SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs491973 | snp | C/T | 0.499393 | 0.0174067 | upstream-variant-2KB, missense | SART1, TSGA10IP | GRCh38.p7 | 11:65959830 | CCATTCTCACCCCCA[C/T]TGACCTGTGGCTCCT | 9092 |
rs493899 | snp | A/C | 0.494651 | 0.0514399 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980481 | TTCTCTCAAAAGCCT[A/C]GGAGGAGGCTGGGAA | 9092 |
rs501353 | snp | G/T | 0.494896 | 0.0502606 | intron-variant | SART1 | GRCh38.p7 | 11:65972078 | atatgaatttagggg[G/T]tacacaaTTCCTAGA | 9092 |
rs542332 | snp | A/G | 0.494651 | 0.0514399 | intron-variant | SART1 | GRCh38.p7 | 11:65976950 | CAGCCCCACCCACTG[A/G]TCACCACCTGCCAGG | 9092 |
rs543952 | snp | A/G | 0.315086 | 0.241379 | intron-variant | SART1 | GRCh38.p7 | 11:65976804 | ATCTCCAGCTTGAGC[A/G]CCCCCAAACGCCCAC | 9092 |
rs550435 | snp | A/G | 0.497165 | 0.0375428 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965180 | GCGGGAGAAGCTGGC[A/G]GCTGCCAAGGAGAAG | 9092 |
rs552130 | snp | A/G | 0.493136 | 0.0581782 | intron-variant | SART1 | GRCh38.p7 | 11:65965329 | TTCCTGAAGAGGGGA[A/G]AAAGTGATGCTCAAG | 9092 |
rs556643 | snp | A/G | 0.498774 | 0.0247239 | intron-variant | SART1 | GRCh38.p7 | 11:65965818 | CAGGGGACACTGGTG[A/G]CCTTGCTACCGGAAT | 9092 |
rs586921 | snp | A/G | 0.26326 | 0.249648 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980230 | TTCTGCACGGCTAGA[A/G]CTGCGGGGCTGAGTC | 9092 |
rs593525 | snp | A/G | 0.495927 | 0.0449436 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960328 | GGCTCCCTGTGTGGC[A/G]CAACTCAGCATGTGT | 9092 |
rs622779 | snp | C/T | 0.329005 | 0.237188 | intron-variant | SART1 | GRCh38.p7 | 11:65976776 | CACCCCCCAGCGGCG[C/T]GGCCCTCACATCCTG | 9092 |
rs642293 | snp | A/G | 0.49306 | 0.0584955 | intron-variant | SART1 | GRCh38.p7 | 11:65962746 | ccaggaaaccaggag[A/G]gctataggccagggg | 9092 |
rs649000 | snp | A/G | 0.486398 | 0.0813386 | intron-variant | SART1 | GRCh38.p7 | 11:65975462 | cacaccactgcactc[A/G]aaagagtgggcaaga | 9092 |
rs649066 | snp | C/T | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65975408 | aaaaaaaaaaaaaTT[C/T]TTCCAGGggccgggt | 9092 |
rs660118 | snp | C/G | 0.498429 | 0.0279843 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967703 | AGCACCTGCGGGGAC[C/G]CCGGCGGTGGAGCTC | 9092 |
rs679581 | snp | A/G | 0.485049 | 0.0851591 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979182 | AGGTGAGACCTGGCC[A/G]TCAAATGACACAAAC | 9092 |
rs688862 | snp | A/G | 0.49783 | 0.0328695 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965922 | AATGGCATGCTCCAC[A/G]GTGAGGCCCTGCAGG | 9092 |
rs754532 | snp | C/T | 0.343701 | 0.231776 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979586 | CTGGGTCACTGTACA[C/T]GGGACAAGTCTCCCA | 9092 |
rs879509 | snp | A/G | 0.0232847 | 0.105357 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65979723 | GGTGTACGTGGGGCC[A/G]GGCACCAGTATCCTG | 9092 |
rs948478 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65977508 | AGCCACAGCTCCAGG[G/T]CCGCCTGAGAAGGCA | 9092 |
rs1144796 | snp | C/T | 0.00501711 | 0.0498336 | intron-variant | SART1 | GRCh38.p7 | 11:65966072 | TGCTCTGTGCTGCCC[C/T]CAGGCGTGCTGCAGG | 9092 |
rs1151505 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | SART1 | GRCh38.p7 | 11:65967068 | AAGGTACTTAACCTC[C/T]CTGTGCCCCAGTTTC | 9092 |
rs1151506 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65975393 | TCCCGGGGggccggg[G/T]ggttgccccctttta | 9092 |
rs1151508 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SART1 | GRCh38.p7 | 11:65976308 | GGGTCCTCCCTGGCA[A/G]CAGCCAGACAGGCCA | 9092 |
rs1192168 | snp | G/T | 0.495745 | 0.0459295 | intron-variant | SART1 | GRCh38.p7 | 11:65963474 | AGGAAAGGAAGAGtt[G/T]tttttttgttttgtt | 9092 |
rs1204011 | snp | C/T | 0.26326 | 0.249648 | intron-variant | SART1 | GRCh38.p7 | 11:65973615 | GGTGGGCCCCGGGCA[C/T]GCACACATTCCCTCT | 9092 |
rs1211380 | snp | C/T | 0.128288 | 0.218372 | intron-variant | SART1 | GRCh38.p7 | 11:65972863 | TTCTATGTAGTTACA[C/T]GTTCACTTTTTTCTT | 9092 |
rs1211729 | snp | G/T | 0.496999 | 0.0386216 | intron-variant | SART1 | GRCh38.p7 | 11:65974392 | cacccggctGATATG[G/T]ttttttttttttttt | 9092 |
rs1212282 | snp | G/T | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65963694 | agaagttcaagacca[G/T]cctggccaagatggt | 9092 |
rs1786169 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65973028 | aatacaaaaaaatta[A/C]ccagacgtggtggcg | 9092 |
rs2276015 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | SART1 | GRCh38.p7 | 11:65976832 | GAGGCTCTGGACACC[A/G]AGCCCGGTGCTCATC | 9092 |
rs2276016 | snp | A/G | 0.289399 | 0.246876 | intron-variant | SART1 | GRCh38.p7 | 11:65976794 | TGAGCACCCCCAAAC[A/G]CCCACCCCCCAGCGG | 9092 |
rs2508192 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65963654 | GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 9092 |
rs2509757 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65963530 | tccattgcccaggct[A/G]gagtgcagtggcgca | 9092 |
rs2845569 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960811 | TCAGTGTATCCCTGG[A/G]ACCCCTGGAATTGAA | 9092 |
rs2845575 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65970824 | CCCACCATCCCCCTC[A/C]TCAGCTCATGAATCC | 9092 |
rs2845576 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65970777 | CAGCAGCTCATGAAT[C/T]CCACCATCCCCCTCC | 9092 |
rs2845581 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65963543 | AGTGAGCTGAGATCG[C/T]GCCACTGCACTCTAG | 9092 |
rs2847724 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65963585 | ctcctgggttcaagc[A/C]attctcctacctcag | 9092 |
rs2847725 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65963608 | tacctcagcctcccg[A/G]gtatctgggattaca | 9092 |
rs3016188 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65963582 | aggtaggagaatggc[G/T]tgaacccaggaggca | 9092 |
rs4930331 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | SART1 | GRCh38.p7 | 11:65967074 | CTTAACCTCCCTGTG[C/T]CCCAGTTTCCCTAGC | 9092 |
rs5792377 | in-del | -/AAAAAC/AAAAC | 0.642672 | 0.0904971 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961205 | CCTATCTCAAGGGAA[-/AAAAAC/AAAAC]AAAACAAAACAAAAC | 9092 |
rs7940585 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SART1 | GRCh38.p7 | 11:65968403 | CATTGGTGAACAGGA[C/T]AGCCATGGGGCCCTG | 9092 |
rs7948137 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SART1 | GRCh38.p7 | 11:65976049 | AAACCGGAGTTTGTC[A/G]GGGGAGGGGCAGGTG | 9092 |
rs7952056 | snp | C/T | 0.432939 | 0.170391 | intron-variant | SART1 | GRCh38.p7 | 11:65977126 | TCAGGGCAGCCATGA[C/T]TTGGGTGGGCTTGGG | 9092 |
rs9326363 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65978255 | GTAGGCCGCCCGACC[C/G]TCCTGCCCTACCACT | 9092 |
rs9988860 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | SART1 | GRCh38.p7 | 11:65978306 | GGGGTTTGTCTCCCT[C/G]CAGCCCCAGCCCCAG | 9092 |
rs10791834 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SART1 | GRCh38.p7 | 11:65973131 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 9092 |
rs10896069 | snp | C/T | 0.100588 | 0.200439 | intron-variant | SART1 | GRCh38.p7 | 11:65970667 | GGTGGTGCAAAGAGA[C/T]GGGAGATGCTGTTCT | 9092 |
rs10896070 | snp | C/T | 0.340108 | 0.233197 | intron-variant | SART1 | GRCh38.p7 | 11:65972997 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAA | 9092 |
rs10896071 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | SART1 | GRCh38.p7 | 11:65974955 | TGAGGCAGGAGAATG[C/G]TGTGAACCCAGGAGG | 9092 |
rs11227367 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65972130 | TGTCCATCTCATGTA[A/G]TTCATTTCTAGGTTA | 9092 |
rs11227368 | snp | C/T | 0.490943 | 0.0666801 | intron-variant | SART1 | GRCh38.p7 | 11:65972899 | GAACGTGGCCGGGCG[C/T]GATGGCTCACGCCTG | 9092 |
rs11227369 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | SART1 | GRCh38.p7 | 11:65978514 | GGGTCAATCAACACC[C/T]GCCCTGTTATTATAC | 9092 |
rs11227370 | snp | C/T | 0.356811 | 0.226034 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980222 | GCTGTCGCTTCTGCA[C/T]GGCTAGAGCTGCGGG | 9092 |
rs11545221 | snp | G/T | 0.125087 | 0.216557 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978665 | GAAGACAGAGCGGCG[G/T]ATGAAGAAGCTGGAC | 9092 |
rs11606402 | snp | G/T | 0.44252 | 0.159487 | intron-variant | SART1 | GRCh38.p7 | 11:65963482 | AAGAGtttttttttt[G/T]ttttgttttgttttt | 9092 |
rs11821955 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SART1 | GRCh38.p7 | 11:65974852 | catccaggctagtac[A/G]gtgaaaccccatctc | 9092 |
rs12288643 | snp | A/T | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65978181 | CACCTGCGTGAGCCC[A/T]TCACTGGCTTTCCTG | 9092 |
rs12575514 | snp | A/C | 0.183568 | 0.241012 | intron-variant | SART1 | GRCh38.p7 | 11:65970344 | CCAAAATGTCTTTTT[A/C]GTTTTTTGTTGTAAG | 9092 |
rs12575735 | snp | C/T | 0.0254355 | 0.109867 | intron-variant | SART1 | GRCh38.p7 | 11:65977760 | CTCCTCTGTCTCGGG[C/T]CAGGGCCATCGATGA | 9092 |
rs12577625 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | SART1 | GRCh38.p7 | 11:65970428 | ATTCTAGAGTATGTG[A/G]GAGACACATTTATGA | 9092 |
rs12785894 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65975276 | cctggttgatctttg[G/T]gttttttgtagagac | 9092 |
rs12797319 | snp | A/G | 0.466618 | 0.124806 | intron-variant | SART1 | GRCh38.p7 | 11:65968201 | GATCTGCCTGCCTCT[A/G]CCTCCGAAAATGCTA | 9092 |
rs12806587 | snp | G/T | | | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965772 | AGGAGTTCGGGCAGA[G/T]GCGGCAGGTGAGGCT | 9092 |
rs12808163 | snp | A/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65975248 | gctgagactacaggc[A/T]tacaccaccatgcct | 9092 |
rs12808809 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65975287 | tttgtgttttttgta[A/G]agactgtgcttcacc | 9092 |
rs28372938 | snp | G/T | 0.0898077 | 0.191933 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961528 | CCGGGTTAATTCCGC[G/T]TCCCTTGAGGAGCGC | 9092 |
rs34227638 | in-del | -/C | | | intron-variant, utr-variant-5-prime | SART1 | GRCh38.p7 | 11:65965080 | AGCCTCACGTCTGGG[-/C]CCCCCTTCCAGAGGC | 9092 |
rs34450536 | multinucleotide-polymorphism | AG/GA | | | intron-variant | SART1 | GRCh38.p7 | 11:65963545 | AGAGTGCAGTGGCAC[AG/GA]TCTCAGCTCACTGCA | 9092 |
rs34639848 | in-del | -/A | | | intron-variant | SART1 | GRCh38.p7 | 11:65970073 | ACACACTGTGCAGGC[-/A]AAAAAGTGGAAAGCC | 9092 |
rs34797583 | in-del | -/AAACA | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961206 | AAACAAAACAAAACA[-/AAACA]GGGAACGTGGGAAGG | 9092 |
rs34922998 | snp | C/G | 0.0298439 | 0.118454 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966444 | GCGGCACGGCTGATG[C/G]CCTGCGGGAGCGGGA | 9092 |
rs34924971 | in-del | -/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65970704 | TGGAGAGCAGATACA[-/C]CCTGGGAGAAGAGCA | 9092 |
rs35036096 | snp | G/T | 0.197531 | 0.244432 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967544 | CCTCAGCCCCTGCCG[G/T]CGGACGACACCCGAG | 9092 |
rs35056344 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967698 | GGTGGAGCTCCACCG[-/C]CCGGGGTCCCCGCAG | 9092 |
rs35186856 | snp | C/T | 0.00199787 | 0.0315427 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978819 | GATGAGCTCCAGCGA[C/T]ACGCCCCTGGGCACC | 9092 |
rs35216160 | in-del | -/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65967967 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 9092 |
rs35239693 | in-del | -/T | 0.498734 | 0.0251279 | intron-variant | SART1 | GRCh38.p7 | 11:65970625 | CCGATTGTTCTGGTG[-/T]TTTTCCAGTGAAGAG | 9092 |
rs35262635 | in-del | -/C | | | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980393 | TCACCTTGGCTGCTT[-/C]CCTTGGCTTCCTCAG | 9092 |
rs35322123 | in-del | -/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65976330 | GAGGACCCTTAGGTT[-/C]CCTGGGTCTCAATGG | 9092 |
rs35807911 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967569 | CCGAGTGGAGAACAT[-/G]GGACATCAGTGATGA | 9092 |
rs35831021 | in-del | -/A | 0.0554779 | 0.157039 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65980111 | GTCAGACCCTGTCTC[-/A]AAAAAAATAAAAAAA | 9092 |
rs35842560 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977881 | GATGAGACGGGCCGG[-/A]AAACTCACACCCAAG | 9092 |
rs35869960 | in-del | -/G | | | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979433 | TGGGGATTGGGCTTT[-/G]GGGTAGGGCACAGGT | 9092 |
rs36014546 | in-del | -/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65978197 | CACTGGCTTTCCTGG[-/C]CCCGCAGGGCCATTC | 9092 |
rs55704213 | snp | A/C | 0.466721 | 0.124627 | intron-variant | SART1 | GRCh38.p7 | 11:65962531 | GAATCGTGTAGGGCG[A/C]ATGGTAGAGAAATGA | 9092 |
rs55723810 | snp | A/G | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65971102 | GAGCTGAGGAGGGGG[A/G]TGGTGGGATTCATGA | 9092 |
rs55928757 | snp | A/G | 0.485118 | 0.0849685 | intron-variant | SART1 | GRCh38.p7 | 11:65974299 | GAATCACTTGAACCC[A/G]AGAGGTGGAGGTTGC | 9092 |
rs55992629 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65971095 | GATTCATGAGCTGAG[A/G]AGGGGGATGGTGGGA | 9092 |
rs55994535 | in-del | -/AA | | | intron-variant | SART1 | GRCh38.p7 | 11:65974391 | AAAAAAAAAAAAAAA[-/AA]CCATATCAGCCGGGT | 9092 |
rs56154109 | snp | C/T | 0.495056 | 0.049474 | intron-variant | SART1 | GRCh38.p7 | 11:65975367 | CTCGGCCTCCCAAAG[C/T]GCTAGGATTATAGAT | 9092 |
rs56159637 | in-del | -/C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65975431 | TTTTTTTTTTTTTTT[-/C/T]CGAGACGGGGTTTCA | 9092 |
rs56239996 | snp | A/T | 0.466721 | 0.124627 | intron-variant | SART1 | GRCh38.p7 | 11:65962532 | AATCGTGTAGGGCGC[A/T]TGGTAGAGAAATGAG | 9092 |
rs56365031 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65971204 | GGGATGGTGGGATTC[A/G]TGAGCTG | 9092 |
rs56663613 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SART1 | GRCh38.p7 | 11:65966972 | CAGCTGGCGCGGTAG[A/G]CGTCTTCCTCAGTGG | 9092 |
rs57209570 | in-del | -/CTG | | | intron-variant | SART1 | GRCh38.p7 | 11:65970881 | GGGATTCATGAGCTG[-/CTG]AGGAGGGGGATGGTG | 9092 |
rs57343901 | in-del | -/ACAAAA | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961209 | TCTCAAGGGAAAAAA[-/ACAAAA]CAAAACAAAACAAAA | 9092 |
rs57968007 | snp | C/T | 0.186421 | 0.24178 | intron-variant | SART1 | GRCh38.p7 | 11:65962209 | AAACCCCCAAGCTGT[C/T]TACCAGCTCTATTAA | 9092 |
rs58609655 | snp | G/T | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65970874 | GGATGGTGGGATTCA[G/T]GAGCTGCTGAGGAGG | 9092 |
rs58905199 | snp | C/T | 0.186421 | 0.24178 | intron-variant | SART1 | GRCh38.p7 | 11:65962206 | AGGAAACCCCCAAGC[C/T]GTTTACCAGCTCTAT | 9092 |
rs59143048 | in-del | -/CTG | | | intron-variant | SART1 | GRCh38.p7 | 11:65970851 | GGGATTCATGAGCTG[-/CTG]AGGAGGGGGATGGTG | 9092 |
rs59156593 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SART1 | GRCh38.p7 | 11:65966966 | GGTAGACAGCTGGCG[C/T]GGTAGGCGTCTTCCT | 9092 |
rs59415516 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SART1 | GRCh38.p7 | 11:65962654 | ATGGATGTGAGTTGA[A/G]GAGTGAGTTGCTCAG | 9092 |
rs59473144 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | SART1 | GRCh38.p7 | 11:65962507 | GGCAAGAAAAACCTG[G/T]TATTGGACGAATCGT | 9092 |
rs60109456 | snp | A/G | 0.421368 | 0.182025 | intron-variant | SART1 | GRCh38.p7 | 11:65974812 | AGGCCAAGGCAGGCA[A/G]ATCACGAGGTCAGGA | 9092 |
rs61629316 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65962218 | AGCTGTTTACCAGCT[A/C]TATTAAATAGTCTTT | 9092 |
rs61740577 | snp | A/G | 0.0199959 | 0.0979727 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967543 | GCCTCAGCCCCTGCC[A/G]TCGGACGACACCCGA | 9092 |
rs61746328 | snp | C/G/T | 0.000434387 | 0.0147313 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65964120 | CTCCTCACTCAGCAT[C/G/T]GAGGAGACTAAGTGA | 9092 |
rs61893935 | snp | G/T | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65970906 | GGATGGTGGGATTCA[G/T]GAGCTGAGGAGGGGG | 9092 |
rs61893936 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SART1 | GRCh38.p7 | 11:65971582 | TTCATGAGCTGCTGA[A/G]GAGGGGGATGGTGGG | 9092 |
rs61893937 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | SART1 | GRCh38.p7 | 11:65972901 | ACGTGGCCGGGCGCG[A/G]TGGCTCACGCCTGTA | 9092 |
rs61893938 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SART1 | GRCh38.p7 | 11:65974029 | GCTGCCCCAGCCCCA[A/G]GGAGAGGGACATGGG | 9092 |
rs61893939 | snp | G/T | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65975122 | TTTTTTTTTTTTTTG[G/T]AGACAGGGTATTGCT | 9092 |
rs67232706 | snp | G/T | 0.186421 | 0.24178 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960136 | CCCCTTCTCTGCTCC[G/T]GAGGAGTGGGGACAT | 9092 |
rs67530871 | snp | A/G | 0.141573 | 0.225263 | upstream-variant-2KB, synonymous-codon | SART1, TSGA10IP | GRCh38.p7 | 11:65959868 | TCCTCAGAGGCCCCC[A/G]AGGACAGAACCCACC | 9092 |
rs71455795 | snp | A/G | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65969858 | CTCCTGAGTAGCTGG[A/G]ACTACAGGTGCATGC | 9092 |
rs71455796 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SART1 | GRCh38.p7 | 11:65970329 | TTTTCCAGTTATCCC[A/C]CAAAATGTCTTTTTA | 9092 |
rs71455797 | snp | G/T | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65971484 | GGGTGGTGGGATTCA[G/T]GAGCTGCTGAGGAGG | 9092 |
rs71462355 | snp | G/T | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65971266 | GGATGGTGGGATTCA[G/T]GAGCTGAGGAGGGGG | 9092 |
rs71462356 | snp | C/G | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65971424 | GGTGGGATTCATGAG[C/G]TGCTGAGGAGGGGGG | 9092 |
