| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs14987 | snp | G/T | | | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88506082 | ATaggggtatccaag[G/T]gagagaatacagtca | 51191 |
| rs2629564 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499704 | AACAAGAGCTGTGAA[C/G]CAGGCAGGCAGCCTG | 51191 |
| rs2629565 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499705 | ACAAGAGCTGTGAAG[C/G]AGGCAGGCAGCCTGC | 51191 |
| rs2717532 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | HERC5 | GRCh38.p7 | 4:88502800 | gatatccaaacagcc[A/G]ataagcatataaagt | 51191 |
| rs3733446 | snp | G/T | 0.164546 | 0.234942 | intron-variant | HERC5 | GRCh38.p7 | 4:88499805 | CGCAGAGAAAGAGGT[G/T]CTGTGAACTATACCT | 51191 |
| rs4132726 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481117 | tgcagtgagccgaga[C/G]tgcgccactgcactc | 51191 |
| rs4544677 | snp | A/G | 0.0116955 | 0.0755709 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461048 | GTAGGGTAATAGAGG[A/G]GAATTCGAAGTCAAG | 51191 |
| rs4585264 | snp | A/C | 0.472522 | 0.113946 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468489 | AGGGTTCTAGTATCC[A/C]AGTTTGGTGAATTCC | 51191 |
| rs6816627 | snp | A/C/G/T | 0.0547245 | 0.156101 | intron-variant | HERC5 | GRCh38.p7 | 4:88471284 | GTAGAAAACAATGTA[A/C/G/T]AAACAATATGATCCa | 51191 |
| rs6826311 | snp | A/T | 0.105569 | 0.204058 | intron-variant | HERC5 | GRCh38.p7 | 4:88488155 | TTCTCTCCTGATTTT[A/T]AACAAGGTTCCAGAG | 51191 |
| rs6832416 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HERC5 | GRCh38.p7 | 4:88501886 | tcactgcaacctccg[C/T]ctcccgggttcaagc | 51191 |
| rs6847262 | snp | A/G | 0.00480766 | 0.0487926 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456407 | gtaggggtggggggg[A/G]gggtAGCTGCCTGCA | 51191 |
| rs6857425 | snp | C/T | 0.00236951 | 0.0343386 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88494245 | CAATGTTGCCAACCT[C/T]CCTTTCCCACTGGCA | 51191 |
| rs7437274 | snp | A/T | 0 | 0 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461056 | ATAGAGGGGAATTCG[A/T]AGTCAAGGGAATTTT | 51191 |
| rs7663568 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | HERC5 | GRCh38.p7 | 4:88487451 | AGTTGGCAGTGGCAG[C/T]CTGTAGTCTTCTGAA | 51191 |
| rs7667551 | snp | A/G | 0.217851 | 0.247924 | intron-variant | HERC5 | GRCh38.p7 | 4:88472755 | CACATATATGCATAC[A/G]CATTCGTAGAGGGAA | 51191 |
| rs7681411 | snp | C/T | 0.388775 | 0.207946 | intron-variant | HERC5 | GRCh38.p7 | 4:88495492 | ttgagctcaggaggt[C/T]gaagctgcagtgagc | 51191 |
| rs7687886 | snp | C/T | 0.0803491 | 0.183626 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468747 | CTTTGCAGGCCAGTA[C/T]TAAGAAAGACACCAA | 51191 |
| rs7688056 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HERC5 | GRCh38.p7 | 4:88503591 | CCTGGTATATGACTC[A/G]GTTGTCATTAGTAAA | 51191 |
| rs7699006 | snp | A/G | 0.492876 | 0.0592575 | missense | HERC5 | GRCh38.p7 | 4:88475940 | CTCCCAGAATGTCCT[A/G]TGATGCATATTTCCA | 51191 |
| rs9784397 | snp | A/G | 0.497445 | 0.0356514 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455565 | gcacaaaagcttgtg[A/G]ggcaggtcagagatt | 51191 |
| rs10049671 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HERC5 | GRCh38.p7 | 4:88498385 | aaacttaggagccca[A/T]ccccaaacccagtgt | 51191 |
| rs10516808 | snp | A/G | 0.170408 | 0.236992 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462511 | AGAATCAGTCCAAGA[A/G]GCATACATAGTGTGG | 51191 |
| rs10516809 | snp | A/G | 0.140899 | 0.224938 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88499935 | CCTTAGGAATTTGCA[A/G]ACACTTCTGGATGAT | 51191 |
| rs11722508 | snp | A/C | 0.164873 | 0.23506 | intron-variant | HERC5 | GRCh38.p7 | 4:88496349 | agaatagccagaaat[A/C]attcttaaggcaaat | 51191 |
| rs11946864 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458021 | GCGTTCTTTAAAATT[A/T]TGCCCATCTGTGGAG | 51191 |
| rs11947119 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | HERC5 | GRCh38.p7 | 4:88482751 | GGTCCTAGGGCTGTA[G/T]tcccaagtacctggg | 51191 |
| rs12331773 | snp | C/T | 0.493107 | 0.0583 | intron-variant | HERC5 | GRCh38.p7 | 4:88489975 | GATCATGCCACTGCA[C/T]TCCGGCCTGGGTGAC | 51191 |
| rs12505811 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468006 | TTATAGCCAGCAGTC[A/G]TTGCTTAAATCTTGA | 51191 |
| rs13119367 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482231 | aggagagtcgcttga[A/T]tccaggaggcagagg | 51191 |
| rs13146052 | snp | A/G | 0.0186899 | 0.0948454 | intron-variant | HERC5 | GRCh38.p7 | 4:88474000 | GAGGTTCTGCGATAC[A/G]GACTCTCAGACCTTT | 51191 |
| rs13147515 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475342 | ttttttttttttttt[G/T]gagatggagtcttgc | 51191 |
| rs13148298 | snp | A/C | 0 | 0 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462031 | CATCAGTGCAAAGGT[A/C]CAATATTGTGATATT | 51191 |
| rs13152493 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458391 | CATTTTTGTAGTAAT[G/T]TTAAGGTTTTTTTTT | 51191 |
| rs17014143 | snp | A/G/T | 0.0131427 | 0.0799923 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463975 | AGAGTGACTCAGATA[A/G/T]CATGTGGAAGGTAAG | 51191 |
| rs17014146 | snp | A/T | 0.214239 | 0.247429 | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467923 | ACGAACAGAGTTATT[A/T]CCTTAAGCAGCATGT | 51191 |
| rs17014147 | snp | G/T | 0.0464069 | 0.145088 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468323 | GACTTTCTAAAACTC[G/T]TACTCTTTGTGCATC | 51191 |
| rs17014153 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469986 | CATTAGTTTGTGTAC[C/G]TGTTATTCTTAGCTG | 51191 |
| rs17014156 | snp | G/T | 0.125182 | 0.216612 | intron-variant | HERC5 | GRCh38.p7 | 4:88473813 | GTCTGTGAAGGGAAG[G/T]GATTGGATCAGTTCA | 51191 |
| rs28410134 | snp | G/T | 0.492287 | 0.0616198 | intron-variant | HERC5 | GRCh38.p7 | 4:88482047 | GGTGTGGTGGCTCAT[G/T]CCTGTAATCCCAGCA | 51191 |
| rs28441580 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475390 | GTGACACAATCTCGG[C/G]TCACTGCAACCTCTG | 51191 |
| rs28517536 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88486360 | TCCTCAAAATCTATG[C/T]AATTTTGCAGTCAGA | 51191 |
| rs28569005 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469526 | AAAATCTGTAGGGCA[A/G]GCCAGCAGGCTGGAG | 51191 |
| rs34100798 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458530 | AATACTTCCTTTTTT[-/T]CAACTGATTTGAAAT | 51191 |
| rs34182426 | in-del | -/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470116 | ATGGCTTTCTAATTC[-/C]TGGAAAATGATTGTA | 51191 |
| rs34457268 | in-del | -/C | | | frameshift-variant | HERC5 | GRCh38.p7 | 4:88494216 | TTCTATGTGGACTTT[-/C]CCCTGTTCAATTGCA | 51191 |
| rs34778861 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488254 | TTTTTTTTTTTGAGA[A/G]AGAGTCTCCCTCTGT | 51191 |
| rs34823613 | snp | A/G | 0.0076247 | 0.0612716 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88472445 | TGTTTATTTGGACTT[A/G]AATAAAGCAAGAAAC | 51191 |
| rs34840817 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HERC5 | GRCh38.p7 | 4:88500359 | ATTCTCCAATAGGCT[A/G]GCTGAGGCTTTTGAA | 51191 |
| rs34980419 | in-del | -/C | | | upstream-variant-2KB, frameshift-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457079 | GCAGGCCCCGCCCCC[-/C]AAACAGCACGTGGGG | 51191 |
| rs35087151 | in-del | -/T | | | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88506077 | CCCGTGACTGTATTC[-/T]TCTCCCTTGGATACC | 51191 |
| rs35414633 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503253 | GAACCTATAGATCAA[-/T]TTTTTGAAAAAATTG | 51191 |
| rs35420686 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488256 | TTTTTTTTTGAGAGA[A/G]AGTCTCCCTCTGTTG | 51191 |
| rs35438949 | in-del | -/T | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88477080 | TTTTTTTTTTTTTTT[-/T]AAGAATCTCATTTGA | 51191 |
| rs35511740 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472790 | TCAACTCAGGGCTTT[-/T]AGGAAGATGATTAAG | 51191 |
| rs35749883 | in-del | -/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474929 | CAAATGATTACTGTG[-/C]ATCTAAGCACACATA | 51191 |
| rs35999083 | in-del | -/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502221 | TGTTGGTATGTAACT[-/G]GGGAGAAGTGCTTGG | 51191 |
| rs36021764 | in-del | -/C | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460610 | ATTCAAGGATCTCCC[-/C]TAGCCCTGTAGTATT | 51191 |
| rs55816888 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455249 | AATTTTTGCTCCTTA[A/G]CTCAGCTAAAATCCA | 51191 |
| rs55990584 | snp | C/T | 0.0233443 | 0.105486 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88470620 | CTAATATAGGGAAAT[C/T]CAAGAGATATTTTCA | 51191 |
| rs56006160 | snp | A/G | 0.021333 | 0.101051 | intron-variant | HERC5 | GRCh38.p7 | 4:88471190 | GGCCAGGCTGGTCTC[A/G]AACTCCTGAGCTCAG | 51191 |
| rs57966410 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466439 | ATTGCCCGGATAGTT[A/G]AACTTAATCTCCAGC | 51191 |
| rs58490237 | in-del | -/GTT | | | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505946 | GTTGTTGTTGTTGTT[-/GTT]TCTCTACTTTGTTTT | 51191 |
| rs58497654 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | HERC5 | GRCh38.p7 | 4:88501590 | CTGGCCTACATCACA[A/T]CTTTTTCCACGATTT | 51191 |
| rs58577205 | in-del | -/A | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480085 | AAAAAAAAAAAAAAA[-/A]GAAATAACCTGTGTG | 51191 |
| rs59412540 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | HERC5 | GRCh38.p7 | 4:88483408 | AGACAGGGCCTAACT[A/G]TGTTGCTCAGGCTGG | 51191 |
| rs59421640 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | HERC5 | GRCh38.p7 | 4:88472934 | TTCTTTTTTTTTTTT[C/T]TTTTCCATTCTACTT | 51191 |
| rs60661158 | snp | A/G | 0.125874 | 0.217008 | intron-variant | HERC5 | GRCh38.p7 | 4:88502577 | TTGGAGGCGAAAGGG[A/G]AAAAAGGAGGAGTGG | 51191 |
| rs61337796 | in-del | -/TT | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502910 | CTAGATGCAAGTCTT[-/TT]GTTGGTTATATGTAC | 51191 |
| rs61755702 | snp | A/G | 0.000286149 | 0.0119579 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462157 | GCTTTTTGCCTGGGG[A/G]CAGAACCTGCATGGG | 51191 |
| rs62308681 | snp | G/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88476297 | AAATTTCACAGAGAA[G/T]TTGAAAGAATAGTAT | 51191 |
| rs62308682 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483034 | TTTCTTTTTCCAGTC[A/C]ATATACGTTTTATTA | 51191 |
| rs62308683 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | HERC5 | GRCh38.p7 | 4:88502649 | ACACTTTCATCAGTA[A/G]GGTACGACAGTTCTA | 51191 |
| rs66502916 | snp | C/T | 0.390277 | 0.206936 | intron-variant | HERC5 | GRCh38.p7 | 4:88502093 | GTGAGCCACTGCGCC[C/T]GGCCTATCTGTAGTA | 51191 |
| rs71609527 | snp | A/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88501650 | AAGTATAACCTATAT[A/T]ACAGAATTTTGCACA | 51191 |
| rs72879395 | snp | A/G | 0.00809425 | 0.0631 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459319 | ATAATCAAAGTGACA[A/G]TAGTTCCTGGTTGGA | 51191 |
| rs72881108 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | HERC5 | GRCh38.p7 | 4:88478286 | TTGTAATTATAATAT[A/G]TACTAAAATATTTTG | 51191 |
| rs72881116 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | HERC5 | GRCh38.p7 | 4:88498318 | CACTAATGTGTGAGA[G/T]CCTCTAGGGGTGGGC | 51191 |
| rs73841943 | snp | A/G | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457992 | TCTCATCGAAGTGGG[A/G]GAAATAGTTGCCCGC | 51191 |
| rs73841944 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467417 | TTCAGATTAGGATTA[A/C]TGTGAATTTAAATGA | 51191 |
| rs73841945 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | HERC5 | GRCh38.p7 | 4:88472757 | CATATATGCATACAC[A/G]TTCGTAGAGGGAAGT | 51191 |
| rs73841946 | snp | G/T | 0.00639822 | 0.0561976 | intron-variant | HERC5 | GRCh38.p7 | 4:88479534 | TTTAGAAACCTCTGT[G/T]TTTTTATCTAGCTGT | 51191 |
| rs73841947 | snp | A/G | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88496746 | GACATGCAGTGTACC[A/G]ACAGTAAAGAAAAGA | 51191 |
| rs73841948 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HERC5 | GRCh38.p7 | 4:88497717 | GTAAAGAATGCAAAC[A/G]TGTTTGGAAGAGAGC | 51191 |
| rs74374958 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | HERC5 | GRCh38.p7 | 4:88497160 | TAAATGGACTAAGGG[A/T]AATTGCTACCAAGAA | 51191 |
| rs74581848 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | HERC5 | GRCh38.p7 | 4:88492099 | ACCTTCATCTCCCGG[A/G]TTCAAGTGAGTCTCC | 51191 |
| rs74632998 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458422 | TTAAGTTAAAATTTT[A/T]CGTACGCTTGGAATT | 51191 |
| rs74658427 | snp | C/T | 0.216649 | 0.247765 | intron-variant | HERC5 | GRCh38.p7 | 4:88499388 | GAAATAATTTAAAAA[C/T]TGGTTACTGTCCATT | 51191 |
| rs74782314 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | HERC5 | GRCh38.p7 | 4:88478058 | CAAGTTTGTAGTTGT[A/G]TTAACTGTAAAGGAA | 51191 |
| rs74876955 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | HERC5 | GRCh38.p7 | 4:88494400 | ATATTTAAGTACACA[C/T]GCTTCATAATATTTC | 51191 |
| rs74945477 | snp | A/T | 0.5 | 0 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459156 | TTCTAATTAAAAAAA[A/T]TCTATGTCAAGACCG | 51191 |
| rs74958280 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | HERC5 | GRCh38.p7 | 4:88484910 | AATGCCTTTAAACAT[A/G]TTTGTTACAGCTTTT | 51191 |
| rs75070724 | snp | A/G | 0.00640729 | 0.0562369 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459389 | AGATACATTCCGTGG[A/G]CCAAGGAGCAGAGCA | 51191 |
| rs75121676 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HERC5 | GRCh38.p7 | 4:88495541 | CTCCAGCCTGGGCGA[C/T]AGTAGAAGACCCTGT | 51191 |
| rs75124661 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462570 | CAGGGCTGTGTGTGA[A/G]ACGGGAAAGGGCATT | 51191 |
| rs75362741 | snp | C/T | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88471984 | CTTCCCTTCCTTCTT[C/T]CTTTTCTTTTTTTCT | 51191 |
| rs75376862 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HERC5 | GRCh38.p7 | 4:88501123 | AAGTTGGTGTGTGTT[A/G]TATGTGTTTTGACAT | 51191 |
| rs75842378 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464728 | GGAATAGCTAGGATT[A/G/T]CAGGCGTGCACTGCC | 51191 |
| rs76041741 | snp | A/C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464726 | CTGGAATAGCTAGGA[A/C/T]TACAGGCGTGCACTG | 51191 |
| rs76095623 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HERC5 | GRCh38.p7 | 4:88501126 | TTGGTGTGTGTTGTA[C/T]GTGTTTTGACATATA | 51191 |
| rs76145679 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464727 | TGGAATAGCTAGGAT[G/T]ACAGGCGTGCACTGC | 51191 |
| rs76166651 | snp | C/T | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88471985 | TTCCCTTCCTTCTTT[C/T]TTTTCTTTTTTTCTT | 51191 |
| rs76392973 | snp | A/G | 0.100231 | 0.200173 | intron-variant | HERC5 | GRCh38.p7 | 4:88494536 | CATAACTAGACTTCA[A/G]TGTTTGCATTAATCT | 51191 |
| rs76555004 | snp | A/C | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88479286 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 51191 |
| rs76603756 | snp | C/G | 0.0194277 | 0.0966252 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505908 | CAACAGCCTTATTTT[C/G]TTGTTGTTATCGTTG | 51191 |
| rs76630192 | snp | A/G | 0.217851 | 0.247924 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506402 | TATGGTAGGAGTGGC[A/G]TTGTTCTCAGTCTTA | 51191 |
| rs76807720 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467471 | GCATATGCAGCTCTC[A/G]TTCCAGTTTGCAAGA | 51191 |
| rs77117111 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HERC5 | GRCh38.p7 | 4:88505603 | TTTGTGAATAAATAG[A/T]TTTTTTTCTCTGTAA | 51191 |
| rs77278996 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464729 | GAATAGCTAGGATTA[C/G]AGGCGTGCACTGCCA | 51191 |
| rs77297677 | snp | G/T | 0.0839998 | 0.186933 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455918 | GAACTCAATAATATA[G/T]AAAGAACTCTTAGAT | 51191 |
| rs77340050 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | HERC5 | GRCh38.p7 | 4:88491543 | GAAAGCAAGGGAGAA[G/T]ATTGTGTCAAGGAAA | 51191 |
| rs77477357 | snp | A/C | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465061 | AGGCATGAGCCACTG[A/C]ACCTGGCCACAACCG | 51191 |
| rs77711968 | snp | C/T | 0.101658 | 0.201233 | intron-variant | HERC5 | GRCh38.p7 | 4:88471897 | CTTCCTTCCTTCCTT[C/T]GAAAAACCTTTATCT | 51191 |
| rs77880491 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | HERC5 | GRCh38.p7 | 4:88502234 | ACTGGGAGAAGTGCT[C/T]GGTGCCTTGTGGTTG | 51191 |
| rs77902409 | snp | C/T | 0.031825 | 0.122064 | intron-variant | HERC5 | GRCh38.p7 | 4:88480189 | CGGGATAATCATTCC[C/T]TTGCTCTTACTATTT | 51191 |
| rs78059579 | snp | G/T | 0.5 | 0 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464607 | TTGGTTTTTTTTTTT[G/T]AGGCAGAGTATTGCT | 51191 |
| rs78300932 | snp | C/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456354 | CCGGGAATACGGGAA[C/T]ACGTAGCGGAGCGGG | 51191 |
| rs78308763 | in-del | -/CAT | 0.387453 | 0.208822 | intron-variant | HERC5 | GRCh38.p7 | 4:88479649 | TTTTTTTTAAAATTA[-/CAT]CATACATATAAAGGA | 51191 |
| rs78393149 | snp | A/G | 0.00327337 | 0.0403233 | synonymous-codon, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469243 | TGTGGAGACTAAACG[A/G]TGGCAGAGCACAAAA | 51191 |
