SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs537793977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479776 | GTACTTTAGAAATAC[C/G]TGTGTGCTGGGCCGG | 51191 |
rs537930074 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456588 | CACCTCAGCCTCCCG[A/G]GTAGCTGGGACTACA | 51191 |
rs537934627 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499682 | GGTAGGGAATTTAAG[A/G]TAAAGGAACAAGAGC | 51191 |
rs537943044 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456759 | CGTGAATCACCGCGC[C/T]CGGCCGCGGCGCACA | 51191 |
rs538005887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481576 | TTTAAACTTTTTTTC[C/T]CCCATAAAGGTTTTA | 51191 |
rs538006100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472706 | CACAGGTTACAGATA[C/T]TCTAAATAGTGTGTC | 51191 |
rs538122278 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88480389 | GAATATACCATACTT[A/T]GCTTATCCATTCCAA | 51191 |
rs538208133 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88480446 | AATTCTTGTGTGTGT[G/T]TTTTTTTTTTGTCTT | 51191 |
rs538244065 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474437 | ACAGTAATTCTAAGG[A/G]TTTGGAATAGGTGAG | 51191 |
rs538271434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488241 | TTTTTTTTCTTTTTT[C/T]TTTTTTTTGAGAGAG | 51191 |
rs538332449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466172 | GCTTACTGCAGCCTT[A/G]ACCTCCCAGGCTCAA | 51191 |
rs538344469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465461 | TTTTCTTATGATCTT[A/G]GAGTAGAATTACATA | 51191 |
rs538395816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489978 | CATGCCACTGCATTC[C/T]GGCCTGGGTGACGGA | 51191 |
rs538455189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489471 | AGGGTTCCTCTGATT[C/G]CCTAGTTGCCTTTGA | 51191 |
rs538456969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498941 | AGAACAGTTCACCGC[C/T]TTCCCCACAAAAACA | 51191 |
rs538520896 | snp | C/G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473604 | TGGGACCCTACAACA[C/G/T]TTAGTGCTGCCTGTA | 51191 |
rs538587358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481417 | ACTACTCCTTTGTCA[A/G]TGATATGTGTTGCAA | 51191 |
rs538763225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497277 | CCCTATAGAGCAGTT[C/T]TGGCAAGGGCTCAGA | 51191 |
rs538794061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466369 | TTACAGGCATGAGCC[A/G]CCACACCCCACCTAA | 51191 |
rs538805422 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503533 | GTTTCTTTAAGTTTC[A/G]TTATTACTAAGCACA | 51191 |
rs538885372 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88491001 | TATATATTGTTCATT[C/G]AGTTTTTAAATTCAG | 51191 |
rs538890749 | snp | C/T | 3.33756e-05 | 0.00408493 | intron-variant | HERC5 | GRCh38.p7 | 4:88494155 | TTAAGATTTTTTTTT[C/T]GCTTTTCAGCCTAAA | 51191 |
rs538902285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88473456 | AACTAGCATTTTCTA[C/T]TTCAGCTGCAAGTTT | 51191 |
rs538905372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491901 | CATCCTCTTGGGAGG[A/G]ATTGGTGTCAGCAGT | 51191 |
rs539125604 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458775 | ACAGTTTAATCTCTT[A/G]ACTTCAGAAAGGGCC | 51191 |
rs539202347 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460932 | GAGTTTGAGGCTGCA[G/T]TGAGCCATGATCGTG | 51191 |
rs539218806 | in-del | -/T | 0.000574269 | 0.0169353 | intron-variant | HERC5 | GRCh38.p7 | 4:88494145 | CATAATACTTTAAGA[-/T]TTTTTTTTTCGCTTT | 51191 |
rs539232241 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499849 | CAGAATAGCTATACA[C/T]TTGACATTTATTTTA | 51191 |
rs539260852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482490 | CCACAGACCCTCCGT[A/G]GCCAACCCTGAGACT | 51191 |
rs539272273 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455313 | TGTGAATACATTGCA[A/G]GGTGAAGAGTGGCAT | 51191 |
rs539353496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88490112 | GATTTGACCATGTTC[A/G]GAAGATCTTTAACTG | 51191 |
rs539418362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502635 | TAAAAAATGGAGGCA[C/T]ACTTTCATCAGTAGG | 51191 |
rs539510327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88501163 | GGAGTTTATATTGTG[A/G]TAAGGAATGGAAATG | 51191 |
rs539528929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462644 | TTACTAACTGCAAGC[C/T]TTGCCCAGTCACTAA | 51191 |
rs539572437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88478300 | TATACTAAAATATTT[C/T]GTTATGTGTATCAAA | 51191 |
rs539588751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479087 | GGTCAGGAGTTCAAG[A/G]CCAGCCTGGCCAACA | 51191 |
rs539644036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88496459 | TGGTGCAGGTTTTCC[A/G]ATAGAACAGACGATA | 51191 |
rs539646672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88505557 | AATGCACTGTCAAAT[A/G]TAGGACACTGCACAT | 51191 |
rs539657811 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HERC5 | GRCh38.p7 | 4:88486053 | TGATAATCTAATTAA[C/T]AGCTATTAAGCAAAA | 51191 |
rs539657978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88494802 | GTATCCAAGAAGGCA[A/G]CCTGGCAAAGAAGCA | 51191 |
rs539736732 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455494 | TCCTGGTGCAGTGGG[C/T]CCCCAAGTCCCTTGT | 51191 |
rs539748872 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464581 | TTGTTTGTTTGTTTG[G/T]TTTTTGGTTTTTGGT | 51191 |
rs539917279 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88479607 | CTCGTGTGAGACATA[C/T]GAAGTTTATATTGCT | 51191 |
rs540011431 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88506066 | GGCCGGTTAGAACCC[A/G]TGACTGTATTCTCTC | 51191 |
rs540025994 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486601 | TCCTTTTTTATTTTC[C/T]GAAAATACAGTTGAA | 51191 |
rs540259758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88495550 | GGGCGACAGTAGAAG[A/G]CCCTGTCTCAATTAA | 51191 |
rs540333162 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88472267 | AATCATGTTTACTAC[A/G]TTGCATTTGGATTTA | 51191 |
rs540361880 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486898 | TTTATATACCTTTCA[C/T]TGATACATATAAAAC | 51191 |
rs540408544 | in-del | -/ATTAT | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88478366 | TAAAATTACGTGATA[-/ATTAT]ATTTACCTTCCTTGT | 51191 |
rs540423330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479843 | GAGGCCAAGGCGGGC[A/G]GATCACGAGGTCAGG | 51191 |
rs540453845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470783 | CATCCCTTTTTAAAA[A/T]TTTTTTTTAACAAAA | 51191 |
rs540564568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88478566 | CATATCGTATTAGGG[A/G]TTTTATTGTTGTTAA | 51191 |
rs540704217 | in-del | -/GAG | 0.0115144 | 0.0749975 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461967 | ACTGTCACTGCTAAA[-/GAG]AAGATTCTGTGTTTT | 51191 |
rs540708958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459140 | TATACATCAATATTT[C/T]TTCTAATTAAAAAAA | 51191 |
rs540853025 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88470835 | AAAATGTCAAAAATA[C/T]ACACAATAAAAAGAA | 51191 |
rs540876572 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88491378 | CGTATGGGTGGTAAA[A/C]AAAGTTTAAGGAGAA | 51191 |
rs540890344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88496519 | GAACTTTATTAGAGG[C/T]GACATATTTGATCAA | 51191 |
rs540891812 | snp | A/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464782 | TATTTATTTATTATT[A/T]TTTTTTGAGACGGAG | 51191 |
rs540914237 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88491108 | ATCTTGTGGGAAAAC[-/TG]AGGTTTTATGAGGTT | 51191 |
rs541004788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499629 | TCACTATCAGTGAAC[A/G]TTAGAATCCTTTTCT | 51191 |
rs541163278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484236 | ATTTTCCTTTTATTT[A/G]TCTGAATATATATGC | 51191 |
rs541207523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502747 | GTAGTATTCCATTGT[A/G]GTTTTAATTTGCATT | 51191 |
rs541289593 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479092 | GGAGTTCAAGACCAG[C/T]CTGGCCAACATGGTG | 51191 |
rs541290989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88490856 | TCTCAAGGAAAAAAA[A/T]ATATATATTGCAGTT | 51191 |
rs541405422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460948 | TGAGCCATGATCGTG[C/G]CACTGCACTACAGCC | 51191 |
rs541439853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468597 | GTATTTTCCCACAAA[A/G]ATCAGCAGATTTTTC | 51191 |
rs541607952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459815 | AATTTGTGAGACTTT[C/T]CCCTAGTAGATTATA | 51191 |
rs541615989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476576 | CTGAACTATTTGAAA[A/G]TAAGTTGAAGACATG | 51191 |
rs541654195 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88502117 | TGTAGTATTTTTGAC[A/C]GACATAGTGTATTTC | 51191 |
rs541675140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484344 | GTTGTGATTTGTGTA[C/T]GTGTGAGAGCTGTCT | 51191 |
rs541785665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461957 | AGGAAGTGTAACTGT[C/T]ACTGCTAAAGAGAAG | 51191 |
rs541800708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491439 | AGGACAGAAGTGTTA[C/G]GATAGAACTGTCTGC | 51191 |
rs541855965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88500803 | GCTTTTATGACAAAA[A/T]TGTACATTTTAACAC | 51191 |
rs541900123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469970 | CATTTGATCCTGGAA[C/G]CATTAGTTTGTGTAC | 51191 |
rs541961619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469376 | CCAGAGAAACAAACT[C/T]ATAGGATATGTGTGT | 51191 |
rs542008587 | snp | A/G | 8.49784e-05 | 0.00651782 | intron-variant | HERC5 | GRCh38.p7 | 4:88494351 | GTAAACAGAGTTCCT[A/G]AGAAAGGACCCTTTC | 51191 |
rs542137737 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88483818 | TACAGGCATGAGCCA[C/T]TGCGCCTGGCCTTCT | 51191 |
rs542174874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88492244 | CCTGACCTCACATGA[C/T]CCGCCCACCTCGGCC | 51191 |
rs542280278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465025 | TCCACCTGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 51191 |
rs542285745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461068 | TCGAAGTCAAGGGAA[A/T]TTTTGTTAATATATA | 51191 |
rs542346974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88472329 | AAAGGTAATTTTGTT[A/G]AAATGGGGCAAGCTC | 51191 |
rs542351127 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88477008 | ATAATATTATCCAAT[A/G]TCTAGGTCATTCAAA | 51191 |
rs542352900 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471452 | CTCAAGCAAAACTCC[C/T]ACCTTAGCCTTCCAC | 51191 |
rs542406088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498547 | GGGAATGTCTATCCT[A/T]TGCCTGTTCCACTGT | 51191 |
rs542481505 | in-del | -/TC | | | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506263 | ATAGATTAAGCTGTG[-/TC]TCTCACACAATGTTT | 51191 |
rs542485516 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506472 | GGTGGCAGTGGTGAC[A/G]GTTATTGGGAGAAGC | 51191 |
rs542488053 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88479672 | TATAAAGGAATATAT[-/A]ATATAATACCTATTT | 51191 |
rs542570025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465637 | TCCTTTTGAGTAGCA[C/T]GTATTACAAGAGAAG | 51191 |
rs542661932 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88471517 | TGCTAATTTTTTAGC[C/T]TTTGTAAAGACAGCA | 51191 |
rs542673329 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88490528 | GAAAGATTGACTTTA[C/G]CAAGTCTCAAGATAC | 51191 |
rs542811611 | in-del | -/CTT | 0.00199481 | 0.0315187 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463734 | GTATGTAGGACTGTC[-/CTT]CTGATATTTAGGAGC | 51191 |
rs542916884 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501749 | AAATATAACATTTCC[A/G]GCTATATAGTTGTGT | 51191 |
rs542951489 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | HERC5 | GRCh38.p7 | 4:88480742 | AAATTATGGTTTTAA[-/T]TGTATTTCCCTGGTT | 51191 |
rs542955034 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457087 | CCGCCCCCAAACAGC[A/G]CGTGGGGGGCGTGGC | 51191 |
rs542998549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474086 | GTAATGATGACTCGA[C/T]GAAGAATAAAAGAGA | 51191 |
rs543093425 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457138 | GCTGAGGCTGCGGTT[C/T]CCCGACGCCACGCAG | 51191 |
rs543095179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466500 | CAGGCCAGGAGAGCT[C/T]TCCCAGGATCCTGCC | 51191 |
rs543156233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465731 | ACTGGAAAGACTCAC[A/G]AACTTACTAAAAGCT | 51191 |
rs543192211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88473879 | TGATTGTGCCACAAA[A/G]AGAACATATGGTATG | 51191 |
rs543201763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88490742 | CCAGCTGCTTGGGAG[G/T]CTGAGGCAGTGAGAA | 51191 |
rs543213908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499540 | GAGTTACTGATACCT[A/G]AAATTTAATATGAGA | 51191 |
rs543213970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489751 | TGGTGACTCACACCT[A/G]TAATCCCGGCGCTTT | 51191 |
rs543276532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498643 | TGGTGCAATCTGGGC[C/T]CACTGCAACCTCCAC | 51191 |
rs543323367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88471962 | TTCCTCCCTCCCTCC[C/T]TCCCTCCTTCCCTTC | 51191 |
rs543346554 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458137 | TCTTTGCCTGGCTTT[C/T]AGAAATTTGAGTTGT | 51191 |
rs543383610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474802 | CTGTGTTAGGGAGAA[A/C]CTATAATAAGGGTTA | 51191 |
rs543383661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88500155 | CAGTTAGATTTTACT[A/G]TGTAACAGCCAACCC | 51191 |
rs543404922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88475764 | TTCCAGCCTCTACAC[C/G]TTGTTTTATTACCAT | 51191 |
rs543427878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483590 | CTGGAGTGCAGTGGC[A/C]CGATCTTGGCTTACT | 51191 |
rs543792953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467909 | TTTCTTGTAGGAAAA[C/T]GAACAGAGTTATTTC | 51191 |
rs543813043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474942 | GTGATCTAAGCACAC[A/G]TAACAAAAATTCAGA | 51191 |
rs543878661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88478700 | CACTGCAGCCTCCAC[C/T]TCCCAGTCTCAAGCG | 51191 |
rs543922816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482824 | TTTGTAGAGACGAGG[C/T]TTCACCATGTTGGCC | 51191 |
rs543937265 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501111 | ACTAAGGCAGAGAAG[A/T]TGGTGTGTGTTGTAT | 51191 |
rs544000902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460804 | GACCAGCCTGGACAA[C/T]ATGGGGAGACTTCAT | 51191 |
rs544109209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459976 | GTACTGAATGTGATG[C/G]AGTAAATTGAAAGTT | 51191 |
rs544150452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88479224 | TGGGAGGCAGAGGAT[A/G]TAGTGAGCTGAGATC | 51191 |
rs544169962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468487 | TAAGGGTTCTAGTAT[C/T]CCAGTTTGGTGAATT | 51191 |
rs544211889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486887 | TAAACATTCTCTTTA[C/T]ATACCTTTCATTGAT | 51191 |
rs544230859 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462855 | CATGAAGAAACATGT[A/G]ATTTCCATTATTGAA | 51191 |
rs544402835 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492126 | CTCCTGCCTCAGCCT[A/C]CTGAGTAGCTGGGAT | 51191 |
rs544493551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464166 | CATGGTTGTTTTCTT[C/T]GATTTTTTTTTTTTT | 51191 |
rs544560927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88471369 | TTTGAGACAAGGTCT[C/T]ACTCCATCACCCAGG | 51191 |
rs544604620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479928 | GAAAATTAGCTGGGC[A/G]TGGTGGCGGGCGCCT | 51191 |
rs544607818 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88497518 | TTTTGTGGAAAGTCA[G/T]ATTCTTAACAATGAA | 51191 |
rs544637515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464299 | TTAATTGTTTATTTG[A/G]GAAAAATAAAATGTA | 51191 |
rs544693171 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455644 | AGAATAATTCATTTT[A/C]AATATAATGAAGACC | 51191 |
rs544701108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471516 | CTGCTAATTTTTTAG[C/G]TTTTGTAAAGACAGC | 51191 |
rs544723933 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464275 | CTTTTGTCTTAAAAA[A/G]ACAAGTCATTAATTG | 51191 |
rs544753299 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467295 | CAAAGAAAGCAACAT[A/G]TGACTATGAAGGGAG | 51191 |
rs544921534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498649 | AATCTGGGCTCACTG[C/T]AACCTCCACCTCCCA | 51191 |
rs544949636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488585 | GGTTTCAGAATGGAC[A/G]TTCTGTCTGTCTGTC | 51191 |
rs545004352 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463254 | AAATATCTAATGTGC[C/T]GCAATTAAAGTGAAT | 51191 |
rs545166325 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506299 | GACTTGGCCTGAAGG[A/G]ATACTCTTTACCTTA | 51191 |
rs545170326 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478344 | TTTTTACCTTCAACA[A/G]TCTAAGTAAAATTAC | 51191 |
rs545182894 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88502515 | GGGAAATTTAAGCCA[C/T]GCAGCCATCAGTGGG | 51191 |
rs545190187 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456874 | CTCGAAAGCCATTCC[C/G]TCCAGGAGTTAAGGT | 51191 |
rs545306648 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455816 | CAGTGCTTCAAAAGA[C/T]ACTTAAAATGAAGAG | 51191 |
rs545332687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464944 | CCTGGCTAATTTTTT[A/G]TATTTTTAGTAAAGA | 51191 |
rs545416982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489613 | TAAGAGGTCCAGTCC[C/T]TTCTGAGGTCTGGCC | 51191 |
rs545430431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488670 | AATTCTCCCTTAAAA[C/T]CTCTTGTCTTGGTTT | 51191 |
rs545457088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497688 | GATTTGGAAATTCTC[A/T]GGCTGGCCATGTTGT | 51191 |
rs545543258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502006 | GGTTTCACCGTGTTA[G/T]CCAGGATGGTCTCCA | 51191 |
rs545694328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88477038 | ATTTCTCTTCTTTTC[C/T]CAAAAAAAGTAAAAA | 51191 |
rs545855589 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88504045 | GCATTCCAGCCCAGG[C/T]GACAGTGCGAGACTC | 51191 |
rs545871121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463149 | TAATCATGAAGAAAA[G/T]AAGAGGTAGTGTCAG | 51191 |
rs545997833 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88489662 | CCTTGAAGGGTTTCA[A/G]TGAGATGGTTAGCAT | 51191 |
rs546114358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476649 | AATCTGGCCGGGCAC[A/G]GTGGCTCATGCCTGT | 51191 |
rs546152903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88494417 | CTTCATAATATTTCC[A/G]TGTTCAACAGCAGCA | 51191 |
rs546252634 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484113 | GCTATTAATACTACC[C/T]TTTAAGTTTTTATTT | 51191 |
rs546274830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469489 | GGAATTGGCTTATGA[A/G]ATTGTAGGGGCTGGC | 51191 |
rs546389698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88495509 | AAGCTGCAGTGAGCC[A/G]TGATCATACCACTGC | 51191 |
rs546402614 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473267 | TTTTCTCTCTGGGTC[A/G]CACTGTAGTTCCTTC | 51191 |
rs546407526 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488263 | TTGAGAGAGAGTCTC[C/T]CTCTGTTGCCCAGAC | 51191 |
rs546440941 | snp | A/G/T | 0.000133788 | 0.00817779 | intron-variant | HERC5 | GRCh38.p7 | 4:88504631 | AATAGATCTGTAATC[A/G/T]TATGTCTTTTTAATG | 51191 |
rs546567360 | snp | A/G | | | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506469 | ACAGGTGGCAGTGGT[A/G]ACAGTTATTGGGAGA | 51191 |
rs546683661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485770 | TCTATAAGTGGTATA[C/T]TATTAAGTCCTAAAG | 51191 |
rs546685244 | snp | A/C | | | synonymous-codon | HERC5 | GRCh38.p7 | 4:88493092 | GTTTGCAGAGATGAT[A/C]CAGCCGGAATATGGG | 51191 |
rs546689335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88476220 | CTAATACTTTTTTAG[A/G]TTCCTTGGATACACA | 51191 |
rs546742553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471638 | GCTACCGCACCCAGC[C/T]GGTAACATAATTTAA | 51191 |
rs546748077 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490016 | TCTGTCTCAAAAAAA[A/T]CAAAAATAATAACCT | 51191 |
rs546795678 | snp | C/T | 1.92513e-05 | 0.00310246 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462407 | GATATACTTGTTAGA[C/T]GAATTTAATGGACCT | 51191 |
rs546806698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471072 | TGCCTCCTAGGCTCA[A/G]GCAGTCCTCCCACCT | 51191 |
rs546855882 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481295 | TGAGCTCAAATGATT[C/G]ACCCACCTCAGTCTC | 51191 |
rs546906064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470176 | TAATTTGCAGAGCAT[A/G]AATAATTAAGAACTG | 51191 |
rs546917240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88478908 | TGAGCCACCATGCCT[A/G]GCCTACCAAAAAAAT | 51191 |
rs547085282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88504130 | CCATGGCACATGGTA[A/G]GTACTCAATAACTGT | 51191 |
rs547122916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498723 | TTACTGGCACATGCC[A/C]CCATGCCTGGCTAAT | 51191 |
rs547184025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88475284 | ATCTATTGTTCATTG[A/G]GTGTAATTCTTGCAC | 51191 |
rs547196187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482960 | TATATTCAGCAAATT[A/T]GCCAAATTCTCATGT | 51191 |
rs547498772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459562 | TCTTGTCCCCTGCTT[C/T]ATATAGTAGCATCTT | 51191 |
rs547534373 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468643 | ATCAGTGTGATTTCC[A/G]TAGGCTATACTTACC | 51191 |