rs72928814 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SART1 | GRCh38.p7 | 11:65965537 | CCAGAGAGGTGAGAC[A/G]GGGCTTGGAGAAGGG | 9092 |
rs72928826 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | SART1 | GRCh38.p7 | 11:65970728 | AAGAGCAGGCCTGCC[A/C]GTGGCAGTGTGGATG | 9092 |
rs72928828 | snp | A/G | 0.184203 | 0.241186 | intron-variant | SART1 | GRCh38.p7 | 11:65971887 | GTCAATGAGCTAGAA[A/G]GAAAGGCTGGAGAGA | 9092 |
rs72928830 | snp | C/G | 0.184521 | 0.241273 | intron-variant | SART1 | GRCh38.p7 | 11:65971910 | TGGAGAGAACAGAAA[C/G]GATCCTTGGAATTGA | 9092 |
rs72928831 | snp | C/T | 0.184838 | 0.241358 | intron-variant | SART1 | GRCh38.p7 | 11:65972586 | CAAGACCACCCCCCC[C/T]ACCAACCCCATCTCT | 9092 |
rs72928843 | snp | A/G | 0.128632 | 0.218563 | intron-variant | SART1 | GRCh38.p7 | 11:65976039 | TAGAGTCCTGAAACC[A/G]GAGTTTGTCGGGGGA | 9092 |
rs72928851 | snp | G/T | 0.0221141 | 0.102801 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979331 | GAAACTCATCACCCT[G/T]CTCTCTCCTGGCCTC | 9092 |
rs72928854 | snp | C/G | 0.0225045 | 0.103662 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979347 | CTCTCTCCTGGCCTC[C/G]GGGGCTGCACAGGTC | 9092 |
rs72928860 | snp | C/T | 0.128632 | 0.218563 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980269 | AAAATGCACGGTTGG[C/T]ACTGACACCATTACT | 9092 |
rs73496487 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SART1 | GRCh38.p7 | 11:65974713 | GCATTAGATATACCT[C/T]GTTTTATGTTTACAA | 9092 |
rs74188201 | snp | A/G | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65971012 | CTGCTGAGGAGGGGG[A/G]TGGTGGGATTCAGGA | 9092 |
rs74465357 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65969231 | CTGTGCTGTTATAGG[A/G]AAAACAGCCAAGACA | 9092 |
rs74611402 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | SART1 | GRCh38.p7 | 11:65973520 | CAAGCCTGACAGTAG[C/T]GAGTAGGAGTAAAGG | 9092 |
rs74736604 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | SART1 | GRCh38.p7 | 11:65970523 | GAGTGAAGCCAGCTC[A/G]TGTCATCATTTATTT | 9092 |
rs74743258 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | SART1 | GRCh38.p7 | 11:65968391 | GGCTGAGAAGGTCAT[C/T]GGTGAACAGGATAGC | 9092 |
rs74833309 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SART1 | GRCh38.p7 | 11:65978460 | AGCGTCTGTGCTCTT[C/T]TCCCATCCCCTTCCC | 9092 |
rs74949878 | snp | C/T | 0.0270952 | 0.113196 | intron-variant | SART1 | GRCh38.p7 | 11:65978552 | GGGCACAGGTGGCTC[C/T]GGCCCCACCCAGGGC | 9092 |
rs74994319 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65971177 | GATGGTGGGATTCAG[A/G]AGCTGAGGAGGGGGA | 9092 |
rs75094826 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SART1 | GRCh38.p7 | 11:65968640 | GAGGAGCCAGCCTTG[C/T]GGGGGGTTAGGGGTG | 9092 |
rs75132850 | snp | A/G | 0.0316293 | 0.121714 | upstream-variant-2KB, missense | SART1, TSGA10IP | GRCh38.p7 | 11:65959884 | AGGACAGAACCCACC[A/G]GCAGCCAGCCTGACA | 9092 |
rs75194122 | snp | A/G | 0.00519327 | 0.0506918 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966486 | TCCGGGCCAAGCTGC[A/G]GCTGCAGGCTCAGTC | 9092 |
rs75306341 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | SART1 | GRCh38.p7 | 11:65970160 | TCTTTTCTTTCTCTT[C/T]TTTTTTTCCTGACCA | 9092 |
rs75463996 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960411 | TGTGTGCACTGCGCT[C/T]TTTTTTTTTTTTTTT | 9092 |
rs75665959 | snp | A/G | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65971044 | GTGCTGAGGAGGGGG[A/G]TGGTGGGATTCAGGA | 9092 |
rs75686353 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | SART1 | GRCh38.p7 | 11:65978283 | ACTCAGCTGCCCCCT[A/T]GCTCTCTGGGGTTTG | 9092 |
rs75807038 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | SART1 | GRCh38.p7 | 11:65970444 | GAGACACATTTATGA[C/T]GGAAGAAGAAAAAGA | 9092 |
rs76039799 | snp | A/G | 0.000812018 | 0.0201333 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967710 | ACCGCCGGGGTCCCC[A/G]CAGGTGCTGGAGGAG | 9092 |
rs76576260 | in-del | -/A/AAAAA/AAAAAA | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961203 | ATCCTATCTCAAGGG[-/A/AAAAA/AAAAAA]AAAAAACAAAACAAA | 9092 |
rs76640991 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SART1 | GRCh38.p7 | 11:65966838 | CCCCATCTGGAATGG[C/T]AGTGACAGGAGCCGC | 9092 |
rs76654835 | snp | A/G | 0.0321132 | 0.122578 | upstream-variant-2KB, missense | SART1, TSGA10IP | GRCh38.p7 | 11:65959844 | AATGGGGGTGAGAAT[A/G]GAGCACTCTCCTCAG | 9092 |
rs76705937 | snp | A/G | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65970798 | TGAGCTGCTGAGGGA[A/G]GGGGATGGTGGGATT | 9092 |
rs76720395 | snp | A/G | 0.0869089 | 0.189476 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960371 | ACCACTGGGTGAGGG[A/G]AGGGGTTTCAGGAGA | 9092 |
rs77078616 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961227 | AAACAAAACAAAACA[C/G]GGAACGTGGGAAGGA | 9092 |
rs77493707 | snp | G/T | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65971603 | GGATGGTGGGATTCA[G/T]GAGCTGCTGAGGAGG | 9092 |
rs77575681 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65965510 | CTGACGGCACTGAGG[C/T]GGGGGCCAACCCCAG | 9092 |
rs77806697 | snp | G/T | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65971057 | GGGTGGTGGGATTCA[G/T]GAGCTGAGGAGGGGG | 9092 |
rs78162580 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | SART1 | GRCh38.p7 | 11:65976040 | AGAGTCCTGAAACCG[A/G]AGTTTGTCGGGGGAG | 9092 |
rs78346567 | snp | C/G | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65975940 | GAACCTGCTTTCTTG[C/G]TGAAGCAGGAAGCGA | 9092 |
rs78473730 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65971439 | CTGCTGAGGAGGGGG[A/G]TGGTGGGATTCATGA | 9092 |
rs78664826 | snp | A/C/G | 0.019064 | 0.0957593 | intron-variant | SART1 | GRCh38.p7 | 11:65977932 | CAGGCGGAGGCCCGG[A/C/G]CTGCCACAGGGAGGC | 9092 |
rs78744926 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SART1 | GRCh38.p7 | 11:65976260 | GTGGAGTTAGGCGGC[A/C]GATAGCAGCTGGGCC | 9092 |
rs78889112 | snp | A/G | 0.127254 | 0.217792 | intron-variant | SART1 | GRCh38.p7 | 11:65970663 | AGGTGGTGGTGCAAA[A/G]AGATGGGAGATGCTG | 9092 |
rs79177013 | snp | A/G | 0.0600325 | 0.162519 | intron-variant | SART1 | GRCh38.p7 | 11:65965994 | GGACAAAGGTAATGC[A/G]AGCTGGGTGCCCTGG | 9092 |
rs79180914 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65976225 | GAGCAGAAGAGTGAC[C/T]CCAGTGAAAGAGGTG | 9092 |
rs79370352 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65973418 | ACCAGGAAAATACCC[A/G]GTGAATCCAGTTTCA | 9092 |
rs79453766 | snp | G/T | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65975120 | TTTTTTTTTTTTTTT[G/T]GGAGACAGGGTATTG | 9092 |
rs79619042 | snp | C/T | 0 | 0 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960409 | ATTGTGTGCACTGCG[C/T]TTTTTTTTTTTTTTT | 9092 |
rs79938829 | snp | A/G | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65965225 | AAAGCTGGGGTGAGG[A/G]GTCCTGGCCAGGGCA | 9092 |
rs79995003 | snp | C/G | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65971029 | GGTGGGATTCATGAG[C/G]TGCTGAGGAGGGGGG | 9092 |
rs80294146 | snp | A/C | 0.0460142 | 0.144533 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961168 | CACGCCACTGCACTC[A/C]AGCCTGAGCAACAGA | 9092 |
rs111291053 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65971963 | GTGTCTCACTTTGTC[A/C]CCCAGGCTGGGGTGC | 9092 |
rs111435679 | snp | G/T | 2.01306e-05 | 0.00317253 | splice-donor-variant | SART1 | GRCh38.p7 | 11:65967588 | CATCAGTGATGAGGG[G/T]GAGGGCCCGGCCAGG | 9092 |
rs111521324 | snp | C/T | 0.00185106 | 0.0303662 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966214 | GCGTGGACGACCTGG[C/T]GCAGGCACGGCCTGG | 9092 |
rs111558508 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65971627 | GAGGAGGGGGATGGT[A/G]GGATTCAGGAGCTGA | 9092 |
rs111587926 | snp | A/G | 0.0212928 | 0.100961 | intron-variant | SART1 | GRCh38.p7 | 11:65977922 | GGGCCTTTTGCAGGC[A/G]GAGGCCCGGCCTGCC | 9092 |
rs111668992 | in-del | -/G | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65967949 | TTGTTTTCTGGGTTT[-/G]TTTTTTTTTTTTTTT | 9092 |
rs111719377 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960685 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 9092 |
rs111729833 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | SART1 | GRCh38.p7 | 11:65968980 | GCCCTACCCCACACT[G/T]CTCACCTAGGAAGAA | 9092 |
rs111836354 | snp | A/G | | | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976413 | GTGGAGATTGTGAAG[A/G]AGCTGGAGTCTCGCC | 9092 |
rs111880698 | snp | C/G/T | 0 | 0 | splice-acceptor-variant | SART1 | GRCh38.p7 | 11:65977013 | GCCACGTGTCCCGTA[C/G/T]TTCTCTGCTTCCTCC | 9092 |
rs111899187 | snp | A/G | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65976861 | TCAGCCTCCTCATCC[A/G]GAGTGGGCTCTGCAG | 9092 |
rs111900320 | snp | C/G | 0.00109675 | 0.0233917 | intron-variant | SART1 | GRCh38.p7 | 11:65978937 | GCTCGAGGCTGGTGG[C/G]GTAGGGTGTGGTGGG | 9092 |
rs112013136 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65978692 | GGACGAGGAGGCGGT[C/G]GGTGCCCTTGGGGAT | 9092 |
rs112242340 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | SART1 | GRCh38.p7 | 11:65964387 | TTCCCAGTGTCCTAG[G/T]CTGCCTGGGGCAGAC | 9092 |
rs112397623 | snp | C/G | | | splice-donor-variant | SART1 | GRCh38.p7 | 11:65978690 | CTGGACGAGGAGGCG[C/G]TGGGTGCCCTTGGGG | 9092 |
rs112567853 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SART1 | GRCh38.p7 | 11:65968150 | AGACGGGGTTTCACT[A/G]TGTTGGCCAGGCTGG | 9092 |
rs112569137 | snp | A/T | 0 | 0 | splice-acceptor-variant | SART1 | GRCh38.p7 | 11:65976654 | GGTCTTTTGTGCCCC[A/T]GGACTTTGAACGGGA | 9092 |
rs112820198 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966108 | GAGGACGTGCTGGTG[A/G]ACGTGAACCTGGTGG | 9092 |
rs112895669 | snp | A/G | 0.5 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65974356 | TCCAGCCTGGCCAAC[A/G]GTGAGACTCTGTCTC | 9092 |
rs113017251 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | SART1 | GRCh38.p7 | 11:65970155 | ACAGTTCTTTTCTTT[-/C]TCTTCTTTTTTTCCT | 9092 |
rs113042741 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SART1 | GRCh38.p7 | 11:65974901 | AAAAATTAGCTGGGC[C/G]TGGTGGCGGGCGCCT | 9092 |
rs113070755 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65962111 | GAGGAGGCGGGGCCT[C/G]CGCAGGGGGCGGGTC | 9092 |
rs113296365 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967700 | GTGGAGCTCCACCGC[C/T]GGGGTCCCCGCAGGT | 9092 |
rs113375330 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976499 | CGCCACGTCCGAGTT[C/T]TGCCGCACCTTGGGG | 9092 |
rs113428761 | snp | C/G | 0.001105 | 0.0234793 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967298 | AGGGTGAAGAAAATC[C/G]GCAAGAAGGAGAAGG | 9092 |
rs113451511 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65963279 | GTTAGAAGGAGGGAG[C/T]GATCAGCAGTCCCAC | 9092 |
rs113675122 | snp | A/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65971611 | GGATTCAGGAGCTGC[A/T]GAGGAGGGGGATGGT | 9092 |
rs113710714 | snp | A/G | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961764 | GCGGCAGCCGGGCTC[A/G]GAGTGGACGTGCCAC | 9092 |
rs113713957 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961866 | GTGCCACCGAGCAGC[C/T]GCCGCGGCACCGGGA | 9092 |
rs113764989 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65975763 | GGACTTTGCTGTCTG[A/G]GCTGCAGGGTTGAGG | 9092 |
rs113987587 | snp | G/T | | | splice-donor-variant | SART1 | GRCh38.p7 | 11:65976767 | AAGCAGCAGCAGGAT[G/T]TGAGGGCCGCGCCGC | 9092 |
rs114322131 | snp | C/G | 0.0460142 | 0.144533 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961170 | CGCCACTGCACTCCA[C/G]CCTGAGCAACAGAGT | 9092 |
rs114758666 | snp | A/G | 0.0117307 | 0.0756818 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967746 | GGCGGAGCTGGAGCT[A/G]CAGAAGCAGCTGGAG | 9092 |
rs115004657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65964665 | AGGTTCAGCACTGTT[C/T]AGTGGTCTTACACAT | 9092 |
rs115168680 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SART1 | GRCh38.p7 | 11:65969132 | GGGCTGAACCCGGGA[C/T]GGAGGCCAGGCTTAC | 9092 |
rs115237748 | snp | C/T | 0.00103847 | 0.0227631 | intron-variant | SART1 | GRCh38.p7 | 11:65977550 | GGGAGTCTCACAACC[C/T]CTCCATCCCTAGGGC | 9092 |
rs115743368 | snp | C/T | 0.0154538 | 0.0865337 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980471 | CACAGTCTGTTTCTC[C/T]CAAAAGCCTAGGAGG | 9092 |
rs116126957 | snp | A/G | 0.0162398 | 0.0886349 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979609 | TGACCCAGAAAGATG[A/G]GATTCCTTGGCCTGA | 9092 |
rs116267709 | snp | A/G | 0.00688414 | 0.0582639 | intron-variant | SART1 | GRCh38.p7 | 11:65978985 | GTGCCCGCCTCTGCA[A/G]CCTCACGCCCCTGTT | 9092 |
rs116614074 | snp | A/C/G | 0.00169766 | 0.0290863 | intron-variant | SART1 | GRCh38.p7 | 11:65976633 | GCTGGGGCCTGGGCC[A/C/G]ACCCTGGTCTTTTGT | 9092 |
rs117259742 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SART1 | GRCh38.p7 | 11:65967153 | GGGAAGCGCTCAGGA[C/T]GCTGGCTAGCACAGA | 9092 |
rs117293758 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SART1 | GRCh38.p7 | 11:65975632 | GCTGGTCTCGATCTC[C/T]GGAACTCAAGCAGTC | 9092 |
rs117835634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65962451 | CAGATTCTCAATAAA[C/T]ATGTTGAATGAGTGA | 9092 |
rs137867012 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65967949 | TTGTTTTCTGGGTTT[G/T]TTTTTTTTTTTTTTT | 9092 |
rs137940965 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SART1 | GRCh38.p7 | 11:65965629 | TTTTTGCACTCCGCT[C/T]GGTAGAGCCCTGAGT | 9092 |
rs137990779 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SART1 | GRCh38.p7 | 11:65972943 | TTGGGAGGCCAAGGC[A/G]GGCGGATCACGAGGT | 9092 |
rs138011111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65962672 | GTGAGTTGCTCAGAT[C/G]CGTATTTTGTAAACA | 9092 |
rs138059558 | snp | A/G | 1.65941e-05 | 0.00288041 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977582 | GCTGGAGACCACAGT[A/G]CAGAAGGTGGCCCGG | 9092 |
rs138334211 | snp | C/T | 0.0185938 | 0.0946107 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979274 | CTGTCGGTCACACCT[C/T]TGCAGGGCCGGCTCT | 9092 |
rs138417683 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65968955 | CATCATTCCAGAGGC[C/T]ACACTTTTAGCCCTA | 9092 |
rs138652501 | snp | C/T | 5.23839e-05 | 0.00511754 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977848 | CGGCTACAAACCCGA[C/T]GTTAAGATCGAATAC | 9092 |
rs138794561 | snp | C/T | 1.66402e-05 | 0.00288441 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966401 | GAGCTTGAAGGGGAG[C/T]GGCCACATTCCTTCC | 9092 |
rs138981987 | snp | C/T | 0.0375453 | 0.131771 | intron-variant | SART1 | GRCh38.p7 | 11:65978742 | CCGGGGCAGGGGTGG[C/T]TGGTGTGTGGGGCCT | 9092 |
rs139015845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973486 | ACCTGCCACCTGCCA[A/G]CAATTCCGCAGAAAG | 9092 |
rs139095381 | snp | C/T | 0.000335777 | 0.0129528 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976425 | AAGAAGCTGGAGTCT[C/T]GCCAGCGGGGCTGGG | 9092 |
rs139408234 | snp | C/T | 0.000112581 | 0.00750185 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966532 | GCCCCGGCTGGCCTC[C/T]GAATACCTCACGCCT | 9092 |
rs139418255 | snp | C/T | 3.52727e-05 | 0.00419942 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965114 | CACCAAGGAGGAGCC[C/T]GTGACAGCTGATGTC | 9092 |
rs139631513 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SART1 | GRCh38.p7 | 11:65970470 | AAAGATCTCGGCAGG[C/T]GGTGCTGGGGCCTAG | 9092 |
rs139806126 | snp | A/T | 0.000203231 | 0.0100784 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965387 | CTGGCTGGACGACAC[A/T]GCAGCCTGGATCGAG | 9092 |
rs139839037 | snp | C/T | 1.69261e-05 | 0.00290908 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967525 | GGAGGAGAAGGAGCC[C/T]GTGCCTCAGCCCCTG | 9092 |
rs140009945 | snp | A/G | 0.000336525 | 0.0129672 | intron-variant | SART1 | GRCh38.p7 | 11:65967235 | TGTGGCCCCCGCTCC[A/G]TGTCTCGCCCCTCTT | 9092 |
rs140132582 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978874 | AAGGCTCAGAAGACC[C/G]CCTACATCGTGCTCA | 9092 |
rs140173581 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SART1 | GRCh38.p7 | 11:65972909 | GGGCGCGATGGCTCA[C/T]GCCTGTAATCCCAGC | 9092 |
rs140187496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65969995 | CCAAAGTGCTGGAAT[C/T]AGAGGCATGAACCAC | 9092 |
rs140383962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65968641 | AGGAGCCAGCCTTGC[A/G]GGGGGTTAGGGGTGG | 9092 |
rs140704257 | snp | C/G | 0.00452108 | 0.0473297 | intron-variant | SART1 | GRCh38.p7 | 11:65978987 | GCCCGCCTCTGCAGC[C/G]TCACGCCCCTGTTCT | 9092 |
rs140812562 | snp | C/T | 0.00472348 | 0.0483677 | intron-variant | SART1 | GRCh38.p7 | 11:65964615 | GGGAAAGAGGCCATC[C/T]GAAGGGGTCTTTGAA | 9092 |
rs140946620 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65963127 | CTGTGACATGAGAAG[A/T]GGGGGTCAGGACTAG | 9092 |
rs140955513 | snp | A/G/T | 0.0185938 | 0.0946107 | intron-variant | SART1 | GRCh38.p7 | 11:65978417 | CCAAGCTGGTCTCCC[A/G/T]GCCTCTGCTGGGGCC | 9092 |
rs141130425 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961601 | AGACGGCGCGAATGT[A/G]CAGTCGAGCGCTGAT | 9092 |
rs141256442 | snp | C/T | 9.15692e-05 | 0.00676581 | missense, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965095 | CCCCCCTTCCAGAGG[C/T]GGGCACCAAGGAGGA | 9092 |
rs141291031 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SART1 | GRCh38.p7 | 11:65963885 | GCACAGAAGAGGCAG[A/G]GCTCTGAGACTGGAC | 9092 |
rs141299262 | snp | C/T | 0.0126979 | 0.078662 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960853 | AGCTCCTAAACAATC[C/T]TAACAGTTCACGGGG | 9092 |
