SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs749902 | snp | A/G | 0.414803 | 0.187989 | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117118132 | ATAAGATACGCTTCT[A/G]TCCTCAGGAGAAAGC | 80263 |
rs755592 | snp | A/G | 0.486725 | 0.0803809 | intron-variant | TRIM45 | GRCh38.p7 | 1:117117509 | GAACACTCGTTAAAA[A/G]AAACCATTTTTTCCC | 80263 |
rs755593 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | TRIM45 | GRCh38.p7 | 1:117117569 | TTTAAATGCCAGTAA[A/G]GTTGATGTGAACCAA | 80263 |
rs1048635 | snp | C/T | 0.114387 | 0.210022 | utr-variant-3-prime, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117112236 | GAGGACCCAGACCTT[C/T]GTTCATTCTAAAGAG | 80263 |
rs1289655 | snp | C/T | 0.206706 | 0.246223 | intron-variant | TRIM45 | GRCh38.p7 | 1:117117986 | AATCTTCACACACCA[C/T]CTCCCTGTCCACTGC | 80263 |
rs1289657 | snp | A/G | 0.114387 | 0.210022 | intron-variant | TRIM45 | GRCh38.p7 | 1:117115180 | GAACACAGTTGAGAG[A/G]GTTATGCCCCCTCCT | 80263 |
rs1289658 | snp | A/G | 0.485378 | 0.0842442 | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117113466 | TGCTTTCTCCTCACC[A/G]TCACAGTGAATGGCG | 80263 |
rs1289659 | snp | C/T | 0.114738 | 0.210248 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111959 | Ctttttttttctttt[C/T]tttttttttttaaag | 80263 |
rs1289660 | snp | C/T | 0.114738 | 0.210248 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111821 | agctgggattacagg[C/T]tcccccccaccttcc | 80263 |
rs1289661 | snp | A/G | 0.262159 | 0.249704 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111800 | CCCACCTTCCCCCAC[A/G]CCCAGCTAATTTTTG | 80263 |
rs1289662 | snp | C/T | 0.114738 | 0.210248 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111732 | ggctggtctcaaact[C/T]ctgacctcgtgatcc | 80263 |
rs1290530 | snp | C/T | 0.483708 | 0.088773 | intron-variant | TRIM45 | GRCh38.p7 | 1:117113654 | GCATCTGTGTCTGCC[C/T]CCTCTCAGCTGAGCA | 80263 |
rs1325510 | snp | A/G | 0.079617 | 0.182947 | downstream-variant-500B, utr-variant-3-prime | TRIM45 | GRCh38.p7 | 1:117110881 | GAAAAGGGTGAGAAC[A/G]CAGAGAACATCTTAG | 80263 |
rs1325511 | snp | A/G | 0.089084 | 0.191327 | intron-variant | TRIM45 | GRCh38.p7 | 1:117116144 | GAGAGAGAATTGAAT[A/G]CAAAACCCACACAAG | 80263 |
rs2296445 | snp | C/T | 0.089084 | 0.191327 | intron-variant | TRIM45 | GRCh38.p7 | 1:117115233 | AAATATAATCTAGCT[C/T]AGGATTTTCCAGTTT | 80263 |
rs2296446 | snp | A/T | 0.089084 | 0.191327 | intron-variant | TRIM45 | GRCh38.p7 | 1:117112562 | TTCTTAGATATTTTC[A/T]CTCCCATGAATCTGC | 80263 |
rs2764859 | snp | A/G | 0.114387 | 0.210022 | intron-variant | TRIM45 | GRCh38.p7 | 1:117119955 | TAGGATTAGCCTAAA[A/G]TAGGTTTCGGGTTCT | 80263 |
rs3738413 | snp | C/T | 0.187385 | 0.242032 | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117116730 | GCCGTCTGTTTCTCC[C/T]GGGCTCTGTGGAGGT | 80263 |
rs3795655 | snp | C/T | 0.357877 | 0.225527 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117121291 | ACCCAAAGAGAAAGT[C/T]TCCAGAACTTGAACA | 80263 |