| rs78430807 | snp | A/C/T | 0.0150606 | 0.0854603 | intron-variant | HERC5 | GRCh38.p7 | 4:88505230 | TCTGTGAAGTTCCTT[A/C/T]TCCTGCCTTGAACCT | 51191 |
| rs78431852 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88484866 | TAAGTTTTTGACCTG[A/T]TTATTCCATATCTAC | 51191 |
| rs78443383 | snp | A/G | 0.308414 | 0.24308 | intron-variant | HERC5 | GRCh38.p7 | 4:88477014 | TTATCCAATATCTAG[A/G]TCATTCAAATTTCTC | 51191 |
| rs78613619 | snp | C/G | 0.0141832 | 0.0830087 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463979 | TGACTCAGATAGCAT[C/G]TGGAAGGTAAGTTGT | 51191 |
| rs78637918 | snp | G/T | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88478629 | AAATATTTTTTTTTT[G/T]GAGATGGGGTCTTAC | 51191 |
| rs78746347 | snp | G/T | 0.5 | 0 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464606 | TTTGGTTTTTTTTTT[G/T]GAGGCAGAGTATTGC | 51191 |
| rs78893196 | snp | C/T | 0.00512826 | 0.0503769 | intron-variant | HERC5 | GRCh38.p7 | 4:88494374 | ACCCTTTCTAACATA[C/T]ATTTAGGCAAATATT | 51191 |
| rs79030806 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HERC5 | GRCh38.p7 | 4:88486576 | GGTAGAGTGTCTTGG[A/G]TGTAAGCACTCCTTT | 51191 |
| rs79103658 | in-del | -/AAA | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482322 | CTCAAAAAAAAAAAA[-/AAA]GGGAAAAGAAAAGAA | 51191 |
| rs79154499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502211 | GCAGGCATTTCTGTT[A/G]GTATGTAACTGGGAG | 51191 |
| rs79380028 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467774 | TCTGGAGTTGAACCC[A/G]TGCCCTTTATGACCT | 51191 |
| rs79421641 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460027 | AATTAAATACTATTA[A/G]TAGTTCTAAAATCCA | 51191 |
| rs79718711 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | HERC5 | GRCh38.p7 | 4:88496195 | TAAAGGCCCAAGGAT[G/T]CCCAAGAATTGCTGG | 51191 |
| rs79813277 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | HERC5 | GRCh38.p7 | 4:88488124 | AACTTTGTTTTGCTT[C/T]AACTCTTATAACCTA | 51191 |
| rs111241260 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476705 | GCAGGCAGATCACCT[A/G]AGGTCAGGAGTTCAA | 51191 |
| rs111247941 | snp | C/T | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88479681 | AATATATATATAATA[C/T]CTATTTAGAATTCAA | 51191 |
| rs111323592 | snp | C/T | 0.5 | 0 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88487095 | AAATGTACAATGCTG[C/T]GTCATATTCAGTCAC | 51191 |
| rs111384872 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501884 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 51191 |
| rs111485718 | snp | C/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88489397 | AAACATAAAAGAATG[C/T]GGCAAAGGGTTTCAT | 51191 |
| rs111492791 | snp | A/G | 0.5 | 0 | missense | HERC5 | GRCh38.p7 | 4:88470651 | TCTCCTGCTTGTCTA[A/G]CTGGAAGTTTTTTAA | 51191 |
| rs111667763 | snp | C/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88504454 | TTAAATTCAGTTTTC[C/T]TTCCTATTTCCTCAA | 51191 |
| rs111770036 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88477414 | AAGGGGAGGGGAAGG[A/G]GAAGGTGAAGGGAAG | 51191 |
| rs111780472 | snp | A/G | 0.329084 | 0.237162 | intron-variant | HERC5 | GRCh38.p7 | 4:88479796 | TGCTGGGCCGGGCGC[A/G]TTGGCTCACGCCTGT | 51191 |
| rs111923801 | snp | C/T | 9.88484e-05 | 0.00702954 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463875 | GCTGCTGTTTACTTT[C/T]GGTGCTGGAAAACAT | 51191 |
| rs112140140 | in-del | -/A | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88476920 | GTGAGACTCCGTCCC[-/A]AAAAAAAAAGAACAT | 51191 |
| rs112154548 | snp | A/G | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88476248 | ACACATGGCTTTGTC[A/G]TGATTTCCTTAGTTT | 51191 |
| rs112230023 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | HERC5 | GRCh38.p7 | 4:88492299 | GTGAGCCACCACGCC[C/T]GGCCAATTTTTATGA | 51191 |
| rs112291038 | snp | A/G | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88497665 | TTAGAAAAAAAGCCA[A/G]ACTTAAAGATTTGGA | 51191 |
| rs112312942 | snp | C/G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455594 | TTCTCCAGGGACCCT[C/G/T]CCTTATCTGCCTCCA | 51191 |
| rs112357547 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HERC5 | GRCh38.p7 | 4:88481128 | CGCAGTCTCGGCTCA[C/T]TGCAACCTCTGCCTC | 51191 |
| rs112377824 | snp | G/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88479257 | GCCACTGCACTCCAG[G/T]CTGGGCAACAGGGTG | 51191 |
| rs112390542 | snp | A/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88486568 | ACCCTGTGGGTAGAG[A/T]GTCTTGGGTGTAAGC | 51191 |
| rs112476417 | snp | C/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88489638 | CTGGCCTAGCCTGGC[C/T]AGCACCACCCTTGAA | 51191 |
| rs112890151 | snp | A/G | 0.5 | 0 | missense | HERC5 | GRCh38.p7 | 4:88489299 | TTTTGAATCAGCTAA[A/G]TCAATTTGAGAATGA | 51191 |
| rs112961590 | snp | C/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88504425 | GAAAAGGTACATCAT[C/T]AAGTCTAAGTTGATT | 51191 |
| rs113251292 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | HERC5 | GRCh38.p7 | 4:88484051 | TGGATGGTATTTCTT[C/T]AGCCCTATCTTCCAG | 51191 |
| rs113417210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88477683 | TCCCACATCCAGATA[A/G]TCTGACCGTTTCCTA | 51191 |
| rs113470579 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88477439 | GGGAAGGGAAAGGGA[C/G]GGGGAGGGGAAGGTG | 51191 |
| rs113582153 | in-del | -/TA | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88472738 | GTACACAAACACACA[-/TA]CACATATATGCATAC | 51191 |
| rs113583484 | snp | A/T | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88488737 | CATAACCTGGATTTT[A/T]TTTCCTGCAGCCTGT | 51191 |
| rs113807638 | snp | C/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88505201 | CACCTTGCACCTTCC[C/T]ACCTCCAGGCCTTTC | 51191 |
| rs113894669 | snp | C/G | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88481586 | TTTTCTCCCATAAAG[C/G]TTTTAAATTATTACC | 51191 |
| rs113914112 | snp | C/T | 0.5 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88501373 | GTATGTATTCTTCAC[C/T]GCTGTATATTCAGTA | 51191 |
| rs114087952 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC5 | GRCh38.p7 | 4:88473027 | TACTGCTATCTTTAG[A/G]TTTTCTTTTTGCAGG | 51191 |
| rs114278656 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88491233 | TGGAAGAGGCAGCAT[C/G]TAAATAAATAAACTG | 51191 |
| rs114399832 | snp | G/T | 0.00747167 | 0.0606631 | intron-variant | HERC5 | GRCh38.p7 | 4:88505648 | CCATGTAAAACAGAT[G/T]GCCTAATTTTATTCT | 51191 |
| rs114566307 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HERC5 | GRCh38.p7 | 4:88474497 | AAGGAGGTAGAATGC[A/G]TGTGTACTAATAAGA | 51191 |
| rs114571059 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HERC5 | GRCh38.p7 | 4:88470408 | TTTATTTCCCATGTT[C/T]GCCACTGAAATTTTG | 51191 |
| rs114675715 | snp | C/T | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455185 | TGGAACGACTGGAAA[C/T]CCATAAGGAAAAAAA | 51191 |
| rs114749403 | snp | A/G | 4.99305e-05 | 0.00499628 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469184 | AATCTGAAGAGGACA[A/G]TTCCTACTCTGAATG | 51191 |
| rs114876930 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466413 | ATTGCTGAGGCATGA[C/T]TGGTTAAATCATTGC | 51191 |
| rs115025674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485372 | TGTAAGGCCAAGATC[A/G]TCAGATCCAGAGGGC | 51191 |
| rs115033892 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88474613 | AGGTAATTATAACAA[C/T]TCGTACATTTACAGA | 51191 |
| rs115070022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497915 | GACAGAACTATGTCA[A/G]GAGTGGCTTTGTGTG | 51191 |
| rs115292865 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466785 | GTGACTCAAACTGAT[A/G]TTGAAAAATGAGCAG | 51191 |
| rs115314038 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88470420 | GTTTGCCACTGAAAT[G/T]TTGAGATTTACCAAA | 51191 |
| rs115345184 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HERC5 | GRCh38.p7 | 4:88483200 | TAGTATCATTTACTT[A/G]TAGGGGTTTGCTGTT | 51191 |
| rs115628318 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | HERC5 | GRCh38.p7 | 4:88505016 | ACTTTCTCATTTTCT[A/G]TTTCCTTACTTTTGA | 51191 |
| rs115746924 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | HERC5 | GRCh38.p7 | 4:88500504 | GTACCTCACATGGCC[A/G]TGCCGAGATTCAGTG | 51191 |
| rs115808046 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HERC5 | GRCh38.p7 | 4:88498542 | GAAATGGGAATGTCT[A/G]TCCTATGCCTGTTCC | 51191 |
| rs115842334 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HERC5 | GRCh38.p7 | 4:88476185 | ATAACAATTACCATG[A/G]TCATCTAAAATAGAT | 51191 |
| rs116024969 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466991 | AGTTTTGGCAATTTA[C/T]TGTATTGCTAAACAC | 51191 |
| rs116131470 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HERC5 | GRCh38.p7 | 4:88477029 | GTCATTCAAATTTCT[C/T]TTCTTTTCCCAAAAA | 51191 |
| rs116612766 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HERC5 | GRCh38.p7 | 4:88489742 | GGACAGGCATGGTGA[C/T]TCACACCTGTAATCC | 51191 |
| rs117571651 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469528 | AATCTGTAGGGCAGG[A/C]CAGCAGGCTGGAGAC | 51191 |
| rs117583526 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455292 | ATGACCAGGAACAAT[C/T]AGGCATGTGAATACA | 51191 |
| rs117936564 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88505167 | CCAAATAATCCCATT[C/G]TCTGAACACTCCTGA | 51191 |
| rs118103566 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HERC5 | GRCh38.p7 | 4:88476593 | AAGTTGAAGACATGA[A/G]ATTTCACTCATAATA | 51191 |
| rs137915296 | snp | C/G | 0.000153988 | 0.00877328 | missense | HERC5 | GRCh38.p7 | 4:88504246 | GGAGAGACTATGTTT[C/G]TAAGTATATCAATTA | 51191 |
| rs137966388 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | HERC5 | GRCh38.p7 | 4:88472704 | CACACAGGTTACAGA[A/T]ATTCTAAATAGTGTG | 51191 |
| rs138057004 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468639 | TCTAATCAGTGTGAT[C/T]TCCATAGGCTATACT | 51191 |
| rs138065090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481635 | GCTTTTTTCTGGAAA[C/G]GACCAGATAGTAAAT | 51191 |
| rs138084118 | snp | G/T | 1.64814e-05 | 0.00287061 | missense | HERC5 | GRCh38.p7 | 4:88493126 | TTCATGTATCCTGAA[G/T]GGGCTTCCTGCATGT | 51191 |
| rs138354720 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HERC5 | GRCh38.p7 | 4:88498340 | GGGGTGGGCTTTGCC[C/T]AGCAAAGTCATGGGT | 51191 |
| rs138435954 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HERC5 | GRCh38.p7 | 4:88494987 | TTTCAGGTATTATTC[A/G]TGGAAATATAAATTG | 51191 |
| rs138498285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460245 | GCCAGTAGAATGTCT[A/G]TATTTCACTTGTAAC | 51191 |
| rs138651900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482776 | CCTGGGATTACAGGC[A/G]TGCACCACCATGCCT | 51191 |
| rs138766192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487659 | ATAAAAGAGGTTTGT[A/G]CAGATTCCTCCCTTT | 51191 |
| rs138781114 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC5 | GRCh38.p7 | 4:88487568 | CTAATGAAAAGATAC[A/G]GTAGCAGGAATAGAA | 51191 |
| rs138904059 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467766 | GTGGTTTGTCTGGAG[C/T]TGAACCCGTGCCCTT | 51191 |
| rs139012623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88498888 | CCATTGTATTTTAGA[A/G]GCAGGTAACTTGTTC | 51191 |
| rs139078447 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88489908 | CAGCTACTCGGGAGG[G/T]TGAAACATGAGAATC | 51191 |
| rs139137489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470733 | ACCGTGAAAGAGGAT[A/G]AAAAAATGATTGGAG | 51191 |
| rs139310661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88495684 | CCCATAATGGCAGAA[C/T]GATGATCTGAACACA | 51191 |
| rs139423505 | snp | A/G/T | 6.59069e-05 | 0.00574019 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475981 | GAGCCTTGTGGTTCC[A/G/T]TTTGCAAAGGTTGTT | 51191 |
| rs139433823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463280 | TGAATCAAGTCATAA[A/C]TGAGAACAGGCTTTG | 51191 |
| rs139514664 | snp | C/G/T | 3.2955e-05 | 0.00405914 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475867 | CCTCAAAGATAATCT[C/G/T]CTCAAAAGACTTCCA | 51191 |
| rs139586816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476276 | TTTCCAACTTTTCAC[G/T]ATGAAAAATTTCACA | 51191 |
| rs139684539 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HERC5 | GRCh38.p7 | 4:88476813 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51191 |
| rs139731879 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455383 | CCAACAGGCTCCCAG[C/G]TCACAGACTGAATAA | 51191 |
| rs139854497 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88488126 | CTTTGTTTTGCTTCA[A/G]CTCTTATAACCTATT | 51191 |
| rs139868572 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | HERC5 | GRCh38.p7 | 4:88496754 | GTGTACCAACAGTAA[A/T]GAAAAGATTTAATAC | 51191 |
| rs140060115 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464965 | TTAGTAAAGACGGGG[C/T]TTCACTGTGTTAGCC | 51191 |
| rs140090204 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88481041 | GTGTCTTGTTTTAAA[A/C]TTCTTTTCTCCCATA | 51191 |
| rs140221853 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491943 | CTCCTCGGGGAGCAA[A/C]CAGCCACTTCAGCAA | 51191 |
| rs140375739 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC5 | GRCh38.p7 | 4:88497457 | GTGCTCCTTGTTACT[A/G]TATAAAGTGGCAGAG | 51191 |
| rs140500541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465819 | GGAAGACACATAAGG[A/G]CAGGGTATAGGAGGG | 51191 |
| rs140526163 | snp | A/C | 4.99771e-05 | 0.0049986 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469182 | TTAATCTGAAGAGGA[A/C]AATTCCTACTCTGAA | 51191 |
| rs140537045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459069 | CTTAATAAACAAGAA[A/C]CTAAAAGCAGATATT | 51191 |
| rs140547631 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HERC5 | GRCh38.p7 | 4:88472156 | ACTGGGAAATATTAA[C/T]TTTTTTAATCTATTA | 51191 |
| rs140660520 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464057 | AATTTAATAAAATTT[C/G]TTTCAGTTTCTTTGA | 51191 |
| rs140792151 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88491312 | TTGAACAGGCCGTTG[G/T]AAGTGACTGTCAATC | 51191 |
| rs140831528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487000 | CATCAGGGATGTAAG[C/G]CTATGAGGTAAAGTG | 51191 |
| rs140887404 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88505042 | TTTGAGAAATATTTA[A/T]CTTCTATTTTTATTT | 51191 |
| rs140909398 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88485586 | AGTCAAATACTAACA[A/G]TCACTAATGTCTGAA | 51191 |
| rs141001025 | snp | A/G | 0.000313007 | 0.0125062 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467182 | TCCAGTGAAAGTATC[A/G]TCAAGTGAAGAACTC | 51191 |
| rs141024373 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HERC5 | GRCh38.p7 | 4:88489623 | AGTCCCTTCTGAGGT[C/G]TGGCCTAGCCTGGCT | 51191 |
| rs141103897 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466647 | ACAGTATAGTGGAAT[A/G]TACAAACCAGCAAAT | 51191 |
| rs141173285 | in-del | -/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456408 | TAGGGGTGGGGGGGA[-/G]GGGTAGCTGCCTGCA | 51191 |
| rs141212897 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462757 | CTGTTAGTGTATTAT[C/T]ACAAAAGAATACTAA | 51191 |
| rs141289100 | snp | C/T | 4.94238e-05 | 0.00497086 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489258 | GTTTGATCTAACAGT[C/T]AGAAGGAATCACTTG | 51191 |
| rs141362172 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506191 | ATTCACTATTCAATG[C/T]GTTTACCAGCTCTTT | 51191 |
| rs141369302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470174 | CATAATTTGCAGAGC[A/G]TAAATAATTAAGAAC | 51191 |
| rs141433499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499537 | TCAGAGTTACTGATA[C/G]CTGAAATTTAATATG | 51191 |
| rs141482515 | snp | C/G/T | 3.2954e-05 | 0.00405908 | HERC5 | 4 | allele_origin=T(somatic)/C(germline) | 4:88493044 | AATTGGGTATGACCT[C/G/T]GGAGGAGTCAAGAAA | 51191 |
| rs141622783 | snp | A/G | 0.00379005 | 0.0433666 | missense | HERC5 | GRCh38.p7 | 4:88504356 | AAATTATTCCACCCC[A/G]AAGAACTGAAGGATG | 51191 |
| rs141746893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487625 | GCCCAATAAATGGCT[A/G]CTACTCTGTGATGGT | 51191 |
| rs141751539 | snp | A/G | 1.81628e-05 | 0.00301348 | intron-variant | HERC5 | GRCh38.p7 | 4:88494132 | TACTGGTAAAAACTC[A/G]TAATACTTTAAGATT | 51191 |
| rs141783783 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HERC5 | GRCh38.p7 | 4:88482984 | CTCATGTTATATCTA[C/G]TATTTACTTATAGAT | 51191 |
| rs141870419 | snp | G/T | 6.59957e-05 | 0.005744 | missense | HERC5 | GRCh38.p7 | 4:88470628 | GGGAAATCCAAGAGA[G/T]ATTTTCATCTCCTGC | 51191 |
| rs142080961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472872 | AAATGTAGAAATGAG[A/G]ACATTTTTTCTGATA | 51191 |
| rs142189085 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457708 | GCTGTCTTTTATCCC[G/T]GTCAGTGTCAGGCGC | 51191 |
| rs142266505 | in-del | -/GTT | | | cds-indel | HERC5 | GRCh38.p7 | 4:88505920 | TTTGTTGTTGTTATC[-/GTT]GTTGTTGTTGTTGTT | 51191 |
| rs142318892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465418 | TCTTATAAAAAACTA[G/T]CATGAATACTTTCAG | 51191 |
