SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3019 | snp | C/T | 0.0966517 | 0.197444 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699833 | GTAGTTCTAGAACTT[C/T]AGAAGCTCCATCTTT | 22954 |
rs700150 | snp | A/C | 0 | 0 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692173 | CCATGGGGTGGTTCT[A/C]TAGATATCTCCATTT | 22954 |
rs803894 | snp | C/T | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687423 | ACTGGGGACCGCGGC[C/T]GGAGTCGTGGGCCGT | 22954 |
rs803895 | snp | A/T | 0.0984431 | 0.198823 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685979 | ACTTTGCACCCGTTT[A/T]AAATTTTTTTTTTTC | 22954 |
rs803896 | snp | C/T | 0.467845 | 0.122652 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685471 | AGGAGTTTACCTTGC[C/T]CACTGCCTAGACAGA | 22954 |
rs803930 | snp | A/G | 0.273318 | 0.24891 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696652 | CTTAGTTTTTATTTC[A/G]TTTATAGTACCACTT | 22954 |
rs803931 | snp | C/T | 0.385168 | 0.210309 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696405 | ATTTTATTTTCTCCA[C/T]CTTTAAAATGGAAAA | 22954 |
rs803932 | snp | A/G | 0.394904 | 0.203722 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695741 | TAGGTCACTGTCAAC[A/G]TATACCCCAAATCAG | 22954 |
rs803933 | snp | C/T | 0.185155 | 0.241444 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695434 | GCAATCTGACAAATA[C/T]ATAGCAGCAGACATG | 22954 |
rs803934 | snp | C/T | 0.286564 | 0.247312 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695402 | ACAATTATCTAAAGT[C/T]AATCCTTCCTCCCTG | 22954 |
rs803935 | snp | C/G | 0.343924 | 0.231686 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694675 | GACCATCCTGGCTAA[C/G]ACGGTGAAACTCCGT | 22954 |
rs803936 | snp | A/G | 0.095934 | 0.196885 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694387 | GTTCTCTCTTCTATC[A/G]TCTGGGACAACAGAC | 22954 |
rs803937 | snp | A/G | 0.095934 | 0.196885 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692534 | CTCAGTTTATCTATG[A/G]AAAGGGACTTTAAAA | 22954 |
rs803938 | snp | A/T | 0.200182 | 0.244986 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691790 | ATCACTGTGCCACCA[A/T]AGGCCACTCGTTAGC | 22954 |
rs803939 | snp | A/G | 0.476314 | 0.106217 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691176 | GATGAGAATTTTGGG[A/G]AGACTAGCAGAGACT | 22954 |
rs803940 | snp | A/G | 0.218151 | 0.247963 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690860 | GCTAACACTCTTAAA[A/G]CAACTACTATTTATT | 22954 |
rs803941 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690688 | attcaaatcccagTA[A/T]CAACTCCCAGCCATA | 22954 |
rs803942 | snp | C/T | 0.449218 | 0.151037 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690026 | TGTTTCTGAACTGGC[C/T]TCAGCAACCCTGTAG | 22954 |
rs803943 | snp | A/T | 0.449091 | 0.151204 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689790 | TCCTTATCTAGCCCC[A/T]GGTCTTGGTCTAAGG | 22954 |
rs803944 | snp | C/T | 0.199564 | 0.24486 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688959 | tcctaggagacaaag[C/T]cagacttggttaaga | 22954 |
rs811457 | snp | C/G | 0.0667028 | 0.170006 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687191 | CGGGGCAAGGCGGCC[C/G]TGCAGGGGTGAGCTT | 22954 |
rs1058686 | snp | A/T | 0 | 0 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697821 | ATCTGCATGGAGTCC[A/T]TCACAGAAGAGCAGC | 22954 |
rs1058687 | snp | C/T | | | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699557 | CCATTTTCCTAAGGG[C/T]GGGGGCTATAGTGTC | 22954 |
rs1661300 | snp | A/G | 0.194975 | 0.243869 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698996 | CATTGATAGCTTTGT[A/G]CTAAGCTTCCTTGGG | 22954 |
rs1661307 | snp | G/T | 0 | 0 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701131 | ATATATCTTACTCTA[G/T]GTGCAGGGCTGATGG | 22954 |
rs1661309 | snp | A/G | 0.201418 | 0.245234 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701341 | AAAGCCCCATATTCT[A/G]ATTATGAAATTGCAT | 22954 |
rs2281627 | snp | C/T | 0.392325 | 0.205532 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700910 | ACTATTATGTAAAGA[C/T]AATAATCCAAATCTT | 22954 |
rs2900134 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693542 | GCTAGTACAGTATGG[A/T]ATGGGATGTACAGTA | 22954 |
rs3215687 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687522 | CGGATCTGGGGGGGG[-/G]CAGGACTAGGGTGGG | 22954 |
rs3747833 | snp | A/C/G | 6.59506e-05 | 0.0057421 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698402 | GTCCAATAGTCAAGT[A/C/G]GTAGAGGAGCAGAGT | 22954 |
rs3747834 | snp | C/G | 0.00141788 | 0.0265881 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698512 | CACTACTGGAGGAGA[C/G]AGCTGATGAGGAGGA | 22954 |
rs3747835 | snp | C/T | 0.00286212 | 0.037721 | TRIM32, ASTN2 | 9 | allele_origin=T(germline)/C(germline) | 9:116698964 | TTTTTGAAGGAAATC[C/T]GCCGCAGCCCCAGTG | 22954 |
rs3789308 | snp | A/T | 0.203882 | 0.245709 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695358 | ACTAGATGCATAGTT[A/T]CCCTTGCAGTACAAA | 22954 |
rs7852360 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690560 | TCCCTCCATCTTGTC[C/T]TTCTGGTAAAACAAT | 22954 |
rs10712697 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691431 | TTCTAGGTCCTGCAG[-/T]TTTAGAGGAAGACAG | 22954 |
rs10983304 | snp | C/T | 0.0533436 | 0.154358 | upstream-variant-2KB, intron-variant, missense | TRIM32, ASTN2 | GRCh38.p7 | 9:116686700 | GTTCCCGGGTACCTT[C/T]AGTCTGCAGGGACAG | 22954 |
rs10983305 | snp | A/C | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693829 | ACTGAAGTCAAATTG[A/C]CCTTCTATCTGAGTC | 22954 |
rs10983306 | snp | A/C | 0.186737 | 0.241863 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697004 | GGTTTTCTTTGCTTA[A/C]AGTACCTTTATCCTC | 22954 |
rs10983307 | snp | C/T | 0.187053 | 0.241946 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701599 | AAATGAGGCCAGGAA[C/T]CCTCCAGCTGTCTGT | 22954 |
rs11340280 | in-del | -/T | 0.463559 | 0.129972 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694628 | ACCACGCCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 22954 |
rs11400163 | in-del | -/A | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696966 | AAAAAAAAAAAAAAA[-/A]GCCTCCACACTTTTG | 22954 |
rs11556350 | snp | A/G/T | 6.59163e-05 | 0.00574054 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697948 | GCAGCAAGATTACCC[A/G/T]CATAACCAGCTTGAC | 22954 |
rs11790014 | snp | C/G | 0.338296 | 0.233889 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686951 | TCAGATGGAAAAACA[C/G]ATTCAGTAAGGTGCC | 22954 |
rs11793648 | snp | A/G | 0.337614 | 0.234145 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690999 | ATCACAGTTCACTGC[A/G]GCCTCAACCTCCTAG | 22954 |
rs12237968 | snp | G/T | 0.180383 | 0.240111 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689601 | CGTATATTCCCGCTT[G/T]CCTTGCTTCTTCCTT | 22954 |
rs12342207 | snp | C/G | 0.380919 | 0.21298 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687330 | GCGTGCGCAGAGGGA[C/G]GCAGGCGGGTGGGCT | 22954 |
rs12685304 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696825 | TAGGAGGATAGATGC[A/G]TGGAAAATGTGTATT | 22954 |
rs16933828 | snp | A/G | 0.174932 | 0.238463 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690904 | AGGCAGTGCTGGAAG[A/G]GAACTAAGTGTTGCT | 22954 |
rs16933830 | snp | G/T | 0.0952156 | 0.196321 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691622 | TCAGGAGCATGCCTG[G/T]GTTTCCCTATAAGCC | 22954 |
rs16933832 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695698 | TGCTGACTTTATCAT[A/G]TGCCTCAACTTGCTA | 22954 |
rs16933835 | snp | A/G | 0.0287284 | 0.116357 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700293 | TACACAAGCCCTTTA[A/G]GAAGCAGTACCTCTC | 22954 |
rs16933836 | snp | A/G | 0.0252325 | 0.109451 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701586 | GCAGGCTGAAGGTAA[A/G]TGAGGCCAGGAATCC | 22954 |
rs17220476 | snp | A/G | 0.202959 | 0.245534 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689841 | GCAGGATGAGGTGCA[A/G]CGGACTATAGGGTGA | 22954 |
rs34052323 | in-del | -/G | 0.0287284 | 0.116357 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693540 | GTGCTAGTACAGTAT[-/G]GTATGGGATGTACAG | 22954 |
rs34641147 | in-del | -/C | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695067 | CTATAAGGCAGCATT[-/C]CCCCAGAGCGTGGTC | 22954 |
rs34641332 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688879 | AACAACAACCACCAG[-/A]AAAAAAAAAAGGGAA | 22954 |
rs34961636 | in-del | -/A | 0.462472 | 0.13174 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696951 | CTCTGTGACATGATT[-/A]AAAAAAAAAAAAAAA | 22954 |
rs35041669 | in-del | -/G | 0.202959 | 0.245534 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688642 | CCACCGGTCCCCCGG[-/G]CCCACTGAAAGTGGT | 22954 |
rs35331277 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688299 | ATTGAATCGTGGGGT[-/G]GGAGATGTCCTAACT | 22954 |
rs35662624 | in-del | -/T | | | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698199 | GACTTTGGAGAGAAG[-/T]TAACTCGTCTGCGGG | 22954 |
rs35783369 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688991 | CATTAGGCAATGTCT[-/G]GGAGATGTTTTTTGG | 22954 |
rs35848094 | in-del | -/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693663 | GAAACAGACATTCAA[-/G]GGGATCATGAAGGGA | 22954 |
rs35891915 | snp | A/G | 0.202959 | 0.245534 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689947 | AGTAACTACTGTTCT[A/G]TATGGTCTCTTTTGG | 22954 |
rs35904234 | in-del | -/T | | | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699110 | CTCAAGGTATATACC[-/T]TTGGATGGCCACTGC | 22954 |
rs41266677 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700781 | TCTTTTAATTAAATA[C/T]GGAATTTTGGAGATG | 22954 |
rs41308922 | snp | A/G | 0.135143 | 0.222054 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686877 | CACTGCCCTTCCTAG[A/G]GAGTCCCGGTTCTCG | 22954 |
rs56666915 | in-del | -/CTTT/TTTT | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694460 | AGTTGTAATTTCTCT[-/CTTT/TTTT]TTTTTTTTTTTTTTT | 22954 |
rs57108535 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697145 | CATTATGTGGACTTG[C/G]ATGTTATACTTATTC | 22954 |
rs57116587 | in-del | -/A | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685982 | AAAAAAAATTTTAAA[-/A]CGGGTGCAAAGTCTC | 22954 |
rs57186221 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697015 | CTTAAAGTACCTTTA[A/T]CCTCATTCCTTCATT | 22954 |
rs57483164 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685976 | CAGGAAAAAAAAAAA[A/T]TTTAAACGGGTGCAA | 22954 |
rs62574187 | snp | C/T | 0.134119 | 0.221521 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695716 | CCTCAACTTGCTAGA[C/T]CTATTCATTCTGATT | 22954 |
rs71502076 | in-del | -/T | 0.5 | 0 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701560 | TGGAGAGAGAAATAT[-/T]AATATTGTGGGCAGG | 22954 |
rs71505580 | snp | C/T | 0.5 | 0 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689377 | AGTAAACTAGCATGC[C/T]TAGGATCTGGCACAT | 22954 |
rs73515222 | snp | C/G | 0.089084 | 0.191327 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696620 | CAGATTGGAATGACT[C/G]CTCAACCCCCATCAA | 22954 |
rs73515229 | snp | A/G | 0.089084 | 0.191327 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697564 | GTTAAGTAAGGGAAT[A/G]ACTGAATGACTGGTC | 22954 |
rs73655470 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688506 | GAACAAAGTGATAAA[C/T]CTTCAGTTCAGATAA | 22954 |
rs73655471 | snp | C/T | 0.5 | 0 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691929 | GGAGCGTGTCAATAG[C/T]AGGATGGACCTTTAT | 22954 |
rs76727272 | snp | A/T | 0.5 | 0 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690836 | AGAACATATAAAAAA[A/T]TGCCTGACAATAAAT | 22954 |
rs76973802 | snp | C/T | 0.134802 | 0.221877 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688069 | TGCAGGAGATGGGGG[C/T]TCAGATTGAGGGAGA | 22954 |
rs77548643 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685376 | GACTTGAGTAATCAT[A/G]AAACTCCAGTCTCCC | 22954 |
rs80202265 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692477 | TGCTTTACACACATA[A/T]TCTCATTTAATCTTT | 22954 |
rs80267639 | snp | A/C | 0.330482 | 0.236691 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693757 | GAAAATGGGCAGCTT[A/C]CTTAAAGATTTGGAA | 22954 |
rs80319306 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701145 | AGGTGCAGGGCTGAT[A/G]GCAAGCCAAAGAGCA | 22954 |
rs111033570 | snp | A/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699201 | CAGTTTGTAGTAACC[A/G]ATGTGGAAGGTGGAA | 22954 |
rs111033571 | snp | C/T | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698130 | GAGGCAGACCATCAG[C/T]CTCCTGGCCACTGTA | 22954 |
rs111309723 | snp | C/T | 0.0287284 | 0.116357 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700549 | ACCTCTCTCTTCTGG[C/T]CTGTGTCTAAGGAAT | 22954 |
rs111482128 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686999 | TACCCTGGAGGCTAC[C/G]GTTTTGTGAAGGGGT | 22954 |
rs112521383 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686980 | CCAACGCTTTGCTGA[C/G]GACTACCCTGGAGGC | 22954 |
rs112643631 | snp | C/T | 0.168135 | 0.236216 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687467 | GGCGGGGGAACGTGC[C/T]GGCGTGCAGCGGCCG | 22954 |
rs113050442 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688822 | TTGAAGGGGCAGTGG[C/G]TCTGTGAGTGAGGTG | 22954 |
rs113316792 | snp | G/T | 0.5 | 0 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690244 | TTGTTGAGTGCTTAT[G/T]ATGTGCATTATCTTA | 22954 |
rs113347165 | snp | A/G/T | 0.0357947 | 0.129549 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694232 | GATATTCCAGAAAGC[A/G/T]TGGGAAATAATTTGC | 22954 |
rs113632200 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687478 | GTGCCGGCGTGCAGC[A/G]GCCGCGCCCGAATGG | 22954 |
rs113850994 | snp | G/T | 0.0356815 | 0.128715 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685828 | GATCCCCAGGAGTAT[G/T]TTTAACACTCCTCTG | 22954 |
rs113989286 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691324 | GAGGTCCCTGAGAAG[C/G]GGCTATTGATTTTTC | 22954 |
rs114026634 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685882 | CTGTATTGATACATA[C/T]ACACACATATATAAT | 22954 |
rs114029413 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695047 | GTTATGGAGAAAATG[C/T]GTATGCTATAAGGCA | 22954 |
rs114572089 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691235 | TGATCCTTTAATCAT[A/G]ATCTCATGATTAAAT | 22954 |
rs114597839 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, splice-acceptor-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697371 | TTACTTCTATTTTAC[A/G]GATGAGTGATGGGGA | 22954 |
rs115588463 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700677 | GTTTTCCTCAAGTCA[C/G]TACATACTATTTGGT | 22954 |
rs115660886 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694875 | CATCAGACCTCATAC[A/G]CTCATGATATATGGT | 22954 |
rs115808405 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695977 | TCCACTCACCTTTCA[A/T]ATCTTACTGACTATA | 22954 |
rs116058338 | snp | C/G | 0.00795532 | 0.062565 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700396 | TATTGATGACTTCAG[C/G]CTGGAAATTGCTTGC | 22954 |
rs116464901 | snp | C/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688750 | GATAGCAGATAGAAA[C/G]TGAGACCTCCAGGGG | 22954 |
rs117078203 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693015 | TTCAAAACTGACCAG[A/C/T]CCTTTTATTAATCTT | 22954 |
rs117083975 | snp | A/G | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685781 | TAAGGGAGAAGAGAG[A/G]TTTTTTTTTTTCAAG | 22954 |
rs117120242 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693962 | AGTGTTTTCAAGTCA[C/T]GGAAGTGGGAAAAGT | 22954 |
rs117599771 | snp | C/G | 0.00409784 | 0.0450791 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698300 | TAAAGCAGTTCTCCA[C/G]GAGTATGGGCATGAG | 22954 |
rs121434447 | snp | A/G | 8.27219e-05 | 0.00643072 | TRIM32, ASTN2 | 9 | allele_origin=G(germline)/A(germline) | 9:116698923 | ACCGTGGTAACTATC[A/G]TATACAAGTCTTTAC | 22954 |
rs137906049 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695864 | CAGAGGGTACTCTAA[A/G]CCAGAAATAAACTGT | 22954 |
rs137947083 | snp | C/G | 5.0192e-05 | 0.00500934 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698108 | GGTGTTATGTGAGCC[C/G]TGCCGGGAGGCAGAC | 22954 |
rs138056275 | snp | A/G/T | 0.000181255 | 0.00951822 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699430 | ATGGGCAGCTGGGTC[A/G/T]CCAGATTAGCCACTT | 22954 |
rs138462089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696890 | AATCATCACAATTTT[C/G]TGCTTCTGTGGATGA | 22954 |
rs138525985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690819 | GTTATTATGAGACTA[C/T]GAGAACATATAAAAA | 22954 |
rs138699534 | snp | C/T | 0.000346526 | 0.0131584 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698263 | CCTTGGAAGGTGTCT[C/T]CAAGGACCTTCAGGC | 22954 |
rs138735929 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699665 | GGATCATTGCATCAA[A/G]ATCTACAGCTACCAT | 22954 |
rs139113969 | snp | A/G | 0.000131891 | 0.00811962 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698430 | AGTTACCTGCTTAAC[A/G]TTGCAGAGGTGCAGG | 22954 |