rs547568005 | snp | C/G | 0.00153108 | 0.027626 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467073 | GGTGGCACACACTTG[C/G]CTATGTTTCTGATTT | 51191 |
rs547680309 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88491565 | TCAAGGAAAAGGACA[C/T]GATCAGAAGTGGAAA | 51191 |
rs547750937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88500116 | GTGAAAAAGGTATTG[A/T]TCTTCATCATGATCT | 51191 |
rs547767523 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472666 | AGTTTGCCCTTTTAG[A/G]GTGAAATAGTTGGCA | 51191 |
rs547772680 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481952 | GACAAATAAACCTTC[A/G]TAATGACAGGGAGGG | 51191 |
rs547864344 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491366 | GAAGGTTAAATACGT[A/G]TGGGTGGTAAACAAA | 51191 |
rs547907001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458856 | AGATAGTCCCCCAAA[C/T]ATAATCCTTCCTTTT | 51191 |
rs547932523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468791 | GCAAATAAAAAGTCC[A/G]TAACTTCCCTGCCCT | 51191 |
rs547953181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492466 | TTTAGGCTGTAGGCC[A/G]GGTGTGGTGGCTCAT | 51191 |
rs547995143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468114 | ATATTTGTATTATGT[A/G]TATTAAACTGATGTC | 51191 |
rs548001263 | snp | A/G | 1.64743e-05 | 0.00287 | missense | HERC5 | GRCh38.p7 | 4:88475955 | ATGATGCATATTTCC[A/G]ACAACTGGGAGAGCC | 51191 |
rs548002153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88483947 | TTGAAATTCCAGTTA[C/T]TGACATGTTAGACTT | 51191 |
rs548037651 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88491043 | CATTTACCATTTGCA[G/T]GCTCTGTGTGAGGCA | 51191 |
rs548154846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491727 | AAGTTTGGCAAGAGT[A/G]GAAGGAGCCCGTGTT | 51191 |
rs548227121 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88501374 | TATGTATTCTTCACC[A/G]CTGTATATTCAGTAC | 51191 |
rs548232896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489951 | GAAGCAGAGGTTGCA[A/G]TGAGCCGAGATCATG | 51191 |
rs548316697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459585 | AGCATCTTAAGTAAA[C/T]AATAAATTCTGAACT | 51191 |
rs548439655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492606 | AAAAAATTAGCCAGG[C/T]GTGGTGGTGCATATC | 51191 |
rs548484153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476816 | ATCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 51191 |
rs548500666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484749 | TCCCTAATTTGAACA[A/G]TCTAGGCTTTGCCTC | 51191 |
rs548554278 | snp | A/G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505978 | TTTTAGGCTTTTAGC[A/G/T]GCCTGAAGCCATGGT | 51191 |
rs548614272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88505293 | CCATCCTTAAAGGTC[C/T]GGCATAATTCTGAAC | 51191 |
rs548662232 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456082 | GATTTTCGGTGACCC[C/T]TCAGAGGGCAAAGGG | 51191 |
rs548664908 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88477024 | TCTAGGTCATTCAAA[G/T]TTCTCTTCTTTTCCC | 51191 |
rs548680623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88495994 | GGTTGGTTACATCTG[C/T]CAATATTTACGGGAT | 51191 |
rs548813165 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88493593 | TTATTTGGTTTTTTA[-/TTTG]TTTGTTTGTTTTGTT | 51191 |
rs548827444 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465479 | GTAGAATTACATAAA[C/T]GGGTAATATTATTAA | 51191 |
rs548831372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497037 | CCCTTTAGATTCAGA[C/T]ACCGAATCTGCTGGC | 51191 |
rs549001179 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88480592 | GCTACGGATATGTGT[C/G]TGTTGTTCTTTACTG | 51191 |
rs549153935 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88480192 | GATAATCATTCCCTT[A/G/T]CTCTTACTATTTTAG | 51191 |
rs549350392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466036 | AATCTGCCATCTAGT[C/T]AGAGGAGTTCACCCA | 51191 |
rs549353209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488187 | TAATTTCGTAGAAGT[A/G]ATATTTGACTACTCC | 51191 |
rs549390186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458614 | AACTGTTTTGGTTCC[C/T]CTAGCATTTGTAATA | 51191 |
rs549509699 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456253 | AAAGCATTGTGCTAA[A/G]TTAAAAAAGCCAGAC | 51191 |
rs549576353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498823 | TGATCCACCCGCCTC[A/G]GCCTCCCAAATTGCT | 51191 |
rs549638630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489117 | AATTTTTACTTAGAG[A/T]GGGCCAATGGTAAAA | 51191 |
rs549697929 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468089 | TCAAATATTTGCATT[C/T]TATATATAAATATTT | 51191 |
rs549737287 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466807 | AATGAGCAGAGGGCA[A/C]GGGGAGGTGCTTGTT | 51191 |
rs549759499 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465603 | CTTATCACCTCTTTG[G/T]ATTCTTCATTACATA | 51191 |
rs549946598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88473354 | TTTTAATCTCTCTCT[C/G]TGTTCATATCCCTCT | 51191 |
rs549968767 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503506 | ATCTATACTATACAT[A/G]TGGATATGAGTGTTT | 51191 |
rs550034208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474205 | ACACTTCACTGTCTT[C/T]GCTAGTGCCTGGCTT | 51191 |
rs550154574 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458686 | CATTAGCACTGAAGA[C/T]GAAACAAGGTCCCAA | 51191 |
rs550383030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88490965 | GCCAGTCAGTCTACT[C/T]GATTATTTGAGTTCC | 51191 |
rs550408979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499234 | GCAGTGATATCTTAG[C/T]CTCAACTTTACATCC | 51191 |
rs550500110 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88493643 | ACAGAATCTCACTCT[G/T]TCACCCAGGCTGGAG | 51191 |
rs550506457 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | HERC5 | GRCh38.p7 | 4:88472247 | TTTTTGGTATTTTAG[-/A]AAAAAATCATGTTTA | 51191 |
rs550524232 | in-del | -/GCGCCCGCCACCAC | 0.00199481 | 0.0315187 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464914 | TAGCTGGGACTACAG[-/GCGCCCGCCACCAC]GCCTGGCTAATTTTT | 51191 |
rs550535705 | snp | A/G | 3.31972e-05 | 0.004074 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459443 | GAAAACCATTTGAGT[A/G]TGACAACTATAGCAT | 51191 |
rs550551626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462558 | TGAGACATGTTTCAG[A/G]GCTGTGTGTGAGACG | 51191 |
rs550608952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470349 | TGACCATAAATCAAG[C/T]CTTTCCTCTTTATTT | 51191 |
rs550662608 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458398 | GTAGTAATTTTAAGG[-/T]TTTTTTTTTTAAGTT | 51191 |
rs550677843 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88477681 | TGTCCCACATCCAGA[G/T]AGTCTGACCGTTTCC | 51191 |
rs550770716 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88494734 | CAGTAAAAGGGTTTT[A/C]ATATCCCTGCTGTGT | 51191 |
rs550845501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503524 | GATATGAGTGTTTCT[C/T]TAAGTTTCGTTATTA | 51191 |
rs550888350 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485283 | CCACCTCAGCAGGAG[A/G]CCACCAGGAACCATG | 51191 |
rs550931666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463309 | TGGGAAGTGGTTTGA[C/T]CCTTTCACAGGTGGG | 51191 |
rs550944089 | snp | A/G | 0.00047493 | 0.0154026 | intron-variant | HERC5 | GRCh38.p7 | 4:88479550 | TTTTTATCTAGCTGT[A/G]AAAATTCCCTTCCTT | 51191 |
rs551058333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88495718 | TGGCTCCAGAGTCTA[C/T]TAATCGTTTATACTA | 51191 |
rs551153053 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | HERC5 | GRCh38.p7 | 4:88492393 | TCAATTTAGGTAAAA[A/C]TTTTACCTAAAGTGG | 51191 |
rs551286000 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459063 | GTTCGTCTTAATAAA[C/G]AAGAACCTAAAAGCA | 51191 |
rs551404590 | snp | A/G | 4.95462e-05 | 0.00497701 | missense | HERC5 | GRCh38.p7 | 4:88504326 | TTTTATAAAATGTGC[A/G]ACGAAGACATTATCA | 51191 |
rs551423563 | in-del | -/A | 0.030351 | 0.119391 | intron-variant | HERC5 | GRCh38.p7 | 4:88482310 | CAAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAG | 51191 |
rs551490995 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464835 | GAGTGCGGTGGCGCA[A/G]TCTCGGCTCACTGCA | 51191 |
rs551516778 | snp | G/T | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457412 | ACCGCGCGCTGCTCC[G/T]GAGGGTGGAGGTGAC | 51191 |
rs551532465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462717 | GTTTGGATGAGATGA[C/T]CTTTAAAGCCTTTGC | 51191 |
rs551585316 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88487306 | GTGGCATTCAAGGAG[C/G]TTATACTCTAATGAA | 51191 |
rs551612665 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455517 | TCCCTTGTGGGCATG[A/C]CCAGACAAGACCCTG | 51191 |
rs551674152 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494508 | TCTAAAATTAGGAAG[C/T]GTTGATTATTCCCAT | 51191 |
rs551702969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465882 | CCTTGGAGCAGGTGG[A/G]TGGTGTTATCTCTTC | 51191 |
rs551806568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479996 | GGCGTGAACCCGGGA[G/T]GCGGAGCTTGCAGTG | 51191 |
rs551824215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88473130 | GGAGTCCAGTGGTGC[A/G]ATCTCGGCTTACTGC | 51191 |
rs551879096 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488447 | ATGTTGGCCAGGCTG[A/G]TCTCAAACTCCTGAC | 51191 |
rs551975789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460432 | GTGAAAATTTTCTGA[A/G]TAATCAAAACTGTTT | 51191 |
rs552048080 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88506069 | CGGTTAGAACCCGTG[A/C]CTGTATTCTCTCCCT | 51191 |
rs552088579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465207 | GGGGTGAGCCACCAC[A/G]CCACTATTTAATTTT | 51191 |
rs552138784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88493717 | GCTCAAGCCATTCTC[C/T]TGCCTCAGCCTGGCG | 51191 |
rs552142795 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481699 | ACAACTGCAGCTATT[C/T]AGTTGTTCAGGAGTA | 51191 |
rs552162009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88475466 | TGGGACTACAGGCAC[G/T]CACCGTCACGCCCAG | 51191 |
rs552211645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483877 | GTTAAGGATATTTCC[A/C]TCCTTTTAGAAATTG | 51191 |
rs552222211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468924 | ATTTGTATAAAGTGC[C/T]GAGTGTTGAGTCCTC | 51191 |
rs552342940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502313 | TGGATATTGATATGG[A/T]TGATGCCATATGTAA | 51191 |
rs552353471 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88478759 | TGGGCCACAGACATG[C/T]GCCACCACGCCCTGC | 51191 |
rs552371061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469452 | ATGTATCTATGGAGG[A/G]GAGAGAGAGAGATTA | 51191 |
rs552427016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485683 | AACCCTGATCATATC[A/G]TATGGGATGGAGGGT | 51191 |
rs552507176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88477719 | GTATTTCCAGTACAC[C/T]GCAAGTAAGTTCTAG | 51191 |
rs552551746 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474210 | TCACTGTCTTCGCTA[G/T]TGCCTGGCTTAGAAT | 51191 |
rs552581952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503105 | CTATGAATATATTCC[C/T]CTGTATTTTCTTCTA | 51191 |
rs552708770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459783 | TAACCTAGAAAAAAT[A/T]CACATTATCATGAAA | 51191 |
rs552890088 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463057 | GTCAGTGTTAGAAAA[A/G]TATTCAAAGGAGAGA | 51191 |
rs552930793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460491 | ACCCTTTTCCAGAAA[C/T]TGCTTCCCTTTTCCT | 51191 |
rs552941205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88477992 | ATACTATTTCATCTG[C/T]ACAAAGAATGTGATT | 51191 |
rs552941488 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469846 | CATCACAACTAGCAT[G/T]TAAGCGCCATGAGGA | 51191 |
rs552942845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469014 | ATTGATTACTTATTT[G/T]TTGAGTATCACTTTG | 51191 |
rs552955595 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476951 | GGAATCCTGTATTAC[A/C/T]CTGGCATCATTATCA | 51191 |
rs552982143 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88484852 | ATGCCACTTTCATTT[-/A]AGTTTTTGACCTGAT | 51191 |
rs553017025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88476499 | ATGGTATTAGAGTCA[A/G]CAATAATAAGTATGT | 51191 |
rs553254856 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483119 | GGGGAACAGTGGATA[C/G]TTATTTGTGATTTTA | 51191 |
rs553263195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88501879 | TCTTGGCTCACTGCA[A/G]CCTCCGCCTCCCGGG | 51191 |
rs553280678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470548 | ATGTCTCATGCTGTA[A/G]AGAAAGAGGCTGTAT | 51191 |
rs553318638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88500515 | GGCCATGCCGAGATT[C/T]AGTGGCTGAAGAGAT | 51191 |
rs553333499 | snp | C/T | 3.39945e-05 | 0.00412263 | intron-variant | HERC5 | GRCh38.p7 | 4:88500041 | TTTAATCTGATTAAC[C/T]CTTTACATATTTAAC | 51191 |
rs553398497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484977 | CTAATATATCATACT[A/G]CTGAAGAAAAAAATC | 51191 |
rs553409280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488352 | TTCTCCTGACTCAGC[C/T]TCCCGAGTAGCTGGG | 51191 |
rs553416468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461781 | AGAGAAAACAGTAGC[A/G]CTGGGGTTTTTCATA | 51191 |
rs553419365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479830 | CCTAGCACTTTAGGA[C/G]GCCAAGGCGGGCGGA | 51191 |
rs553419371 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495427 | AATTAGCTGGGCATG[G/T]TGGCACATGCCAGGA | 51191 |
rs553537369 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471128 | CACATGGCACTACAC[C/T]CAGCTAATTTTTGTA | 51191 |
rs553545841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462776 | AAAGAATACTAAAAT[A/T]ATATTTAAGAACTCA | 51191 |
rs553547947 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455938 | AACTCTTAGATAAAA[A/C]GTCAAGCTAGCTAAT | 51191 |
rs553604606 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497299 | GGGCTCAGAAGAAGA[A/C/G]GAGACCTCTAGAGAA | 51191 |
rs553717193 | in-del | -/TT | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475173 | TGGAGTTCTGATGCA[-/TT]TTTACTCTTGAAAAA | 51191 |
rs553861148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88490195 | GAATCATAATGACCA[C/G]TAGATCTTTTGAGTG | 51191 |
rs554005896 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457871 | CGTCCCCCGCCCGCC[A/G]CATCTCCCACTGTCT | 51191 |
rs554020087 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456972 | TTGCCTTTGGCCGCC[G/T]GCCAAGTCACTCTCA | 51191 |
rs554062800 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461794 | GCGCTGGGGTTTTTC[A/G]TAGAGGTAGATTGCT | 51191 |
rs554118857 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487545 | GCACCTATGTAAGGA[C/G]GCACAATCTAATGAA | 51191 |
rs554131094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474357 | GTGGAAGGATATTCG[A/G]GGCAGCTAGAAAAGC | 51191 |
rs554270166 | in-del | -/ACTC | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465725 | CAATTCACTGGAAAG[-/ACTC]ACGAACTTACTAAAA | 51191 |
rs554330902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481534 | GTCTGTCCGTTTCTT[G/T]ATATAATTTTACTCC | 51191 |
rs554333629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467613 | TATACCTGGCACTGA[A/G]CTGTGCTCAGCACTT | 51191 |
rs554397748 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503563 | ATAACAGATTTTTGA[A/G]TTGTTTTACCTTCCT | 51191 |
rs554397749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88475582 | TCGGCCTCCCAAAGT[A/G]CTGGTTAGGTGTGCT | 51191 |
rs554410156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483384 | CAGCTAATTGTTTCA[C/T]TTTTGGAGAGACAGG | 51191 |
rs554411797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474631 | GTACATTTACAGATA[C/T]CACTTAGCCACTATC | 51191 |
rs554471350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482564 | CACGGGGAGAGGCCT[G/T]TGCCAGAAGCAGGCT | 51191 |
rs554485939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458928 | TGTTTATTACTGTTA[C/T]TTGCTTTTTGGGAGA | 51191 |
rs554498697 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HERC5 | GRCh38.p7 | 4:88471749 | AAGAAATTATTGGTC[A/G]GAAGCCCTCTCTTTT | 51191 |
rs554557943 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88493786 | ACCTGGGTAGTTTTT[C/G]TATTTTTTGTAGAGA | 51191 |
rs554582557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491192 | CTACAAAGATTTTTA[G/T]TATTTCACTATTTCA | 51191 |
rs554643133 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88483490 | AGTGCAAGGATTACC[C/T]GGGTAAGCCACCACA | 51191 |
rs554668482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499484 | TTAAGCTTGATGATA[C/T]TGGGACAAGAGGTGC | 51191 |
rs554833279 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458773 | GGACAGTTTAATCTC[-/TT]AACTTCAGAAAGGGC | 51191 |
rs554879462 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458111 | TCCTTTTTCGGTAAA[A/T]TGCCTGTTTATCTTT | 51191 |
rs554930910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88475636 | AATTGAATGGAGAGA[A/T]TACTAATTGTATATC | 51191 |
rs555148137 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88476277 | TTCCAACTTTTCACT[A/G]TGAAAAATTTCACAG | 51191 |
rs555193697 | snp | C/T | 3.81781e-05 | 0.00436894 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469136 | TAAATTATTGTATTT[C/T]ACTTTCCTGTTTGTT | 51191 |
rs555193739 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469717 | GCTTTACTCAGTTTA[C/T]CATTTTAAATGTTAA | 51191 |
rs555255366 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466233 | CTGGGACCACAGGTC[C/T]ACCATGCCCAGCTAA | 51191 |
rs555316644 | snp | A/C | 0.000181628 | 0.00952789 | missense | HERC5 | GRCh38.p7 | 4:88504330 | ATAAAATGTGCGACG[A/C]AGACATTATCAAATT | 51191 |
rs555393128 | in-del | -/AAAC | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495388 | ACCTCATCTCTACAA[-/AAAC]AAACAAACAAAAACA | 51191 |
rs555425292 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456723 | GCCCGCCTCGGCCCC[C/G]CAAAGTGCTGGGATT | 51191 |
rs555454425 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491933 | GGGGTGCAGCCTCCT[C/T]GGGGAGCAAACAGCC | 51191 |
rs555595711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471948 | CTTCCCTCCCTTCTT[C/T]CCTCCCTCCCTCCCT | 51191 |
rs555658484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489396 | AAAACATAAAAGAAT[A/G]TGGCAAAGGGTTTCA | 51191 |
rs555799469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486996 | AAACCATCAGGGATG[G/T]AAGGCTATGAGGTAA | 51191 |
rs555801250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88496330 | ATGGATGAACAAAGG[G/T]TCAAGAATAGCCAGA | 51191 |
rs555906991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88480792 | TTTCATGTTTGTAAT[G/T]GCAATATTTGTTTCC | 51191 |
rs555931135 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88504738 | ATCCTCTGTGTCCCA[A/C/G]CATCAAAAAACAAAT | 51191 |
rs555964590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488501 | CCTCCCAAACTGCTG[A/G]GATTAACAGGCGTGA | 51191 |
rs555996501 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501561 | GAGTGGCAAAGAGAT[C/G]TCTAGGAAGCGTGCT | 51191 |
rs556000459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88505511 | TTGAGGACAGTGACT[A/G]TGTGTCAGACATTGT | 51191 |
rs556096511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472710 | GGTTACAGATATTCT[A/G]AATAGTGTGTCTGTA | 51191 |
rs556120514 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506183 | AAAGTCTTATTCACT[A/G]TTCAATGTGTTTACC | 51191 |
rs556195586 | snp | A/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460321 | TCTTAAAGTAAATAC[A/T]TAATGAGAGAATTCT | 51191 |
rs556256912 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456767 | ACCGCGCCCGGCCGC[A/G]GCGCACAACGCTTAA | 51191 |
rs556389454 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465537 | CTCTTCACCAAAGAA[A/G]CGTTCTCTTCAATAT | 51191 |
rs556396590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472018 | TTTCTTTTTCTGAGG[C/T]AGGATCTTGCTCTGT | 51191 |
rs556401734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464857 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACA | 51191 |
rs556467630 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495651 | AAACACAGAAAGATT[A/G]GGTAACTTGCTCAAG | 51191 |
rs556549598 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486696 | TCTCCTTCTAGCACA[G/T]CAAGTCTTGCCCAGC | 51191 |
rs556616902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457731 | TCAGGCGCGGGGTGA[A/G]CGGGATACTGGCGAC | 51191 |
rs556642011 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499790 | TTTAGACTATCAGTA[C/T]GCAGAGAAAGAGGTG | 51191 |
rs556705151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88473885 | TGCCACAAAAAGAAC[A/G]TATGGTATGTAAATG | 51191 |
rs556728425 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456761 | TGAATCACCGCGCCC[A/G]GCCGCGGCGCACAAC | 51191 |
rs556764793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481617 | CTAAATCAGGGGTCG[A/G]CAGCTTTTTTCTGGA | 51191 |
rs556844703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489985 | CTGCATTCCGGCCTG[A/G]GTGACGGAGCGAGAC | 51191 |
rs556925278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88485210 | ATCTTCAGGGGATCC[C/T]GCTTTGTCCTTTGAC | 51191 |
rs556927380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471116 | TGGGGCTTCAGACAC[A/G]TGGCACTACACCCAG | 51191 |
rs557260575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463750 | TTCTGATATTTAGGA[G/T]CTTTACTTTGACAGT | 51191 |
rs557311460 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501802 | TATTTATCTGTAGAA[-/T]TTTTTTTTTCTTTTG | 51191 |