| rs142382132 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HERC5 | GRCh38.p7 | 4:88489761 | CACCTGTAATCCCGG[C/T]GCTTTGGGATGCTGA | 51191 |
| rs142446290 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88471499 | GCACGTGCCACCACC[C/T]CCTGCTAATTTTTTA | 51191 |
| rs142448263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498458 | TTAAGATTTAATGTT[A/G]CATGCCATTTTGAGT | 51191 |
| rs142509922 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HERC5 | GRCh38.p7 | 4:88475465 | CTGGGACTACAGGCA[C/T]GCACCGTCACGCCCA | 51191 |
| rs142534489 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88503769 | TATGATGGAGTTGTT[A/G]TAAAAATTACATTAG | 51191 |
| rs142563973 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HERC5 | GRCh38.p7 | 4:88479002 | CCTCAAATATACCCA[A/G]TAAGCTGGTGAGGTG | 51191 |
| rs142679937 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88481768 | CATGGCTATGTTCCA[A/G]TAAGACTATAAAAAT | 51191 |
| rs142762471 | snp | C/T | 4.94613e-05 | 0.00497275 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88494266 | CCCACTGGCACTGTT[C/T]AAGAAACTTTTGGAC | 51191 |
| rs142920571 | snp | C/G/T | 4.94241e-05 | 0.00497092 | missense | HERC5 | GRCh38.p7 | 4:88489242 | TCGCTTTGAGGCCCA[C/G/T]GTTTGATCTAACAGT | 51191 |
| rs142944410 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | HERC5 | GRCh38.p7 | 4:88496185 | ATGAACTCTGTAAAG[G/T]CCCAAGGATTCCCAA | 51191 |
| rs143121208 | snp | G/T | 3.3012e-05 | 0.00406262 | missense | HERC5 | GRCh38.p7 | 4:88494179 | GCCTAAATTTGAGAA[G/T]AAAAGATACTTCTTT | 51191 |
| rs143126476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88496804 | AAAGAACTTCTTTCT[C/T]CATCAAGAGGGTGTT | 51191 |
| rs143295323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502516 | GGAAATTTAAGCCAC[A/G]CAGCCATCAGTGGGT | 51191 |
| rs143343865 | snp | C/G/T | 0.0162398 | 0.0886349 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461586 | TAGATATTGTCAGCT[C/G/T]TATCAGATAACATCT | 51191 |
| rs143417798 | snp | C/T | 0.0248432 | 0.108648 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469667 | GGCTCACTCACATTA[C/T]GGAAGGTCCTTTCTT | 51191 |
| rs143427466 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88486357 | GACTCCTCAAAATCT[A/G]TGCAATTTTGCAGTC | 51191 |
| rs143456779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463443 | ATGAGAACTGTTGTC[A/G]CTGGGTTGAGAAGCA | 51191 |
| rs143589817 | snp | C/G | 8.26262e-05 | 0.006427 | missense | HERC5 | GRCh38.p7 | 4:88470655 | CTGCTTGTCTAACTG[C/G]AAGTTTTTTAAGGAA | 51191 |
| rs143785832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88495347 | TGAGCCCAGGAGTTT[C/G]AGACCTGCCTGACCA | 51191 |
| rs143872346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488829 | TTTCAGTGGATACCA[A/G]TACATCTCTTAGCCT | 51191 |
| rs143917469 | snp | A/C | 6.60055e-05 | 0.00574442 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463563 | CCTTATTGAAGGACT[A/C]GACAATCAGAAAGTT | 51191 |
| rs144118380 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HERC5 | GRCh38.p7 | 4:88470974 | GGTTCTTTGTTTTTT[C/T]CTTTTTTTTTTTGAG | 51191 |
| rs144282953 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | HERC5 | GRCh38.p7 | 4:88483040 | TTTCCAGTCCATATA[C/T]GTTTTATTATTTTCC | 51191 |
| rs144318965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476446 | TAGTAATTGTATTTA[G/T]TCACTGAAAAGTTTA | 51191 |
| rs144372118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88505535 | ACATTGTTCGAATAC[A/T]ATCCCCAATGCACTG | 51191 |
| rs144447890 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455146 | GACAGGGATGCCAAG[A/G]CAATTCCATGGGGAT | 51191 |
| rs144598457 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HERC5 | GRCh38.p7 | 4:88473999 | TGAGGTTCTGCGATA[C/T]GGACTCTCAGACCTT | 51191 |
| rs144631199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491363 | TCTGAAGGTTAAATA[C/T]GTATGGGTGGTAAAC | 51191 |
| rs144720450 | in-del | -/GTTGTT | 0.221007 | 0.28405 | cds-indel | HERC5 | GRCh38.p7 | 4:88505920 | TTTGTTGTTGTTATC[-/GTTGTT]GTTGTTGTTGTTGTT | 51191 |
| rs144746644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488024 | TGCATTTACCATAAT[A/G]AAAATGGGAAATTGA | 51191 |
| rs144855704 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88495769 | AAAAAAAAATCAAAA[C/G]CACAAGATTTAGAAA | 51191 |
| rs144866645 | snp | C/T | 0.000591079 | 0.0171811 | intron-variant | HERC5 | GRCh38.p7 | 4:88487225 | AAATCACATGCTAAG[C/T]GCCTTCTTAATCATG | 51191 |
| rs144879231 | in-del | -/AGAA | 0.0209421 | 0.100162 | intron-variant | HERC5 | GRCh38.p7 | 4:88495642 | CAGAAACTAAAACAC[-/AGAA]AGATTAGGTAACTTG | 51191 |
| rs144890220 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467204 | GAAGAACTCAAACTT[A/G]GTAAATTCTATAGGA | 51191 |
| rs144962395 | snp | C/G | 0.000353372 | 0.0132876 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469252 | TAAACGGTGGCAGAG[C/G]ACAAAAAGGTACACC | 51191 |
| rs145132833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88497812 | TGGTGCTATTCATCA[C/T]GACAATGGAAGAATG | 51191 |
| rs145203134 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | HERC5 | GRCh38.p7 | 4:88505064 | TTTTATTTTTGTGGA[-/T]TAACATGTATGTTAG | 51191 |
| rs145240865 | snp | C/T | 6.68382e-05 | 0.00578054 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469241 | GATGTGGAGACTAAA[C/T]GGTGGCAGAGCACAA | 51191 |
| rs145458874 | in-del | -/TGT | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483212 | CTTATAGGGGTTTGC[-/TGT]TGTTGTTGTTGTTTT | 51191 |
| rs145487863 | snp | A/G | 0.000198318 | 0.00995588 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88486131 | TAAACCAGGTGAAAT[A/G]TCAACTACCTGAAAG | 51191 |
| rs145513876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88477899 | ATGTTTTCTGTAAGA[A/G]TTAAACACCTCAGAC | 51191 |
| rs145572233 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464443 | AGTATAAGACATAGT[C/T]AGTGATGGTTTGAGT | 51191 |
| rs145637132 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HERC5 | GRCh38.p7 | 4:88485502 | GACACATGGTTTCAG[C/T]GCATATAGCCAAGAT | 51191 |
| rs145662907 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466002 | TTTTTATTTTGGAGA[A/C]AGGGTACAGGATGTA | 51191 |
| rs145752002 | in-del | -/TAAT | 0.00199481 | 0.0315187 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456212 | ACACAAATGAATTAC[-/TAAT]TAAACACAATAGTAT | 51191 |
| rs145844917 | snp | C/T | 0.000494519 | 0.0157167 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486162 | TATTTTCCAAGTAGA[C/T]GAACTCTTGCACCGT | 51191 |
| rs145851876 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88479811 | GTTGGCTCACGCCTG[A/T]CATCCTAGCACTTTA | 51191 |
| rs145883437 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459580 | ATAGTAGCATCTTAA[A/G]TAAATAATAAATTCT | 51191 |
| rs145957630 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88498198 | CTGCAGAGAGCCCCC[A/G]CTAAGGCAATGCCTA | 51191 |
| rs145991643 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88482177 | TAGCTGGGTGTGGTG[G/T]CGTATGCCTGTAATC | 51191 |
| rs146002396 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HERC5 | GRCh38.p7 | 4:88476275 | GTTTCCAACTTTTCA[C/T]TATGAAAAATTTCAC | 51191 |
| rs146126637 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HERC5 | GRCh38.p7 | 4:88501680 | AAGTCATAAATGTAC[A/T]GTTTAGTGAATTTCA | 51191 |
| rs146222921 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | HERC5 | GRCh38.p7 | 4:88502598 | GGAGGAGTGGGACTT[A/G]AAAGCTGTTAGTAAG | 51191 |
| rs146318143 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88498460 | AAGATTTAATGTTGC[A/G]TGCCATTTTGAGTTT | 51191 |
| rs146331546 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HERC5 | GRCh38.p7 | 4:88471008 | GGGTCTTGCCCTGTC[A/G]TTGCCCATGCTTTAA | 51191 |
| rs146520117 | in-del | -/ACGA | 0.0126979 | 0.078662 | intron-variant | HERC5 | GRCh38.p7 | 4:88477944 | GAAAGTTGTGCATTC[-/ACGA]ACGATTTTTAATTTA | 51191 |
| rs146522189 | snp | A/T | 0.00597247 | 0.0543191 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506606 | ATAAATGTAAATTAC[A/T]CTTTGATAATGTAAA | 51191 |
| rs146552197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88471287 | ATCATATTGTTTATA[C/T]ATTGTTTTCTACCTA | 51191 |
| rs146622089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466620 | TGGGCAAGGCAGATT[C/T]CTTGCTACACAACAG | 51191 |
| rs146670892 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88497363 | CATGATCAGAATGTT[A/C]GTAGAAACGTAGACA | 51191 |
| rs146793069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458667 | ACACGAATAGATTCT[A/G]TTTCATTAGCACTGA | 51191 |
| rs146794302 | snp | A/G | 0.000131787 | 0.00811641 | missense | HERC5 | GRCh38.p7 | 4:88493099 | GAGATGATCCAGCCG[A/G]AATATGGGATGTTCA | 51191 |
| rs146826580 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465729 | TCACTGGAAAGACTC[A/C]CGAACTTACTAAAAG | 51191 |
| rs146953973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468435 | GAGGTAAAAATAGAT[C/T]TCCAGGTGTTCTATA | 51191 |
| rs147100883 | snp | C/G/T | 0.00117718 | 0.0242339 | intron-variant | HERC5 | GRCh38.p7 | 4:88472539 | GAGAAAGAAAATACA[C/G/T]CAGAATATTTCTTAA | 51191 |
| rs147141570 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469838 | AACTAACCCATCACA[A/G]CTAGCATGTAAGCGC | 51191 |
| rs147217025 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463768 | TTACTTTGACAGTGC[A/T]ATTTATTAGTGATTC | 51191 |
| rs147247901 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HERC5 | GRCh38.p7 | 4:88495606 | GATTCTAGTATTATT[A/G]TCATCCCTCTTTTAC | 51191 |
| rs147324367 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489588 | CAGGTAGATAGTTCA[C/G/T]TGTTGGCCCTAAGAG | 51191 |
| rs147345085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463198 | AATTTGAAAGAAAGG[A/C]ATTGCTATGTTCATT | 51191 |
| rs147348706 | snp | G/T | 1.64738e-05 | 0.00286995 | missense | HERC5 | GRCh38.p7 | 4:88475948 | ATGTCCTATGATGCA[G/T]ATTTCCAACAACTGG | 51191 |
| rs147649544 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456110 | GGGGAAGTTTTCTCC[C/T]GTTCCCTACAACCGA | 51191 |
| rs147724568 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HERC5 | GRCh38.p7 | 4:88478088 | ACTTTTCCAGGATGT[G/T]AAATTATTAGTAGTA | 51191 |
| rs147753522 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88485520 | ATATAGCCAAGATGA[C/G]TTTTTAGAAGACCAC | 51191 |
| rs147757779 | snp | C/T | 0.000214131 | 0.010345 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467147 | GGAAATGGTGGAACA[C/T]GTGACCAGCTGATGC | 51191 |
| rs147829814 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88506015 | TTTCTGTCTCTAGTG[A/G]TAAGCAGGAAAGAGG | 51191 |
| rs148027798 | snp | A/G | 0.000395348 | 0.0140541 | missense | HERC5 | GRCh38.p7 | 4:88493045 | ATTGGGTATGACCTC[A/G]GAGGAGTCAAGAAAG | 51191 |
| rs148035671 | snp | C/T | 3.30006e-05 | 0.00406192 | missense | HERC5 | GRCh38.p7 | 4:88472428 | ACTACAGAAATGATG[C/T]CTGTTTATTTGGACT | 51191 |
| rs148072740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474955 | ACATAACAAAAATTC[A/G]GAATTCCATTCCATT | 51191 |
| rs148209752 | snp | A/G | 0.00305772 | 0.0389809 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462101 | TGCTGCATTTTAAAT[A/G]GAATAAAACAGCATT | 51191 |
| rs148230180 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88480419 | ATATTGACAGATATA[A/T]ATGCTGTTTGCAATT | 51191 |
| rs148399592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503760 | TAAGCAGCATATGAT[A/G]GAGTTGTTATAAAAA | 51191 |
| rs148556308 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HERC5 | GRCh38.p7 | 4:88495892 | TACATGAACTAAAAG[A/G]TCTTTAAATTTGTAT | 51191 |
| rs148569726 | snp | A/G | 5.16418e-05 | 0.00508116 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88487096 | AATGTACAATGCTGC[A/G]TCATATTCAGTCACT | 51191 |
| rs148681180 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88470094 | ATCTTTTAGAAATAT[G/T]TTTAGGTATGGCTTT | 51191 |
| rs148735571 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465100 | TTGTATTTTTAGTAG[A/C]GTCGGGGTTTCACCG | 51191 |
| rs148757029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88483508 | GTAAGCCACCACACC[A/G]GCTCTATAGGCTTTT | 51191 |
| rs148852557 | snp | A/G | 4.94645e-05 | 0.00497291 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486198 | TTTTTTTGTAGAAGT[A/G]TGCAGAAGGTACTTG | 51191 |
| rs148931573 | snp | A/G | | | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467725 | CTTGGAGAGAAAAGG[A/G]TTAGCCACTTAATCA | 51191 |
| rs149084453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498127 | CACCTAGATATCAAA[G/T]GATACTCCACAGAGC | 51191 |
| rs149210921 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88471333 | ACATTTTATTCTATC[C/T]TTTTTGGTAATTTTT | 51191 |
| rs149253362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88473904 | GGTATGTAAATGAAA[C/T]AATCATAGGGCATCC | 51191 |
| rs149381951 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88487906 | GCCTCACACAAAGCA[A/C]CCAAAGGGTTGGGTA | 51191 |
| rs149436515 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | HERC5 | GRCh38.p7 | 4:88495725 | AGAGTCTATTAATCG[G/T]TTATACTAACTGTAC | 51191 |
| rs149523231 | snp | C/T | 0.000115412 | 0.00759556 | missense | HERC5 | GRCh38.p7 | 4:88493132 | TATCCTGAAGGGGCT[C/T]CCTGCATGTGGTTTC | 51191 |
| rs149597564 | in-del | -/AACC/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491943 | TCCTCGGGGAGCAAA[-/AACC/C]CAGCCACTTCAGCAA | 51191 |
| rs149613437 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460637 | TATTTCCCATTTTCT[A/G]TCAGACACTGTCATG | 51191 |
| rs149708039 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464403 | ACCAGAGTTCTTTCA[C/T]TGTAGCCTGCCCTGA | 51191 |
| rs149783393 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88476877 | TTGAGCCAAGATCAC[A/G]CCATTGCACTCCAGC | 51191 |
| rs149837380 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88486012 | TATTCTGGTCATTAT[A/G]AGAGTGTTTCATTTA | 51191 |
| rs149952857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497660 | TATCATTAGAAAAAA[A/G]GCCAAACTTAAAGAT | 51191 |
| rs150044503 | snp | A/G | 0.000179314 | 0.00946705 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88505836 | GGAAACAGTTGAAGA[A/G]GCGCTTCAAGAAGCC | 51191 |
| rs150060489 | in-del | -/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472921 | GGGACTGCCTGGATT[-/C]TTTTTTTTTTTTTTT | 51191 |
| rs150165322 | in-del | -/TT | 0.0256215 | 0.110247 | intron-variant | HERC5 | GRCh38.p7 | 4:88502908 | TTCTAGATGCAAGTC[-/TT]TTGTTGGTTATATGT | 51191 |
| rs150183626 | snp | G/T | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458538 | CTTTTTTTCAACTGA[G/T]TTGAAATGCTGAGAC | 51191 |
| rs150236658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467502 | GACTTACTAATTCTT[A/G]TAATTAGTTGTTTAC | 51191 |
| rs150351580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487631 | TAAATGGCTACTACT[C/T]TGTGATGGTGCCATA | 51191 |
| rs150378907 | snp | A/G | 4.94344e-05 | 0.00497139 | missense | HERC5 | GRCh38.p7 | 4:88493123 | ATGTTCATGTATCCT[A/G]AAGGGGCTTCCTGCA | 51191 |
| rs150387057 | in-del | -/G | 0.203575 | 0.245652 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457609 | GAGGGGCGGGCAGCC[-/G]GGGGGTCCGCGCCTG | 51191 |
| rs150425904 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HERC5 | GRCh38.p7 | 4:88494769 | CATTCCTACACATCC[A/G]TAAGAAATATTCACA | 51191 |
| rs150431696 | snp | A/G | 9.95289e-05 | 0.00705369 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469197 | CAATTCCTACTCTGA[A/G]TGAAGGGACTGTAAA | 51191 |
| rs150546747 | snp | A/G | 0.000395948 | 0.0140648 | missense | HERC5 | GRCh38.p7 | 4:88472500 | GACTGGATTACTAAC[A/G]TGGTATCTTCAGATT | 51191 |
| rs150648465 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | HERC5 | GRCh38.p7 | 4:88476759 | AACCCTGACTCTACT[A/G]AAAATACAAAAATTA | 51191 |
| rs150763091 | snp | C/T | | | synonymous-codon | HERC5 | GRCh38.p7 | 4:88494251 | TGCCAACCTTCCTTT[C/T]CCACTGGCACTGTTT | 51191 |
| rs150804850 | snp | C/G | 0.039522 | 0.134904 | intron-variant | HERC5 | GRCh38.p7 | 4:88470389 | CTGAGTATGTATAAA[C/G]TTTTTTATTTCCCAT | 51191 |
| rs150827761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484268 | TTATAACTCAGGTAT[C/G]TGAAGTCTTTGCAGG | 51191 |
| rs150917306 | snp | A/G | 1.7086e-05 | 0.00292279 | missense | HERC5 | GRCh38.p7 | 4:88504517 | GTTATGAACCAGGAT[A/G]TAACAGTTCACATCC | 51191 |
| rs150937365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486699 | CCTTCTAGCACATCA[A/G]GTCTTGCCCAGCAAA | 51191 |
| rs150997178 | snp | A/G | 0.0012483 | 0.0249518 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504542 | ACATCCCACCATAGT[A/G]ATGTTTTGGAAGGCT | 51191 |
| rs151062847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457796 | GGGGCATGCGGGCAC[C/G]GTCTTCATCCTTTTA | 51191 |
| rs151070041 | snp | A/G/T | 0.000280033 | 0.0118297 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489243 | CGCTTTGAGGCCCAC[A/G/T]TTTGATCTAACAGTC | 51191 |
| rs151303993 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88489788 | CTGAAGCAGGTGGAT[C/T]ACCTGAGGTCAGGAG | 51191 |
| rs151305721 | snp | C/G | 0.00123831 | 0.024852 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468404 | GAATCAAAGCATTTT[C/G]CTCTGGATAAAGAAA | 51191 |