rs3841707 | in-del | -/GTTA | 0.356383 | 0.226236 | utr-variant-3-prime, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117112156 | AGTGCTCTTTTGTTA[-/GTTA]TTCACTGATTGTACT | 80263 |
rs6657335 | snp | C/T | 0.35894 | 0.225016 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117121424 | TTCCACTGCATCCCA[C/T]ACCAGACACGCCCAC | 80263 |
rs6691149 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122344 | CTAGCGTGCTGGGTA[C/T]AAGCACTCCCGCGGC | 80263 |
rs10923206 | snp | A/G | 0.348134 | 0.229934 | downstream-variant-500B, utr-variant-3-prime | TRIM45 | GRCh38.p7 | 1:117110660 | ACGTAACAGAGCAAG[A/G]CTCTGTCTCAAAAAA | 80263 |
rs10923207 | snp | A/G | 0.347032 | 0.230401 | downstream-variant-500B, utr-variant-3-prime | TRIM45 | GRCh38.p7 | 1:117110758 | GGCTGAGTGACAGAA[A/G]GAGTGAGGAAGAGCA | 80263 |
rs10923208 | snp | A/G | 0.464735 | 0.128019 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111879 | TTTGAACCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 80263 |
rs11355900 | in-del | -/A | | | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117123042 | TAACCCCAAAATATG[-/A]AAAAAAAAAAAAAAA | 80263 |
rs11806143 | snp | C/T | 0.0402882 | 0.136092 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122865 | CTCCAGTTGCGTCAG[C/T]TTGTCTACTGGGCCC | 80263 |
rs12032692 | snp | A/G | 0 | 0 | missense, intron-variant, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117121146 | GAGTTCCCAAGTGCA[A/G]TCCCACTAGTGAGTT | 80263 |
rs12118664 | snp | G/T | 0.439502 | 0.163061 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117112016 | CCTAGACCCTTCAGT[G/T]CCAATGGAATAGATA | 80263 |
rs12747360 | snp | A/G | 0.492871 | 0.0592773 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122955 | TCACTTGATTCCTTC[A/G]TTATCTGTTTCATGC | 80263 |
rs34010882 | snp | C/T | | | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122870 | GTTGCGTCAGCTTGT[C/T]TACTGGGCCCTCACT | 80263 |
rs34128202 | in-del | -/G | | | intron-variant | TRIM45 | GRCh38.p7 | 1:117119855 | AGCAAGACAGTCGCA[-/G]GGGACTATCACATAA | 80263 |
rs34257983 | snp | C/T | 0.0327071 | 0.123628 | synonymous-codon, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117115668 | CCCATCCTTGTTATC[C/T]TGGACCATTGTTCTG | 80263 |
rs34513357 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122963 | TTCCTTCGTTATCTG[C/T]TTCATGCTATAGGCA | 80263 |
rs34644534 | snp | C/T | 0.001862 | 0.0304554 | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117113404 | CGGTTTTCTGGCCCC[C/T]GCTGGAGCAGAAGGT | 80263 |
rs34781363 | snp | A/G | 0.0066041 | 0.0570827 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117121172 | GAGTTTGCTTACAAA[A/G]CCCAGCAGCGGTTTT | 80263 |
rs34863850 | snp | C/T | 0.0106991 | 0.0723538 | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117118198 | TTCAGCTTCCTGAGC[C/T]GTTCTACCACCACCC | 80263 |
rs35074348 | snp | C/T | 0.00374157 | 0.0430904 | missense, intron-variant, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117121126 | GGGGGCAGTGAGTCT[C/T]GCCTGAGTTCCCAAG | 80263 |