rs139275673 | snp | C/T | 0.000461262 | 0.0151795 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699351 | GGCTTAGGCCTCAAT[C/T]TGGAGAATCGGCAGA | 22954 |
rs139277710 | snp | C/G | 1.65241e-05 | 0.00287433 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698881 | TCAGTCTCTACGTGA[C/G]CAGTCAAGGTGAAGT | 22954 |
rs139362681 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692403 | TGCTACTGCTAATAA[C/T]AATAAAAACTATTAT | 22954 |
rs139857671 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686596 | GCCAGATGCCTAGTG[C/T]CCCAGATTCCCTCAA | 22954 |
rs139909800 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700648 | ACAGCAAAACTATTG[G/T]TTTGTTATTCTGTGT | 22954 |
rs140059042 | snp | C/T | 6.61934e-05 | 0.00575259 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698940 | ATACAAGTCTTTACC[C/T]GCAAAGGCTTTTTGA | 22954 |
rs140261676 | snp | A/C/G | 0.00279258 | 0.0372817 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701268 | AGCTGCCAAAGGATA[A/C/G]GTAAAGAGGTCATTA | 22954 |
rs140296854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695055 | GAAAATGCGTATGCT[A/G]TAAGGCAGCATTCCC | 22954 |
rs140589523 | snp | C/T | 0.000478623 | 0.0154623 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698018 | TACAGCTGGGCTCAG[C/T]GAGGCTGTGGGGCTG | 22954 |
rs140701310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692612 | AGAGCTTGAATTCAA[A/G]TCCAGGAAAGCCTGA | 22954 |
rs140747003 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701709 | TCAAGTAAAGCAGTT[A/G]TCTGTTGGCTCAAAA | 22954 |
rs140762965 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688353 | GAGTAGATTTGTGGA[C/T]TGGTGTCTTGGGCTG | 22954 |
rs140862380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689848 | GAGGTGCAACGGACT[A/G]TAGGGTGAGGTATGG | 22954 |
rs141308099 | snp | C/T | | | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698499 | CAGGCAGATGTAGCA[C/T]TACTGGAGGAGACAG | 22954 |
rs141352486 | snp | G/T | 0.000578125 | 0.016992 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697748 | AGGAAGAGCAATGGC[G/T]GCAGCAGCAGCTTCT | 22954 |
rs141560856 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691403 | AATGTTTGTGAAAGA[C/T]GCAAGGGAGTCTTTC | 22954 |
rs141586818 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691801 | GCCTTTGGTGGCACA[A/G]TGATAGTTTTGCACT | 22954 |
rs141806013 | snp | A/G | 0.000165289 | 0.00908941 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698754 | GTTGCCAGCCCTAGG[A/G]CCTCACCTGCTAAAC | 22954 |
rs141943847 | in-del | -/TGT | 0.0391387 | 0.134304 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693598 | AAGATGGTAGGCTGA[-/TGT]TGTTAGATGAGGTGG | 22954 |
rs141953092 | snp | C/T | 0.000418638 | 0.0144618 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698146 | CTCCTGGCCACTGTA[C/T]ACTCCCTGTCAAAGA | 22954 |
rs141965401 | snp | C/T | 0.000164905 | 0.00907884 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699200 | CCAGTTTGTAGTAAC[C/T]GATGTGGAAGGTGGA | 22954 |
rs142702527 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693501 | CAGCTTAAGGGACAG[A/T]TTCTCATCGGGAGCT | 22954 |
rs142715198 | snp | C/T | 1.65247e-05 | 0.00287438 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698882 | CAGTCTCTACGTGAC[C/T]AGTCAAGGTGAAGTA | 22954 |
rs142781513 | snp | A/C/G | 0.000400877 | 0.0141524 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699705 | TATTCCACCCCATAG[A/C/G]GGATGAGAAATTATC | 22954 |
rs142997889 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699036 | CCCAACCTCACTCCT[C/T]TCTCAGTGGCAATGA | 22954 |
rs143186354 | snp | A/G/T | 0.000439271 | 0.0148136 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699635 | TAAGGGGCAGCTGCT[A/G/T]GTCTTGGACTGTTGG | 22954 |
rs143568516 | snp | C/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698779 | CTAAACAGCGGGGTC[C/G]TGAGGCAGCCTCCAA | 22954 |
rs143760041 | snp | A/G/T | 4.94385e-05 | 0.0049716 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697876 | GCCATACCATCTGCC[A/G/T]CCAGTGCCTGGAGAA | 22954 |
rs143839165 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696776 | TAGTACAGAACAAGA[C/T]ACCTAAACTTAGATG | 22954 |
rs143913303 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692494 | CTCATTTAATCTTTG[A/C]AATAACTTTGTGAGG | 22954 |
rs144031102 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697301 | CTATACTAAGCACAT[C/T]ATATTTATCTTGTTA | 22954 |
rs144172952 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700216 | TATTCCCGTAACATT[A/T]TGTCTCAGTCTGATC | 22954 |
rs144532174 | snp | A/G | 1.65682e-05 | 0.00287817 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698649 | CCCCGGACAGTTAAC[A/G]TGGAAGATTCCTGGG | 22954 |
rs144587882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692752 | TTAGTTTTCTCATCT[A/G]TTTTACAACTTGAGA | 22954 |
rs144651222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694874 | ACATCAGACCTCATA[C/T]GCTCATGATATATGG | 22954 |
rs144716630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690108 | CCTAAAAGAAAATAT[A/G]TCATGGGAATTAAAT | 22954 |
rs144793422 | snp | G/T | 0.0299144 | 0.118585 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687228 | TGGGGCCAGCTGCAC[G/T]ACAAGCCCCAGCATG | 22954 |
rs145003353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689310 | CTTCATCTGTAAAAT[A/G]GGGTTATGATAACAA | 22954 |
rs145449915 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687793 | GCCCCGATGAGATTT[C/G]AGGAAATCTGGGGGC | 22954 |
rs145721012 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693233 | TCATTACAGTACTCT[C/T]TTTATAAACTAAGAA | 22954 |
rs145728860 | snp | A/C/G | 9.88849e-05 | 0.00703091 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699272 | CAAATACAGCTGCCT[A/C/G]TGTAGTGCTGTGCGG | 22954 |
rs145828717 | snp | A/G | 6.62745e-05 | 0.00575612 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698968 | TGAAGGAAATCCGCC[A/G]CAGCCCCAGTGGCAT | 22954 |
rs145907585 | snp | C/T | 0.000149471 | 0.00864367 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698209 | AGAAGTTAACTCGTC[C/T]GCGGGAACTTATGGG | 22954 |
rs146094774 | snp | A/G | 6.61726e-05 | 0.00575169 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698911 | TACTAGTCGCTGACC[A/G]TGGTAACTATCGTAT | 22954 |
rs146167094 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686238 | CTTAGGTATATGTGG[C/G]CTTGTGTAACCACCT | 22954 |
rs147280518 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692567 | CTACAGAAGTATTAA[C/T]AACTTGCTCACGTCT | 22954 |
rs147304059 | snp | C/T | 4.94752e-05 | 0.00497344 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698343 | CAGGATGAGCTGGCT[C/T]GCTCTCGGAAGTTCT | 22954 |
rs147656324 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687935 | GTGGGGTGAGTTCTT[C/G]AGGGACTCTATCTTG | 22954 |
rs147803099 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699360 | CTCAATCTGGAGAAT[C/T]GGCAGAATGAGCACC | 22954 |
rs148027625 | snp | A/G | 9.93723e-05 | 0.00704814 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698715 | GTTACTTTTAGAGAG[A/G]TGGACATGAGCCCGG | 22954 |
rs148367669 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691644 | CTATAAGCCCCTACT[C/T]GTTGAGTTTATCTTA | 22954 |
rs148469577 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693424 | TGGTGCTAGAAGAGG[C/T]GAGATTAATATGGAA | 22954 |
rs149419526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696037 | CATTTCCACCACCTG[C/T]TCCCTAGTTCAGACT | 22954 |
rs149509191 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699584 | TGTCCTTATTCGAGA[A/G]GGACTTACCTGTCCG | 22954 |
rs149833926 | snp | C/T | 0.000120824 | 0.00777158 | upstream-variant-2KB, intron-variant, stop-gained | TRIM32, ASTN2 | GRCh38.p7 | 9:116686761 | TCTGCTGTCGGCCTC[C/T]CAGCTGAGTAGGCAA | 22954 |
rs149956877 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699881 | ATGTCCCCCTCCCCG[C/T]TTCCCACCTAAATTT | 22954 |
rs150289087 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695673 | AGCTGTAGGATTTGC[A/G]TTTATGAAATGCTGA | 22954 |
rs150318692 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699401 | TGGCTTTTCCATTGG[C/T]TCTGTAGGCCCTGAT | 22954 |
rs150342900 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688902 | AAAGGGAACCCTTAG[A/G]TATTGAGCATTTAGT | 22954 |
rs150477945 | snp | C/G | 0.000383759 | 0.0138467 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698081 | CCGGCAATTCTGCCG[C/G]AGCTGTGGTTTGGTG | 22954 |
rs150586381 | snp | A/C | 3.30551e-05 | 0.00406528 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698760 | AGCCCTAGGGCCTCA[A/C]CTGCTAAACAGCGGG | 22954 |
rs150813870 | snp | C/T | 0.000413904 | 0.0143799 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699017 | CTTCCTTGGGGCAGA[C/T]CTACCCAACCTCACT | 22954 |
rs150864995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691907 | CAAAAAACCCAGTCA[A/T]ACCAGGGGAGCGTGT | 22954 |
rs150928412 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701697 | ATGCCTTTTCCCTCA[A/G]GTAAAGCAGTTATCT | 22954 |
rs150981665 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693718 | GATACTCATTCTGAT[C/T]GGTTGTACAGTTGAT | 22954 |
rs151116227 | snp | C/G | 6.59554e-05 | 0.00574224 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699142 | TGGCCTGTCACAGGA[C/G]CCAGCTGAGCAAACC | 22954 |
rs151231525 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688585 | TATTAAACAAAGATC[C/G]GTTATCATGAGGCAG | 22954 |
rs151330357 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697879 | ATACCATCTGCCGCC[A/G]GTGCCTGGAGAAGCT | 22954 |
rs180759209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694920 | TGAGGTATGGATTTG[A/C]GTCATAATGGGTTGC | 22954 |
rs181050598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688847 | GAGGTGTTTGGGCTC[A/G]GAGACAGACAAAACA | 22954 |
rs181519489 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686431 | GTCACATAGCTAAGG[A/G]GAATTTCAAATCCAA | 22954 |
rs181673266 | snp | A/G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695619 | TCCTCCTTCTCCTGG[A/G/T]TGGTTGACCATCTGC | 22954 |
rs182327824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689388 | ATGCCTAGGATCTGG[C/T]ACATAGTAAGTTCTC | 22954 |
rs182399889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697237 | CACCAAATATGAAAA[G/T]AATCATTAGCTCATT | 22954 |
rs182718256 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690686 | TTTATGGCTGGGAGT[C/T]GATACTGGGATTTGA | 22954 |
rs182744179 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691780 | AGTCAGTCCTGCTAA[C/T]GAGTGGCCTTTGGTG | 22954 |
rs183136193 | snp | A/G | 0.000165659 | 0.00909956 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698965 | TTTTGAAGGAAATCC[A/G]CCGCAGCCCCAGTGG | 22954 |
rs183199482 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696706 | ACATGTCTTGTCTTT[C/T]ATAAAGTTTGAATAT | 22954 |
rs184103246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692823 | GTAGCATCATCACAG[A/C]TCACTGCAACCTCCA | 22954 |
rs184193712 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686575 | CCTGTATCAGACCTC[C/G]TCCTTGCCAGATGCC | 22954 |
rs184489068 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694524 | TGGAGTGCAGTGGCG[A/C/T]GTCTCGGCTCACTGC | 22954 |
rs184509791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693224 | TTTCCATAGTCATTA[C/T]AGTACTCTTTTTATA | 22954 |
rs184974217 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700759 | TTCTTCATCTCTGGT[A/G]TTCATGTCTTTTAAT | 22954 |
rs185274826 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685771 | ATTTTTGTTTTAAGG[C/G]AGAAGAGAGATTTTT | 22954 |
rs185845262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695847 | GTTTGTATTGGGTGA[C/T]GCAGAGGGTACTCTA | 22954 |
rs186074712 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689105 | TGTGTGGGATACGCC[C/G]TTCCCCCCCGCAGTA | 22954 |
rs186206606 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697080 | TTGGGAAGCCTTCCC[A/C]AAGTCTGTTAGGTAG | 22954 |
rs187054436 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689596 | AACTCCGTATATTCC[C/T]GCTTTCCTTGCTTCT | 22954 |
rs187391824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695495 | GTAATGTATATCTCT[A/G]CATTAACTCCCCTTC | 22954 |
rs187467050 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700076 | GGCTTTGATGCCCTT[G/T]ATCCATTGTTTCCTT | 22954 |
rs187684745 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687070 | TCCTGACTTACTGAG[C/T]GAACTTGAGCAGGTC | 22954 |
rs188064768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697597 | AGCTATTCTCTAAAT[C/G]TTTCTTGAGTGAATT | 22954 |
rs188529467 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687982 | AGCTGGCTGAGGTGT[A/G]AAGGCAGCACATGAC | 22954 |
rs188598117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693114 | GCGTTATTAATACTA[A/G]TACTAGTTATTGTTA | 22954 |
rs188871286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693396 | CTCATTTCATGGAAT[A/G]GGGAAAACCCAGTGG | 22954 |
rs189168345 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695587 | GTCCTTAAAATCAAA[C/T]GAACTTGCCCTCCAC | 22954 |
rs189381768 | snp | C/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700955 | GTGTACAGAATCATC[C/G]CCCAAGGTTTAGAGT | 22954 |
rs189523962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694714 | CTGACCTCATGATTC[A/G]CCCACCTCAGCCTCC | 22954 |
rs190065311 | snp | A/G | 0 | 0 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691760 | GACCTCACTGAATTC[A/G]TTAAAGTCAGTCCTG | 22954 |
rs190170575 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685984 | AAAAAAATTTTAAAC[A/G]GGTGCAAAGTCTCCC | 22954 |
rs190204413 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696171 | ATGACGCTCAAAAAT[C/T]TCATTTTGGCTCTGA | 22954 |
rs190500188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689171 | AGTTGAGGCACTCTG[A/G]CCTAGAGTCAGATAC | 22954 |
rs191049736 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697084 | GAAGCCTTCCCCAAG[C/T]CTGTTAGGTAGAATC | 22954 |
rs191705012 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693933 | CCATTTCAGGCTAAG[A/T]TCCTTCACAAAGCAG | 22954 |
rs192200916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693223 | TTTTCCATAGTCATT[A/G]CAGTACTCTTTTTAT | 22954 |
rs192516080 | snp | A/G | 3.33895e-05 | 0.00408579 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698083 | GGCAATTCTGCCGGA[A/G]CTGTGGTTTGGTGTT | 22954 |
rs192725208 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701628 | GTGCTTTTGAAAGAG[A/G]TGCCATCACTGAGTG | 22954 |
rs192837427 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700234 | TCTCAGTCTGATCGT[C/T]TTTACCAGTATGAAA | 22954 |
rs193133240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692049 | CACCAGTACCGTTCA[C/T]AGGGCCAGACACATA | 22954 |
rs193247731 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685437 | AACTATTGCAATTCC[A/C]CTGTCTTGATGAATC | 22954 |
rs199664043 | snp | C/T | 0.000115322 | 0.00759261 | stop-gained, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699579 | TATAGTGTCCTTATT[C/T]GAGAGGGACTTACCT | 22954 |
rs199699832 | snp | C/G/T | 0.000132636 | 0.00814259 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698221 | GTCTGCGGGAACTTA[C/G/T]GGGGGAGCTGCAGCG | 22954 |
rs199704873 | snp | A/G | 0.00199798 | 0.0315436 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699580 | ATAGTGTCCTTATTC[A/G]AGAGGGACTTACCTG | 22954 |
rs199863390 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697840 | CAGAAGAGCAGCTGC[A/G]TCCCAAGCTTCTGCA | 22954 |
rs200085883 | snp | A/G | 6.61277e-05 | 0.00574974 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698243 | GCTGCAGCGGCGGAA[A/G]GCAGCCTTGGAAGGT | 22954 |
rs200196832 | snp | A/G | 0.000629754 | 0.0177336 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698222 | TCTGCGGGAACTTAT[A/G]GGGGAGCTGCAGCGG | 22954 |
rs200244154 | snp | C/T | 1.64933e-05 | 0.00287165 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699125 | CTTGGATGGCCACTG[C/T]GTGGCCTGTCACAGG | 22954 |
rs200326473 | snp | C/T | 0.000230833 | 0.0107407 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697999 | CAGTGCTAAAGATCA[C/T]TGATACAGCTGGGCT | 22954 |
rs200374340 | snp | A/G | 1.6571e-05 | 0.0028784 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698709 | ACCTCTGTTACTTTT[A/G]GAGAGATGGACATGA | 22954 |
rs200638331 | snp | G/T | 0.00199803 | 0.031544 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699707 | TTCCACCCCATAGGG[G/T]ATGAGAAATTATCAG | 22954 |
rs200994877 | in-del | -/C | 0.0119091 | 0.0762411 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696081 | TCTTCTCTGATGTTT[-/C]CCCCACTCCATTCCT | 22954 |
rs200997003 | snp | C/T | 0.000569057 | 0.0168584 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698151 | GGCCACTGTACACTC[C/T]CTGTCAAAGAAGCAG | 22954 |
rs201035561 | snp | A/T | 0.00199792 | 0.0315431 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697966 | TAACCAGCTTGACCC[A/T]GCTGACAGACAATCT | 22954 |
rs201083322 | snp | A/G | 3.29592e-05 | 0.00405938 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699365 | TCTGGAGAATCGGCA[A/G]AATGAGCACCACCTG | 22954 |
rs201130164 | snp | C/T | 0.000215651 | 0.0103817 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698055 | TGTCGGTCCTGTGGG[C/T]GGCGTCTGCCCCGGC | 22954 |
rs201288003 | snp | A/T | 3.32105e-05 | 0.00407482 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697702 | AATACTGTGCTGTTC[A/T]GTTCTGAGCTGTGCT | 22954 |