rs557316306 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486451 | AAAAAGGAAAGGGTA[A/G]AAATCTGTCTATACT | 51191 |
rs557403053 | snp | A/C/G | 0.00059332 | 0.0172138 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463998 | AAGGTAAGTTGTAAA[A/C/G]TATCAATAAGAATTG | 51191 |
rs557500751 | snp | G/T | 0.000214346 | 0.0103502 | missense | HERC5 | GRCh38.p7 | 4:88493136 | CTGAAGGGGCTTCCT[G/T]CATGTGGTTTCCTGT | 51191 |
rs557965598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88479120 | GTGAAACCTTGTCTC[C/T]ATAAAAATACAAAAA | 51191 |
rs558027516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486675 | CCTTTCTCTGAAGGT[G/T]ATAATTCTCCTTCTA | 51191 |
rs558031272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88478360 | TCTAAGTAAAATTAC[A/G]TGATAATTATATTTA | 51191 |
rs558123883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459017 | GTTATATTTTCTTAT[A/G]GACCTTTTCATCTTT | 51191 |
rs558186001 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88486726 | CAAAATTCATGTATG[A/T]GCTAACCAGCTACCC | 51191 |
rs558455112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459644 | GCAGGTATCATGTGT[C/T]GTTTTGGCATTTAAA | 51191 |
rs558504072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88500430 | GTTACAGAGAGGAAG[C/T]GATAGCAAGCCCCAC | 51191 |
rs558520681 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468264 | GACTACGTTTAAGAA[C/G]AATCTGAAGTTATTT | 51191 |
rs558574395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484145 | AAGTAGTAATGTTTT[C/T]CATTTCTAGATACTC | 51191 |
rs558584102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483592 | GGAGTGCAGTGGCAC[C/G]ATCTTGGCTTACTGC | 51191 |
rs558584436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491921 | GTGTCAGCAGTAGGG[G/T]TGCAGCCTCCTCGGG | 51191 |
rs558596122 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463764 | AGCTTTACTTTGACA[C/G]TGCTATTTATTAGTG | 51191 |
rs558662553 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468927 | TGTATAAAGTGCTGA[A/G]TGTTGAGTCCTCAAA | 51191 |
rs558700370 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478756 | AGCTGGGCCACAGAC[A/G]TGTGCCACCACGCCC | 51191 |
rs558815243 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HERC5 | GRCh38.p7 | 4:88497615 | GCTTATACCAAAATG[C/T]AAGCAGGGAGAATTA | 51191 |
rs559097027 | snp | A/G | 4.94262e-05 | 0.00497098 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475882 | GCTCAAAAGACTTCC[A/G]TTTCATTCTCCACCC | 51191 |
rs559113511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499709 | GAGCTGTGAAGCAGG[C/G]AGGCAGCCTGCAGAA | 51191 |
rs559118772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469733 | CATTTTAAATGTTAA[A/T]CTCATCTAAAAAAAT | 51191 |
rs559160531 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88475323 | TTCTTTTTCTTTCTT[G/T]CTTTTTTTTTTTTTT | 51191 |
rs559160880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483657 | CCTCAGCTTCCTGAG[G/T]AGCCAGGAATATAGG | 51191 |
rs559173077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88482969 | CAAATTTGCCAAATT[C/T]TCATGTTATATCTAG | 51191 |
rs559227527 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470510 | AGAGGTTGGAAGGAT[A/G]GTTATAAGATGTGGT | 51191 |
rs559328160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469315 | TCAAGTATCATTTCC[C/T]AAACTGGTTCTGCAC | 51191 |
rs559387786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498794 | CAGGCTGGTCTCAAA[C/T]TCTTGACCTCAAGTG | 51191 |
rs559403064 | snp | C/T | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88490888 | GAGTTGGTATTTCCA[C/T]GTATTTTTGCACACA | 51191 |
rs559426494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459183 | ACCGTTGTCTTTCCT[A/G]ATTTGCTTTGCCTAC | 51191 |
rs559488768 | snp | C/G | 6.20687e-05 | 0.0055705 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460203 | ATTAATAGTTTTGTA[C/G]AAGTAATACCTGTGT | 51191 |
rs559518498 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88472860 | TATGCAAAGCATAAA[A/T]GTAGAAATGAGAACA | 51191 |
rs559551218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491395 | AAGTTTAAGGAGAAA[A/G]TGAGCATCCAGGGAA | 51191 |
rs559557609 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88502776 | TTTCTCTGATTACTA[A/G]TGTTAAGCACTTTAT | 51191 |
rs559619312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502121 | GTATTTTTGACCGAC[A/G]TAGTGTATTTCAAGT | 51191 |
rs559687792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460976 | GCCTGGGTAACTGAG[C/T]GAGACCCTGTCTCAA | 51191 |
rs559723715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492491 | GCTCATGGCTGTAAT[A/C]TCAGCGCTTTGGGAG | 51191 |
rs559760436 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HERC5 | GRCh38.p7 | 4:88476814 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51191 |
rs559820920 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488781 | ATCTGAACTTCTCTT[C/T]GGAATGAGAGAGCAT | 51191 |
rs559882831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465012 | CCTGACCTTGTGATC[C/T]ACCTGCCTCGGCCTC | 51191 |
rs559896840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472296 | TAGACAATTTATTAT[A/T]GTTACACACTTGAGA | 51191 |
rs560012530 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505919 | TTTTGTTGTTGTTAT[C/T]GTTGTTGTTGTTGTT | 51191 |
rs560095766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464342 | TTATTCATTAAATGT[A/G]ATCACCCTCTCTGAC | 51191 |
rs560206017 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467392 | CAAAATAATTATTCT[A/G]TATTACTCCTTCAGA | 51191 |
rs560339819 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88488682 | AAATCTCTTGTCTTG[G/T]TTTTTTTTTTCCTGG | 51191 |
rs560472301 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455865 | GAAAACATTTCAAAA[C/T]GTATAGCTAATAAAG | 51191 |
rs560485627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88473186 | TCTTAATGTAGTTTT[C/T]ATTATTTCCCTATTT | 51191 |
rs560485682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481734 | GAAAGCAGCCACAGG[C/T]AATACAAAAATGAAT | 51191 |
rs560508660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458523 | ATTTCTTAATACTTC[C/T]TTTTTTTCAACTGAT | 51191 |
rs560521128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466637 | TTGCTACACAACAGT[A/G]TAGTGGAATATACAA | 51191 |
rs560614026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472888 | ACATTTTTTCTGATA[C/T]GAATATCCCTCTCAC | 51191 |
rs560616194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465075 | GCACCTGGCCACAAC[C/T]GGCTAATTTTTGTAT | 51191 |
rs560715551 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457104 | GTGGGGGGCGTGGCG[G/T]CCCGGCAGGGGCTCA | 51191 |
rs560732529 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471589 | CAAGCAGTCCTCCCA[C/T]CTCAGCCTCCTGGTG | 51191 |
rs560735526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474005 | TCTGCGATACGGACT[C/T]TCAGACCTTTGGCAT | 51191 |
rs560772423 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465578 | TTCGGTATCTCTTAA[C/T]CAAAGCAGTCTTATC | 51191 |
rs560785259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498553 | GTCTATCCTATGCCT[A/G]TTCCACTGTTGTATT | 51191 |
rs560802040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465984 | TTTTTGTTTTTTCTG[G/T]TTTTTTTATTTTGGA | 51191 |
rs560825976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88480606 | TGTGTTGTTCTTTAC[C/T]GGTAGTGACAAACTT | 51191 |
rs560847510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497891 | GGCCCTGAGTGCCAA[A/G]GCCTGGAGGACAGAA | 51191 |
rs560849682 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506579 | ATGTTGTACATACTC[A/G]TTAACATAGTGATAA | 51191 |
rs561146288 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88503827 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGCAGGCA | 51191 |
rs561174284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488986 | CAGGTCCCTTGTTTC[C/T]TCTGCTCACTGAGAC | 51191 |
rs561244479 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88474823 | ATAAGGGTTAAATGA[C/G]CTAATTAATATATGT | 51191 |
rs561250604 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466939 | GATGATTTTCATCCT[C/T]TAAGAGATGTTTAGT | 51191 |
rs561300300 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464295 | GTCATTAATTGTTTA[C/T]TTGGGAAAAATAAAA | 51191 |
rs561313393 | snp | A/G | 0 | 0 | intron-variant | HERC5 | GRCh38.p7 | 4:88474123 | CCCTGTGCTTTAGAA[A/G]CTCATGGTGTAGTAA | 51191 |
rs561523517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459901 | ATAATATTTTATTAT[A/T]ATTATGTAATGCATA | 51191 |
rs561642769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88478652 | GGTCTTACTCTGTCA[C/T]CCAGGTTGGAGTGCT | 51191 |
rs561652700 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458252 | CTCACTTTGCCTTTT[-/G]TGCATGTTGTTTTTA | 51191 |
rs561705277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88477182 | AGATAGATAGATAGA[C/T]AGTGAAACCCCATCT | 51191 |
rs561713129 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496424 | AGCTGTATTAGTCAG[G/T]ACAGTATGATGTATG | 51191 |
rs561834754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88493279 | TATAATTATGGAGAT[A/G]ATGTATAATTCTAAT | 51191 |
rs561924050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472341 | GTTGAAATGGGGCAA[A/G]CTCTAGAAGAAACTT | 51191 |
rs561984182 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484999 | AAAAAAATCTGCCAT[A/G]CTATTGAAAAACAAT | 51191 |
rs562163052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88494557 | GCATTAATCTTTCAA[C/G]TTTTTCTGTGTAGGA | 51191 |
rs562164723 | snp | C/T | 0.000689271 | 0.0185516 | intron-variant | HERC5 | GRCh38.p7 | 4:88504186 | CCCCTCACCATTTTG[C/T]TCAGGATATTGCAGT | 51191 |
rs562183968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479883 | CAATCATGACTAACA[C/T]GGTGAAACCCCGTCT | 51191 |
rs562195919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88487835 | TCAGATAATCCCTGC[C/T]GCATTGCAATTTAAT | 51191 |
rs562330655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471468 | ACCTTAGCCTTCCAC[A/G]TAGCTGGGACTACAG | 51191 |
rs562381787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88496574 | AATGGAACTGGAAAA[A/G]AATGATATCTATCTG | 51191 |
rs562394281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479229 | GGCAGAGGATGTAGT[G/T]AGCTGAGATCGTGCC | 51191 |
rs562419662 | snp | A/G | 0.000402923 | 0.014188 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88487072 | TTCCATTTTTAGGAC[A/G]CTTCAGAAAATGTAC | 51191 |
rs562449492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463386 | GAGGCGTAGAACTTG[A/G]TCCTAAACATGGCAA | 51191 |
rs562514562 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497867 | CTGGGGGCTGTCACT[C/T]CCATCATAGGCCCTG | 51191 |
rs562517327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463219 | TATGTTCATTAAAAG[C/T]AATTCTAGATGGCTG | 51191 |
rs562565824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88478710 | TCCACCTCCCAGTCT[C/G]AAGCGGTTCTCCCAC | 51191 |
rs562581356 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458454 | TCAGTACTGAGGTAG[A/G]AGGGGAGCTAGATTT | 51191 |
rs562669239 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455733 | GCAAAAATGTCTTAA[C/G]TAGGACAAAAAAGGT | 51191 |
rs562669892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88505062 | TATTTTTATTTTTGT[A/G]GATAACATGTATGTT | 51191 |
rs562700463 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496127 | AGAATGTGAAAATAG[A/G]CAAATAACATCTTAA | 51191 |
rs562742697 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464192 | TTTTTTTTTTTTTTT[A/T]AATGAGCAGATACAA | 51191 |
rs562984762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88473090 | TATTTTTTTGGAAAC[A/G]GAGTCTCGCTTTGTT | 51191 |
rs562997798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88480918 | CTTTTGTCAATGATA[C/T]GTGTTGCAAATACTG | 51191 |
rs563047024 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488044 | TGGGAAATTGATTTA[C/T]GAGTTCTGAGTATGA | 51191 |
rs563127801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469437 | TCTGTCTGTCCATCT[A/G]TGTATCTATGGAGGG | 51191 |
rs563140989 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88492256 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 51191 |
rs563195615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488592 | GAATGGACATTCTGT[C/G]TGTCTGTCTGTCTCT | 51191 |
rs563206083 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478302 | TACTAAAATATTTTG[G/T]TATGTGTATCAAAAA | 51191 |
rs563216392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479935 | AGCTGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 51191 |
rs563350610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461993 | GTGTTTTTCTGTGGC[A/T]GACATAGGGTAACTG | 51191 |
rs563362156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88500820 | GTACATTTTAACACA[C/T]TCTTTTTAGAAAGTA | 51191 |
rs563368854 | in-del | -/G | 0.312593 | 0.242037 | intron-variant | HERC5 | GRCh38.p7 | 4:88477328 | GGGAAGGGGAAGGGA[-/G]GGGGAGGGGGGAGAG | 51191 |
rs563388822 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462604 | TAGGGATGAGAACCT[-/G]GGATTCTGATTCCCA | 51191 |
rs563411825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461137 | GGGATTCAAGGGAAG[C/T]TAATAATTAGTGAGT | 51191 |
rs563426348 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501570 | AGAGATCTCTAGGAA[A/G]CGTGCTGGCCTACAT | 51191 |
rs563460047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483832 | ATTGCGCCTGGCCTT[C/G]TATTAGGTTTTTGAA | 51191 |
rs563561319 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88484372 | TCTGTTTTCCTTGGA[A/G]CTTTATCTTTTGGAA | 51191 |
rs563615864 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HERC5 | GRCh38.p7 | 4:88479630 | ATATTGCTATTTTTT[A/T]AATTTTTTTTTAAAA | 51191 |
rs563636454 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88493470 | TCCTAATGAATTTGA[A/T]GACAAAGGCTGTGGA | 51191 |
rs563721595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479703 | AGAATTCAAGGAAAA[A/G]TAATAAAATAAACAT | 51191 |
rs563743483 | in-del | -/T | 0.399073 | 0.200692 | intron-variant | HERC5 | GRCh38.p7 | 4:88480444 | CAATTCTTGTGTGTG[-/T]TTTTTTTTTTTTGTC | 51191 |
rs563763522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485646 | TCACGACATGCCAGG[A/G]TGTTCATGTGTCTGT | 51191 |
rs564012212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502801 | CTTTATATGCTTATT[C/G]GCTGTTTGGATATCC | 51191 |
rs564152522 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489568 | TGTTCTCCCCACACC[C/T]TGCTCAGGTAGATAG | 51191 |
rs564187036 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88491555 | GAAGATTGTGTCAAG[A/G]AAAAGGACATGATCA | 51191 |
rs564191372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469477 | AGATTATTTTAAGGA[A/G]TTGGCTTATGAGATT | 51191 |
rs564226232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502011 | CACCGTGTTAGCCAG[A/G]ATGGTCTCCATCTCC | 51191 |
rs564317927 | snp | A/T | 3.51451e-05 | 0.00419181 | intron-variant | HERC5 | GRCh38.p7 | 4:88479324 | TAAAACTCATTTTTT[A/T]AAAAATTTGCTTTCC | 51191 |
rs564331424 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HERC5 | GRCh38.p7 | 4:88477063 | TAAAAAGTATTTATA[A/G]CTTTTTTTTTTTTTT | 51191 |
rs564352851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470171 | CATCATAATTTGCAG[A/C]GCATAAATAATTAAG | 51191 |
rs564382614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487015 | GCTATGAGGTAAAGT[A/G]TAAGGTTTCTCTGTC | 51191 |
rs564382620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88478801 | AGTTCTGGTAGAGAC[C/T]GAGTTTCTCTATGTT | 51191 |
rs564392327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486331 | ATAGCAGGACTTGTG[A/G]GAAACATTAAGACTC | 51191 |
rs564397453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463176 | TCAGGTGATGACACT[A/G]GTAGATAATTTGAAA | 51191 |
rs564420686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503217 | GGTTTTATTTTTTCA[A/G]TTTTTGAAACTGATT | 51191 |
rs564537802 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88504051 | CAGCCCAGGTGACAG[A/T]GCGAGACTCCGTCTC | 51191 |
rs564606622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466514 | TCTCCCAGGATCCTG[C/T]CATGAATAATAAAGA | 51191 |
rs564612502 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457170 | TGCGCGCAGCTGGTT[C/T]CCGCTCTGCAGCGCA | 51191 |
rs564682114 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480641 | AGCAGTTGGACCAAT[A/T]TAAATTCTCTCCAGA | 51191 |
rs564724391 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471625 | ATTATAGGTGTGAGC[A/T]ACCGCACCCAGCCGG | 51191 |
rs564769867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88490753 | GGAGGCTGAGGCAGT[G/T]AGAATCTCTTGAACC | 51191 |
rs565059390 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88482901 | CTCCCAAAGTGCTGG[G/T]ATTACAGGTGTGAGC | 51191 |
rs565179909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499592 | AAAAGCTTCAATAAA[A/G]GTAACACCAGTTTGA | 51191 |
rs565194226 | snp | A/C | 0.000148452 | 0.00861418 | missense | HERC5 | GRCh38.p7 | 4:88472442 | GCCTGTTTATTTGGA[A/C]TTAAATAAAGCAAGA | 51191 |
rs565253369 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462450 | GGTTCAAATCTTCAC[-/T]TTTCATTTTCACTGC | 51191 |
rs565264565 | snp | A/G | 0.000326716 | 0.012777 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459474 | GAAACATCTAAGGTA[A/G]GGAACTTTTTTCTTT | 51191 |
rs565309198 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478305 | TAAAATATTTTGTTA[C/T]GTGTATCAAAAAATT | 51191 |
rs565325742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88475778 | CCTTGTTTTATTACC[A/G]TCAGTTGCACCCTGC | 51191 |
rs565639553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498207 | GCCCCCACTAAGGCA[A/G]TGCCTAGTGGAGTCA | 51191 |
rs565651163 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC5 | GRCh38.p7 | 4:88482217 | TGGGAGGCTGAGGCA[A/G]GAGAGTCGCTTGAAT | 51191 |
rs565651655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88473664 | ATTTCATCAACATTT[A/G]TTAGAGCTCATTTTC | 51191 |
rs565656949 | in-del | -/A | 0.0559142 | 0.157578 | intron-variant | HERC5 | GRCh38.p7 | 4:88482310 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 51191 |
rs565718747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458857 | GATAGTCCCCCAAAC[A/G]TAATCCTTCCTTTTA | 51191 |
rs566100605 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485835 | TGGGATATTGCATTG[-/T]TTTTTTTTTTCTTCC | 51191 |
rs566106338 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465726 | AATTCACTGGAAAGA[C/T]TCACGAACTTACTAA | 51191 |
rs566131974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459569 | CCCTGCTTTATATAG[C/T]AGCATCTTAAGTAAA | 51191 |
rs566289537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483953 | TTCCAGTTATTGACA[C/T]GTTAGACTTTTTCAG | 51191 |
rs566351008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491611 | CAAGGAGATGAGATA[A/T]GAGAAAAAGTCCTTG | 51191 |
rs566361835 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473556 | CCCACTGGGGGTCCG[A/T]GGTGAAATGGTTCCC | 51191 |
rs566645077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88495825 | TTTTACTGGAAACAT[C/T]GAAGATAACCTAAAT | 51191 |
rs566702307 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459292 | ATAATGAAGTTAGTA[A/G]TACAGTGGGTAATAA | 51191 |
rs566761633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88494893 | TAACGTGAGAGGCTA[A/G]TTTATACTTCAAGTT | 51191 |
rs566787056 | snp | A/C | 0.0158469 | 0.0875917 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456417 | GGGGGAGGGTAGCTG[A/C]CTGCATAGCTCTGCC | 51191 |
rs566886159 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505983 | GGCTTTTAGCAGCCT[A/G]AAGCCATGGTTTTTC | 51191 |
rs566908361 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HERC5 | GRCh38.p7 | 4:88471927 | TTTTTTCTATGGCCC[A/G]CCCTTCTTCCCTCCC | 51191 |
rs566915894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472591 | AAATGTTTTGTGTTA[A/G]GGGATTCTCCGAGAC | 51191 |
rs566925961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88480113 | GTGCTTTAGAAATAC[C/T]GTGTACCCCTCATGG | 51191 |
rs566985052 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HERC5 | GRCh38.p7 | 4:88479642 | TTTTAATTTTTTTTT[A/T]AAATTACATCATACA | 51191 |
rs567000032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88505470 | CTTCACAAGAATCTA[A/C]TATTCCCAGTCAGAC | 51191 |
rs567017476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88497346 | GAGATTACCTAAGTG[A/G]TCATGATCAGAATGT | 51191 |
rs567054294 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457413 | CCGCGCGCTGCTCCG[G/T]AGGGTGGAGGTGACG | 51191 |
rs567157543 | snp | A/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88506144 | AATATTTTTCAAAAA[A/T]AAAATAACCGAAAAA | 51191 |
rs567230372 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465514 | GACCAAATTATCGGA[A/G]TATGAGTCTCTTCAC | 51191 |
rs567297668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503332 | TGTTTAAATCGTCTT[C/T]TGTCATTCTTGAAAA | 51191 |
rs567359600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499418 | TTTGATGTGACCTCT[A/G]TTCTCACAAATGCCC | 51191 |
rs567386666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88480357 | TCATTTTCACTCTGC[A/G]GTATAGTTCATTGTA | 51191 |
rs567536202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457668 | GCGCGCCTGGCTCGG[A/T]TAGTTTCGCCGACGG | 51191 |
rs567550729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479727 | TAAACATTAGTGTCC[C/T]TACCACCCATGTTAA | 51191 |
rs567561265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487506 | CTTGGGCTTGATTAG[G/T]TGTAACAGACTTGGG | 51191 |
rs567719039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465454 | AGGCATATTTTCTTA[C/T]GATCTTGGAGTAGAA | 51191 |
