SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12605 | snp | C/T | 0.449979 | 0.150028 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP45, TSTD3 | GRCh38.p7 | 6:99432255 | AGATCAAGGTGCCAG[C/T]AGACTTGGGGTCTGG | 85015 |
rs733615 | snp | A/C | 0.243061 | 0.249904 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99497918 | tctgttccctttttg[A/C]ccagataatttctag | 85015 |
rs912338 | snp | A/G | 0.128976 | 0.218754 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99498009 | ccagtcgaatgttag[A/G]tactattccaaattg | 85015 |
rs994197 | snp | C/T | 0.127944 | 0.218179 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99512818 | CTTCTCCCTCCAAAC[C/T]TCCTCATCTACTCTC | 85015 |
rs994198 | snp | C/T | 0.122758 | 0.215196 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99512885 | TATCCCCTTCTCTGA[C/T]AGCAACTTCCCAGTT | 85015 |
rs1134718 | snp | C/T | 0.288646 | 0.246995 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | USP45, TSTD3 | GRCh38.p7 | 6:99432504 | CAGCTGTGTAACTTA[C/T]TGAGCGTTATTTTGG | 85015 |
rs1323717 | snp | C/G | 0.145642 | 0.227177 | utr-variant-5-prime, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99514858 | CTCACAACCACCTTA[C/G]GAGATAAGTTGCTAT | 85015 |
rs1853522 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99485079 | tcacgcctgtaatcc[C/T]agcattttgggaggc | 85015 |
rs2181687 | snp | A/G | 0.121369 | 0.214369 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99488099 | TTTTTAAGCCCCCTG[A/G]CTACTATCTTAGTTG | 85015 |
rs2209156 | snp | C/G | 0.493432 | 0.0569306 | upstream-variant-2KB, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99516090 | CTCCGCCCCCACACC[C/G]CCGCCGCCCCCTGAA | 85015 |
rs2209157 | snp | C/T | 0.274393 | 0.248807 | upstream-variant-2KB, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99516136 | CTAACATTCGTCATA[C/T]ATTATTGTGGTTTTT | 85015 |
rs2397338 | snp | A/C | 0.216649 | 0.247765 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99492624 | CTCAGTCTCCTAAGT[A/C]GTTGGGATTACAGGC | 85015 |
rs2397339 | snp | C/T | 0.121369 | 0.214369 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99492738 | CTCAAGTGATCTGCA[C/T]GCCTTGGCCTCCCAA | 85015 |
rs3087961 | snp | A/G | 0.479502 | 0.0991411 | utr-variant-3-prime, nc-transcript-variant, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99433190 | TTAAAACTTGTGAAG[A/G]CCACCTTTTTAGGTA | 85015 |
rs3886048 | snp | C/T | 0.120674 | 0.21395 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99447516 | ATTATACATATAATA[C/T]TAACAGTTGGTAAAC | 85015 |
rs3886049 | snp | A/G | 0.121022 | 0.21416 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99447459 | AACAAGTTCCACTCC[A/G]CTGAATTTATATAGT | 85015 |
rs4144163 | snp | A/T | 0.49655 | 0.04139 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99441591 | AAATTGCTTTCTAGC[A/T]GGTGTTACCAACTTA | 85015 |
rs4240578 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99441392 | caaaaattagccagg[C/T]gtggtggtgggtgcc | 85015 |
rs4240579 | snp | A/C | 0.320335 | 0.239902 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99479012 | aatctattgcaacaa[A/C]aaaaaaaaaaacagg | 85015 |
rs4403271 | snp | A/G | 0.468148 | 0.122112 | intron-variant, utr-variant-3-prime, nc-transcript-variant | USP45, TSTD3 | GRCh38.p7 | 6:99460640 | AATCTATTTTGAAGT[A/G]TATTGATAGATACCG | 85015 |
rs4428510 | snp | C/T | 0.0352966 | 0.128072 | intron-variant, downstream-variant-500B | USP45, TSTD3 | GRCh38.p7 | 6:99456951 | gagaaagagaatgcg[C/T]gcctgggggtaggcc | 85015 |
rs4431441 | snp | C/T | 0.0456336 | 0.143994 | intron-variant, utr-variant-3-prime, nc-transcript-variant | USP45, TSTD3 | GRCh38.p7 | 6:99460978 | ATTGAATTTAAGAGC[C/T]GAGTCTCAAAGAGCT | 85015 |
rs4448102 | snp | C/T | 0.315758 | 0.241197 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99478293 | GATTTCTAGACTCTA[C/T]GATGGAGCCTATCTG | 85015 |
rs4487587 | snp | A/G | 0.455858 | 0.141853 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99449257 | aagacccatcagtgt[A/G]ctgtattcaggagac | 85015 |