rs201877419 | snp | A/C | 4.95774e-05 | 0.00497858 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698034 | GAGGCTGTGGGGCTG[A/C]TCATGTGTCGGTCCT | 22954 |
rs201891227 | snp | C/G | 0.000148474 | 0.00861482 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697769 | AGCAGCTTCTCACCT[C/G]AACCTGGATGCCCTC | 22954 |
rs202186657 | in-del | -/ATA | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701247 | TCTTTGGATTGTATC[-/ATA]ATAATAGCTGCCAAA | 22954 |
rs367574371 | snp | A/C | 0.00014885 | 0.00862571 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698605 | TAGGTCATGTTGGCC[A/C]CCTCCAAATTGGACA | 22954 |
rs368048867 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690209 | AGCCTCAATCTATTA[A/G]AAATGCAAATGATTA | 22954 |
rs368240408 | snp | C/G/T | 0.000153988 | 0.00877328 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699597 | GAGGGACTTACCTGT[C/G/T]CGGTGGGCATAGCCC | 22954 |
rs368380803 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689820 | AGAGGAGCCTGAGGT[C/T]ATCAGGCAGGATGAG | 22954 |
rs368455215 | snp | A/C | 4.94597e-05 | 0.00497266 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698435 | CCTGCTTAACATTGC[A/C]GAGGTGCAGGCTGTG | 22954 |
rs368850903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691026 | CTAGGCTCAAGTGAT[C/T]CTCCCATCTCAGCCT | 22954 |
rs368895262 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698811 | ATCCAGCAGTGCCTC[C/T]TTCTCAAGAAGATGG | 22954 |
rs368901621 | snp | A/G | 6.59022e-05 | 0.00573993 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699321 | GATGCTGAGGGCACC[A/G]TCTACTTCACCCAGG | 22954 |
rs369246436 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688222 | TTGACGAGGGTTGCA[A/G/T]TATACAGCCCCAAAG | 22954 |
rs369671745 | snp | G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691979 | AATATTTTACATGTT[G/T]TCTAGTTTTTAGGGG | 22954 |
rs369862143 | snp | A/G | 1.65029e-05 | 0.00287248 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698012 | CATTGATACAGCTGG[A/G]CTCAGCGAGGCTGTG | 22954 |
rs369869399 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687239 | GCACGACAAGCCCCA[A/G]CATGCTGGGGAGGCG | 22954 |
rs369919296 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695263 | ATAATAAAAATATTA[C/G]CACTTCATAGTGTCA | 22954 |
rs370191610 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688564 | AAGGGCAGAATCTTC[-/TTC]ATTTATTAAACAAAG | 22954 |
rs370216046 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696668 | TTTATAGTACCACTT[C/T]CTGCCTTCATTATTA | 22954 |
rs370216394 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116687566 | GGGGCAGGCTCGGGA[G/T]GGATTCGTGGGGCTG | 22954 |
rs370383245 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695839 | TGTTCATGGTTTGTA[C/T]TGGGTGACGCAGAGG | 22954 |
rs370534929 | snp | C/T | 1.64874e-05 | 0.00287113 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698367 | AAGTTCTTCACAGGC[C/T]CTTTGGCTGAAGTTG | 22954 |
rs370691123 | snp | A/C | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699872 | TTATTTGTTATGTCC[A/C]CCTCCCCGCTTCCCA | 22954 |
rs370951769 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694522 | TCTGGAGTGCAGTGG[C/T]GCGTCTCGGCTCACT | 22954 |
rs371002754 | snp | G/T | 1.64876e-05 | 0.00287116 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699174 | TGGGGTATCACAGCC[G/T]TGCCATCTGGCCAGT | 22954 |
rs371233848 | snp | C/G | 1.64923e-05 | 0.00287156 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699230 | AAAGCTTTGGTGTTT[C/G]ACAGTTGATCGAGGA | 22954 |
rs371331075 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687118 | TCGGTTTCTTCATCT[A/G]CACCAAGGAGACGGA | 22954 |
rs372044621 | snp | C/T | 6.59196e-05 | 0.00574068 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699404 | CTTTTCCATTGGCTC[C/T]GTAGGCCCTGATGGG | 22954 |
rs372116948 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696039 | TTTCCACCACCTGCT[C/T]CCTAGTTCAGACTCC | 22954 |
rs372298402 | snp | C/G/T | 0.000148673 | 0.00862073 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698553 | ACTGCCAGCTTGCCT[C/G/T]GGGAGCTCACCCTGC | 22954 |
rs372518768 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697042 | CATTTCTTTCAAGAC[A/G]TATCTTAGGAGTGAA | 22954 |
rs372594074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696979 | AAAGCCTCCACACTT[C/T]TGCTTACATGGTTTT | 22954 |
rs373015960 | snp | A/G/T | 8.27621e-05 | 0.00643234 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698941 | TACAAGTCTTTACCC[A/G/T]CAAAGGCTTTTTGAA | 22954 |
rs373060450 | in-del | -/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694645 | TTTTTTTTTTTTTTT[-/G]TATTTTTAGTAGAGA | 22954 |
rs373287765 | snp | A/G | 0.000297989 | 0.0122027 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698721 | TTTAGAGAGATGGAC[A/G]TGAGCCCGGAGGAAG | 22954 |
rs373465703 | in-del | -/AGAT | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686190 | AGAGAGTGGGTTCTC[-/AGAT]AGAATTGGGTACAAA | 22954 |
rs373469245 | snp | G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694255 | TAATTTGCTGCTATT[G/T]TTACAAGTTGGCAGC | 22954 |
rs373567403 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687757 | GGGTGCAGAATTTCA[A/G]AAATATGAAGGAACT | 22954 |
rs373660071 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699836 | GTTCTAGAACTTCAG[A/G]AGCTCCATCTTTTAA | 22954 |
rs373853273 | snp | A/G/T | 9.8942e-05 | 0.00703294 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698320 | ATGGGCATGAGGAGC[A/G/T]CAGGGTCCAGGATGA | 22954 |
rs374055553 | snp | A/C/T | 3.32382e-05 | 0.00407654 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698205 | GGAGAGAAGTTAACT[A/C/T]GTCTGCGGGAACTTA | 22954 |
rs374136376 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699158 | CCAGCTGAGCAAACC[A/G]TGGGGTATCACAGCC | 22954 |
rs374237296 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116687039 | GACTGGAGTCAGATA[C/T]GCATTCTGGCTTATC | 22954 |
rs374248541 | snp | A/G | 8.24328e-05 | 0.00641947 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698392 | AAGTTGAGAAGTCCA[A/G]TAGTCAAGTGGTAGA | 22954 |
rs374251322 | in-del | -/AATA | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701253 | GATTGTATCATAATA[-/AATA]GCTGCCAAAGGATAG | 22954 |
rs374471533 | snp | C/G | 1.6489e-05 | 0.00287128 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699243 | TTCACAGTTGATCGA[C/G]GATCAGGGGTGGTCA | 22954 |
rs375442860 | snp | A/G/T | 6.63059e-05 | 0.00575755 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698681 | CATGGAGGCCACAGC[A/G/T]TCTGCTGCCTCTACC | 22954 |
rs375537493 | snp | A/G | 1.65323e-05 | 0.00287505 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698588 | TGTGGAGCTCCTTAA[A/G]GTAGGTCATGTTGGC | 22954 |
rs375637102 | in-del | -/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691802 | CCTTTGGTGGCACAG[-/T]GATAGTTTTGCACTT | 22954 |
rs375894217 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687515 | GTGGGGACCGGATCT[-/G]GGGGGGGGCAGGACT | 22954 |
rs376007099 | snp | A/C/T | 1.64914e-05 | 0.00287149 | synonymous-codon, missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698349 | GAGCTGGCTCGCTCT[A/C/T]GGAAGTTCTTCACAG | 22954 |
rs376113966 | snp | A/G | 3.29832e-05 | 0.00406085 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699214 | CCGATGTGGAAGGTG[A/G]AAAGCTTTGGTGTTT | 22954 |
rs376526398 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688724 | CCTTTTTCCCTGTAC[C/T]CCCAAGCTACGATAG | 22954 |
rs376668333 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700833 | ATGCCATTTTGCTTC[C/T]TTATCTCACTGTGTT | 22954 |
rs376970949 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687432 | CGCGGCCGGAGTCGT[A/G]GGCCGTGGCTCAGCG | 22954 |
rs377026732 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687095 | CAGGTCCCTTTCGCC[C/T]ATGGGCGTCGGTTTC | 22954 |
rs377181799 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695789 | GATCTCTCTGGGTCA[A/T]CTTCATAAGTATATG | 22954 |
rs377368040 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699868 | GTTTTTATTTGTTAT[A/G]TCCCCCTCCCCGCTT | 22954 |
rs377510422 | snp | C/T | 9.93328e-05 | 0.00704674 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698728 | AGATGGACATGAGCC[C/T]GGAGGAAGTGGTTGC | 22954 |
rs377669059 | snp | A/C | 1.64811e-05 | 0.00287059 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697968 | ACCAGCTTGACCCAG[A/C]TGACAGACAATCTGA | 22954 |
rs386361511 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688889 | ACCAGAAAAAAAAAA[-/A]GGGAACCCTTAGGTA | 22954 |
rs398124253 | snp | C/T | | | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698420 | AGAGGAGCAGAGTTA[C/T]CTGCTTAACATTGCA | 22954 |
rs527286297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689695 | GTGAGTATCACTGAC[C/T]ATCAGATTGAACTCT | 22954 |
rs527395517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688895 | AAAAAAAAAAGGGAA[C/T]CCTTAGGTATTGAGC | 22954 |
rs527671692 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699799 | GAATAGACTCAGCCT[A/G]TGTCCTGATTCCAGC | 22954 |
rs527953664 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700332 | GATCTGTGCCATCTT[G/T]GATTGAGAATTGCAG | 22954 |
rs527961381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691007 | TCACTGCAGCCTCAA[C/T]CTCCTAGGCTCAAGT | 22954 |
rs528520101 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688061 | CGATGGAATGCAGGA[A/G]ATGGGGGCTCAGATT | 22954 |
rs528552111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693812 | TGTAGTCTTTTGGGG[A/G]AACTGAAGTCAAATT | 22954 |
rs528609321 | in-del | -/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694629 | CCACGCCCAGCTAAT[-/T]TTTTTTTTTTTTTTT | 22954 |
rs529201438 | snp | A/C | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701534 | CTCAGGCCTTTGGCA[A/C]ACAGTTTGCAGTGGA | 22954 |
rs529340694 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701461 | TCTGTGGGGGCACCC[A/C]GCAGCAGGAGATCTG | 22954 |
rs529912349 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687069 | CTCCTGACTTACTGA[C/G]TGAACTTGAGCAGGT | 22954 |
rs530217734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696659 | TTTATTTCGTTTATA[A/G]TACCACTTTCTGCCT | 22954 |
rs530705016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694791 | TTGTAATTTCTATCA[A/G]TATGTCTATGCTATT | 22954 |
rs530859799 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693101 | TTGTAAACTGAATGC[A/G]TTATTAATACTAGTA | 22954 |
rs530869339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694038 | TTTAGTGAGGGGAAC[A/G]CAGGTTTTCCTGGCA | 22954 |
rs530876238 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685894 | ATATACACACATATA[A/T]AATATGTATATATGT | 22954 |
rs531319468 | in-del | -/GCA | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687224 | CGCTTGGGGCCAGCT[-/GCA]CGACAAGCCCCAGCA | 22954 |
rs531988466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695719 | CAACTTGCTAGACCT[A/G]TTCATTCTGATTTGG | 22954 |
rs532051101 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688413 | GGGAGACAGAGGGAG[-/T]TCAGGGGACCCAAGG | 22954 |
rs532084545 | snp | C/T | 3.38312e-05 | 0.00411272 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699733 | ATCAGTTTCTTCTGC[C/T]CCCAAGCCAACTTCC | 22954 |
rs532269538 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687116 | CGTCGGTTTCTTCAT[C/T]TGCACCAAGGAGACG | 22954 |
rs532401930 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696267 | TCCCACAGTTTTAAT[C/G]TAAGGATAATAAAAA | 22954 |
rs532572905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688961 | TTAACCAAGTCTGGC[C/T]TTGTCTCCTAGGAGA | 22954 |
rs532729383 | snp | C/T | 1.66999e-05 | 0.00288958 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698181 | GCTGAGGAGCGGCGT[C/T]GGGACTTTGGAGAGA | 22954 |
rs533209692 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699844 | ACTTCAGAAGCTCCA[C/T]CTTTTAATGTTTTTA | 22954 |
rs533236140 | snp | C/T | 4.94629e-05 | 0.00497283 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698479 | ACTTCCTGGCCAAGA[C/T]CAAGCAGGCAGATGT | 22954 |
rs533288656 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700435 | GAAGCATATATGGGT[C/T]GGAATTATGCCAAAG | 22954 |
rs533301609 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695998 | ACTGACTATACTTCT[A/G]GATATTGCTCAAATG | 22954 |
rs533336111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691838 | GCATTCTGTTAGAAT[A/G]CATGAGGAATAAAGT | 22954 |
rs533616801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688141 | GCGGGGCTGAGTGTG[A/G]CAGAGATTTGGAAAT | 22954 |
rs533687160 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695947 | TCTCTGCTCTTCACC[A/C]CTCCCCCACCATAAT | 22954 |
rs533925126 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690069 | GTCTGACAGCAAGAC[C/T]TAGCTGGAATATCTG | 22954 |
rs534126880 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689288 | TTAACCACCCAGTGC[C/T]TTGGCTCTTCATCTG | 22954 |
rs534259071 | snp | A/G | 0.000214251 | 0.0103479 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697832 | GTCCTTCACAGAAGA[A/G]CAGCTGCGTCCCAAG | 22954 |
rs534626362 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700053 | AAATCCTTGATTTTT[C/T]CCCATTTGGCTTTGA | 22954 |
rs535219105 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693586 | CAAGGGATGTGGGAA[C/G]ATGGTAGGCTGATGT | 22954 |
rs535366004 | snp | A/C | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689495 | GTATTCAGTTTTACA[A/C]ATGAGGAAACTAAGG | 22954 |
rs535411189 | in-del | -/ATGT | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700013 | TTAGCCCTTTGTGCC[-/ATGT]ATGTTTGAAATTTGC | 22954 |
rs535526192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692169 | AAGGAAATGGAGATA[C/T]CTAGAGAACCACCCC | 22954 |
rs535532791 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696989 | CACTTTTGCTTACAT[A/G]GTTTTCTTTGCTTAA | 22954 |
rs535743394 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693833 | AAGTCAAATTGACCT[A/T]CTATCTGAGTCATTC | 22954 |
rs535929967 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701796 | TGTGCTTAGTACAGT[C/T]GATGTTTAATTATCT | 22954 |
rs535970392 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693360 | CTTTTGTTTTGTTTG[C/T]TTTTTCTACTACCTT | 22954 |
rs536432160 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687216 | GCCCCGCGCGCTTGG[C/G]GCCAGCTGCACGACA | 22954 |
rs537002542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695926 | CTAGGCTTGAGTCTT[C/T]GGCTATCTCTGCTCT | 22954 |
rs537061404 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701668 | ATTTAGATCTCTACC[C/G]ATCTAAACCAGTCAT | 22954 |
rs537362342 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697644 | GGAAAATGAATAATG[A/G]TTTCTTTTTCTCTTT | 22954 |
rs537393304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694586 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 22954 |
rs537479224 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700571 | CTAAGGAATTGTACA[A/G]CATAGGCCAGGGCCA | 22954 |
rs537592373 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687209 | CCGCCTTGCCCCGCG[C/T]GCTTGGGGCCAGCTG | 22954 |
rs537699914 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685643 | AGGATATGTCAAGCT[A/G]TAAGATAAAAATTGA | 22954 |
rs538227887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688473 | GTATATGAAGATGAG[C/T]AGAGTTCAGGTGCTG | 22954 |
rs538387691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696881 | CCTAAAACTAATCAT[C/T]ACAATTTTCTGCTTC | 22954 |
rs538761159 | snp | A/C/G | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685392 | AAACTCCAGTCTCCC[A/C/G]CACAGCTGACTCTGC | 22954 |
rs538766979 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695025 | ACTATATTAGTGTTC[C/G/T]TTCTGTGTTATGGAG | 22954 |
rs538918400 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687360 | TGCCGGCGGTGGACT[C/G]GTCGGAGCCGCGGGC | 22954 |
rs539357455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688298 | GGATTGAATCGTGGG[G/T]TGGAGATGTCCTAAC | 22954 |
rs539376933 | snp | A/G | 0.000280452 | 0.0118384 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698007 | AAGATCATTGATACA[A/G]CTGGGCTCAGCGAGG | 22954 |
rs539378996 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693530 | TGAAGAGATGTGCTA[-/G]GTACAGTATGGTATG | 22954 |
rs539458612 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699880 | TATGTCCCCCTCCCC[A/G]CTTCCCACCTAAATT | 22954 |
rs539842210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692579 | TAATAACTTGCTCAC[A/G]TCTCCACAATAAGTA | 22954 |
rs539903665 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689757 | AGGGAGGAGCCCTGG[A/T]CTTTGTTCTTGGTTT | 22954 |
rs540004929 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687405 | CGGGAAGGAGGGTTG[A/G]GGACTGGGGACCGCG | 22954 |
rs540442765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687706 | CGGGGTGTAGCATGT[A/G]GGAGATGGGAGGGAA | 22954 |
rs540547141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696234 | TTCCAAGTCTGTTAC[C/T]CTATTCCCCATATAT | 22954 |
rs540682122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688635 | TCCATTCTGACCACC[A/G]GTCCCCCGGCCCACT | 22954 |
rs540790986 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700814 | AAGAGGGATAACCTG[C/T]GCTATGCCATTTTGC | 22954 |