rs141499780 | snp | A/G | 0.000584166 | 0.0170804 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966215 | CGTGGACGACCTGGC[A/G]CAGGCACGGCCTGGG | 9092 |
rs141735982 | snp | C/T | 0.00116837 | 0.0241417 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976484 | GGCCATCGTGTTCAA[C/T]GCCACGTCCGAGTTC | 9092 |
rs141881804 | snp | C/G | | | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966186 | GACTACCTGCCCTAT[C/G]CCGAGGACGAGAGCG | 9092 |
rs141911207 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65970143 | ATAAACATTGTTACA[A/G]TTCTTTTCTTTCTCT | 9092 |
rs141923813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968776 | AGAGTGAGGGGTGGC[A/G]TGAGCTGAGATGGAG | 9092 |
rs142276907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972566 | ACCAGCCTGGGGCAA[C/T]ACAGCAAGACCACCC | 9092 |
rs142289846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65973795 | GAAACTGATGAGCTA[C/T]AGCCGTGTGCATCAG | 9092 |
rs142409678 | snp | A/G | 1.67287e-05 | 0.00289207 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966111 | GACGTGCTGGTGAAC[A/G]TGAACCTGGTGGATA | 9092 |
rs142477091 | in-del | -/CA | | | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980456 | AGGACTTGGGGCAGT[-/CA]CAGTCTGTTTCTCTC | 9092 |
rs142515674 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SART1 | GRCh38.p7 | 11:65977215 | GTCCCAATGCTGGAG[C/T]CAGCTGTCCGGCCCA | 9092 |
rs142561129 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977591 | CACAGTGCAGAAGGT[A/G]GCCCGGGTGAAGGCC | 9092 |
rs142676468 | snp | A/C/T | 2.32702e-05 | 0.00341094 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966513 | AGTCCCTGAGCACAG[A/C/T]GGGGCCCCGGCTGGC | 9092 |
rs142745462 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SART1 | GRCh38.p7 | 11:65963444 | AGGAGAAGGTAGGAT[A/G]CAGGATGGGAATGCA | 9092 |
rs142979429 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SART1 | GRCh38.p7 | 11:65969755 | TTGAGACGGAGTCTC[G/T]CTCTGTCACCAGGCT | 9092 |
rs143171385 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961294 | AGCTGGGCTGTGGAA[C/T]TGGAGATCTCGGGAA | 9092 |
rs143241490 | snp | C/T | 1.72261e-05 | 0.00293475 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976684 | ATGAGGAGCGCTCAG[C/T]CAACGGTGGCTCCGA | 9092 |
rs143497003 | snp | C/T | 0.00056339 | 0.0167743 | intron-variant | SART1 | GRCh38.p7 | 11:65965828 | TGGTGGCCTTGCTAC[C/T]GGAATCCCGAGGTTG | 9092 |
rs143564275 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SART1 | GRCh38.p7 | 11:65962767 | AGGCCAGGGGAGGGC[C/T]GATGGTGGCCTGCAC | 9092 |
rs143605991 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65971058 | GGTGGTGGGATTCAG[A/G]AGCTGAGGAGGGGGA | 9092 |
rs143607098 | snp | C/T | 0.00617528 | 0.0552223 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967697 | AAGGTGGAGCTCCAC[C/T]GCCGGGGTCCCCGCA | 9092 |
rs143726227 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SART1 | GRCh38.p7 | 11:65963902 | CTCTGAGACTGGACT[C/T]GGGCAGAGGAGCTGC | 9092 |
rs143757952 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65969388 | ATGACTGAAATGAAC[A/T]TAAGGGTTTCTAGCC | 9092 |
rs143988028 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SART1 | GRCh38.p7 | 11:65964843 | GCAGACTGCGCTGTG[C/T]GGGGGTGGGTTTCTT | 9092 |
rs144123570 | snp | C/T | 3.47228e-05 | 0.00416656 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965123 | GGAGCCCGTGACAGC[C/T]GATGTCATCAACCCT | 9092 |
rs144235182 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65980072 | GGGCCCTGATTGAGC[C/T]ACCACACTGCAGCCT | 9092 |
rs144454090 | snp | A/G | 1.96142e-05 | 0.00313157 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977884 | TGAGACGGGCCGGAA[A/G]CTCACACCCAAGGAG | 9092 |
rs144548769 | snp | C/T | 3.85832e-05 | 0.00439205 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966485 | ATCCGGGCCAAGCTG[C/T]GGCTGCAGGCTCAGT | 9092 |
rs144821079 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SART1 | GRCh38.p7 | 11:65963385 | GGGGAGCCTGGAGAG[G/T]TTGGGATCCATGGCC | 9092 |
rs145104842 | snp | A/G | 0.00193094 | 0.031012 | intron-variant | SART1 | GRCh38.p7 | 11:65978592 | CCTCTCATGCCCCGC[A/G]TCCCCAGGCTTTCCG | 9092 |
rs145111989 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65973355 | AACAGGAAAATAGGC[A/G]AAAGATGTAGATAAG | 9092 |
rs145444854 | snp | C/T | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961144 | GTCGAGGCTGCAGTG[C/T]GCTGTGATCACGCCA | 9092 |
rs145544619 | snp | C/T | 6.60589e-05 | 0.00574675 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978891 | CTACATCGTGCTCAG[C/T]GGCAGCGGCAAGAGC | 9092 |
rs145553277 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SART1 | GRCh38.p7 | 11:65970396 | ACCCGCAAAGGAGCC[G/T]TTTCTGACTACCGGA | 9092 |
rs145648559 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SART1 | GRCh38.p7 | 11:65976948 | TGCCTGGCAGGTGGT[A/G]ACCAGTGGGTGGGGC | 9092 |
rs145672074 | snp | A/G | 6.69064e-05 | 0.00578349 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977088 | AGCTGCCCTGCTCCT[A/G]TGTCAGAACAAAGGT | 9092 |
rs145691687 | snp | G/T | 3.64764e-05 | 0.00427046 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976485 | GCCATCGTGTTCAAC[G/T]CCACGTCCGAGTTCT | 9092 |
rs145763267 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65972844 | GTTTCTTCAAGAAAC[C/T]ATGAAGAAAAAAGTG | 9092 |
rs145777558 | snp | A/C | 0.00358779 | 0.0422022 | | | GRCh38.p7 | 11:65968846 | TCGTCGCTGCCCCAG[A/C]GGCACAGTGGGCCGG | 9092 |
rs146043538 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977839 | GGAGAAGGACGGCTA[C/T]AAACCCGACGTTAAG | 9092 |
rs146054065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65967144 | CTCATGTGTGGGAAG[C/T]GCTCAGGACGCTGGC | 9092 |
rs146142946 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | SART1 | GRCh38.p7 | 11:65969846 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGAACT | 9092 |
rs146560628 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SART1 | GRCh38.p7 | 11:65963544 | TAGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG | 9092 |
rs146564888 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960062 | CTTAGCTCTGTCCCC[A/G]CACCCCCTCCCCACC | 9092 |
rs146823521 | snp | C/T | 0.00124554 | 0.0249242 | intron-variant | SART1 | GRCh38.p7 | 11:65964153 | ACTGTCTCCCTTGTT[C/T]CTACTTTGTTTTTCT | 9092 |
rs147016976 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SART1 | GRCh38.p7 | 11:65968651 | CTTGCGGGGGGTTAG[A/G]GGTGGCAGCAGGTGG | 9092 |
rs147105474 | snp | C/T | 0.000649897 | 0.0180146 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966188 | CTACCTGCCCTATGC[C/T]GAGGACGAGAGCGTG | 9092 |
rs147158365 | snp | A/G | 0.00238343 | 0.0344389 | intron-variant | SART1 | GRCh38.p7 | 11:65965829 | GGTGGCCTTGCTACC[A/G]GAATCCCGAGGTTGG | 9092 |
rs147204944 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65976278 | TAGCAGCTGGGCCTG[A/C]ATGGGCTGTGGGCGT | 9092 |
rs147294445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65963057 | AATCCAGAGTTTGGA[C/T]TGGATAAAGCCATTG | 9092 |
rs147353641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65962381 | GAGGTTGACTTTCTC[C/T]ACTCAGCTGCTTGAG | 9092 |
rs147646312 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65968737 | TTAGAGTGCCTGAGG[G/T]CCAGGGAGGCTGGAG | 9092 |
rs147708849 | snp | C/T | 0.000115608 | 0.00760201 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978897 | CGTGCTCAGCGGCAG[C/T]GGCAAGAGCATGAAC | 9092 |
rs147744540 | snp | A/G | 7.26216e-05 | 0.00602541 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976490 | CGTGTTCAACGCCAC[A/G]TCCGAGTTCTGCCGC | 9092 |
rs147917964 | snp | A/G | 0.00187047 | 0.0305243 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966133 | TGGTGGATAAGGAGC[A/G]GGCAGAGAAAAATGT | 9092 |
rs147934496 | snp | C/T | 0.000566795 | 0.0168249 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976481 | GGGGGCCATCGTGTT[C/T]AACGCCACGTCCGAG | 9092 |
rs148093839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65974346 | GCCACTTCACTCCAG[C/T]CTGGCCAACAGTGAG | 9092 |
rs148277686 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961515 | TGGGATCCCACCTCC[A/G]GGTTAATTCCGCTTC | 9092 |
rs148286104 | snp | C/G/T | 0.0001773 | 0.00941401 | missense, synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976745 | CACGGTGAACCTGGA[C/G/T]GAGGAGAAGCAGCAG | 9092 |
rs148394152 | snp | A/G | 0.00192508 | 0.030965 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978617 | TTTCCGGCAGCTGTC[A/G]CACCGCTTCCATGGC | 9092 |
rs148535660 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65967988 | AGAGTTTCGCTCTTT[C/T]GCCCAGGCTGGAATG | 9092 |
rs148588114 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65963389 | AGCCTGGAGAGGTTG[G/T]GATCCATGGCCCAGG | 9092 |
rs148815205 | snp | C/T | 0.00198764 | 0.0314622 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977061 | GGAACCGATCGTGAA[C/T]AGGGGGCTGGCAGCT | 9092 |
rs149149066 | snp | A/G/T | 3.44015e-05 | 0.00414724 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976678 | AACGGGATGAGGAGC[A/G/T]CTCAGCCAACGGTGG | 9092 |
rs149203052 | snp | A/G/T | 3.345e-05 | 0.00408951 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966109 | AGGACGTGCTGGTGA[A/G/T]CGTGAACCTGGTGGA | 9092 |
rs149311843 | snp | C/T | 0.000106775 | 0.00730589 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977857 | ACCCGACGTTAAGAT[C/T]GAATACGTGGATGAG | 9092 |
rs149365770 | snp | A/C | 1.68332e-05 | 0.00290109 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966434 | TTGGAGCAGGGCGGC[A/C]CGGCTGATGGCCTGC | 9092 |
rs149551290 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65979787 | ATTTTAAAAATGAAA[C/T]CAAAAAATAAATTGA | 9092 |
rs149700997 | snp | A/G | 4.97797e-05 | 0.00498873 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965765 | GTGGAGGAGGAGTTC[A/G]GGCAGAGGCGGCAGG | 9092 |
rs149754263 | snp | C/T | 0.000690203 | 0.0185641 | intron-variant | SART1 | GRCh38.p7 | 11:65976601 | CCGCCCTCTGCTTCC[C/T]TCGGCTGGGTGGGCT | 9092 |
rs149897859 | snp | A/C/T | 0.000112967 | 0.00751469 | synonymous-codon, missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976461 | GATGAGGATCCCGAG[A/C/T]GGAAGGGGGCCATCG | 9092 |
rs150018115 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SART1 | GRCh38.p7 | 11:65970368 | TTGTAAGCAGCATCC[A/G]ATCAAGTTTCCCACC | 9092 |
rs150143836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65964646 | GAAGGTGGGGTTAGA[A/G]GGCAGGTTCAGCACT | 9092 |
rs150231146 | snp | C/T | 6.64474e-05 | 0.00576362 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966359 | TTGCAGCAAAAACCT[C/T]GCTCTATCCTGTCCA | 9092 |
rs150316451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65972936 | CAGCACTTTGGGAGG[C/T]CAAGGCGGGCGGATC | 9092 |
rs150474893 | snp | A/G/T | 0.0021702 | 0.0328697 | intron-variant | SART1 | GRCh38.p7 | 11:65978992 | CCTCTGCAGCCTCAC[A/G/T]CCCCTGTTCTTCTCT | 9092 |
rs150808292 | snp | A/G | 0.000159536 | 0.00892988 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965111 | GGGCACCAAGGAGGA[A/G]CCCGTGACAGCTGAT | 9092 |
rs150837563 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65970266 | CGCATAGCCACACTG[C/T]CCTAACAAGCCCATA | 9092 |
rs150945862 | snp | C/T | 0.000399281 | 0.0141238 | stop-gained, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977813 | TACCGAGGCTTCACA[C/T]AGGACTTCAAGGAGA | 9092 |
rs151206894 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65968547 | CCAAGATAACGTGCC[A/G]GGGGTTGGGATCTTA | 9092 |
rs180776533 | snp | A/G | 0.00597247 | 0.0543191 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980560 | GGATCACTTGAGGCC[A/G]GGAGTTCAAGACCAG | 9092 |
rs180785159 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961297 | TGGGCTGTGGAATTG[A/G]AGATCTCGGGAAAAC | 9092 |
rs180877613 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65971056 | GGGGTGGTGGGATTC[A/G]GGAGCTGAGGAGGGG | 9092 |
rs180938697 | snp | C/G/T | 0.00403372 | 0.0447291 | intron-variant | SART1 | GRCh38.p7 | 11:65966023 | GGGTGGGGGCACAGC[C/G/T]TCTGCTGAGTTGCGG | 9092 |
rs180956538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65975065 | AAAAATTAAAAGACA[A/G]ACAAACAAACAAATG | 9092 |
rs181041637 | snp | C/T | 0.00511725 | 0.0503233 | intron-variant | SART1 | GRCh38.p7 | 11:65967413 | GGTGGTGGGGCGAGA[C/T]GGCTGGGCTGGGGTG | 9092 |
rs181125809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65974430 | TCACACCTATAGTCC[C/T]AGCACTTTGGGAGGC | 9092 |
rs181590526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65970252 | TCAGGGCCTTCTCCC[A/G]CATAGCCACACTGCC | 9092 |
rs181767417 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65962453 | GATTCTCAATAAATA[C/T]GTTGAATGAGTGAAT | 9092 |
rs181793391 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961446 | CAGGGAGGCCGGGGA[A/G]GAACTTAAAGCCACG | 9092 |
rs181880927 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65966923 | GGTGTGCGTGGATTC[C/T]GTCCACAGGGTGACT | 9092 |
rs181957387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969898 | CAGCTGATTTTTGTA[C/T]TTTTTAGAAGAAACA | 9092 |
rs182295892 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979541 | GTATTTGGTGCACGC[A/G]GTATGGGGAGGGCTG | 9092 |
rs182710991 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65967891 | CACCTGTGTCATAGG[C/T]GACAGCCACATTCCT | 9092 |
rs182868363 | snp | C/T | 9.91998e-05 | 0.00704202 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978816 | GAAGATGAGCTCCAG[C/T]GACACGCCCCTGGGC | 9092 |
rs183146633 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SART1 | GRCh38.p7 | 11:65972905 | GGCCGGGCGCGATGG[C/T]TCACGCCTGTAATCC | 9092 |
rs183150285 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65964710 | AGGCATGAGGTCCCT[C/G/T]CTTGCTGGTATAATG | 9092 |
rs183617338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968575 | TTAGATGGGAGAGTG[C/T]AGGGAAGACCTTTCC | 9092 |
rs183642250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65971781 | CTGAGTCTAAACTGG[C/G]TAATGAGGGACATAA | 9092 |
rs183872120 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960429 | TTTTTTTTTTTTTAA[C/G]ACAGAGTCTCGCTCT | 9092 |
rs184041967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969053 | TTCTGATACTACTGG[A/G]AGGCAAAGTGGGGAC | 9092 |
rs184201286 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65965522 | AGGCGGGGGCCAACC[A/C]CAGAGAGGTGAGACG | 9092 |
rs184498165 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SART1 | GRCh38.p7 | 11:65974159 | CAAGATCAGGAGATT[A/G]AGACCATCCTGGCTA | 9092 |
rs184545172 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65969567 | GGATCCTCCTGCCTC[A/G]GGCTCTCAAGTAGCT | 9092 |
rs184598648 | snp | C/T | | | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980316 | TGCGGGGCTGAGTCT[C/T]TGGGTGCCCTTCCTT | 9092 |
rs184739906 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979708 | GCCACCTTGGGTGCC[C/T]AGGATACTGGTGCCT | 9092 |
rs184743948 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960061 | GCTTAGCTCTGTCCC[C/T]GCACCCCCTCCCCAC | 9092 |
rs184748936 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960728 | GGGTTTTAAGTCCCA[A/G]TAGTTTTAAGTTAGG | 9092 |
rs185279706 | snp | A/G | 5.34736e-05 | 0.00517049 | intron-variant | SART1 | GRCh38.p7 | 11:65965246 | GGCCAGGGCAGGCAA[A/G]GGAAGGGCTGGGGAG | 9092 |
rs185411829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970346 | AAAATGTCTTTTTAG[A/T]TTTTTGTTGTAAGCA | 9092 |
rs185422016 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65973760 | GGAGCATCCAGCTCA[C/T]GGGCTGTGATTCCAT | 9092 |
rs185492007 | snp | A/T | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961405 | CGTGAGGTAGTGAAC[A/T]CCCCGTTGCCGGTGA | 9092 |
rs185539698 | snp | A/C/G | 3.3465e-05 | 0.0040904 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966099 | CAGGAGGAGGAGGAC[A/C/G]TGCTGGTGAACGTGA | 9092 |
rs185565535 | snp | C/T | 0.000648121 | 0.01799 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967542 | TGCCTCAGCCCCTGC[C/T]GTCGGACGACACCCG | 9092 |
rs185708409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65970215 | CTGCATCCTTAACGA[C/T]TTCAGTAGGCATCTG | 9092 |
rs185941895 | snp | A/G | 1.65512e-05 | 0.00287669 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977052 | CCTGGACGAGGAACC[A/G]ATCGTGAATAGGGGG | 9092 |
rs186382362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65975641 | GATCTCCGGAACTCA[A/G]GCAGTCCACCCGCCT | 9092 |
rs186432084 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65963903 | TCTGAGACTGGACTC[A/G]GGCAGAGGAGCTGCT | 9092 |
rs186497808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65972726 | CAGCTATGATAGACT[A/G]TAGCTGACTATATCA | 9092 |
rs186512493 | snp | A/G/T | 0.000165623 | 0.00909882 | intron-variant | SART1 | GRCh38.p7 | 11:65964598 | CTGAGGATAGGGTTT[A/G/T]GGGGAAAGAGGCCAT | 9092 |
rs186565396 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65974761 | GTGTTCCTGGCCAGG[C/T]GCGGTGGCTCACGTC | 9092 |
rs186949347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65966973 | AGCTGGCGCGGTAGG[C/T]GTCTTCCTCAGTGGG | 9092 |
rs187173913 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65972946 | GGAGGCCAAGGCGGG[A/C]GGATCACGAGGTCAG | 9092 |
rs187186669 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961759 | GCTCGGCGGCAGCCG[A/G]GCTCGGAGTGGACGT | 9092 |
rs187226680 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65969188 | TTGAGGTTTAAGGGC[A/G]TATGGTCTCTGTTAG | 9092 |