rs567722893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88473312 | CTTCCCTCCTCCCCT[C/T]CTTCCTCCCTCTAGC | 51191 |
rs567920060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458655 | TTTGAGATTTTTACA[C/T]GAATAGATTCTATTT | 51191 |
rs568006486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460504 | AACTGCTTCCCTTTT[C/T]CTAACACCTTTCCAA | 51191 |
rs568028011 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461396 | ACAGAAAGAATAAAA[A/G]TTGGGGAAGCAAGAA | 51191 |
rs568101374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469498 | TTATGAGATTGTAGG[A/G]GCTGGCAAGTCCAAA | 51191 |
rs568115620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469090 | CTCTCTAGAGTGTAC[C/G]TAAAAGTTGGGTGCC | 51191 |
rs568134552 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88492864 | ATGTAGAGATTAAAT[A/G]TGATAATATAAGTAG | 51191 |
rs568150742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88478000 | TCATCTGCACAAAGA[A/G]TGTGATTAATTTTGC | 51191 |
rs568224922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503456 | AAAATTTTTTTGTCT[G/T]CTTTTCTGTTAGTTA | 51191 |
rs568235120 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490520 | AGATTAAAGAAAGAT[C/T]GACTTTACCAAGTCT | 51191 |
rs568298347 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486280 | CAGTGAGTTAATACA[A/G]GCATTTCTTGTCCTC | 51191 |
rs568355339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88471677 | TGACCTTCCATTAGA[A/G]GGTCTTCCATGAGAA | 51191 |
rs568374814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471079 | TAGGCTCAAGCAGTC[C/G]TCCCACCTCAGCCTG | 51191 |
rs568424057 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481674 | CTTTATGAGGCATGT[C/G]GTTTCTGTCACAACT | 51191 |
rs568539806 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88485909 | AGAGGTTTATCATTA[C/T]ATCATCAATCTCTAC | 51191 |
rs568551845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88493893 | TTCTGGGATTACAAG[C/T]GTGAGAGTGGCAGGG | 51191 |
rs568683655 | snp | A/G | 3.32596e-05 | 0.00407783 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463660 | TTTGGCTGTATTTTT[A/G]GAAGAACAGTTTGTA | 51191 |
rs568935954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461560 | CTCTGGTGTATTTTT[A/T]TAGACTCTATTAGAT | 51191 |
rs568992389 | in-del | -/TGTT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458306 | GTCAATTTTTTTGTC[-/TGTT]AAGGCTTATGGGTTT | 51191 |
rs568993721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469585 | AAGTCTGAAGGCAAT[C/T]TAAAAGCAGAATTTC | 51191 |
rs569038185 | snp | G/T | 0.000115625 | 0.00760258 | missense | HERC5 | GRCh38.p7 | 4:88504322 | AGGATTTTATAAAAT[G/T]TGCGACGAAGACATT | 51191 |
rs569060831 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490926 | GTATAACTCTAATGG[A/G]CTCGTTATGTGATTC | 51191 |
rs569096075 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456277 | GCCAGACATCACTTA[A/G]ATATGGTTCCGTTTG | 51191 |
rs569131888 | in-del | -/AG | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475699 | AGAAGGGATGTAAAC[-/AG]GGGTTTTAGAAAACT | 51191 |
rs569155618 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88493988 | CTTTTAATGGCAAAA[A/C]CTGCAATTACTTTTG | 51191 |
rs569157293 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465110 | AGTAGAGTCGGGGTT[A/T]CACCGTGTTGGCCAG | 51191 |
rs569157511 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455447 | TCATCCCTGCTGCAT[A/G]AGGCTGAATTCCCTC | 51191 |
rs569169665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464524 | GGTAAAATGTCTTGC[C/T]CAGACTCCTTAGTTT | 51191 |
rs569176275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88503561 | ACATAACAGATTTTT[G/T]AATTGTTTTACCTTC | 51191 |
rs569191152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88479586 | TGGCTTGAATCTTTA[A/G]GTAGACTCGTGTGAG | 51191 |
rs569213737 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492497 | GGCTGTAATCTCAGC[A/G]CTTTGGGAGGCTGAG | 51191 |
rs569331119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88479061 | GAGGCAAAGGTGGGC[A/G]GATCACCTGAGGTCA | 51191 |
rs569470768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88471877 | CTGTGGTCAGTCCTT[C/T]CTTCCTTCCTTCCTT | 51191 |
rs569559646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468837 | ATCGAGTTCCTCACA[C/T]TTCTGCACACAGCTC | 51191 |
rs569559676 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459613 | ACTGACCAGTAAAGT[C/T]CTTATGTCCCCCAGG | 51191 |
rs569571718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468217 | TAATTGGCAGAAAAT[A/G]TACTAAGTTTTGTCT | 51191 |
rs569604291 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485396 | AGAGGGCCATAGTTA[A/C]AGGGTGAAACAGTCT | 51191 |
rs569646821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482281 | CGTCACTGCACTCCA[A/G]CCTGGGTGACAGAGC | 51191 |
rs569669858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88483094 | TCTAATATGATGTTA[A/C]ATAGAAGTGGGGGAA | 51191 |
rs569685108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88491869 | GTGACTGAAGGAGCA[A/G]AGATGGGTTATGATA | 51191 |
rs569765959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88490944 | CGTTATGTGATTCTA[C/T]GCTTTGCCAGTCAGT | 51191 |
rs569958950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88475421 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 51191 |
rs570037177 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458407 | TTAAGGTTTTTTTTT[-/TT]AAGTTAAAATTTTTC | 51191 |
rs570219889 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498681 | GTTCAAGCGATTCTC[A/G]TCCCTCAGCCTCCTG | 51191 |
rs570237109 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473811 | GCGTCTGTGAAGGGA[A/G]GGGATTGGATCAGTT | 51191 |
rs570262546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476819 | CCAGCTACTCGGGAG[C/G]CTGAGGCAGGAGAAT | 51191 |
rs570298145 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470223 | ATGAAACTGAGCATA[C/T]TCCTTCCCCCATTTA | 51191 |
rs570315747 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461281 | GTTCGGATTATGAAG[A/G]TGAAACACACAAGCC | 51191 |
rs570325007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88484764 | GTCTAGGCTTTGCCT[C/G]CTTTCCCCAAAGCCC | 51191 |
rs570392815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468290 | TATTTAAATTGAACA[C/T]GCATGTTTGTGCCAA | 51191 |
rs570405581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468967 | TTTCAGTCTAAGCCC[C/T]CTTGGACAAGAAAGT | 51191 |
rs570406670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88475507 | TATTTTAAGTAGAGA[C/T]AGGGTTTCACCATGT | 51191 |
rs570453463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485674 | TGTCATAATAACCCT[A/G]ATCATATCATATGGG | 51191 |
rs570457226 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88487948 | TTTACATATGCAGAC[-/AT]ATGTTATATGTATGT | 51191 |
rs570468502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476114 | GCAAAACTAAGATAC[C/T]TAGAAATGTATTCAT | 51191 |
rs570526058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88501679 | CAAGTCATAAATGTA[C/T]AGTTTAGTGAATTTC | 51191 |
rs570541144 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88484947 | TTTCTAGGTGTTTTC[A/G]GTGGATCAGGGTACC | 51191 |
rs570589574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88482805 | CTGGCTAATTTTTGT[A/G]TTTTTTGTAGAGACG | 51191 |
rs570786500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88493719 | TCAAGCCATTCTCTT[C/G]CCTCAGCCTGGCGGG | 51191 |
rs570825901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88485715 | GGAAAATTTCCTCTC[G/T]GTAGGGGAATGTTCC | 51191 |
rs570827787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476903 | CCAGCCTGGGCGACA[A/G]AGTGAGACTCCGTCC | 51191 |
rs570915705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492741 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAACAAAA | 51191 |
rs570933961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88502378 | GGCTTTTTGGGGAGA[A/G]CTGCACAGGCATCCA | 51191 |
rs570941120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488239 | CTTTTTTTTTCTTTT[C/T]TTTTTTTTTTGAGAG | 51191 |
rs570977720 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88491448 | GTGTTAGGATAGAAC[C/T]GTCTGCAATTCTGTT | 51191 |
rs571067631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470496 | TAGGAGACAAATGGA[G/T]AGGTTGGAAGGATAG | 51191 |
rs571125518 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474581 | AGGAGTCCAATATAA[C/T]GTTTTAATATAAAAA | 51191 |
rs571163471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481260 | GTTTCGCCATGTAGC[C/T]CAGGCTGGTCTCGAA | 51191 |
rs571226239 | snp | C/T | 1.69905e-05 | 0.00291461 | intron-variant | HERC5 | GRCh38.p7 | 4:88489158 | TATTTCTGTTTCTGT[C/T]TTCCTAGAGTAAAAA | 51191 |
rs571252396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88498144 | ATACTCCACAGAGCC[A/G]TGGGGTCCAGGCAGA | 51191 |
rs571261814 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88506055 | GAGGGTTTACTGGCC[A/G]GTTAGAACCCGTGAC | 51191 |
rs571305102 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HERC5 | GRCh38.p7 | 4:88489879 | CCGTGTGTGGTGGTG[A/G]GTGCCTGTAATCCCA | 51191 |
rs571494745 | in-del | -/TTGTTTGT | 0.00438332 | 0.0466095 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464562 | GGTTTTTTGGTTTTC[-/TTGTTTGT]TTGTTTGTTTGTTTT | 51191 |
rs571528132 | snp | C/G | | | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468366 | CATACCTCAGAAAAG[C/G]AGTTAATAATGATTG | 51191 |
rs571535352 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88480425 | ACAGATATATATGCT[G/T]TTTGCAATTCTTGTG | 51191 |
rs571654509 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465605 | TATCACCTCTTTGGA[C/T]TCTTCATTACATACA | 51191 |
rs571672449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466363 | CTGGGATTACAGGCA[C/T]GAGCCACCACACCCC | 51191 |
rs571675016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467011 | TTGCTAAACACTCTC[A/G]TCATTGTGGATAATT | 51191 |
rs571718046 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503513 | CTATACATGTGGATA[A/T]GAGTGTTTCTTTAAG | 51191 |
rs571722412 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456406 | GGTAGGGGTGGGGGG[A/G]AGGGTAGCTGCCTGC | 51191 |
rs571735652 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88474270 | TTGAGTCATTATTAG[A/G]GCAGTGAATGGTTAG | 51191 |
rs571741481 | in-del | -/TAT | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88475271 | TATTAGTTCTGAATC[-/TAT]TATTGTTCATTGAGT | 51191 |
rs571798687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88472303 | TTTATTATAGTTACA[C/T]ACTTGAGAAAAAAGG | 51191 |
rs571899981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88490987 | TTGAGTTCCACTTTT[A/G]TATATTGTTCATTCA | 51191 |
rs572108076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488381 | GGATTACAGGTGCCC[A/G]CCGCCACACCCAGCT | 51191 |
rs572193825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88499464 | AGTCTAATTTCAGGT[A/G]TTTCTTAAGCTTGAT | 51191 |
rs572245071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457980 | CTTCTCCCACATTCT[C/T]ATCGAAGTGGGGGAA | 51191 |
rs572354698 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HERC5 | GRCh38.p7 | 4:88502283 | CAGAATCAATGCTCC[C/T]ACCTGAAATTCATTT | 51191 |
rs572444117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88481765 | GGTCATGGCTATGTT[C/T]CAATAAGACTATAAA | 51191 |
rs572712097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88475600 | GGTTAGGTGTGCTTG[A/G]TCTCCTTCATGCACC | 51191 |
rs572774541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474638 | TACAGATATCACTTA[A/G]CCACTATCTCATAAT | 51191 |
rs572774603 | in-del | -/A | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500078 | TGTCAACTTTTACTT[-/A]AAAAAAAAACCTGAA | 51191 |
rs572787027 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88482636 | CAGCCCAATCTAGAA[A/G]GGGATGTGTGGGCTG | 51191 |
rs572836259 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495936 | ACTTTTAGGTCTTAA[A/G]ATTCTCTTAAAAATA | 51191 |
rs572859267 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463185 | GACACTAGTAGATAA[G/T]TTGAAAGAAAGGAAT | 51191 |
rs572871448 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HERC5 | GRCh38.p7 | 4:88494489 | TTGGATGATAATTTC[A/G]TTTTCTAAAATTAGG | 51191 |
rs572943268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502703 | GTATTACTAGTCTTT[C/T]TTAAATTAGCCATTC | 51191 |
rs573011530 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471916 | AAACCTTTATCTTTT[C/T]TCTATGGCCCGCCCT | 51191 |
rs573020140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88470774 | CTGTGTGTTCATCCC[G/T]TTTTAAAAATTTTTT | 51191 |
rs573098936 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88479137 | TAAAAATACAAAAAT[G/T]AGCCGGGCATGGTGG | 51191 |
rs573215919 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491723 | TCTGAAGTTTGGCAA[C/G]AGTGGAAGGAGCCCG | 51191 |
rs573226312 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88504734 | GAACATCCTCTGTGT[C/G/T]CCAACATCAAAAAAC | 51191 |
rs573269870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471209 | TCCTGAGCTCAGGCA[A/G]TCTACCAGCCTTGGC | 51191 |
rs573305505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463196 | ATAATTTGAAAGAAA[A/G]GAATTGCTATGTTCA | 51191 |
rs573445302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88496477 | AGAACAGACGATAGA[G/T]CTCAGAAATGGACCC | 51191 |
rs573530545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88495542 | TCCAGCCTGGGCGAC[A/C]GTAGAAGACCCTGTC | 51191 |
rs573701219 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500843 | AGAAAGTATGCTCCA[A/G]AGTGTTTTTATTGAT | 51191 |
rs573734740 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456282 | ACATCACTTAGATAT[C/G]GTTCCGTTTGTATGC | 51191 |
rs573853068 | in-del | -/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492044 | AGTCTCACTCTGTTG[-/C]CCAGGCTGGAGAGCA | 51191 |
rs573916867 | snp | C/T | 0.000119416 | 0.00772618 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88487133 | TTATCTTTAATAATC[C/T]GTCGAAAATTAAACT | 51191 |
rs574006884 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455609 | CCCTTATCTGCCTCC[A/C]GCATCTATCGATACT | 51191 |
rs574023494 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456733 | GCCCCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 51191 |
rs574099995 | snp | A/G | 3.47778e-05 | 0.00416985 | missense | HERC5 | GRCh38.p7 | 4:88505816 | CTCCCTAAATATTCT[A/G]CAATGGAAACAGTTG | 51191 |
rs574120452 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88480873 | ACTTTTTCTTACTGA[A/T]TATAGAATTCTTTTA | 51191 |
rs574201610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464793 | TATTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGC | 51191 |
rs574235559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC5 | GRCh38.p7 | 4:88488580 | CATTTGGTTTCAGAA[C/T]GGACATTCTGTCTGT | 51191 |
rs574256744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88489414 | GCAAAGGGTTTCATA[G/T]AGAGGAAGTTATCTT | 51191 |
rs574318997 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88487861 | TTAATAATGATTAAA[A/T]TTGTTAATATAGGTA | 51191 |
rs574432123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459802 | ATTATCATGAAATAA[C/T]TTGTGAGACTTTTCC | 51191 |
rs574444854 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88500625 | CATTTTTGTAAATCT[A/G]CCATACTGGGTCTAT | 51191 |
rs574467895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459274 | AGATGTTTTAAGTGT[A/G]TTATAATGAAGTTAG | 51191 |
rs574529278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469966 | GTCCCATTTGATCCT[A/G]GAACCATTAGTTTGT | 51191 |
rs574547131 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88484329 | TTTATGCTCATGTAT[G/T]TTGTGATTTGTGTAT | 51191 |
rs574592652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476952 | GAATCCTGTATTACC[C/T]TGGCATCATTATCAT | 51191 |
rs574605138 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88476525 | TATGTTGTCATTTGT[G/T]CTTTCTGTTTATGTA | 51191 |
rs574784428 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483162 | TTTCATGGACTATTC[C/T]TAGTTTCCAAAGGAA | 51191 |
rs574845558 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88485073 | GGGAAAGGTTAATGA[A/C]AAATAATTTGTGTTT | 51191 |
rs574990641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462797 | TAAGAACTCACATAT[C/T]CTGATCTTATTCTAT | 51191 |
rs575269666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462963 | ACCCAGCTGTGGTAC[G/T]GTATGCATTACCCTG | 51191 |
rs575279747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88492295 | AGGTGTGAGCCACCA[C/T]GCCCGGCCAATTTTT | 51191 |
rs575280788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88502000 | AGACAGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 51191 |
rs575435574 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460703 | TAAAGAAACTTGACT[A/G]TGAGGCCAGGCTTGG | 51191 |
rs575480148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88486026 | TAAGAGTGTTTCATT[C/T]ATAATTTAATCTGAT | 51191 |
rs575525122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88471081 | GGCTCAAGCAGTCCT[C/T]CCACCTCAGCCTGAG | 51191 |
rs575618342 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501572 | AGATCTCTAGGAAGC[C/G]TGCTGGCCTACATCA | 51191 |
rs575668602 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466446 | GGATAGTTAAACTTA[A/G]TCTCCAGCACTGCCC | 51191 |
rs575728911 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478620 | GCTTTAAAAAAATAT[A/T]TTTTTTTTTGAGATG | 51191 |
rs575798633 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475822 | TGAATCCCTTTTCCC[C/T]GTTCCTTTCTGACCA | 51191 |
rs575889454 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458986 | TGTTCTTGAAATGAG[A/T]TTATGTTGTCTTAAA | 51191 |
rs575912754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498570 | TCCACTGTTGTATTT[A/T]ATTTAATTTATTTAT | 51191 |
rs576094746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88481574 | GTTTTAAACTTTTTT[C/T]CTCCCATAAAGGTTT | 51191 |
rs576174304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88500235 | CTGGGCCGACTTGGC[C/T]AGGCTGGATGGTCTA | 51191 |
rs576174337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88490696 | TAAAAATACAAAAAT[C/T]AGTTGGGTGTGGTGG | 51191 |
rs576281393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458288 | TTTTTTGGGGGGTAG[C/T]CTGTCAATTTTTTTG | 51191 |
rs576329796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88474937 | TTACTGTGATCTAAG[C/T]ACACATAACAAAAAT | 51191 |
rs576408321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459653 | ATGTGTTGTTTTGGC[A/G]TTTAAAGGAAATGAT | 51191 |
rs576659128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476308 | AGAAGTTGAAAGAAT[A/G]GTATGGTATACCATA | 51191 |
rs576682742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88475755 | AGAATGACATTCCAG[C/T]CTCTACACCTTGTTT | 51191 |
rs576745542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459958 | TAAAAAATAATTTTA[A/G]ATGTACTGAATGTGA | 51191 |
rs576806704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468483 | AAACTAAGGGTTCTA[G/T]TATCCCAGTTTGGTG | 51191 |
rs576811243 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501055 | GAGCTCTAAAAATTC[C/T]TTTTAGCTCTTTAAT | 51191 |
rs576823855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467573 | CACAGTCATATAAAA[C/G]CCTCAGAATAATGAG | 51191 |
rs576853298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88476444 | AATAGTAATTGTATT[C/T]ATTCACTGAAAAGTT | 51191 |
rs576877675 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466515 | CTCCCAGGATCCTGC[C/G]ATGAATAATAAAGAC | 51191 |
rs576915571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88484160 | TCATTTCTAGATACT[C/T]GAATTTGTTCTTTAA | 51191 |
rs577057314 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476582 | TATTTGAAAATAAGT[G/T]GAAGACATGAGATTT | 51191 |
rs577102185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88499608 | GTAACACCAGTTTGA[A/G]TGAATTCACTATCAG | 51191 |
rs577255722 | snp | C/G | 1.64838e-05 | 0.00287083 | intron-variant | HERC5 | GRCh38.p7 | 4:88475836 | CTGTTCCTTTCTGAC[C/G]ACAGATAACCACCTG | 51191 |
rs577258729 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498302 | AATCAAAAGCACCCA[A/T]CACTAATGTGTGAGA | 51191 |
rs577402425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461717 | TATTTGGGATCTTGT[A/T]ATTTCAAATGAATTT | 51191 |
rs577422157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469782 | AGAATAATATTTGAC[C/T]AAATATCTTGGTACC | 51191 |
rs577556585 | in-del | -/T | 0.312837 | 0.241974 | intron-variant | HERC5 | GRCh38.p7 | 4:88477064 | AAAAGTATTTATAGC[-/T]TTTTTTTTTTTTTTT | 51191 |
rs577561068 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476897 | TGCACTCCAGCCTGG[G/T]CGACAGAGTGAGACT | 51191 |
rs577595834 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HERC5 | GRCh38.p7 | 4:88479805 | GGGCGCGTTGGCTCA[C/T]GCCTGTCATCCTAGC | 51191 |
rs577596736 | snp | A/G | | | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467175 | TGCCGCTTCCAGTGA[A/G]AGTATCATCAAGTGA | 51191 |
rs577597223 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470939 | CAAATGTATTCTTTT[A/T]AAAAAAATGAGATCA | 51191 |
rs577655592 | in-del | -/TAT | 0.00159617 | 0.0282053 | intron-variant | HERC5 | GRCh38.p7 | 4:88504936 | TTTTTACTGTTCCTA[-/TAT]TATTAATACTATATT | 51191 |
rs577778535 | snp | C/T | | | upstream-variant-2KB, stop-gained, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456877 | GAAAGCCATTCCGTC[C/T]AGGAGTTAAGGTGGC | 51191 |
rs577890120 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456786 | CACAACGCTTAACAA[A/C]CTTTGGCTTCCGTTA | 51191 |