rs4499939 | snp | C/T | 0.485799 | 0.0830599 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99444903 | tatctcctgatcttt[C/T]agcctcaccgtacct | 85015 |
rs4504482 | snp | C/T | 0.447593 | 0.153157 | synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B | USP45, TSTD3 | GRCh38.p7 | 6:99446062 | GTCAAAATCTTGATC[C/T]CCAGTTACAGTGCTG | 85015 |
rs4526201 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99457476 | GAACCTATGTGAATA[C/T]TGGGGCAGGTTCCCC | 85015 |
rs4555918 | snp | C/T | 0.5 | 0 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99462854 | CCGGGCATGGTGGTG[C/T]GCACATGTAGTCCCA | 85015 |
rs4613830 | snp | A/G | 0.462144 | 0.132269 | intron-variant, downstream-variant-500B | USP45, TSTD3 | GRCh38.p7 | 6:99457099 | aattttggtcagacc[A/G]ggtgctctcaaaacc | 85015 |
rs4618534 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99446820 | ACAATCACAGCTCAC[C/T]GCAGCCTCAAACTCT | 85015 |
rs4618535 | snp | C/T | 0.310386 | 0.242597 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99487793 | gcgacagagcgagac[C/T]ccgtctcaaaaaaaa | 85015 |
rs4839748 | snp | C/T | 0.364817 | 0.222075 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99442039 | TGCTCCCTACAATGC[C/T]CAAACCCTGGGAATA | 85015 |
rs4840043 | snp | A/G | 0.369142 | 0.219784 | utr-variant-3-prime, nc-transcript-variant, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99433185 | TCAGCTACCTAAAAA[A/G]GTGGTCTTCACAAGT | 85015 |
rs4840044 | snp | A/G | 0.492727 | 0.0598633 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99440137 | AAATAAATTCAATAT[A/G]AAAGCTAAGCTACTG | 85015 |
rs4840045 | snp | A/C | 0.349671 | 0.229272 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99455118 | CAAAAAACAAAAAAA[A/C]AAAACACAACAGTAT | 85015 |
rs4840046 | snp | A/G | 0.0402882 | 0.136092 | intron-variant, upstream-variant-2KB | USP45, TSTD3 | GRCh38.p7 | 6:99470106 | tccagagtgacacct[A/G]tacatcagatatgag | 85015 |
rs4840048 | snp | C/T | 0.318415 | 0.240457 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99480205 | ctaacaaaatatgtg[C/T]gggatttgtatgctg | 85015 |
rs4840049 | snp | A/G | 0 | 0 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99480404 | ggaccggccaggcgc[A/G]gtggctcacgcctgt | 85015 |
rs4840052 | snp | A/G | 0.225301 | 0.248777 | intron-variant, downstream-variant-500B | USP45, TSTD3 | GRCh38.p7 | 6:99482070 | TAGATATACAAAAAC[A/G]CAAGCTCATATTCAA | 85015 |
rs4840053 | snp | A/G | 0.121369 | 0.214369 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99491053 | TTCAGATATTAAGGA[A/G]CTATTTTTAACTCCC | 85015 |
rs4840054 | snp | C/T | 0.121369 | 0.214369 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99493654 | aggcgtccaccacta[C/T]gtccagctaattttt | 85015 |
rs4840055 | snp | A/G | 0.122758 | 0.215196 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99508153 | TTTGTGTGAAATAAT[A/G]AAGATTTCTCTTATT | 85015 |
rs5878580 | in-del | -/T/TT/TTT | 0.172028 | 0.23753 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99472221 | AACTTCACTTACTAA[-/T/TT/TTT]TTTTTTTTTTTTTTG | 85015 |
rs5878581 | in-del | -/T | 0.0376037 | 0.131863 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99475818 | TTACTTACTTAGTTG[-/T]TTTTTTGTTTGTTTG | 85015 |
rs5878582 | in-del | -/T | 0.122064 | 0.214785 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99492666 | GCCTAACTTTTTGTA[-/T]TTTTTAGTAGAGATG | 85015 |
rs5878583 | in-del | -/C | 0.494013 | 0.0543839 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99512833 | TTCCTCATCTACTCT[-/C]CCCTACAGTTCCACC | 85015 |
rs5878584 | in-del | -/A | 0.123452 | 0.215605 | intron-variant, utr-variant-5-prime | USP45, TSTD3 | GRCh38.p7 | 6:99514670 | GCCCATATCCTTAAG[-/A]AAAAAAAATCCTTTT | 85015 |
rs6570063 | snp | C/T | 0.0836354 | 0.186609 | utr-variant-3-prime, nc-transcript-variant, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99435252 | AAAGCACATAAAACA[C/T]GGAATATGATTGCTC | 85015 |
rs6570064 | snp | A/G | 0.492871 | 0.0592773 | utr-variant-3-prime, nc-transcript-variant, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99435261 | AAAACACGGAATATG[A/G]TTGCTCAAAACAAGA | 85015 |