rs187449112 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | SART1 | GRCh38.p7 | 11:65973148 | CACTGCACTCCAGCC[A/T]GGGTGACAGAGCAAG | 9092 |
rs187750348 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979583 | TCCTGGGAGACTTGT[C/T]CCGTGTACAGTGACC | 9092 |
rs188094916 | snp | A/G | 0.00150389 | 0.0273803 | intron-variant | SART1 | GRCh38.p7 | 11:65965679 | TGGCCTGAAGTCCTA[A/G]GTCACCCCTCCCTGT | 9092 |
rs188208800 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65968806 | GAGGTAGGGGGCCAA[C/G]GCAGGGGGAGCCTTG | 9092 |
rs188245267 | snp | C/T | 0.000727431 | 0.0190575 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965381 | TGACCCCTGGCTGGA[C/T]GACACTGCAGCCTGG | 9092 |
rs188326606 | snp | C/T | 0.0119091 | 0.0762411 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979515 | GTGAAACTCCCAGGG[C/T]TGGGCTGGGAGTATT | 9092 |
rs188658887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970471 | AAGATCTCGGCAGGC[A/G]GTGCTGGGGCCTAGA | 9092 |
rs188752597 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65979986 | GGCGTGGTGGTGAGC[A/G]CCTGTAGTCCCAGCT | 9092 |
rs188784068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65978407 | CATCCACTAGCCAAG[C/G]TGGTCTCCCGGCCTC | 9092 |
rs188830907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970217 | GCATCCTTAACGACT[C/T]CAGTAGGCATCTGGC | 9092 |
rs188839960 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SART1 | GRCh38.p7 | 11:65964720 | TCCCTCCTTGCTGGT[A/G]TAATGGGGATCTGGG | 9092 |
rs188965763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968369 | TGTGAGTAGTGCATT[A/G]TTCTTGGGCTGAGAA | 9092 |
rs189426635 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961438 | TGCAAGCGCAGGGAG[A/G]CCGGGGAGGAACTTA | 9092 |
rs189465452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65973779 | CTGTGATTCCATAGT[A/G]GAAACTGATGAGCTA | 9092 |
rs189580211 | snp | C/T | 0.000222944 | 0.0105557 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967549 | GCCCCTGCCGTCGGA[C/T]GACACCCGAGTGGAG | 9092 |
rs189728196 | snp | A/C | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961075 | GTGGTAGCGTACTCT[A/C]GTAGTCCCAGCTACT | 9092 |
rs189728908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65964691 | CACATGCATATTTGC[C/T]GGAAGGCATGAGGTC | 9092 |
rs189973843 | snp | G/T | 0.0103295 | 0.0711199 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980463 | GGGGCAGTCACAGTC[G/T]GTTTCTCTCAAAAGC | 9092 |
rs190061310 | snp | A/G | 0.0158469 | 0.0875917 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960591 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTTAC | 9092 |
rs190494963 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SART1 | GRCh38.p7 | 11:65972897 | GAGAACGTGGCCGGG[C/T]GCGATGGCTCACGCC | 9092 |
rs190508463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65966727 | CAGGTGTGGATGGGT[C/G]AGGGCTGCTGAGCCA | 9092 |
rs190544110 | snp | A/G | 3.31225e-05 | 0.00406941 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967269 | TTAAGGTGACCTTTA[A/G]AAAGACCAAGCGGAG | 9092 |
rs190605797 | snp | A/G | 0.00159808 | 0.0282221 | intron-variant | SART1 | GRCh38.p7 | 11:65969662 | TCAAACGATCCTCTC[A/G]CCTCCACCTCCCAAA | 9092 |
rs191063669 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SART1 | GRCh38.p7 | 11:65971678 | ATGCCCTGAAGCAGT[A/G]GATGGTGGGATTGAG | 9092 |
rs191135306 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SART1 | GRCh38.p7 | 11:65976280 | GCAGCTGGGCCTGCA[G/T]GGGCTGTGGGCGTGG | 9092 |
rs191355920 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SART1 | GRCh38.p7 | 11:65969323 | GGGACATAGTTTGCC[C/T]GGCTAAAAAGGAACA | 9092 |
rs191381809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65964379 | CAGGGCCCTTCCCAG[G/T]GTCCTAGGCTGCCTG | 9092 |
rs191711866 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SART1 | GRCh38.p7 | 11:65962396 | CACTCAGCTGCTTGA[A/G]GACAGAGGGCTTCTG | 9092 |
rs191894984 | snp | C/T | 0.000279551 | 0.0118194 | intron-variant | SART1 | GRCh38.p7 | 11:65978589 | TCTCCTCTCATGCCC[C/T]GCGTCCCCAGGCTTT | 9092 |
rs191909806 | snp | A/G/T | 0.000310135 | 0.0124493 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965417 | GAGGAGCCGGCAGCT[A/G/T]CAGAAGGAGAAGGAC | 9092 |
rs192006699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65974091 | TCAGCCGCTGGGTGC[A/G]GTGGCTCACACCTGT | 9092 |
rs192121846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968393 | CTGAGAAGGTCATTG[A/G]TGAACAGGATAGCCA | 9092 |
rs192159537 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SART1 | GRCh38.p7 | 11:65968860 | GAGGCACAGTGGGCC[A/G]GGCACTGCTCACATG | 9092 |
rs192255821 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979540 | AGTATTTGGTGCACG[C/T]GGTATGGGGAGGGCT | 9092 |
rs192658387 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979614 | CAGAAAGATGAGATT[C/T]CTTGGCCTGAACTCT | 9092 |
rs192760334 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973463 | AAGGTGAACCAAAAC[A/C/G]GTGAGGCACCTGCCA | 9092 |
rs192789186 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65973042 | AACCAGACGTGGTGG[C/T]GGGCACCTGTAGTCC | 9092 |
rs192946346 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960628 | GGCCAGGATGGTCTC[A/G]ATCTCTTGACCTCGT | 9092 |
rs193076697 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SART1 | GRCh38.p7 | 11:65964740 | GGGGATCTGGGGCTC[C/T]GCCTGCTCTCTGAGT | 9092 |
rs193173936 | snp | C/T | 0.00874735 | 0.0655527 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980220 | ATGCTGTCGCTTCTG[C/T]ACGGCTAGAGCTGCG | 9092 |
rs199576447 | snp | A/G | 0.000168079 | 0.00916575 | intron-variant | SART1 | GRCh38.p7 | 11:65965698 | ACCCCTCCCTGTCCC[A/G]TAGGCCAAGTTACTG | 9092 |
rs199590563 | snp | A/G | 3.3222e-05 | 0.00407553 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966374 | CGCTCTATCCTGTCC[A/G]AGTATGACGAAGAGC | 9092 |
rs199692927 | snp | G/T | 0.000681759 | 0.0184503 | intron-variant | SART1 | GRCh38.p7 | 11:65967456 | GTGCTCACCAGAGAG[G/T]CCTCCTTCCCTCAGA | 9092 |
rs199739878 | snp | A/G/T | 4.98031e-05 | 0.00498994 | intron-variant | SART1 | GRCh38.p7 | 11:65965797 | GAGGCTGCAGCAGGG[A/G/T]TGGTACAGGGGACAC | 9092 |
rs199764575 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979168 | GTCTGGCTCCTGCTA[G/T]GTGAGACCTGGCCAT | 9092 |
rs199843654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65976789 | CCGCGCCGCTGGGGG[G/T]TGGGCGTTTGGGGGT | 9092 |
rs199929714 | in-del | -/GCT | | | intron-variant | SART1 | GRCh38.p7 | 11:65970937 | TGGTGGGATTCATGA[-/GCT]GCTGAGGAGGGGGAT | 9092 |
rs199970730 | in-del | -/GGAGC | | | intron-variant | SART1 | GRCh38.p7 | 11:65971635 | GGATGGTGGGATTCA[-/GGAGC]TGAGGAGGGGGATGG | 9092 |
rs200075642 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967303 | GAAGAAAATCCGCAA[C/G]AAGGAGAAGGAGGTA | 9092 |
rs200211612 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967574 | GTGGAGAACATGGAC[A/G]TCAGTGATGAGGGTG | 9092 |
rs200247501 | snp | C/G | 0.0335 | 0.125011 | missense, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65962042 | CGCAGCCAGGCAGAG[C/G]CCTCCGAGCGGCGCG | 9092 |
rs200286107 | snp | C/T | 0.000165098 | 0.00908415 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967380 | ATGGGGACTTTGGTT[C/T]CAGGTGGGCTTGGAC | 9092 |
rs200289737 | snp | C/T | 5.01132e-05 | 0.0050054 | splice-donor-variant | SART1 | GRCh38.p7 | 11:65966220 | ACGACCTGGCGCAGG[C/T]ACGGCCTGGGCAGGC | 9092 |
rs200375835 | snp | A/G | 8.35541e-05 | 0.00646297 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965706 | CTGTCCCGTAGGCCA[A/G]GTTACTGGAGGAGAT | 9092 |
rs200401091 | snp | A/G | 4.29378e-05 | 0.00463326 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965361 | ATAAAGACCCTAGGA[A/G]AGGATGACCCCTGGC | 9092 |
rs200411744 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966373 | TCGCTCTATCCTGTC[C/T]AAGTATGACGAAGAG | 9092 |
rs200419057 | in-del | -/AT | | | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65980115 | ACCCTGTCTCAAAAA[-/AT]AAATAAAAAAAATTT | 9092 |
rs200425467 | snp | A/C | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961205 | TCCTATCTCAAGGGA[A/C]AAAACAAAACAAAAC | 9092 |
rs200457088 | snp | C/T | 3.32425e-05 | 0.00407678 | intron-variant | SART1 | GRCh38.p7 | 11:65966343 | ACCTGTACCTCTTGC[C/T]TTGCAGCAAAAACCT | 9092 |
rs200461701 | in-del | -/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65972578 | AACACAGCAAGACCA[-/C]CCCCCCCTACCAACC | 9092 |
rs200524670 | snp | A/G | 1.66023e-05 | 0.00288113 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965775 | AGTTCGGGCAGAGGC[A/G]GCAGGTGAGGCTGCA | 9092 |
rs200608651 | snp | A/G | 0.000635384 | 0.0178126 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976671 | GACTTTGAACGGGAT[A/G]AGGAGCGCTCAGCCA | 9092 |
rs200648701 | snp | A/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966549 | AATACCTCACGCCTG[A/T]GGAGATGGTGAGCCC | 9092 |
rs200869280 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967533 | AGGAGCCTGTGCCTC[A/G]GCCCCTGCCGTCGGA | 9092 |
rs200870704 | snp | C/G | 0.000121466 | 0.00779218 | intron-variant, utr-variant-5-prime | SART1 | GRCh38.p7 | 11:65964044 | TTGGCCCTGTGTTCA[C/G]CTCCTGAGCCATGCT | 9092 |
rs200878652 | snp | A/G | 6.60786e-05 | 0.0057476 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965896 | CCTTAGGACCTGTAC[A/G]GTGCCCGGGACCTGC | 9092 |
rs200956510 | in-del | -/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65963482 | AAGAGTTTTTTTTTT[-/G]TTTTGTTTTGTTTTT | 9092 |
rs200958331 | snp | C/T | 0.00336134 | 0.0408579 | intron-variant | SART1 | GRCh38.p7 | 11:65966568 | GATGGTGAGCCCTCC[C/T]GTGCCTTATACTCGG | 9092 |
rs201006690 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966200 | TGCCGAGGACGAGAG[C/T]GTGGACGACCTGGCG | 9092 |
rs201043732 | snp | C/G | 0.000415196 | 0.0144023 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967800 | ACAGCAGCTACAGCA[C/G]CTGCGAGACAGTGGC | 9092 |
rs201159110 | in-del | -/A | | | intron-variant | SART1 | GRCh38.p7 | 11:65973182 | CGTCTCAAAAAAAAA[-/A]GAAATTGAGAACGTA | 9092 |
rs201202822 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65971635 | GGATGGTGGGATTCA[G/T]GAGCTGAGGAGGGGG | 9092 |
rs201218299 | snp | C/G | 0.000231838 | 0.0107641 | intron-variant | SART1 | GRCh38.p7 | 11:65967418 | TGGGGCGAGATGGCT[C/G]GGCTGGGGTGGCCTG | 9092 |
rs201276041 | in-del | -/GTG | | | intron-variant | SART1 | GRCh38.p7 | 11:65971029 | GGTGGGATTCATGAG[-/GTG]CTGAGGAGGGGGGTG | 9092 |
rs201326498 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65970907 | GATGGTGGGATTCAG[A/G]AGCTGAGGAGGGGGA | 9092 |
rs201336410 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967348 | TGACTTGCTGCCTCT[C/T]GGGGACCAGACTCAG | 9092 |
rs201351683 | in-del | -/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65962531 | GAATCGTGTAGGGCG[-/C]ATGGTAGAGAAATGA | 9092 |
rs201364567 | in-del | -/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65963471 | GCAGGAAAGGAAGAG[-/T]TTTTTTTTTTGTTTT | 9092 |
rs201368685 | snp | A/G | 0.000483249 | 0.0155368 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966189 | TACCTGCCCTATGCC[A/G]AGGACGAGAGCGTGG | 9092 |
rs201422595 | in-del | -/GCT | | | intron-variant | SART1 | GRCh38.p7 | 11:65970818 | TGGTGGGATTCATGA[-/GCT]GCTGAGGAGGGGGAT | 9092 |
rs201519291 | snp | A/G | 0.000122639 | 0.00782972 | intron-variant | SART1 | GRCh38.p7 | 11:65976350 | GGTCTCAATGGCATC[A/G]CCCCAGAAACTGCTG | 9092 |
rs201529113 | snp | A/C/T | 0.000166215 | 0.00911499 | intron-variant | SART1 | GRCh38.p7 | 11:65966342 | AACCTGTACCTCTTG[A/C/T]CTTGCAGCAAAAACC | 9092 |
rs201560941 | snp | C/T | 0.000535871 | 0.01636 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966521 | AGCACAGTGGGGCCC[C/T]GGCTGGCCTCCGAAT | 9092 |
rs201607938 | snp | C/T | 0.000154723 | 0.00879418 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976679 | ACGGGATGAGGAGCG[C/T]TCAGCCAACGGTGGC | 9092 |
rs201634204 | in-del | -/CAAA | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961210 | TCTCAAGGGAAAAAA[-/CAAA]ACAAAACAAAACAGG | 9092 |
rs201806167 | snp | A/G | 0.000232303 | 0.0107749 | intron-variant | SART1 | GRCh38.p7 | 11:65965811 | GGTGGTACAGGGGAC[A/G]CTGGTGGCCTTGCTA | 9092 |
rs201941438 | in-del | -/AAA | | | intron-variant | SART1 | GRCh38.p7 | 11:65974516 | AACCCTGTCTCTACT[-/AAA]AAAAATACAAAAATT | 9092 |
rs201965311 | snp | C/T | 0.000232169 | 0.0107717 | intron-variant | SART1 | GRCh38.p7 | 11:65978782 | CTTTCTGAGTGGCCC[C/T]GACCCCTCAGCTCCT | 9092 |
rs201995541 | snp | A/G | 0.000340994 | 0.013053 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977834 | TTCAAGGAGAAGGAC[A/G]GCTACAAACCCGACG | 9092 |
rs202007981 | in-del | -/TGC | | | intron-variant | SART1 | GRCh38.p7 | 11:65971300 | GTGGGATTCATGAGC[-/TGC]TGAGGAGGGGGATGG | 9092 |
rs202057886 | snp | A/G | 0.0053959 | 0.0516608 | intron-variant | SART1 | GRCh38.p7 | 11:65965319 | AGCTGGGCTCCTTGA[A/G]CATCACTTTTTCCCC | 9092 |
rs202095327 | snp | C/T | 1.66799e-05 | 0.00288785 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966206 | GGACGAGAGCGTGGA[C/T]GACCTGGCGCAGGCA | 9092 |
rs202123592 | snp | A/G | 1.66424e-05 | 0.0028846 | intron-variant | SART1 | GRCh38.p7 | 11:65978976 | GCGTGGCCTGTGCCC[A/G]CCTCTGCAGCCTCAC | 9092 |
rs202145026 | snp | C/G | 0.000141682 | 0.00841551 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961810 | GAAGCATCGCGGAGA[C/G]AAGGAGGCGGCCGGG | 9092 |
rs202186196 | snp | A/G | 0.000843627 | 0.0205208 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967781 | GACGCCGGCTGCGAC[A/G]GTTACAGCAGCTACA | 9092 |
rs202240319 | snp | G/T | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961211 | CTCAAGGGAAAAAAC[G/T]AAACAAAACAAAACA | 9092 |
rs267603120 | snp | C/T | | | upstream-variant-2KB, missense | SART1, TSGA10IP | GRCh38.p7 | 11:65959935 | GACCCGGAGTGCAGT[C/T]CCTGAGATAAAATTA | 9092 |
rs267603121 | snp | C/T | | | upstream-variant-2KB, missense | SART1, TSGA10IP | GRCh38.p7 | 11:65959936 | ACCCGGAGTGCAGTC[C/T]CTGAGATAAAATTAA | 9092 |
rs367604433 | in-del | -/GTG | | | intron-variant | SART1 | GRCh38.p7 | 11:65970656 | GTGGCAGAGGTGGTG[-/GTG]CAAAGAGATGGGAGA | 9092 |
rs367624927 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65976282 | AGCTGGGCCTGCATG[A/G]GCTGTGGGCGTGGCC | 9092 |
rs367722063 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976477 | GGAAGGGGGCCATCG[A/T]GTTCAACGCCACGTC | 9092 |
rs367740935 | snp | G/T | 6.73253e-05 | 0.00580156 | intron-variant, synonymous-codon | SART1 | GRCh38.p7 | 11:65964060 | CTCCTGAGCCATGCT[G/T]CTTCTTGTTCCAGCT | 9092 |
rs367820057 | snp | C/T | 0.000183647 | 0.00958071 | upstream-variant-2KB, synonymous-codon | SART1, TSGA10IP | GRCh38.p7 | 11:65959883 | AAGGACAGAACCCAC[C/T]GGCAGCCAGCCTGAC | 9092 |
rs367869405 | snp | A/G/T | 0.000133381 | 0.00816542 | intron-variant | SART1 | GRCh38.p7 | 11:65966012 | CTGGGTGCCCTGGGT[A/G/T]GGGGCACAGCCTCTG | 9092 |
rs368042991 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SART1 | GRCh38.p7 | 11:65973099 | GAATGGTGTGAACCC[A/G]GGAGGCGGAGCTTGC | 9092 |
rs368107466 | snp | A/G | 1.64993e-05 | 0.00287218 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967362 | TCGGGGACCAGACTC[A/G]GGATGGGGACTTTGG | 9092 |
rs368109327 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65962263 | GAGCCCAGGAGTTAG[A/C]GGCTGCAGTGAGCTG | 9092 |
rs368110835 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979171 | TGGCTCCTGCTAGGT[A/G]AGACCTGGCCATCAA | 9092 |
rs368174170 | snp | C/G/T | 0.00039157 | 0.0139874 | intron-variant | SART1 | GRCh38.p7 | 11:65977526 | TGGAGCTGTGGCTCT[C/G/T]GAGGGGTTGGGAGTC | 9092 |
rs368223220 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65972113 | ACAATATATTGTCAA[C/G]ATGTCCATCTCATGT | 9092 |
rs368297502 | snp | C/T | 0.000167079 | 0.00913846 | utr-variant-3-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979070 | CCTCAACCTTCATAT[C/T]AAATAAAGCTCCCTC | 9092 |
rs368302542 | snp | A/G | 8.26603e-05 | 0.00642832 | intron-variant | SART1 | GRCh38.p7 | 11:65965870 | GGAGGTTCCTGACTC[A/G]CCGATTCTTCCCTTA | 9092 |
rs368385142 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65977219 | CAATGCTGGAGCCAG[A/C]TGTCCGGCCCAGAGC | 9092 |
rs368428982 | snp | A/C | 3.42759e-05 | 0.00413966 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965148 | AACCCTATGGCCTTG[A/C]GACAGCGAGAGGAGC | 9092 |
rs368449173 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65963594 | TCAAGCAATTCTCCT[A/C]CCTCAGCCTCCCGAG | 9092 |
rs368563983 | in-del | -/C | 0.000101254 | 0.00711454 | intron-variant | SART1 | GRCh38.p7 | 11:65965695 | GTCACCCCTCCCTGT[-/C]CCGTAGGCCAAGTTA | 9092 |
rs368588379 | snp | C/G | 3.53451e-05 | 0.00420372 | upstream-variant-2KB, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65959954 | GAGATAAAATTAAAG[C/G]CTTTATGGCAAACAC | 9092 |
rs368652945 | in-del | -/GCT | 0.00557542 | 0.0525036 | intron-variant | SART1 | GRCh38.p7 | 11:65971574 | TGGTGGGATTCATGA[-/GCT]GCTGAAGAGGGGGAT | 9092 |
rs368698198 | snp | A/G | 0.000398314 | 0.0141067 | intron-variant | SART1 | GRCh38.p7 | 11:65967632 | AGGGACAGGAGCCGC[A/G]GGTTGGAGGAGATGG | 9092 |
rs368847994 | snp | A/G | 8.27931e-05 | 0.00643348 | intron-variant | SART1 | GRCh38.p7 | 11:65977679 | TGGGGCCTGTGCAGG[A/G]CTGAGGGGCCTGTGC | 9092 |
rs368896964 | snp | C/T | 0.00054093 | 0.0164369 | intron-variant | SART1 | GRCh38.p7 | 11:65978597 | CATGCCCCGCGTCCC[C/T]AGGCTTTCCGGCAGC | 9092 |
rs368914489 | snp | C/T | 0.00025832 | 0.0113619 | intron-variant | SART1 | GRCh38.p7 | 11:65976572 | GAGGAGCTCATGGTG[C/T]GTCTGGGGCGGCCCC | 9092 |