| rs151335709 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88471898 | TTCCTTCCTTCCTTC[A/G]AAAAACCTTTATCTT | 51191 |
| rs180672436 | snp | C/T | 3.29946e-05 | 0.00406155 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486211 | GTATGCAGAAGGTAC[C/T]TGTGGAAAATGACTG | 51191 |
| rs180683251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465587 | TCTTAACCAAAGCAG[G/T]CTTATCACCTCTTTG | 51191 |
| rs180942717 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88470989 | TCTTTTTTTTTTTGA[C/G]ACAGGGTCTTGCCCT | 51191 |
| rs180954007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88490066 | AGAATTTTCTCTTTA[A/C]ATCCTACAGTTATTT | 51191 |
| rs180974960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502526 | GCCACGCAGCCATCA[G/T]TGGGTGCCCAGGGAG | 51191 |
| rs181371686 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88501246 | CATCTGTCCCTCTTT[A/T]TCCACTCGTTCTGCT | 51191 |
| rs181381681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466430 | GGTTAAATCATTGCC[C/T]GGATAGTTAAACTTA | 51191 |
| rs181383098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458754 | AGAGTACATTTTTAC[C/T]AGTGGACAGTTTAAT | 51191 |
| rs181391856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486596 | AGCACTCCTTTTTTA[C/T]TTTCTGAAAATACAG | 51191 |
| rs181397573 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481947 | CTTTTGACAAATAAA[A/C]CTTCATAATGACAGG | 51191 |
| rs181435184 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88493884 | CTCCCAAAGTTCTGG[C/G]ATTACAAGCGTGAGA | 51191 |
| rs181491304 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88471844 | GTTTATCTTTTTTCT[A/C/G]TCTTCCTTCCTTCCT | 51191 |
| rs181582021 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476372 | GGTACAGTCATAGCT[C/T]ACTGTAATCTTAAAC | 51191 |
| rs181585901 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496044 | ACACAGGAATACACA[A/G]ATATCTGTTAGCAGA | 51191 |
| rs181611841 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88476738 | CTAGCCTGGCCAACA[C/T]GACAAAACCCTGACT | 51191 |
| rs181616377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88490647 | TCAGGAGTTCGAAAC[C/T]AACCTGACCAGCATG | 51191 |
| rs181802170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88485758 | GCAGAGTGAATGTCT[A/G]TAAGTGGTATATTAT | 51191 |
| rs181983352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88501619 | TTCTTAATCTTTTTT[C/T]TTAAACTTTGTATTG | 51191 |
| rs181988428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88482267 | GTGAGCCAAGATTGC[A/G]TCACTGCACTCCAGC | 51191 |
| rs182054207 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88478682 | TCTGGCACAATCTCA[A/G]CTCACTGCAGCCTCC | 51191 |
| rs182188138 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88496760 | CAACAGTAAAGAAAA[G/T]ATTTAATACATTTAA | 51191 |
| rs182202408 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468477 | TAAGCAAAACTAAGG[A/G]TTCTAGTATCCCAGT | 51191 |
| rs182230315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492192 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 51191 |
| rs182255605 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HERC5 | GRCh38.p7 | 4:88473613 | ACAACACTTAGTGCT[A/G]CCTGTATCAACAACC | 51191 |
| rs182287599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489639 | TGGCCTAGCCTGGCT[A/G]GCACCACCCTTGAAG | 51191 |
| rs182301231 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465104 | ATTTTTAGTAGAGTC[A/G/T]GGGTTTCACCGTGTT | 51191 |
| rs182308726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460252 | GAATGTCTATATTTC[A/G]CTTGTAACAGGACAG | 51191 |
| rs182557157 | snp | A/G | 0.0134176 | 0.0808008 | intron-variant | HERC5 | GRCh38.p7 | 4:88470604 | AACCAGTGTCTTATT[A/G]CTAATATAGGGAAAT | 51191 |
| rs182627284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483260 | TCTGCCCAGGCTGGA[A/G]TGCAGTGGTGCAGTC | 51191 |
| rs182842130 | snp | A/G | 0.000581048 | 0.0170349 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88487137 | CTTTAATAATCTGTC[A/G]AAAATTAAACTACTA | 51191 |
| rs182938130 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461261 | TATTTCATATTATCT[A/C]CTGTGTTCGGATTAT | 51191 |
| rs183019511 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483736 | GTTTCACCACATTGC[C/T]CAGGCTGGTCTCCCA | 51191 |
| rs183027163 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461432 | ACTGGTCATGCTCAT[C/T]ATTATATTCCTGGTG | 51191 |
| rs183033262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503832 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAAATCA | 51191 |
| rs183058729 | snp | A/G | | | missense | HERC5 | GRCh38.p7 | 4:88479443 | AGTTGGATTACTGGG[A/G]TGAAAGTGCTGAGGA | 51191 |
| rs183067179 | snp | A/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455509 | CCCCCAAGTCCCTTG[A/T]GGGCATGCCCAGACA | 51191 |
| rs183073789 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498311 | CACCCAACACTAATG[G/T]GTGAGAGCCTCTAGG | 51191 |
| rs183125935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497040 | TTTAGATTCAGACAC[C/T]GAATCTGCTGGCACT | 51191 |
| rs183134544 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455175 | ATAGGCAAGCTGGAA[C/T]GACTGGAAATCCATA | 51191 |
| rs183375243 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88479173 | GCCTGTAATTCCAGC[C/T]ACTCAGGAAGGTGAG | 51191 |
| rs183385496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474323 | GCCCAGAGGAATTAA[C/G]ATCTTACCAGGTGCT | 51191 |
| rs183411382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472821 | GATTTGTTGAGATTG[A/G]TACACTAGAATAAGA | 51191 |
| rs183501271 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486820 | TTCAGCAGAACAGAC[C/T]CTTTGGGAAAGCATC | 51191 |
| rs183613494 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HERC5 | GRCh38.p7 | 4:88492660 | CTGAGGCAGGAGAAT[C/T]GCTTAAACCCAGGAG | 51191 |
| rs183721006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470682 | GGAAAAGGTAATATA[A/T]GTAATAAATTAATTG | 51191 |
| rs183727025 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467773 | GTCTGGAGTTGAACC[C/T]GTGCCCTTTATGACC | 51191 |
| rs183732346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489698 | AGAATTAAGGGGTTG[C/T]TTTTGTTCTTATGCA | 51191 |
| rs183749097 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HERC5 | GRCh38.p7 | 4:88499845 | CCTTCAGAATAGCTA[A/T]ACACTTGACATTTAT | 51191 |
| rs183776864 | snp | C/G | 0.000181256 | 0.00951816 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475849 | ACCACAGATAACCAC[C/G]TGCCTCAAAGATAAT | 51191 |
| rs183788531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88493411 | ATGGATTAAAAAGGA[A/G]CCCTCTCTTTTTTAG | 51191 |
| rs183875402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487715 | GAGGTGGTTATGTTT[A/G]TAGATGTATCCAGCA | 51191 |
| rs183998794 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462551 | CTGTAATTGAGACAT[C/G]TTTCAGGGCTGTGTG | 51191 |
| rs184002729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491435 | AGAAAGGACAGAAGT[C/G]TTAGGATAGAACTGT | 51191 |
| rs184099603 | snp | C/G/T | 1.79043e-05 | 0.00299196 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469297 | TCTGCTTATATATCA[C/G/T]TCTCAAGTATCATTT | 51191 |
| rs184169009 | snp | C/T | 0.00319098 | 0.0398384 | intron-variant | HERC5 | GRCh38.p7 | 4:88484008 | TTCTGTCATATTTTC[C/T]GTCTCATTGTCTCTC | 51191 |
| rs184278239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88485225 | CGCTTTGTCCTTTGA[C/T]CGTAATAGATAATAT | 51191 |
| rs184305329 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464761 | AACTGGCTAATTTTT[A/T]AATTTTATTTATTTA | 51191 |
| rs184321843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88480958 | CTTTTGCTTTATGGT[A/G]TTTTTTGACAAACAC | 51191 |
| rs184390353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484604 | TTGCCTTGTGGTCCT[A/G]GGGTCAAGGTGGAGG | 51191 |
| rs184439835 | snp | A/C | | | upstream-variant-2KB, missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456853 | CTAGTGGAACTGCAG[A/C]GTTTCCTCGAAAGCC | 51191 |
| rs184484551 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506249 | ATATCAATTATAATA[C/T]AGATTAAGCTGTGTC | 51191 |
| rs184524397 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464426 | TGCCCTGATCACAGT[A/G]AAGTATAAGACATAG | 51191 |
| rs184610189 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88500232 | GAACTGGGCCGACTT[A/G]GCCAGGCTGGATGGT | 51191 |
| rs184644507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458396 | TTGTAGTAATTTTAA[G/T]GTTTTTTTTTTTAAG | 51191 |
| rs184786312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481472 | TCTTTTGCTTTTATG[C/G]TGTTTTTTGACAAAC | 51191 |
| rs184790048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474397 | AGCACAGTGTGTCAG[A/G]CAATAGGACTGGCTC | 51191 |
| rs184803012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88492906 | CAGTGCCTTCCAAAT[A/G]CTTGGGTCCACAATT | 51191 |
| rs185175255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88488052 | TGATTTATGAGTTCT[A/G]AGTATGACTGTAATG | 51191 |
| rs185218959 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HERC5 | GRCh38.p7 | 4:88496927 | ATGAGTAGAATTCAT[C/T]CCCCTATGAAAGAGG | 51191 |
| rs185322477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470041 | AACCATAGAACTCCT[A/G]TAGGTTTACAGAACT | 51191 |
| rs185446308 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465330 | TTTTGGGCAGTTTTT[C/G]CCTCACTAAACGTAG | 51191 |
| rs185495139 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465620 | TTCTTCATTACATAC[A/C]GTCCTTTTGAGTAGC | 51191 |
| rs185559425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88471148 | TAATTTTTGTATTTT[C/T]TTGTAGAGCCAGAGT | 51191 |
| rs185568996 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461326 | CCCAGGGTCTAGAGG[C/T]GTGTATGTACAAGGG | 51191 |
| rs185576528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88490311 | TCCCTCATTTTACAG[A/T]TGGGGAAACTGAGGT | 51191 |
| rs185863885 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482574 | GGCCTGTGCCAGAAG[C/T]AGGCTTGGAACCATT | 51191 |
| rs185879680 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88482083 | CTCGGAGGCTGAGGC[A/G]GGCAGATCACAAGGT | 51191 |
| rs186000202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467004 | TACTGTATTGCTAAA[C/T]ACTCTCATCATTGTG | 51191 |
| rs186016836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486647 | AGGTAGCAGTTGACC[C/T]GAAGTGTTTCTCCCT | 51191 |
| rs186027145 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460466 | CTACATCTGATCCAG[A/G]CCTGGGGCCACCCTT | 51191 |
| rs186040613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88501254 | CCTCTTTATCCACTC[A/G]TTCTGCTTTTTCTTT | 51191 |
| rs186093194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88496461 | GTGCAGGTTTTCCGA[C/T]AGAACAGACGATAGA | 51191 |
| rs186127569 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88477143 | GGTGAAACTTCATCT[C/G]TACTAAAAATATAAT | 51191 |
| rs186131210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486296 | GCATTTCTTGTCCTC[C/T]GCAAAATTGCACAAT | 51191 |
| rs186198431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503569 | GATTTTTGAATTGTT[C/T]TACCTTCCTGGTATA | 51191 |
| rs186246325 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HERC5 | GRCh38.p7 | 4:88478940 | TTAATTTGCTTCACT[A/G]TAGTAACAATTTTAC | 51191 |
| rs186331239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483321 | TCAAGTGATTCTCCT[A/G]CCTCAGCCTCCTGAG | 51191 |
| rs186355601 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491852 | AAGGCAGGAATGGAG[G/T]GGTGACTGAAGGAGC | 51191 |
| rs186584724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88473253 | TCTACTCTCCATTTT[C/T]TTCTCTCTGGGTCGC | 51191 |
| rs186695472 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88476443 | TAATAGTAATTGTAT[G/T]TATTCACTGAAAAGT | 51191 |
| rs186772695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88487289 | CAGTGAAACCAATGG[C/T]TGTGGCATTCAAGGA | 51191 |
| rs186833882 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HERC5 | GRCh38.p7 | 4:88492573 | ACACAGTGAAACCCC[A/G]TCTCTACTTAAAATA | 51191 |
| rs186837633 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88484642 | ATTGATATGGCAGTG[G/T]AGGAAAGAGCTTATT | 51191 |
| rs186876509 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494048 | TTATCTCAGGCTTTA[A/C]ATTTTTCAATTTGAG | 51191 |
| rs186968233 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490649 | AGGAGTTCGAAACCA[A/G]CCTGACCAGCATGGT | 51191 |
| rs187070044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487961 | ACATATGTTATATGT[A/G]TGTATAATATTCAAA | 51191 |
| rs187093277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469325 | TTTCCCAAACTGGTT[C/G]TGCACAGCAATATGA | 51191 |
| rs187157808 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88477491 | AGGGGGAGGGGAAGG[A/G]GAAGGTGAAGGGAAG | 51191 |
| rs187168983 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HERC5 | GRCh38.p7 | 4:88472017 | CTTTCTTTTTCTGAG[A/G]CAGGATCTTGCTCTG | 51191 |
| rs187652489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461569 | ATTTTTTTAGACTCT[A/G]TTAGATATTGTCAGC | 51191 |
| rs187656297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503870 | AGGAGTTTGAGAGCA[A/G]CCTGGCCAACATGGT | 51191 |
| rs187664765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483897 | TTTAGAAATTGTTCC[A/G]CATTTTAAATCTAAA | 51191 |
| rs187682826 | snp | C/T | 5.14302e-05 | 0.00507074 | intron-variant | HERC5 | GRCh38.p7 | 4:88479521 | GGGTAAGAGTTCCTT[C/T]AGAAACCTCTGTGTT | 51191 |
| rs187703822 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455591 | AGATTCTCCAGGGAC[C/T]CTCCCTTATCTGCCT | 51191 |
| rs187820331 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88473858 | TTCTGTTTACTAATT[A/G]TACCTTGATTGTGCC | 51191 |
| rs187958868 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506401 | ATATGGTAGGAGTGG[C/T]ATTGTTCTCAGTCTT | 51191 |
| rs188060473 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HERC5 | GRCh38.p7 | 4:88479190 | CTCAGGAAGGTGAGG[C/T]AGGAGAATTGCTTGA | 51191 |
| rs188361868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497101 | GTGAGCAATAAATTT[C/G]TATTTATAGATTACC | 51191 |
| rs188373100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464427 | GCCCTGATCACAGTA[A/G]AGTATAAGACATAGT | 51191 |
| rs188388742 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HERC5 | GRCh38.p7 | 4:88470890 | ACTTAAGAGTAATAG[C/T]TAGCACTTACGTATA | 51191 |
| rs188405297 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88489925 | GAAACATGAGAATCA[C/T]TTGAACCCAGGAAGC | 51191 |
| rs188524317 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HERC5 | GRCh38.p7 | 4:88492832 | AATTCTCAAGGCCTC[A/G]TTATCTCATAGAATT | 51191 |
| rs188571149 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455193 | CTGGAAATCCATAAG[A/G]AAAAAAAAGAACCTT | 51191 |
| rs188618128 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458427 | TTAAAATTTTTCGTA[C/T]GCTTGGAATTTTCAG | 51191 |
| rs188793028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88474324 | CCCAGAGGAATTAAG[A/G]TCTTACCAGGTGCTC | 51191 |
| rs188870871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484436 | TTCTTCTGCCAGGCT[C/G]CTAGAGATACCACCA | 51191 |
| rs188898131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487014 | GGCTATGAGGTAAAG[C/T]GTAAGGTTTCTCTGT | 51191 |
| rs189046137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485516 | GTGCATATAGCCAAG[A/C]TGAGTTTTTAGAAGA | 51191 |
| rs189076814 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464794 | ATTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGCT | 51191 |
| rs189115986 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88504655 | TTTAATGGGATAAAA[A/T]TTTCCTTTATGATAA | 51191 |
| rs189134365 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462747 | CACTTAAAGTCTGTT[A/T]GTGTATTATTACAAA | 51191 |
| rs189275056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88501571 | GAGATCTCTAGGAAG[C/T]GTGCTGGCCTACATC | 51191 |
| rs189287130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482122 | CAAGACCAGCCTGAC[C/T]AACATAGTGAAACCT | 51191 |
| rs189303265 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459624 | AAGTCCTTATGTCCC[C/T]CAGGGCAGGTATCAT | 51191 |
| rs189314155 | snp | A/G | 1.65272e-05 | 0.0028746 | missense | HERC5 | GRCh38.p7 | 4:88499952 | CACTTCTGGATGATG[A/G]AGGTGATAACTTTGA | 51191 |
| rs189318390 | snp | A/G | 0.0283406 | 0.115616 | upstream-variant-2KB, missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457049 | CAAACATTATGTTTC[A/G]TTTTCCACTGGAGCT | 51191 |
| rs189520175 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88474475 | GAGGTTGTGTCTGAT[A/C/G]ATGAGCAAGGAGGTA | 51191 |
| rs189534383 | snp | C/T | 0.000609359 | 0.0174444 | missense | HERC5 | GRCh38.p7 | 4:88493097 | CAGAGATGATCCAGC[C/T]GGAATATGGGATGTT | 51191 |
| rs189571454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88476340 | GCAATAAATGGTACA[C/T]CTTGCTGGAGTGCAG | 51191 |
| rs189574042 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HERC5 | GRCh38.p7 | 4:88491961 | GCCACTTCAGCAAAC[A/G]CCTTATGTGTGCTCT | 51191 |