rs577936119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88498418 | CCTGAAAGTGGGACA[C/T]TGAGTCAAAGATTAT | 51191 |
rs577951405 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465573 | CCTCATTCGGTATCT[C/G]TTAACCAAAGCAGTC | 51191 |
rs577951415 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455768 | ACTATGTAAAAGAAA[A/C]AAATGGATAAATTAC | 51191 |
rs577962954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464894 | TTCTGCCTCAGCCTC[C/G]GGAGTAGCTGGGACT | 51191 |
rs578045019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC5 | GRCh38.p7 | 4:88488611 | CTGTCTGTCTCTCCC[A/C]CTCTCTCTCCCTGCT | 51191 |
rs578071633 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506264 | TAGATTAAGCTGTGT[C/T]TCTCACACAATGTTT | 51191 |
rs578182110 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492423 | GTAAAAACTTTAGGC[C/T]CTGGGGTTTGACTGA | 51191 |
rs578232580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC5 | GRCh38.p7 | 4:88482488 | CACCACAGACCCTCC[A/G]TAGCCAACCCTGAGA | 51191 |
rs745390567 | snp | C/G | 1.67733e-05 | 0.00289592 | intron-variant | HERC5 | GRCh38.p7 | 4:88476069 | CTTTACCTGTCTTCT[C/G]AGTGGAAAGACATGT | 51191 |
rs745414643 | snp | A/C | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464239 | TCCTTAGTGAAATAC[A/C]TTTGTAACTATTCAG | 51191 |
rs745443819 | in-del | -/A | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497603 | TTTTCTTGACTGCTT[-/A]ATACCAAAATGCAAG | 51191 |
rs745449364 | in-del | -/A | 3.48111e-05 | 0.00417185 | intron-variant | HERC5 | GRCh38.p7 | 4:88489135 | GCCAATGGTAAAATG[-/A]AGTGTAATATTTCTG | 51191 |
rs745458870 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502351 | AGTATGAAAATGTTT[A/G]GTACATAATGGGGCT | 51191 |
rs745472153 | snp | C/T | 3.32231e-05 | 0.00407559 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504256 | TGTTTCTAAGTATAT[C/T]AATTACATTTTCAAC | 51191 |
rs745565375 | snp | G/T | 1.74051e-05 | 0.00294996 | intron-variant | HERC5 | GRCh38.p7 | 4:88479332 | ATTTTTTAAAAAATT[G/T]GCTTTCCTTGTGTTC | 51191 |
rs745602985 | snp | C/G | 2.37397e-05 | 0.00344518 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459510 | AAAATTAATTTTAAT[C/G]AAAAGACAATAATAA | 51191 |
rs745648455 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470495 | ATAGGAGACAAATGG[A/T]GAGGTTGGAAGGATA | 51191 |
rs745678890 | snp | C/G | 1.65263e-05 | 0.00287452 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459387 | GAAGATACATTCCGT[C/G]GACCAAGGAGCAGAG | 51191 |
rs745689176 | snp | C/G | 1.64993e-05 | 0.00287218 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468355 | TTTCAGAAAGCCATA[C/G]CTCAGAAAAGGAGTT | 51191 |
rs745738262 | in-del | -/TTTA | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501785 | ATGAATATATCACAG[-/TTTA]TTTATCTGTAGAATT | 51191 |
rs745769045 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455531 | GCCCAGACAAGACCC[C/T]GGGCAGGCTTCCTCA | 51191 |
rs745785472 | snp | C/G | 1.64947e-05 | 0.00287177 | missense | HERC5 | GRCh38.p7 | 4:88472466 | AGCAAGAAACATCTT[C/G]AAGGAGTTAACCCAA | 51191 |
rs745863921 | snp | A/G | 1.7009e-05 | 0.0029162 | intron-variant | HERC5 | GRCh38.p7 | 4:88504460 | TCAGTTTTCCTTCCT[A/G]TTTCCTCAATAACTT | 51191 |
rs745902972 | snp | A/G | 3.3216e-05 | 0.00407515 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463652 | TGTCTCTTTTTGGCT[A/G]TATTTTTAGAAGAAC | 51191 |
rs745926323 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484433 | ATTTTCTTCTGCCAG[G/T]CTCCTAGAGATACCA | 51191 |
rs745964893 | snp | C/G/T | 3.30073e-05 | 0.00406236 | missense, synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463612 | GGCTCTCACAGTGCC[C/G/T]TACTCACACAGGTGG | 51191 |
rs745965432 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457542 | GACGCCGAGTGAGTG[C/G]GGCTGGTGTGTGAGG | 51191 |
rs745980731 | snp | C/T | 3.29739e-05 | 0.00406028 | intron-variant | HERC5 | GRCh38.p7 | 4:88475827 | CCCTTTTCCCTGTTC[C/T]TTTCTGACCACAGAT | 51191 |
rs746038790 | snp | C/T | 1.66676e-05 | 0.00288679 | intron-variant | HERC5 | GRCh38.p7 | 4:88499889 | TCTAGTGATCATGGT[C/T]ATTACCTTTTTAAAA | 51191 |
rs746046896 | in-del | -/AT | 1.96678e-05 | 0.00313584 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460192 | TTTTCTGTAATATTA[-/AT]AGTTTTGTAGAAGTA | 51191 |
rs746050963 | snp | A/C | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468504 | CAGTTTGGTGAATTC[A/C]AAAATCATCAGTTTA | 51191 |
rs746073656 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463909 | CAACTTGGTCATAAT[G/T]CAACACAGAATGAGC | 51191 |
rs746135371 | snp | C/G | 1.65666e-05 | 0.00287802 | missense | HERC5 | GRCh38.p7 | 4:88494321 | AAAGAACTCAGTCCT[C/G]ATTTGGGAAAGTAAG | 51191 |
rs746141117 | in-del | -/TACTT | 1.66189e-05 | 0.00288256 | intron-variant | HERC5 | GRCh38.p7 | 4:88472384 | GATAATCTAACAAAA[-/TACTT]AATTTATCTTTCTTC | 51191 |
rs746222700 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491914 | GGGATTGGTGTCAGC[A/G]GTAGGGGTGCAGCCT | 51191 |
rs746225726 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490092 | TATTTTGGGGTATAA[C/T]TGTAGATTTGACCAT | 51191 |
rs746227136 | snp | A/G | 3.30196e-05 | 0.00406309 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486138 | GGTGAAATGTCAACT[A/G]CCTGAAAGTATTTTC | 51191 |
rs746265955 | snp | C/T | 3.51377e-05 | 0.00419137 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457334 | CGGGCAAGGCCGCCG[C/T]GACCCAGCCCGCGAA | 51191 |
rs746348512 | snp | C/T | 3.03845e-05 | 0.00389761 | intron-variant | HERC5 | GRCh38.p7 | 4:88505626 | CTCTGTAAAGAGATT[C/T]TGGTCTCCATGTAAA | 51191 |
rs746395520 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462803 | CTCACATATCCTGAT[C/G]TTATTCTATAAGGTA | 51191 |
rs746445067 | snp | A/G | 3.31203e-05 | 0.00406928 | intron-variant | HERC5 | GRCh38.p7 | 4:88486238 | ACTGTGGTAGGTATA[A/G]CATGTTTAAAGGGGG | 51191 |
rs746517242 | snp | G/T | 1.69761e-05 | 0.00291337 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88505767 | GAATGAAAGAGACCC[G/T]ATAAGAGCACTGACA | 51191 |
rs746527360 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480061 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 51191 |
rs746543320 | snp | C/T | 1.66297e-05 | 0.0028835 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462220 | CACCACACCACAGAT[C/T]GTGGAGCACCTCGCA | 51191 |
rs746545085 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | HERC5 | GRCh38.p7 | 4:88493037 | GTGGAGAAATTGGGT[A/G]TGACCTCGGAGGAGT | 51191 |
rs746567146 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460533 | AACTTCCACTCTTCC[A/G]GCTCAGAATCCCCTT | 51191 |
rs746709653 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88493134 | TCCTGAAGGGGCTTC[C/T]TGCATGTGGTTTCCT | 51191 |
rs746755712 | snp | C/T | 0.000517331 | 0.0160748 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457531 | GGCGGCGCCCGGACG[C/T]CGAGTGAGTGGGGCT | 51191 |
rs746768834 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473367 | CTGTGTTCATATCCC[C/T]CTTCTCTTTCCCTCT | 51191 |
rs746769469 | in-del | -/TTT | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465090 | CGGCTAATTTTTGTA[-/TTT]TTAGTAGAGTCGGGG | 51191 |
rs746803233 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486335 | CAGGACTTGTGGGAA[A/G]CATTAAGACTCCTCA | 51191 |
rs746808514 | in-del | -/ATT | 0.000115477 | 0.00759772 | cds-indel | HERC5 | GRCh38.p7 | 4:88472485 | AGTTAACCCAAAAGG[-/ATT]ACTGGATTACTAACA | 51191 |
rs746828656 | snp | A/G | 1.6525e-05 | 0.00287441 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467014 | CTAAACACTCTCATC[A/G]TTGTGGATAATTAAG | 51191 |
rs746869119 | snp | A/G | 1.7357e-05 | 0.00294588 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88487152 | GAAAATTAAACTACT[A/G]CATACAGACACACTT | 51191 |
rs746870132 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469015 | TTGATTACTTATTTG[C/T]TGAGTATCACTTTGT | 51191 |
rs746881153 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470291 | ATAAATAGGACTTGC[A/G]TAGTTGGTGGGGTGG | 51191 |
rs746915886 | snp | C/T | 4.96011e-05 | 0.00497977 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459384 | CATGAAGATACATTC[C/T]GTGGACCAAGGAGCA | 51191 |
rs746986539 | snp | A/T | 3.36519e-05 | 0.00410181 | missense | HERC5 | GRCh38.p7 | 4:88504235 | GTTTTATTAAAGGAG[A/T]GACTATGTTTCTAAG | 51191 |
rs747077893 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496281 | ATCCCAGGAGGCTTT[C/T]TATTAAACTTCACAA | 51191 |
rs747098849 | snp | A/G | 1.67421e-05 | 0.00289323 | missense | HERC5 | GRCh38.p7 | 4:88489169 | CTGTTTTCCTAGAGT[A/G]AAAAACATAAAGCTT | 51191 |
rs747133383 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482761 | CTGTATTCCCAAGTA[C/T]CTGGGATTACAGGCG | 51191 |
rs747134685 | in-del | -/A | 1.6628e-05 | 0.00288335 | frameshift-variant | HERC5 | GRCh38.p7 | 4:88489178 | TAGAGTAAAAAACAT[-/A]AAGCTTATCTTAGGT | 51191 |
rs747184435 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484095 | TTTTCAGATATTTTG[A/G]TTGCTATTAATACTA | 51191 |
rs747206462 | snp | A/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467296 | AAAGAAAGCAACATA[A/T]GACTATGAAGGGAGT | 51191 |
rs747213664 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466264 | TTTTTAAATTTGTTG[G/T]AGAGATAGGGTCTCC | 51191 |
rs747219808 | snp | A/T | 1.64966e-05 | 0.00287194 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463590 | AGTTGAATTTGTCGC[A/T]TGTGGTGGCTCTCAC | 51191 |
rs747308300 | snp | A/C | 4.95323e-05 | 0.00497631 | missense | HERC5 | GRCh38.p7 | 4:88504335 | ATGTGCGACGAAGAC[A/C]TTATCAAATTATTCC | 51191 |
rs747345070 | snp | C/G | 1.64947e-05 | 0.00287177 | missense | HERC5 | GRCh38.p7 | 4:88494282 | AAGAAACTTTTGGAC[C/G]AAATGCCATCATTGG | 51191 |
rs747348644 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472566 | TTAAAAGAACTCAAA[A/G]TTTCAGAAGAAATGT | 51191 |
rs747353577 | snp | C/T | 1.6577e-05 | 0.00287893 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463643 | GTGTACCCTTGTCTC[C/T]TTTTGGCTGTATTTT | 51191 |
rs747355201 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490222 | AGTGCTGTCCTTGTG[A/G]CAAGAACTGTTTTAA | 51191 |
rs747443320 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485805 | AGACATGAAGAACTG[A/G]ACCCCAGAGTACTTT | 51191 |
rs747452750 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466303 | GCCAGGCTGGTCTTA[A/G]ACTTCTGGGTTCAAA | 51191 |
rs747479115 | snp | C/T | | | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506605 | GATAAATGTAAATTA[C/T]ACTTTGATAATGTAA | 51191 |
rs747481300 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491507 | AGAGATAAATAAAAC[C/T]GTGAAGAGTGCTTCA | 51191 |
rs747549849 | snp | C/T | 3.53863e-05 | 0.00420618 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460156 | GGAGATTACCATTCT[C/T]TTGCACTCTCAAAAG | 51191 |
rs747616161 | snp | A/G | 1.66807e-05 | 0.00288792 | intron-variant | HERC5 | GRCh38.p7 | 4:88499886 | GTGTCTAGTGATCAT[A/G]GTTATTACCTTTTTA | 51191 |
rs747644216 | snp | A/G | 3.42155e-05 | 0.00413601 | missense | HERC5 | GRCh38.p7 | 4:88504502 | TTCTCTAGAATGCAC[A/G]TTATGAACCAGGATA | 51191 |
rs747704644 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458603 | TCTTATTACCAAACT[A/G]TTTTGGTTCCCCTAG | 51191 |
rs747750106 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88493029 | TTCATTTAGTGGAGA[A/G]ATTGGGTATGACCTC | 51191 |
rs747762414 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476084 | CAGTGGAAAGACATG[C/T]CTAGTAAAGTTATGG | 51191 |
rs747789900 | snp | A/G | 1.69364e-05 | 0.00290997 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462189 | AGCTTGGAGTTGGAA[A/G]GAAATTTCCCTCAAC | 51191 |
rs747840384 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460346 | AATTCTTGGATCTGT[A/G]AAATGTTCAGGTTTC | 51191 |
rs747842097 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489286 | TTGATTGAGGATGTT[C/T]TGAATCAGCTAAGTC | 51191 |
rs747894300 | in-del | -/T | 0.000138836 | 0.00833059 | intron-variant | HERC5 | GRCh38.p7 | 4:88504473 | TATTTCCTCAATAAC[-/T]TTTTTTTTGTATTTT | 51191 |
rs747908269 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498195 | CAACTGCAGAGAGCC[C/T]CCACTAAGGCAATGC | 51191 |
rs747968407 | in-del | -/TTTA | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469683 | GGAAGGTCCTTTCTT[-/TTTA]TTCACTTGTTCAAGT | 51191 |
rs747968409 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488223 | CTGCTAAAAGCATAG[A/C]CTTTTTTTTTCTTTT | 51191 |
rs747977650 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | HERC5 | GRCh38.p7 | 4:88475949 | TGTCCTATGATGCAT[A/G]TTTCCAACAACTGGG | 51191 |
rs747991317 | snp | C/G | 3.30994e-05 | 0.004068 | intron-variant | HERC5 | GRCh38.p7 | 4:88500885 | CAGAATTATGTTGGA[C/G]ATATTATCTGAGTTC | 51191 |
rs748002273 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484556 | TAGGGGATAATTTTT[C/G]CCCAACTCAGCACCA | 51191 |
rs748009334 | snp | C/G | 1.65853e-05 | 0.00287964 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464033 | AATGAGTGCAGCAAA[C/G]TAGATAGTAATTTAA | 51191 |
rs748091091 | snp | A/G | 1.65581e-05 | 0.00287728 | intron-variant | HERC5 | GRCh38.p7 | 4:88476033 | TCACTGGTTCTGGGT[A/G]AGTTTGATCATTTGA | 51191 |
rs748189556 | snp | C/T | 1.66588e-05 | 0.00288602 | intron-variant | HERC5 | GRCh38.p7 | 4:88486268 | GAAATTGATAATCAG[C/T]GAGTTAATACAGGCA | 51191 |
rs748252354 | snp | C/T | 4.22324e-05 | 0.00459504 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457515 | GCTGCTCGCCGGGAG[C/T]GGCGGCGCCCGGACG | 51191 |
rs748254733 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496092 | ATAGCCTCATGAAAA[C/T]TCTTCTGTTTACTCA | 51191 |
rs748284623 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494899 | GAGAGGCTAATTTAT[A/C]CTTCAAGTTGACAGT | 51191 |
rs748319333 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455380 | CTGCCAACAGGCTCC[C/T]AGCTCACAGACTGAA | 51191 |
rs748331684 | snp | A/G | 0.000103493 | 0.00719276 | missense | HERC5 | GRCh38.p7 | 4:88505807 | GTCCTCTTCCTCCCT[A/G]AATATTCTACAATGG | 51191 |
rs748355683 | snp | A/G | 1.68633e-05 | 0.00290368 | intron-variant | HERC5 | GRCh38.p7 | 4:88470683 | GAAAAGGTAATATAT[A/G]TAATAAATTAATTGT | 51191 |
rs748440675 | in-del | -/TAAAA | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500703 | TTTAATTTGATCAGT[-/TAAAA]TAAGAGAATTCAAGC | 51191 |
rs748469924 | snp | A/G | 1.65002e-05 | 0.00287225 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463573 | GGACTAGACAATCAG[A/G]AAGTTGAATTTGTCG | 51191 |
rs748493849 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502797 | AGCACTTTATATGCT[A/T]ATTGGCTGTTTGGAT | 51191 |
rs748507528 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464832 | CTGGAGTGCGGTGGC[A/G]CAATCTCGGCTCACT | 51191 |
rs748542406 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502007 | GTTTCACCGTGTTAG[C/T]CAGGATGGTCTCCAT | 51191 |
rs748551476 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88472436 | AATGATGCCTGTTTA[C/T]TTGGACTTAAATAAA | 51191 |
rs748552605 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465961 | AAATTCACCCAAGTT[C/G]AGAGTTGTTTTTGTT | 51191 |
rs748612871 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488639 | GCTTGTCTCTCTTCA[A/G]TTAACTTCTTAGGTA | 51191 |
rs748634127 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503917 | TAAAAATACAAAAAA[A/C]TTAGCTGGGCATGGT | 51191 |
rs748637224 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503172 | ATCCACTTTAATTGA[-/T]TTTTTTAGTAAGATG | 51191 |
rs748693566 | snp | A/C/T | 3.47501e-05 | 0.00416822 | intron-variant | HERC5 | GRCh38.p7 | 4:88494141 | AAACTCATAATACTT[A/C/T]AAGATTTTTTTTTCG | 51191 |
rs748773876 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488199 | AGTAATATTTGACTA[C/T]TCCTTTTTCTGCTAA | 51191 |
rs748799957 | snp | A/G | 1.67534e-05 | 0.0028942 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88479495 | CCTAGAAATGTTGAA[A/G]AAGCTGCACAGGGTA | 51191 |
rs748806391 | in-del | -/TTTAAGAT | 3.52634e-05 | 0.00419886 | intron-variant | HERC5 | GRCh38.p7 | 4:88494139 | AAAAACTCATAATAC[-/TTTAAGAT]TTTTTTTTCGCTTTT | 51191 |
rs748829089 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472143 | CTATTTTTTTTAAAC[C/T]GGGAAATATTAATTT | 51191 |
rs748836362 | snp | A/G | 1.65059e-05 | 0.00287275 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467220 | GTAAATTCTATAGGA[A/G]CATAGGGTTTGGCAT | 51191 |
rs748861254 | in-del | -/A | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473544 | CAGAACCACAGCCCC[-/A]CTGGGGGTCCGAGGT | 51191 |
rs748861994 | snp | A/G/T | 5.20701e-05 | 0.00510224 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459520 | TTAATCAAAAGACAA[A/G/T]AATAATTTCTGTAGG | 51191 |
rs748991107 | snp | A/G | 1.651e-05 | 0.0028731 | missense | HERC5 | GRCh38.p7 | 4:88504342 | ACGAAGACATTATCA[A/G]ATTATTCCACCCCGA | 51191 |
rs749105423 | in-del | -/TA | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485126 | AGAGCTCTGGGAAGG[-/TA]TATATTCTAACAAGC | 51191 |
rs749112031 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497850 | AGGCATTTCAGAGAT[C/T]ACTGGGGGCTGTCAC | 51191 |
rs749119503 | snp | C/G | 3.29489e-05 | 0.00405874 | missense | HERC5 | GRCh38.p7 | 4:88489250 | AGGCCCACGTTTGAT[C/G]TAACAGTCAGAAGGA | 51191 |
rs749133554 | snp | A/G | 1.7423e-05 | 0.00295147 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460144 | CAGATCACATGTGGA[A/G]ATTACCATTCTCTTG | 51191 |
rs749154082 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458322 | GTTAAGGCTTATGGG[C/T]TTTATGTTAGGCTGG | 51191 |
rs749154731 | in-del | -/TGTC | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481518 | TAATGTAGATAAATT[-/TGTC]TGTCCGTTTCTTTAT | 51191 |
rs749181028 | in-del | -/TTG | 1.65427e-05 | 0.00287595 | cds-indel | HERC5 | GRCh38.p7 | 4:88505906 | TCCAACAGCCTTATT[-/TTG]TTGTTGTTATCGTTG | 51191 |
rs749250245 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88493000 | GATGTATTATTTGCT[C/T]TGTTTCCTCAGGTTT | 51191 |
rs749295263 | snp | C/G | | | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506286 | ACAATGTTTGCATGA[C/G]TTGGCCTGAAGGGAT | 51191 |
rs749308081 | snp | A/G | 0.000736106 | 0.0191706 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457357 | CCCGCGAAGTCTCCG[A/G]GCGCACAGCTCTGGC | 51191 |
rs749313128 | snp | A/G | 0.000247217 | 0.0111152 | intron-variant | HERC5 | GRCh38.p7 | 4:88475837 | TGTTCCTTTCTGACC[A/G]CAGATAACCACCTGC | 51191 |
rs749371253 | in-del | -/AA | 2.17896e-05 | 0.00330065 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460073 | TATGGTGATTAACAC[-/AA]AGTGTATTTTCCTTC | 51191 |
rs749403305 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463930 | CAGAATGAGCTAAGA[A/C]CCTGTTTGGTGGCTG | 51191 |
rs749408301 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465175 | TCGCCTTGACCCCTC[A/G]GAGTGTTGGGATTAC | 51191 |
rs749426686 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470219 | TAAGATGAAACTGAG[A/C]ATACTCCTTCCCCCA | 51191 |
rs749471663 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88493433 | CTTTTTTAGGTACTC[A/G]TTCTTTGTGTCAGTT | 51191 |
rs749501001 | snp | A/G | 1.66123e-05 | 0.00288199 | intron-variant | HERC5 | GRCh38.p7 | 4:88486253 | GCATGTTTAAAGGGG[A/G]AAATTGATAATCAGT | 51191 |
rs749511746 | snp | G/T | 2.05615e-05 | 0.0032063 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457507 | GTTCACCAGCTGCTC[G/T]CCGGGAGCGGCGGCG | 51191 |
rs749594681 | in-del | -/GAG | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497297 | AAGGGCTCAGAAGAA[-/GAG]GAGACCTCTAGAGAA | 51191 |
rs749614165 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494806 | CCAAGAAGGCAACCT[C/G]GCAAAGAAGCAATAG | 51191 |
rs749646313 | snp | C/G | 0.00010495 | 0.00724321 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469281 | CCCCACAGTCTGACT[C/G]TCTGCTTATATATCA | 51191 |
rs749652923 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478582 | TTTTATTGTTGTTAA[A/G]TAAGTAGATGTTAGC | 51191 |
rs749689788 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462902 | ATTTCTCATGATCCC[A/G]AACAACTCATTAAGA | 51191 |
rs749695511 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495286 | GGCATGATGGCTTAT[A/C]CCTGTAATCCCAGCA | 51191 |
rs749704194 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480186 | TTTCGGGATAATCAT[C/T]CCCTTGCTCTTACTA | 51191 |
rs749716501 | in-del | -/A | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500077 | TGTCAACTTTTACTT[-/A]AAAAAAAAAACCTGA | 51191 |
rs749748925 | snp | G/T | 3.96346e-05 | 0.00445148 | missense | HERC5 | GRCh38.p7 | 4:88505870 | AACAACAACAGAGGA[G/T]TTGGCTGACCAGCTT | 51191 |
rs749753514 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501601 | CACATCTTTTTCCAC[A/G]ATTTCTTAATCTTTT | 51191 |
rs749753634 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501127 | GGTGTGTGTTGTATG[-/T]TGTTTTGACATATAT | 51191 |
rs749754680 | snp | A/G | 4.95405e-05 | 0.00497673 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88493155 | GTGGTTTCCTGTCAA[A/G]GTAAGTTCCCTCTTC | 51191 |
rs749818689 | snp | C/G | 1.65594e-05 | 0.0028774 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462234 | TTGTGGAGCACCTCG[C/G]AGGAGTACCCTTGGC | 51191 |
rs749837998 | snp | C/T | 1.69499e-05 | 0.00291112 | missense | HERC5 | GRCh38.p7 | 4:88505775 | GAGACCCTATAAGAG[C/T]ACTGACATGTTTCAG | 51191 |
rs749867961 | snp | A/T | 1.65192e-05 | 0.00287391 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88470650 | ATCTCCTGCTTGTCT[A/T]ACTGGAAGTTTTTTA | 51191 |
rs749884954 | snp | C/T | 1.65373e-05 | 0.00287548 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463631 | TCACACAGGTGGGTG[C/T]ACCCTTGTCTCTTTT | 51191 |