rs541032542 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700380 | GACCCTAGTTGGTTG[A/G]TATTGATGACTTCAG | 22954 |
rs541146017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689702 | TCACTGACTATCAGA[C/T]TGAACTCTAAAGTTG | 22954 |
rs541387054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692750 | TCTTAGTTTTCTCAT[C/G]TATTTTACAACTTGA | 22954 |
rs541449335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688851 | TGTTTGGGCTCGGAG[A/T]CAGACAAAACAACAA | 22954 |
rs541526451 | in-del | -/AATA | 0.0115144 | 0.0749975 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701249 | TTTGGATTGTATCAT[-/AATA]AATAGCTGCCAAAGG | 22954 |
rs541560500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697112 | ATCCATCATTCCATC[C/T]ACTGTACTCCAGCAG | 22954 |
rs541627561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693529 | GCTGAAGAGATGTGC[C/T]AGTACAGTATGGTAT | 22954 |
rs541767264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690533 | CACACTGATGTGTAA[C/G]CTTTGTGACATTCCC | 22954 |
rs541969351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691447 | TTTAGAGGAAGACAG[A/G]GACAACAGGCAAGCA | 22954 |
rs542432976 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700991 | ATACCCTATTCTGAG[C/G]TTCTGCTGTATGTTT | 22954 |
rs542506728 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699743 | TCTGCTCCCAAGCCA[A/G]CTTCCCTTCCCTTAG | 22954 |
rs542781629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693758 | AAAATGGGCAGCTTA[C/G]TTAAAGATTTGGAAT | 22954 |
rs542874707 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685765 | ACACTGATTTTTGTT[C/T]TAAGGGAGAAGAGAG | 22954 |
rs543431935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692860 | GGTCTCAAGTAAGGA[C/G]ATTGCTACGAATTCT | 22954 |
rs543534409 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700183 | CTGCTCCACCTTTCA[G/T]TGACATTTAAGACAT | 22954 |
rs543666777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693660 | ACAGGAAACAGACAT[A/T]CAAGGGATCATGAAG | 22954 |
rs543682671 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701153 | GGCTGATGGCAAGCC[A/G]AAGAGCAACTGCCTT | 22954 |
rs544675318 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696132 | CTGCTTCAAAACATT[C/T]ATCACCTCACCATGC | 22954 |
rs544675490 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686969 | TCAGTAAGGTGCCAA[C/G]GCTTTGCTGAGGACT | 22954 |
rs544760356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687460 | GCGGCCAGGCGGGGG[A/G]ACGTGCCGGCGTGCA | 22954 |
rs545165682 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694749 | GTGCTGGGATTACAG[A/G]CATGAGCCACCACGC | 22954 |
rs545399307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696305 | TAAAATTCATTAAAG[A/G]CTTTTTTGGTGCAGA | 22954 |
rs545471341 | in-del | -/GAG | 6.60033e-05 | 0.00574433 | cds-indel, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698520 | GAGGAGACAGCTGAT[-/GAG]GAGGAGCCAGAGCTC | 22954 |
rs545515832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695416 | TAACTTTAGATAATT[A/G]TGCATGTCTGCTGCT | 22954 |
rs546242243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694296 | AAACTGATCTGCACT[A/G]CCAGCTCTGGGAAGA | 22954 |
rs546879645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697256 | CATTAGCTCATTAGC[A/T]TTTATTACAAGTATA | 22954 |
rs547167046 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696695 | ATTATTTACCTACAT[G/T]TCTTGTCTTTTATAA | 22954 |
rs547176782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688216 | GAGGAATTGACGAGG[A/G]TTGCAATATACAGCC | 22954 |
rs547881214 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687210 | CGCCTTGCCCCGCGC[A/G]CTTGGGGCCAGCTGC | 22954 |
rs548027917 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689039 | ATACTACTGGCCTCA[A/G]GTGGGTAGATTAAAC | 22954 |
rs548061497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691810 | GGCACAGTGATAGTT[G/T]TGCACTTGATTAGCA | 22954 |
rs548528701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697613 | TTTCTTGAGTGAATT[C/T]ATTTATATAGTCAGA | 22954 |
rs548768572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692345 | TGCTGAAAAGTGCCT[A/G]TTCATTTCTTCTAAT | 22954 |
rs548896925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689982 | CTTTTCCCTGGAACA[G/T]AATTTGGCTCTATCA | 22954 |
rs548935389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690971 | GTCACCCAGGCTGGA[A/G]TGCAGTGGTGCAATC | 22954 |
rs549155360 | snp | A/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699489 | ATTGCTGGCATGTGT[A/G]TGGATGCTCGTGGTG | 22954 |
rs549163904 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701509 | GGACTTGCTGAGGCA[A/G]TAACAGTGGCTCAGG | 22954 |
rs549446083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693049 | ATGCCTTTATATGCC[A/T]TGAAAGGAAAGGTTG | 22954 |
rs549484022 | in-del | -/ACAAGCC | 0.00162074 | 0.0284209 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687229 | GGGGCCAGCTGCACG[-/ACAAGCC]CCAGCATGCTGGGGA | 22954 |
rs549577425 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699857 | CATCTTTTAATGTTT[C/T]TATTTGTTATGTCCC | 22954 |
rs549857802 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700441 | TATATGGGTTGGAAT[C/T]ATGCCAAAGCATAGG | 22954 |
rs550228492 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692798 | CCCCTTTTGCCCAGG[C/T]TGAAGTACAGTAGCA | 22954 |
rs550817273 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685975 | TCAGGAAAAAAAAAA[A/T]TTTTAAACGGGTGCA | 22954 |
rs550892719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694157 | CATAGTAAATTCATT[G/T]TTTTAAACCTGATGT | 22954 |
rs550931339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694802 | ATCAGTATGTCTATG[C/G]TATTGCCCCTAGACA | 22954 |
rs551237407 | snp | A/C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694011 | GTTTGAGACTATTTC[A/C/T]GTGCCTCATGCTTTA | 22954 |
rs551253712 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693142 | TTAATGCTGTTTCTG[A/G]TTATTATTTATTTAG | 22954 |
rs551522802 | snp | A/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699603 | CTTACCTGTCCGGTG[A/G]GCATAGCCCTAACTC | 22954 |
rs551852050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695046 | TGTTATGGAGAAAAT[A/G]CGTATGCTATAAGGC | 22954 |
rs551858118 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688623 | ATTGCCACTAACTCC[A/G]TTCTGACCACCGGTC | 22954 |
rs551886146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695735 | TTCATTCTGATTTGG[C/G]GTATACGTTGACAGT | 22954 |
rs551919008 | snp | A/C | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685461 | ATGAATCAGCTCTGT[A/C]TAGGCAGTGGGCAAG | 22954 |
rs552179581 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687830 | CATCTGGCAAGGACA[A/G]GGTCTGAGATGATAG | 22954 |
rs552819482 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688891 | CCAGAAAAAAAAAAG[A/G]GAACCCTTAGGTATT | 22954 |
rs552865146 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688988 | GAGACATTAGGCAAT[A/G]TCTGGAGATGTTTTT | 22954 |
rs552899331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697543 | ATAGACCTCAATAAA[A/G]TAGTTGTTAAGTAAG | 22954 |
rs552938001 | snp | A/C/G | 6.67695e-05 | 0.00577762 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698182 | CTGAGGAGCGGCGTC[A/C/G]GGACTTTGGAGAGAA | 22954 |
rs553229576 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense | TRIM32, ASTN2 | GRCh38.p7 | 9:116686742 | TGTACTCCCCAAGTC[C/T]GCCTCTGCTGTCGGC | 22954 |
rs553373967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695381 | AGTACAAAGGAAGTG[A/G]GATATCAGGGAGGAA | 22954 |
rs553724316 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697849 | AGCTGCGTCCCAAGC[C/T]TCTGCACTGTGGCCA | 22954 |
rs553842961 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689449 | CTTCTTTACTCAGTT[A/T]TCATGACAGTCCTTC | 22954 |
rs555005550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689113 | ATACGCCCTTCCCCC[C/T]CGCAGTAAGGAATTA | 22954 |
rs555106278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691366 | ATTCCTTGAGTCATA[C/G]TGGCAGCGTAGGTAC | 22954 |
rs555106908 | snp | A/G | 1.65496e-05 | 0.00287655 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698946 | GTCTTTACCCGCAAA[A/G]GCTTTTTGAAGGAAA | 22954 |
rs555217187 | snp | A/G/T | 0.000131818 | 0.00811747 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699452 | TAGCCACTTCTTCTC[A/G/T]GAGAATGAGGATTTC | 22954 |
rs555570915 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700574 | AGGAATTGTACAACA[C/T]AGGCCAGGGCCAACA | 22954 |
rs555611773 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699899 | CCCACCTAAATTTAG[A/T]GCTTTAAAAGATGCA | 22954 |
rs555635894 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701052 | AGTTAGTCTTGTTTT[C/T]AAGATCAGAAGTGGG | 22954 |
rs555711192 | snp | C/T | | | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697767 | GCAGCAGCTTCTCAC[C/T]TGAACCTGGATGCCC | 22954 |
rs555725454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692617 | TTGAATTCAAATCCA[A/G]GAAAGCCTGATCCCT | 22954 |
rs555914032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689444 | ATCTACTTCTTTACT[C/T]AGTTTTCATGACAGT | 22954 |
rs555915611 | snp | C/T | 3.30404e-05 | 0.00406437 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698565 | CCTCGGGAGCTCACC[C/T]TGCAAGATGTGGAGC | 22954 |
rs555952470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690501 | TATAAGGCCCTTAAA[C/G]TAGATCATTGTCTAT | 22954 |
rs556842802 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700212 | ATCATATTCCCGTAA[C/T]ATTATGTCTCAGTCT | 22954 |
rs556969305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692593 | CGTCTCCACAATAAG[C/T]AGTAGAGCTTGAATT | 22954 |
rs557007903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693313 | ACAGTGCTAAGATAT[A/G]ATCTCAGTCCTATAT | 22954 |
rs557209519 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694588 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG | 22954 |
rs557238372 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699839 | CTAGAACTTCAGAAG[C/T]TCCATCTTTTAATGT | 22954 |
rs557476533 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691514 | CCTTGACATAGTTTA[G/T]CTATGTTTAACTTAG | 22954 |
rs557750001 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701178 | TGCCTTACTTTGATG[C/T]AAACAAAATTTGCTA | 22954 |
rs557795910 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700767 | CTCTGGTGTTCATGT[C/T]TTTTAATTAAATACG | 22954 |
rs557939030 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700856 | ACTGTGTTCTTTCAG[A/G]GTGTAGATATCTACC | 22954 |
rs558095719 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697154 | GACTTGCATGTTATA[C/T]TTATTCCTTTTACTG | 22954 |
rs558401622 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686295 | CATCAGCTGCCTTAT[C/G]TCATTAGGTCCTTAT | 22954 |
rs558918995 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687369 | TGGACTCGTCGGAGC[C/T]GCGGGCGGTCAGGTA | 22954 |
rs558962253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696066 | CTCCCCATTATCCCC[A/G]TCTTCTCTGATGTTT | 22954 |
rs559000597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696798 | ACTTAGATGGGTGGA[C/T]AGGTGAGTAAGTAGG | 22954 |
rs559242426 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701527 | ACAGTGGCTCAGGCC[C/T]TTGGCACACAGTTTG | 22954 |
rs559441617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694696 | CAGGATGGTCTCGAT[C/T]TCCTGACCTCATGAT | 22954 |
rs559502933 | snp | A/T | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701781 | GTGAATATTTTAGGC[A/T]GTGCTTAGTACAGTC | 22954 |
rs559813848 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693771 | TACTTAAAGATTTGG[A/C]ATGATAAGACAATTC | 22954 |
rs559939354 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687477 | CGTGCCGGCGTGCAG[C/T]GGCCGCGCCCGAATG | 22954 |
rs560060853 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687729 | GGAGGGAATCAGGGC[C/T]CTGGAGGGACCTGGG | 22954 |
rs560171561 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696253 | TTCCCCATATATACT[C/G]CCACAGTTTTAATCT | 22954 |
rs560377402 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687097 | GGTCCCTTTCGCCCA[C/T]GGGCGTCGGTTTCTT | 22954 |
rs561107355 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686982 | AACGCTTTGCTGAGG[A/T]CTACCCTGGAGGCTA | 22954 |
rs561181017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694816 | GCTATTGCCCCTAGA[C/T]ACTTGGCATTTAAGA | 22954 |
rs561302864 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688871 | CAAAACAACAACAAC[A/C]ACCACCAGAAAAAAA | 22954 |
rs562104353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696367 | ATTATTTCATTCTTA[C/G]ATTAACTCTGTAAAG | 22954 |
rs562106957 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692868 | GTAAGGAGATTGCTA[C/T]GAATTCTAGCATTTC | 22954 |
rs562625645 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688846 | TGAGGTGTTTGGGCT[C/T]GGAGACAGACAAAAC | 22954 |
rs563191272 | snp | C/T | 3.32105e-05 | 0.00407482 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698211 | AAGTTAACTCGTCTG[C/T]GGGAACTTATGGGGG | 22954 |
rs563791818 | snp | G/T | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686503 | AGTATAGTCACCTTG[G/T]AGAGTAGGTGATTGG | 22954 |
rs564184168 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701147 | GTGCAGGGCTGATGG[C/T]AAGCCAAAGAGCAAC | 22954 |
rs564290779 | snp | A/G | 3.29815e-05 | 0.00406075 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698455 | TGCAGGCTGTGTCTC[A/G]CTGTGACTACTTCCT | 22954 |
rs564352159 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695897 | TGATAAGGCACTGCT[A/G]TTTTTTAAATCATCT | 22954 |
rs564372991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691835 | TTAGCATTCTGTTAG[A/G]ATGCATGAGGAATAA | 22954 |
rs565126602 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694763 | GGCATGAGCCACCAC[A/G]CCTGGCCCTGAGTTG | 22954 |
rs565537656 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691474 | AGCATGTTTTCCAGG[-/A]AACCCTATTATTCAT | 22954 |
rs565986492 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700687 | AGTCAGTACATACTA[C/T]TTGGTTTCAGGATTT | 22954 |
rs566081602 | snp | G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696674 | GTACCACTTTCTGCC[G/T]TCATTATTATTTACC | 22954 |
rs566141939 | snp | A/T | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699520 | ATCTCATCGTGGCTG[A/T]CAGTAGTCGCAAGGA | 22954 |
rs566391067 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685996 | AACGGGTGCAAAGTC[G/T]CCCCAACTGGTCTAA | 22954 |
rs566423760 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685311 | CACTGGCTTCCCCCA[A/G]CCCACCAAGTTATCC | 22954 |
rs566580469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694325 | GAACACAGATGTCCC[G/T]GTGCATTGTAAGGTA | 22954 |
rs567071452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696699 | TTTACCTACATGTCT[G/T]GTCTTTTATAAAGTT | 22954 |
rs567077221 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696892 | TCATCACAATTTTCT[A/G]CTTCTGTGGATGATT | 22954 |
rs567551216 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687215 | TGCCCCGCGCGCTTG[G/T]GGCCAGCTGCACGAC | 22954 |
rs567749286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695871 | TACTCTAAGCCAGAA[A/G]TAAACTGTCTTGATA | 22954 |
rs567833792 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688135 | TGAGGTGCGGGGCTG[A/T]GTGTGGCAGAGATTT | 22954 |
rs567913198 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699910 | TTAGAGCTTTAAAAG[A/G]TGCACTGCCCAAATA | 22954 |
rs568153046 | in-del | -/G | 0.34437 | 0.231505 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687514 | GTGGGGACCGGATCT[-/G]GGGGGGGGCAGGACT | 22954 |
rs568240672 | snp | A/C | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689280 | TGAGTTACTTAACCA[A/C]CCAGTGCCTTGGCTC | 22954 |
rs568423338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689116 | CGCCCTTCCCCCCCG[C/T]AGTAAGGAATTATCC | 22954 |
rs568433214 | snp | C/T | 4.94735e-05 | 0.00497336 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698319 | TATGGGCATGAGGAG[C/T]GCAGGGTCCAGGATG | 22954 |
rs568812188 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700232 | TGTCTCAGTCTGATC[A/G]TCTTTACCAGTATGA | 22954 |
rs568935813 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688344 | AAGGACCCTGAGTAG[A/G]TTTGTGGATTGGTGT | 22954 |
rs569426994 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689853 | GCAACGGACTATAGG[C/G]TGAGGTATGGAGGCC | 22954 |
rs569502547 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699874 | ATTTGTTATGTCCCC[C/T]TCCCCGCTTCCCACC | 22954 |
rs569540984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691263 | AATGAACAGATGTTA[C/T]ATGCAGAGAAAGGAA | 22954 |
rs569587415 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689042 | CTACTGGCCTCAAGT[C/G]GGTAGATTAAACATT | 22954 |
rs570088499 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696139 | AAAACATTCATCACC[C/T]CACCATGCCCTTGAA | 22954 |
rs570489446 | in-del | -/GGGCCAGC | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687215 | TGCCCCGCGCGCTTG[-/GGGCCAGC]TGCACGACAAGCCCC | 22954 |
rs570787290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691129 | TTCACTCTGTTGCTC[A/G]GGCTCTTTGCCAGAT | 22954 |
rs570882290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690178 | CCTTGTCAGTAGCTA[C/T]GGCACTTGTCCTGTC | 22954 |