rs35253907 | snp | A/G | 0.0036374 | 0.0424908 | synonymous-codon, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117116738 | TTTCTCCCGGGCTCT[A/G]TGGAGGTCTGAAAAA | 80263 |
rs35451049 | snp | A/C | | | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117123671 | TTTTGCTCTTGTTGC[A/C]TAGGCCGGAATGCAA | 80263 |
rs35745444 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime | TRIM45 | GRCh38.p7 | 1:117110670 | CAAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 80263 |
rs36008981 | snp | A/T | 0.00722684 | 0.0596757 | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117118690 | TGAACAGGACACAGG[A/T]TGGGCTTCCCAATCC | 80263 |
rs41276578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM45 | GRCh38.p7 | 1:117113544 | TAACAGGATGTGCTG[C/T]GCATCACTATGTGCT | 80263 |
rs41276580 | snp | A/G | 0.089084 | 0.191327 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122142 | TCGTCCCACGAACGC[A/G]GACTGGGTTCTCCCA | 80263 |
rs41276582 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122412 | TCAGGCTCGCGTTAC[C/G]GGGACCGGTTCGGGA | 80263 |
rs41276584 | snp | G/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122413 | CAGGCTCGCGTTACG[G/T]GGACCGGTTCGGGAG | 80263 |
rs41296182 | snp | G/T | 0.00238591 | 0.0344566 | stop-gained, intron-variant, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117120939 | AGGATGCCGATCTGC[G/T]ACTGCAGACTTCGTG | 80263 |
rs41301281 | snp | A/G | 0.0659466 | 0.169187 | intron-variant | TRIM45 | GRCh38.p7 | 1:117112471 | ACATGGGACAAAGAG[A/G]AAAGGACAAAAATCA | 80263 |
rs41302819 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TRIM45 | GRCh38.p7 | 1:117112643 | CCTGAGAATTGATCA[C/T]AGCAAATCAACTCAT | 80263 |
rs41306177 | snp | A/G | 0.0821764 | 0.185298 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111491 | ATAGAGACGGAGTAG[A/G]GGGACACCACCAAAA | 80263 |
rs41313987 | snp | C/T | 0.089084 | 0.191327 | intron-variant | TRIM45 | GRCh38.p7 | 1:117112522 | CAGTTACCATTATCA[C/T]GGAAATTAGACCTCC | 80263 |
rs41313989 | snp | C/G | 0.089084 | 0.191327 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111461 | CCAGGCTTTGGGGCA[C/G]AAGGCTGTCATGGCA | 80263 |
rs45573635 | snp | G/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117112180 | AAAGAGCACTTGAAC[G/T]CCAGTGCAAGATAAG | 80263 |
rs58501866 | snp | A/G | 0.095934 | 0.196885 | intron-variant | TRIM45 | GRCh38.p7 | 1:117114819 | CTATTAAATATGAAT[A/G]TTCCTTAGTGCACAA | 80263 |
rs59255120 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122972 | TATCTGTTTCATGCT[A/G]TAGGCATAGTGTCTG | 80263 |
rs61038562 | snp | C/G | 0.00411986 | 0.0451991 | intron-variant | TRIM45 | GRCh38.p7 | 1:117115716 | TAAGAGTCAAAACAC[C/G]ACTCACTTCCACAAG | 80263 |
rs61628531 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime | TRIM45 | GRCh38.p7 | 1:117110690 | AAAAAAAAAAAAAAA[-/A]GAACCACTCATCTCA | 80263 |
rs61642190 | in-del | -/AA | 0.349671 | 0.229272 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117123056 | TAACCCCAAAATATG[-/AA]AAAAAAAAAAAAAAC | 80263 |
rs61758105 | snp | C/T | 0.0317054 | 0.12185 | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117116661 | ACTTGAACGTTGTCT[C/T]CTCCCCTGCCCATGA | 80263 |