| rs189600233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481060 | TTTTCTCCCATAAAG[A/G]GTTTTGATTCGAGAC | 51191 |
| rs189606926 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88473420 | CCTCCTTTCAGCTCC[C/G]GCACTTGCTCTGTTT | 51191 |
| rs189647647 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88481490 | TTTTTTGACAAACTC[A/T]CATTCTTAATTTTAA | 51191 |
| rs189833360 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88493700 | CAACCTCCGCCTCCC[A/G]AGCTCAAGCCATTCT | 51191 |
| rs189875661 | snp | C/T | 1.65026e-05 | 0.00287246 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88494294 | GACCAAATGCCATCA[C/T]TGGAAGACTTGAAAG | 51191 |
| rs189876666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88500508 | CTCACATGGCCATGC[C/T]GAGATTCAGTGGCTG | 51191 |
| rs190204943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466142 | CCCAGGCTGGACTGC[A/G]GTGGTGCTATCATGG | 51191 |
| rs190219377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486362 | CTCAAAATCTATGCA[A/G]TTTTGCAGTCAGAGT | 51191 |
| rs190247439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88483635 | CTGGGTTCAAGCTAT[C/T]GTCGTGCCTCAGCTT | 51191 |
| rs190255650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461347 | TGTACAAGGGTAAAG[G/T]GATATTCAGAGTTTA | 51191 |
| rs190259916 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HERC5 | GRCh38.p7 | 4:88503693 | TGCATAGTGTATCTT[C/T]TTCCCTTCTTTGACT | 51191 |
| rs190286098 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490427 | CTGCTTAATGAAGAC[A/G]GATAAAGATTGGCCT | 51191 |
| rs190358175 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | HERC5 | GRCh38.p7 | 4:88476709 | GCAGATCACCTGAGG[A/T]CAGGAGTTCAAGACT | 51191 |
| rs190371261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88470533 | GATGTGGTATTTATC[A/G]TGTCTCATGCTGTAA | 51191 |
| rs190417497 | snp | A/G | 1.64906e-05 | 0.00287142 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88486203 | TTGTAGAAGTATGCA[A/G]AAGGTACTTGTGGAA | 51191 |
| rs190534597 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88486788 | ACTGAGCTTATTCAC[A/G]TGGTAGAAACTCAGG | 51191 |
| rs190612396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488872 | CTTTGGTATCTTAAG[C/T]ATTAATAATTGTGTG | 51191 |
| rs190681806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88501983 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCAC | 51191 |
| rs190700135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465574 | CTCATTCGGTATCTC[C/T]TAACCAAAGCAGTCT | 51191 |
| rs190894768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460944 | GCAGTGAGCCATGAT[C/T]GTGCCACTGCACTAC | 51191 |
| rs190917508 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88483214 | TATAGGGGTTTGCTG[C/T]TGTTGTTGTTGTTTT | 51191 |
| rs190929618 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HERC5 | GRCh38.p7 | 4:88478438 | GTTACTAGTGGATGG[A/G]GGTGGAAAGGAAATG | 51191 |
| rs190974331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503926 | AAAAAAATTAGCTGG[A/G]CATGGTGGCAGGCAC | 51191 |
| rs190980523 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88483922 | TCTAAATGAATATTG[A/G]CTCTCTTTTTTGAAA | 51191 |
| rs191116465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479028 | AGGTGGCTCATGCCT[A/G]CAATCCCAGCACTTT | 51191 |
| rs191254671 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88475364 | GAGTCTTGCTCTGTG[C/T]CTGGAGTGCAGTGAC | 51191 |
| rs191267157 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88493213 | AAGTACACCATATAC[C/G]ATAGAAAATTAGTTT | 51191 |
| rs191350945 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HERC5 | GRCh38.p7 | 4:88496928 | TGAGTAGAATTCATT[C/T]CCCTATGAAAGAGGC | 51191 |
| rs191446690 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88471171 | GCCAGAGTTTTACCA[C/T]GTTGGCCAGGCTGGT | 51191 |
| rs191459961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467574 | ACAGTCATATAAAAC[A/C]CTCAGAATAATGAGC | 51191 |
| rs191589010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88487622 | GGAGCCCAATAAATG[A/G]CTACTACTCTGTGAT | 51191 |
| rs191598049 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489636 | GTCTGGCCTAGCCTG[C/G]CTAGCACCACCCTTG | 51191 |
| rs191624175 | snp | A/T | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469259 | TGGCAGAGCACAAAA[A/T]GGTACACCCCACAGT | 51191 |
| rs191842272 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506610 | ATGTAAATTACACTT[C/T]GATAATGTAAAATAC | 51191 |
| rs191871034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484703 | AACCCTTTTCGGTCT[C/T]AGACTTGTGGGGATA | 51191 |
| rs191875837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464649 | GCTGGAGTGCAGTGA[C/T]GCAATCTCAGCTCAC | 51191 |
| rs191942514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472641 | AAGTTAAACTCAGAT[A/G]ACATTTAGGAGTTTG | 51191 |
| rs191975349 | snp | C/T | 0.000170294 | 0.00922594 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88487113 | CATATTCAGTCACTT[C/T]CCATTTATCTTTAAT | 51191 |
| rs192008543 | snp | A/G | 0.0101981 | 0.0706808 | intron-variant | HERC5 | GRCh38.p7 | 4:88479317 | AGCACAATAAAACTC[A/G]TTTTTTAAAAAATTT | 51191 |
| rs192043619 | snp | A/G/T | 0.00159649 | 0.0282165 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455295 | ACCAGGAACAATTAG[A/G/T]CATGTGAATACATTG | 51191 |
| rs192166251 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88505568 | AAATGTAGGACACTG[C/T]ACATGGGCTCCAGTG | 51191 |
| rs192183257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462958 | GCTTTACCCAGCTGT[A/G]GTACTGTATGCATTA | 51191 |
| rs192253336 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88490930 | AACTCTAATGGACTC[A/C/G]TTATGTGATTCTATG | 51191 |
| rs192317482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468027 | TAAATCTTGAAAACA[C/T]GGTTTTTAGTAATGG | 51191 |
| rs192466000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461873 | TTGAATTTGATTTAT[A/G]ATCAAATTTATTATG | 51191 |
| rs192593558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484460 | ACCACCAGTTTGGTA[A/G]TACTTTACATTTTTG | 51191 |
| rs192642143 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | HERC5 | GRCh38.p7 | 4:88481151 | TCTGCCTCCCAGGCT[C/T]CTGTGATCCTCCCAC | 51191 |
| rs192692669 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456330 | AAGCACATCACTGTT[C/G]CCAGGCACCCGGGAA | 51191 |
| rs192695609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499368 | CATCATAGGATGATA[C/G]GATGGAAATAATTTA | 51191 |
| rs192709767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479835 | CACTTTAGGAGGCCA[A/G]GGCGGGCGGATCACG | 51191 |
| rs192758164 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88500089 | ACTTAAAAAAAAAAC[C/G]TGAATAAATTAGTGA | 51191 |
| rs192792262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492617 | CAGGCGTGGTGGTGC[A/G]TATCTGTAATCCCAG | 51191 |
| rs192836213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469445 | TCCATCTATGTATCT[A/G]TGGAGGGGAGAGAGA | 51191 |
| rs192838603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497118 | ATTTATAGATTACCC[A/C]GTCTAAGGTATTTTG | 51191 |
| rs192874229 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457597 | GGCTGAGGGCTGTGA[C/G]GGGCGGGCAGCCGGG | 51191 |
| rs193004819 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88474076 | GCTGGGCACTGTAAT[C/G]ATGACTCGATGAAGA | 51191 |
| rs193025512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487970 | ATATGTATGTATAAT[A/G]TTCAAATATATGTCC | 51191 |
| rs193056400 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | HERC5 | GRCh38.p7 | 4:88474334 | TTAAGATCTTACCAG[G/T]TGCTCACGTGGAAGG | 51191 |
| rs193234882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492845 | TCGTTATCTCATAGA[A/G]TTAATGTAGAGATTA | 51191 |
| rs199516439 | snp | C/G | 3.49987e-05 | 0.00418308 | missense | HERC5 | GRCh38.p7 | 4:88505822 | AAATATTCTACAATG[C/G]AAACAGTTGAAGAAG | 51191 |
| rs199682964 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | HERC5 | GRCh38.p7 | 4:88480784 | GAGCATATTTTCATG[-/T]TTGTAATTGCAATAT | 51191 |
| rs199762669 | snp | C/T | | | missense | HERC5 | GRCh38.p7 | 4:88504387 | TGATTGTTGGAAATA[C/T]AGATTATGATTGGAA | 51191 |
| rs199767115 | snp | C/G/T | 3.295e-05 | 0.00405881 | missense | HERC5 | GRCh38.p7 | 4:88475973 | AACTGGGAGAGCCTT[C/G/T]TGGTTCCATTTGCAA | 51191 |
| rs199777857 | snp | A/G | 0.000993843 | 0.0222696 | intron-variant | HERC5 | GRCh38.p7 | 4:88486103 | TTTTTCACAAGTCAT[A/G]TTTTATTTAAGGTAA | 51191 |
| rs199946875 | snp | A/G | 1.66407e-05 | 0.00288446 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468428 | AAAGAAAGAGGTAAA[A/G]ATAGATCTCCAGGTG | 51191 |
| rs199950240 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490250 | TAAGTGCCTTATACC[C/T]AATTTTTTAACCCTT | 51191 |
| rs200010865 | snp | C/G | | | utr-variant-5-prime, missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457141 | GAGGCTGCGGTTCCC[C/G]GACGCCACGCAGCTG | 51191 |
| rs200055854 | snp | C/T | 3.43359e-05 | 0.00414328 | intron-variant | HERC5 | GRCh38.p7 | 4:88479340 | AAAAATTTGCTTTCC[C/T]TGTGTTCCTCAGAAG | 51191 |
| rs200086017 | snp | A/G | 0.000116439 | 0.00762927 | missense | HERC5 | GRCh38.p7 | 4:88489176 | CCTAGAGTAAAAAAC[A/G]TAAAGCTTATCTTAG | 51191 |
| rs200164798 | in-del | -/G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480445 | GTGTTTTTTTTTTTT[-/G/T]GTCTTGTTGGGAGTT | 51191 |
| rs200181971 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488414 | TTTTTGTATTTTTAG[C/T]AGAGACAGGGTTTCA | 51191 |
| rs200245264 | snp | C/T | 0.00108739 | 0.0232919 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88486175 | GACGAACTCTTGCAC[C/T]GTCTCAATTTTTTTG | 51191 |
| rs200318350 | snp | C/G | 8.25566e-05 | 0.00642429 | missense | HERC5 | GRCh38.p7 | 4:88504368 | CCCGAAGAACTGAAG[C/G]ATGTGATTGTTGGAA | 51191 |
| rs200417801 | snp | A/T | 6.63357e-05 | 0.00575877 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460069 | TCATTATGGTGATTA[A/T]CACAAAGTGTATTTT | 51191 |
| rs200437348 | snp | G/T | 0.000534488 | 0.0163389 | intron-variant | HERC5 | GRCh38.p7 | 4:88486071 | CTATTAAGCAAAATT[G/T]TCTTTAAATATAAAA | 51191 |
| rs200442831 | snp | A/G | 1.64806e-05 | 0.00287054 | missense | HERC5 | GRCh38.p7 | 4:88494232 | CCCTGTTCAATTGCA[A/G]TGTTGCCAACCTTCC | 51191 |
| rs200448008 | snp | G/T | 0.000132194 | 0.00812894 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468332 | AAACTCTTACTCTTT[G/T]TGCATCCTTTCAGAA | 51191 |
| rs200500673 | snp | G/T | 1.66382e-05 | 0.00288424 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463661 | TTGGCTGTATTTTTA[G/T]AAGAACAGTTTGTAT | 51191 |
| rs200512267 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480457 | GTGTTTTTTTTTTTT[A/C]TCTTGTTGGGAGTTC | 51191 |
| rs200538566 | snp | A/G | | | missense | HERC5 | GRCh38.p7 | 4:88475935 | TCCTTCTCCCAGAAT[A/G]TCCTNTGATGCATAT | 51191 |
| rs200541371 | snp | A/G | 0.000177773 | 0.00942627 | intron-variant | HERC5 | GRCh38.p7 | 4:88487061 | ATTATTGTCATTTCC[A/G]TTTTTAGGACGCTTC | 51191 |
| rs200562632 | snp | A/G | 3.29734e-05 | 0.00406025 | missense | HERC5 | GRCh38.p7 | 4:88500933 | CACTGGGACAGAAAC[A/G]ACACAAACTTAATTC | 51191 |
| rs200710850 | snp | A/G | 3.39311e-05 | 0.00411879 | missense | HERC5 | GRCh38.p7 | 4:88505768 | AATGAAAGAGACCCT[A/G]TAAGAGCACTGACAT | 51191 |
| rs200721883 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467202 | GTGAAGAACTCAAAC[C/T]TGGTAAATTCTATAG | 51191 |
| rs200742258 | snp | A/G | 0.000181829 | 0.00953317 | intron-variant | HERC5 | GRCh38.p7 | 4:88472405 | ATTTATCTTTCTTCT[A/G]CAGAAGAACTACAGA | 51191 |
| rs200792950 | snp | A/G | 6.59185e-05 | 0.00574064 | missense | HERC5 | GRCh38.p7 | 4:88494226 | GACTTTCCCTGTTCA[A/G]TTGCAATGTTGCCAA | 51191 |
| rs200933186 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491942 | CCTCCTCGGGGAGCA[A/C]ACAGCCACTTCAGCA | 51191 |
| rs201018284 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463635 | ACAGGTGGGTGTACC[C/T]TTGTCTCTTTTTGGC | 51191 |
| rs201021472 | snp | A/G | 0.00199792 | 0.0315431 | missense | HERC5 | GRCh38.p7 | 4:88489311 | TAAGTCAATTTGAGA[A/G]TGAAGACCTGAGGAA | 51191 |
| rs201120262 | snp | A/T | 3.3083e-05 | 0.00406699 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463539 | TTACATAGGTAAAGA[A/T]GATCCATCCCTTATT | 51191 |
| rs201145366 | snp | G/T | 4.99538e-05 | 0.00499744 | intron-variant | HERC5 | GRCh38.p7 | 4:88472376 | TCTAGGGAGATAATC[G/T]AACAAAATACTTAAT | 51191 |
| rs201159551 | snp | A/C | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457851 | TCTGTTCAAGTTTGT[A/C]CCCCCGTCCCCCGCC | 51191 |
| rs201276494 | snp | A/T | 3.29495e-05 | 0.00405877 | missense | HERC5 | GRCh38.p7 | 4:88475961 | CATATTTCCAACAAC[A/T]GGGAGAGCCTTGTGG | 51191 |
| rs201315674 | snp | A/G | 0.000399281 | 0.0141238 | missense | HERC5 | GRCh38.p7 | 4:88505856 | TTCAAGAAGCCATCA[A/G]CAACAACAGAGGATT | 51191 |
| rs201347076 | snp | C/T | 0.000195896 | 0.00989493 | intron-variant | HERC5 | GRCh38.p7 | 4:88487034 | GGTTTCTCTGTCCTT[C/T]AACTTATCAGAATTA | 51191 |
| rs201521313 | snp | A/G | 3.29641e-05 | 0.00405968 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467198 | TCAAGTGAAGAACTC[A/G]AACTTGGTAAATTCT | 51191 |
| rs201540163 | snp | C/T | 0.000115621 | 0.00760245 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504325 | ATTTTATAAAATGTG[C/T]GACGAAGACATTATC | 51191 |
| rs201548154 | snp | G/T | 1.64917e-05 | 0.00287151 | missense | HERC5 | GRCh38.p7 | 4:88494189 | GAGAAGAAAAGATAC[G/T]TCTTTTTTGGGGTTC | 51191 |
| rs201630041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467050 | ACCATATGTGCTTTT[A/G]TTTAATAGGTGGCAC | 51191 |
| rs201793802 | in-del | -/A | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500078 | TACTTAAAAAAAAAA[-/A]CCTGAATAAATTAGT | 51191 |
| rs201816981 | in-del | -/TTGT | 0.02016 | 0.0983543 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464562 | GGTTTTTTGGTTTTC[-/TTGT]TTGTTTGTTTGTTTG | 51191 |
| rs201866694 | in-del | -/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467447 | ATAAAATAGACAATG[-/G]ATTCAGAGGCATATG | 51191 |
| rs201933395 | snp | C/T | 6.62683e-05 | 0.00575585 | intron-variant | HERC5 | GRCh38.p7 | 4:88504630 | GAATAGATCTGTAAT[C/T]GTATGTCTTTTTAAT | 51191 |
| rs201937855 | snp | A/T | 0.00182661 | 0.0301657 | intron-variant | HERC5 | GRCh38.p7 | 4:88479323 | ATAAAACTCATTTTT[A/T]AAAAAATTTGCTTTC | 51191 |
| rs201957323 | snp | A/T | 1.65282e-05 | 0.00287469 | missense | HERC5 | GRCh38.p7 | 4:88499953 | ACTTCTGGATGATGA[A/T]GGTGATAACTTTGAG | 51191 |
| rs201981495 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455833 | CTTAAAATGAAGAGG[G/T]AAGCCACAGACAGGT | 51191 |
| rs202063985 | in-del | -/A | 0.0383715 | 0.133092 | intron-variant | HERC5 | GRCh38.p7 | 4:88495754 | ACTAATAAGACAAGG[-/A]AAAAAAAATCAAAAG | 51191 |
| rs202082513 | snp | C/T | 0.00113785 | 0.023825 | intron-variant | HERC5 | GRCh38.p7 | 4:88500017 | AATAAAAGCAGATAA[C/T]AGATTAGTTTTAATC | 51191 |
| rs202161571 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492005 | TCCTGATTTTTATTA[G/T]TTATTTATTTATTTT | 51191 |
| rs367560354 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502654 | TTCATCAGTAGGGTA[C/T]GACAGTTCTAATTGC | 51191 |
| rs367561890 | snp | C/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469266 | GCACAAAAAGGTACA[C/G]CCCACAGTCTGACTC | 51191 |
| rs367586335 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | HERC5 | GRCh38.p7 | 4:88486507 | TCTGATACCCTTAAA[-/G]TGGTCATAACAAGGC | 51191 |
| rs367588822 | snp | A/G | 1.82091e-05 | 0.00301732 | missense | HERC5 | GRCh38.p7 | 4:88505708 | AGACTACAAATGAAA[A/G]ATTTAAATAATATGA | 51191 |
| rs367799604 | snp | A/G | 8.24382e-05 | 0.00641968 | missense | HERC5 | GRCh38.p7 | 4:88479418 | ATGTTTAAAACAGCC[A/G]TCATATGCCAGTTGG | 51191 |
| rs367942785 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475199 | GAAAAAAGAAACCCA[A/C]GGTGTGATAGTGTAA | 51191 |
| rs367960917 | snp | G/T | 0.000153988 | 0.00877328 | missense | HERC5 | GRCh38.p7 | 4:88504514 | CACGTTATGAACCAG[G/T]ATATAACAGTTCACA | 51191 |
| rs368008464 | snp | A/T | 1.65436e-05 | 0.00287602 | missense | HERC5 | GRCh38.p7 | 4:88499929 | TTTTTTCCTTAGGAA[A/T]TTGCAAACACTTCTG | 51191 |
| rs368075332 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503804 | AGGTGCGGTGGCTAA[C/T]GTCTGTAATCCCAGC | 51191 |
| rs368102756 | in-del | -/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480086 | AAAAAAAAAAAAAAA[-/G]AAATAACCTGTGTGC | 51191 |
| rs368105433 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503101 | AGGGCTATGAATATA[C/T]TCCCCTGTATTTTCT | 51191 |
| rs368119527 | in-del | -/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462606 | GGGATGAGAACCTGG[-/G]ATTCTGATTCCCACT | 51191 |
| rs368127860 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485587 | GTCAAATACTAACAG[A/T]CACTAATGTCTGAAG | 51191 |
| rs368193564 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HERC5 | GRCh38.p7 | 4:88490924 | TTGTATAACTCTAAT[A/G]GACTCGTTATGTGAT | 51191 |
| rs368237480 | snp | G/T | 1.98426e-05 | 0.00314975 | intron-variant | HERC5 | GRCh38.p7 | 4:88504608 | CCTTGGTAAGTATTA[G/T]ATCAAGGAATAGATC | 51191 |
