCTCCAAAATGT[C/T]AAATTTCAGAGGCTT | 56469 |
rs6317557 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Pias1, Gm35574 | Mm_Celera | 9:62978953 | GAAATTGGGATAAAA[A/G]AAACTATCCAAgtca | 56469 |
rs6317585 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Pias1, Gm35574 | Mm_Celera | 9:62978971 | ACTATCCAAgtcagg[A/T]atggtggtgaatgcc | 56469 |
rs6318591 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Pias1, Gm35574 | Mm_Celera | 9:62979146 | GGCGCTATCCATTAA[C/G]ATTTTCTGTCTTAAA | 56469 |
rs6319623 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | Pias1, Gm35574 | Mm_Celera | 9:62979339 | AAGTGTCCAGAAACA[A/C]AGGTAGTGGTCTGCT | 56469 |
rs6337877 | snp | A/G | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62948673 | GACAAGAATCTACAA[A/G]CTTTCTCCTAAAACA | 56469 |
rs6338004 | snp | A/T | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62948754 | ATTCACTGTTGATAT[A/T]TTTTTTTAATTCTTT | 56469 |
rs6361929 | snp | A/G | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62944331 | cacctttgtattcag[A/G]atgctatggcagaag | 56469 |
rs6362531 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Pias1 | Mm_Celera | 9:62944461 | CATAAGAAATAATGT[G/T]CACACTTCAATTTAA | 56469 |
rs29601796 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Pias1 | Mm_Celera | 9:62890769 | CTGTCCAAGTCTGGG[C/T]TGGGCATGAAGGCCA | 56469 |
rs30129977 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pias1 | GRCm38.p3 | 9:62917129 | ACAGTTCATATGTGG[C/T]GAAATAATGTGAAGG | 56469 |
rs30231017 | snp | C/T | 0.197531 | 0.244432 | upstream-variant-2KB, intron-variant | Pias1, Gm35574 | Mm_Celera | 9:62982033 | GGTACTCTATTTCTC[C/T]GCTTTCTTCACTGAA | 56469 |
rs30285417 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pias1 | Mm_Celera | 9:62924041 | CTTTCACTGCCTTCT[A/G]TTTATTTTGAGAAAT | 56469 |
rs30433699 | snp | G/T | 0.5 | 0 | intron-variant | Pias1 | Mm_Celera | 9:62885405 | ATGAGAAGTCGAGCT[G/T]AAGGTTCTACGGCAC | 56469 |
rs33631496 | snp | C/G | 0.375 | 0.216506 | intron-variant | Pias1 | GRCm38.p3 | 9:62970345 | AGAAAAAATAAATAA[C/G]CTTTGGAGAGATACT | 56469 |
rs33659439 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Pias1 | GRCm38.p3 | 9:62932731 | AAGTGTAAATAGAAG[A/G]CATGAAAATTCCCAA | 56469 |
rs33680321 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Pias1, Gm35574 | Mm_Celera | 9:62981396 | AGAAAAAAAAAAAAA[A/T]ATATATATATATATA | 56469 |
rs33717432 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pias1 | Mm_Celera | 9:62931531 | GAAATAACCTGTCAG[C/T]GAACAGAAGAAGAAT | 56469 |
rs33730400 | snp | A/C | 0.375 | 0.216506 | intron-variant | Pias1 | Mm_Celera | 9:62897708 | ATCCCCTTCCCAGTT[A/C]CCCCTCCACAAATCC | 56469 |
rs36251282 | snp | G/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62924704 | CGTTGGTAGGTTGCT[G/T]CCTAGTTAACTCCTG | 56469 |
rs36284715 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Pias1 | Mm_Celera | 9:62952409 | ACATTAATTATAAAA[C/G]AGCCAGGATCAAGCT | 56469 |
rs36299557 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62886271 | CAAGAAAACCAATGG[C/T]CTCATGCTGATGTCC | 56469 |
rs36359997 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Pias1, Gm35574 | Mm_Celera | 9:62982687 | AGACTCAGCTGTGAT[C/T]TTTATTCAACCACCC | 56469 |
rs36369487 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62895060 | GAATCTCAAAATTTG[A/G]TCATGCATCCTCTTA | 56469 |
rs36375980 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Pias1 | GRCm38.p3 | 9:62881475 | AAGGCTGGTAAAATC[C/T]ACGCACACACAAACA | 56469 |
rs36387363 | snp | A/G | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62887759 | GAGATGCTACGGTAA[A/G]ACTATTCATGCAGTC | 56469 |
rs36409534 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62962583 | GTACGACAAAGGAAG[C/T]GGGAAATCTAAGAAA | 56469 |
rs36421925 | snp | A/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Pias1, Gm35574 | Mm_Celera | 9:62982781 | TAGACTGCATCACCA[A/T]ATTCGAATCCAGGCA | 56469 |
rs36423214 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62955668 | TAAAATAAAATCTCT[C/T]GCTTGAAGGATCAAA | 56469 |
rs36427692 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62906156 | AACATCCGGCAGCTC[C/T]TGAAGGAAAATGGCT | 56469 |