rs73006084 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TRIM45 | GRCh38.p7 | 1:117120484 | GCTGCACTTTGTAAA[C/T]TGAAAGGGTTTATTG | 80263 |
rs74430292 | in-del | -/AAAA | | | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111960 | TTTAAAAAAAAAAAA[-/AAAA]GAAAAAAAAAGGGTT | 80263 |
rs74899279 | snp | A/G | 0.00213854 | 0.0326297 | synonymous-codon, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117112341 | TAGACTCCTCGGTGC[A/G]CTCTGCCCACCTGTC | 80263 |
rs75110803 | snp | A/G | 0.089084 | 0.191327 | intron-variant | TRIM45 | GRCh38.p7 | 1:117120039 | CGAAGGGACAAAAGT[A/G]ATCCATCTGACAAAC | 80263 |
rs75119143 | in-del | -/CCAAAGA | | | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111431 | TTTGTATGCCCTTGA[-/CCAAAGA]GTAATCTTCCAGGCT | 80263 |
rs75508623 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122209 | AGTGGGAGACGTTTT[C/T]CGGGCTCCCGAGGTC | 80263 |
rs75895534 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TRIM45 | GRCh38.p7 | 1:117117609 | AAAGGAAAGGAAACC[A/G]TAATCTCATCTTCCT | 80263 |
rs76812052 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TRIM45 | GRCh38.p7 | 1:117120653 | CTCACCGAGGGATTT[A/G]TCTTGACACCTCTTT | 80263 |
rs76838034 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | TRIM45 | GRCh38.p7 | 1:117119780 | AATTTGAAGCTTATA[C/T]GCCTATTCTGGCACC | 80263 |
rs76902778 | snp | C/T | 0.0728114 | 0.176364 | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117116670 | TTGTCTCCTCCCCTG[C/T]CCATGATTTCTCCTG | 80263 |
rs76987957 | snp | C/G | 0.0807149 | 0.183963 | intron-variant | TRIM45 | GRCh38.p7 | 1:117113873 | GCAAAAGCAGAAGCC[C/G]ATGCCACAATAAGCT | 80263 |
rs77781304 | snp | C/T | 0.031825 | 0.122064 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122131 | TGCCCTCGGACTCGT[C/T]CCACGAACGCAGACT | 80263 |
rs77954166 | snp | A/C | | | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117118652 | CACAGAACTCACAGA[A/C]CAGCCTCAGTTCCTC | 80263 |
rs78180333 | snp | A/G | 0.0314385 | 0.121371 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117122428 | GGGACCGGTTCGGGA[A/G]ACCGTGGAGCCGAGG | 80263 |
rs78238731 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117123043 | AACCCCAAAATATGA[A/G]AAAAAAAAAAAAAAC | 80263 |
rs79272318 | snp | A/T | 0.0894459 | 0.191631 | intron-variant | TRIM45 | GRCh38.p7 | 1:117112918 | AGTAATTAGATCCCT[A/T]ACCTAAACTGACTCC | 80263 |
rs79372778 | in-del | -/AAAA | | | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117123054 | ATGAAAAAAAAAAAA[-/AAAA]CCATTATAAAATATA | 80263 |
rs79746092 | snp | C/T | 0.031825 | 0.122064 | intron-variant | TRIM45 | GRCh38.p7 | 1:117117022 | CTTTAAAAATACTCA[C/T]GACTGACCGAGGTAT | 80263 |
rs79788159 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TRIM45 | GRCh38.p7 | 1:117115453 | GGGCTGTTTCTAAAG[C/T]GAAGAAGAAGACATG | 80263 |
rs80064834 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | TRIM45 | GRCh38.p7 | 1:117114041 | AATAAGTAGAATGTC[A/G]CAACCACAAAGATAG | 80263 |