| rs368336450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461742 | GAATTTTACAGTTGT[C/T]TATTTGGGATCATTA | 51191 |
| rs368351629 | snp | A/G | 5.17612e-05 | 0.00508703 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469272 | AAAGGTACACCCCAC[A/G]GTCTGACTCTCTGCT | 51191 |
| rs368438363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470557 | GCTGTAAAGAAAGAG[G/T]CTGTATGTATGTATA | 51191 |
| rs368466221 | snp | G/T | 1.70886e-05 | 0.00292301 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468456 | GTGTTCTATAACCTG[G/T]TATTTTAAGCAAAAC | 51191 |
| rs368506162 | snp | C/T | 0.000248973 | 0.0111546 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457481 | TGGAACGCGGCGGGG[C/T]GGGCGTCCAGGTTCA | 51191 |
| rs368595358 | snp | A/G | 5.6234e-05 | 0.00530225 | intron-variant | HERC5 | GRCh38.p7 | 4:88470694 | ATATGTAATAAATTA[A/G]TTGTATTAAATTGTA | 51191 |
| rs368597927 | snp | A/G/T | 0.000133368 | 0.00816502 | intron-variant | HERC5 | GRCh38.p7 | 4:88493190 | CTTAAGGTATTTTGC[A/G/T]ACAGAAAAAGTACAC | 51191 |
| rs368642534 | snp | A/T | 3.2963e-05 | 0.00405961 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88494254 | CAACCTTCCTTTCCC[A/T]CTGGCACTGTTTAAG | 51191 |
| rs368712793 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462142 | ATGTCAAGGTGGTGA[A/G]CTTTTTGCCTGGGGA | 51191 |
| rs368735393 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88493245 | TCTAGACTATTTCAT[G/T]TTAGAAGAGGAGTAT | 51191 |
| rs368739655 | snp | A/G/T | 0.000150572 | 0.00867554 | intron-variant | HERC5 | GRCh38.p7 | 4:88504418 | AACATTTGAAAAGGT[A/G/T]CATCATCAAGTCTAA | 51191 |
| rs368791165 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88501880 | CTTGGCTCACTGCAA[C/T]CTCCGCCTCCCGGGT | 51191 |
| rs368840895 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88471930 | TTTCTATGGCCCGCC[C/T]TTCTTCCCTCCCTTC | 51191 |
| rs368911479 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489990 | TTCCGGCCTGGGTGA[C/T]GGAGCGAGACTCTGT | 51191 |
| rs369004430 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88486759 | GTTATATCATTCTCC[A/G]TTTATCAAATGCAAC | 51191 |
| rs369216089 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88477675 | GTAGACTGTCCCACA[C/T]CCAGATAGTCTGACC | 51191 |
| rs369260903 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462368 | GAGAGTATGGAACAC[A/G]TTCTCAGATTCCTAT | 51191 |
| rs369280809 | snp | A/G | 3.29717e-05 | 0.00406015 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88486163 | ATTTTCCAAGTAGAC[A/G]AACTCTTGCACCGTC | 51191 |
| rs369379391 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HERC5 | GRCh38.p7 | 4:88487324 | ATACTCTAATGAAGA[C/T]GGCAAGGCAGACTGT | 51191 |
| rs369435919 | snp | C/T | 1.65141e-05 | 0.00287346 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462249 | CAGGAGTACCCTTGG[C/T]TCAGATTTCTGCCGG | 51191 |
| rs369455543 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463376 | CCTTCACCCTGAGGC[A/G]TAGAACTTGATCCTA | 51191 |
| rs369641292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88493950 | TTAGGTTGGTGCAAA[A/G]GTAATTGCAGGTTTT | 51191 |
| rs369683436 | snp | A/G | 3.36253e-05 | 0.00410019 | intron-variant | HERC5 | GRCh38.p7 | 4:88500029 | TAACAGATTAGTTTT[A/G]ATCTGATTAACCCTT | 51191 |
| rs369707936 | snp | C/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458252 | CTCACTTTGCCTTTT[C/G]TGCATGTTGTTTTTA | 51191 |
| rs369739729 | snp | C/T | 0.000118732 | 0.00770402 | intron-variant | HERC5 | GRCh38.p7 | 4:88470720 | TTGTATTAAGAGTAC[C/T]GTGAAAGAGGATAAA | 51191 |
| rs369844675 | snp | C/T | 0.000103546 | 0.00719462 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459314 | GGGTAATAATCAAAG[C/T]GACAATAGTTCCTGG | 51191 |
| rs369873265 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88470798 | ATTTTTTTTAACAAA[A/T]GTAAATATATGTTTG | 51191 |
| rs369910290 | snp | C/T | 0.000153988 | 0.00877328 | missense | HERC5 | GRCh38.p7 | 4:88499975 | AACTTTGAGGAAGTA[C/T]TTTACATCCATTTTA | 51191 |
| rs369926460 | snp | C/T | 1.81069e-05 | 0.00300884 | missense | HERC5 | GRCh38.p7 | 4:88505841 | CAGTTGAAGAAGCGC[C/T]TCAAGAAGCCATCAA | 51191 |
| rs369944873 | snp | A/G | 3.30633e-05 | 0.00406578 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463628 | TACTCACACAGGTGG[A/G]TGTACCCTTGTCTCT | 51191 |
| rs369956338 | snp | C/T | 5.55468e-05 | 0.00526976 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88487071 | TTTCCATTTTTAGGA[C/T]GCTTCAGAAAATGTA | 51191 |
| rs370002822 | snp | A/C/G | 6.59243e-05 | 0.00574094 | missense | HERC5 | GRCh38.p7 | 4:88493025 | AGGTTTCATTTAGTG[A/C/G]AGAAATTGGGTATGA | 51191 |
| rs370049359 | in-del | -/TTTA | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500739 | TTGAAAAAATTTATT[-/TTTA]TTCAGTATGATAGGG | 51191 |
| rs370053122 | snp | G/T | 0.000153988 | 0.00877327 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460077 | GTGATTAACACAAAG[G/T]GTATTTTCCTTCATC | 51191 |
| rs370062005 | snp | A/C | 4.94262e-05 | 0.00497098 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467176 | GCCGCTTCCAGTGAA[A/C]GTATCATCAAGTGAA | 51191 |
| rs370072533 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457815 | TTCATCCTTTTAGCC[A/G]GTCTGGCTTTCTCAT | 51191 |
| rs370084052 | snp | A/G | 0.0232847 | 0.105357 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88506154 | AAAAATAAAATAACC[A/G]AAAAATTAACATAAA | 51191 |
| rs370207981 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474923 | TTTTAAACAAATGAT[C/T]ACTGTGATCTAAGCA | 51191 |
| rs370220097 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483507 | GGTAAGCCACCACAC[A/C]GGCTCTATAGGCTTT | 51191 |
| rs370299747 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488357 | CTGACTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 51191 |
| rs370455399 | snp | A/G | 2.13113e-05 | 0.00326423 | intron-variant | HERC5 | GRCh38.p7 | 4:88487215 | TCATTAGCATAAATC[A/G]CATGCTAAGCGCCTT | 51191 |
| rs370538693 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472262 | GAAAAAATCATGTTT[A/G]CTACATTGCATTTGG | 51191 |
| rs370560085 | snp | C/T | 1.64928e-05 | 0.00287161 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88500968 | TGGAAGTAGCATAAC[C/T]GTCAACCAGACTAAC | 51191 |
| rs370621839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88489600 | TCAGTGTTGGCCCTA[A/G]GAGGTCCAGTCCCTT | 51191 |
| rs370627596 | snp | C/G/T | 0.000646349 | 0.0179657 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460189 | AATTTTTCTGTAATA[C/G/T]TAATAGTTTTGTAGA | 51191 |
| rs370727932 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498463 | ATTTAATGTTGCATG[A/C]CATTTTGAGTTTTGG | 51191 |
| rs370784063 | snp | A/C/G | 6.62065e-05 | 0.00575316 | intron-variant | HERC5 | GRCh38.p7 | 4:88472533 | TATGTGGAGAAAGAA[A/C/G]ATACACCAGAATATT | 51191 |
| rs370796308 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487908 | CTCACACAAAGCACC[C/T]AAAGGGTTGGGTATT | 51191 |
| rs370804659 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473653 | CTCAGTGGACTATTT[C/G]ATCAACATTTGTTAG | 51191 |
| rs370850519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476648 | GAATCTGGCCGGGCA[C/T]GGTGGCTCATGCCTG | 51191 |
| rs370884693 | snp | A/C | 0.000148644 | 0.00861973 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459398 | CCGTGGACCAAGGAG[A/C]AGAGCACATGCTGAT | 51191 |
| rs370900197 | snp | C/T | 6.66856e-05 | 0.00577394 | intron-variant | HERC5 | GRCh38.p7 | 4:88476055 | ATCATTTGAAGATAC[C/T]TTACCTGTCTTCTCA | 51191 |
| rs370912159 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472534 | ATGTGGAGAAAGAAA[A/G]TACACCAGAATATTT | 51191 |
| rs370965985 | snp | C/T | 1.69815e-05 | 0.00291384 | intron-variant | HERC5 | GRCh38.p7 | 4:88504456 | AAATTCAGTTTTCCT[C/T]CCTATTTCCTCAATA | 51191 |
| rs370986699 | snp | A/G | 3.35132e-05 | 0.00409334 | missense | HERC5 | GRCh38.p7 | 4:88504240 | ATTAAAGGAGAGACT[A/G]TGTTTCTAAGTATAT | 51191 |
| rs371148333 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | HERC5 | GRCh38.p7 | 4:88493203 | GCGACAGAAAAAGTA[C/T]ACCATATACCATAGA | 51191 |
| rs371215005 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | HERC5 | GRCh38.p7 | 4:88470268 | ATTTCTACTTCAGTG[G/T]AATAGAAATAAATAG | 51191 |
| rs371218901 | snp | A/G | 1.65789e-05 | 0.0028791 | synonymous-codon, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469201 | TCCTACTCTGAATGA[A/G]GGGACTGTAAAGAGA | 51191 |
| rs371326243 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458723 | CCTAGTTTAATTTTT[C/G]TGAACAAATTAAATA | 51191 |
| rs371365692 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88479430 | GCCGTCATATGCCAG[C/T]TGGATTACTGGGATG | 51191 |
| rs371380843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88481250 | TAGAGATGGGGTTTC[A/G]CCATGTAGCCCAGGC | 51191 |
| rs371466879 | snp | A/G | 1.77824e-05 | 0.00298176 | missense | HERC5 | GRCh38.p7 | 4:88505720 | AAAGATTTAAATAAT[A/G]TGAAAATAACATTTT | 51191 |
| rs371474448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463480 | CAGGTAACTCCACTG[G/T]GAAACTCAGCATTTC | 51191 |
| rs371481479 | snp | A/C | 0.000512299 | 0.0159965 | missense | HERC5 | GRCh38.p7 | 4:88499939 | AGGAATTTGCAAACA[A/C]TTCTGGATGATGAAG | 51191 |
| rs371616410 | snp | C/T | 1.72621e-05 | 0.00293781 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469271 | AAAAGGTACACCCCA[C/T]AGTCTGACTCTCTGC | 51191 |
| rs371634541 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492431 | TTTAGGCTCTGGGGT[G/T]TGACTGATAAAGGAT | 51191 |
| rs371685246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502792 | TGTTAAGCACTTTAT[A/G]TGCTTATTGGCTGTT | 51191 |
| rs371685384 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469656 | CAACTGGATGAGGCT[C/T]ACTCACATTATGGAA | 51191 |
| rs371716039 | in-del | -/CGGGAATA | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456339 | CTGTTGCCAGGCACC[-/CGGGAATA]CGGGAATACGGGAAT | 51191 |
| rs371733825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88493325 | TTTAAAATGGAGTTT[C/T]CTTTTCCTGGGTTCC | 51191 |
| rs371787396 | snp | A/G | 1.76204e-05 | 0.00296814 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462382 | CATTCTCAGATTCCT[A/G]TTACCAACAGATATA | 51191 |
| rs371788516 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462201 | GAAGGAAATTTCCCT[C/T]AACCACCACACCACA | 51191 |
| rs371795309 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486135 | CCAGGTGAAATGTCA[A/G]CTACCTGAAAGTATT | 51191 |
| rs371895637 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478434 | AGTGGTTACTAGTGG[A/G]TGGGGGTGGAAAGGA | 51191 |
| rs371946866 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88491096 | ATCTTTCTGATAATC[C/T]TGTGGGAAAACTGAG | 51191 |
| rs371947036 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456335 | CATCACTGTTGCCAG[A/G]CACCCGGGAATACGG | 51191 |
| rs371988480 | snp | C/T | 0.000564521 | 0.0167911 | intron-variant | HERC5 | GRCh38.p7 | 4:88472386 | TAATCTAACAAAATA[C/T]TTAATTTATCTTTCT | 51191 |
| rs372049085 | snp | A/T | 1.71422e-05 | 0.0029276 | intron-variant | HERC5 | GRCh38.p7 | 4:88494359 | AGTTCCTGAGAAAGG[A/T]CCCTTTCTAACATAT | 51191 |
| rs372129026 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | HERC5 | GRCh38.p7 | 4:88486812 | ACTCAGGTTTCAGCA[-/G]AACAGACTCTTTGGG | 51191 |
| rs372212599 | snp | A/T | 0.000153988 | 0.00877328 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504527 | AGGATATAACAGTTC[A/T]CATCCCACCATAGTG | 51191 |
| rs372309434 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88470635 | CCAAGAGATATTTTC[A/C]TCTCCTGCTTGTCTA | 51191 |
| rs372314449 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470523 | ATAGTTATAAGATGT[A/G]GTATTTATCATGTCT | 51191 |
| rs372362742 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486637 | CCTGCTGCCAAGGTA[A/G]CAGTTGACCCGAAGT | 51191 |
| rs372368706 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485858 | TTTCTTCCTATTGAA[A/C]GTTCTTTAAAAATTT | 51191 |
| rs372485001 | snp | A/T | 1.93613e-05 | 0.00311131 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469133 | GTCTAAATTATTGTA[A/T]TTTACTTTCCTGTTT | 51191 |
| rs372506989 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | HERC5 | GRCh38.p7 | 4:88501024 | TGGTTTGTATATGTA[C/G]TATTTTTATTTTACT | 51191 |
| rs372568620 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465200 | GATTACAGGGGTGAG[C/T]CACCACGCCACTATT | 51191 |
| rs372579236 | snp | C/T | 0.000153988 | 0.00877328 | missense | HERC5 | GRCh38.p7 | 4:88472464 | AAAGCAAGAAACATC[C/T]TCAAGGAGTTAACCC | 51191 |
| rs372581209 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471959 | TCTTTCCTCCCTCCC[G/T]CCCTCCCTCCTTCCC | 51191 |
| rs372623086 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462042 | AGGTACAATATTGTG[A/G]TATTATACTAGGTAG | 51191 |
| rs372632571 | snp | A/G | 0.000115436 | 0.00759637 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464004 | AGTTGTAAAGTATCA[A/G]TAAGAATTGATAAAA | 51191 |
| rs372691147 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455529 | ATGCCCAGACAAGAC[A/C]CTGGGCAGGCTTCCT | 51191 |
| rs372711685 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499846 | CTTCAGAATAGCTAT[A/G]CACTTGACATTTATT | 51191 |
| rs372766151 | snp | G/T | 4.96364e-05 | 0.00498154 | intron-variant | HERC5 | GRCh38.p7 | 4:88500889 | ATTATGTTGGAGATA[G/T]TATCTGAGTTCATTT | 51191 |
| rs372886038 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501811 | TAGAATTTTTTTTTT[-/T]CTTTTGAGATGGCAC | 51191 |
| rs372887262 | snp | G/T | 1.87124e-05 | 0.00305873 | intron-variant | HERC5 | GRCh38.p7 | 4:88470701 | ATAAATTAATTGTAT[G/T]AAATTGTATTAAGAG | 51191 |
| rs373036897 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88498326 | TGTGAGAGCCTCTAG[C/G]GGTGGGCTTTGCCCA | 51191 |
| rs373086607 | snp | A/G | 0.00011906 | 0.00771466 | intron-variant | HERC5 | GRCh38.p7 | 4:88487226 | AATCACATGCTAAGC[A/G]CCTTCTTAATCATGC | 51191 |
| rs373088619 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464167 | ATGGTTGTTTTCTTT[G/T]ATTTTTTTTTTTTTT | 51191 |
| rs373148226 | snp | C/T | 1.65605e-05 | 0.0028775 | intron-variant | HERC5 | GRCh38.p7 | 4:88500868 | ATTGATGATAGATTG[C/T]TCAGAATTATGTTGG | 51191 |
| rs373212378 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479992 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 51191 |
| rs373293044 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506188 | CTTATTCACTATTCA[A/G]TGTGTTTACCAGCTC | 51191 |
| rs373361082 | snp | A/C | 0.000712132 | 0.0188563 | intron-variant | HERC5 | GRCh38.p7 | 4:88487042 | TGTCCTTTAACTTAT[A/C]AGAATTATTGTCATT | 51191 |
| rs373480551 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479604 | AGACTCGTGTGAGAC[A/G]TACGAAGTTTATATT | 51191 |
| rs373594488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487465 | GCCTGTAGTCTTCTG[A/T]ATAGTACTCAAAGAG | 51191 |
| rs373617373 | snp | C/G | 1.66073e-05 | 0.00288156 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463650 | CTTGTCTCTTTTTGG[C/G]TGTATTTTTAGAAGA | 51191 |
| rs373686116 | snp | C/T | 3.36219e-05 | 0.00409998 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88479360 | TTCCTCAGAAGAGTA[C/T]TGGGCAACTCTGCAA | 51191 |
| rs373753270 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498836 | TCGGCCTCCCAAATT[G/T]CTGGGATTACAGGCG | 51191 |
| rs373759496 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488760 | CAGCCTGTTTGCTTT[C/T]TAAACATCTGAACTT | 51191 |
| rs373819357 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457888 | ATCTCCCACTGTCTC[A/G]TTTTGAGAAAGTAGT | 51191 |
| rs373878600 | snp | A/G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497144 | TTTTGTTATGGCAGC[A/G/T]TAAATGGACTAAGGG | 51191 |
| rs373899002 | snp | A/C | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466516 | TCCCAGGATCCTGCC[A/C]TGAATAATAAAGACT | 51191 |
| rs374009669 | snp | A/G | 0.000153988 | 0.00877328 | splice-donor-variant | HERC5 | GRCh38.p7 | 4:88499993 | TACATCCATTTTAAT[A/G]TGAGTAACAATAAAA | 51191 |
| rs374092530 | snp | A/T | 0.000312935 | 0.0125048 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463905 | TGGGCAACTTGGTCA[A/T]AATTCAACACAGAAT | 51191 |
| rs374096805 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471783 | TCCCACTTTTCAGTC[C/G]ATTTAACGGGAAGAA | 51191 |
| rs374125215 | snp | A/G | 3.83752e-05 | 0.0043802 | intron-variant | HERC5 | GRCh38.p7 | 4:88487188 | AATAGAGGTATGTAT[A/G]CCTATTTGTCTTCAT | 51191 |
| rs374132307 | in-del | -/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464169 | GGTTGTTTTCTTTGA[-/T]TTTTTTTTTTTTTTT | 51191 |
| rs374198150 | snp | C/G | 0.000798403 | 0.0199641 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463969 | GGGTATAGAGTGACT[C/G]AGATAGCATGTGGAA | 51191 |
| rs374210638 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467207 | GAACTCAAACTTGGT[A/T]AATTCTATAGGAACA | 51191 |
| rs374267519 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455608 | TCCCTTATCTGCCTC[C/T]AGCATCTATCGATAC | 51191 |
| rs374278831 | snp | A/G/T | 0.000133652 | 0.00817379 | synonymous-codon, missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460095 | ATTTTCCTTCATCAG[A/G/T]TTTGAAAGCATTTTA | 51191 |