rs36441500 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62924890 | AAAACTGCACTTTTC[C/T]AAGATAATTTAATAC | 56469 |
rs36441974 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62906075 | TGAGGGTTTCAATGT[A/G]TCCCATAACGTATCA | 56469 |
rs36473366 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pias1 | Mm_Celera | 9:62899860 | AAAGAGAAAAAGCAT[C/T]TTAATTATTTTTGTT | 56469 |
rs36506374 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62947999 | TATGTGCAGCAGTTT[C/T]CCTCTGTAAAGTCAC | 56469 |
rs36522207 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62913216 | GATTTAAGGCTCTAA[C/T]ATGAAAGAACACTAT | 56469 |
rs36525956 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62937003 | CACAGAGCCTAAAAA[A/T]GGTATCAACACCCAA | 56469 |
rs36543393 | snp | G/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62906178 | AAAATGGCTAGCTGA[G/T]CTGCTGCACTGGAAT | 56469 |
rs36546481 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62911336 | ATAACTCCATCGAGG[C/T]TTTGAAAAAAAAGGA | 56469 |
rs36562263 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62911943 | CAGAATCAAGGTCAG[C/T]CCATCATGCTCCCGA | 56469 |
rs36562349 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62913738 | CTGAGATATGCTACA[C/G]ATGTCCTTACAACTT | 56469 |
rs36586833 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62935646 | CTTTTGGACCGGAGC[A/G]AGCAGAATTGTCCAG | 56469 |
rs36618550 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Pias1 | Mm_Celera | 9:62897107 | ACACAGCCAACAGCC[A/C]TCTCAGACATCACTA | 56469 |
rs36618571 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62892840 | TCTTAGCATTCAGGA[A/G]GCAGAGCCAAGCGAA | 56469 |
rs36625550 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62890353 | AGGATGTCATCTAGT[C/T]CAGGTGGCCCCAAAC | 56469 |
rs36642194 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62933580 | GATCCACTATCAAAT[A/T]TGCATTGCTCTGACC | 56469 |
rs36653920 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Pias1 | GRCm38.p3 | 9:62881177 | CAGACTGCGCATCCA[A/G]GCAGCGTTTGCTCCA | 56469 |
rs36671027 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Pias1 | Mm_Celera | 9:62930728 | ACAAATCAACAAACT[A/G]CTACACAATGACAAC | 56469 |
rs36675334 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62923089 | ATCAGATGCAGCTTC[C/T]GGACTACCCCAGGAG | 56469 |
rs36677194 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62961500 | TCAGTTACAGTTTGT[C/T]ACTGACTCAGGTGAA | 56469 |
rs36685742 | snp | A/C | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62916275 | TGAGATCCAGCTGAA[A/C]AACAAAATGACCAAG | 56469 |
rs36705146 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62887818 | CTCTGAGAACGCAGG[A/C/T]GCAACACCCAGTTGA | 56469 |
rs36708128 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Pias1 | Mm_Celera | 9:62929630 | TCAGATAAGCCAATT[C/T]AAGGGATATTATAAG | 56469 |
rs36758732 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Pias1 | Mm_Celera | 9:62901434 | TTCTTAAAAGAACAA[C/G]AAACTGCCACCCTCT | 56469 |
rs36780286 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Pias1 | Mm_Celera | 9:62917705 | CGAACAGGTGACTAC[C/T]GTATGATTTTGGCAA | 56469 |
rs36803092 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62914405 | GAGATGCTAATCAAC[A/G]TTGTGAGATTCTGGA | 56469 |
rs36825422 | snp | A/G | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62904606 | TTAGTTTGGAAAAGA[A/G]AGTCATCAAGACACT | 56469 |
rs36827509 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pias1 | Mm_Celera | 9:62916878 | ACTGGAAATAGCAAT[A/G]ATAAAAGCACCAGAG | 56469 |
rs36848565 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Pias1 | Mm_Celera | 9:62944986 | ACAGGCGTTATTTCA[A/T]ACTTACAACTATAGA | 56469 |
rs36854103 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62891722 | CTGAGCCCTGGGATT[C/G]AGATCTTTGTGAGTA | 56469 |
rs36865581 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Pias1 | Mm_Celera | 9:62926681 | AAGCACCTCATCATT[A/G]GGTTTCTCCATATTT | 56469 |
rs36875745 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62934903 | AGATCCTTATCTGGC[C/T]TGTGTACTCTCACAC | 56469 |
rs36889255 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pias1 | Mm_Celera | 9:62913402 | CCTAGATCTTAAAGA[C/T]ACTTGACTTGGGCCA | 56469 |