rs368988089 | snp | C/T | 4.95913e-05 | 0.00497928 | intron-variant | SART1 | GRCh38.p7 | 11:65965872 | AGGTTCCTGACTCGC[C/T]GATTCTTCCCTTAGG | 9092 |
rs369030277 | snp | A/C | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65960981 | GGAGTTCGAGACCAG[A/C]CTGGCCAACATAGTG | 9092 |
rs369148455 | snp | C/T | 2.01562e-05 | 0.00317454 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961750 | GTTGTCTGGGCTCGG[C/T]GGCAGCCGGGCTCGG | 9092 |
rs369274842 | snp | A/G | 0.000342123 | 0.0130746 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965382 | GACCCCTGGCTGGAC[A/G]ACACTGCAGCCTGGA | 9092 |
rs369312564 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960037 | AGGTGGCAGGTGGGT[A/G]GGCAGCAGGCTTAGC | 9092 |
rs369336856 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65963487 | TTTTTTTTTTGTTTT[G/T]TTTTGTTTTTTTGAG | 9092 |
rs369344365 | snp | C/T | 0.00127183 | 0.0251852 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967738 | GAGGACGAGGCGGAG[C/T]TGGAGCTGCAGAAGC | 9092 |
rs369346839 | snp | C/T | 1.65507e-05 | 0.00287664 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977612 | GGTGAAGGCCCCCAA[C/T]AAGTCGCTGCCCTCA | 9092 |
rs369415657 | snp | C/T | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978914 | GCAAGAGCATGAACG[C/T]GTGAGTGGCTCGAGG | 9092 |
rs369497387 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65974672 | TGATAGAGTGAGATG[A/G]TCTCAATAAATAAGT | 9092 |
rs369518510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65974913 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 9092 |
rs369677284 | snp | C/T | 0.000132431 | 0.0081362 | intron-variant | SART1 | GRCh38.p7 | 11:65964477 | CATGGCACCCTGTGT[C/T]TTTAATAGCCCCTAA | 9092 |
rs369946855 | snp | C/T | 0.000149809 | 0.00865344 | intron-variant | SART1 | GRCh38.p7 | 11:65978975 | GGCGTGGCCTGTGCC[C/T]GCCTCTGCAGCCTCA | 9092 |
rs369954244 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | SART1 | GRCh38.p7 | 11:65966251 | TGGGTGGCGGGGGCT[C/G]AGGTGGAGAATGTCG | 9092 |
rs369974547 | snp | C/T | 0.000197644 | 0.00993897 | intron-variant | SART1 | GRCh38.p7 | 11:65964157 | TCTCCCTTGTTTCTA[C/T]TTTGTTTTTCTAAGA | 9092 |
rs370163896 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65967605 | AGGGCCCGGCCAGGG[A/G]GTGGGAGGGGCAGGG | 9092 |
rs370201584 | snp | A/G | 0.000874543 | 0.0208927 | intron-variant, utr-variant-5-prime | SART1 | GRCh38.p7 | 11:65965059 | CCACCAGCCATGGGC[A/G]GGCATAGCCTCACGT | 9092 |
rs370207973 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SART1 | GRCh38.p7 | 11:65976984 | AGAGCCGGTATGGCC[C/T]GCTAACCACCCCCGC | 9092 |
rs370263938 | snp | C/T | 0.000117382 | 0.0076601 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966077 | TGTGCTGCCCCCAGG[C/T]GTGCTGCAGGAGGAG | 9092 |
rs370384430 | snp | C/T | 1.6766e-05 | 0.00289529 | intron-variant | SART1 | GRCh38.p7 | 11:65977549 | TGGGAGTCTCACAAC[C/T]CCTCCATCCCTAGGG | 9092 |
rs370390416 | snp | A/C | 1.65688e-05 | 0.00287821 | intron-variant | SART1 | GRCh38.p7 | 11:65965826 | ACTGGTGGCCTTGCT[A/C]CCGGAATCCCGAGGT | 9092 |
rs370478222 | snp | A/G | 1.65244e-05 | 0.00287436 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65964530 | CAAACTCCGGGCAAA[A/G]TTGGGGCTGAAACCC | 9092 |
rs370486013 | snp | C/T | 0.00015076 | 0.00868086 | intron-variant | SART1 | GRCh38.p7 | 11:65966036 | GCCTCTGCTGAGTTG[C/T]GGACAAGTGTGAATG | 9092 |
rs370488726 | snp | C/T | 0.000231773 | 0.0107626 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977776 | CAGGGCCATCGATGA[C/T]AAGTACAGCCGGAGG | 9092 |
rs370491203 | in-del | -/AAA | | | intron-variant | SART1 | GRCh38.p7 | 11:65973012 | TGTCTCTACTAAAAA[-/AAA]TACAAAAAAATTAAC | 9092 |
rs370495034 | snp | A/G | 3.32978e-05 | 0.00408017 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966406 | TGAAGGGGAGCGGCC[A/G]CATTCCTTCCGCTTG | 9092 |
rs370505822 | snp | C/T | 9.05264e-05 | 0.00672718 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966538 | GCTGGCCTCCGAATA[C/T]CTCACGCCTGAGGAG | 9092 |
rs370631644 | snp | A/G | 6.6368e-05 | 0.00576017 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965759 | ACTCTGGTGGAGGAG[A/G]AGTTCGGGCAGAGGC | 9092 |
rs370657310 | snp | C/T | 0.000279981 | 0.0118285 | intron-variant, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976380 | GGGTTTGCCCACAGC[C/T]GCTCCCTCCCCCAGG | 9092 |
rs370669502 | snp | C/T | 1.67066e-05 | 0.00289016 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977083 | CTGGCAGCTGCCCTG[C/T]TCCTGTGTCAGAACA | 9092 |
rs370672268 | snp | C/G/T | 6.6418e-05 | 0.0057624 | utr-variant-3-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979042 | GTGACAGCGCCCTCC[C/G/T]GCCCCGGCCCTGCCT | 9092 |
rs371023991 | snp | C/T | 3.32309e-05 | 0.00407607 | intron-variant | SART1 | GRCh38.p7 | 11:65965993 | AGGACAAAGGTAATG[C/T]GAGCTGGGTGCCCTG | 9092 |
rs371040413 | snp | C/T | 3.33028e-05 | 0.00408048 | intron-variant | SART1 | GRCh38.p7 | 11:65967461 | CACCAGAGAGGCCTC[C/T]TTCCCTCAGACTGCG | 9092 |
rs371147069 | snp | C/T | 3.39824e-05 | 0.0041219 | intron-variant | SART1 | GRCh38.p7 | 11:65965687 | AGTCCTAGGTCACCC[C/T]TCCCTGTCCCGTAGG | 9092 |
rs371154680 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65962415 | AGAGGGCTTCTGTTT[C/T]CCTCAGTTGTCTGGT | 9092 |
rs371186444 | snp | C/T | 6.06006e-05 | 0.00550424 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965399 | CACTGCAGCCTGGAT[C/T]GAGAGGAGCCGGCAG | 9092 |
rs371313304 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SART1 | GRCh38.p7 | 11:65968981 | CCCTACCCCACACTT[C/G]TCACCTAGGAAGAAG | 9092 |
rs371331961 | snp | C/T | 3.37712e-05 | 0.00410907 | intron-variant | SART1 | GRCh38.p7 | 11:65967226 | CTGCCTTTCTGTGGC[C/T]CCCGCTCCATGTCTC | 9092 |
rs371334815 | snp | A/G | 4.98616e-05 | 0.00499283 | utr-variant-3-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979048 | GCGCCCTCCCGCCCC[A/G]GCCCTGCCTCAACCT | 9092 |
rs371435554 | snp | C/G/T | 0.000126957 | 0.00796652 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976493 | GTTCAACGCCACGTC[C/G/T]GAGTTCTGCCGCACC | 9092 |
rs371539247 | snp | A/C/G | 0.000167219 | 0.00914257 | intron-variant | SART1 | GRCh38.p7 | 11:65978926 | ACGCGTGAGTGGCTC[A/C/G]AGGCTGGTGGGGTAG | 9092 |
rs371557283 | snp | C/T | 5.05514e-05 | 0.00502724 | intron-variant | SART1 | GRCh38.p7 | 11:65976997 | CCTGCTAACCACCCC[C/T]GCCACGTGTCCCGTA | 9092 |
rs371593735 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980524 | CCTGTAATCCCAGCA[C/T]TCTGGGAGGCTGAGG | 9092 |
rs371595726 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65964755 | CGCCTGCTCTCTGAG[G/T]TGGAGCTGTGGCCGT | 9092 |
rs371636508 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65970026 | CACACCCGGCCACCT[A/G]GAAGGTTTTTTAAAC | 9092 |
rs371660848 | snp | C/T | 1.65307e-05 | 0.0028749 | intron-variant | SART1 | GRCh38.p7 | 11:65967397 | AGGTGGGCTTGGACA[C/T]GGTGGTGGGGCGAGA | 9092 |
rs371662642 | snp | C/G | 7.62922e-05 | 0.00617578 | intron-variant | SART1 | GRCh38.p7 | 11:65965334 | GCATCACTTTTTCCC[C/G]TCTTCAGGAAGATAA | 9092 |
rs371713910 | snp | C/T | 5.01945e-05 | 0.00500946 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966110 | GGACGTGCTGGTGAA[C/T]GTGAACCTGGTGGAT | 9092 |
rs371814551 | snp | C/T | 3.45781e-05 | 0.00415787 | intron-variant | SART1 | GRCh38.p7 | 11:65976603 | GCCCTCTGCTTCCCT[C/T]GGCTGGGTGGGCTGG | 9092 |
rs371897877 | snp | A/T | 0.000389057 | 0.0139419 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65959981 | ACACAGTATGAGATT[A/T]CTGGTGGTGGGGGTG | 9092 |
rs371918833 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960016 | AAGCTACGGGTTGGA[A/C]GTTGGAGGTGGCAGG | 9092 |
rs372059769 | snp | A/C/G | 1.65198e-05 | 0.00287395 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978828 | CAGCGACACGCCCCT[A/C/G]GGCACCGTGGCCCTG | 9092 |
rs372104972 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65975932 | ATGTCACGGAACCTG[C/T]TTTCTTGGTGAAGCA | 9092 |
rs372158649 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65976621 | CTGGGTGGGCTGGCT[A/G]GGGCCTGGGCCGACC | 9092 |
rs372169365 | snp | A/G | 1.71643e-05 | 0.00292948 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967550 | CCCCTGCCGTCGGAC[A/G]ACACCCGAGTGGAGA | 9092 |
rs372244872 | snp | A/C/G/T | 0.000154892 | 0.0087993 | intron-variant | SART1 | GRCh38.p7 | 11:65976573 | AGGAGCTCATGGTGC[A/C/G/T]TCTGGGGCGGCCCCG | 9092 |
rs372275370 | snp | G/T | 0.000169986 | 0.00921759 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961838 | GGGACGACGGCGGCG[G/T]CCGGCACCGGGGGTG | 9092 |
rs372358365 | snp | A/C/G/T | 0.00087638 | 0.0209149 | intron-variant | SART1 | GRCh38.p7 | 11:65965849 | CCCGAGGTTGGGTGC[A/C/G/T]TGGAGGGAGGTTCCT | 9092 |
rs372409677 | in-del | -/ACAA | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979192 | TGGCCATCAAATGAC[-/ACAA]ACAACTAAACGATGG | 9092 |
rs372588966 | snp | A/G | 5.03715e-05 | 0.00501829 | intron-variant | SART1 | GRCh38.p7 | 11:65967242 | CCCGCTCCATGTCTC[A/G]CCCCTCTTCCCTTAA | 9092 |
rs372733020 | snp | C/G | 1.83071e-05 | 0.00302543 | intron-variant | SART1 | GRCh38.p7 | 11:65964161 | CCTTGTTTCTACTTT[C/G]TTTTTCTAAGAGAGG | 9092 |
rs372766144 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65974933 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 9092 |
rs372801881 | snp | C/G | 3.41676e-05 | 0.00413311 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965155 | TGGCCTTGCGACAGC[C/G]AGAGGAGCTGCGGGA | 9092 |
rs372825547 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979382 | TCCTGTAATGTCTCC[C/T]GGTCAGGGCAGCCCA | 9092 |
rs372960740 | snp | C/T | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961477 | AAGACACTGACTTAA[C/T]GGGCTCTAAGTCCTT | 9092 |
rs372967734 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | SART1 | GRCh38.p7 | 11:65967644 | CGCGGGTTGGAGGAG[A/G]TGGTCTGAGCAGGCA | 9092 |
rs373028782 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SART1 | GRCh38.p7 | 11:65974704 | GCATATGATGCATTA[G/T]ATATACCTCGTTTTA | 9092 |
rs373084839 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65970888 | ATGAGCTGCTGAGGA[A/G]GGGGATGGTGGGATT | 9092 |
rs373094319 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65974831 | ACGAGGTCAGGAGAT[G/T]GAGACCATCCAGGCT | 9092 |
rs373209379 | snp | A/G/T | 0.000181936 | 0.00953618 | intron-variant | SART1 | GRCh38.p7 | 11:65977724 | GGGACCACAGCAGGC[A/G/T]GCAGCTCCTCACACT | 9092 |
rs373320354 | snp | A/G | 1.66103e-05 | 0.00288182 | intron-variant | SART1 | GRCh38.p7 | 11:65978984 | TGTGCCCGCCTCTGC[A/G]GCCTCACGCCCCTGT | 9092 |
rs373342209 | snp | A/G | 1.67265e-05 | 0.00289188 | intron-variant | SART1 | GRCh38.p7 | 11:65977003 | AACCACCCCCGCCAC[A/G]TGTCCCGTAGTTCTC | 9092 |
rs373380190 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65967612 | GGCCAGGGGGTGGGA[G/T]GGGCAGGGACAGGAG | 9092 |
rs373384055 | snp | C/T | 1.86614e-05 | 0.00305456 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976732 | ACATCGGCTGGAGCA[C/T]GGTGAACCTGGACGA | 9092 |
rs373450376 | snp | C/T | 3.44412e-05 | 0.00414963 | intron-variant | SART1 | GRCh38.p7 | 11:65965667 | GGTGATGCTGAGTGG[C/T]CTGAAGTCCTAGGTC | 9092 |
rs373458556 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SART1 | GRCh38.p7 | 11:65965873 | GGTTCCTGACTCGCC[A/G]ATTCTTCCCTTAGGA | 9092 |
rs373499762 | snp | C/G/T | 0.000327301 | 0.0127891 | intron-variant | SART1 | GRCh38.p7 | 11:65976785 | AGGGCCGCGCCGCTG[C/G/T]GGGGTGGGCGTTTGG | 9092 |
rs373540194 | snp | A/G | 0.000163987 | 0.00905352 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967816 | CTGCGAGACAGTGGC[A/G]AGAAGGTGAGGCTGG | 9092 |
rs373569431 | snp | C/T | 0.000132363 | 0.00813411 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977630 | GTCGCTGCCCTCAGC[C/T]GTGTACTGCATCGAG | 9092 |
rs373570526 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65964808 | GTTGTTAGATGGACT[A/G]GAAGATGTGCACACT | 9092 |
rs373615717 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SART1 | GRCh38.p7 | 11:65978991 | GCCTCTGCAGCCTCA[C/T]GCCCCTGTTCTTCTC | 9092 |
rs373665639 | snp | C/T | 0.000401701 | 0.0141665 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966098 | GCAGGAGGAGGAGGA[C/T]GTGCTGGTGAACGTG | 9092 |
rs373700227 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | SART1 | GRCh38.p7 | 11:65977921 | AGGGCCTTTTGCAGG[C/T]GGAGGCCCGGCCTGC | 9092 |
rs373759907 | snp | A/C/T | 1.66037e-05 | 0.00288125 | intron-variant | SART1 | GRCh38.p7 | 11:65967439 | GGGTGGCCTGGGGAC[A/C/T]GGTGCTCACCAGAGA | 9092 |
rs373790467 | snp | A/G | 1.66073e-05 | 0.00288156 | utr-variant-3-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979043 | TGACAGCGCCCTCCC[A/G]CCCCGGCCCTGCCTC | 9092 |
rs373812085 | snp | C/T | 6.88018e-05 | 0.00586483 | intron-variant | SART1 | GRCh38.p7 | 11:65976653 | TGGTCTTTTGTGCCC[C/T]AGGACTTTGAACGGG | 9092 |
rs373877874 | snp | A/G | 0.00143764 | 0.0267722 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967561 | GGACGACACCCGAGT[A/G]GAGAACATGGACATC | 9092 |
rs373938407 | snp | C/G | 1.65496e-05 | 0.00287655 | intron-variant | SART1 | GRCh38.p7 | 11:65977697 | GAGGGGCCTGTGCCA[C/G]CTTGGAGCTTCGGGA | 9092 |
rs373955573 | snp | C/G | 2.32361e-05 | 0.00340845 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966512 | CAGTCCCTGAGCACA[C/G]TGGGGCCCCGGCTGG | 9092 |
rs373968636 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SART1 | GRCh38.p7 | 11:65972893 | AATTGAGAACGTGGC[C/T]GGGCGCGATGGCTCA | 9092 |
rs374131487 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979440 | TTGGGCTTTGGGTAG[A/G]GCACAGGTGCCACCT | 9092 |
rs374274301 | snp | C/T | 1.67464e-05 | 0.0028936 | intron-variant | SART1 | GRCh38.p7 | 11:65967246 | CTCCATGTCTCGCCC[C/T]TCTTCCCTTAAGGTG | 9092 |
rs374274682 | snp | A/G | 3.41425e-05 | 0.0041316 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965167 | AGCGAGAGGAGCTGC[A/G]GGAGAAGCTGGCGGC | 9092 |
rs374342564 | snp | G/T | | | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65980037 | AGGATCACTTGAACC[G/T]GGGAGACACAGGCTG | 9092 |
rs374361529 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65976130 | GGCTTTGGAGGGGGA[C/T]TGGCACAGGCCTGGT | 9092 |
rs374434835 | snp | G/T | 3.33339e-05 | 0.00408238 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966410 | GGGGAGCGGCCACAT[G/T]CCTTCCGCTTGGAGC | 9092 |
rs374516477 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65975293 | TTTTTTGTAGAGACT[A/G]TGCTTCACCTTATTG | 9092 |
rs374728508 | snp | C/T | 0.000151527 | 0.00870289 | missense, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961949 | CGACGGAAGCGGAGC[C/T]GGGAACGTGGGGGCG | 9092 |
rs374733944 | snp | C/T | 7.05567e-05 | 0.00593914 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976529 | GGAGATCCCCACCTA[C/T]GGGCTGGCTGGCAAT | 9092 |
rs374743211 | snp | A/G | 0.000801041 | 0.019997 | intron-variant | SART1 | GRCh38.p7 | 11:65965459 | GAGGGTGAGCACCTG[A/G]GCAGCATGGGGTGGT | 9092 |
rs374906330 | snp | G/T | 1.65518e-05 | 0.00287674 | intron-variant | SART1 | GRCh38.p7 | 11:65964592 | ATGGGGCTGAGGATA[G/T]GGTTTGGGGGAAAGA | 9092 |
rs374913348 | snp | A/G | 0.000114591 | 0.00756852 | intron-variant, utr-variant-5-prime | SART1 | GRCh38.p7 | 11:65965073 | CGGGCATAGCCTCAC[A/G]TCTGGGCCCCCCTTC | 9092 |
rs374974267 | snp | G/T | 7.12818e-05 | 0.00596957 | intron-variant | SART1 | GRCh38.p7 | 11:65967606 | GGGCCCGGCCAGGGG[G/T]TGGGAGGGGCAGGGA | 9092 |
rs375013917 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960697 | AGGCGTGAGCCACCG[C/T]GCCCGGCCTGCACTG | 9092 |
rs375131980 | snp | C/T | 3.30267e-05 | 0.00406353 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978882 | GAAGACCCCCTACAT[C/T]GTGCTCAGCGGCAGC | 9092 |
rs375257855 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65971148 | GATGGGATTCATGAG[C/G]TGCTGAGGAGGGGGA | 9092 |
rs375290813 | snp | A/G | 3.30573e-05 | 0.00406541 | intron-variant | SART1 | GRCh38.p7 | 11:65967398 | GGTGGGCTTGGACAC[A/G]GTGGTGGGGCGAGAT | 9092 |
rs375336025 | snp | C/T | 0.000100835 | 0.00709982 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967490 | CGGGGACGGGGTCGC[C/T]GCCGAGTGTCCGAAG | 9092 |
rs375398781 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65978201 | TGGCTTTCCTGGCCC[A/G]CAGGGCCATTCCAGC | 9092 |
rs375455328 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SART1 | GRCh38.p7 | 11:65968095 | GCTGGGATTACAGGC[A/G]CACGCCACCAGACCC | 9092 |
rs375550218 | snp | A/G | 0.000120522 | 0.00776187 | intron-variant | SART1 | GRCh38.p7 | 11:65976588 | GTCTGGGGCGGCCCC[A/G]CCCTCTGCTTCCCTC | 9092 |
rs375583517 | snp | C/T | 3.3123e-05 | 0.00406945 | intron-variant | SART1 | GRCh38.p7 | 11:65964471 | AATGCACATGGCACC[C/T]TGTGTCTTTAATAGC | 9092 |
rs375720342 | snp | A/G | 3.32801e-05 | 0.00407908 | intron-variant | SART1 | GRCh38.p7 | 11:65978763 | TGTGGGGCCTGCTGC[A/G]GCCCTTTCTGAGTGG | 9092 |
rs375789520 | snp | C/T | 5.09628e-05 | 0.00504765 | intron-variant | SART1 | GRCh38.p7 | 11:65978962 | GGTGGGGAGGGGTGG[C/T]GTGGCCTGTGCCCGC | 9092 |
rs375799235 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SART1 | GRCh38.p7 | 11:65970691 | CTGTTCTGGAGAGTG[A/G]AGAGCAGATACACCC | 9092 |
rs375907218 | snp | A/G | 1.68616e-05 | 0.00290353 | intron-variant | SART1 | GRCh38.p7 | 11:65967230 | CTTTCTGTGGCCCCC[A/G]CTCCATGTCTCGCCC | 9092 |
rs375911359 | snp | C/T | 0.000827362 | 0.0203223 | intron-variant | SART1 | GRCh38.p7 | 11:65977669 | GTGAGTGTGGTGGGG[C/T]CTGTGCAGGGCTGAG | 9092 |