rs749950989 | in-del | -/ACT | 1.71905e-05 | 0.00293172 | cds-indel, intron-variant | HERC5 | GRCh38.p7 | 4:88487146 | TCTGTCGAAAATTAA[-/ACT]ACTACATACAGACAC | 51191 |
rs750020276 | in-del | -/TGAGGGCTGTGAGGGGTGAGGGC | 0.00103252 | 0.0226979 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457562 | GGTGTGTGAGGGCTG[-/TGAGGGCTGTGAGGGGTGAGGGC]TGAGGGCTGTGAGGG | 51191 |
rs750051380 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466582 | GGTTACCTCCTAGGA[A/G]CAGGGCACCAGCCAG | 51191 |
rs750066872 | snp | G/T | 1.64852e-05 | 0.00287094 | missense | HERC5 | GRCh38.p7 | 4:88479433 | GTCATATGCCAGTTG[G/T]ATTACTGGGATGAAA | 51191 |
rs750110923 | in-del | -/AGAT | 1.64746e-05 | 0.00287002 | frameshift-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463970 | GGTATAGAGTGACTC[-/AGAT]AGCATGTGGAAGGTA | 51191 |
rs750222594 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489725 | TGCAATAACCTAAAT[C/T]GGGACAGGCATGGTG | 51191 |
rs750283371 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88505067 | TTATTTTTGTGGATA[A/G]CATGTATGTTAGAAG | 51191 |
rs750307083 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473487 | TCTCATTCGCTCCTT[C/T]CTTTCAAGGAAAGAT | 51191 |
rs750338408 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490824 | CACTCTAGCCTGGGC[A/G]ACAGAGCAAGATTCT | 51191 |
rs750355148 | snp | C/T | 1.82941e-05 | 0.00302435 | missense | HERC5 | GRCh38.p7 | 4:88504591 | GAAGAAAAGAAAAAA[C/T]TCCTTGGTAAGTATT | 51191 |
rs750369071 | snp | A/G | 1.67209e-05 | 0.00289139 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469242 | ATGTGGAGACTAAAC[A/G]GTGGCAGAGCACAAA | 51191 |
rs750381278 | snp | A/C/G | 3.59391e-05 | 0.00423892 | missense, synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460113 | TGAAAGCATTTTACA[A/C/G]GAAAAAAAAATAATT | 51191 |
rs750432822 | snp | C/T | 6.60589e-05 | 0.00574675 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504328 | TTATAAAATGTGCGA[C/T]GAAGACATTATCAAA | 51191 |
rs750445969 | snp | A/T | 1.64749e-05 | 0.00287005 | stop-gained | HERC5 | GRCh38.p7 | 4:88475908 | CACCCCAAGAAGCTT[A/T]AGAAATTTTCTTCCT | 51191 |
rs750469669 | snp | A/G | 1.83707e-05 | 0.00303068 | missense | HERC5 | GRCh38.p7 | 4:88505704 | TGACAGACTACAAAT[A/G]AAAGATTTAAATAAT | 51191 |
rs750518598 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500403 | CTTTATTCTTCACAT[A/G]GTGGCCTTAGGGTTA | 51191 |
rs750524329 | in-del | -/AT | 1.8105e-05 | 0.00300868 | frameshift-variant, intron-variant | HERC5 | GRCh38.p7 | 4:88487174 | GACACACTTTTAAAA[-/AT]AGAGGTATGTATGCC | 51191 |
rs750528125 | in-del | -/TTG | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478572 | GTATTAGGGATTTTA[-/TTG]TTGTTAAATAAGTAG | 51191 |
rs750541819 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496505 | CCCATGCCTATGTGG[A/T]ACTTTATTAGAGGTG | 51191 |
rs750575617 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486758 | TGTTATATCATTCTC[C/T]GTTTATCAAATGCAA | 51191 |
rs750581308 | snp | C/T | 0.000180717 | 0.009504 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462119 | ATAAAACAGCATTTG[C/T]TTTGTTTATGTCAAG | 51191 |
rs750676191 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487536 | GCTTGACTAGCACCT[A/T]TGTAAGGAGGCACAA | 51191 |
rs750691497 | snp | A/C | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469901 | TCCAGGCCTCTGTTT[A/C]TGTATATTGTGACTC | 51191 |
rs750700319 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88493095 | TGCAGAGATGATCCA[A/G]CCGGAATATGGGATG | 51191 |
rs750720998 | snp | A/C | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467134 | AGATGGACAACTGGG[A/C]AATGGTGGAACACGT | 51191 |
rs750735560 | snp | C/T | 0.000129946 | 0.00805954 | stop-gained, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457489 | GGCGGGGCGGGCGTC[C/T]AGGTTCACCAGCTGC | 51191 |
rs750823444 | snp | A/G | 1.64876e-05 | 0.00287116 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464000 | GGTAAGTTGTAAAGT[A/G]TCAATAAGAATTGAT | 51191 |
rs750826517 | snp | C/G | 1.68803e-05 | 0.00290515 | intron-variant | HERC5 | GRCh38.p7 | 4:88500034 | GATTAGTTTTAATCT[C/G]ATTAACCCTTTACAT | 51191 |
rs750904209 | in-del | -/G | 1.75157e-05 | 0.00295932 | intron-variant | HERC5 | GRCh38.p7 | 4:88504206 | GATATTGCAGTAAGT[-/G]GAAATAACATTTTGT | 51191 |
rs751004347 | snp | A/T | 1.68989e-05 | 0.00290674 | splice-donor-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462358 | GGGCCACACTGAGAG[A/T]ATGGAACACATTCTC | 51191 |
rs751020170 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492930 | CACAATTAATGTTAG[C/G]TATTTACTATTATTA | 51191 |
rs751031685 | snp | G/T | 1.65971e-05 | 0.00288067 | intron-variant | HERC5 | GRCh38.p7 | 4:88501000 | AGTAGGTACAAAAAA[G/T]GAAATAGTTGGTTTG | 51191 |
rs751044987 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483417 | CTAACTATGTTGCTC[A/T]GGCTGGTCTTGAGCT | 51191 |
rs751055364 | snp | C/G | 1.64991e-05 | 0.00287215 | missense | HERC5 | GRCh38.p7 | 4:88470626 | TAGGGAAATCCAAGA[C/G]ATATTTTCATCTCCT | 51191 |
rs751116510 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494463 | ACCAGTTTTAACTTT[A/G]ACAAGAATTGTTGGA | 51191 |
rs751122057 | in-del | -/AA | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455966 | AATAAATAAATGGTC[-/AA]AAGATTTGAATACAC | 51191 |
rs751171705 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479204 | GCAGGAGAATTGCTT[A/G]AACCTGGGAGGCAGA | 51191 |
rs751174030 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481384 | TTAGTGCTTACAAGA[A/G]TTCTTTCTATTTTGG | 51191 |
rs751206373 | snp | A/G | 0.000322026 | 0.012685 | intron-variant | HERC5 | GRCh38.p7 | 4:88493204 | CGACAGAAAAAGTAC[A/G]CCATATACCATAGAA | 51191 |
rs751270068 | snp | A/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464756 | GCCACAACTGGCTAA[A/T]TTTTAAATTTTATTT | 51191 |
rs751272883 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463911 | ACTTGGTCATAATTC[A/G]ACACAGAATGAGCTA | 51191 |
rs751293985 | snp | A/G | 1.833e-05 | 0.00302732 | missense | HERC5 | GRCh38.p7 | 4:88505846 | GAAGAAGCGCTTCAA[A/G]AAGCCATCAACAACA | 51191 |
rs751343604 | snp | A/T | 1.64806e-05 | 0.00287054 | missense | HERC5 | GRCh38.p7 | 4:88494231 | TCCCTGTTCAATTGC[A/T]ATGTTGCCAACCTTC | 51191 |
rs751344156 | snp | C/G | 1.64871e-05 | 0.00287111 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88479420 | GTTTAAAACAGCCGT[C/G]ATATGCCAGTTGGAT | 51191 |
rs751357880 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502238 | GGAGAAGTGCTTGGT[C/G]CCTTGTGGTTGCCCC | 51191 |
rs751379978 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461130 | AGAATCTGGGATTCA[A/G]GGGAAGTTAATAATT | 51191 |
rs751454598 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465341 | TTTTCCCTCACTAAA[C/T]GTAGAGCAAAATTCA | 51191 |
rs751457431 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487980 | ATAATATTCAAATAT[A/G]TGTCCTTAAAGCAGA | 51191 |
rs751510218 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471731 | ACTTTATATTGAAGT[A/T]CTAAGAAATTATTGG | 51191 |
rs751510594 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489607 | TGGCCCTAAGAGGTC[C/T]AGTCCCTTCTGAGGT | 51191 |
rs751540435 | snp | C/T | 1.77332e-05 | 0.00297763 | intron-variant | HERC5 | GRCh38.p7 | 4:88479556 | TCTAGCTGTAAAAAT[C/T]CCCTTCCTTTCAGCT | 51191 |
rs751643701 | snp | C/T | 5.09187e-05 | 0.00504547 | intron-variant | HERC5 | GRCh38.p7 | 4:88504455 | TAAATTCAGTTTTCC[C/T]TCCTATTTCCTCAAT | 51191 |
rs751671079 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494485 | ATTGTTGGATGATAA[-/T]TTCGTTTTCTAAAAT | 51191 |
rs751691739 | in-del | -/TTTAAA | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484171 | TACTCGAATTTGTTC[-/TTTAAA]TTTAGTTTCTTGCTC | 51191 |
rs751703947 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant | HERC5 | GRCh38.p7 | 4:88475798 | TTGCACCCTGCTTCT[A/G]CTGAGTTTTGAATCC | 51191 |
rs751737341 | snp | C/G | 1.74406e-05 | 0.00295296 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468466 | ACCTGGTATTTTAAG[C/G]AAAACTAAGGGTTCT | 51191 |
rs751737428 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497558 | TTGGCAGAAGCAATC[G/T]CTAAGCAAAGTGGTA | 51191 |
rs751750069 | snp | A/G | 1.66657e-05 | 0.00288662 | intron-variant | HERC5 | GRCh38.p7 | 4:88492969 | TTCATATATAGCAAT[A/G]TAGAGCCCTGGAAGT | 51191 |
rs751834219 | in-del | -/AA | 1.68761e-05 | 0.00290478 | intron-variant | HERC5 | GRCh38.p7 | 4:88504441 | AAGTCTAAGTTGATT[-/AA]ATTCAGTTTTCCTTC | 51191 |
rs751863114 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474255 | ATATTTTTGGATGAA[C/T]TGAGTCATTATTAGG | 51191 |
rs751883222 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463880 | TGTTTACTTTCGGTG[C/G]TGGAAAACATGGGCA | 51191 |
rs751977442 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475897 | ATTTCATTCTCCACC[C/T]CAAGAAGCTTTAGAA | 51191 |
rs751988901 | snp | A/G | 1.6722e-05 | 0.00289149 | intron-variant | HERC5 | GRCh38.p7 | 4:88500013 | TAACAATAAAAGCAG[A/G]TAACAGATTAGTTTT | 51191 |
rs751996660 | snp | A/C | 1.64849e-05 | 0.00287092 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463997 | GAAGGTAAGTTGTAA[A/C]GTATCAATAAGAATT | 51191 |
rs752033370 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486648 | GGTAGCAGTTGACCC[A/G]AAGTGTTTCTCCCTT | 51191 |
rs752148971 | snp | A/C/T | 3.43149e-05 | 0.00414204 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469267 | CACAAAAAGGTACAC[A/C/T]CCACAGTCTGACTCT | 51191 |
rs752182626 | snp | C/T | 1.65367e-05 | 0.00287543 | splice-donor-variant, intron-variant | HERC5 | GRCh38.p7 | 4:88486230 | GGAAAATGACTGTGG[C/T]AGGTATAGCATGTTT | 51191 |
rs752197681 | snp | A/T | 2.3079e-05 | 0.0033969 | intron-variant | HERC5 | GRCh38.p7 | 4:88487045 | CCTTTAACTTATCAG[A/T]ATTATTGTCATTTCC | 51191 |
rs752283704 | snp | A/T | 3.29723e-05 | 0.00406018 | missense | HERC5 | GRCh38.p7 | 4:88500952 | CAAACTTAATTCCTA[A/T]TGGAAGTAGCATAAC | 51191 |
rs752306776 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491219 | TTCACCAAGAGGAAT[G/T]GAAGAGGCAGCATCT | 51191 |
rs752345242 | snp | A/G | 1.64963e-05 | 0.00287192 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88470617 | TTACTAATATAGGGA[A/G]ATCCAAGAGATATTT | 51191 |
rs752346083 | snp | A/G | 1.70831e-05 | 0.00292254 | stop-gained | HERC5 | GRCh38.p7 | 4:88505751 | GCTGTCCTGAAAGTT[A/G]GAATGAAAGAGACCC | 51191 |
rs752355965 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492685 | CAGGAGGCGGAGGTT[A/G]CAGTGAGCCGAGATC | 51191 |
rs752399699 | in-del | -/AGGCTG | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495456 | GAGGCACACCTCAGA[-/AGGCTG]AGGCAGGTGGATAGA | 51191 |
rs752411073 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88477682 | GTCCCACATCCAGAT[A/T]GTCTGACCGTTTCCT | 51191 |
rs752447516 | snp | A/G | 1.66078e-05 | 0.00288161 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463528 | TATTTTTTTCCTTAC[A/G]TAGGTAAAGATGATC | 51191 |
rs752493374 | snp | C/T | | | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462285 | CCCACAGCATGGCCT[C/T]ATCCATGTCTGGCAA | 51191 |
rs752508110 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455434 | GAAGACTTCTTGCTC[A/T]TCCCTGCTGCATAAG | 51191 |
rs752546199 | snp | C/T | 1.80062e-05 | 0.00300046 | missense | HERC5 | GRCh38.p7 | 4:88505838 | AAACAGTTGAAGAAG[C/T]GCTTCAAGAAGCCAT | 51191 |
rs752557460 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492302 | AGCCACCACGCCCGG[C/T]CAATTTTTATGATTT | 51191 |
rs752649629 | snp | C/T | | | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463605 | TTGTGGTGGCTCTCA[C/T]AGTGCCCTACTCACA | 51191 |
rs752653353 | snp | A/C | 1.81082e-05 | 0.00300895 | intron-variant | HERC5 | GRCh38.p7 | 4:88479316 | AAGCACAATAAAACT[A/C]ATTTTTTAAAAAATT | 51191 |
rs752705019 | snp | C/T | 1.70081e-05 | 0.00291612 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459340 | CCTGGTTGGATTTGC[C/T]CTGTAGAATGCATTA | 51191 |
rs752742355 | snp | A/G | 1.66996e-05 | 0.00288956 | intron-variant | HERC5 | GRCh38.p7 | 4:88493196 | GTATTTTGCGACAGA[A/G]AAAGTACACCATATA | 51191 |
rs752834709 | snp | C/G | | | upstream-variant-2KB, missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457088 | CGCCCCCAAACAGCA[C/G]GTGGGGGGCGTGGCG | 51191 |
rs752836833 | snp | C/T | 1.71047e-05 | 0.00292439 | intron-variant | HERC5 | GRCh38.p7 | 4:88489153 | TGTAATATTTCTGTT[C/T]CTGTTTTCCTAGAGT | 51191 |
rs752839723 | snp | A/C | 3.29489e-05 | 0.00405874 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467174 | ATGCCGCTTCCAGTG[A/C]AAGTATCATCAAGTG | 51191 |
rs752839887 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473258 | TCTCCATTTTTTTCT[C/T]TCTGGGTCGCACTGT | 51191 |
rs752848714 | snp | G/T | 1.64923e-05 | 0.00287156 | missense | HERC5 | GRCh38.p7 | 4:88479408 | ACTGGTCCAGATGTT[G/T]AAAACAGCCGTCATA | 51191 |
rs752899204 | snp | C/G | 3.32729e-05 | 0.00407864 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459447 | ACCATTTGAGTATGA[C/G]AACTATAGCATGAAA | 51191 |
rs752988739 | snp | A/C | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459843 | ATATGAATTAGAACT[A/C]ATTTTCATCTTGCAT | 51191 |
rs753034336 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88505613 | AATAGATTTTTTTCT[C/T]TGTAAAGAGATTTTG | 51191 |
rs753049034 | snp | C/T | 1.6601e-05 | 0.00288101 | intron-variant | HERC5 | GRCh38.p7 | 4:88472549 | ATACACCAGAATATT[C/T]CTTAAAAGAACTCAA | 51191 |
rs753052752 | in-del | -/A | 1.64866e-05 | 0.00287106 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467207 | GAACTCAAACTTGGT[-/A]AATTCTATAGGAACA | 51191 |
rs753133847 | snp | G/T | 1.6477e-05 | 0.00287024 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489222 | GGAAGAAAGAGAGTC[G/T]GAATTCGCTTTGAGG | 51191 |
rs753228414 | in-del | -/AGGT | 1.7051e-05 | 0.0029198 | splice-donor-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459469 | AGCATGAAACATCTA[-/AGGT]AGGGAACTTTTTTCT | 51191 |
rs753255642 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | HERC5 | GRCh38.p7 | 4:88475880 | CTGCTCAAAAGACTT[C/T]CATTTCATTCTCCAC | 51191 |
rs753349675 | snp | A/G | 1.76111e-05 | 0.00296736 | intron-variant | HERC5 | GRCh38.p7 | 4:88494375 | CCCTTTCTAACATAT[A/G]TTTAGGCAAATATTT | 51191 |
rs753414690 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466940 | ATGATTTTCATCCTC[C/T]AAGAGATGTTTAGTT | 51191 |
rs753422617 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503695 | CATAGTGTATCTTTT[G/T]CCCTTCTTTGACTTT | 51191 |
rs753444883 | snp | G/T | 1.64787e-05 | 0.00287038 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463851 | TGACATTCCCTTTCC[G/T]TAGGATGGGCTGCTG | 51191 |
rs753455544 | snp | A/G | 1.64928e-05 | 0.00287161 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486207 | AGAAGTATGCAGAAG[A/G]TACTTGTGGAAAATG | 51191 |
rs753467776 | snp | A/T | | | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467816 | CTCTGAAACACTCCA[A/T]TGTAGAAGCACCTTG | 51191 |
rs753495657 | snp | G/T | 0.000389087 | 0.0139425 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469141 | TATTGTATTTTACTT[G/T]CCTGTTTGTTTACAG | 51191 |
rs753513671 | snp | A/G | 1.79832e-05 | 0.00299854 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462156 | AGCTTTTTGCCTGGG[A/G]ACAGAACCTGCATGG | 51191 |
rs753543501 | snp | C/T | 1.78423e-05 | 0.00298678 | intron-variant | HERC5 | GRCh38.p7 | 4:88486087 | TCTTTAAATATAAAA[C/T]TTTTTCACAAGTCAT | 51191 |
rs753545690 | snp | A/G | 1.65905e-05 | 0.0028801 | missense | HERC5 | GRCh38.p7 | 4:88499990 | TTTTACATCCATTTT[A/G]ATGTGAGTAACAATA | 51191 |
rs753593835 | snp | A/G | 1.6788e-05 | 0.00289719 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469248 | AGACTAAACGGTGGC[A/G]GAGCACAAAAAGGTA | 51191 |
rs753599467 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487783 | TTTACCACCAAAGTA[A/G]TAAAATTGGGCAATT | 51191 |
rs753618416 | snp | C/T | 4.94295e-05 | 0.00497115 | missense | HERC5 | GRCh38.p7 | 4:88475869 | TCAAAGATAATCTGC[C/T]CAAAAGACTTCCATT | 51191 |
rs753695435 | snp | A/G | 1.98344e-05 | 0.00314909 | intron-variant | HERC5 | GRCh38.p7 | 4:88504609 | CTTGGTAAGTATTAT[A/G]TCAAGGAATAGATCT | 51191 |
rs753726190 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492465 | ATTTAGGCTGTAGGC[C/T]GGGTGTGGTGGCTCA | 51191 |
rs753797209 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462282 | AAGCCCACAGCATGG[C/T]CTTATCCATGTCTGG | 51191 |
rs753801454 | snp | A/T | 0.00229864 | 0.0338236 | intron-variant | HERC5 | GRCh38.p7 | 4:88479309 | AAAAAAAAAGCACAA[A/T]AAAACTCATTTTTTA | 51191 |
rs753832149 | snp | A/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467245 | TGGCATAGTATCTTT[A/T]TAGAGAAAATGATTT | 51191 |
rs753859865 | snp | A/G | 1.65108e-05 | 0.00287317 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464025 | ATTGATAAAATGAGT[A/G]CAGCAAACTAGATAG | 51191 |
rs753872945 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470157 | GCACAAAATAGTTGC[A/G]TCATAATTTGCAGAG | 51191 |
rs753903126 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502156 | GACTATTATGAATAA[C/T]GCTCTTGTGAACATT | 51191 |
rs753907822 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487636 | GGCTACTACTCTGTG[A/C]TGGTGCCATAAAAGA | 51191 |
rs753940402 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486908 | TTTCATTGATACATA[C/T]AAAACACATTTTCTA | 51191 |
rs753955360 | snp | A/G | 1.67211e-05 | 0.00289142 | intron-variant | HERC5 | GRCh38.p7 | 4:88501021 | AGTTGGTTTGTATAT[A/G]TACTATTTTTATTTT | 51191 |
rs753957699 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471537 | TAAAGACAGCAGCTT[G/T]GCTATGTTGCCCAGG | 51191 |
rs753979561 | snp | A/G | 1.65168e-05 | 0.00287369 | missense | HERC5 | GRCh38.p7 | 4:88476024 | GACCAGTCTTCACTG[A/G]TTCTGGGTAAGTTTG | 51191 |
rs754059043 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467148 | GAAATGGTGGAACAC[A/G]TGACCAGCTGATGCC | 51191 |
rs754094395 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473136 | CAGTGGTGCGATCTC[A/G]GCTTACTGCATGCTT | 51191 |
rs754126010 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455307 | TAGGCATGTGAATAC[A/T]TTGCAAGGTGAAGAG | 51191 |
rs754165352 | snp | C/T | 1.65518e-05 | 0.00287674 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459433 | TCATCAGATGGAAAA[C/T]CATTTGAGTATGACA | 51191 |
rs754227812 | in-del | -/CT | 3.4805e-05 | 0.00417149 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469279 | CACCCCACAGTCTGA[-/CT]CTCTGCTTATATATC | 51191 |
rs754231341 | snp | C/G | 1.65318e-05 | 0.002875 | missense | HERC5 | GRCh38.p7 | 4:88504302 | GTTTATGAAGAATTT[C/G]GGAGAGGATTTTATA | 51191 |
rs754254407 | in-del | -/TTCA | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461226 | AATTGATCATTTGAC[-/TTCA]TTCATTCATGAACAA | 51191 |
rs754255221 | snp | C/T | 1.71976e-05 | 0.00293232 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459325 | AAAGTGACAATAGTT[C/T]CTGGTTGGATTTGCT | 51191 |
rs754262723 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497022 | GGGTCGTCACCTATT[A/C]CCTTTAGATTCAGAC | 51191 |
rs754282551 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495924 | ATTGTTTCTCAAACT[G/T]TTAGGTCTTAAGATT | 51191 |
rs754304407 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482116 | GGAGTTCAAGACCAG[C/T]CTGACCAACATAGTG | 51191 |
rs754357857 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483581 | TTGCTCAGGCTGGAG[C/T]GCAGTGGCACGATCT | 51191 |
rs754363045 | snp | A/G | 1.6483e-05 | 0.00287076 | missense | HERC5 | GRCh38.p7 | 4:88489208 | TCGGCAGCAATTGAG[A/G]AAGAAAGAGAGTCTG | 51191 |
rs754391072 | in-del | -/ATAAT | 8.31871e-05 | 0.00644877 | intron-variant | HERC5 | GRCh38.p7 | 4:88486260 | TAAAGGGGGAAATTG[-/ATAAT]CAGTGAGTTAATACA | 51191 |
rs754478218 | snp | A/T | 3.53419e-05 | 0.00420354 | intron-variant | HERC5 | GRCh38.p7 | 4:88486089 | TTTAAATATAAAACT[A/T]TTTCACAAGTCATAT | 51191 |
rs754550903 | snp | A/T | 1.7433e-05 | 0.00295232 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460145 | AGATCACATGTGGAG[A/T]TTACCATTCTCTTGC | 51191 |
rs754553147 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88505310 | GCATAATTCTGAACT[C/G]TTGGAAATCCCCTCA | 51191 |
rs754632535 | snp | G/T | 1.78134e-05 | 0.00298436 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469148 | TTTTACTTTCCTGTT[G/T]GTTTACAGAATTCAT | 51191 |
rs754788369 | snp | C/T | 1.77492e-05 | 0.00297898 | missense | HERC5 | GRCh38.p7 | 4:88505721 | AAGATTTAAATAATA[C/T]GAAAATAACATTTTG | 51191 |
rs754802437 | snp | C/T | 1.65187e-05 | 0.00287386 | missense | HERC5 | GRCh38.p7 | 4:88476025 | ACCAGTCTTCACTGG[C/T]TCTGGGTAAGTTTGA | 51191 |
rs754833853 | in-del | -/AT | 1.70907e-05 | 0.00292319 | intron-variant | HERC5 | GRCh38.p7 | 4:88489386 | TGAGAAAAGAAAAAC[-/AT]AAAAGAATGTGGCAA | 51191 |
rs754890021 | snp | A/C | 1.64754e-05 | 0.00287009 | missense | HERC5 | GRCh38.p7 | 4:88493114 | GAATATGGGATGTTC[A/C]TGTATCCTGAAGGGG | 51191 |
rs754912842 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499762 | TGACATGTTTAGTTG[A/G]GGTCTGGCCCTGTTT | 51191 |
rs755027453 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487657 | CCATAAAAGAGGTTT[A/G]TACAGATTCCTCCCT | 51191 |
rs755068107 | snp | A/T | 5.38112e-05 | 0.00518678 | intron-variant | HERC5 | GRCh38.p7 | 4:88479311 | AAAAAAAGCACAATA[A/T]AACTCATTTTTTAAA | 51191 |
rs755115909 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465342 | TTTCCCTCACTAAAC[A/G]TAGAGCAAAATTCAG | 51191 |
rs755135564 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467406 | TATATTACTCCTTCA[A/G]ATTAGGATTAATGTG | 51191 |
rs755136527 | in-del | -/C | 3.41012e-05 | 0.0041291 | intron-variant | HERC5 | GRCh38.p7 | 4:88504473 | CTATTTCCTCAATAA[-/C]TTTTTTTTGTATTTT | 51191 |