rs36912057 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62916901 | CACCAGAGGAATTAC[A/G]GATGCAGGACAACTA | 56469 |
rs36927637 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62943123 | TGTGACATAATTAGC[A/G]GGATTAACATTCACA | 56469 |
rs36928525 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62907048 | GGGACTTTTTTCTGT[A/G]TAAATAATCTGAATC | 56469 |
rs36930359 | snp | G/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62889572 | AGGTGCTACAGTACC[G/T]GATTCTTTCCAGTTG | 56469 |
rs36933482 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pias1 | Mm_Celera | 9:62899550 | TCAGCCATGCTAGGG[C/T]TCATGATGCTGCATG | 56469 |
rs36971370 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Pias1 | GRCm38.p3 | 9:62932173 | CAACAGTCTTAACTG[C/G/T]GAAATGCAAACCAAA | 56469 |
rs37002524 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Pias1 | Mm_Celera | 9:62969423 | TTGACCTAGATATAC[A/C]CAGGGAAACACCAGG | 56469 |
rs37025222 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62904141 | ATACGTGATCACACC[A/G]TGTGGTTTGGAATTT | 56469 |
rs37040295 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62921562 | GCAGCAACACCCTCT[C/T]TTGATTGAACAACCA | 56469 |
rs37062027 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62919118 | AGGCTAAATAGTGGT[A/T]TATTCTTATCACCAT | 56469 |
rs37091388 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62926559 | ATCCTTTTCCTTCAG[C/T]CTGTCCAGTGCTGGG | 56469 |
rs37197500 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62923701 | TAAAGGTCATCAGTA[C/T]AGACATAGCCAGAAC | 56469 |
rs37222395 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62924441 | AGGCACGGCACGTGA[C/G]AGCAGGAATTTCTCT | 56469 |
rs37242938 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Pias1 | Mm_Celera | 9:62951713 | TAAAGTCTAAGAAAA[A/C]CGCTAAGCACAGCAT | 56469 |
rs37278126 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Pias1 | Mm_Celera | 9:62905313 | GGCCCAGCGGGCACC[G/T]CCTACACAGTAATGG | 56469 |
rs37279037 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62909715 | AGGTGTTGGAATTGC[C/T]CTCCTTGCTCCTCCT | 56469 |
rs37285614 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pias1 | Mm_Celera | 9:62895554 | GTTTGATCCTCAAAA[C/T]ATAGATGGTAGAAGA | 56469 |
rs37317312 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62960752 | TGTAGATGTGCTAGA[A/G]ACGCTTCTTCCACGG | 56469 |
rs37319013 | snp | A/G | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62902487 | GTCCTGTTTGAATTA[A/G]TGGAGTATGGAAACA | 56469 |
rs37365815 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pias1 | Mm_Celera | 9:62948469 | CTGTAGTGCTGCACG[C/T]CAGTAGTGATGGAAT | 56469 |
rs37368445 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62911819 | ATGAGCTGCTATTAG[C/T]AAGTCATCTTAAGAG | 56469 |
rs37403686 | snp | C/T | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62891632 | ACTAGCCTTGCGGAG[C/T]CAATCCTCTCCTTCC | 56469 |
rs37412361 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62884402 | CTTTGCTACCAACAT[C/T]GAGTACTCACAGACT | 56469 |
rs37432282 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Pias1 | Mm_Celera | 9:62953850 | AAACTGCTGAGCACA[A/G]TGGCCAACAACTGAA | 56469 |
rs37437309 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Pias1 | Mm_Celera | 9:62885400 | AAACTATGAGAAGTC[A/G]AGCTGAAGGTTCTAC | 56469 |
rs37499379 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Pias1 | Mm_Celera | 9:62929981 | CAAGCTCAGTATAAC[A/T]GCAAAACTACTATGA | 56469 |
rs37508314 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62912083 | CTTGAAGCCAGGAAG[C/T]CCACTTTTAGATCTT | 56469 |
rs37542893 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62911437 | GTCTCCGACTCATGA[C/T]GCCTCCATTTCCTTA | 56469 |
rs37579773 | snp | A/G | 0.32 | 0.24 | intron-variant | Pias1 | Mm_Celera | 9:62909364 | TGTCTGAGCATTGTC[A/G]CCTGTGCACTCACAT | 56469 |
rs37595153 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pias1 | Mm_Celera | 9:62916790 | AACTTAAGTAGGAAA[C/T]AGCCACAAACCAGTA | 56469 |
rs37628803 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pias1 | Mm_Celera | 9:62925790 | TGTGACACTGAAAAG[A/G]CTATCATAAACTTTC | 56469 |
rs37634360 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pias1 | Mm_Celera | 9:62911417 | GTCAGGACCCTTTCT[C/T]TCTTGTCTCCGACTC | 56469 |