rs571019638 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695400 | ATCAGGGAGGAAGGA[C/T]TAACTTTAGATAATT | 22954 |
rs571526516 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699788 | TGGCACATGCAGAAT[A/C]GACTCAGCCTATGTC | 22954 |
rs572039781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690607 | TTCTAGGTGCCCTTA[C/G]CAACCTCTCAGCCAG | 22954 |
rs572052810 | snp | C/T | 0.0012718 | 0.0251849 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698112 | TTATGTGAGCCCTGC[C/T]GGGAGGCAGACCATC | 22954 |
rs572074758 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700782 | CTTTTAATTAAATAC[A/G]GAATTTTGGAGATGA | 22954 |
rs572584943 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693509 | GGGACAGATTCTCAT[C/G]GGGAGCTGAAGAGAT | 22954 |
rs572600335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692695 | GTCTTTTAGTCCTAG[C/T]TCTGTTGTGTGATTT | 22954 |
rs572604510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693868 | TATTACAGTAATGAC[C/T]AGATGTGCCCTTCTG | 22954 |
rs572618351 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690224 | AAAATGCAAATGATT[A/G]TAATTTGTTGAGTGC | 22954 |
rs572710748 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701120 | TTTACTAAGTAATAT[A/G]TCTTACTCTAGGTGC | 22954 |
rs573190873 | snp | C/T | 0.0018128 | 0.0300518 | upstream-variant-2KB, intron-variant, missense | TRIM32, ASTN2 | GRCh38.p7 | 9:116686751 | CAAGTCTGCCTCTGC[C/T]GTCGGCCTCCCAGCT | 22954 |
rs573622329 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700950 | TACATGTGTACAGAA[C/T]CATCCCCCAAGGTTT | 22954 |
rs573732326 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700602 | ACAAAGTGGAGAGGT[A/G]GACACATTTTCATGT | 22954 |
rs573783882 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692595 | TCTCCACAATAAGTA[C/G]TAGAGCTTGAATTCA | 22954 |
rs573889604 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686608 | GTGCCCCAGATTCCC[C/T]CAAATCTCAGGCCAG | 22954 |
rs573961489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694652 | TTTTTTTTGTATTTT[C/T]AGTAGAGACGGAGTT | 22954 |
rs573999550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695279 | CACTTCATAGTGTCA[A/T]CATGAAGATTAAAAG | 22954 |
rs573999660 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685474 | GTCTAGGCAGTGGGC[A/G]AGGTAAACTCCTCAG | 22954 |
rs574543133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696177 | CTCAAAAATCTCATT[C/T]TGGCTCTGAAGACCT | 22954 |
rs574718662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116687654 | CGGTTGCAGCATCTC[G/T]GGAGGTATGAGGTAA | 22954 |
rs575633576 | snp | C/T | 1.64857e-05 | 0.00287099 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697811 | AGAATGCCCCATCTG[C/T]ATGGAGTCCTTCACA | 22954 |
rs575695746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695230 | TCTGAGCATTCGTTT[C/T]CTCATCTGTAAAATA | 22954 |
rs575734376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688392 | ATTTTCCTTAAATCG[C/T]TGCATGGGAGACAGA | 22954 |
rs575772581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695491 | TGTTGTAATGTATAT[C/T]TCTACATTAACTCCC | 22954 |
rs575809349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696067 | TCCCCATTATCCCCG[C/T]CTTCTCTGATGTTTC | 22954 |
rs575825332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690504 | AAGGCCCTTAAAGTA[G/T]ATCATTGTCTATGCA | 22954 |
rs575937203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689485 | AGGCTCTACTGTATT[C/T]AGTTTTACACATGAG | 22954 |
rs575937254 | snp | C/T | 1.65663e-05 | 0.002878 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698648 | GCCCCGGACAGTTAA[C/T]GTGGAAGATTCCTGG | 22954 |
rs576963223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688768 | AGACCTCCAGGGGAA[C/T]GAGTGGAATAATTTA | 22954 |
rs577002302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689325 | GGGGTTATGATAACA[A/G]GACCAATGTCACAGA | 22954 |
rs577072407 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697006 | TTTTCTTTGCTTAAA[A/G]TACCTTTATCCTCAT | 22954 |
rs577555648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691518 | GACATAGTTTAGCTA[C/T]GTTTAACTTAGTAAT | 22954 |
rs577667095 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690740 | TTTTGAGACCTTGGA[C/G]AGGCTACTTTCTCTG | 22954 |
rs577805788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694530 | GCAGTGGCGCGTCTC[A/G]GCTCACTGCAAGCTC | 22954 |
rs577814903 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700096 | ATTGTTTCCTTCCTA[A/C]TATAATGTGCTTCAT | 22954 |
rs577916622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693643 | ATGGCACAAAGTGCA[C/T]AACAGGAAACAGACA | 22954 |
rs577967994 | snp | C/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701274 | CAAAGGATAGGTAAA[C/G]AGGTCATTAAAATGA | 22954 |
rs745324847 | snp | A/G | 1.65946e-05 | 0.00288046 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697710 | GCTGTTCAGTTCTGA[A/G]CTGTGCTAGCAATAC | 22954 |
rs745396502 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701118 | TGTTTACTAAGTAAT[A/G]TATCTTACTCTAGGT | 22954 |
rs745426698 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686403 | TTTGTTTATTGTTTT[A/G]TCATTGTGCAGGGTC | 22954 |
rs745543294 | snp | G/T | 0.000121825 | 0.00780369 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686677 | GAGCAAAACTACACT[G/T]GGTTTGGGTTCCCGG | 22954 |
rs745663214 | snp | A/C | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688915 | AGGTATTGAGCATTT[A/C]GTCCTGTGCTAGACT | 22954 |
rs745730451 | snp | A/C | 1.64895e-05 | 0.00287132 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698311 | TCCAGGAGTATGGGC[A/C]TGAGGAGCGCAGGGT | 22954 |
rs745937688 | snp | A/G | 1.65222e-05 | 0.00287417 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698800 | CAGCCTCCAATATCC[A/G]GCAGTGCCTCTTTCT | 22954 |
rs746066557 | in-del | -/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693920 | TGTCTCTTAGCTCCA[-/T]TTTCAGGCTAAGATC | 22954 |
rs746197672 | snp | C/T | 1.65457e-05 | 0.00287621 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698043 | GGGCTGCTCATGTGT[C/T]GGTCCTGTGGGCGGC | 22954 |
rs746232692 | in-del | -/TG | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701612 | AATCCTCCAGCTGTC[-/TG]TGCTTTTGAAAGAGG | 22954 |
rs746299779 | snp | A/G | 9.88598e-05 | 0.00702995 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699599 | GGGACTTACCTGTCC[A/G]GTGGGCATAGCCCTA | 22954 |
rs746321506 | in-del | -/GACA | 1.64806e-05 | 0.00287054 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697970 | CAGCTTGACCCAGCT[-/GACA]GACAATCTGACAGTG | 22954 |
rs746368262 | snp | C/T | 4.94368e-05 | 0.00497152 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697959 | ACCCGCATAACCAGC[C/T]TGACCCAGCTGACAG | 22954 |
rs746383181 | snp | A/G | 6.61715e-05 | 0.00575164 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699048 | CCTCTCTCAGTGGCA[A/G]TGAACTGCCAGGGGC | 22954 |
rs746450893 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693625 | GTGGGAGGTCAAGAA[C/T]TAATGGCACAAAGTG | 22954 |
rs746472238 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699331 | GCACCGTCTACTTCA[C/T]CCAGGGCTTAGGCCT | 22954 |
rs746590049 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699451 | TTAGCCACTTCTTCT[C/T]GGAGAATGAGGATTT | 22954 |
rs746676204 | snp | C/G | 1.64822e-05 | 0.00287068 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697833 | TCCTTCACAGAAGAG[C/G]AGCTGCGTCCCAAGC | 22954 |
rs746815723 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691750 | GTCAGGTGATGACCT[C/T]ACTGAATTCGTTAAA | 22954 |
rs746890090 | snp | A/T | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699505 | TGGATGCTCGTGGTG[A/T]TCTCATCGTGGCTGA | 22954 |
rs747040382 | in-del | -/C | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693534 | AGAGATGTGCTAGTA[-/C]AGTATGGTATGGGAT | 22954 |
rs747057835 | snp | A/G | | | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698504 | AGATGTAGCACTACT[A/G]GAGGAGACAGCTGAT | 22954 |
rs747067557 | snp | A/C/T | 4.94877e-05 | 0.00497411 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699096 | AGCTATGATAACTCC[A/C/T]TCAAGGTATATACCT | 22954 |
rs747266069 | snp | A/T | 1.65496e-05 | 0.00287655 | stop-gained, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698943 | CAAGTCTTTACCCGC[A/T]AAGGCTTTTTGAAGG | 22954 |
rs747533628 | snp | A/G | 1.67391e-05 | 0.00289297 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698118 | GAGCCCTGCCGGGAG[A/G]CAGACCATCAGCCTC | 22954 |
rs747685252 | in-del | -/G | 4.94605e-05 | 0.0049727 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698433 | TACCTGCTTAACATT[-/G]CAGAGGTGCAGGCTG | 22954 |
rs747692895 | snp | A/G | 0.000120576 | 0.00776361 | upstream-variant-2KB, intron-variant, synonymous-codon | TRIM32, ASTN2 | GRCh38.p7 | 9:116686788 | GCAAAACATTCCTTT[A/G]CAGAGCAATGTGTTC | 22954 |
rs747723402 | snp | A/G | 1.64866e-05 | 0.00287106 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698439 | CTTAACATTGCAGAG[A/G]TGCAGGCTGTGTCTC | 22954 |
rs747829781 | snp | C/T | 4.94311e-05 | 0.00497123 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699468 | GAGAATGAGGATTTC[C/T]GCTGCATTGCTGGCA | 22954 |
rs747954415 | snp | C/T | 1.64933e-05 | 0.00287165 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699116 | GGTATATACCTTGGA[C/T]GGCCACTGCGTGGCC | 22954 |
rs748106080 | snp | A/G | 1.65048e-05 | 0.00287265 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698525 | GACAGCTGATGAGGA[A/G]GAGCCAGAGCTCACT | 22954 |
rs748185117 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690619 | TTACCAACCTCTCAG[C/G]CAGACTTTGTCTAAA | 22954 |
rs748208744 | snp | A/G | 1.67624e-05 | 0.00289498 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698129 | GGAGGCAGACCATCA[A/G]CCTCCTGGCCACTGT | 22954 |
rs748277314 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696237 | CAAGTCTGTTACTCT[A/G]TTCCCCATATATACT | 22954 |
rs748324526 | snp | A/G | 3.33061e-05 | 0.00408068 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698068 | GGCGGCGTCTGCCCC[A/G]GCAATTCTGCCGGAG | 22954 |
rs748404804 | snp | G/T | 1.64928e-05 | 0.00287161 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699204 | TTTGTAGTAACCGAT[G/T]TGGAAGGTGGAAAGC | 22954 |
rs748468497 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699709 | CCACCCCATAGGGGA[C/T]GAGAAATTATCAGTT | 22954 |
rs748493211 | snp | G/T | 1.65781e-05 | 0.00287902 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698684 | GGAGGCCACAGCGTC[G/T]GCTGCCTCTACCTCT | 22954 |
rs748502403 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686806 | GAGCAATGTGTTCAT[A/G]GATAAACTTGTCTCT | 22954 |
rs748575389 | snp | C/G | 1.65261e-05 | 0.0028745 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698764 | CTAGGGCCTCACCTG[C/G]TAAACAGCGGGGTCC | 22954 |
rs748613689 | snp | A/G | 1.65304e-05 | 0.00287488 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697739 | ACCCTTCAAAGGAAG[A/G]GCAATGGCTGCAGCA | 22954 |
rs748896830 | snp | C/G | 5.1113e-05 | 0.00505508 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699748 | TCCCAAGCCAACTTC[C/G]CTTCCCTTAGTTCTT | 22954 |
rs748952234 | snp | A/C/G | 3.29779e-05 | 0.00406055 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698458 | AGGCTGTGTCTCGCT[A/C/G]TGACTACTTCCTGGC | 22954 |
rs749100046 | snp | A/G | 1.67522e-05 | 0.0028941 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698137 | ACCATCAGCCTCCTG[A/G]CCACTGTACACTCCC | 22954 |
rs749146435 | snp | A/C/G | 3.29518e-05 | 0.00405894 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699312 | GTCACCTGTGATGCT[A/C/G]AGGGCACCGTCTACT | 22954 |
rs749206703 | snp | G/T | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686060 | CCCCTACCTGCTAAT[G/T]ACAATTTTTCAAATA | 22954 |
rs749242181 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686989 | TGCTGAGGACTACCC[C/T]GGAGGCTACCGTTTT | 22954 |
rs749255121 | snp | A/G | 1.66139e-05 | 0.00288213 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697698 | CATGAATACTGTGCT[A/G]TTCAGTTCTGAGCTG | 22954 |
rs749382323 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693555 | GGTATGGGATGTACA[A/G]TATTAATCATTAGGT | 22954 |
rs749537116 | snp | C/G/T | 3.32167e-05 | 0.00407522 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698207 | AGAGAAGTTAACTCG[C/G/T]CTGCGGGAACTTATG | 22954 |
rs749660270 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689154 | AATGTCAGTAATGCC[A/G]AAGTTGAGGCACTCT | 22954 |
rs749689590 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697947 | TGCAGCAAGATTACC[C/T]GCATAACCAGCTTGA | 22954 |
rs749696299 | in-del | -/GTTAACTC | 6.65203e-05 | 0.00576678 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698198 | GGACTTTGGAGAGAA[-/GTTAACTC]GTCTGCGGGAACTTA | 22954 |
rs749760133 | snp | A/T | 0.000181748 | 0.00953104 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698782 | AACAGCGGGGTCCTG[A/T]GGCAGCCTCCAATAT | 22954 |
rs749761958 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692148 | CACCAAAGGCTGATA[C/T]AGGTAAAGGAAATGG | 22954 |
rs749899402 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689181 | TCTGACCTAGAGTCA[-/C]GATACCCTGGGTTCA | 22954 |
rs749903497 | snp | A/G | 1.65296e-05 | 0.00287481 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698751 | GTGGTTGCCAGCCCT[A/G]GGGCCTCACCTGCTA | 22954 |
rs750062920 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700428 | TTTTAAAGAAGCATA[C/T]ATGGGTTGGAATTAT | 22954 |
rs750269792 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690580 | GGTAAAACAATCAAA[C/T]TTAAAAATCATTTCT | 22954 |
rs750300057 | snp | A/G | 3.29484e-05 | 0.00405871 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699529 | TGGCTGACAGTAGTC[A/G]CAAGGAAATTCTCCA | 22954 |
rs750316476 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697896 | TGCCTGGAGAAGCTA[C/T]TGGCCAGTAGCATCA | 22954 |
rs750466433 | snp | A/G | 4.94719e-05 | 0.00497328 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698486 | GGCCAAGATCAAGCA[A/G]GCAGATGTAGCACTA | 22954 |
rs750550251 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696824 | GTAGGAGGATAGATG[C/T]GTGGAAAATGTGTAT | 22954 |
rs750626801 | snp | C/T | 1.65745e-05 | 0.00287871 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699681 | ATCTACAGCTACCAT[C/T]TGAGAAGATATTCCA | 22954 |
rs750797541 | snp | A/G | 5.02155e-05 | 0.00501051 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698113 | TATGTGAGCCCTGCC[A/G]GGAGGCAGACCATCA | 22954 |
rs751028044 | snp | A/G/T | 6.5908e-05 | 0.00574023 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697921 | GCATCAATGGTGTCC[A/G/T]CTGTCCCTTTTGCAG | 22954 |
rs751224092 | snp | C/T | 1.65364e-05 | 0.0028754 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698903 | AGGTGAAGTACTAGT[C/T]GCTGACCGTGGTAAC | 22954 |
rs751447830 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694343 | GCATTGTAAGGTAAC[A/G]TTCTAGATTCAAACT | 22954 |
rs751460354 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699561 | TTTCCTAAGGGTGGG[A/G]GCTATAGTGTCCTTA | 22954 |
rs751527505 | snp | G/T | 0.000120547 | 0.00776267 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686824 | TAAACTTGTCTCTAG[G/T]GCAGCTCTCTGTCAG | 22954 |
rs751662240 | snp | A/C | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700101 | TTCCTTCCTACTATA[A/C]TGTGCTTCATCTGTG | 22954 |
rs751714214 | snp | C/T | 1.65515e-05 | 0.00287671 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698624 | CCAAATTGGACAAGC[C/T]GTTAAGAAGCCCCGG | 22954 |
rs751757854 | snp | C/T | 1.6489e-05 | 0.00287128 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699189 | TTGCCATCTGGCCAG[C/T]TTGTAGTAACCGATG | 22954 |
rs751787826 | in-del | -/ACTT | 1.64776e-05 | 0.00287028 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699441 | GTCGCCAGATTAGCC[-/ACTT]ACTTCTTCTCGGAGA | 22954 |
rs751975292 | snp | G/T | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701379 | TCAAAGATTGGGTAA[G/T]TGAGAGGAAATTGAT | 22954 |
rs752016708 | snp | C/T | 9.9295e-05 | 0.0070454 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698238 | GGGGAGCTGCAGCGG[C/T]GGAAGGCAGCCTTGG | 22954 |
rs752129261 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699280 | GCTGCCTATGTAGTG[C/T]TGTGCGGCCCAAATT | 22954 |
rs752165418 | snp | C/T | 1.67172e-05 | 0.00289108 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698100 | TGTGGTTTGGTGTTA[C/T]GTGAGCCCTGCCGGG | 22954 |
rs752319293 | snp | A/G | 1.68071e-05 | 0.00289884 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699722 | GATGAGAAATTATCA[A/G]TTTCTTCTGCTCCCA | 22954 |
rs752329242 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698028 | CTCAGCGAGGCTGTG[A/G]GGCTGCTCATGTGTC | 22954 |
rs752379777 | snp | C/T | 1.64876e-05 | 0.00287116 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699169 | AACCATGGGGTATCA[C/T]AGCCTTGCCATCTGG | 22954 |
rs752394920 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689830 | GAGGTTATCAGGCAG[A/G]ATGAGGTGCAACGGA | 22954 |
rs752475495 | in-del | -/AAC | | | cds-indel, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699613 | GGTGGGCATAGCCCT[-/AAC]AACTCCTAAGGGGCA | 22954 |
