SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs185272 | snp | C/G | 0.0560713 | 0.157771 | synonymous-codon, nc-transcript-variant | TRIM41 | GRCh38.p7 | 5:181234256 | CCGCCTGGCAGAGCG[C/G]CGGCAGGAGGTTGCT | 90933 |
rs1044207 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | TRIM41 | GRCh38.p7 | 5:181235517 | GCTCATCCCACCCCA[A/C]ACCCCTCCCAGGTCT | 90933 |
rs2241371 | snp | C/T | 0.000627145 | 0.0176969 | missense, nc-transcript-variant | TRIM41 | GRCh38.p7 | 5:181234195 | GCCGGGTGAGCCGTG[C/T]CAGGGTCCAGCGTCA | 90933 |
rs2241372 | snp | A/G | 0.191147 | 0.242974 | intron-variant | TRIM41 | GRCh38.p7 | 5:181233340 | CTGCACAGGGACAGC[A/G]TTCCCCGATCTCCAG | 90933 |
rs2259749 | snp | C/T | 0.49995 | 0.00499176 | intron-variant | TRIM41 | GRCh38.p7 | 5:181225241 | GTCAGACCCAAATGC[C/T]CTGCACTTGCCTCCC | 90933 |
rs2261114 | snp | C/G | 0.496348 | 0.0425753 | downstream-variant-500B | TRIM41 | GRCh38.p7 | 5:181236035 | AGATGTTTGCCACAC[C/G]TAGTTGAAACTGAAG | 90933 |
rs2545098 | snp | A/G | 0.49995 | 0.00499176 | | | GRCh38.p7 | 5:181223744 | CAGGTGGCTCTGAGT[A/G]CAAGTCTGCCCCAAT | 90933 |
rs2545099 | snp | C/G | 0.185472 | 0.241529 | | | GRCh38.p7 | 5:181222125 | GCTTCTTAGTATTTG[C/G]ACAGTGGAAACGTGC | 90933 |
rs2545100 | snp | C/T | 0.185318 | 0.241943 | | | GRCh38.p7 | 5:181222091 | CACCTCTGAGGGTAA[C/T]CTCCATCTTCAGAGA | 90933 |
rs2546388 | snp | C/T | 0.39709 | 0.20215 | | | GRCh38.p7 | 5:181236293 | GGCCCTCAATCCCCC[C/T]ACACACAAACACAGT | 90933 |
rs2546389 | snp | C/T | 0.0973687 | 0.197999 | | | GRCh38.p7 | 5:181233971 | CCCCCAGCCTGGCTC[C/T]TCCTGCCACTCCACC | 90933 |
rs2546390 | snp | C/T | 0.350764 | 0.228794 | | | GRCh38.p7 | 5:181233831 | CCTGGGGCCCAACTT[C/T]CCTCAGGACCCAGTC | 90933 |
rs2546392 | snp | C/T | 0.0887219 | 0.191022 | | | GRCh38.p7 | 5:181223658 | TAGCTTCCGGCCTCC[C/T]TCCCAACACTTCCGG | 90933 |
rs2770957 | snp | C/G | 0.499954 | 0.00479211 | intron-variant | TRIM41 | GRCh38.p7 | 5:181229734 | TTGGTGCCCTGGGAA[C/G]TCATGTATTAGATAT | 90933 |
rs2770987 | snp | G/T | 0.1652 | 0.235179 | upstream-variant-2KB, downstream-variant-500B | TRIM41, MIR4638 | GRCh38.p7 | 5:181222336 | GCGCAGGGACACACA[G/T]GTCCTTCCTGCCACG | 90933 |
rs3215868 | in-del | -/AGTC | 0.496999 | 0.0386216 | downstream-variant-500B | TRIM41 | GRCh38.p7 | 5:181236134 | ATGCTGTAGTTGCTT[-/AGTC]TAGCACAGAAAATTG | 90933 |
rs6601178 | snp | A/G | 0.148384 | 0.228417 | missense, upstream-variant-2KB, nc-transcript-variant | TRIM41, MIR4638 | GRCh38.p7 | 5:181224231 | GTGGAGGCTGTGGGG[A/G]CTGGCGCGGGGTGGG | 90933 |
rs6601179 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TRIM41 | GRCh38.p7 | 5:181230116 | GGGCACCCCTGGAAA[A/G]ACTCTGGTGCGGGGC | 90933 |
rs6876339 | snp | C/T | | | downstream-variant-500B | TRIM41 | GRCh38.p7 | 5:181236170 | TAGTGGGGTCTCAGC[C/T]GCATGTTGAACCATT | 90933 |
rs6892994 | snp | A/C/G/T | 0.257416 | 0.250502 | upstream-variant-2KB | TRIM41 | GRCh38.p7 | 5:181221971 | AACCTTTCCAAAAAG[A/C/G/T]GAAATTACGCCCAAC | 90933 |
rs7706515 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM41 | GRCh38.p7 | 5:181225830 | AAGGCAGCCAGCACA[A/G]ATAGCACTACTTAGT | 90933 |