rs376037779 | snp | C/G | 0.000334756 | 0.0129331 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967717 | GGGTCCCCGCAGGTG[C/G]TGGAGGAGGACGAGG | 9092 |
rs376068517 | snp | C/T | 0.000289409 | 0.0120258 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976721 | CGGGGAGGAGAACAT[C/T]GGCTGGAGCACGGTG | 9092 |
rs376129477 | snp | A/G | 0.000114305 | 0.00755907 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966533 | CCCCGGCTGGCCTCC[A/G]AATACCTCACGCCTG | 9092 |
rs376172148 | snp | A/G | 0.000169986 | 0.00921759 | intron-variant | SART1 | GRCh38.p7 | 11:65967834 | AAGGTGAGGCTGGGC[A/G]TGGGCAGGGTGACTG | 9092 |
rs376240417 | snp | C/G | 1.89009e-05 | 0.0030741 | upstream-variant-2KB, missense | SART1, TSGA10IP | GRCh38.p7 | 11:65959920 | TACAACCCCAGCCTG[C/G]ACCCGGAGTGCAGTC | 9092 |
rs376278814 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65962540 | AGGGCGCATGGTAGA[G/T]AAATGAGGGAGTAAG | 9092 |
rs376324863 | snp | A/G | 0.000237107 | 0.0108857 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967778 | AGGGACGCCGGCTGC[A/G]ACAGTTACAGCAGCT | 9092 |
rs376362292 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65978294 | CCCTTGCTCTCTGGG[G/T]TTTGTCTCCCTGCAG | 9092 |
rs376362379 | snp | C/T | 9.92211e-05 | 0.00704278 | intron-variant | SART1 | GRCh38.p7 | 11:65976775 | GCAGGATGTGAGGGC[C/T]GCGCCGCTGGGGGGT | 9092 |
rs376376577 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960630 | CCAGGATGGTCTCGA[G/T]CTCTTGACCTCGTGA | 9092 |
rs376513721 | snp | C/G | 2.01965e-05 | 0.00317771 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961747 | TGCGTTGTCTGGGCT[C/G]GGCGGCAGCCGGGCT | 9092 |
rs376516240 | snp | A/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65975294 | TTTTTGTAGAGACTG[A/T]GCTTCACCTTATTGT | 9092 |
rs376528664 | snp | C/T | 0.00036422 | 0.0134899 | intron-variant | SART1 | GRCh38.p7 | 11:65976632 | GGCTGGGGCCTGGGC[C/T]GACCCTGGTCTTTTG | 9092 |
rs376611219 | snp | C/G | 1.65381e-05 | 0.00287555 | intron-variant | SART1 | GRCh38.p7 | 11:65965862 | GCGTGGAGGGAGGTT[C/G]CTGACTCGCCGATTC | 9092 |
rs376695466 | snp | A/C/G | 9.96122e-05 | 0.00705671 | intron-variant | SART1 | GRCh38.p7 | 11:65967440 | GGTGGCCTGGGGACC[A/C/G]GTGCTCACCAGAGAG | 9092 |
rs376749982 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965719 | CAAGTTACTGGAGGA[A/G]ATGGACCAAGAGTTT | 9092 |
rs376847340 | snp | C/G/T | 0.00025953 | 0.011389 | intron-variant | SART1 | GRCh38.p7 | 11:65976786 | GGGCCGCGCCGCTGG[C/G/T]GGGTGGGCGTTTGGG | 9092 |
rs377049028 | snp | C/G | 1.65364e-05 | 0.0028754 | intron-variant | SART1 | GRCh38.p7 | 11:65977713 | CTTGGAGCTTCGGGA[C/G]CACAGCAGGCGGCAG | 9092 |
rs377261046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65962220 | CTGTTTACCAGCTCT[A/G]TTAAATAGTCTTTCT | 9092 |
rs377299485 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65973233 | TTTACAAAACATACC[A/G]TGAAGAATATAAAAA | 9092 |
rs377339635 | snp | C/T | 1.65537e-05 | 0.0028769 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977034 | TGCTTCCTCCACCAC[C/T]ATCCTGGACGAGGAA | 9092 |
rs377348569 | snp | C/T | 3.32138e-05 | 0.00407502 | utr-variant-3-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979044 | GACAGCGCCCTCCCG[C/T]CCCGGCCCTGCCTCA | 9092 |
rs377371371 | snp | C/T | 1.73222e-05 | 0.00294292 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966455 | GATGGCCTGCGGGAG[C/T]GGGAGCTGGAGGAGA | 9092 |
rs377376434 | snp | A/C/T | 1.71275e-05 | 0.00292634 | intron-variant | SART1 | GRCh38.p7 | 11:65976974 | GGGGCTGAGAAGAGC[A/C/T]GGTATGGCCTGCTAA | 9092 |
rs377409653 | in-del | -/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65976370 | GAAACTGCTGGGTTT[-/C]GCCCACAGCCGCTCC | 9092 |
rs377459006 | snp | C/G | 0.000163986 | 0.00905352 | intron-variant | SART1 | GRCh38.p7 | 11:65978553 | GGCACAGGTGGCTCC[C/G]GCCCCACCCAGGGCC | 9092 |
rs377565304 | snp | C/T | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967325 | AAGGAGGTAGTAGTG[C/T]GGGCAGATGACTTGC | 9092 |
rs377767199 | snp | C/T | 1.66424e-05 | 0.0028846 | intron-variant | SART1 | GRCh38.p7 | 11:65967458 | GCTCACCAGAGAGGC[C/T]TCCTTCCCTCAGACT | 9092 |
rs386374024 | in-del | -/AAACA | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961222 | AACAAAACAAAACAA[-/AAACA]AACAGGGAACGTGGG | 9092 |
rs386754407 | multinucleotide-polymorphism | AAC/CAG | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961168 | CACGCCACTGCACTC[AAC/CAG]CCTGAGCAACAGAGT | 9092 |
rs386754408 | multinucleotide-polymorphism | AT/CA | | | intron-variant | SART1 | GRCh38.p7 | 11:65962531 | GAATCGTGTAGGGCG[AT/CA]TGGTAGAGAAATGAG | 9092 |
rs386754409 | multinucleotide-polymorphism | AA/GG | | | intron-variant | SART1 | GRCh38.p7 | 11:65976039 | TAGAGTCCTGAAACC[AA/GG]AGTTTGTCGGGGGAG | 9092 |
rs386754410 | multinucleotide-polymorphism | AAT/GAC | | | intron-variant | SART1 | GRCh38.p7 | 11:65976948 | TGCCTGGCAGGTGGT[AAT/GAC]CAGTGGGTGGGGCTG | 9092 |
rs397723728 | in-del | -/TGTTT | 0 | 0 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961226 | CCTTCCCACGTTCCC[-/TGTTT]TGTTTTGTTTTGTTT | 9092 |
rs527346196 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961570 | GACCACTCGCTCAAA[G/T]AACCCACCCGACCCG | 9092 |
rs527388598 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65968533 | GGGCACTCAGTAAAC[C/G]AAGATAACGTGCCGG | 9092 |
rs527397719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65962151 | TCCCGGAACGCGTGG[G/T]TCTGGGTGTGCGCGC | 9092 |
rs527512212 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980373 | ATCTGACTCTTGATT[C/G]TGTTTTCACCTTGGC | 9092 |
rs527665511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65963078 | AAAGCCATTGGGAGT[C/T]AGTATCTGGGTGGCC | 9092 |
rs527736599 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SART1 | GRCh38.p7 | 11:65974900 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGGGCGCC | 9092 |
rs527821831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968699 | CAGTAGACCAACCAG[C/T]AGGTGTCTCAGGAGA | 9092 |
rs527822267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65975727 | GTGGACATAGTGACT[C/G]GAACCTTCACTGAGG | 9092 |
rs528254318 | snp | C/T | 9.79768e-05 | 0.00699848 | intron-variant | SART1 | GRCh38.p7 | 11:65965456 | GAAGAGGGTGAGCAC[C/T]TGGGCAGCATGGGGT | 9092 |
rs528329246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972911 | GCGCGATGGCTCACG[C/T]CTGTAATCCCAGCAC | 9092 |
rs528348040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65976833 | ATGAGCACCGGGCTC[C/G]GTGTCCAGAGCCTCA | 9092 |
rs528438861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970497 | CTAGAGTGCAAGTGG[A/G]GGGTGGGCTTGAGTG | 9092 |
rs528668451 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65978185 | TGCGTGAGCCCTTCA[C/T]TGGCTTTCCTGGCCC | 9092 |
rs528829485 | snp | A/G | 1.65567e-05 | 0.00287716 | intron-variant | SART1 | GRCh38.p7 | 11:65977667 | ATGTGAGTGTGGTGG[A/G]GCCTGTGCAGGGCTG | 9092 |
rs528935524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65978517 | TCAATCAACACCCGC[C/G]CTGTTATTATACACC | 9092 |
rs528996460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65972981 | TGAGACCATCCTGGT[C/T]AACACAGTGAAACCC | 9092 |
rs529112764 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65964417 | CTTTGTGTTTGGGAC[C/T]ACTCACTCCCACCCT | 9092 |
rs529255112 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979573 | GCTCAGTGCCTCCTG[A/G]GAGACTTGTCCCGTG | 9092 |
rs529270039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973537 | AGTAGGAGTAAAGGA[C/T]ATGGAGCGGCCAGAG | 9092 |
rs529432974 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979212 | CAACTAAACGATGGA[A/G]GAGAGAGCGAGCCCG | 9092 |
rs529505764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968577 | AGATGGGAGAGTGCA[A/G]GGAAGACCTTTCCAA | 9092 |
rs529531968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65974156 | TCACAAGATCAGGAG[A/G]TTGAGACCATCCTGG | 9092 |
rs529801453 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65964151 | GTACTGTCTCCCTTG[C/T]TTCTACTTTGTTTTT | 9092 |
rs530104928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969324 | GGACATAGTTTGCCC[A/G]GCTAAAAAGGAACAG | 9092 |
rs530143447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SART1 | GRCh38.p7 | 11:65964012 | TTCCTGCAGCTGGAG[C/T]CAACGATGCTGGCTT | 9092 |
rs530143514 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65970017 | ATGAACCACCACACC[C/T]GGCCACCTAGAAGGT | 9092 |
rs530288972 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65969569 | ATCCTCCTGCCTCAG[C/G]CTCTCAAGTAGCTGA | 9092 |
rs530411149 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65970603 | GGGAAGTCAAGGCAG[C/G]CCATGGCCGATTGTT | 9092 |
rs530474006 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65971892 | TGAGCTAGAAAGAAA[C/G]GCTGGAGAGAACAGA | 9092 |
rs530512587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65977361 | CCCTGGTGTTAGGAC[C/T]CCAGCTCTGCCATTT | 9092 |
rs530569762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65976889 | CAGACCTCCCAGGGC[A/G]ATCTGAGGAGTAAAT | 9092 |
rs530668857 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65963607 | CTACCTCAGCCTCCC[A/G]AGTATCTGGGATTAC | 9092 |
rs530721949 | snp | C/T | 0.000797819 | 0.0199568 | intron-variant | SART1 | GRCh38.p7 | 11:65966338 | TCCCAACCTGTACCT[C/T]TTGCCTTGCAGCAAA | 9092 |
rs530755098 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960069 | CTGTCCCCGCACCCC[C/G]TCCCCACCAGGAGCT | 9092 |
rs530808128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65971915 | AGAACAGAAAGGATC[C/T]TTGGAATTGAGGGGT | 9092 |
rs530839286 | snp | C/G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65973354 | CAACAGGAAAATAGG[C/G/T]GAAAGATGTAGATAA | 9092 |
rs530917377 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960358 | CACAGACTGAGCAAC[C/T]ACTGGGTGAGGGGAG | 9092 |
rs531117702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65973035 | AAAAATTAACCAGAC[A/G]TGGTGGCGGGCACCT | 9092 |
rs531205282 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961470 | AGCCACGAAGACACT[G/T]ACTTAATGGGCTCTA | 9092 |
rs531279210 | snp | A/G | 0.000191608 | 0.00978607 | intron-variant | SART1 | GRCh38.p7 | 11:65978571 | CCCACCCAGGGCCCT[A/G]CATCTCCTCTCATGC | 9092 |
rs531281005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973361 | AAAATAGGCGAAAGA[C/T]GTAGATAAGACAGGC | 9092 |
rs531316332 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960709 | CCGCGCCCGGCCTGC[A/T]CTGGGGTTTTAAGTC | 9092 |
rs531346026 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65968843 | TGGTCGTCGCTGCCC[C/T]AGAGGCACAGTGGGC | 9092 |
rs531593647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65974798 | CCCAACACTTTGGGA[C/G]GCCAAGGCAGGCAAA | 9092 |
rs531620339 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65969269 | AGTGAGTGGGCGTGG[A/C]TGGGTTCCAGTAATA | 9092 |
rs531718421 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65974601 | GGAGGATCACTTGAA[A/C]CTGGGAGGTGGAGGT | 9092 |
rs531718764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968237 | ACAGGTGTGTGCCAC[C/T]GTGCCCAGCCCTCTA | 9092 |
rs531738763 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980318 | CGGGGCTGAGTCTTT[G/T]GGTGCCCTTCCTTGA | 9092 |
rs531881640 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65974328 | GCAGTGAGCCAAGAT[C/T]GTGCCACTTCACTCC | 9092 |
rs531940411 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SART1 | GRCh38.p7 | 11:65963483 | AGAGTTTTTTTTTTG[G/T]TTTGTTTTGTTTTTT | 9092 |
rs531946236 | in-del | -/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65975412 | GCCCCTGGAAGAATT[-/T]TTTTTTTTTTTTTTT | 9092 |
rs532055270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65962986 | AAGCAGATTTGGAGC[G/T]GGGGTGGGGGGAGAT | 9092 |
rs532064486 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65966762 | GGCCCCAGTCTGTTT[C/T]GGCTCTGCCATGCTG | 9092 |
rs532399839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65975870 | TGCTGGTGCCCGTGT[A/G]GGGGTCGCTGGATTC | 9092 |
rs532585709 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65972494 | TTTGGTAGAAAAGAT[C/T]TTTTAAGTTGTCAGC | 9092 |
rs532745068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972791 | ATCCTGTCTCAAAAA[A/C]AAAAAAAAACCAAGA | 9092 |
rs532814556 | snp | G/T | 0.000355255 | 0.013323 | intron-variant | SART1 | GRCh38.p7 | 11:65977532 | TGTGGCTCTCGAGGG[G/T]TTGGGAGTCTCACAA | 9092 |
rs532901917 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65977953 | ACAGGGAGGCCAAGC[C/G]CAGGGCCATGCAATG | 9092 |
rs532970934 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960620 | ACCATGTAGGCCAGG[A/G]TGGTCTCGATCTCTT | 9092 |
rs533269108 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960140 | TTCTCTGCTCCTGAG[C/G]AGTGGGGACATCTCA | 9092 |
rs533616558 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979131 | ATTCCAGGGTTGGAT[A/C]TTTGGTTGGGTGTGG | 9092 |
rs533622356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973090 | GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGGC | 9092 |
rs533753377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65974395 | AAAAAAAAAAAACCA[C/T]ATCAGCCGGGTGTGG | 9092 |
rs533864965 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65973690 | CAGTGGGCCTGCAGC[C/T]GCAGTACTTGGGACA | 9092 |
rs533986089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65968372 | GAGTAGTGCATTGTT[C/T]TTGGGCTGAGAAGGT | 9092 |
rs534008759 | snp | C/G | 0.000698777 | 0.0186789 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967743 | CGAGGCGGAGCTGGA[C/G]CTGCAGAAGCAGCTG | 9092 |
rs534048583 | snp | A/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65972917 | TGGCTCACGCCTGTA[A/T]TCCCAGCACTTTGGG | 9092 |
rs534094670 | snp | C/T | 1.72394e-05 | 0.00293589 | intron-variant | SART1 | GRCh38.p7 | 11:65976592 | GGGGCGGCCCCGCCC[C/T]CTGCTTCCCTCGGCT | 9092 |
rs534570282 | snp | A/G | 5.02449e-05 | 0.00501198 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65964126 | ACTCAGCATCGAGGA[A/G]ACTAAGTGAGTACTG | 9092 |
rs534583115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969585 | CTCTCAAGTAGCTGA[A/G]ACTACAGGCGTGCGC | 9092 |
rs534755214 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65968906 | TTCATTCCATCCTCC[C/T]AGCAACACCCTATGA | 9092 |
rs534870547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972107 | GATAGGACAATATAT[A/T]GTCAAGATGTCCATC | 9092 |
rs534943641 | in-del | -/C | 0.00557542 | 0.0525036 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65960997 | TGGCCAACATAGTGA[-/C]CCCCACCCCCTACCC | 9092 |
rs534960447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65964772 | GGAGCTGTGGCCGTC[A/G]CATACTCACTCTGGC | 9092 |
rs535035551 | snp | A/T | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961512 | TTCTGGGATCCCACC[A/T]CCGGGTTAATTCCGC | 9092 |
rs535099092 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960227 | AAATTCAAGCATGAA[C/T]AAGATGAAATGACTC | 9092 |
rs535573892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65975652 | CTCAAGCAGTCCACC[C/T]GCCTCAGAAGATTTT | 9092 |
rs535612080 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960672 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 9092 |
rs535658262 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SART1 | GRCh38.p7 | 11:65978415 | AGCCAAGCTGGTCTC[C/T]CGGCCTCTGCTGGGG | 9092 |
rs535833998 | snp | C/T | 3.36134e-05 | 0.00409946 | intron-variant | SART1 | GRCh38.p7 | 11:65967241 | CCCCGCTCCATGTCT[C/T]GCCCCTCTTCCCTTA | 9092 |
rs535909626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65972900 | AACGTGGCCGGGCGC[A/G]ATGGCTCACGCCTGT | 9092 |
rs535999286 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65966784 | GCCATGCTGCCAGCT[C/G]GTGCCTTGGATAAAC | 9092 |
rs536022403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968781 | GAGGGGTGGCGTGAG[C/T]TGAGATGGAGAGGTA | 9092 |
rs536164111 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961682 | GCAGCCGCTCTTAGT[C/T]TCCGGCAACACGACA | 9092 |
rs536287389 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65970135 | CAGTAATTATAAACA[C/T]TGTTACAGTTCTTTT | 9092 |
rs536468505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65976092 | CTGGAGGAAGGAGTT[G/T]GAGGCTGAGGTAGTG | 9092 |
rs536495080 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65966914 | GACTGGAGAGGTGTG[C/T]GTGGATTCTGTCCAC | 9092 |
rs536709409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969747 | GTTGTTGTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 9092 |
rs537111180 | snp | G/T | 0.000155289 | 0.00881024 | intron-variant | SART1 | GRCh38.p7 | 11:65976609 | TGCTTCCCTCGGCTG[G/T]GTGGGCTGGCTGGGG | 9092 |
rs537176344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65977165 | CAGGTGCAGGCAGGG[C/T]CCCCTCCGGTCCCCT | 9092 |
rs537390747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972876 | ACGTGTAACTACATA[C/G]AAATTGAGAACGTGG | 9092 |
rs537664596 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979284 | CACCTCTGCAGGGCC[A/G]GCTCTCTGATAGAAA | 9092 |
rs537710991 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65972274 | AACAGAACAGAGAGA[A/C/T]CAGACAGCGGGGCCC | 9092 |
rs537909607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972649 | GCATGTGTCTGAAGC[C/T]TCAGCTACGCCGGAG | 9092 |
rs537993475 | snp | A/G | 0.000185874 | 0.00963858 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967729 | GTGCTGGAGGAGGAC[A/G]AGGCGGAGCTGGAGC | 9092 |
rs538288690 | snp | A/G | 1.6552e-05 | 0.00287676 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967271 | AAGGTGACCTTTAAA[A/G]AGACCAAGCGGAGGG | 9092 |