rs755146276 | snp | C/T | 1.71399e-05 | 0.0029274 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459330 | GACAATAGTTCCTGG[C/T]TGGATTTGCTCTGTA | 51191 |
rs755162025 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455366 | AAACAAGGAGGGTCC[G/T]GCCAACAGGCTCCCA | 51191 |
rs755192370 | snp | A/T | 1.71443e-05 | 0.00292777 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88487100 | TACAATGCTGCGTCA[A/T]ATTCAGTCACTTTCC | 51191 |
rs755205666 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501288 | TATCACACATTACCT[A/G]CCTTTAGGGTTTATT | 51191 |
rs755237879 | snp | C/T | 4.94205e-05 | 0.0049707 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467163 | GTGACCAGCTGATGC[C/T]GCTTCCAGTGAAAGT | 51191 |
rs755238030 | snp | C/G | 0.000165741 | 0.00910182 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457509 | TCACCAGCTGCTCGC[C/G]GGGAGCGGCGGCGCC | 51191 |
rs755252956 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496032 | TAAATATTTTAAACA[C/T]AGGAATACACAAATA | 51191 |
rs755256004 | snp | A/G | 1.68556e-05 | 0.00290302 | intron-variant | HERC5 | GRCh38.p7 | 4:88501032 | ATATGTACTATTTTT[A/G]TTTTACTGAGCTCTA | 51191 |
rs755340399 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482154 | GTCTCTACTAAAAAT[A/G]CAAAAGTTAGCTGGG | 51191 |
rs755344537 | in-del | -/GTGAGGG | 0.000620155 | 0.0175981 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457569 | AGGGCTGTGAGGGCT[-/GTGAGGG]GTGAGGGGTGAGGGC | 51191 |
rs755388589 | snp | A/C | 7.01311e-05 | 0.0059212 | intron-variant | HERC5 | GRCh38.p7 | 4:88489121 | TTTACTTAGAGAGGG[A/C]CAATGGTAAAATGAA | 51191 |
rs755474468 | snp | A/G | 1.65021e-05 | 0.00287241 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463567 | ATTGAAGGACTAGAC[A/G]ATCAGAAAGTTGAAT | 51191 |
rs755513470 | snp | A/G | 2.02571e-05 | 0.00318247 | missense | HERC5 | GRCh38.p7 | 4:88505874 | ACAACAGAGGATTTG[A/G]CTGACCAGCTTGCTT | 51191 |
rs755538110 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465689 | TTAATGCACATCAGG[A/G]CAATACCCCTACTAA | 51191 |
rs755587880 | snp | C/G | 1.64996e-05 | 0.0028722 | missense | HERC5 | GRCh38.p7 | 4:88472429 | CTACAGAAATGATGC[C/G]TGTTTATTTGGACTT | 51191 |
rs755595031 | snp | C/T | 4.96282e-05 | 0.00498113 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463633 | ACACAGGTGGGTGTA[C/T]CCTTGTCTCTTTTTG | 51191 |
rs755613359 | snp | A/C | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465615 | TTGGATTCTTCATTA[A/C]ATACAGTCCTTTTGA | 51191 |
rs755614466 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464381 | GTGGCCAACATACTT[C/T]TTAATTACCAGAGTT | 51191 |
rs755655857 | snp | A/C | 1.64961e-05 | 0.00287189 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468372 | TCAGAAAAGGAGTTA[A/C]TAATGATTGCTGGAG | 51191 |
rs755697075 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502495 | TGCAACCCAGAGCAT[A/G]CGTGGGGAAATTTAA | 51191 |
rs755715949 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487424 | TGGCCTAGTTGTCGG[G/T]TTTTTACCTGAAGTT | 51191 |
rs755743691 | snp | A/T | 3.29696e-05 | 0.00406001 | missense | HERC5 | GRCh38.p7 | 4:88479434 | TCATATGCCAGTTGG[A/T]TTACTGGGATGAAAG | 51191 |
rs755781516 | snp | C/G | 1.73667e-05 | 0.0029467 | intron-variant | HERC5 | GRCh38.p7 | 4:88494370 | AAGGACCCTTTCTAA[C/G]ATATATTTAGGCAAA | 51191 |
rs755844063 | in-del | -/C | 1.70764e-05 | 0.00292197 | frameshift-variant | HERC5 | GRCh38.p7 | 4:88504531 | TATAACAGTTCACAT[-/C]CCACCATAGTGATGT | 51191 |
rs755895776 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503676 | TCATTTTGGTTGATG[G/T]TTGCATAGTGTATCT | 51191 |
rs755909096 | snp | G/T | 6.80492e-05 | 0.00583266 | intron-variant | HERC5 | GRCh38.p7 | 4:88504461 | CAGTTTTCCTTCCTA[G/T]TTCCTCAATAACTTT | 51191 |
rs755945792 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473602 | ATTGGGACCCTACAA[C/T]ACTTAGTGCTGCCTG | 51191 |
rs755946171 | snp | C/T | 1.66098e-05 | 0.00288177 | intron-variant | HERC5 | GRCh38.p7 | 4:88492984 | ATAGAGCCCTGGAAG[C/T]GATGTATTATTTGCT | 51191 |
rs756034225 | snp | C/T | 1.87278e-05 | 0.00305999 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504596 | AAAGAAAAAATTCCT[C/T]GGTAAGTATTATATC | 51191 |
rs756069557 | snp | A/T | 0.000115254 | 0.00759037 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462126 | AGCATTTGCTTTGTT[A/T]ATGTCAAGGTGGTGA | 51191 |
rs756100413 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485696 | TCATATGGGATGGAG[A/G]GTTGGAAAATTTCCT | 51191 |
rs756106887 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458188 | ATGGAAGAGGTATTT[A/G]AATATTGAATAAGAA | 51191 |
rs756180608 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475933 | CTTCCTTCTCCCAGA[A/G]TGTCCTATGATGCAT | 51191 |
rs756251623 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496933 | AGAATTCATTCCCCT[A/G]TGAAAGAGGCCCAAG | 51191 |
rs756269089 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500631 | TGTAAATCTACCATA[C/G]TGGGTCTATGCTGTA | 51191 |
rs756270691 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468577 | TTATTGTCTAAACTA[C/T]ATCAGTATTTTCCCA | 51191 |
rs756309773 | snp | A/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462082 | AATGCTTTAGGGTAA[A/T]GTCTGCTGCATTTTA | 51191 |
rs756320554 | snp | C/T | 5.90458e-05 | 0.00543318 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457342 | GCCGCCGCGACCCAG[C/T]CCGCGAAGTCTCCGG | 51191 |
rs756350549 | snp | A/G | 3.37393e-05 | 0.00410713 | intron-variant | HERC5 | GRCh38.p7 | 4:88500035 | ATTAGTTTTAATCTG[A/G]TTAACCCTTTACATA | 51191 |
rs756376700 | snp | C/G | 3.29946e-05 | 0.00406155 | missense | HERC5 | GRCh38.p7 | 4:88476014 | TAAAATGAGTGACCA[C/G]TCTTCACTGGTTCTG | 51191 |
rs756431103 | snp | C/T | 1.65671e-05 | 0.00287807 | intron-variant | HERC5 | GRCh38.p7 | 4:88486239 | CTGTGGTAGGTATAG[C/T]ATGTTTAAAGGGGGA | 51191 |
rs756449535 | snp | G/T | 0.000127787 | 0.00799233 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457492 | GGGGCGGGCGTCCAG[G/T]TTCACCAGCTGCTCG | 51191 |
rs756487030 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494693 | TAAGTTAAAAGACAA[A/G]CCACCACCTCACCAA | 51191 |
rs756544897 | snp | A/G | 1.66405e-05 | 0.00288443 | intron-variant | HERC5 | GRCh38.p7 | 4:88501007 | ACAAAAAATGAAATA[A/G]TTGGTTTGTATATGT | 51191 |
rs756595934 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479597 | TTTAAGTAGACTCGT[G/T]TGAGACATACGAAGT | 51191 |
rs756624869 | in-del | -/GAC | 2.49116e-05 | 0.00352919 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459515 | TAATTTTAATCAAAA[-/GAC]AATAATAATTTCTGT | 51191 |
rs756633895 | in-del | -/T | 1.65503e-05 | 0.00287661 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467242 | GTTTGGCATAGTATC[-/T]TTTTAGAGAAAATGA | 51191 |
rs756681304 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495827 | TTACTGGAAACATCG[A/C]AGATAACCTAAATAA | 51191 |
rs756694449 | snp | C/T | 9.32236e-05 | 0.00682665 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88505851 | AGCGCTTCAAGAAGC[C/T]ATCAACAACAACAGA | 51191 |
rs756696421 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494469 | TTTAACTTTGACAAG[A/T]ATTGTTGGATGATAA | 51191 |
rs756708717 | snp | A/G | 1.65179e-05 | 0.00287379 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88472412 | TTTCTTCTACAGAAG[A/G]ACTACAGAAATGATG | 51191 |
rs756735015 | snp | C/T | 1.74698e-05 | 0.00295544 | stop-gained, intron-variant | HERC5 | GRCh38.p7 | 4:88487087 | GCTTCAGAAAATGTA[C/T]AATGCTGCGTCATAT | 51191 |
rs756765184 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478099 | ATGTTAAATTATTAG[C/T]AGTATTTTTTAATAG | 51191 |
rs756770241 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483822 | GGCATGAGCCATTGC[A/G]CCTGGCCTTCTATTA | 51191 |
rs756803870 | snp | C/T | 3.47126e-05 | 0.00416594 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462371 | AGTATGGAACACATT[C/T]TCAGATTCCTATTAC | 51191 |
rs756896848 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501477 | TATTTTGACTTCCCA[A/G]CATCTAATGGAATGC | 51191 |
rs756900772 | snp | C/T | 1.65214e-05 | 0.0028741 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463547 | GTAAAGATGATCCAT[C/T]CCTTATTGAAGGACT | 51191 |
rs757024586 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502276 | ATGCAGGCAGAATCA[A/G]TGCTCCTACCTGAAA | 51191 |
rs757050596 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488037 | ATAAAAATGGGAAAT[G/T]GATTTATGAGTTCTG | 51191 |
rs757091193 | snp | G/T | 1.84272e-05 | 0.00303534 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459487 | TAGGGAACTTTTTTC[G/T]TTTATTAAAAATTAA | 51191 |
rs757106083 | snp | C/T | 1.6486e-05 | 0.00287102 | missense | HERC5 | GRCh38.p7 | 4:88479424 | AAAACAGCCGTCATA[C/T]GCCAGTTGGATTACT | 51191 |
rs757110207 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465465 | CTTATGATCTTGGAG[C/T]AGAATTACATAAATG | 51191 |
rs757155310 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464856 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 51191 |
rs757193879 | in-del | -/ATG | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496576 | TGGAACTGGAAAAAA[-/ATG]ATATCTATCTGGGGA | 51191 |
rs757268042 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496387 | GAGAACTTGGTCTGT[C/G]AGCTATCAAGAATTA | 51191 |
rs757300259 | snp | A/C | 1.65064e-05 | 0.00287279 | splice-acceptor-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468344 | TTTGTGCATCCTTTC[A/C]GAAAGCCATACCTCA | 51191 |
rs757301857 | snp | C/G/T | 2.27327e-05 | 0.00337132 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460063 | TAACTTTCATTATGG[C/G/T]GATTAACACAAAGTG | 51191 |
rs757363165 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497639 | AGAATTATTTAAAGT[A/G]GAATTTATCATTAGA | 51191 |
rs757382529 | snp | A/C | 1.64749e-05 | 0.00287005 | missense | HERC5 | GRCh38.p7 | 4:88475899 | TTCATTCTCCACCCC[A/C]AGAAGCTTTAGAAAT | 51191 |
rs757389006 | in-del | -/T | 1.64746e-05 | 0.00287002 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469291 | GACTCTCTGCTTATA[-/T]TATCACTCTCAAGTA | 51191 |
rs757412670 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484348 | TGATTTGTGTATGTG[G/T]GAGAGCTGTCTGTTT | 51191 |
rs757465761 | snp | C/T | 5.00521e-05 | 0.00500236 | intron-variant | HERC5 | GRCh38.p7 | 4:88493192 | TAAGGTATTTTGCGA[C/T]AGAAAAAGTACACCA | 51191 |
rs757525016 | snp | A/C | 1.66707e-05 | 0.00288705 | intron-variant | HERC5 | GRCh38.p7 | 4:88492975 | TATAGCAATATAGAG[A/C]CCTGGAAGTGATGTA | 51191 |
rs757532227 | snp | G/T | 1.66746e-05 | 0.00288739 | intron-variant | HERC5 | GRCh38.p7 | 4:88499887 | TGTCTAGTGATCATG[G/T]TTATTACCTTTTTAA | 51191 |
rs757550987 | snp | A/T | 1.64923e-05 | 0.00287156 | intron-variant | HERC5 | GRCh38.p7 | 4:88475815 | TGAGTTTTGAATCCC[A/T]TTTCCCTGTTCCTTT | 51191 |
rs757556463 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474295 | GGTTAGCTCTTTTTA[C/G]TCAAAACAAGTTGCC | 51191 |
rs757574787 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463893 | TGCTGGAAAACATGG[C/G]CAACTTGGTCATAAT | 51191 |
rs757609063 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485634 | TATTCATTGTCTTCA[C/T]GACATGCCAGGGTGT | 51191 |
rs757683006 | in-del | -/A | 8.33083e-05 | 0.00645347 | intron-variant | HERC5 | GRCh38.p7 | 4:88486266 | GGGAAATTGATAATC[-/A]GTGAGTTAATACAGG | 51191 |
rs757685865 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471476 | CTTCCACGTAGCTGG[A/G]ACTACAGGCACGTGC | 51191 |
rs757720417 | snp | A/G | 1.65446e-05 | 0.00287612 | intron-variant | HERC5 | GRCh38.p7 | 4:88486232 | AAAATGACTGTGGTA[A/G]GTATAGCATGTTTAA | 51191 |
rs757731807 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469798 | AAATATCTTGGTACC[A/G]TGGCCTAGCCAAGTT | 51191 |
rs757780297 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475325 | CTTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 51191 |
rs757845281 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492957 | ATTAAATGAGACTTC[A/G]TATATAGCAATATAG | 51191 |
rs757905588 | snp | A/G | 8.02343e-05 | 0.0063333 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457275 | CAAAGCGGCGATGGA[A/G]CGGAGGTCGCGGAGG | 51191 |
rs757987321 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476097 | TGTCTAGTAAAGTTA[C/T]GGCAAAACTAAGATA | 51191 |
rs757995107 | snp | A/G | 1.65094e-05 | 0.00287305 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462317 | ATTTATTCATGGGGA[A/G]AAAATGAATGTGGAC | 51191 |
rs758016475 | snp | A/G | 5.11592e-05 | 0.00505737 | missense | HERC5 | GRCh38.p7 | 4:88505754 | GTCCTGAAAGTTGGA[A/G]TGAAAGAGACCCTAT | 51191 |
rs758084674 | snp | C/G | 1.67111e-05 | 0.00289055 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462210 | TTCCCTCAACCACCA[C/G]ACCACAGATTGTGGA | 51191 |
rs758181606 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88477701 | TGACCGTTTCCTATC[C/T]CTGTATTTCCAGTAC | 51191 |
rs758205592 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501156 | ATATCATGGAGTTTA[C/T]ATTGTGGTAAGGAAT | 51191 |
rs758213002 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460486 | GGGCCACCCTTTTCC[A/G]GAAACTGCTTCCCTT | 51191 |
rs758258292 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496047 | CAGGAATACACAAAT[A/G]TCTGTTAGCAGAGCA | 51191 |
rs758267111 | snp | C/G/T | 3.35043e-05 | 0.00409283 | intron-variant | HERC5 | GRCh38.p7 | 4:88493200 | TTTGCGACAGAAAAA[C/G/T]TACACCATATACCAT | 51191 |
rs758301850 | snp | A/G | 1.65166e-05 | 0.00287368 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463622 | GTGCCCTACTCACAC[A/G]GGTGGGTGTACCCTT | 51191 |
rs758337163 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486915 | GATACATATAAAACA[C/T]ATTTTCTACTACTGG | 51191 |
rs758368305 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488606 | TCTGTCTGTCTGTCT[C/G]TCCCACTCTCTCTCC | 51191 |
rs758387037 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455504 | GTGGGCCCCCAAGTC[C/G]CTTGTGGGCATGCCC | 51191 |
rs758400140 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502158 | CTATTATGAATAATG[C/T]TCTTGTGAACATTCT | 51191 |
rs758417506 | snp | A/G | 5.04062e-05 | 0.00502002 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459352 | TGCTCTGTAGAATGC[A/G]TTAAATTAGGAAAAA | 51191 |
rs758440949 | snp | A/G | 3.30387e-05 | 0.00406427 | missense | HERC5 | GRCh38.p7 | 4:88504320 | AGAGGATTTTATAAA[A/G]TGTGCGACGAAGACA | 51191 |
rs758486816 | snp | C/T | 4.94287e-05 | 0.00497111 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489228 | AAGAGAGTCTGAATT[C/T]GCTTTGAGGCCCACG | 51191 |
rs758516147 | snp | C/G/T | 4.96088e-05 | 0.00498019 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468326 | TTTCTAAAACTCTTA[C/G/T]TCTTTGTGCATCCTT | 51191 |
rs758540520 | snp | A/C | | | utr-variant-5-prime, missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457268 | GACCCCGCAAAGCGG[A/C]GATGGAGCGGAGGTC | 51191 |
rs758557919 | in-del | -/TCTAAG | 1.67161e-05 | 0.00289098 | cds-indel | HERC5 | GRCh38.p7 | 4:88504245 | AGGAGAGACTATGTT[-/TCTAAG]TATATCAATTACATT | 51191 |
rs758574879 | in-del | -/TG | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470905 | TAGCACTTACGTATA[-/TG]TGATTATATTTTTTC | 51191 |
rs758575801 | snp | G/T | 1.64966e-05 | 0.00287194 | missense | HERC5 | GRCh38.p7 | 4:88472438 | TGATGCCTGTTTATT[G/T]GGACTTAAATAAAGC | 51191 |
rs758626243 | snp | A/G | | | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467758 | GCCAGTAAGTGGTTT[A/G]TCTGGAGTTGAACCC | 51191 |
rs758680856 | snp | A/C | 3.32546e-05 | 0.00407752 | intron-variant | HERC5 | GRCh38.p7 | 4:88472550 | TACACCAGAATATTT[A/C]TTAAAAGAACTCAAA | 51191 |
rs758710760 | snp | A/G | 4.99097e-05 | 0.00499524 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459448 | CCATTTGAGTATGAC[A/G]ACTATAGCATGAAAC | 51191 |
rs758719606 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467210 | CTCAAACTTGGTAAA[C/T]TCTATAGGAACATAG | 51191 |
rs758753358 | in-del | -/GTAAAATGAAGTGTA | 1.74845e-05 | 0.00295668 | intron-variant | HERC5 | GRCh38.p7 | 4:88489127 | TAGAGAGGGCCAATG[-/GTAAAATGAAGTGTA]ATATTTCTGTTTCTG | 51191 |
rs758757171 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497371 | GAATGTTAGTAGAAA[C/T]GTAGACAATAAAGGC | 51191 |
rs758880759 | snp | A/G | 1.78509e-05 | 0.0029875 | intron-variant | HERC5 | GRCh38.p7 | 4:88494381 | CTAACATATATTTAG[A/G]CAAATATTTAAGTAC | 51191 |
rs758930705 | snp | G/T | 1.64841e-05 | 0.00287085 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88494257 | CCTTCCTTTCCCACT[G/T]GCACTGTTTAAGAAA | 51191 |
rs758962475 | snp | A/G | 1.66288e-05 | 0.00288343 | intron-variant | HERC5 | GRCh38.p7 | 4:88499999 | CATTTTAATGTGAGT[A/G]ACAATAAAAGCAGAT | 51191 |
rs758986538 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88505564 | TGTCAAATGTAGGAC[A/T]CTGCACATGGGCTCC | 51191 |
rs759010039 | snp | C/T | 1.65715e-05 | 0.00287845 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463640 | TGGGTGTACCCTTGT[C/T]TCTTTTTGGCTGTAT | 51191 |
rs759051729 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500072 | TAAACATGTCAACTT[C/T]TACTTAAAAAAAAAA | 51191 |
rs759060645 | in-del | -/T | 0.000574269 | 0.0169353 | intron-variant | HERC5 | GRCh38.p7 | 4:88494146 | CATAATACTTTAAGA[-/T]TTTTTTTTCGCTTTT | 51191 |
rs759069410 | snp | C/G | | | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467835 | AGAAGCACCTTGGAG[C/G]ATTTCTGTTACTTGT | 51191 |
rs759119934 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463977 | AGTGACTCAGATAGC[A/G]TGTGGAAGGTAAGTT | 51191 |
rs759233377 | snp | C/G | 2.14071e-05 | 0.00327156 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457544 | CGCCGAGTGAGTGGG[C/G]CTGGTGTGTGAGGGC | 51191 |
rs759258899 | in-del | -/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474991 | CTAAACAGTTGCATT[-/C]TGAATTGGGGAAACT | 51191 |
rs759319386 | snp | G/T | 0.000181265 | 0.0095184 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467061 | TTTTATTTAATAGGT[G/T]GCACACACTTGCCTA | 51191 |
rs759319513 | snp | A/C | 1.87387e-05 | 0.00306088 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457453 | TGCTGCTCGCCGGGG[A/C]GCCTCGCGGTCTTGG | 51191 |
rs759343670 | snp | C/T | 3.85304e-05 | 0.00438905 | intron-variant | HERC5 | GRCh38.p7 | 4:88487189 | ATAGAGGTATGTATG[C/T]CTATTTGTCTTCATT | 51191 |
rs759384657 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492678 | TTAAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 51191 |
rs759437964 | snp | A/G | 7.3574e-05 | 0.00606478 | intron-variant | HERC5 | GRCh38.p7 | 4:88494128 | ATTGTACTGGTAAAA[A/G]CTCATAATACTTTAA | 51191 |
rs759448631 | snp | A/G | 1.66638e-05 | 0.00288645 | intron-variant | HERC5 | GRCh38.p7 | 4:88493191 | TTAAGGTATTTTGCG[A/G]CAGAAAAAGTACACC | 51191 |
rs759461028 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478983 | TCCCATTACATTTTG[C/T]AGACCTCAAATATAC | 51191 |
rs759463125 | in-del | -/GGGC | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473705 | AAAATCCTCCTGTGG[-/GGGC]GGGCCAGTTTAACTT | 51191 |
rs759478846 | snp | C/T | 3.12319e-05 | 0.00395158 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505918 | ATTTTGTTGTTGTTA[C/T]CGTTGTTGTTGTTGT | 51191 |
rs759493528 | snp | A/G | 3.35587e-05 | 0.00409613 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463514 | TTGGTCACTTCAGCT[A/G]TTTTTTTCCTTACAT | 51191 |
rs759539784 | snp | C/G/T | 5.00775e-05 | 0.00500366 | intron-variant | HERC5 | GRCh38.p7 | 4:88472358 | TCTAGAAGAAACTTT[C/G/T]CATCTAGGGAGATAA | 51191 |
rs759566754 | snp | A/G | 1.76092e-05 | 0.0029672 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88505827 | TTCTACAATGGAAAC[A/G]GTTGAAGAAGCGCTT | 51191 |
rs759586971 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503330 | TTTGTTTAAATCGTC[C/T]TTTGTCATTCTTGAA | 51191 |
rs759618896 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473140 | GGTGCGATCTCGGCT[C/T]ACTGCATGCTTCGTT | 51191 |
rs759624799 | snp | C/T | 1.6569e-05 | 0.00287824 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468310 | GTTTGTGCCAAATGA[C/T]TTTCTAAAACTCTTA | 51191 |
rs759639763 | snp | A/G | | | missense | HERC5 | GRCh38.p7 | 4:88504522 | GAACCAGGATATAAC[A/G]GTTCACATCCCACCA | 51191 |
rs759641992 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489518 | GTGGGCACTCACTCA[C/G]TATGTTTGGGCTAAG | 51191 |
rs759673086 | snp | A/G | 1.65201e-05 | 0.00287398 | missense | HERC5 | GRCh38.p7 | 4:88494174 | TTTCAGCCTAAATTT[A/G]AGAAGAAAAGATACT | 51191 |
rs759696970 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490466 | TTAGTAAATGGAGTA[C/T]TTTTTATTGGGGACC | 51191 |
rs759721077 | snp | A/C | 6.68717e-05 | 0.00578199 | missense | HERC5 | GRCh38.p7 | 4:88479368 | AAGAGTATTGGGCAA[A/C]TCTGCAAGAATCCAC | 51191 |
rs759874836 | in-del | -/T | 0.00058326 | 0.0170672 | intron-variant | HERC5 | GRCh38.p7 | 4:88501012 | AAATGAAATAGTTGG[-/T]TTGTATATGTACTAT | 51191 |
rs759895396 | snp | C/T | 1.65985e-05 | 0.00288079 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459442 | GGAAAACCATTTGAG[C/T]ATGACAACTATAGCA | 51191 |
rs759939032 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474439 | AGTAATTCTAAGGGT[G/T]TGGAATAGGTGAGGA | 51191 |
rs759939062 | snp | G/T | 1.66175e-05 | 0.00288244 | missense | HERC5 | GRCh38.p7 | 4:88504399 | ATACAGATTATGATT[G/T]GAAAACATTTGAAAA | 51191 |
rs759946816 | snp | G/T | 6.74696e-05 | 0.00580777 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468443 | AATAGATCTCCAGGT[G/T]TTCTATAACCTGGTA | 51191 |
rs759953021 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497047 | TCAGACACCGAATCT[G/T]CTGGCACTTTGATCT | 51191 |