rs7711424 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TRIM41 | GRCh38.p7 | 5:181230087 | CCTGTGAAGGGGAAG[A/G]GGACCAAAGGTGAGG | 90933 |
rs7727787 | snp | A/G | 0.15665 | 0.231917 | intron-variant | TRIM41 | GRCh38.p7 | 5:181226039 | GTTTCTCAGCTCTGA[A/G]TGGTACAGCTAGACA | 90933 |
rs7728896 | snp | C/T | 0.209693 | 0.246729 | intron-variant | TRIM41 | GRCh38.p7 | 5:181226102 | CTTTTACAGAGTGGC[C/T]ttttttttttttaat | 90933 |
rs7735783 | snp | C/T | 0.0182019 | 0.0936463 | downstream-variant-500B | TRIM41 | GRCh38.p7 | 5:181235858 | CAGGATTTCTTCCTT[C/T]GCCGCCCCTGCAGTG | 90933 |
rs10050604 | snp | A/G | 0.0455778 | 0.143915 | upstream-variant-2KB | TRIM41 | GRCh38.p7 | 5:181222052 | CTGAGCTAGCCGGGC[A/G]GCCATGTCTGTATTC | 90933 |
rs10059653 | snp | A/C/T | 0.00052366 | 0.0161731 | missense, nc-transcript-variant | TRIM41 | GRCh38.p7 | 5:181234174 | TCCCTCCCTCCCAAG[A/C/T]GGACCTGACGCTGGA | 90933 |
rs11347848 | in-del | -/T | 0.451483 | 0.148002 | intron-variant | TRIM41 | GRCh38.p7 | 5:181226878 | TTTTCTTTTCCCCCC[-/T]TTTTTTTTTTTTGAG | 90933 |
rs11741493 | snp | A/C | 0.5 | 0 | intron-variant | TRIM41 | GRCh38.p7 | 5:181228952 | aaaaaaaaaaaaaaa[A/C]aaaaaaCAGTAAATG | 90933 |
rs11743501 | snp | A/G | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181227986 | ttgctgtgttgctca[A/G]gctggtcttgaacca | 90933 |
rs11744527 | snp | A/G | 0.157311 | 0.232183 | intron-variant | TRIM41 | GRCh38.p7 | 5:181229074 | TCATGCTATTGTCAC[A/G]AGTTGACTATAATTC | 90933 |
rs11949220 | snp | C/T | 0.00912139 | 0.0669141 | intron-variant | TRIM41 | GRCh38.p7 | 5:181230711 | GGGCAGGTGCCTCTC[C/T]CAGCCCCCACTTTTC | 90933 |
rs11954812 | snp | C/G | 0.0644444 | 0.167538 | upstream-variant-2KB, downstream-variant-500B | TRIM41, MIR4638 | GRCh38.p7 | 5:181222388 | ATCTCCCGAACAGAC[C/G]AAAACgtgtttccgc | 90933 |
rs11958114 | snp | A/G | 0.0422008 | 0.138995 | upstream-variant-2KB | TRIM41 | GRCh38.p7 | 5:181222056 | gctagccgggcGGCC[A/G]TGTCTGTATTCTAAC | 90933 |
rs11958790 | snp | C/T | 0.185472 | 0.241529 | upstream-variant-2KB | TRIM41 | GRCh38.p7 | 5:181222057 | CTAGCCGGGCGGCCA[C/T]GTCTGTATTCTAACT | 90933 |
rs12108987 | snp | A/G | 0.217851 | 0.247924 | intron-variant | TRIM41 | GRCh38.p7 | 5:181228190 | cagtgagctgagatc[A/G]cgccactgcactcca | 90933 |
rs12651805 | snp | C/T | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181228907 | ctgctgcactccatt[C/T]taggcgacagagcaa | 90933 |
rs12655848 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM41 | GRCh38.p7 | 5:181228827 | taatctcagctactc[A/G]ggaggctgaggcagg | 90933 |
rs13158204 | snp | A/G | 0 | 0 | intron-variant | TRIM41 | GRCh38.p7 | 5:181229951 | AAGGCGTTGAGTGTA[A/G]AGGTGAGGCTGGAAG | 90933 |
rs13158211 | snp | A/G | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181229953 | GGCGTTGAGTGTAGA[A/G]GTGAGGCTGGAAGTG | 90933 |
rs13179344 | snp | A/G | 0.49995 | 0.00499176 | intron-variant | TRIM41 | GRCh38.p7 | 5:181230236 | CGGTGGCTCACGCCT[A/G]TAATCTCAGTACTTT | 90933 |