rs6570065 | snp | C/T | 0.0102441 | 0.0708325 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99435828 | TGGCCTGCTGATTCA[C/T]TATCAGCCGCTTTCA | 85015 |
rs6570074 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99447937 | tccaggcaaacaggg[C/T]ctggagtggacctcc | 85015 |
rs6570079 | snp | A/T | 0.459574 | 0.136304 | intron-variant, utr-variant-3-prime, nc-transcript-variant | USP45, TSTD3 | GRCh38.p7 | 6:99461856 | ATTAACAGCTTCACT[A/T]ATCAGCAAAACAAGA | 85015 |
rs6570082 | snp | A/C | 0.456095 | 0.141508 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99475398 | CTCGGCTCACTGCAA[A/C]CTCCACCCTTGGGGT | 85015 |
rs6570100 | snp | C/T | 0.122411 | 0.214991 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99500924 | ACTGTCTCATTAGGG[C/T]GATGGCTAACAAAAA | 85015 |
rs6900331 | snp | C/G | 0.106278 | 0.204558 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99465445 | AGACTAGACATTTTT[C/G]GTTAGCTTAGGGCTG | 85015 |
rs6902279 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99481119 | aaaaaatacataaaa[A/C]TCTTCAAATAATGTT | 85015 |
rs6903138 | snp | C/G | 0.040671 | 0.13668 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99453035 | cctgttgtggggtgg[C/G]gggagcagggaggga | 85015 |
rs6904812 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99505695 | GCTACATTACATGTT[C/T]ACAATCTTCTTACCC | 85015 |
rs6904832 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99505719 | CTTACCCACCTTTTT[C/G]TAATTcagtaattct | 85015 |
rs6904927 | snp | C/T | 0.460925 | 0.134204 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99448031 | acatccacaccaaaa[C/T]cccatctgtcagtca | 85015 |
rs6905020 | snp | C/T | 0.12932 | 0.218944 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99505821 | TCCACCCCAGAACTA[C/T]TAAATTAGAATTTCT | 85015 |
rs6907845 | snp | A/T | 0.45889 | 0.13735 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99451675 | cacagaattggaaaa[A/T]actactttaaagttc | 85015 |
rs6912228 | snp | C/G | 0.462363 | 0.131916 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99467303 | AACCTGAGGTTGGGA[C/G]AAAATGGATTAAACA | 85015 |
rs6915401 | snp | A/T | 0.492823 | 0.0594727 | utr-variant-3-prime, nc-transcript-variant, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99432963 | ATAAGAGAACAGGCA[A/T]CAACTATTCTTTGAA | 85015 |
rs6916603 | snp | G/T | 0.393065 | 0.205018 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99457682 | CCAGAATCCAATTAA[G/T]CTAATTCTGATTGaa | 85015 |
rs6916617 | snp | C/T | 0.390277 | 0.206936 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99457698 | CTAATTCTGATTGaa[C/T]agtttccaaattcag | 85015 |
rs6918880 | snp | C/T | 0.457853 | 0.138915 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99486570 | CTTTTCGACTATATA[C/T]ACATATATATATGGT | 85015 |
rs6919202 | snp | C/T | 0.493432 | 0.0569306 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99510942 | GAGCTGGATGAGCCA[C/T]ACTGGATCAAAAATG | 85015 |
rs6922192 | snp | G/T | 0.456803 | 0.140473 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99464453 | tgggatatatatagt[G/T]agtatacaagtagcc | 85015 |
rs6925132 | snp | A/G | 0 | 0 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99453018 | aagatcacacacagg[A/G]gcctgttgtggggtg | 85015 |
rs6926881 | snp | A/C | 0.12932 | 0.218944 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99505748 | CTTAAACTGTGGTCT[A/C]CAGACCAGCAGCACT | 85015 |
rs6932460 | snp | A/G | 0.0930568 | 0.194599 | upstream-variant-2KB, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99515900 | ctgccttagcctccc[A/G]agtagctgggactac | 85015 |
rs6932681 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99448784 | ccagagagaaaggtc[A/G]ggttacccgcaaagg | 85015 |
rs6934517 | snp | C/T | 0.121369 | 0.214369 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99486228 | AACCAACTCAAAGAA[C/T]AGTGCCACAGCTCAG | 85015 |
rs6934692 | snp | A/G | 0.256518 | 0.249915 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99503874 | ATAACACCTGAAAAA[A/G]TATAAAATTTAAGAA | 85015 |