rs752567476 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694828 | AGACACTTGGCATTT[A/G]AGAATTTACCATTCA | 22954 |
rs752582017 | snp | A/C | 0.00012062 | 0.00776501 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686845 | TCTCTGTCAGAGCAC[A/C]GAACATGAGGCCAAA | 22954 |
rs752667526 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699306 | AAATTTGTCACCTGT[A/G]ATGCTGAGGGCACCG | 22954 |
rs752855496 | snp | C/T | 1.64936e-05 | 0.00287168 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697781 | CCTGAACCTGGATGC[C/T]CTCCGGGAAGTGCTA | 22954 |
rs752860146 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699390 | CACCTGGAGGGTGGC[C/T]TTTCCATTGGCTCTG | 22954 |
rs752864284 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687339 | GAGGGAGGCAGGCGG[A/G]TGGGCTGCCGGCGGT | 22954 |
rs752937052 | snp | C/G | 1.64909e-05 | 0.00287144 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698347 | ATGAGCTGGCTCGCT[C/G]TCGGAAGTTCTTCAC | 22954 |
rs753215766 | snp | G/T | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701486 | GATCTGTCTTTGCTG[G/T]CAGTGGGGGACTTGC | 22954 |
rs753234105 | snp | G/T | 1.65072e-05 | 0.00287286 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698258 | GGCAGCCTTGGAAGG[G/T]GTCTCCAAGGACCTT | 22954 |
rs753259162 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700187 | TCCACCTTTCAGTGA[C/T]ATTTAAGACATCATA | 22954 |
rs753319373 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689939 | TGAAGGAGAGTAACT[A/G]CTGTTCTGTATGGTC | 22954 |
rs753330152 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691292 | AATTGAAAGAGAGAG[A/G]GGGTTGAGGTTAGTT | 22954 |
rs753431772 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700974 | AAGGTTTAGAGTCAC[C/T]AATACCCTATTCTGA | 22954 |
rs753519978 | snp | A/G | 6.68527e-05 | 0.00578117 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698176 | AAGCAGCTGAGGAGC[A/G]GCGTCGGGACTTTGG | 22954 |
rs753539210 | in-del | -/TGCATTA | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690247 | TGAGTGCTTATTATG[-/TGCATTA]TGCATTATCTTAGTG | 22954 |
rs753585764 | snp | G/T | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687994 | TGTGAAGGCAGCACA[G/T]GACATTCAGTGCATA | 22954 |
rs753650301 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697792 | ATGCCCTCCGGGAAG[C/T]GCTAGAATGCCCCAT | 22954 |
rs753733923 | snp | A/C/G | 3.30689e-05 | 0.00406615 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698742 | CCGGAGGAAGTGGTT[A/C/G]CCAGCCCTAGGGCCT | 22954 |
rs753738560 | snp | C/T | 3.29598e-05 | 0.00405941 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697875 | GGCCATACCATCTGC[C/T]GCCAGTGCCTGGAGA | 22954 |
rs753819969 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698293 | CAAGGTATAAAGCAG[C/T]TCTCCAGGAGTATGG | 22954 |
rs753866301 | snp | A/G | 3.29478e-05 | 0.00405867 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699513 | CGTGGTGATCTCATC[A/G]TGGCTGACAGTAGTC | 22954 |
rs753960738 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698375 | CACAGGCTCTTTGGC[C/T]GAAGTTGAGAAGTCC | 22954 |
rs754071735 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699414 | GGCTCTGTAGGCCCT[A/G]ATGGGCAGCTGGGTC | 22954 |
rs754088922 | snp | G/T | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686209 | AGAATTGGGTACAAA[G/T]TTGGGCTCCAACACT | 22954 |
rs754182702 | snp | G/T | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701679 | TACCCATCTAAACCA[G/T]TCATGCCTTTTCCCT | 22954 |
rs754192979 | snp | A/G | 3.31214e-05 | 0.00406935 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699020 | CCTTGGGGCAGATCT[A/G]CCCAACCTCACTCCT | 22954 |
rs754362159 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687859 | AGGAGCAAGGTCTAG[A/G]GCGATCCTAAGTGCT | 22954 |
rs754449534 | snp | A/G | 6.60306e-05 | 0.00574551 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698019 | ACAGCTGGGCTCAGC[A/G]AGGCTGTGGGGCTGC | 22954 |
rs754554333 | snp | C/T | 6.61594e-05 | 0.00575112 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698910 | GTACTAGTCGCTGAC[C/T]GTGGTAACTATCGTA | 22954 |
rs754641107 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688007 | CATGACATTCAGTGC[A/G]TAAGAGGAAGGAGCA | 22954 |
rs754722456 | snp | A/G | 1.65004e-05 | 0.00287227 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698517 | CTGGAGGAGACAGCT[A/G]ATGAGGAGGAGCCAG | 22954 |
rs755010346 | snp | A/G | 1.67525e-05 | 0.00289413 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699715 | CATAGGGGATGAGAA[A/G]TTATCAGTTTCTTCT | 22954 |
rs755075876 | snp | A/G | 1.64904e-05 | 0.00287139 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699197 | TGGCCAGTTTGTAGT[A/G]ACCGATGTGGAAGGT | 22954 |
rs755258236 | snp | A/G | 0.00012046 | 0.00775987 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686827 | ACTTGTCTCTAGTGC[A/G]GCTCTCTGTCAGAGC | 22954 |
rs755332171 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697242 | AATATGAAAATAATC[A/G]TTAGCTCATTAGCAT | 22954 |
rs755369647 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699282 | TGCCTATGTAGTGCT[A/G]TGCGGCCCAAATTTG | 22954 |
rs755416418 | snp | A/C | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701533 | GCTCAGGCCTTTGGC[A/C]CACAGTTTGCAGTGG | 22954 |
rs755478136 | snp | C/T | 1.67441e-05 | 0.0028934 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698119 | AGCCCTGCCGGGAGG[C/T]AGACCATCAGCCTCC | 22954 |
rs755561234 | snp | A/G | 1.66535e-05 | 0.00288556 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698190 | CGGCGTCGGGACTTT[A/G]GAGAGAAGTTAACTC | 22954 |
rs755672567 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688147 | CTGAGTGTGGCAGAG[A/G]TTTGGAAATAGGGAT | 22954 |
rs755732550 | snp | C/G | 1.65149e-05 | 0.00287353 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698029 | TCAGCGAGGCTGTGG[C/G]GCTGCTCATGTGTCG | 22954 |
rs755938925 | snp | G/T | 1.66076e-05 | 0.00288158 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697692 | CTAGGGCATGAATAC[G/T]GTGCTGTTCAGTTCT | 22954 |
rs755947560 | snp | C/G | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685780 | TTAAGGGAGAAGAGA[C/G]ATTTTTTTTTTTCAA | 22954 |
rs756049046 | snp | C/G | 3.30142e-05 | 0.00406276 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698537 | GGAGGAGCCAGAGCT[C/G]ACTGCCAGCTTGCCT | 22954 |
rs756141939 | snp | A/G | 1.65633e-05 | 0.00287774 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698642 | TAAGAAGCCCCGGAC[A/G]GTTAACGTGGAAGAT | 22954 |
rs756317694 | snp | A/G | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701732 | GCTCAAAATGGAAGT[A/G]TGATCTGAGTCTTTT | 22954 |
rs756350336 | snp | C/T | 3.29881e-05 | 0.00406115 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697782 | CTGAACCTGGATGCC[C/T]TCCGGGAAGTGCTAG | 22954 |
rs756356270 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116687590 | GGGGCTGAGGAGATC[A/C]GAGGAGATGCAGCTG | 22954 |
rs756404391 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699307 | AATTTGTCACCTGTG[A/G]TGCTGAGGGCACCGT | 22954 |
rs756454902 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693449 | ATGGAATATAATTAT[A/G]TAATTTTTCTGAGTC | 22954 |
rs756695941 | in-del | -/C | 1.66704e-05 | 0.00288703 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698186 | GGAGCGGCGTCGGGA[-/C]TTTGGAGAGAAGTTA | 22954 |
rs756704681 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691315 | GGTTAGTTGGAGGTC[C/G]CTGAGAAGGGGCTAT | 22954 |
rs756710806 | snp | C/G | 1.65688e-05 | 0.00287821 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698659 | TTAACGTGGAAGATT[C/G]CTGGGCCATGGAGGC | 22954 |
rs757287996 | snp | C/G | 4.9467e-05 | 0.00497303 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697797 | CTCCGGGAAGTGCTA[C/G]AATGCCCCATCTGCA | 22954 |
rs757348387 | in-del | -/C | 0.000120707 | 0.00776782 | upstream-variant-2KB, intron-variant, frameshift-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686774 | TCCCAGCTGAGTAGG[-/C]AAAACATTCCTTTAC | 22954 |
rs757432259 | snp | A/T | 1.64781e-05 | 0.00287033 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699424 | GCCCTGATGGGCAGC[A/T]GGGTCGCCAGATTAG | 22954 |
rs757439739 | in-del | -/TTTT/TTTTT/TTTTTT | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694459 | GAGTTGTAATTTCTC[-/TTTT/TTTTT/TTTTTT]TTTTTTTTTTTTTTT | 22954 |
rs757524831 | snp | A/G | 3.29484e-05 | 0.00405871 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699522 | CTCATCGTGGCTGAC[A/G]GTAGTCGCAAGGAAA | 22954 |
rs757526804 | snp | C/G | 4.94703e-05 | 0.0049732 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698297 | GTATAAAGCAGTTCT[C/G]CAGGAGTATGGGCAT | 22954 |
rs757634856 | snp | C/G | 1.65586e-05 | 0.00287733 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699027 | GCAGATCTACCCAAC[C/G]TCACTCCTCTCTCAG | 22954 |
rs757752867 | snp | C/G | 3.3094e-05 | 0.00406766 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698933 | CTATCGTATACAAGT[C/G]TTTACCCGCAAAGGC | 22954 |
rs757842932 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697828 | TGGAGTCCTTCACAG[A/G]AGAGCAGCTGCGTCC | 22954 |
rs757902820 | snp | A/C | 1.65315e-05 | 0.00287498 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698897 | CAGTCAAGGTGAAGT[A/C]CTAGTCGCTGACCGT | 22954 |
rs758004405 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700429 | TTTAAAGAAGCATAT[A/G]TGGGTTGGAATTATG | 22954 |
rs758054761 | snp | C/T | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701707 | CCTCAAGTAAAGCAG[C/T]TATCTGTTGGCTCAA | 22954 |
rs758118499 | snp | A/C | 1.64743e-05 | 0.00287 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699530 | GGCTGACAGTAGTCG[A/C]AAGGAAATTCTCCAT | 22954 |
rs758130716 | in-del | -/AATA | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701114 | TGGTGTTTACTAAGT[-/AATA]AATATATCTTACTCT | 22954 |
rs758299221 | snp | A/G | 3.29549e-05 | 0.00405911 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697905 | AAGCTATTGGCCAGT[A/G]GCATCAATGGTGTCC | 22954 |
rs758381917 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691462 | AGACAACAGGCAAGC[A/G]TGTTTTCCAGGAAAC | 22954 |
rs758495606 | snp | C/T | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698539 | AGGAGCCAGAGCTCA[C/T]TGCCAGCTTGCCTCG | 22954 |
rs758553325 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698403 | TCCAATAGTCAAGTG[A/G]TAGAGGAGCAGAGTT | 22954 |
rs758672160 | snp | G/T | 1.64912e-05 | 0.00287147 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698492 | GATCAAGCAGGCAGA[G/T]GTAGCACTACTGGAG | 22954 |
rs758786326 | snp | A/G | 5.0213e-05 | 0.00501039 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698116 | GTGAGCCCTGCCGGG[A/G]GGCAGACCATCAGCC | 22954 |
rs758882829 | snp | A/G | 4.96471e-05 | 0.00498208 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698044 | GGCTGCTCATGTGTC[A/G]GTCCTGTGGGCGGCG | 22954 |
rs758934164 | snp | C/T | 3.30437e-05 | 0.00406457 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699067 | ACTGCCAGGGGCTGA[C/T]TGGTGTGACTGACAG | 22954 |
rs759016258 | snp | C/T | 3.29761e-05 | 0.00406041 | stop-gained, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699144 | GCCTGTCACAGGAGC[C/T]AGCTGAGCAAACCAT | 22954 |
rs759024082 | snp | A/C | 1.64882e-05 | 0.00287121 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699178 | GTATCACAGCCTTGC[A/C]ATCTGGCCAGTTTGT | 22954 |
rs759025665 | snp | A/G | 1.64904e-05 | 0.00287139 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699241 | GTTTCACAGTTGATC[A/G]AGGATCAGGGGTGGT | 22954 |
rs759344939 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696184 | ATCTCATTTTGGCTC[A/T]GAAGACCTTTTATAA | 22954 |
rs759347153 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700207 | AAGACATCATATTCC[C/T]GTAACATTATGTCTC | 22954 |
rs759376012 | in-del | -/A | 3.30371e-05 | 0.00406417 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698849 | AGGCAGCACTCCAGG[-/A]ATGTTCAATCTTCCA | 22954 |
rs759526539 | in-del | -/CTAT | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697501 | GTCTGGTTTGTTTCC[-/CTAT]CTGTCACCCTCACGT | 22954 |
rs759596991 | snp | A/T | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701371 | TCCGATTTTCAAAGA[A/T]TGGGTAATTGAGAGG | 22954 |
rs759604705 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687218 | CCCGCGCGCTTGGGG[A/C]CAGCTGCACGACAAG | 22954 |
rs759707001 | snp | C/T | 0.000132461 | 0.00813714 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698720 | TTTTAGAGAGATGGA[C/T]ATGAGCCCGGAGGAA | 22954 |
rs759724372 | snp | C/T | 4.94409e-05 | 0.00497172 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697850 | GCTGCGTCCCAAGCT[C/T]CTGCACTGTGGCCAT | 22954 |
rs759742371 | snp | A/G | 0.000380691 | 0.0137913 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698631 | GGACAAGCTGTTAAG[A/G]AGCCCCGGACAGTTA | 22954 |
rs759785845 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699483 | CGCTGCATTGCTGGC[A/G]TGTGTGTGGATGCTC | 22954 |
rs759793253 | snp | C/G | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685747 | ACATTAAAGAAGAGT[C/G]AAACACTGATTTTTG | 22954 |
rs759830190 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692348 | TGAAAAGTGCCTATT[C/T]ATTTCTTCTAATAGG | 22954 |
rs759945386 | snp | A/G | 8.27027e-05 | 0.00642997 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698239 | GGGAGCTGCAGCGGC[A/G]GAAGGCAGCCTTGGA | 22954 |
rs759997807 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700174 | CAGTGGGATCTGCTC[C/T]ACCTTTCAGTGACAT | 22954 |
rs760108488 | snp | A/T | 1.64798e-05 | 0.00287047 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699368 | GGAGAATCGGCAGAA[A/T]GAGCACCACCTGGAG | 22954 |
rs760180890 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699171 | CCATGGGGTATCACA[A/G]CCTTGCCATCTGGCC | 22954 |
rs760202414 | snp | A/G | 3.34549e-05 | 0.00408978 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698172 | AAAGAAGCAGCTGAG[A/G]AGCGGCGTCGGGACT | 22954 |
rs760241996 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700894 | AAATTCAGCCAAAAG[C/T]ACTATTATGTAAAGA | 22954 |
rs760400497 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699262 | CAGGGGTGGTCAAAT[A/G]CAGCTGCCTATGTAG | 22954 |
rs760513760 | snp | A/G | 0.00013242 | 0.00813586 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698729 | GATGGACATGAGCCC[A/G]GAGGAAGTGGTTGCC | 22954 |
rs760532086 | snp | G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696494 | CTTTGCCTTTTATAC[G/T]TTGTTAAGGTTGTGC | 22954 |
rs760537269 | in-del | -/GGAGCTCACCCTGCAAGATGT | 1.65232e-05 | 0.00287425 | cds-indel, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698554 | TGCCAGCTTGCCTCG[-/GGAGCTCACCCTGCAAGATGT]GGAGCTCACCCTGCA | 22954 |
rs760730435 | snp | A/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698059 | GGTCCTGTGGGCGGC[A/G]TCTGCCCCGGCAATT | 22954 |
rs760820148 | snp | C/T | 3.29652e-05 | 0.00405974 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697980 | CAGCTGACAGACAAT[C/T]TGACAGTGCTAAAGA | 22954 |
rs760918075 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698465 | GTCTCGCTGTGACTA[C/T]TTCCTGGCCAAGATC | 22954 |
rs760924488 | snp | C/G | 1.65187e-05 | 0.00287386 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698844 | GCCAAAGGCAGCACT[C/G]CAGGAATGTTCAATC | 22954 |
rs761012752 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697856 | TCCCAAGCTTCTGCA[C/T]TGTGGCCATACCATC | 22954 |
rs761193342 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699613 | CGGTGGGCATAGCCC[C/T]AACTCCTAAGGGGCA | 22954 |
rs761382746 | snp | C/G | 1.64898e-05 | 0.00287135 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698328 | GAGGAGCGCAGGGTC[C/G]AGGATGAGCTGGCTC | 22954 |
rs761458746 | in-del | -/TGGT | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701219 | TCAAAATTGTTTTTA[-/TGGT]TGGTAGTAGTGTTTC | 22954 |
rs761503419 | snp | A/G | 3.29576e-05 | 0.00405928 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699361 | TCAATCTGGAGAATC[A/G]GCAGAATGAGCACCA | 22954 |
rs761580782 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690524 | TTGTCTATGCACACT[A/G]ATGTGTAACCTTTGT | 22954 |
rs761591526 | snp | A/G/T | 4.96564e-05 | 0.00498258 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698236 | TGGGGGAGCTGCAGC[A/G/T]GCGGAAGGCAGCCTT | 22954 |
rs761682659 | snp | A/G | 1.65244e-05 | 0.00287436 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698879 | AGTCAGTCTCTACGT[A/G]ACCAGTCAAGGTGAA | 22954 |
rs761684552 | snp | A/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699567 | AAGGGTGGGGGCTAT[A/G]GTGTCCTTATTCGAG | 22954 |
rs761878106 | snp | C/T | 1.64827e-05 | 0.00287073 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699634 | CTAAGGGGCAGCTGC[C/T]GGTCTTGGACTGTTG | 22954 |
rs762108943 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692610 | GTAGAGCTTGAATTC[A/G]AATCCAGGAAAGCCT | 22954 |
rs762110851 | in-del | -/TGA | 1.64746e-05 | 0.00287002 | cds-indel, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699503 | TGTGGATGCTCGTGG[-/TGA]TCTCATCGTGGCTGA | 22954 |
rs762250542 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698476 | ACTACTTCCTGGCCA[A/G]GATCAAGCAGGCAGA | 22954 |
rs762271347 | snp | A/T | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687867 | GGTCTAGGGCGATCC[A/T]AAGTGCTATTGAGAA | 22954 |