rs17714046 | snp | C/T | 0.0817981 | 0.184954 | utr-variant-3-prime, missense, nc-transcript-variant, synonymous-codon | TRIM41 | GRCh38.p7 | 5:181234980 | CCTTCTCTCACCTAC[C/T]ATGTCTGTCCAACAG | 90933 |
rs34347124 | in-del | -/A | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181228934 | CAAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 90933 |
rs34534964 | in-del | -/C | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181233528 | TCTCCTTCCTTCCCC[-/C]AGGACCTGAGTTTCC | 90933 |
rs34891840 | snp | A/G | 0.0106695 | 0.0722558 | intron-variant | TRIM41 | GRCh38.p7 | 5:181230915 | TTCCCACTCTCACAG[A/G]GAGTGACTTGGTCCC | 90933 |
rs35032551 | snp | G/T | 0.142947 | 0.22592 | intron-variant | TRIM41 | GRCh38.p7 | 5:181233259 | TGGGGTGGTTGAAAT[G/T]GATGTGTGTTCATTG | 90933 |
rs35202141 | in-del | -/A | | | upstream-variant-2KB, downstream-variant-500B | TRIM41, MIR4638 | GRCh38.p7 | 5:181222263 | GTGAGGGGCGAGACC[-/A]TGAATTTACTTGAGT | 90933 |
rs35398057 | in-del | -/C | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181230421 | GAATCGCTTGAATCC[-/C]GGGAGGTGGAGGTTC | 90933 |
rs35664724 | in-del | -/G | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181226235 | CAGCCTCCTGAGTAT[-/G]CTGGGATTACAGGCA | 90933 |
rs35719413 | snp | C/T | 0.142781 | 0.225841 | synonymous-codon, nc-transcript-variant | TRIM41 | GRCh38.p7 | 5:181232796 | TGCAAGGCGACTAGC[C/T]GCGGCTCCCGCACGC | 90933 |
rs35761564 | in-del | -/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | TRIM41 | GRCh38.p7 | 5:181234912 | CCCCCTTGACCCCAG[-/G]CCCCTGCTTCTCCCT | 90933 |
rs35905834 | in-del | -/C | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181231383 | TTGTTGTTTTTTTCC[-/C]ATTATTGCTCGCCCT | 90933 |
rs35905886 | in-del | -/T | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181229687 | GTGTGGGCAGGGACT[-/T]CCGCAGTGTCCTGGA | 90933 |
rs36085853 | in-del | -/C | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181233348 | GGGGAACGCTGTCCC[-/C]TGTGCAGCTGACACT | 90933 |
rs55810697 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | TRIM41 | GRCh38.p7 | 5:181225870 | GATGGGTTTGAAGCA[C/G]TGGGACCAGGAGGAG | 90933 |
rs55855372 | snp | A/G | 0.0034767 | 0.0415483 | intron-variant | TRIM41 | GRCh38.p7 | 5:181233601 | CCCTCTGGGAATATC[A/G]TGGTCCCACCCCCTG | 90933 |
rs55879636 | snp | A/C | 0.189576 | 0.242588 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRIM41, MIR4638 | GRCh38.p7 | 5:181223537 | GTTCTCTAGTGCGGA[A/C]TAGAGCGTCTCCTCG | 90933 |
rs55899220 | snp | A/C | 0.191147 | 0.242974 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRIM41, MIR4638 | GRCh38.p7 | 5:181223421 | GAAGTTTCTCCCCAG[A/C]GGCGGGGGATGGGGG | 90933 |
rs55909571 | snp | C/T | 0.0376037 | 0.131863 | upstream-variant-2KB | TRIM41 | GRCh38.p7 | 5:181221732 | CACGATAGCCCGCGG[C/T]GCTGGCCTGCAGGAA | 90933 |
rs55928464 | snp | C/G | 0.200776 | 0.245106 | intron-variant | TRIM41 | GRCh38.p7 | 5:181233447 | ATAGGTGTGTTCCCA[C/G]TCTTTGCCCTTCGTG | 90933 |
rs56159207 | snp | C/T | 0.356383 | 0.226236 | intron-variant | TRIM41 | GRCh38.p7 | 5:181227020 | GGGATTACAGGCATG[C/T]GCCACCACACCTGGC | 90933 |