rs538643720 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65964750 | GGCTCCGCCTGCTCT[C/T]TGAGTTGGAGCTGTG | 9092 |
rs538651311 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65974997 | GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC | 9092 |
rs538739713 | snp | A/G/T | 3.46308e-05 | 0.00416104 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967557 | CGTCGGACGACACCC[A/G/T]AGTGGAGAACATGGA | 9092 |
rs538763820 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65974620 | GGAGGTGGAGGTTGC[A/G]GTGAGCCTATATCGC | 9092 |
rs538778894 | in-del | -/TT | | | intron-variant | SART1 | GRCh38.p7 | 11:65970158 | GTTCTTTTCTTTCTC[-/TT]CTTTTTTTCCTGACC | 9092 |
rs538860795 | snp | A/G | 0.000342983 | 0.013091 | intron-variant | SART1 | GRCh38.p7 | 11:65976975 | GGGCTGAGAAGAGCC[A/G]GTATGGCCTGCTAAC | 9092 |
rs538961022 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65969441 | ACATTAGACTCACCT[A/G]GGAGGTTGTTTTTGT | 9092 |
rs539114847 | snp | A/G | 2.30955e-05 | 0.00339812 | intron-variant | SART1 | GRCh38.p7 | 11:65965022 | GCTGGAAGGGGGCAG[A/G]GTGAGTGGCTCCCTC | 9092 |
rs539560282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65965566 | GGAAGGGCCGTGGTC[A/G]GTAGCATCTACTTTG | 9092 |
rs539645434 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65972953 | AAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATGA | 9092 |
rs539717642 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SART1, TSGA10IP | GRCh38.p7 | 11:65959705 | AGTCACTTTGCCCAG[A/G]ATCACACAGCAAGCC | 9092 |
rs539733917 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65975354 | GTGATCCTCCAGCCT[C/T]GGCCTCCCAAAGTGC | 9092 |
rs539936191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65977972 | GGCCATGCAATGCCC[C/T]GGGCCATGCAATGCC | 9092 |
rs539969537 | snp | A/G | 0 | 0 | intron-variant | SART1 | GRCh38.p7 | 11:65978335 | AGCCCCAGCGTCCAG[A/G]CCCAGCCCCTGCGTG | 9092 |
rs539971363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65972439 | CAAAGTAAAAACTTC[A/G]CATTTCGGAATCAAA | 9092 |
rs539972337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65978498 | CCCAGGCCTGGCATT[A/G]GGGTCAATCAACACC | 9092 |
rs540067099 | in-del | -/ACAA | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65973315 | TGGTGTCAAGAGTAT[-/ACAA]ACAGACAAAACAAAT | 9092 |
rs540078488 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65966667 | TTGTGTTCACAAAGC[A/G]CTTGGCCTCGCGGGT | 9092 |
rs540127670 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65973183 | CGTCTCAAAAAAAAA[A/G]AAATTGAGAACGTAA | 9092 |
rs540851048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65974664 | AGCATGGGTGATAGA[A/G]TGAGATGGTCTCAAT | 9092 |
rs540955566 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65980083 | GAGCCACCACACTGC[A/G]GCCTAGGTGACAGTC | 9092 |
rs540959281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65974077 | TTTTAAAAACTATAT[C/G]AGCCGCTGGGTGCGG | 9092 |
rs540990552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65973614 | GAGAGGGAATGTGTG[C/T]GTGCCCGGGGCCCAC | 9092 |
rs541048625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65969990 | GCCTCCCAAAGTGCT[A/G]GAATTAGAGGCATGA | 9092 |
rs541126436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65975728 | TGGACATAGTGACTC[A/G]AACCTTCACTGAGGA | 9092 |
rs541558901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65973152 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 9092 |
rs541712672 | in-del | -/AGG | 6.70938e-05 | 0.00579158 | cds-indel, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966084 | CCCCAGGCGTGCTGC[-/AGG]AGGAGGAGGAGGACG | 9092 |
rs541842359 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960533 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGACTAC | 9092 |
rs541854013 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65971571 | GGATGGTGGGATTCA[G/T]GAGCTGCTGAAGAGG | 9092 |
rs541939998 | snp | C/T | 3.30803e-05 | 0.00406682 | intron-variant | SART1 | GRCh38.p7 | 11:65964502 | CCCTAACACTTGTAT[C/T]TCTTGTTGTCAGCAA | 9092 |
rs542107090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65977282 | TCTGCTCTGCCTTTG[A/G]GGCTCCACACCTGCT | 9092 |
rs542179334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65971896 | CTAGAAAGAAAGGCT[A/G]GAGAGAACAGAAAGG | 9092 |
rs542240296 | snp | C/G | 3.35284e-05 | 0.00409427 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967483 | CAGACTGCGGGGACG[C/G]GGTCGCCGCCGAGTG | 9092 |
rs542303302 | snp | A/G | 0.000251705 | 0.0112156 | intron-variant | SART1 | GRCh38.p7 | 11:65966244 | GGCAGGCTGGGTGGC[A/G]GGGGCTGAGGTGGAG | 9092 |
rs542349404 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960052 | GGGCAGCAGGCTTAG[C/T]TCTGTCCCCGCACCC | 9092 |
rs542380135 | snp | A/G | 5.17005e-05 | 0.00508405 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976687 | AGGAGCGCTCAGCCA[A/G]CGGTGGCTCCGAATC | 9092 |
rs542392680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973288 | TGCCCATATATACCA[C/T]CAAGAATGGGTTGGT | 9092 |
rs542418791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65978530 | GCCCTGTTATTATAC[A/G]CCTTGTGGGCACAGG | 9092 |
rs542473398 | snp | A/G | 0.000316206 | 0.0125699 | intron-variant | SART1 | GRCh38.p7 | 11:65967851 | GGGCAGGGTGACTGC[A/G]TCAGCAGTCACCTGT | 9092 |
rs542705380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65972987 | CATCCTGGTCAACAC[A/G]GTGAAACCCTGTCTC | 9092 |
rs542717851 | in-del | -/GTTTTTT | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65973199 | AAATTGAGAACGTAA[-/GTTTTTT]GTTTTTTGTTTTTTT | 9092 |
rs543340890 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SART1 | GRCh38.p7 | 11:65975634 | TGGTCTCGATCTCCG[A/G]AACTCAAGCAGTCCA | 9092 |
rs543369146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968599 | CCTTTCCAAGGTACT[A/G]GTTCATCTGAGACTT | 9092 |
rs543805527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65977944 | CGGCCTGCCACAGGG[A/G]GGCCAAGCCCAGGGC | 9092 |
rs544089729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65978447 | CCTGCAGGGTGCCAG[C/T]GTCTGTGCTCTTTTC | 9092 |
rs544100223 | snp | C/T | 4.95438e-05 | 0.00497689 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65965919 | GGACCTGCAGGGCCT[C/T]ACCGTGGAGCATGCC | 9092 |
rs544531038 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65972584 | AGCAAGACCACCCCC[C/G]CTACCAACCCCATCT | 9092 |
rs544592549 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961158 | GCGCTGTGATCACGC[C/T]ACTGCACTCCAGCCT | 9092 |
rs544620509 | snp | A/G | 0.00114482 | 0.0238977 | intron-variant | SART1 | GRCh38.p7 | 11:65962105 | GCCGGTGAGGAGGCG[A/G]GGCCTGCGCAGGGGG | 9092 |
rs544669222 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960609 | GACGGGGTTTTACCA[C/T]GTAGGCCAGGATGGT | 9092 |
rs544769879 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65973954 | GCCATGAAGACAAGC[C/T]GGTGAGTCATGACCA | 9092 |
rs544803519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65967912 | CCACATTCCTGTCTG[A/C]AGCCTCTTTTCCATT | 9092 |
rs545003847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968444 | GCTGGCTTTCTAGAG[C/T]GTGTGGGGGAGAGCG | 9092 |
rs545006741 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65975671 | TCAGAAGATTTTTTT[A/T]AAAAAATGAATGTAA | 9092 |
rs545037634 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65963337 | AACCGAAAAGAACCC[A/G]CTAGATTTAGAAACG | 9092 |
rs545078495 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980348 | AGCTCTGTATTCTCT[A/G]TAGTTTGACATCTGA | 9092 |
rs545090377 | snp | C/T | 1.65192e-05 | 0.00287391 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978834 | CACGCCCCTGGGCAC[C/T]GTGGCCCTGCTCCAG | 9092 |
rs545289750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65976234 | AGTGACCCCAGTGAA[A/G]GAGGTGCAGAGTGGA | 9092 |
rs545387084 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65965500 | TTCTGGTGGCCTGAC[A/G]GCACTGAGGCGGGGG | 9092 |
rs545599670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65964470 | AAATGCACATGGCAC[A/C]CTGTGTCTTTAATAG | 9092 |
rs545697562 | in-del | -/AAA | 0.00318978 | 0.0398085 | intron-variant | SART1 | GRCh38.p7 | 11:65973007 | AACCCTGTCTCTACT[-/AAA]AAAAATACAAAAAAA | 9092 |
rs545713979 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SART1 | GRCh38.p7 | 11:65969884 | CATGCCACCACGCCC[A/G]GCTGATTTTTGTATT | 9092 |
rs546138370 | snp | G/T | 7.1163e-05 | 0.0059646 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65959990 | GAGATTTCTGGTGGT[G/T]GGGGTGGTGGAAGCT | 9092 |
rs546197475 | in-del | -/GCT | | | intron-variant | SART1 | GRCh38.p7 | 11:65970847 | TGGTGGGATTCATGA[-/GCT]GCTGAGGAGGGGGAT | 9092 |
rs546286061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972081 | TGAATTTAGGGGTTA[C/T]ACAATTCCTAGATAG | 9092 |
rs546297393 | snp | A/G | 0.000218489 | 0.0104497 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966431 | CGCTTGGAGCAGGGC[A/G]GCACGGCTGATGGCC | 9092 |
rs546321993 | snp | C/T | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65960953 | GCCAAGGCGGGTGTA[C/T]AGCCTGAGCTCAGGA | 9092 |
rs546322932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972796 | GTCTCAAAAAAAAAA[A/C]AAAACCAAGAAACCC | 9092 |
rs546532584 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960207 | ATGTATATGTTGGGT[A/C]CTATAAATTCAAGCA | 9092 |
rs546592209 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SART1, TSGA10IP | GRCh38.p7 | 11:65959720 | GATCACACAGCAAGC[C/T]GGCACTGAAGCAGGG | 9092 |
rs546652717 | snp | A/G | 0.00034263 | 0.0130843 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978671 | AGAGCGGCGGATGAA[A/G]AAGCTGGACGAGGAG | 9092 |
rs546655570 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65964706 | CGGAAGGCATGAGGT[C/T]CCTCCTTGCTGGTAT | 9092 |
rs546979464 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65979139 | GTTGGATCTTTGGTT[A/G]GGTGTGGCACAGAGT | 9092 |
rs547163677 | snp | A/C/T | 0.00557933 | 0.0525774 | intron-variant | SART1 | GRCh38.p7 | 11:65974402 | AAAAACCATATCAGC[A/C/T]GGGTGTGGTGGTTCA | 9092 |
rs547214860 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65969652 | ATTCCTGAGCTCAAA[C/T]GATCCTCTCGCCTCC | 9092 |
rs547308852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973515 | AGGTCCAAGCCTGAC[A/G]GTAGCGAGTAGGAGT | 9092 |
rs547361658 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65979744 | CACGTACACCCACAT[A/G]CTTCTCAGATGGCTC | 9092 |
rs547426809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65962180 | GCAGTGTCAGCGAAG[C/G]TCTTCAGGCCAGGAA | 9092 |
rs547720205 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65975019 | CACTCCAGCCTGGGC[A/G]ACAAAGTGAGACTCT | 9092 |
rs547886190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65976856 | GAGCCTCAGCCTCCT[C/T]ATCCAGAGTGGGCTC | 9092 |
rs548186561 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65970707 | AGAGCAGATACACCC[G/T]GGGAGAAGAGCAGGC | 9092 |
rs548219759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970232 | TCAGTAGGCATCTGG[C/T]GAAATCAGGGCCTTC | 9092 |
rs548337900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972168 | CTCCAGTAAAAATCC[A/C]AATAGGGATTATTTT | 9092 |
rs548466532 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65978247 | GCACTCTCGTAGGCC[A/G/T]CCCGACCGTCCTGCC | 9092 |
rs548502130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65964812 | TTAGATGGACTGGAA[C/G]ATGTGCACACTTGCT | 9092 |
rs548592396 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960696 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTGCACT | 9092 |
rs549073557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973544 | GTAAAGGACATGGAG[C/T]GGCCAGAGTCCTCAG | 9092 |
rs549098718 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960295 | GGATCCTTAAAGGGG[C/T]GCATACAACATAGCC | 9092 |
rs549186014 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979232 | GAGCGAGCCCGGGTC[C/T]TCTAAGGCTCCTTCC | 9092 |
rs549348095 | in-del | -/T | 0.217551 | 0.247885 | intron-variant | SART1 | GRCh38.p7 | 11:65975102 | GATGTCCTGGAAGAC[-/T]TTTTTTTTTTTTTTT | 9092 |
rs549674041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968833 | CTTGACCCCATGGTC[A/G]TCGCTGCCCCAGAGG | 9092 |
rs549686855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968179 | GGTCTCCAACTCCTG[A/C]CCTCATGATCTGCCT | 9092 |
rs549686893 | snp | G/T | 0.000221477 | 0.0105209 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961739 | TCCCATTTTGCGTTG[G/T]CTGGGCTCGGCGGCA | 9092 |
rs549835993 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65969929 | GGGTTTCACCGTGTT[A/G]GTCAGGCTGGTCTCA | 9092 |
rs549839251 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980506 | TGGGAACAGTGGCAC[A/G]TGCCTGTAATCCCAG | 9092 |
rs549851887 | snp | C/T | 2.8129e-05 | 0.00375016 | intron-variant, utr-variant-5-prime | SART1 | GRCh38.p7 | 11:65964019 | AGCTGGAGCCAACGA[C/T]GCTGGCTTCTTGGCC | 9092 |
rs549910292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65975834 | TGGCTGGGCATCTGC[A/G]ACAGGAGGGAAAGCA | 9092 |
rs550124980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65977384 | TGCCATTTCCCTGGC[A/C]AGTGACCCTTGGCAA | 9092 |
rs550151264 | snp | C/T | 1.73592e-05 | 0.00294606 | intron-variant | SART1 | GRCh38.p7 | 11:65976631 | TGGCTGGGGCCTGGG[C/T]CGACCCTGGTCTTTT | 9092 |
rs550173304 | snp | C/T | | | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980262 | TAGCCTGAAAATGCA[C/T]GGTTGGCACTGACAC | 9092 |
rs550308031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972004 | TCTCAGCTCACTGCA[A/G]TTTCCACCTCCTAAA | 9092 |
rs550431883 | in-del | -/ACAA | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65975062 | AATAAAAATTAAAAG[-/ACAA]ACAAACAAACAAATG | 9092 |
rs550517646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970608 | GTCAAGGCAGCCCAT[A/G]GCCGATTGTTCTGGT | 9092 |
rs550684589 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65963989 | CTGGTGAGGGGCCCT[C/T]ATTTTTGTTCCTGCA | 9092 |
rs550817129 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960096 | AGCTTTGGCTCTTTT[A/G]GTTCCCCCCACCCAG | 9092 |
rs550897793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65967108 | CCAGTGGAATTGAGA[C/T]AGTAACCACCCCACA | 9092 |
rs551133211 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979296 | GCCGGCTCTCTGATA[A/G]AAAGTGGAAGGCGGT | 9092 |
rs551233761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972887 | CATAGAAATTGAGAA[C/T]GTGGCCGGGCGCGAT | 9092 |
rs551453812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968318 | GGGGATCCTTTCCTT[A/G]CCTCTCTCTTCTGTG | 9092 |
rs551490558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65962318 | TGGGCAACAAAGCGA[C/G]ACTCTGTCTCAAAAA | 9092 |
rs552043086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65963021 | CACTTTTGGGGTTGT[C/T]AAGGTTGATGGTAAT | 9092 |
rs552176648 | in-del | -/TAGA | | | intron-variant | SART1 | GRCh38.p7 | 11:65964798 | CTGGCTGTGAGTTGT[-/TAGA]TGGACTGGAAGATGT | 9092 |
rs552181689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969474 | TTGTTTTAAGAAACA[A/G]GGTCTCGCTCGGTTG | 9092 |
rs552211504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65975942 | ACCTGCTTTCTTGGT[A/G]AAGCAGGAAGCGAGA | 9092 |
rs552323027 | snp | C/T | 8.33063e-05 | 0.00645339 | intron-variant | SART1 | GRCh38.p7 | 11:65977009 | CCCCGCCACGTGTCC[C/T]GTAGTTCTCTGCTTC | 9092 |
rs552323775 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65969007 | AGAAGCCAAGAAAGC[A/G]TGTCCAGGAGAGGGA | 9092 |
rs552788434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65965625 | GCCCTTTTTGCACTC[C/T]GCTTGGTAGAGCCCT | 9092 |
rs553377219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972898 | AGAACGTGGCCGGGC[A/G]CGATGGCTCACGCCT | 9092 |
rs553387944 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960444 | GACAGAGTCTCGCTC[C/T]GTCACCAGGCCGGAG | 9092 |
rs553399245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973198 | GAAATTGAGAACGTA[A/C]GTTTTTTGTTTTTTG | 9092 |
rs553449212 | snp | C/G | 1.66521e-05 | 0.00288544 | intron-variant | SART1 | GRCh38.p7 | 11:65978941 | GAGGCTGGTGGGGTA[C/G]GGTGTGGTGGGGAGG | 9092 |
rs553489414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65972464 | ATCAAATTAAGGAAA[C/T]TACATTTATAACTTT | 9092 |
rs553491579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65978390 | CTGCCCCCATGGCAG[C/T]GCATCCACTAGCCAA | 9092 |
rs553633934 | in-del | -/AGC | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65976264 | AGTTAGGCGGCAGAT[-/AGC]AGCTGGGCCTGCATG | 9092 |
rs553663694 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961076 | TGGTAGCGTACTCTC[A/G]TAGTCCCAGCTACTG | 9092 |
rs553695614 | snp | G/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65962018 | CGGAGCAGCACGCAC[G/T]GGCGGGAGCGCAGCC | 9092 |
rs553778380 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979336 | TCATCACCCTGCTCT[C/T]TCCTGGCCTCGGGGG | 9092 |
rs553959418 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65970895 | GCTGAGGAGGGGGAT[G/T]GTGGGATTCAGGAGC | 9092 |
rs554230676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65963460 | CAGGATGGGAATGCA[A/G]GAAAGGAAGAGTTTT | 9092 |
rs554579369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969611 | TGCGCCTGTGGGTCT[C/T]AGTGTGTTGCCCGGG | 9092 |
rs554584536 | snp | A/G/T | 0.00119752 | 0.0244452 | intron-variant | SART1 | GRCh38.p7 | 11:65970369 | TGTAAGCAGCATCCA[A/G/T]TCAAGTTTCCCACCC | 9092 |
rs554817787 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65970791 | GAATTCATGAGCTGC[G/T]GAGGGAGGGGGATGG | 9092 |
rs554865168 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65968104 | ACAGGCGCACGCCAC[C/G]AGACCCGGCTAATTT | 9092 |