rs6937597 | snp | C/T | 0 | 0 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99471163 | AATTTATATTCTCTA[C/T]TCCAAACTGTTTAAA | 85015 |
rs6940360 | snp | C/T | 0.121369 | 0.214369 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99487064 | gctctggttgaataa[C/T]ctgaaggtgggtttc | 85015 |
rs7453739 | snp | A/G | 0 | 0 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99458339 | CAGCTATTACGATTG[A/G]CAGCAATCATGAGAA | 85015 |
rs7454755 | snp | A/G | 0.396909 | 0.202282 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99446837 | CAGCCTCAAACTCTC[A/G]GACTCAAGTGATCCT | 85015 |
rs7738617 | snp | C/T | 0.401392 | 0.198948 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99512571 | GGCTAAGCAACATCG[C/T]AATTTTCATGGTTGC | 85015 |
rs7744845 | snp | C/T | 0.440645 | 0.161723 | missense, utr-variant-5-prime, nc-transcript-variant, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99508684 | AGAATCTTCTTTCTT[C/T]TAAACATTCTGAGCA | 85015 |
rs7745005 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99435966 | ATTTTACCTGAGAAG[C/T]CTGTTTTTTCTTGGG | 85015 |
rs7745012 | snp | C/T | 0.241053 | 0.24984 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99473946 | GTTTATGATCAAATA[C/T]GTAAAAGTAGAGAGG | 85015 |
rs7745189 | snp | C/T | 0.163564 | 0.234582 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99508892 | TAAAAAGCACAGAGA[C/T]TGAACACACAAAATA | 85015 |
rs7749062 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99470584 | CTGAAATACACTTAT[A/G]TACTATAAAGAAATC | 85015 |
rs7753232 | snp | C/T | 0.122758 | 0.215196 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99513336 | CTTCTTCACTTTCCT[C/T]AAACCTCTAACCCCT | 85015 |
rs7755530 | snp | A/G | 0.318656 | 0.240388 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99496175 | AATAAATAGAGATAG[A/G]GTCATGTTATGTTGT | 85015 |
rs7759598 | snp | C/T | 0.401392 | 0.198948 | upstream-variant-2KB, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99516809 | GCAAACTTGAGCAAA[C/T]CTAAATAATTTGCAT | 85015 |
rs7760158 | snp | C/T | 0.396546 | 0.202545 | intron-variant, utr-variant-3-prime, nc-transcript-variant | USP45, TSTD3 | GRCh38.p7 | 6:99459410 | tttaggttgattcca[C/T]gtctttgctattgtg | 85015 |
rs7760472 | snp | C/T | 0.447291 | 0.153545 | intron-variant, utr-variant-3-prime, nc-transcript-variant | USP45, TSTD3 | GRCh38.p7 | 6:99459570 | agccacactgctttc[C/T]gcaacggttgaacta | 85015 |
rs7763359 | snp | C/G | 0.444133 | 0.157519 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99451911 | ctttgacaaacctga[C/G]aaaaacaagcaatgg | 85015 |
rs7764482 | snp | A/C | 0.444 | 0.157683 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99451921 | cctgagaaaaacaag[A/C]aatggggaaaggatt | 85015 |
rs7767049 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | USP45, TSTD3 | GRCh38.p7 | 6:99470291 | TGCTGCCTGGATAAG[C/G]AGAAGACACTCATGA | 85015 |
rs7767584 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99458149 | cctcaacctcccaag[G/T]agctggattacaggc | 85015 |
rs7772838 | snp | C/T | 0.419135 | 0.184101 | utr-variant-3-prime, nc-transcript-variant, intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99434201 | TTTGTATACTATTAC[C/T]GTCTTTAATTACAGT | 85015 |
rs7772948 | snp | A/G | 0.493432 | 0.0569306 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99513304 | ACTTACATACTATCC[A/G]CAGAGCCATTTCAAA | 85015 |
rs7775207 | snp | A/G | 0.401037 | 0.199218 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99512232 | atcaggccagtgcat[A/G]agtcaccttgagggt | 85015 |
rs7775372 | snp | C/G | 0.401392 | 0.198948 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99512348 | tgctgggggcccata[C/G]aatactctttcgaca | 85015 |
rs9321562 | snp | C/T | 0.121022 | 0.21416 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99483769 | CGTGAACCCGGGAAG[C/T]GGAGCTTGCAGTGAG | 85015 |
rs9321565 | snp | C/T | 0.121369 | 0.214369 | intron-variant | USP45, TSTD3 | GRCh38.p7 | 6:99495452 | TTTTGCATTTAGAGT[C/T]GGATAGTTTGAGAGT | 85015 |