| rs374301235 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488135 | GCTTCAACTCTTATA[A/T]CCTATTCTCTCCTGA | 51191 |
| rs374301967 | snp | A/G | 0.000221588 | 0.0105235 | intron-variant | HERC5 | GRCh38.p7 | 4:88504469 | CTTCCTATTTCCTCA[A/G]TAACTTTTTTTTGTA | 51191 |
| rs374330750 | in-del | -/TCTGCCAG | 0.00557542 | 0.0525036 | intron-variant | HERC5 | GRCh38.p7 | 4:88484425 | CGCAGAGAATTTTCT[-/TCTGCCAG]GCTCCTAGAGATACC | 51191 |
| rs374367912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88501346 | AATGATAGTGAATGC[A/G]GCAGGGACTTGGTAT | 51191 |
| rs374378187 | snp | A/G | 1.6495e-05 | 0.0028718 | intron-variant | HERC5 | GRCh38.p7 | 4:88470585 | ATACCATGTGATTTG[A/G]TTTAACCAGTGTCTT | 51191 |
| rs374382804 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485870 | GAAAGTTCTTTAAAA[A/G]TTTCCTATGAATTAA | 51191 |
| rs374414663 | in-del | -/GAAAA | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88482327 | AAAAAAAAAAAAAGG[-/GAAAA]GAAAAGAAAAGAGAA | 51191 |
| rs374464415 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456651 | TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACC | 51191 |
| rs374467671 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492001 | AATATCCTGATTTTT[A/G]TTATTTATTTATTTA | 51191 |
| rs374593770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485296 | AGGCCACCAGGAACC[A/G]TGAAGATGAAGTACC | 51191 |
| rs374596221 | snp | A/G | 6.60066e-05 | 0.00574447 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489195 | AGCTTATCTTAGGTC[A/G]GCAGCAATTGAGGAA | 51191 |
| rs374791377 | snp | C/T | 8.35206e-05 | 0.00646168 | intron-variant | HERC5 | GRCh38.p7 | 4:88501018 | AATAGTTGGTTTGTA[C/T]ATGTACTATTTTTAT | 51191 |
| rs374801710 | snp | A/G | 2.31994e-05 | 0.00340576 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460044 | AGTTCTAAAATCCAT[A/G]TTGTAACTTTCATTA | 51191 |
| rs374842725 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | HERC5 | GRCh38.p7 | 4:88472396 | AAATACTTAATTTAT[C/G]TTTCTTCTACAGAAG | 51191 |
| rs374895568 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | HERC5 | GRCh38.p7 | 4:88486240 | TGTGGTAGGTATAGC[A/G]TGTTTAAAGGGGGAA | 51191 |
| rs374952246 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475063 | AGACAGTTGCTCTTA[C/T]GGAAGATAATGAGAA | 51191 |
| rs375001054 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460909 | GCAGGAGGATCCCTT[A/G]AGCCCAGGAGTTTGA | 51191 |
| rs375026279 | in-del | -/CTC | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484723 | TTGTGGGGATAACTT[-/CTC]CTATGGACTCCCTAA | 51191 |
| rs375087072 | snp | A/T | 4.94849e-05 | 0.00497393 | synonymous-codon, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468380 | GGAGTTAATAATGAT[A/T]GCTGGAGGGAATCAA | 51191 |
| rs375091350 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485068 | CAAAAGGGAAAGGTT[A/G]ATGAAAAATAATTTG | 51191 |
| rs375122262 | snp | A/G | 1.79464e-05 | 0.00299548 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469296 | CTCTGCTTATATATC[A/G]CTCTCAAGTATCATT | 51191 |
| rs375133286 | snp | A/G | 0.000153988 | 0.00877328 | missense | HERC5 | GRCh38.p7 | 4:88470642 | ATATTTTCATCTCCT[A/G]CTTGTCTAACTGGAA | 51191 |
| rs375334253 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476661 | CACGGTGGCTCATGC[C/T]TGTAATCTCAGCACT | 51191 |
| rs375422646 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486714 | AGTCTTGCCCAGCAA[A/C]ATTCATGTATGAGCT | 51191 |
| rs375430185 | snp | A/G | 4.9588e-05 | 0.00497911 | missense | HERC5 | GRCh38.p7 | 4:88504303 | TTTATGAAGAATTTC[A/G]GAGAGGATTTTATAA | 51191 |
| rs375670181 | snp | G/T | 0.000153988 | 0.00877328 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462246 | TCGCAGGAGTACCCT[G/T]GGCTCAGATTTCTGC | 51191 |
| rs375673452 | snp | A/G | 0.000101092 | 0.00710884 | intron-variant | HERC5 | GRCh38.p7 | 4:88476079 | CTTCTCAGTGGAAAG[A/G]CATGTCTAGTAAAGT | 51191 |
| rs375752991 | snp | G/T | 5.10712e-05 | 0.00505302 | intron-variant | HERC5 | GRCh38.p7 | 4:88504227 | AACATTTTGTTTTAT[G/T]AAAGGAGAGACTATG | 51191 |
| rs375807965 | snp | C/T | 1.65113e-05 | 0.00287322 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463619 | ACAGTGCCCTACTCA[C/T]ACAGGTGGGTGTACC | 51191 |
| rs375852237 | snp | C/T | 0.000181652 | 0.00952852 | intron-variant | HERC5 | GRCh38.p7 | 4:88500906 | ATCTGAGTTCATTTG[C/T]GGTTACAGGTGCACT | 51191 |
| rs375932425 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460303 | TATGGTTCCGAGTAC[A/G]ATTCTTAAAGTAAAT | 51191 |
| rs376012411 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463943 | GACCCTGTTTGGTGG[C/G]TGAGCTTGTTGGGTA | 51191 |
| rs376039327 | snp | G/T | 1.73736e-05 | 0.00294729 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88487090 | TCAGAAAATGTACAA[G/T]GCTGCGTCATATTCA | 51191 |
| rs376253040 | in-del | -/A | 0.493107 | 0.0583 | intron-variant | HERC5 | GRCh38.p7 | 4:88479285 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51191 |
| rs376271813 | in-del | -/C | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457766 | GGATCCTCCGCTCAG[-/C]AAAGTGGCCGGTGCG | 51191 |
| rs376284875 | snp | A/T | 1.82121e-05 | 0.00301757 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462397 | ATTACCAACAGATAT[A/T]CTTGTTAGATGAATT | 51191 |
| rs376373013 | snp | A/G | 1.82274e-05 | 0.00301883 | intron-variant | HERC5 | GRCh38.p7 | 4:88479308 | AAAAAAAAAAGCACA[A/G]TAAAACTCATTTTTT | 51191 |
| rs376433962 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455553 | GCTTCCTCAGCTGCA[A/C]AAAAGCTTGTGAGGC | 51191 |
| rs376445249 | in-del | -/T | 0.0271762 | 0.113356 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456468 | CCGGCGCACAACGCA[-/T]TTTTTTTTTTTGATA | 51191 |
| rs376489828 | snp | A/T | 1.71843e-05 | 0.00293119 | missense | HERC5 | GRCh38.p7 | 4:88504553 | TAGTGATGTTTTGGA[A/T]GGCTTTCCACAAATT | 51191 |
| rs376568622 | snp | A/G/T | 0.000214171 | 0.0103464 | missense | HERC5 | GRCh38.p7 | 4:88489229 | AGAGAGTCTGAATTC[A/G/T]CTTTGAGGCCCACGT | 51191 |
| rs376578004 | snp | A/G | 1.98513e-05 | 0.00315044 | intron-variant | HERC5 | GRCh38.p7 | 4:88470721 | TGTATTAAGAGTACC[A/G]TGAAAGAGGATAAAA | 51191 |
| rs376609358 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495532 | ACCACTGCACTCCAG[A/C]CTGGGCGACAGTAGA | 51191 |
| rs376617022 | snp | A/G | 5.43345e-05 | 0.00521194 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88505839 | AACAGTTGAAGAAGC[A/G]CTTCAAGAAGCCATC | 51191 |
| rs376687144 | snp | C/T | 9.91998e-05 | 0.00704202 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88499962 | TGATGAAGGTGATAA[C/T]TTTGAGGAAGTATTT | 51191 |
| rs376848674 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463837 | TCTAGCATCTGATAT[A/G]ACATTCCCTTTCCTT | 51191 |
| rs376853356 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | HERC5 | GRCh38.p7 | 4:88494830 | GCAATAGAAATGCTT[C/T]CTAAATAAAAATGTC | 51191 |
| rs376853452 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462904 | TTCTCATGATCCCAA[A/G]CAACTCATTAAGAGT | 51191 |
| rs376865548 | snp | A/G | 1.65974e-05 | 0.0028807 | synonymous-codon, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469195 | GACAATTCCTACTCT[A/G]AATGAAGGGACTGTA | 51191 |
| rs377060874 | snp | A/G | 1.89863e-05 | 0.00308104 | intron-variant | HERC5 | GRCh38.p7 | 4:88470709 | ATTGTATTAAATTGT[A/G]TTAAGAGTACCGTGA | 51191 |
| rs377081826 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465317 | TATACACTTATTCTT[G/T]TGGGCAGTTTTTCCC | 51191 |
| rs377086844 | snp | A/G | 3.29881e-05 | 0.00406115 | missense | HERC5 | GRCh38.p7 | 4:88472467 | GCAAGAAACATCTTC[A/G]AGGAGTTAACCCAAA | 51191 |
| rs377114085 | snp | A/G | 3.89492e-05 | 0.00441283 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460188 | TAATTTTTCTGTAAT[A/G]TTAATAGTTTTGTAG | 51191 |
| rs377146328 | snp | C/T | 0.000131907 | 0.00812009 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489300 | TTTGAATCAGCTAAG[C/T]CAATTTGAGAATGAA | 51191 |
| rs377292897 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475117 | ATTTTCGGATTTTGT[C/T]TTTTTTTTTTTTTTT | 51191 |
| rs377409594 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473421 | CTCCTTTCAGCTCCC[A/G]CACTTGCTCTGTTTG | 51191 |
| rs377415064 | snp | A/C | 6.37058e-05 | 0.00564348 | intron-variant | HERC5 | GRCh38.p7 | 4:88487214 | TTCATTAGCATAAAT[A/C]ACATGCTAAGCGCCT | 51191 |
| rs377473460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88482119 | GTTCAAGACCAGCCT[A/G]ACCAACATAGTGAAA | 51191 |
| rs377491497 | in-del | -/TCT | 0.0109695 | 0.0732422 | intron-variant | HERC5 | GRCh38.p7 | 4:88493166 | TCAAGGTAAGTTCCC[-/TCT]TCTTTGCTTAAGGTA | 51191 |
| rs377553054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88483639 | GTTCAAGCTATCGTC[A/G]TGCCTCAGCTTCCTG | 51191 |
| rs377595074 | snp | G/T | 1.64984e-05 | 0.00287209 | missense | HERC5 | GRCh38.p7 | 4:88472485 | GAGTTAACCCAAAAG[G/T]ACTGGATTACTAACA | 51191 |
| rs377680094 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487735 | TGTATCCAGCAAAGT[A/G]GATGGATATTTTACC | 51191 |
| rs377712274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88480694 | ATGTCTGACTTTAAC[A/G]TTTTGAAAATATTTT | 51191 |
| rs377737513 | snp | A/T | 0.000103197 | 0.00718248 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459323 | TCAAAGTGACAATAG[A/T]TCCTGGTTGGATTTG | 51191 |
| rs377738502 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488356 | CCTGACTCAGCCTCC[A/C]GAGTAGCTGGGATTA | 51191 |
| rs377741809 | snp | C/T | 3.32094e-05 | 0.00407475 | intron-variant | HERC5 | GRCh38.p7 | 4:88476042 | CTGGGTAAGTTTGAT[C/T]ATTTGAAGATACTTT | 51191 |
| rs377751795 | snp | G/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468460 | TCTATAACCTGGTAT[G/T]TTAAGCAAAACTAAG | 51191 |
| rs377758029 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480743 | AATTATGGTTTTAAT[-/T]GTATTTCCCTGGTTC | 51191 |
| rs397994435 | in-del | -/G | 0 | 0 | upstream-variant-2KB, frameshift-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456908 | CGCTGCCCGCCCGGG[-/G]ACACTTTCTCAGTCC | 51191 |
| rs527282427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88505251 | CCTTGAACCTCACCT[A/G]CCTCCTTGTTGCCTT | 51191 |
| rs527311401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465022 | TGATCCACCTGCCTC[G/T]GCCTCCCAAAGTGCT | 51191 |
| rs527391815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464390 | ATACTTTTTAATTAC[C/T]AGAGTTCTTTCATTG | 51191 |
| rs527395255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471533 | TTTGTAAAGACAGCA[C/G]CTTTGCTATGTTGCC | 51191 |
| rs527441463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497787 | AGGTTAGTGTGGATG[G/T]GTGGAAGCCTGGTGC | 51191 |
| rs527516376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88496960 | CAAGGGAGCCTGTTC[A/G]CCCCTTCCACCATGA | 51191 |
| rs527608868 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505954 | TTGTTGTTTCTCTAC[C/T]TTGTTTTGTTTTAGG | 51191 |
| rs527624144 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498601 | TTTGAGACAGAGTCT[C/T]ACTCTGTGGCCCAGG | 51191 |
| rs527660259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88473210 | CCTATTTTATTTTAC[C/T]GGTTGATATGGGGAT | 51191 |
| rs527696893 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490966 | CCAGTCAGTCTACTC[A/G]ATTATTTGAGTTCCA | 51191 |
| rs527773859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88481122 | CAGTGGCGCAGTCTC[A/G]GCTCACTGCAACCTC | 51191 |
| rs527971957 | snp | A/C | 0.00025468 | 0.0112816 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457529 | GCGGCGGCGCCCGGA[A/C]GCCGAGTGAGTGGGG | 51191 |
| rs528052610 | in-del | -/TGAATATACCATACT | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88480373 | GTATAGTTCATTGTA[-/TGAATATACCATACT]TAGCTTATCCATTCC | 51191 |
| rs528066028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465686 | GTCTTAATGCACATC[A/G]GGGCAATACCCCTAC | 51191 |
| rs528108820 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88504758 | AAAAAACAAATGTTA[A/G]TATCTATAAGCAATC | 51191 |
| rs528116144 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492907 | AGTGCCTTCCAAATA[C/T]TTGGGTCCACAATTA | 51191 |
| rs528170756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484491 | GCTTGAAGCTTTTTA[A/G]AATTTGGTGGCAAAG | 51191 |
| rs528212544 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88492429 | ACTTTAGGCTCTGGG[G/T]TTTGACTGATAAAGG | 51191 |
| rs528213411 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484077 | TCCAGTTCATGAATT[C/T]TCTTTTCAGATATTT | 51191 |
| rs528305264 | snp | A/T | 1.64912e-05 | 0.00287147 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462287 | CACAGCATGGCCTTA[A/T]CCATGTCTGGCAACA | 51191 |
| rs528378097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461294 | AGATGAAACACACAA[G/T]CCCTGCCTTTAAGAA | 51191 |
| rs528390122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469482 | ATTTTAAGGAATTGG[C/T]TTATGAGATTGTAGG | 51191 |
| rs528437415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88494522 | GTGTTGATTATTCCC[A/G]TAACTAGACTTCAAT | 51191 |
| rs528508527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88504072 | ACTCCGTCTCAAAAA[A/G]AAAAAAAAATTACAT | 51191 |
| rs528509788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88493788 | CTGGGTAGTTTTTGT[A/G]TTTTTTGTAGAGATG | 51191 |
| rs528575628 | in-del | -/G | 0 | 0 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456407 | TAGGGGTGGGGGGGA[-/G]GGGTAGCTGCCTGCA | 51191 |
| rs528614402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503243 | TGATTATACTGAACC[C/T]ATAGATCAATTTTTT | 51191 |
| rs528645760 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484437 | TCTTCTGCCAGGCTC[C/G]TAGAGATACCACCAG | 51191 |
| rs528702409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88480902 | TATTTTGGACACTAC[G/T]CTTTTGTCAATGATA | 51191 |
| rs528745788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88478853 | CTGAGCTCAGACAAT[C/T]CACCTGCCTCAGCCT | 51191 |
| rs528863674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470347 | TCTGACCATAAATCA[A/G]GCCTTTCCTCTTTAT | 51191 |
| rs528949293 | in-del | -/TAGTGTGTCTGT | 0.0154538 | 0.0865337 | intron-variant | HERC5 | GRCh38.p7 | 4:88472713 | TACAGATATTCTAAA[-/TAGTGTGTCTGT]ACACAAACACACATA | 51191 |
| rs528978938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88477514 | AAGGGAAGGGAACGG[A/C]AAGGAAGGGGGAGGG | 51191 |
| rs529025542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485561 | TTTATTTCAGGATAA[C/T]GCCCATCCAAGTCAA | 51191 |
| rs529055995 | snp | A/G | 1.65644e-05 | 0.00287783 | missense | HERC5 | GRCh38.p7 | 4:88504270 | TCAATTACATTTTCA[A/G]CGACTCTGTAAAGGC | 51191 |
| rs529210575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88470800 | TTTTTTTAACAAAAG[C/T]AAATATATGTTTGCT | 51191 |
| rs529368454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486542 | AGACTCATCAGGAGC[C/T]AAGAGCCAAGACCCT | 51191 |
| rs529450863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88494621 | TGCAAAATCTGCTAG[C/T]GATATTTATGTTAAA | 51191 |
| rs529526806 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485064 | TTTACAAAAGGGAAA[C/G]GTTAATGAAAAATAA | 51191 |
| rs529576200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479894 | AACATGGTGAAACCC[C/T]GTCTCTATTAAAAAT | 51191 |
| rs529589686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481710 | TATTCAGTTGTTCAG[G/T]AGTAGCATGAAAGCA | 51191 |
| rs529604537 | snp | A/G | 3.49162e-05 | 0.00417814 | intron-variant | HERC5 | GRCh38.p7 | 4:88479540 | AACCTCTGTGTTTTT[A/G]TCTAGCTGTAAAAAT | 51191 |
| rs529736558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499756 | TAAATTTGACATGTT[C/T]AGTTGAGGTCTGGCC | 51191 |
| rs529810414 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472761 | TATGCATACACATTC[A/G]TAGAGGGAAGTTTTT | 51191 |
| rs529814466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468064 | AATTAAACTGATAAC[A/G]TTTAGCTAATCAAAT | 51191 |
| rs529848982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498822 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAATTGC | 51191 |
| rs529919788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88475328 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTG | 51191 |
| rs529933327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483686 | GGCACATGCCACCCC[A/G]CTTGGCTAATTTTTG | 51191 |
| rs529969651 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476128 | TTAGAAATGTATTCA[-/T]TTTTTTTTTAGTTCG | 51191 |
| rs530071659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461001 | TCTCAAAAAAAAAGA[A/C]ACTTACTGTGAATGG | 51191 |
| rs530203878 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472788 | TTTTCAACTCAGGGC[G/T]TTAGGAAGATGATTA | 51191 |
| rs530205616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460242 | GGAGCCAGTAGAATG[C/T]CTATATTTCACTTGT | 51191 |
| rs530356937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502160 | ATTATGAATAATGCT[A/C]TTGTGAACATTCTTG | 51191 |
| rs530361749 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464747 | GCGTGCACTGCCACA[A/G]CTGGCTAATTTTTAA | 51191 |