rs762337721 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689460 | AGTTTTCATGACAGT[C/T]CTTCTAAGTAGGCTC | 22954 |
rs762342489 | snp | C/T | 4.96126e-05 | 0.00498035 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698600 | TAAGGTAGGTCATGT[C/T]GGCCCCCTCCAAATT | 22954 |
rs762478436 | in-del | -/A | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695117 | TTGTTATGTGACAGT[-/A]AAAAAATAGCTTGAA | 22954 |
rs762785784 | snp | C/T | 3.33823e-05 | 0.00408534 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698079 | CCCCGGCAATTCTGC[C/T]GGAGCTGTGGTTTGG | 22954 |
rs762815981 | snp | A/C | 1.6566e-05 | 0.00287797 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698986 | GCCCCAGTGGCATTG[A/C]TAGCTTTGTGCTAAG | 22954 |
rs762840200 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692919 | GGAGCTACAGCAGCT[C/G]ATTTTCTGGGCAAGA | 22954 |
rs762878990 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696758 | CTAAAGACCTCTTGT[A/G]TCTAGTACAGAACAA | 22954 |
rs762905941 | snp | A/G | 3.29843e-05 | 0.00406092 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699128 | GGATGGCCACTGCGT[A/G]GCCTGTCACAGGAGC | 22954 |
rs762907412 | snp | C/T | 1.65466e-05 | 0.00287628 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698614 | TTGGCCCCCTCCAAA[C/T]TGGACAAGCTGTTAA | 22954 |
rs763077693 | snp | A/G | 0.000240993 | 0.0109744 | upstream-variant-2KB, intron-variant, missense | TRIM32, ASTN2 | GRCh38.p7 | 9:116686793 | ACATTCCTTTACAGA[A/G]CAATGTGTTCATGGA | 22954 |
rs763124613 | snp | G/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699890 | TCCCCGCTTCCCACC[G/T]AAATTTAGAGCTTTA | 22954 |
rs763172140 | snp | A/G | 1.66635e-05 | 0.00288643 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699696 | CTGAGAAGATATTCC[A/G]CCCCATAGGGGATGA | 22954 |
rs763188009 | snp | A/C | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701058 | TCTTGTTTTTAAGAT[A/C]AGAAGTGGGTGAGAG | 22954 |
rs763424304 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689768 | CTGGACTTTGTTCTT[C/G]GTTTGCCCTTAGACC | 22954 |
rs763453251 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686978 | TGCCAACGCTTTGCT[C/G]AGGACTACCCTGGAG | 22954 |
rs763454337 | snp | C/T | 1.651e-05 | 0.0028731 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697759 | TGGCTGCAGCAGCAG[C/T]TTCTCACCTGAACCT | 22954 |
rs763720824 | snp | C/T | 5.01744e-05 | 0.00500846 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698175 | GAAGCAGCTGAGGAG[C/T]GGCGTCGGGACTTTG | 22954 |
rs763779010 | snp | C/T | | | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698036 | GGCTGTGGGGCTGCT[C/T]ATGTGTCGGTCCTGT | 22954 |
rs763817002 | snp | C/T | 1.64822e-05 | 0.00287068 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699269 | GGTCAAATACAGCTG[C/T]CTATGTAGTGCTGTG | 22954 |
rs763955829 | snp | C/T | 1.67559e-05 | 0.00289442 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698133 | GCAGACCATCAGCCT[C/T]CTGGCCACTGTACAC | 22954 |
rs763986341 | snp | C/G | 1.65201e-05 | 0.00287398 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698845 | CCAAAGGCAGCACTC[C/G]AGGAATGTTCAATCT | 22954 |
rs763988582 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697790 | GGATGCCCTCCGGGA[A/G]GTGCTAGAATGCCCC | 22954 |
rs764047562 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696497 | TGCCTTTTATACTTT[C/G]TTAAGGTTGTGCCTT | 22954 |
rs764134507 | snp | A/T | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687784 | AACTGGGGGGCCCCG[A/T]TGAGATTTGAGGAAA | 22954 |
rs764186649 | snp | A/G | 1.65405e-05 | 0.00287576 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698736 | ATGAGCCCGGAGGAA[A/G]TGGTTGCCAGCCCTA | 22954 |
rs764366522 | snp | A/G | 4.94385e-05 | 0.0049716 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697869 | CACTGTGGCCATACC[A/G]TCTGCCGCCAGTGCC | 22954 |
rs764373255 | in-del | -/A | 1.64885e-05 | 0.00287123 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699248 | AGTTGATCGAGGATC[-/A]GGGGTGGTCAAATAC | 22954 |
rs764467077 | snp | A/T | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701665 | AGCATTTAGATCTCT[A/T]CCCATCTAAACCAGT | 22954 |
rs764665307 | snp | C/T | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686085 | CAAATATAGTTATCA[C/T]TAAGTGCAAACTACC | 22954 |
rs764730016 | snp | A/G | 3.29772e-05 | 0.00406048 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698471 | CTGTGACTACTTCCT[A/G]GCCAAGATCAAGCAG | 22954 |
rs764793062 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691322 | TGGAGGTCCCTGAGA[A/G]GGGGCTATTGATTTT | 22954 |
rs764873959 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692837 | GCTCACTGCAACCTC[C/T]ACTTCCTGGTCTCAA | 22954 |
rs764957636 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698003 | GCTAAAGATCATTGA[C/T]ACAGCTGGGCTCAGC | 22954 |
rs765158423 | snp | C/T | 1.65666e-05 | 0.00287802 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698967 | TTGAAGGAAATCCGC[C/T]GCAGCCCCAGTGGCA | 22954 |
rs765208184 | snp | A/C | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690573 | TCTTTCTGGTAAAAC[A/C]ATCAAATTTAAAAAT | 22954 |
rs765348678 | snp | C/G | 1.64743e-05 | 0.00287 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699528 | GTGGCTGACAGTAGT[C/G]GCAAGGAAATTCTCC | 22954 |
rs765555919 | snp | G/T | 1.65573e-05 | 0.00287721 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699673 | GCATCAAGATCTACA[G/T]CTACCATCTGAGAAG | 22954 |
rs765617425 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687927 | TTGAGGGGGTGGGGT[A/G]AGTTCTTGAGGGACT | 22954 |
rs765666809 | snp | C/T | 6.59489e-05 | 0.00574196 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699172 | CATGGGGTATCACAG[C/T]CTTGCCATCTGGCCA | 22954 |
rs765686224 | snp | A/G | 1.65411e-05 | 0.00287581 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698602 | AGGTAGGTCATGTTG[A/G]CCCCCTCCAAATTGG | 22954 |
rs765874460 | snp | C/T | 3.31307e-05 | 0.00406992 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698990 | CAGTGGCATTGATAG[C/T]TTTGTGCTAAGCTTC | 22954 |
rs765931929 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694330 | CAGATGTCCCTGTGC[A/G]TTGTAAGGTAACGTT | 22954 |
rs766064961 | in-del | -/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689519 | ACTAAGGCTTAGGAA[-/G]TGACTTGCCTAAGTT | 22954 |
rs766074937 | snp | C/T | 1.65359e-05 | 0.00287536 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698902 | AAGGTGAAGTACTAG[C/T]CGCTGACCGTGGTAA | 22954 |
rs766267880 | snp | A/G | 3.3379e-05 | 0.00408514 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698080 | CCCGGCAATTCTGCC[A/G]GAGCTGTGGTTTGGT | 22954 |
rs766289627 | snp | C/T | 3.30066e-05 | 0.00406229 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698015 | TGATACAGCTGGGCT[C/T]AGCGAGGCTGTGGGG | 22954 |
rs766439806 | snp | A/G | 8.28233e-05 | 0.00643465 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698638 | CTGTTAAGAAGCCCC[A/G]GACAGTTAACGTGGA | 22954 |
rs766457847 | snp | C/T | 0.000120489 | 0.0077608 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686819 | ATGGATAAACTTGTC[C/T]CTAGTGCAGCTCTCT | 22954 |
rs766491249 | snp | A/C | 1.64925e-05 | 0.00287158 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698495 | CAAGCAGGCAGATGT[A/C]GCACTACTGGAGGAG | 22954 |
rs766687896 | snp | G/T | 1.65496e-05 | 0.00287655 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698615 | TGGCCCCCTCCAAAT[G/T]GGACAAGCTGTTAAG | 22954 |
rs766830255 | snp | C/T | 3.30142e-05 | 0.00406276 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697760 | GGCTGCAGCAGCAGC[C/T]TCTCACCTGAACCTG | 22954 |
rs766851159 | snp | C/G | 1.64792e-05 | 0.00287042 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699362 | CAATCTGGAGAATCG[C/G]CAGAATGAGCACCAC | 22954 |
rs767024504 | snp | A/G | 1.66952e-05 | 0.00288917 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698089 | TCTGCCGGAGCTGTG[A/G]TTTGGTGTTATGTGA | 22954 |
rs767055461 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699273 | AAATACAGCTGCCTA[C/T]GTAGTGCTGTGCGGC | 22954 |
rs767176438 | snp | C/G | 1.65594e-05 | 0.0028774 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699018 | TTCCTTGGGGCAGAT[C/G]TACCCAACCTCACTC | 22954 |
rs767396315 | snp | A/C | 1.6736e-05 | 0.0028927 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698161 | CACTCCCTGTCAAAG[A/C]AGCAGCTGAGGAGCG | 22954 |
rs767423594 | snp | C/T | 1.65603e-05 | 0.00287747 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698634 | CAAGCTGTTAAGAAG[C/T]CCCGGACAGTTAACG | 22954 |
rs767493404 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696276 | TTTAATCTAAGGATA[A/G]TAAAAAAGAGAACTA | 22954 |
rs767582051 | snp | C/G | 0.000602083 | 0.0173401 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TRIM32, ASTN2 | GRCh38.p7 | 9:116686831 | GTCTCTAGTGCAGCT[C/G]TCTGTCAGAGCACAG | 22954 |
rs767649701 | snp | A/G | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701451 | AGCCACTTTATCTGT[A/G]GGGGCACCCAGCAGC | 22954 |
rs767818381 | snp | C/T | 0.000131965 | 0.0081219 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697774 | CTTCTCACCTGAACC[C/T]GGATGCCCTCCGGGA | 22954 |
rs767885077 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699378 | CAGAATGAGCACCAC[C/T]TGGAGGGTGGCTTTT | 22954 |
rs767937527 | snp | C/T | 4.94711e-05 | 0.00497324 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698345 | GGATGAGCTGGCTCG[C/T]TCTCGGAAGTTCTTC | 22954 |
rs768024209 | snp | A/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700186 | CTCCACCTTTCAGTG[A/T]CATTTAAGACATCAT | 22954 |
rs768135611 | snp | C/T | 3.295e-05 | 0.00405881 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699498 | ATGTGTGTGGATGCT[C/T]GTGGTGATCTCATCG | 22954 |
rs768228994 | snp | A/C | 3.29652e-05 | 0.00405974 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697836 | TTCACAGAAGAGCAG[A/C]TGCGTCCCAAGCTTC | 22954 |
rs768229782 | snp | C/G | 1.65699e-05 | 0.00287831 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698225 | GCGGGAACTTATGGG[C/G]GAGCTGCAGCGGCGG | 22954 |
rs768280505 | snp | C/G | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685366 | TCAGGGAGATGACTT[C/G]AGTAATCATAAAACT | 22954 |
rs768336228 | in-del | -/AC | 1.64974e-05 | 0.00287201 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698269 | AAGGTGTCTCCAAGG[-/AC]CTTCAGGCAAGGTAT | 22954 |
rs768347084 | snp | A/G | | | intron-variant, upstream-variant-2KB, splice-donor-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687666 | CTCGGGAGGTATGAG[A/G]TAATGTCGGGGCCCT | 22954 |
rs768452232 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689107 | GTGGGATACGCCCTT[-/C]CCCCCCCGCAGTAAG | 22954 |
rs768741902 | snp | A/G/T | 1.64743e-05 | 0.00287 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699510 | GCTCGTGGTGATCTC[A/G/T]TCGTGGCTGACAGTA | 22954 |
rs768786063 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690424 | TAGTTTTATTAGAAG[C/G]CTTTTCCAACCCTTC | 22954 |
rs768844180 | snp | G/T | 3.32452e-05 | 0.00407695 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698063 | CTGTGGGCGGCGTCT[G/T]CCCCGGCAATTCTGC | 22954 |
rs769040262 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697985 | GACAGACAATCTGAC[A/G]GTGCTAAAGATCATT | 22954 |
rs769128859 | snp | C/T | 3.29603e-05 | 0.00405944 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699618 | GGCATAGCCCTAACT[C/T]CTAAGGGGCAGCTGC | 22954 |
rs769410403 | snp | C/T | 3.29761e-05 | 0.00406041 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698454 | GTGCAGGCTGTGTCT[C/T]GCTGTGACTACTTCC | 22954 |
rs769518349 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699469 | AGAATGAGGATTTCC[A/G]CTGCATTGCTGGCAT | 22954 |
rs769607018 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699587 | CCTTATTCGAGAGGG[A/G]CTTACCTGTCCGGTG | 22954 |
rs769607026 | snp | C/G | 1.64923e-05 | 0.00287156 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698336 | CAGGGTCCAGGATGA[C/G]CTGGCTCGCTCTCGG | 22954 |
rs769863991 | snp | A/G | 1.64928e-05 | 0.00287161 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699210 | GTAACCGATGTGGAA[A/G]GTGGAAAGCTTTGGT | 22954 |
rs769877788 | snp | C/G | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685448 | TTCCCCTGTCTTGAT[C/G]AATCAGCTCTGTCTA | 22954 |
rs769958781 | snp | C/T | 1.67649e-05 | 0.0028952 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698132 | GGCAGACCATCAGCC[C/T]CCTGGCCACTGTACA | 22954 |
rs769987584 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699732 | TATCAGTTTCTTCTG[C/T]TCCCAAGCCAACTTC | 22954 |
rs769992168 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691909 | AAAAACCCAGTCAAA[C/G]CAGGGGAGCGTGTCA | 22954 |
rs770015462 | snp | A/G | 5.00046e-05 | 0.00499998 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698072 | GCGTCTGCCCCGGCA[A/G]TTCTGCCGGAGCTGT | 22954 |
rs770128543 | snp | G/T | 1.65269e-05 | 0.00287457 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698771 | CTCACCTGCTAAACA[G/T]CGGGGTCCTGAGGCA | 22954 |
rs770278877 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690713 | TTGAATCCTTGCTCT[A/G]TTACTTATTGGTTTT | 22954 |
rs770328940 | snp | A/G | 1.65784e-05 | 0.00287905 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698685 | GAGGCCACAGCGTCT[A/G]CTGCCTCTACCTCTG | 22954 |
rs770577221 | snp | C/T | 1.70496e-05 | 0.00291967 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699749 | CCCAAGCCAACTTCC[C/T]TTCCCTTAGTTCTTG | 22954 |
rs770696637 | snp | A/G | 1.67497e-05 | 0.00289389 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698145 | CCTCCTGGCCACTGT[A/G]CACTCCCTGTCAAAG | 22954 |
rs770788386 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699933 | CCCAAATAGGACACA[C/T]GATGGTGTTAGCTGA | 22954 |
rs770795697 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688460 | TGAAACTGGATGAGT[A/G]TATGAAGATGAGCAG | 22954 |
rs770803017 | snp | A/G | 1.6489e-05 | 0.00287128 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699140 | CGTGGCCTGTCACAG[A/G]AGCCAGCTGAGCAAA | 22954 |
rs770884964 | in-del | -/T | 1.65544e-05 | 0.00287696 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698626 | AAATTGGACAAGCTG[-/T]TAAGAAGCCCCGGAC | 22954 |
rs771081250 | in-del | -/T | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686383 | CAAAGATGTTAGTCA[-/T]TGTTTTTGTTTATTG | 22954 |
rs771175196 | snp | A/G | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701326 | TCTTTTCATCTGGAG[A/G]AAGCCCCATATTCTG | 22954 |
rs771427815 | snp | G/T | 1.65258e-05 | 0.00287448 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698784 | CAGCGGGGTCCTGAG[G/T]CAGCCTCCAATATCC | 22954 |
rs771433979 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689285 | TACTTAACCACCCAG[A/T]GCCTTGGCTCTTCAT | 22954 |
rs771473463 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697847 | GCAGCTGCGTCCCAA[A/G]CTTCTGCACTGTGGC | 22954 |
rs771507617 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693566 | TACAGTATTAATCAT[A/T]AGGTCAAGGGATGTG | 22954 |
rs771537352 | in-del | -/GCAGG | 1.64882e-05 | 0.00287121 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698482 | CCTGGCCAAGATCAA[-/GCAGG]GCAGGCAGATGTAGC | 22954 |
rs771595639 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692155 | GGCTGATATAGGTAA[A/T]GGAAATGGAGATATC | 22954 |
rs771805940 | snp | A/G | 1.65455e-05 | 0.00287619 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697733 | AGCAATACCCTTCAA[A/G]GGAAGAGCAATGGCT | 22954 |
rs771838323 | in-del | -/A | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696951 | TCTGTGACATGATTA[-/A]AAAAAAAAAAAAAAA | 22954 |
rs771841455 | snp | A/G | 3.29783e-05 | 0.00406055 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698318 | GTATGGGCATGAGGA[A/G]CGCAGGGTCCAGGAT | 22954 |
rs772028299 | snp | C/G | 1.64808e-05 | 0.00287057 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697851 | CTGCGTCCCAAGCTT[C/G]TGCACTGTGGCCATA | 22954 |
rs772100034 | snp | G/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700502 | TAGTCAGCAAATTTG[G/T]ATAGTCTCTAGGGCT | 22954 |
rs772291469 | snp | G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693677 | AAGGGATCATGAAGG[G/T]AGCCAAGATGATACA | 22954 |
rs772336687 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699602 | ACTTACCTGTCCGGT[A/G]GGCATAGCCCTAACT | 22954 |
rs772461592 | snp | C/T | 3.30442e-05 | 0.0040646 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698807 | CAATATCCAGCAGTG[C/T]CTCTTTCTCAAGAAG | 22954 |
rs772844579 | snp | C/T | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685466 | TCAGCTCTGTCTAGG[C/T]AGTGGGCAAGGTAAA | 22954 |
rs772903453 | snp | C/G | 1.66832e-05 | 0.00288814 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698075 | TCTGCCCCGGCAATT[C/G]TGCCGGAGCTGTGGT | 22954 |
rs772922696 | snp | A/G | 3.29864e-05 | 0.00406105 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699126 | TTGGATGGCCACTGC[A/G]TGGCCTGTCACAGGA | 22954 |
rs772990865 | snp | A/T | 1.64901e-05 | 0.00287137 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698338 | GGGTCCAGGATGAGC[A/T]GGCTCGCTCTCGGAA | 22954 |