rs80280718 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TRIM45 | GRCh38.p7 | 1:117116031 | TACCAAAGGGAGACT[A/G]AATTTTGAAAAGGGT | 80263 |
rs111458367 | snp | A/G | | | intron-variant | TRIM45 | GRCh38.p7 | 1:117113025 | TTGGAATTTATTTAA[A/G]GTTCTAAAAGGAATA | 80263 |
rs111567538 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117123626 | ACCTCTACCTTTCCC[-/T]TTTTTTTTTTTTCTT | 80263 |
rs111819012 | snp | A/G | 0.5 | 0 | intron-variant | TRIM45 | GRCh38.p7 | 1:117117930 | TCCCCACCTTTGGTA[A/G]CCTGGTCAGTAGGGC | 80263 |
rs112110082 | snp | A/G | 0.5 | 0 | intron-variant | TRIM45 | GRCh38.p7 | 1:117115470 | AAGAAGAAGACATGG[A/G]GATTCTATTCAATCT | 80263 |
rs112306956 | snp | A/G | 0.5 | 0 | intron-variant | TRIM45 | GRCh38.p7 | 1:117115714 | GATAAGAGTCAAAAC[A/G]CCACTCACTTCCACA | 80263 |
rs112383862 | snp | A/G | 0.0352966 | 0.128072 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117121327 | CATGGGGACTCCCTC[A/G]CTGACAAATAAAAGG | 80263 |
rs112655636 | snp | A/C/T | 1.64982e-05 | 0.00287208 | synonymous-codon, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117112359 | CTGCCCACCTGTCCA[A/C/T]GTGCATTCAGATTTC | 80263 |
rs112720783 | snp | C/T | 0 | 0 | intron-variant | TRIM45 | GRCh38.p7 | 1:117120102 | CACCCCAATTAACAC[C/T]TACCAGCCCACCTCA | 80263 |
rs113129701 | snp | A/G | 0.5 | 0 | intron-variant | TRIM45 | GRCh38.p7 | 1:117115552 | ATCCAGGGAGCTCAG[A/G]GAAGCACGTGCACCA | 80263 |
rs113160987 | snp | C/T | 0.5 | 0 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | TRIM45 | GRCh38.p7 | 1:117121467 | CCCGCAAGTCCTCCC[C/T]GGATGCGCTTCCAGG | 80263 |
rs113286499 | snp | A/G | 0 | 0 | intron-variant | TRIM45 | GRCh38.p7 | 1:117117668 | GATCTAGGAATCCAG[A/G]GCCTGCCATGCTCCT | 80263 |
rs113463400 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | TRIM45 | GRCh38.p7 | 1:117115604 | CTTTGATGCAGACCC[A/G]CACAGTATAGACGCC | 80263 |
rs113811830 | snp | C/G | 0.5 | 0 | intron-variant | TRIM45 | GRCh38.p7 | 1:117114899 | TCAGTGTTGATTTCT[C/G]TGGAGGGAAACCTCT | 80263 |
rs113824510 | snp | C/T | 0.5 | 0 | intron-variant | TRIM45 | GRCh38.p7 | 1:117117947 | CTGGTCAGTAGGGCA[C/T]GCTTCCTAGCAGAAC | 80263 |
rs113838673 | in-del | -/G | 0.0894459 | 0.191631 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111813 | GGTGTGGGGGAAGGT[-/G]GGGGGGAACCTGTAA | 80263 |
rs113976601 | snp | C/T | 0.5 | 0 | intron-variant | TRIM45 | GRCh38.p7 | 1:117113568 | ATGTGCTAAACAGAG[C/T]CTGAGGCACAGGGCC | 80263 |
rs114050025 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | TRIM45 | GRCh38.p7 | 1:117111259 | TCCCAGTTAACTTTC[C/T]AGGTATATAGATAAC | 80263 |
rs114439025 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TRIM45 | GRCh38.p7 | 1:117116856 | TTACTGTAACCACCC[C/T]GGGTCCCTTTGTTTT | 80263 |
rs114616811 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM45 | GRCh38.p7 | 1:117113125 | GAAGCACAGGGCTCA[C/T]AGGAGCTGTACCAAA | 80263 |
rs114635718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM45 | GRCh38.p7 | 1:117113923 | TCTGCCTCACTCTAT[A/C]CTTGTATGAAGTATA | 80263 |