| rs530495396 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88483875 | AGGTTAAGGATATTT[C/T]CCTCCTTTTAGAAAT | 51191 |
| rs530601685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491508 | GAGATAAATAAAACC[A/G]TGAAGAGTGCTTCAT | 51191 |
| rs530646214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460384 | ACTATTCCTAAATTT[G/T]GTTTCATGTTTTTAT | 51191 |
| rs530664221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88490953 | ATTCTATGCTTTGCC[A/G]GTCAGTCTACTCGAT | 51191 |
| rs530704268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468853 | TTCTGCACACAGCTC[C/T]TTCAGGATCTTCCCT | 51191 |
| rs530766648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492653 | CTGGGGGCTGAGGCA[A/G]GAGAATCGCTTAAAC | 51191 |
| rs530772033 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88502876 | TTGCTTTTTTTTTTC[C/T]TGTCAGTTTATGAGA | 51191 |
| rs530821896 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479972 | CTCGGGAGGCTGAGG[C/T]AGGAGAATGGCGTGA | 51191 |
| rs530831889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484429 | GAGAATTTTCTTCTG[C/T]CAGGCTCCTAGAGAT | 51191 |
| rs530839547 | snp | A/G | 0.000214265 | 0.0103483 | missense | HERC5 | GRCh38.p7 | 4:88476005 | GGTTGTTTGTAAAAT[A/G]AGTGACCAGTCTTCA | 51191 |
| rs530865754 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462053 | TGTGATATTATACTA[G/T]GTAGAGCATGCATAA | 51191 |
| rs530925543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461164 | GAGTATTTGACCTTC[A/G]TTGCAAGGCCTGTTG | 51191 |
| rs530976395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486295 | GGCATTTCTTGTCCT[C/T]TGCAAAATTGCACAA | 51191 |
| rs531083222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88477129 | AGCCTGGCCAACATG[A/G]TGAAACTTCATCTCT | 51191 |
| rs531101334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88477706 | GTTTCCTATCCCTGT[A/G]TTTCCAGTACACCGC | 51191 |
| rs531228480 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505989 | TAGCAGCCTGAAGCC[A/G]TGGTTTTTCATTTCT | 51191 |
| rs531303660 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456194 | GACTACCATTCAACA[A/G]TAACACAAATGAATT | 51191 |
| rs531371074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481195 | GTAGCTTGGACTACA[C/T]GTGCAAGCCACCAAA | 51191 |
| rs531374542 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457125 | CAGGGGCTCAGTAGC[G/T]GAGGCTGCGGTTCCC | 51191 |
| rs531484290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489083 | ACTTATAAGCAGAAC[A/C]AGTTTATTCTGCTTT | 51191 |
| rs531550251 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465562 | CAATATTTATACCTC[A/G]TTCGGTATCTCTTAA | 51191 |
| rs531613025 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489806 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGTC | 51191 |
| rs531715809 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | HERC5 | GRCh38.p7 | 4:88473343 | CTCACCCCATTTTTT[A/C]ATCTCTCTCTGTGTT | 51191 |
| rs531747813 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503440 | ATCTTCTCTGTCCTT[A/G]AAAATTTTTTTGTCT | 51191 |
| rs531822415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474173 | GCATACATCAGTGCA[A/G]AGACCTGGTGTGTTT | 51191 |
| rs532023988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498156 | GCCATGGGGTCCAGG[C/T]AGAGAACTGGCACAG | 51191 |
| rs532030597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458407 | TTAAGGTTTTTTTTT[C/T]TAAGTTAAAATTTTT | 51191 |
| rs532041831 | snp | C/T | 1.65209e-05 | 0.00287405 | stop-gained, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459391 | ATACATTCCGTGGAC[C/T]AAGGAGCAGAGCACA | 51191 |
| rs532053321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467785 | ACCCGTGCCCTTTAT[C/G]ACCTCAGAGTCTGAG | 51191 |
| rs532082638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88498721 | AATTACTGGCACATG[C/T]CACCATGCCTGGCTA | 51191 |
| rs532090497 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457206 | TGAGGCAGTGGGCGC[C/G]CTCAGTCCCGGGACC | 51191 |
| rs532138024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482915 | GGATTACAGGTGTGA[A/G]CCACTGCACCTGGCC | 51191 |
| rs532249539 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88490760 | GAGGCAGTGAGAATC[G/T]CTTGAACCCAGGAGG | 51191 |
| rs532251580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482139 | ACATAGTGAAACCTC[A/G]TCTCTACTAAAAATA | 51191 |
| rs532295563 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470975 | TTCTTTGTTTTTTTC[-/T]TTTTTTTTTTTGAGA | 51191 |
| rs532356275 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88472602 | GTTAAGGGATTCTCC[A/G]AGACCTTGTAGCATA | 51191 |
| rs532430940 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468535 | CCAGGCTGACTTTTT[G/T]GGGGATAGCTGGACA | 51191 |
| rs532582357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459523 | ATCAAAAGACAATAA[C/T]AATTTCTGTAGGAAA | 51191 |
| rs532631920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88467983 | TGGGCTTAAAGTACT[C/T]ATATTCTTTATAGCC | 51191 |
| rs532640182 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88475020 | CTATAAGGAAATTGG[A/T]GGGGCTAGAAACTAG | 51191 |
| rs532702930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491564 | GTCAAGGAAAAGGAC[A/G]TGATCAGAAGTGGAA | 51191 |
| rs532753314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88501227 | TCCAAAATTACAACA[C/G]CAACATCTGTCCCTC | 51191 |
| rs532872940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460042 | ATAGTTCTAAAATCC[A/G]TGTTGTAACTTTCAT | 51191 |
| rs532878106 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464371 | ACAATGCCTTGTGGC[C/T]AACATACTTTTTAAT | 51191 |
| rs532879764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88470897 | AGTAATAGCTAGCAC[C/T]TACGTATATGATTAT | 51191 |
| rs532890365 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88478715 | CTCCCAGTCTCAAGC[A/G]GTTCTCCCACCTCAG | 51191 |
| rs532913713 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88491804 | AAGGGGGACCTTAAC[-/A]TGTTTGTGAATGGAA | 51191 |
| rs532936554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88495754 | ACTAATAAGACAAGG[A/G]AAAAAAAATCAAAAG | 51191 |
| rs533004432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88505129 | TTTCCAGTCTTAACT[C/T]CTAGAGGAAATTTTT | 51191 |
| rs533006035 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476866 | CAGAGGTTGCATTGA[A/G]CCAAGATCACGCCAT | 51191 |
| rs533028212 | snp | A/C/G | 3.32928e-05 | 0.00407987 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459449 | CATTTGAGTATGACA[A/C/G]CTATAGCATGAAACA | 51191 |
| rs533103901 | snp | A/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458579 | AAACCGTTAGTCTGC[A/T]GGACCATTTCTTATT | 51191 |
| rs533110048 | snp | C/T | 8.51462e-05 | 0.00652425 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505883 | GATTTGGCTGACCAG[C/T]TTGCTTGTCCAACAG | 51191 |
| rs533166290 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498186 | GGGTTGAGGCAACTG[C/T]AGAGAGCCCCCACTA | 51191 |
| rs533212637 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455154 | TGCCAAGGCAATTCC[A/T]TGGGGATAGGCAAGC | 51191 |
| rs533279057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464207 | AAATGAGCAGATACA[A/G]TTCACTTTCTGCTGT | 51191 |
| rs533328345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88479946 | GTGGCGGGCGCCTGT[A/G]GTCCCAGCTACTCGG | 51191 |
| rs533507027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88496831 | TGTTAGAAAAATGCA[A/G]AAGGGAAGGTGTTGT | 51191 |
| rs533549374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88494934 | TGAAGTGTTGATGCT[A/G]TATAGTATTAGCAAG | 51191 |
| rs533599403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465853 | CAAATGCTGAGCTTG[C/T]GGCTGTCACCTCCCC | 51191 |
| rs533665734 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88473129 | TGGAGTCCAGTGGTG[C/T]GATCTCGGCTTACTG | 51191 |
| rs533895018 | snp | A/G | 0.000495958 | 0.0157395 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463541 | ACATAGGTAAAGATG[A/G]TCCATCCCTTATTGA | 51191 |
| rs533932516 | snp | A/G | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88479650 | TTTTTTTAAAATTAC[A/G]TCATACATATAAAGG | 51191 |
| rs533939662 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495079 | CAACTCAACAATTCT[A/T]CTTCTAGACATTTAA | 51191 |
| rs533997169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479157 | GGGCATGGTGGTAGG[C/T]GCCTGTAATTCCAGC | 51191 |
| rs534000065 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491837 | GAAGGATTCCAGGAA[A/G]AGGCAGGAATGGAGG | 51191 |
| rs534017132 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464733 | AGCTAGGATTACAGG[A/C]GTGCACTGCCACAAC | 51191 |
| rs534125616 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88488478 | CTCAAGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 51191 |
| rs534137055 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88497349 | ATTACCTAAGTGGTC[A/G]TGATCAGAATGTTAG | 51191 |
| rs534145652 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455652 | TCATTTTAAATATAA[C/T]GAAGACCAACAATTA | 51191 |
| rs534173244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88495074 | CTTTTCAACTCAACA[A/G]TTCTACTTCTAGACA | 51191 |
| rs534285907 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484454 | AGAGATACCACCAGT[G/T]TGGTAGTACTTTACA | 51191 |
| rs534294806 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468968 | TTCAGTCTAAGCCCC[A/C]TTGGACAAGAAAGTG | 51191 |
| rs534388179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498248 | GCTGCTCTAGAGACC[C/T]GAGAAGAGCCACCAG | 51191 |
| rs534508187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502394 | CTGCACAGGCATCCA[A/G]GCTGATCTGTTTGGC | 51191 |
| rs534514816 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456480 | CGCATTTTTTTTTTT[G/T]ATACATAGTCTCGCT | 51191 |
| rs534525171 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482996 | CTAGTATTTACTTAT[A/G]GATTCTTTTGAATTA | 51191 |
| rs534582734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459684 | TAAATAGTCTGCCTA[A/G]CCCTAAATTGGACTT | 51191 |
| rs534621865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460484 | TGGGGCCACCCTTTT[C/T]CAGAAACTGCTTCCC | 51191 |
| rs534660795 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88476920 | GTGAGACTCCGTCCC[A/C]AAAAAAAAAGAACAT | 51191 |
| rs534719580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484964 | TGGATCAGGGTACCT[A/T]ATATATCATACTGCT | 51191 |
| rs534759162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88475548 | GGTCACGATCTCCTG[A/G]CCTTGTGATCTGCCT | 51191 |
| rs534765865 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485779 | GGTATATTATTAAGT[C/G]CTAAAGACTAAGACA | 51191 |
| rs534813901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88492066 | TGGAGAGCAGTGGTG[C/T]GACCTTGGCTCATGG | 51191 |
| rs535034291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88477973 | ATTTAATTTTTAACA[C/T]ATTATACTATTTCAT | 51191 |
| rs535052523 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474978 | ATTCCATTTTTTCCT[A/G]AACAGTTGCATTCTG | 51191 |
| rs535080359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461408 | AAAGTTGGGGAAGCA[A/G]GAAAAGAAACTGGTC | 51191 |
| rs535424256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470562 | AAAGAAAGAGGCTGT[A/G]TGTATGTATACCATG | 51191 |
| rs535517969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460526 | CCTTTCCAACTTCCA[C/G]TCTTCCGGCTCAGAA | 51191 |
| rs535525957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469508 | GTAGGGGCTGGCAAG[G/T]CCAAAATCTGTAGGG | 51191 |
| rs535592062 | snp | C/T | 4.07938e-05 | 0.00451611 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469108 | AAAGTTGGGTGCCTA[C/T]CTCTGATGTGTCTAA | 51191 |
| rs535592976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88485156 | CTTTTGCCACTTACA[A/G]GGAGAATCACAAGAA | 51191 |
| rs535600703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88493905 | AAGCGTGAGAGTGGC[A/G]GGGATTTAAATTGAC | 51191 |
| rs535617564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485953 | ATATTCTTTATGTTC[A/G]TGAAAATTTGGGGCT | 51191 |
| rs535650452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88504474 | TATTTCCTCAATAAC[G/T]TTTTTTTGTATTTTC | 51191 |
| rs535663919 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490586 | CAGTGGCTCATGCCT[A/G]TAATCCTAGCACTTT | 51191 |
| rs535664048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492865 | TGTAGAGATTAAATA[C/T]GATAATATAAGTAGG | 51191 |
| rs535666156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503509 | TATACTATACATGTG[A/G]ATATGAGTGTTTCTT | 51191 |
| rs535727122 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486336 | AGGACTTGTGGGAAA[C/T]ATTAAGACTCCTCAA | 51191 |
| rs535748845 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462842 | GTCTGTAAACACACA[G/T]GAAGAAACATGTAAT | 51191 |
| rs535803372 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88473688 | CATTTTCTTTTGTTT[C/T]CTAAAATCCTCCTGT | 51191 |
| rs535830299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482235 | GAGTCGCTTGAATCC[A/C]GGAGGCAGAGGTTGT | 51191 |
| rs535861516 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478417 | GAGATAGATAATAAA[A/C]TAGTGGTTACTAGTG | 51191 |
| rs535920334 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475310 | TGCACATGTTTTTTT[A/C]TTTTTCTTTCTTTCT | 51191 |
| rs536050845 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468151 | CCACCTTGTGAATTA[C/T]CTATGTTTGCCAACT | 51191 |
| rs536191634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88474341 | CTTACCAGGTGCTCA[C/T]GTGGAAGGATATTCG | 51191 |
| rs536201162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466434 | AAATCATTGCCCGGA[G/T]AGTTAAACTTAATCT | 51191 |
| rs536252698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88500168 | CTATGTAACAGCCAA[C/G]CCTAAAACCTAGTGC | 51191 |
| rs536263388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481506 | CATTCTTAATTTTAA[G/T]GTAGATAAATTTGTC | 51191 |
| rs536377402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499472 | TTCAGGTGTTTCTTA[A/T]GCTTGATGATATTGG | 51191 |
| rs536378308 | snp | C/T | 1.69318e-05 | 0.00290957 | intron-variant | HERC5 | GRCh38.p7 | 4:88489371 | TAATGTTTTTGCTGC[C/T]GAGAAAAGAAAAACA | 51191 |
| rs536421061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458869 | AACATAATCCTTCCT[C/T]TTAAGAATATAGGCA | 51191 |
| rs536508759 | snp | A/G | | | synonymous-codon | HERC5 | GRCh38.p7 | 4:88493059 | CGGAGGAGTCAAGAA[A/G]GAGTTCTTCTACTGT | 51191 |
| rs536574607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491699 | TGGGTTTGGAAGTTG[A/G]CGTATATCTCTGAAG | 51191 |
| rs536644193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88491150 | TCCTTAGTAAGAAGA[A/G]GGGGAAGGGTTTGAC | 51191 |
| rs536785996 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478714 | CCTCCCAGTCTCAAG[C/T]GGTTCTCCCACCTCA | 51191 |
| rs536791170 | snp | C/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469109 | AAGTTGGGTGCCTAT[C/G]TCTGATGTGTCTAAA | 51191 |
| rs536847807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466229 | GTAGCTGGGACCACA[A/G]GTCCACCATGCCCAG | 51191 |
| rs536858296 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88475625 | TGCACCCTGATAATT[C/G]AATGGAGAGAATACT | 51191 |
| rs536917733 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503761 | AAGCAGCATATGATG[A/G]AGTTGTTATAAAAAT | 51191 |
| rs536949057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468255 | AGAAAAGATGACTAC[A/G]TTTAAGAAGAATCTG | 51191 |
| rs536949087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458997 | TGAGATTATGTTGTC[C/T]TAAAGTTATATTTTC | 51191 |
| rs536985052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483437 | GGTCTTGAGCTCCTG[A/G]CCTCAAGTGATTCTC | 51191 |
| rs537000825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484110 | GTTGCTATTAATACT[A/G]CCTTTTAAGTTTTTA | 51191 |
| rs537126012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482449 | GACACCTCAGCCCAT[A/G]TGTCTGAATTCCATC | 51191 |
| rs537130106 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88474400 | ACAGTGTGTCAGACA[A/G]TAGGACTGGCTCGAG | 51191 |
| rs537173926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491307 | AAATGTTGAACAGGC[C/T]GTTGGAAGTGACTGT | 51191 |
| rs537193082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482418 | CACCAGAAGGGGTGT[C/T]ACATGCCCGTATGTG | 51191 |
| rs537216510 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462462 | TCACTTTCATTTTCA[C/G]TGCTCTTCCTGATTA | 51191 |
| rs537321009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476835 | CTGAGGCAGGAGAAT[C/T]GCTTGACCTGAGAGG | 51191 |
| rs537387220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484831 | GGGCAGATGCTCTCA[A/G]GGCAAATGCCACTTT | 51191 |
| rs537396907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487509 | GGGCTTGATTAGGTG[G/T]AACAGACTTGGGCTT | 51191 |
| rs537578175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88495213 | GATATATTTTTGGTA[C/T]ACTTATGCAAATGGA | 51191 |
| rs537582329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88505509 | GCTTGAGGACAGTGA[C/T]TATGTGTCAGACATT | 51191 |
| rs537792019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488162 | CTGATTTTAAACAAG[G/T]TTCCAGAGATAATTT | 51191 |