rs773172434 | snp | A/C | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692903 | TTAGTCTCTGCTTGA[A/C]GGAGCTACAGCAGCT | 22954 |
rs773467531 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691983 | TTTTACATGTTGTCT[A/G]GTTTTTAGGGGAAAG | 22954 |
rs773505805 | snp | C/T | 1.65231e-05 | 0.00287424 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697750 | GAAGAGCAATGGCTG[C/T]AGCAGCAGCTTCTCA | 22954 |
rs773666256 | snp | A/G | | | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697718 | GTTCTGAGCTGTGCT[A/G]GCAATACCCTTCAAA | 22954 |
rs773701865 | snp | G/T | 1.65721e-05 | 0.0028785 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698705 | CTCTACCTCTGTTAC[G/T]TTTAGAGAGATGGAC | 22954 |
rs773872830 | snp | A/G | 4.95679e-05 | 0.0049781 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698554 | CTGCCAGCTTGCCTC[A/G]GGAGCTCACCCTGCA | 22954 |
rs773911535 | in-del | -/TGT | 1.64961e-05 | 0.00287189 | cds-indel, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698270 | GGTGTCTCCAAGGAC[-/TGT]CTTCAGGCAAGGTAT | 22954 |
rs773943651 | snp | A/C | 0.000122033 | 0.00781035 | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686663 | CTCCACCTTCACCCG[A/C]GCAAAACTACACTTG | 22954 |
rs773963132 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116696160 | TGCCCTTGAAAATGA[C/T]GCTCAAAAATCTCAT | 22954 |
rs774265676 | snp | A/G | 1.64914e-05 | 0.00287149 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699233 | GCTTTGGTGTTTCAC[A/G]GTTGATCGAGGATCA | 22954 |
rs774289005 | snp | C/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700196 | CAGTGACATTTAAGA[C/T]ATCATATTCCCGTAA | 22954 |
rs774316527 | snp | C/G | 0.000181751 | 0.00953112 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698788 | GGGGTCCTGAGGCAG[C/G]CTCCAATATCCAGCA | 22954 |
rs774419345 | snp | A/T | 1.65608e-05 | 0.00287752 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698719 | CTTTTAGAGAGATGG[A/T]CATGAGCCCGGAGGA | 22954 |
rs774511117 | snp | A/C | 6.60033e-05 | 0.00574433 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697766 | AGCAGCAGCTTCTCA[A/C]CTGAACCTGGATGCC | 22954 |
rs774621148 | snp | C/G | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685724 | ATAATTCATTTAACT[C/G]GTAATAAACATTAAA | 22954 |
rs774789988 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692166 | GTAAAGGAAATGGAG[A/G]TATCTAGAGAACCAC | 22954 |
rs774822384 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699256 | GAGGATCAGGGGTGG[C/T]CAAATACAGCTGCCT | 22954 |
rs774825642 | snp | C/T | 6.59055e-05 | 0.00574007 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699470 | GAATGAGGATTTCCG[C/T]TGCATTGCTGGCATG | 22954 |
rs774834352 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700683 | CTCAAGTCAGTACAT[A/G]CTATTTGGTTTCAGG | 22954 |
rs774914398 | snp | C/G | 1.67321e-05 | 0.00289236 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698163 | CTCCCTGTCAAAGAA[C/G]CAGCTGAGGAGCGGC | 22954 |
rs774975492 | snp | A/G | 0.000231451 | 0.0107551 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697738 | TACCCTTCAAAGGAA[A/G]AGCAATGGCTGCAGC | 22954 |
rs775116209 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699325 | CTGAGGGCACCGTCT[A/G]CTTCACCCAGGGCTT | 22954 |
rs775563324 | snp | A/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698041 | TGGGGCTGCTCATGT[A/G]TCGGTCCTGTGGGCG | 22954 |
rs775576184 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697852 | TGCGTCCCAAGCTTC[C/T]GCACTGTGGCCATAC | 22954 |
rs775738712 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697978 | CCCAGCTGACAGACA[A/G]TCTGACAGTGCTAAA | 22954 |
rs775843254 | snp | A/G | 1.65203e-05 | 0.002874 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698829 | CTCAAGAAGATGGGG[A/G]CCAAAGGCAGCACTC | 22954 |
rs775844916 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699509 | TGCTCGTGGTGATCT[C/T]ATCGTGGCTGACAGT | 22954 |
rs775856458 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699604 | TTACCTGTCCGGTGG[G/T]CATAGCCCTAACTCC | 22954 |
rs775940650 | snp | C/T | 3.3129e-05 | 0.00406982 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698230 | AACTTATGGGGGAGC[C/T]GCAGCGGCGGAAGGC | 22954 |
rs775944156 | snp | C/T | 1.64895e-05 | 0.00287132 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698462 | TGTGTCTCGCTGTGA[C/T]TACTTCCTGGCCAAG | 22954 |
rs775968992 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693727 | TCTGATTGGTTGTAC[A/G]GTTGATAGCTGGCAG | 22954 |
rs776139143 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116692446 | AATTGCATGCCTGGC[C/T]TGGTACTGTACTTAG | 22954 |
rs776230323 | snp | A/G | 1.64904e-05 | 0.00287139 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698325 | CATGAGGAGCGCAGG[A/G]TCCAGGATGAGCTGG | 22954 |
rs776360378 | in-del | -/G | 1.65269e-05 | 0.00287457 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698773 | CACCTGCTAAACAGC[-/G]GGGTCCTGAGGCAGC | 22954 |
rs776448126 | snp | C/T | 8.26071e-05 | 0.00642625 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698876 | TCCAGTCAGTCTCTA[C/T]GTGACCAGTCAAGGT | 22954 |
rs776504480 | snp | A/C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699512 | TCGTGGTGATCTCAT[A/C/T]GTGGCTGACAGTAGT | 22954 |
rs776626466 | snp | G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689371 | TAGTGAAGTAAACTA[G/T]CATGCCTAGGATCTG | 22954 |
rs776734216 | snp | G/T | 1.64811e-05 | 0.00287059 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699625 | CCCTAACTCCTAAGG[G/T]GCAGCTGCTGGTCTT | 22954 |
rs776776794 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695801 | TCAACTTCATAAGTA[A/T]ATGTATATCAAGAGG | 22954 |
rs776796546 | snp | C/T | 1.66488e-05 | 0.00288515 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698067 | GGGCGGCGTCTGCCC[C/T]GGCAATTCTGCCGGA | 22954 |
rs776840916 | in-del | -/GAGG | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116687902 | TTTTCGGAGTGGGCT[-/GAGG]GTGAGATTGAGGGGG | 22954 |
rs776918693 | snp | A/G | 1.65373e-05 | 0.00287548 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698598 | CTTAAGGTAGGTCAT[A/G]TTGGCCCCCTCCAAA | 22954 |
rs776989459 | snp | C/G | 1.6486e-05 | 0.00287102 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697994 | TCTGACAGTGCTAAA[C/G]ATCATTGATACAGCT | 22954 |
rs777077560 | snp | A/C | 0.00024216 | 0.011001 | upstream-variant-2KB, intron-variant, missense | TRIM32, ASTN2 | GRCh38.p7 | 9:116686731 | GGGCTGCAGAGTGTA[A/C]TCCCCAAGTCTGCCT | 22954 |
rs777110882 | snp | C/G | 1.6489e-05 | 0.00287128 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698472 | TGTGACTACTTCCTG[C/G]CCAAGATCAAGCAGG | 22954 |
rs777215889 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688235 | CAATATACAGCCCCA[A/G]AGATTGGAATTTGGA | 22954 |
rs777277975 | snp | A/G | 3.39213e-05 | 0.00411819 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699739 | TTCTTCTGCTCCCAA[A/G]CCAACTTCCCTTCCC | 22954 |
rs777285202 | snp | C/G | 3.29527e-05 | 0.00405898 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699595 | GAGAGGGACTTACCT[C/G]TCCGGTGGGCATAGC | 22954 |
rs777455523 | snp | C/T | 3.30327e-05 | 0.0040639 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698552 | CACTGCCAGCTTGCC[C/T]CGGGAGCTCACCCTG | 22954 |
rs777563978 | snp | C/G | 1.64931e-05 | 0.00287163 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699211 | TAACCGATGTGGAAG[C/G]TGGAAAGCTTTGGTG | 22954 |
rs777865829 | in-del | -/A | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686377 | GTGTTCAAAGATGTT[-/A]AGTCATTGTTTTTGT | 22954 |
rs777911858 | snp | A/G | 1.65012e-05 | 0.00287234 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698266 | TGGAAGGTGTCTCCA[A/G]GGACCTTCAGGCAAG | 22954 |
rs777914761 | snp | A/G | 1.66112e-05 | 0.00288189 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698206 | GAGAGAAGTTAACTC[A/G]TCTGCGGGAACTTAT | 22954 |
rs777921394 | snp | A/G | 1.66186e-05 | 0.00288254 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697693 | TAGGGCATGAATACT[A/G]TGCTGTTCAGTTCTG | 22954 |
rs777938900 | snp | C/G | 3.29516e-05 | 0.00405891 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699310 | TTGTCACCTGTGATG[C/G]TGAGGGCACCGTCTA | 22954 |
rs777958344 | snp | C/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693517 | TTCTCATCGGGAGCT[C/G]AAGAGATGTGCTAGT | 22954 |
rs778038121 | snp | A/G | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700372 | AATGGATTGACCCTA[A/G]TTGGTTGGTATTGAT | 22954 |
rs778138359 | snp | A/G | 4.95823e-05 | 0.00497882 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698773 | CACCTGCTAAACAGC[A/G]GGGTCCTGAGGCAGC | 22954 |
rs778141507 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697839 | ACAGAAGAGCAGCTG[C/T]GTCCCAAGCTTCTGC | 22954 |
rs778148713 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116689115 | ACGCCCTTCCCCCCC[A/G]CAGTAAGGAATTATC | 22954 |
rs778153636 | snp | A/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695205 | AGCTGTGTGACCTTG[A/T]GCAAGTTTTTCTGAG | 22954 |
rs778321975 | snp | A/G | 4.95995e-05 | 0.00497969 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698746 | AGGAAGTGGTTGCCA[A/G]CCCTAGGGCCTCACC | 22954 |
rs778428905 | snp | C/T | 1.65718e-05 | 0.00287848 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698665 | TGGAAGATTCCTGGG[C/T]CATGGAGGCCACAGC | 22954 |
rs778601240 | snp | A/G | 1.66054e-05 | 0.00288139 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697703 | ATACTGTGCTGTTCA[A/G]TTCTGAGCTGTGCTA | 22954 |
rs778620127 | snp | C/G/T | 4.94306e-05 | 0.00497124 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699320 | TGATGCTGAGGGCAC[C/G/T]GTCTACTTCACCCAG | 22954 |
rs778694090 | snp | A/C | 1.6486e-05 | 0.00287102 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697803 | GAAGTGCTAGAATGC[A/C]CCATCTGCATGGAGT | 22954 |
rs778701960 | snp | G/T | 1.64787e-05 | 0.00287038 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699425 | CCCTGATGGGCAGCT[G/T]GGTCGCCAGATTAGC | 22954 |
rs778727373 | snp | A/G | | | | | GRCh38.p7 | 9:116688853 | TTTGGGCTCGGAGAC[A/G]GACAAAACAACAACA | 22954 |
rs778781864 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRIM32, ASTN2 | GRCh38.p7 | 9:116688112 | GGTGAGGAATTGGGG[C/T]GTTGAACTGAGGTGC | 22954 |
rs778832308 | snp | G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689995 | CAGAATTTGGCTCTA[G/T]CATTTCCAGGACTAG | 22954 |
rs778921810 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116685554 | ATTAAAATGCTGAAT[-/AA]AGAGTGTTTAAAGCA | 22954 |
rs779090548 | snp | C/T | 1.65556e-05 | 0.00287707 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699029 | AGATCTACCCAACCT[C/T]ACTCCTCTCTCAGTG | 22954 |
rs779100984 | snp | G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695210 | TGTGACCTTGAGCAA[G/T]TTTTTCTGAGCATTC | 22954 |
rs779171695 | in-del | -/GATA | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689317 | GTAAAATGGGGTTAT[-/GATA]GATAACAAGACCAAT | 22954 |
rs779215839 | snp | C/T | | | upstream-variant-2KB, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116686387 | GATGTTAGTCATTGT[C/T]TTTGTTTATTGTTTT | 22954 |
rs779273254 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693590 | GGATGTGGGAAGATG[A/G]TAGGCTGATGTTAGA | 22954 |
rs779343712 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691579 | ACTTCCTTCTGGATC[A/G]TTTTGTTTGCCCCAG | 22954 |
rs779432836 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697912 | TGGCCAGTAGCATCA[A/G]TGGTGTCCGCTGTCC | 22954 |
rs779442616 | snp | A/C | 1.65479e-05 | 0.0028764 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698939 | TATACAAGTCTTTAC[A/C]CGCAAAGGCTTTTTG | 22954 |
rs779530342 | snp | C/T | 3.29587e-05 | 0.00405934 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697954 | AGATTACCCGCATAA[C/T]CAGCTTGACCCAGCT | 22954 |
rs779667568 | snp | A/T | | | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116700452 | GAATTATGCCAAAGC[A/T]TAGGAAGCTGGGAAT | 22954 |
rs779669603 | snp | A/G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690810 | CTTTACATGGTTATT[A/G/T]TGAGACTATGAGAAC | 22954 |
rs779755416 | snp | A/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699438 | CTGGGTCGCCAGATT[A/G]GCCACTTCTTCTCGG | 22954 |
rs779779169 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116691539 | ACTTAGTAATTTAGC[C/T]AAAGTTTTCTTTCTC | 22954 |
rs779843649 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699555 | CTCCATTTTCCTAAG[A/G]GTGGGGGCTATAGTG | 22954 |
rs779854612 | snp | A/G | 3.29554e-05 | 0.00405914 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699439 | TGGGTCGCCAGATTA[A/G]CCACTTCTTCTCGGA | 22954 |
rs779861222 | snp | G/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116690126 | ATGGGAATTAAATCA[G/T]CCCTGTCTAAACTCC | 22954 |
rs779933628 | snp | A/G | 1.64887e-05 | 0.00287125 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698423 | GGAGCAGAGTTACCT[A/G]CTTAACATTGCAGAG | 22954 |
rs780303807 | snp | A/G | 1.65149e-05 | 0.00287353 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699074 | GGGGCTGATTGGTGT[A/G]ACTGACAGCTATGAT | 22954 |
rs780411500 | snp | A/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698493 | ATCAAGCAGGCAGAT[A/G]TAGCACTACTGGAGG | 22954 |
rs780528671 | in-del | -/T | 1.66668e-05 | 0.00288672 | frameshift-variant, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698186 | GAGCGGCGTCGGGAC[-/T]TTTGGAGAGAAGTTA | 22954 |
rs780605878 | snp | A/C | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116695643 | CATCTGCAGATCACA[A/C]GACTGCACAGATACA | 22954 |
rs780679793 | snp | C/G | 1.64882e-05 | 0.00287121 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699184 | CAGCCTTGCCATCTG[C/G]CCAGTTTGTAGTAAC | 22954 |
rs780679942 | snp | G/T | 1.65666e-05 | 0.00287802 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698049 | CTCATGTGTCGGTCC[G/T]GTGGGCGGCGTCTGC | 22954 |
rs780765510 | snp | A/G | 1.67393e-05 | 0.00289299 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698117 | TGAGCCCTGCCGGGA[A/G]GCAGACCATCAGCCT | 22954 |
rs780799984 | snp | C/T | 0.000247164 | 0.011114 | synonymous-codon, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697943 | CTTTTGCAGCAAGAT[C/T]ACCCGCATAACCAGC | 22954 |
rs780867714 | snp | A/G | 3.295e-05 | 0.00405881 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699582 | AGTGTCCTTATTCGA[A/G]AGGGACTTACCTGTC | 22954 |
rs780885702 | snp | C/T | 1.6513e-05 | 0.00287336 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698026 | GGCTCAGCGAGGCTG[C/T]GGGGCTGCTCATGTG | 22954 |
rs780958079 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698437 | TGCTTAACATTGCAG[A/G]GGTGCAGGCTGTGTC | 22954 |
rs781108150 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116693112 | ATGCGTTATTAATAC[C/T]AGTACTAGTTATTGT | 22954 |
rs781242319 | snp | C/T | 1.67922e-05 | 0.00289755 | utr-variant-3-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699720 | GGGATGAGAAATTAT[C/T]AGTTTCTTCTGCTCC | 22954 |
rs781333763 | snp | A/G | 1.65061e-05 | 0.00287277 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698523 | GAGACAGCTGATGAG[A/G]AGGAGCCAGAGCTCA | 22954 |
rs781359060 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699286 | TATGTAGTGCTGTGC[A/G]GCCCAAATTTGTCAC | 22954 |
rs781450516 | snp | C/G | 1.67475e-05 | 0.00289369 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698121 | CCCTGCCGGGAGGCA[C/G]ACCATCAGCCTCCTG | 22954 |
rs781475334 | snp | C/T | 3.29891e-05 | 0.00406122 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116699103 | ATAACTCCCTCAAGG[C/T]ATATACCTTGGATGG | 22954 |
rs781488306 | snp | A/G | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698857 | CTCCAGGAATGTTCA[A/G]TCTTCCAGTCAGTCT | 22954 |
rs781563722 | snp | C/T | 1.65787e-05 | 0.00287907 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698683 | TGGAGGCCACAGCGT[C/T]TGCTGCCTCTACCTC | 22954 |
rs781578048 | snp | C/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697247 | GAAAATAATCATTAG[C/T]TCATTAGCATTTATT | 22954 |
rs781716459 | in-del | -/A | 1.65767e-05 | 0.00287891 | utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116697721 | CTGAGCTGTGCTAGC[-/A]ATACCCTTCAAAGGA | 22954 |
rs781758209 | snp | C/G | 3.32375e-05 | 0.00407647 | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698203 | TTGGAGAGAAGTTAA[C/G]TCGTCTGCGGGAACT | 22954 |
rs794727284 | snp | C/T | | | missense, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116698680 | CCATGGAGGCCACAG[C/T]GTCTGCTGCCTCTAC | 22954 |
rs796117352 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687235 | AGCTGCACGACAAGC[C/G]CCAGCATGCTGGGGA | 22954 |
rs796205260 | snp | A/G | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116689623 | TTCTTCCTTGCTAGG[A/G]CCTGCTTAGTCTTAT | 22954 |
rs796223238 | in-del | -/T | | | intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116694644 | TTTTTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG | 22954 |
rs796941540 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116687233 | CCAGCTGCACGACAA[G/T]CCCCAGCATGCTGGG | 22954 |
rs796948539 | snp | G/T | | | downstream-variant-500B, intron-variant | TRIM32, ASTN2 | GRCh38.p7 | 9:116701655 | AGTGACATTCAGCAT[G/T]TAGATCTCTACCCAT | 22954 |