rs554956130 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SART1 | GRCh38.p7 | 11:65972661 | AGCCTCAGCTACGCC[A/G]GAGGCTAAGGCAGGA | 9092 |
rs555188697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65975809 | GAGGGGAGATGGTAA[C/T]CATTGTGTGTGGCTG | 9092 |
rs555277187 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65979872 | AATCACAGCACTTTA[A/G]GAGGCTGAGGCAGGA | 9092 |
rs555491337 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65978251 | TCTCGTAGGCCGCCC[A/G]ACCGTCCTGCCCTAC | 9092 |
rs555652627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65977928 | TTTGCAGGCGGAGGC[C/T]CGGCCTGCCACAGGG | 9092 |
rs555763221 | snp | C/T | 6.671e-05 | 0.00577499 | intron-variant | SART1 | GRCh38.p7 | 11:65967253 | TCTCGCCCCTCTTCC[C/T]TTAAGGTGACCTTTA | 9092 |
rs555782802 | snp | C/T | 0.000323468 | 0.0127133 | intron-variant | SART1 | GRCh38.p7 | 11:65967853 | GCAGGGTGACTGCGT[C/T]AGCAGTCACCTGTCC | 9092 |
rs555806417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65973137 | CGAGATCGCACCACT[A/G]CACTCCAGCCTGGGT | 9092 |
rs555841457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65973800 | TGATGAGCTACAGCC[A/G]TGTGCATCAGGGTTA | 9092 |
rs555942493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65963309 | CATACCACAGGAGAT[C/T]AAGCAAAACCAGAAC | 9092 |
rs556002689 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979350 | TCTCCTGGCCTCGGG[A/G]GCTGCACAGGTCACT | 9092 |
rs556167038 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65974462 | GAGGTGAGTGGATCA[C/T]TTGAAGCTGGTTTTG | 9092 |
rs556351316 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65972979 | GATGAGACCATCCTG[C/G]TCAACACAGTGAAAC | 9092 |
rs556402703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968408 | GTGAACAGGATAGCC[A/T]TGGGGCCCTGGGCTC | 9092 |
rs556672452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65976103 | AGTTTGAGGCTGAGG[C/T]AGTGTGTGAGGGGCT | 9092 |
rs556963417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65964875 | TTTTTCTTTAAAGCA[C/T]GATTTGAGGGGCTTT | 9092 |
rs557103231 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | SART1, TSGA10IP | GRCh38.p7 | 11:65959901 | CAGCCAGCCTGACAG[G/T]CACTACAACCCCAGC | 9092 |
rs557118831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972321 | CCCAGTGGGAAGAGT[C/T]GCTCGTCAGTGCAGC | 9092 |
rs557276842 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SART1 | GRCh38.p7 | 11:65971667 | TGGTGGGATTAATGC[C/T]CTGAAGCAGTGGATG | 9092 |
rs557291420 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65976256 | CAGAGTGGAGTTAGG[C/T]GGCAGATAGCAGCTG | 9092 |
rs557368285 | snp | C/G/T | 1.66045e-05 | 0.00288132 | intron-variant | SART1 | GRCh38.p7 | 11:65965795 | GTGAGGCTGCAGCAG[C/G/T]GGTGGTACAGGGGAC | 9092 |
rs557506309 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SART1 | GRCh38.p7 | 11:65977172 | AGGCAGGGCCCCCTC[C/G]GGTCCCCTCTGCTGC | 9092 |
rs557539048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973620 | GAATGTGTGCGTGCC[C/T]GGGGCCCACCCCACA | 9092 |
rs557614243 | snp | A/G | 9.91408e-05 | 0.00703993 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65978822 | GAGCTCCAGCGACAC[A/G]CCCCTGGGCACCGTG | 9092 |
rs557634116 | snp | A/G | 0.000187886 | 0.0096906 | intron-variant | SART1 | GRCh38.p7 | 11:65965015 | CCCCTGAGCTGGAAG[A/G]GGGCAGGGTGAGTGG | 9092 |
rs557639370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65973169 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAGA | 9092 |
rs557650553 | in-del | -/GGGCCATGCAATGCCCC | 0.00279162 | 0.0372561 | intron-variant | SART1 | GRCh38.p7 | 11:65977956 | GGGAGGCCAAGCCCA[-/GGGCCATGCAATGCCCC]GGGCCATGCAATGCC | 9092 |
rs557676171 | snp | A/G | 3.30284e-05 | 0.00406363 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967284 | AAAAGACCAAGCGGA[A/G]GGTGAAGAAAATCCG | 9092 |
rs558152094 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65961830 | AGGCGGCCGGGACGA[C/T]GGCGGCGGCCGGCAC | 9092 |
rs558227079 | snp | A/G | 0.000292298 | 0.0120857 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65967734 | GGAGGAGGACGAGGC[A/G]GAGCTGGAGCTGCAG | 9092 |
rs558238982 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65968449 | CTTTCTAGAGTGTGT[C/G]GGGGAGAGCGTGGGG | 9092 |
rs558276869 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961261 | GTTCCCTGACGATAC[A/T]GGTTATAGCGGGTCT | 9092 |
rs558414393 | snp | G/T | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961534 | TAATTCCGCTTCCCT[G/T]GAGGAGCGCATGCGC | 9092 |
rs558435010 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65980002 | CCTGTAGTCCCAGCT[A/G]CTTGGGATGCTGAGG | 9092 |
rs558614355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970239 | GCATCTGGCGAAATC[A/G]GGGCCTTCTCCCGCA | 9092 |
rs558667215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65974629 | GGTTGCAGTGAGCCT[A/C]TATCGCCCCATTGCA | 9092 |
rs558668906 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980598 | AACACGGTAAAACTC[C/T]GTCTTTGACTAAAAA | 9092 |
rs558859990 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65972302 | CCCCGAGACAGAATC[A/G]TGTCCCAGTGGGAAG | 9092 |
rs559071951 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SART1 | GRCh38.p7 | 11:65974911 | TGGGCGTGGTGGCGG[C/G]CGCCTGTAGTCCCAG | 9092 |
rs559514382 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65970311 | GCAGCTCGCATGCCA[A/G]CATTTTCCAGTTATC | 9092 |
rs559549829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65977225 | TGGAGCCAGCTGTCC[A/G]GCCCAGAGCCACTCC | 9092 |
rs559636078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65971793 | TGGGTAATGAGGGAC[A/G]TAACAGAGAATGATG | 9092 |
rs559670827 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65972980 | ATGAGACCATCCTGG[C/T]CAACACAGTGAAACC | 9092 |
rs559700576 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960021 | ACGGGTTGGAAGTTG[A/G]AGGTGGCAGGTGGGT | 9092 |
rs559725195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65978145 | TCAGACAGGCACTCG[A/G]GACCTCTGCCCTCCT | 9092 |
rs559830933 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SART1 | GRCh38.p7 | 11:65972801 | AAAAAAAAAAAAAAA[A/C]CAAGAAACCCACAGG | 9092 |
rs560051151 | snp | C/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65968305 | GCCTGCTTTAGTAGG[C/G]GATCCTTTCCTTGCC | 9092 |
rs560251766 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65966994 | CCTCAGTGGGTAAGA[A/G]CAGGACTCTGGAGCC | 9092 |
rs560269380 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961400 | AAGACCGTGAGGTAG[C/T]GAACACCCCGTTGCC | 9092 |
rs560560472 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979565 | AGGGCTGAGCTCAGT[G/T]CCTCCTGGGAGACTT | 9092 |
rs560560925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65962204 | CCAGGAAACCCCCAA[A/G]CTGTTTACCAGCTCT | 9092 |
rs560619038 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SART1 | GRCh38.p7 | 11:65968110 | GCACGCCACCAGACC[C/T]GGCTAATTTTTATAT | 9092 |
rs560742491 | snp | C/T | 0.00128172 | 0.0252828 | intron-variant | SART1 | GRCh38.p7 | 11:65963974 | CAGCAGGCCCAGGTG[C/T]TGGTGAGGGGCCCTC | 9092 |
rs561269813 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65968882 | GCTCACATGTTCTGT[A/G]TTTGTTGATTCATTC | 9092 |
rs561558855 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65977299 | GCTCCACACCTGCTT[C/G]GGGAAGGAGAGGGGA | 9092 |
rs561718114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65976859 | CCTCAGCCTCCTCAT[C/T]CAGAGTGGGCTCTGC | 9092 |
rs561818933 | snp | A/T | 3.30666e-05 | 0.00406598 | intron-variant | SART1 | GRCh38.p7 | 11:65965868 | AGGGAGGTTCCTGAC[A/T]CGCCGATTCTTCCCT | 9092 |
rs561904217 | snp | C/T | 6.68393e-05 | 0.00578059 | intron-variant | SART1 | GRCh38.p7 | 11:65966304 | GGTGGCTCAGTGGCT[C/T]TTCAGGAGCCAGCCT | 9092 |
rs562186793 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961447 | AGGGAGGCCGGGGAG[A/G]AACTTAAAGCCACGA | 9092 |
rs562421314 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65962074 | GAAGCGGGAGAAGCG[C/T]GATGACGGCTACGAG | 9092 |
rs562487195 | snp | A/G | | | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961590 | CACCCGACCCGAGAC[A/G]GCGCGAATGTGCAGT | 9092 |
rs562502156 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65968671 | GCAGCAGGTGGACAG[A/G]CTGGCATTTAGGCAG | 9092 |
rs562622461 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65973289 | GCCCATATATACCAC[C/G]AAGAATGGGTTGGTG | 9092 |
rs562896901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969001 | CTAGGAAGAAGCCAA[A/G]AAAGCGTGTCCAGGA | 9092 |
rs562930361 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SART1 | GRCh38.p7 | 11:65974772 | CAGGCGCGGTGGCTC[A/G]CGTCTGTAACCCCAA | 9092 |
rs563027847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SART1 | GRCh38.p7 | 11:65962864 | CAGAACTCAGCACTT[A/G]TATGAGGGTGGGAAG | 9092 |
rs563046172 | in-del | -/A | | | intron-variant | SART1 | GRCh38.p7 | 11:65972786 | ACAAGATCCTGTCTC[-/A]AAAAAAAAAAAAAAC | 9092 |
rs563249232 | in-del | -/C | 0.00239521 | 0.0345234 | intron-variant | SART1 | GRCh38.p7 | 11:65969663 | CAAACGATCCTCTCG[-/C]CTCCACCTCCCAAAG | 9092 |
rs563457471 | snp | C/G | 0.000105094 | 0.00724817 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976431 | CTGGAGTCTCGCCAG[C/G]GGGGCTGGGAGGAGG | 9092 |
rs563543036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970109 | CAGTGAACACCTTTG[A/T]CCTCTAGAGTCAGTA | 9092 |
rs563695525 | snp | C/T | 5.96356e-05 | 0.00546024 | intron-variant | SART1 | GRCh38.p7 | 11:65977947 | CCTGCCACAGGGAGG[C/T]CAAGCCCAGGGCCAT | 9092 |
rs563858391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65977462 | GCTTTCCAGAGGCAA[A/G]GAAAGGGAGGTGCCC | 9092 |
rs564069140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972021 | TTCCACCTCCTAAAG[A/G]TGCTCTGTCCACATA | 9092 |
rs564143092 | snp | C/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65969227 | AATGCTGTGCTGTTA[C/T]AGGGAAAACAGCCAA | 9092 |
rs564275444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65966933 | GATTCTGTCCACAGG[G/T]TGACTGTGTGAACGT | 9092 |
rs564280501 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | SART1, TSGA10IP | GRCh38.p7 | 11:65960618 | TTACCATGTAGGCCA[A/G]GATGGTCTCGATCTC | 9092 |
rs564628147 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SART1 | GRCh38.p7 | 11:65979533 | GGCTGGGAGTATTTG[G/T]TGCACGCGGTATGGG | 9092 |
rs564735825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65962583 | GTGAACACAAAGGAC[C/T]CTGTACTGTAGTCTC | 9092 |
rs564773893 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980351 | TCTGTATTCTCTATA[G/T]TTTGACATCTGACTC | 9092 |
rs564868703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65962133 | GGGCGGGTCGGGCGG[A/G]GGTCCCGGAACGCGT | 9092 |
rs564898603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65975687 | AAAAAATGAATGTAA[C/T]ATAAAATGAAAGAGG | 9092 |
rs564975548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65967981 | TTGAGACAGAGTTTC[A/G]CTCTTTCGCCCAGGC | 9092 |
rs565308684 | snp | C/G/T | 4.96548e-05 | 0.0049825 | intron-variant | SART1 | GRCh38.p7 | 11:65964486 | CTGTGTCTTTAATAG[C/G/T]CCCTAACACTTGTAT | 9092 |
rs565327921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969133 | GGCTGAACCCGGGAC[A/G]GAGGCCAGGCTTACT | 9092 |
rs565559208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65963716 | TGAACTTCTGACCTC[A/G]TGATCCATCTGCCTC | 9092 |
rs565669187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65976038 | CTAGAGTCCTGAAAC[C/T]GGAGTTTGTCGGGGG | 9092 |
rs565698575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65964768 | AGTTGGAGCTGTGGC[C/T]GTCGCATACTCACTC | 9092 |
rs565705871 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65969548 | TTGAACTCCTGGGCT[C/T]AAGGGATCCTCCTGC | 9092 |
rs565714376 | snp | A/G | 1.72157e-05 | 0.00293386 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65976559 | TCGCGAGGAGCAGGA[A/G]GAGCTCATGGTGCGT | 9092 |
rs565732348 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SART1 | GRCh38.p7 | 11:65980599 | ACACGGTAAAACTCC[A/G]TCTTTGACTAAAAAT | 9092 |
rs565783420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65975315 | ACCTTATTGTCCAGG[C/G]TGGTCTCGAACTCCT | 9092 |
rs565925659 | snp | C/T | 0.000132396 | 0.00813512 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977619 | GCCCCCAACAAGTCG[C/T]TGCCCTCAGCCGTGT | 9092 |
rs565925763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970706 | GAGAGCAGATACACC[C/T]TGGGAGAAGAGCAGG | 9092 |
rs565958852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972101 | TTCCTAGATAGGACA[A/G]TATATTGTCAAGATG | 9092 |
rs565978227 | snp | A/G | 1.66799e-05 | 0.00288785 | missense, utr-variant-5-prime, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65964092 | CCAGCTCCAAAACTA[A/G]CTCAGGCGATGCCTC | 9092 |
rs566033145 | snp | C/T | 0.000231646 | 0.0107596 | synonymous-codon, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65977043 | CACCACCATCCTGGA[C/T]GAGGAACCGATCGTG | 9092 |
rs566083988 | snp | A/T | 6.89834e-05 | 0.00587256 | missense, nc-transcript-variant | SART1 | GRCh38.p7 | 11:65966453 | CTGATGGCCTGCGGG[A/T]GCGGGAGCTGGAGGA | 9092 |
rs566306362 | snp | C/T | 0.00414676 | 0.0453452 | upstream-variant-2KB, intron-variant | SART1, TSGA10IP | GRCh38.p7 | 11:65959807 | AGGGGCCTCTATCTG[C/T]GTCTTGAAGGAGCCA | 9092 |
rs566458236 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65966056 | AAGTGTGAATGGCCA[C/G]TGCTCTGTGCTGCCC | 9092 |
rs566511005 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960213 | ATGTTGGGTCCTATA[A/C]ATTCAAGCATGAATA | 9092 |
rs566579350 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65972438 | TCAAAGTAAAAACTT[A/C]ACATTTCGGAATCAA | 9092 |
rs566860856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SART1 | GRCh38.p7 | 11:65973129 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 9092 |
rs566951370 | snp | A/G | | | intron-variant | SART1 | GRCh38.p7 | 11:65970044 | AGGTTTTTTAAACAT[A/G]TGAGCCACACCCCAC | 9092 |
rs566956998 | snp | G/T | 7.38075e-05 | 0.0060744 | intron-variant | SART1 | GRCh38.p7 | 11:65978713 | CCTTGGGGATGTGGG[G/T]GGCCCTGTGCCTGCC | 9092 |
rs567007033 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961673 | GCGACGGAAGCAGCC[A/G]CTCTTAGTTTCCGGC | 9092 |
rs567028341 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960284 | GGAGAGGGGGTGGAT[C/T]CTTAAAGGGGCGCAT | 9092 |
rs567067338 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SART1 | GRCh38.p7 | 11:65961107 | GGAAGGCTGAGGTGG[A/G]AGGATCACTTGAGCC | 9092 |
rs567275343 | snp | A/T | 0.000121293 | 0.00778664 | intron-variant | SART1 | GRCh38.p7 | 11:65963980 | GCCCAGGTGCTGGTG[A/T]GGGGCCCTCATTTTT | 9092 |
rs567437259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65963199 | ATGTTACCAAAAAAA[A/G]GAGACAGAGTAACCA | 9092 |
rs567518339 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65979782 | TTAAGATTTTAAAAA[C/T]GAAACCAAAAAATAA | 9092 |
rs568066835 | snp | A/G | 6.92953e-05 | 0.00588582 | intron-variant | SART1 | GRCh38.p7 | 11:65976604 | CCCTCTGCTTCCCTC[A/G]GCTGGGTGGGCTGGC | 9092 |
rs568090977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65970544 | TCATTTATTTCAGGA[A/G]GGAAGGTGGGGAGGG | 9092 |
rs568092939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65964839 | TGCTGCAGACTGCGC[A/T]GTGCGGGGGTGGGTT | 9092 |
rs568379848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65965511 | TGACGGCACTGAGGC[A/G]GGGGCCAACCCCAGA | 9092 |
rs568396310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65977712 | GCTTGGAGCTTCGGG[A/G]CCACAGCAGGCGGCA | 9092 |
rs568630328 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | SART1, TSGA10IP | GRCh38.p7 | 11:65960299 | CCTTAAAGGGGCGCA[C/T]ACAACATAGCCTAAC | 9092 |
rs568631031 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SART1 | GRCh38.p7 | 11:65972873 | TGAACGTGTAACTAC[A/G]TAGAAATTGAGAACG | 9092 |
rs568680519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65972246 | GCAGTGTGGGATTGC[A/G]TAAGGATAGACTAAC | 9092 |
rs569012988 | snp | G/T | | | intron-variant | SART1 | GRCh38.p7 | 11:65972631 | AATTAGCTGGGCATG[G/T]TAGCATGTGTCTGAA | 9092 |
rs569233272 | snp | A/C | | | intron-variant | SART1 | GRCh38.p7 | 11:65970092 | AAGTGGAAAGCCTAT[A/C]ACAGTGAACACCTTT | 9092 |
rs569470995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65963319 | GAGATCAAGCAAAAC[C/G]AGAACCGAAAAGAAC | 9092 |
rs569552969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65962211 | ACCCCCAAGCTGTTT[A/G]CCAGCTCTATTAAAT | 9092 |
rs569561364 | snp | C/T | 1.79338e-05 | 0.00299443 | intron-variant, utr-variant-5-prime | SART1 | GRCh38.p7 | 11:65964038 | GGCTTCTTGGCCCTG[C/T]GTTCAGCTCCTGAGC | 9092 |
rs569665829 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SART1 | GRCh38.p7 | 11:65974964 | AGAATGCTGTGAACC[C/T]AGGAGGCGGAGCTTG | 9092 |
rs569681210 | in-del | -/TGG | 0.0256215 | 0.110247 | intron-variant | SART1 | GRCh38.p7 | 11:65971530 | AGCTGAGGAGGGGGA[-/TGG]TGGGATTCATGAGCT | 9092 |
rs569711169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65969435 | GCCTGCACATTAGAC[C/T]CACCTAGGAGGTTGT | 9092 |
rs569774197 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SART1 | GRCh38.p7 | 11:65979985 | AGGCGTGGTGGTGAG[C/T]GCCTGTAGTCCCAGC | 9092 |
rs569870417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65975862 | GCAGAGGGTGCTGGT[C/G]CCCGTGTGGGGGTCG | 9092 |
rs569955100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SART1 | GRCh38.p7 | 11:65968835 | TGACCCCATGGTCGT[C/T]GCTGCCCCAGAGGCA | 9092 |