rs56180100 | in-del | -/TCAG | | | downstream-variant-500B | TRIM41 | GRCh38.p7 | 5:181236136 | GCTGTAGTTGCTTAG[-/TCAG]CACAGAAAATTGCAA | 90933 |
rs57140600 | snp | A/G | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181228246 | TCTCAAAAAAAAAAA[A/G]AAAAAATGTTTTGAG | 90933 |
rs57318614 | snp | G/T | 0.360421 | 0.224293 | intron-variant | TRIM41 | GRCh38.p7 | 5:181231374 | CCCGCTTTTTTTGTT[G/T]TTTTTTTCCATTATT | 90933 |
rs57863187 | snp | C/T | 0.191147 | 0.242974 | intron-variant | TRIM41 | GRCh38.p7 | 5:181232063 | GCTTTTGGGTGACTT[C/T]CTTAAGGTCACTGTG | 90933 |
rs58238754 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TRIM41 | GRCh38.p7 | 5:181229007 | GAATTAATGGAGAAA[C/T]TATTGACTAGAAAAG | 90933 |
rs58539433 | snp | A/G | 0.137527 | 0.223271 | intron-variant | TRIM41 | GRCh38.p7 | 5:181232156 | CAAAAATTTTTACCA[A/G]GTGCCTACTCTGATT | 90933 |
rs58715056 | in-del | -/G | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181228948 | AAAAAAAAAAAAAAA[-/G]AAAAAAAAAACAGTA | 90933 |
rs59079840 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | TRIM41 | GRCh38.p7 | 5:181231359 | GCACACCCCGACCCC[C/T]CCGCTTTTTTTGTTG | 90933 |
rs59361996 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRIM41 | GRCh38.p7 | 5:181228060 | GGATTACTGTGTCTG[C/T]CCGACAGTTAAATGT | 90933 |
rs59521877 | snp | A/G | 0.0896358 | 0.19179 | upstream-variant-2KB, downstream-variant-500B | TRIM41, MIR4638 | GRCh38.p7 | 5:181222526 | CGGCTGAGACGGCCG[A/G]GATAGCTCTAGGCAA | 90933 |
rs59697106 | snp | C/T | 0.183568 | 0.241012 | intron-variant | TRIM41 | GRCh38.p7 | 5:181227096 | CAGACTGATCTCGAA[C/T]GCCTGACCTCAGGTG | 90933 |
rs60401553 | snp | C/T | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181226878 | TTTTCTTTTCCCCCC[C/T]TTTTTTTTTTTTGAG | 90933 |
rs60815823 | in-del | -/AAAA | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181230523 | AAAAAAAAAAAAAAA[-/AAAA]TACACACAGGGCTTC | 90933 |
rs61384174 | snp | C/G | | | intron-variant | TRIM41 | GRCh38.p7 | 5:181228177 | GCGGTGGAGCTTGCA[C/G]TGAGCTGAGATCACG | 90933 |
rs61758103 | snp | C/T | 0.0543571 | 0.155647 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TRIM41, MIR4638 | GRCh38.p7 | 5:181224383 | GTGGGAGGAGGAGGA[C/T]GAGGAGGAAGACCTG | 90933 |
rs70973984 | in-del | -/AAA | 0 | 0 | intron-variant | TRIM41 | GRCh38.p7 | 5:181230526 | AAAAAAAAAAAAAAA[-/AAA]TACACACAGGGCTTC | 90933 |
rs71613496 | snp | C/T | 0.0303794 | 0.119444 | utr-variant-3-prime, intron-variant, nc-transcript-variant | TRIM41 | GRCh38.p7 | 5:181234889 | TTGTTACTGTGTTGC[C/T]TCCCACTCCCCCTTG | 90933 |
rs71658378 | in-del | -/AGTC | | | downstream-variant-500B | TRIM41 | GRCh38.p7 | 5:181236135 | TGCTGTAGTTGCTTA[-/AGTC]GCACAGAAAATTGCA | 90933 |
rs71963223 | in-del | -/TT | 0.104149 | 0.203046 | utr-variant-3-prime, intron-variant | TRIM41 | GRCh38.p7 | 5:181235149 | TGCTCTTCAACCTCT[-/TT]ATCAGTTCTGAGGCT | 90933 |
rs72821733 | snp | A/C/G/T | 0.00438571 | 0.0466605 | upstream-variant-2KB, downstream-variant-500B | TRIM41, MIR4638 | GRCh38.p7 | 5:181222486 | CTTGGCTACTTTCCT[A/C/G/T]CCGGCATCGTCCTGA | 90933 |
rs72821734 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM41 | GRCh38.p7 | 5:181225308 | TGTCTTCAAGGACTT[C/T]GGTTGGCTCTGTGTC | 90933 |
rs73364099 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | TRIM41, MIR4638 | GRCh38.p7 | 5:181223149 | TGGGGCGTCTGCTGC[C/T]CTAACCCGCGAAGCG | 90933 |
rs73365903 | snp | A/G | 0.00773254 | 0.0616966 | missense, upstream-variant-2KB, nc-transcript-variant | TRIM41, MIR4638 | GRCh38.p7 | 5:181224184 | ATGAGTTAGATCGGG[A/G]GGAGGAGGAGGAGGA | 90933 |
rs73365905 | snp | C/G | 0.0188509 | 0.0952371 | intron-variant | TRIM41 | GRCh38.p7 | 5:181224861 | GTGGGGGGATGGAGA[C/G]GAAGTAAGGGGACCT | 90933 |
rs73365970 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | TRIM41 | GRCh38.p7 | 5:181229423 | TCAAAGAAAAGGAGA[C/G]AGGCTAGTAGAAGAC | 90933 |
rs73814525 | snp | A/G | 0.0471551 | 0.14613 | upstream-variant-2KB | TRIM41 | GRCh38.p7 | 5:181222032 | AGAGTCTCATGCTCT[A/G]CCGACTGAGCTAGCC | 90933 |
rs73814538 | snp | G/T | 0.0209036 | 0.100074 | upstream-variant-2KB, nc-transcript-variant | TRIM41, MIR4638 | GRCh38.p7 | 5:181222632 | TCCACCGCAGCCGAG[G/T]CCGCAGGTCCTGTAA | 90933 |
rs73814539 | snp | C/T | 0.00203472 | 0.0318311 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TRIM41, MIR4638 | GRCh38.p7 | 5:181224548 | GAGGTGCTTCACATG[C/T]CCTCAGTGCCGAAAG | 90933 |
rs74365536 | snp | C/T | 0.0081877 | 0.0634572 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TRIM41, MIR4638 | GRCh38.p7 | 5:181224515 | CGTCACCCCACTGCC[C/T]CCGCCTCCAGCCCCT | 90933 |
rs74778386 | snp | G/T | 0.5 | 0 | intron-variant | TRIM41 | GRCh38.p7 | 5:181226890 | CCCTTTTTTTTTTTT[G/T]GAGACAGAATTTCAC | 90933 |
rs75309992 | snp | A/G | 0.00138614 | 0.0262897 | intron-variant | TRIM41 | GRCh38.p7 | 5:181233600 | AGGGGGTGGGACCAC[A/G]ATATTCCCAGAGGGA | 90933 |
rs75538078 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, downstream-variant-500B | TRIM41, MIR4638 | GRCh38.p7 | 5:181222282 | ATTTACTTGAGTAGT[A/G]CTCTCCTTCAGTTTT | 90933 |
rs75896174 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | TRIM41 | GRCh38.p7 | 5:181225030 | GACCAGGGAAGGATG[A/G]CTTCCTCAAAGCAAA | 90933 |
rs76528977 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM41 | GRCh38.p7 | 5:181229398 | GAGCTCTCCTACCCT[A/G]TATTCTCTCTCAAAG | 90933 |
rs76878637 | snp | A/C | 0 | 0 | intron-variant | TRIM41 | GRCh38.p7 | 5:181228935 | CAAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 90933 |
rs77172445 | snp | A/C | 0.0252325 | 0.109451 | upstream-variant-2KB, downstream-variant-500B | TRIM41, MIR4638 | GRCh38.p7 | 5:181222343 | GACACACATGTCCTT[A/C]CTGCCACGTAAGGCC | 90933 |
rs77281389 | snp | C/T | 0.0108197 | 0.0727517 | intron-variant | TRIM41 | GRCh38.p7 | 5:181224897 | AAGGAAACATCTCTT[C/T]ACCCACCAAAGAACC | 90933 |
rs77505387 | snp | C/G | 0.0125423 | 0.078191 | utr-variant-3-prime, missense, nc-transcript-variant | TRIM41 | GRCh38.p7 | 5:181234948 | AGCCTAAAGAACCCT[C/G]CTGGCCTCCAGCTCA | 90933 |
rs77567667 | snp | A/G | 0.00111962 | 0.0236338 | missense, nc-transcript-variant | TRIM41 | GRCh38.p7 | 5:181233683 | CTATGGGGTTGGCAC[A/G]GGTCAGGGGACCAGA | 90933 |