rs759987670 | snp | A/G | 4.96479e-05 | 0.00498212 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459432 | CTCATCAGATGGAAA[A/G]CCATTTGAGTATGAC | 51191 |
rs760017280 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498702 | CAGCCTCCTGAGTAA[C/T]TGGAATTACTGGCAC | 51191 |
rs760076500 | snp | A/C | 1.69026e-05 | 0.00290706 | intron-variant | HERC5 | GRCh38.p7 | 4:88489367 | CACTTAATGTTTTTG[A/C]TGCTGAGAAAAGAAA | 51191 |
rs760078102 | snp | C/T | 3.31972e-05 | 0.004074 | intron-variant | HERC5 | GRCh38.p7 | 4:88472540 | AGAAAGAAAATACAC[C/T]AGAATATTTCTTAAA | 51191 |
rs760089558 | snp | C/T | 2.20383e-05 | 0.00331944 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460070 | CATTATGGTGATTAA[C/T]ACAAAGTGTATTTTC | 51191 |
rs760156831 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496959 | CCAAGGGAGCCTGTT[C/G]GCCCCTTCCACCATG | 51191 |
rs760166040 | snp | A/G | 6.59174e-05 | 0.00574059 | missense | HERC5 | GRCh38.p7 | 4:88489214 | GCAATTGAGGAAGAA[A/G]GAGAGTCTGAATTCG | 51191 |
rs760210219 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483406 | AGAGACAGGGCCTAA[C/G]TATGTTGCTCAGGCT | 51191 |
rs760212347 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498445 | TTATTCTCAAGCCTT[A/C]AGATTTAATGTTGCA | 51191 |
rs760218502 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491388 | GTAAACAAAGTTTAA[A/G]GAGAAAATGAGCATC | 51191 |
rs760258188 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458792 | CTTCAGAAAGGGCCA[A/G]ATGTGCACTAATGCC | 51191 |
rs760263219 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484786 | CCAAAGCCCCAACCA[C/T]TGAAAATTGAAGTTT | 51191 |
rs760371054 | snp | A/T | 1.64887e-05 | 0.00287125 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88486199 | TTTTTTGTAGAAGTA[A/T]GCAGAAGGTACTTGT | 51191 |
rs760376855 | snp | G/T | 1.64735e-05 | 0.00286993 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463965 | TGTTGGGTATAGAGT[G/T]ACTCAGATAGCATGT | 51191 |
rs760416118 | snp | A/G | 0.000556948 | 0.0166782 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457414 | CGCGCGCTGCTCCGG[A/G]GGGTGGAGGTGACGC | 51191 |
rs760447619 | snp | A/G | 1.65233e-05 | 0.00287426 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463826 | TATTTTATTTTTCTA[A/G]CATCTGATATGACAT | 51191 |
rs760474767 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | HERC5 | GRCh38.p7 | 4:88475963 | TATTTCCAACAACTG[C/G]GAGAGCCTTGTGGTT | 51191 |
rs760559992 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469544 | CAGCAGGCTGGAGAC[C/T]TGGGGAGGAGTTGAT | 51191 |
rs760600916 | snp | A/G | 1.83276e-05 | 0.00302712 | missense | HERC5 | GRCh38.p7 | 4:88505705 | GACAGACTACAAATG[A/G]AAGATTTAAATAATA | 51191 |
rs760609084 | snp | G/T | 8.24708e-05 | 0.00642095 | intron-variant | HERC5 | GRCh38.p7 | 4:88470563 | AAGAAAGAGGCTGTA[G/T]GTATGTATACCATGT | 51191 |
rs760632109 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467019 | CACTCTCATCATTGT[A/G]GATAATTAAGAATTG | 51191 |
rs760663348 | snp | C/T | 3.49247e-05 | 0.00417865 | missense | HERC5 | GRCh38.p7 | 4:88505820 | CTAAATATTCTACAA[C/T]GGAAACAGTTGAAGA | 51191 |
rs760703522 | snp | C/T | 2.50485e-05 | 0.00353888 | intron-variant | HERC5 | GRCh38.p7 | 4:88487025 | AAAGTGTAAGGTTTC[C/T]CTGTCCTTTAACTTA | 51191 |
rs760726895 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492397 | TTTAGGTAAAACTTT[C/T]ACCTAAAGTGGTAAA | 51191 |
rs760732463 | in-del | -/GGTG | 1.65166e-05 | 0.00287368 | frameshift-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463622 | TGCCCTACTCACACA[-/GGTG]GGTGGGTGTACCCTT | 51191 |
rs760796082 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463249 | GTTGGAAATATCTAA[C/T]GTGCTGCAATTAAAG | 51191 |
rs760830679 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480847 | ACTTTTGTTCATTTA[A/G]ATGATGTTTGACTTT | 51191 |
rs760845697 | snp | A/C | 0.000488232 | 0.0156166 | intron-variant | HERC5 | GRCh38.p7 | 4:88479306 | AAAAAAAAAAAAGCA[A/C]AATAAAACTCATTTT | 51191 |
rs760846705 | snp | A/G | 3.29821e-05 | 0.00406078 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462275 | GCCGGAGAAGCCCAC[A/G]GCATGGCCTTATCCA | 51191 |
rs760854685 | snp | C/T | 3.33433e-05 | 0.00408296 | intron-variant | HERC5 | GRCh38.p7 | 4:88493189 | GCTTAAGGTATTTTG[C/T]GACAGAAAAAGTACA | 51191 |
rs760864621 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487565 | AATCTAATGAAAAGA[C/T]ACGGTAGCAGGAATA | 51191 |
rs761018066 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502947 | ATATCTTCTTACATA[C/T]TGTGGCTTGTCTTTT | 51191 |
rs761039567 | snp | C/G | 1.70679e-05 | 0.00292124 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463490 | CACTGTGAAACTCAG[C/G]ATTTCCTTTTGGTCA | 51191 |
rs761043953 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467137 | TGGACAACTGGGAAA[C/T]GGTGGAACACGTGAC | 51191 |
rs761067861 | snp | A/G | 1.65343e-05 | 0.00287521 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459424 | CTGATTCTCTCATCA[A/G]ATGGAAAACCATTTG | 51191 |
rs761071166 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488966 | CCACAAAGGCTTTGA[C/T]TCTTCAGGTCCCTTG | 51191 |
rs761101932 | in-del | -/CCTT | 1.77543e-05 | 0.0029794 | intron-variant | HERC5 | GRCh38.p7 | 4:88479558 | TAGCTGTAAAAATTC[-/CCTT]CCTTTCAGCTGGCTT | 51191 |
rs761115190 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482082 | GCTCGGAGGCTGAGG[C/T]GGGCAGATCACAAGG | 51191 |
rs761196699 | snp | A/G | 2.18224e-05 | 0.00330314 | intron-variant | HERC5 | GRCh38.p7 | 4:88487217 | ATTAGCATAAATCAC[A/G]TGCTAAGCGCCTTCT | 51191 |
rs761196873 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474316 | ACAAGTTGCCCAGAG[A/G]AATTAAGATCTTACC | 51191 |
rs761240422 | snp | A/G/T | 3.30574e-05 | 0.00406544 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467234 | AACATAGGGTTTGGC[A/G/T]TAGTATCTTTTTAGA | 51191 |
rs761284663 | snp | A/G | 1.65422e-05 | 0.0028759 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504286 | CGACTCTGTAAAGGC[A/G]GTTTATGAAGAATTT | 51191 |
rs761320899 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | HERC5 | GRCh38.p7 | 4:88475851 | CACAGATAACCACCT[A/G]CCTCAAAGATAATCT | 51191 |
rs761393280 | snp | A/G/T | 3.2967e-05 | 0.00405988 | synonymous-codon, missense | HERC5 | GRCh38.p7 | 4:88489207 | GTCGGCAGCAATTGA[A/G/T]GAAGAAAGAGAGTCT | 51191 |
rs761400309 | in-del | -/AGCTA | 1.64727e-05 | 0.00286986 | frameshift-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463921 | ATTCAACACAGAATG[-/AGCTA]AGCTAAGACCCTGTT | 51191 |
rs761414824 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495663 | ATTAGGTAACTTGCT[C/G]AAGGCCCCATAATGG | 51191 |
rs761420635 | snp | G/T | 1.64944e-05 | 0.00287175 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460046 | TTCTAAAATCCATGT[G/T]GTAACTTTCATTATG | 51191 |
rs761424576 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455869 | ACATTTCAAAACGTA[C/T]AGCTAATAAAGAACA | 51191 |
rs761441515 | in-del | -/TGTGAGGGC | 0.00163399 | 0.0285363 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457551 | TGAGTGGGGCTGGTG[-/TGTGAGGGC]TGTGAGGGCTGTGAG | 51191 |
rs761467808 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481697 | TCACAACTGCAGCTA[G/T]TCAGTTGTTCAGGAG | 51191 |
rs761502802 | snp | C/G | 3.40426e-05 | 0.00412554 | intron-variant | HERC5 | GRCh38.p7 | 4:88494353 | AAACAGAGTTCCTGA[C/G]AAAGGACCCTTTCTA | 51191 |
rs761514049 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496877 | TCCCCCACAAAATTC[A/C]TATTTTGAAGCCTCA | 51191 |
rs761521148 | snp | C/T | 0.000182241 | 0.00954398 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463808 | CAGTGAATACTACTT[C/T]TTTATTTTATTTTTC | 51191 |
rs761559843 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88505485 | TATTCCCAGTCAGAC[-/T]TTTAAGCTGCTTGAG | 51191 |
rs761565792 | snp | C/G | 1.65748e-05 | 0.00287874 | intron-variant | HERC5 | GRCh38.p7 | 4:88472537 | TGGAGAAAGAAAATA[C/G]ACCAGAATATTTCTT | 51191 |
rs761697271 | snp | C/T | 1.7783e-05 | 0.00298181 | intron-variant | HERC5 | GRCh38.p7 | 4:88479559 | AGCTGTAAAAATTCC[C/T]TTCCTTTCAGCTGGC | 51191 |
rs761745897 | snp | A/G | | | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467672 | CAGTTCCTGGGAGGT[A/G]TATTCTGTCACTCCT | 51191 |
rs761768572 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88493923 | GATTTAAATTGACTT[A/G]ATGACCAAATATTAG | 51191 |
rs761829936 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481801 | CAGAGGGCTAGATTA[A/G]GTCTGCAAAACTGCC | 51191 |
rs761880204 | snp | C/T | 1.72961e-05 | 0.00294071 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504560 | GTTTTGGAAGGCTTT[C/T]CACAAATTGACTCTG | 51191 |
rs761984324 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88493077 | GTTCTTCTACTGTCT[A/G]TTTGCAGAGATGATC | 51191 |
rs761993429 | snp | C/T | 3.82614e-05 | 0.0043737 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88505692 | TCTTACAGGAACTGA[C/T]AGACTACAAATGAAA | 51191 |
rs761996316 | snp | C/G | 1.65963e-05 | 0.0028806 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469223 | GTAAAGAGATGGATT[C/G]CTGATGTGGAGACTA | 51191 |
rs762106443 | snp | C/T | 1.64982e-05 | 0.00287208 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462262 | GGCTCAGATTTCTGC[C/T]GGAGAAGCCCACAGC | 51191 |
rs762160999 | snp | A/G | 6.5962e-05 | 0.00574253 | missense | HERC5 | GRCh38.p7 | 4:88500963 | CCTAATGGAAGTAGC[A/G]TAACTGTCAACCAGA | 51191 |
rs762177633 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467097 | CTGATTTGGGAAAGG[G/T]CTTTTCCTTTGGTTC | 51191 |
rs762192535 | snp | C/T | 2.24223e-05 | 0.00334823 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460222 | TAATACCTGTGTGTA[C/T]ATGTGGAGCCAGTAG | 51191 |
rs762217360 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501785 | ATGAATATATCACAG[C/T]TTATTTATCTGTAGA | 51191 |
rs762252125 | snp | G/T | 1.64803e-05 | 0.00287052 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475996 | ATTTGCAAAGGTTGT[G/T]TGTAAAATGAGTGAC | 51191 |
rs762302692 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487418 | GACAACTGGCCTAGT[G/T]GTCGGGTTTTTACCT | 51191 |
rs762346659 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479302 | AAAAAAAAAAAAAAA[A/G]GCACAATAAAACTCA | 51191 |
rs762355685 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470922 | GATTATATTTTTTCA[C/T]GCAAATGTATTCTTT | 51191 |
rs762361652 | snp | C/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469672 | ACTCACATTATGGAA[C/G]GTCCTTTCTTTTTAT | 51191 |
rs762375734 | snp | A/G | 1.73171e-05 | 0.00294249 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459300 | GTTAGTAATACAGTG[A/G]GTAATAATCAAAGTG | 51191 |
rs762448170 | in-del | -/TAT | 1.65488e-05 | 0.00287647 | intron-variant | HERC5 | GRCh38.p7 | 4:88500887 | GAATTATGTTGGAGA[-/TAT]TATCTGAGTTCATTT | 51191 |
rs762465610 | snp | C/T | 1.65329e-05 | 0.0028751 | missense | HERC5 | GRCh38.p7 | 4:88489187 | AAACATAAAGCTTAT[C/T]TTAGGTCGGCAGCAA | 51191 |
rs762515665 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504271 | CAATTACATTTTCAA[C/T]GACTCTGTAAAGGCG | 51191 |
rs762547084 | in-del | -/ATT | 1.65318e-05 | 0.002875 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467014 | CTAAACACTCTCATC[-/ATT]GTGGATAATTAAGAA | 51191 |
rs762552479 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466431 | GTTAAATCATTGCCC[A/G]GATAGTTAAACTTAA | 51191 |
rs762624638 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495397 | CTACAAAAACAAACA[A/C]ACAAAAACAACAAAA | 51191 |
rs762637716 | in-del | -/G | 0.000211696 | 0.0102861 | intron-variant | HERC5 | GRCh38.p7 | 4:88479303 | AAAAAAAAAAAAAAA[-/G]CACAATAAAACTCAT | 51191 |
rs762707799 | snp | A/T | 2.10192e-05 | 0.00324178 | intron-variant | HERC5 | GRCh38.p7 | 4:88487213 | CTTCATTAGCATAAA[A/T]CACATGCTAAGCGCC | 51191 |
rs762740352 | snp | C/T | 1.65688e-05 | 0.00287821 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463533 | TTTTCCTTACATAGG[C/T]AAAGATGATCCATCC | 51191 |
rs762808313 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479189 | ACTCAGGAAGGTGAG[A/G]CAGGAGAATTGCTTG | 51191 |
rs762914058 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465213 | AGCCACCACGCCACT[A/G]TTTAATTTTTTTGAT | 51191 |
rs762946617 | snp | C/T | 9.89299e-05 | 0.00703244 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88479417 | GATGTTTAAAACAGC[C/T]GTCATATGCCAGTTG | 51191 |
rs762948463 | snp | A/C | 1.68627e-05 | 0.00290363 | intron-variant | HERC5 | GRCh38.p7 | 4:88494344 | AAAGTAAGTAAACAG[A/C]GTTCCTGAGAAAGGA | 51191 |
rs762970774 | snp | A/G | 1.64999e-05 | 0.00287222 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462310 | TGGCAACATTTATTC[A/G]TGGGGAAAAAATGAA | 51191 |
rs762986053 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490604 | ATCCTAGCACTTTAG[A/G]AGACTGAGGTGGGCA | 51191 |
rs763030555 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459880 | CTGCATCCTAAAATT[A/G]TTTGCATAATATTTT | 51191 |
rs763037841 | snp | A/G | 6.59359e-05 | 0.00574139 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88494206 | CTTTTTTGGGGTTCT[A/G]TGTGGACTTTCCCTG | 51191 |
rs763039082 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475240 | AGAATATGGTACTTA[C/T]GACTGAGAAGGCTGT | 51191 |
rs763057263 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474201 | TTTTACACTTCACTG[G/T]CTTCGCTAGTGCCTG | 51191 |
rs763063088 | snp | C/T | 2.00576e-05 | 0.00316676 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460087 | CAAAGTGTATTTTCC[C/T]TCATCAGGTTTGAAA | 51191 |
rs763096715 | snp | A/G | 3.41799e-05 | 0.00413385 | missense | HERC5 | GRCh38.p7 | 4:88504537 | AGTTCACATCCCACC[A/G]TAGTGATGTTTTGGA | 51191 |
rs763291929 | snp | A/C | 8.74801e-05 | 0.00661305 | intron-variant | HERC5 | GRCh38.p7 | 4:88505643 | GGTCTCCATGTAAAA[A/C]AGATTGCCTAATTTT | 51191 |
rs763306719 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486529 | TAACAAGGCAGTGAG[A/C]CTCATCAGGAGCCAA | 51191 |
rs763323131 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475975 | CTGGGAGAGCCTTGT[A/G]GTTCCATTTGCAAAG | 51191 |
rs763359321 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461206 | TATGAACTTGTATTG[A/G]AAGAAATTGATCATT | 51191 |
rs763367418 | snp | A/G | 1.70947e-05 | 0.00292354 | intron-variant | HERC5 | GRCh38.p7 | 4:88489386 | TGAGAAAAGAAAAAC[A/G]TAAAAGAATGTGGCA | 51191 |
rs763383153 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499000 | TCTGTTACTTCACAA[C/T]ACAGTAATTTAAAAA | 51191 |
rs763440850 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500182 | ACCCTAAAACCTAGT[A/G]CCCTAAAAGAACAAA | 51191 |
rs763467980 | in-del | -/GTT/GTTGTT | 0.149014 | 0.228696 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505919 | TTTGTTGTTGTTATC[-/GTT/GTTGTT]GTTGTTGTTGTTGTT | 51191 |
rs763476320 | snp | C/T | | | synonymous-codon | HERC5 | GRCh38.p7 | 4:88470638 | AGAGATATTTTCATC[C/T]CCTGCTTGTCTAACT | 51191 |
rs763639462 | snp | A/G | 1.64988e-05 | 0.00287213 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88470623 | ATATAGGGAAATCCA[A/G]GAGATATTTTCATCT | 51191 |
rs763733008 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460636 | GTATTTCCCATTTTC[C/T]ATCAGACACTGTCAT | 51191 |
rs763767204 | snp | A/G | 0.000231669 | 0.0107602 | missense | HERC5 | GRCh38.p7 | 4:88504278 | ATTTTCAACGACTCT[A/G]TAAAGGCGGTTTATG | 51191 |
rs763782648 | in-del | -/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88505261 | ACCTACCTCCTTGTT[-/G]GCCTTTCTAAACCTT | 51191 |
rs763824668 | snp | A/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464668 | ATCTCAGCTCACTGC[A/T]ACCTCCGCCTCCCAG | 51191 |
rs763846467 | snp | G/T | 3.30333e-05 | 0.00406393 | splice-donor-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463624 | GCCCTACTCACACAG[G/T]TGGGTGTACCCTTGT | 51191 |
rs763935263 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463695 | AAGTTAGTGTTTCCC[A/G]GAGAAGAAAGGTCAT | 51191 |
rs763946161 | snp | A/T | 1.69086e-05 | 0.00290758 | intron-variant | HERC5 | GRCh38.p7 | 4:88494347 | GTAAGTAAACAGAGT[A/T]CCTGAGAAAGGACCC | 51191 |
rs763990710 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465249 | GATATATCAGTCCAC[A/G]TCTTGCCAGAGGGAT | 51191 |
rs764036732 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503532 | TGTTTCTTTAAGTTT[C/T]GTTATTACTAAGCAC | 51191 |
rs764084976 | in-del | -/T/TTTTTTTTTTTTTTTTTTT | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475117 | TTTTCGGATTTTGTC[-/T/TTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 51191 |
rs764105143 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496084 | AATATCATATAGCCT[C/T]ATGAAAACTCTTCTG | 51191 |
rs764120713 | snp | A/C | 1.67837e-05 | 0.00289682 | intron-variant | HERC5 | GRCh38.p7 | 4:88504426 | AAAAGGTACATCATC[A/C]AGTCTAAGTTGATTA | 51191 |
rs764154998 | snp | C/T | 2.17167e-05 | 0.00329513 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460213 | TTGTAGAAGTAATAC[C/T]TGTGTGTATATGTGG | 51191 |
rs764167775 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459989 | TGCAGTAAATTGAAA[A/G]TTTTTTCTTGAGCTT | 51191 |
rs764237686 | snp | A/G | 1.73492e-05 | 0.00294522 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468464 | TAACCTGGTATTTTA[A/G]GCAAAACTAAGGGTT | 51191 |
rs764275926 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474206 | CACTTCACTGTCTTC[A/G]CTAGTGCCTGGCTTA | 51191 |
rs764322521 | in-del | -/A | 1.81467e-05 | 0.00301214 | intron-variant | HERC5 | GRCh38.p7 | 4:88486082 | ATTGTCTTTAAATAT[-/A]AAAACTTTTTCACAA | 51191 |
rs764329743 | snp | A/C | 5.29227e-05 | 0.00514379 | intron-variant | HERC5 | GRCh38.p7 | 4:88479554 | TATCTAGCTGTAAAA[A/C]TTCCCTTCCTTTCAG | 51191 |
rs764345587 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461300 | AACACACAAGCCCTG[C/T]CTTTAAGAAGCCCAG | 51191 |
rs764347168 | snp | A/T | 1.64751e-05 | 0.00287007 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475891 | ACTTCCATTTCATTC[A/T]CCACCCCAAGAAGCT | 51191 |
rs764397675 | snp | A/G | 3.86593e-05 | 0.00439638 | splice-acceptor-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460093 | GTATTTTCCTTCATC[A/G]GGTTTGAAAGCATTT | 51191 |
rs764433933 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499078 | CCTTTCCCAATGTCA[C/T]GTATCCCTTCAGAAA | 51191 |
rs764437186 | snp | C/T | 3.33923e-05 | 0.00408596 | intron-variant | HERC5 | GRCh38.p7 | 4:88492965 | AGACTTCATATATAG[C/T]AATATAGAGCCCTGG | 51191 |
rs764567572 | in-del | -/CCTTT | 1.66585e-05 | 0.00288599 | intron-variant | HERC5 | GRCh38.p7 | 4:88499894 | TGATCATGGTTATTA[-/CCTTT]TTAAAAGCAAGATTA | 51191 |
rs764584509 | in-del | -/TA | 1.64732e-05 | 0.0028699 | frameshift-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463957 | GCTGAGCTTGTTGGG[-/TA]TAGAGTGACTCAGAT | 51191 |
rs764604728 | snp | C/T | 3.29723e-05 | 0.00406018 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88500935 | CTGGGACAGAAACGA[C/T]ACAAACTTAATTCCT | 51191 |
rs764636731 | in-del | -/ATA | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459886 | CCTAAAATTGTTTGC[-/ATA]ATATTTTATTATAAT | 51191 |
rs764680547 | snp | A/G | 1.65343e-05 | 0.00287521 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486228 | GTGGAAAATGACTGT[A/G]GTAGGTATAGCATGT | 51191 |
rs764686453 | snp | G/T | | | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467867 | TCTGAAAGCTTAGTG[G/T]TGACCTCAAGTAACA | 51191 |
rs764686857 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491084 | ATGACCCCTGTAATC[C/T]TTCTGATAATCTTGT | 51191 |
rs764699077 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469774 | AAACATCCAGAATAA[C/T]ATTTGACCAAATATC | 51191 |
rs764726505 | snp | A/G | 8.23689e-05 | 0.00641698 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463876 | CTGCTGTTTACTTTC[A/G]GTGCTGGAAAACATG | 51191 |
rs764834927 | snp | C/T | 0.000357249 | 0.0133603 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457455 | CTGCTCGCCGGGGCG[C/T]CTCGCGGTCTTGGAA | 51191 |
rs764845694 | snp | A/G | 3.34236e-05 | 0.00408787 | intron-variant | HERC5 | GRCh38.p7 | 4:88500012 | GTAACAATAAAAGCA[A/G]ATAACAGATTAGTTT | 51191 |
rs764886834 | in-del | -/AA | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464270 | GTGCACTTTTGTCTT[-/AA]AAAAACAAGTCATTA | 51191 |
rs764929989 | in-del | -/TGTGAGGGC | 0.00163399 | 0.0285363 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457550 | TGAGTGGGGCTGGTG[-/TGTGAGGGC]TGTGAGGGCTGTGAG | 51191 |
rs765006268 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492682 | ACCCAGGAGGCGGAG[A/G]TTGCAGTGAGCCGAG | 51191 |
rs765028936 | snp | C/T | 2.15901e-05 | 0.00328551 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457549 | AGTGAGTGGGGCTGG[C/T]GTGTGAGGGCTGTGA | 51191 |
rs765048709 | snp | A/G | 1.64961e-05 | 0.00287189 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462302 | TCCATGTCTGGCAAC[A/G]TTTATTCATGGGGAA | 51191 |
rs765078361 | snp | A/T | 0.00014844 | 0.00861383 | intron-variant | HERC5 | GRCh38.p7 | 4:88470608 | AGTGTCTTATTACTA[A/T]TATAGGGAAATCCAA | 51191 |
rs765107612 | snp | A/T | 1.67674e-05 | 0.00289541 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463515 | TGGTCACTTCAGCTA[A/T]TTTTTTCCTTACATA | 51191 |
rs765136357 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463476 | AGTCCAGGTAACTCC[A/G]CTGTGAAACTCAGCA | 51191 |
rs765233734 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489530 | TCAGTATGTTTGGGC[A/T]AAGGAGCAGCAGGCA | 51191 |
rs765251764 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479156 | CGGGCATGGTGGTAG[A/G]CGCCTGTAATTCCAG | 51191 |
rs765280435 | snp | A/G | 0.000186933 | 0.00966601 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505920 | TTTGTTGTTGTTATC[A/G]TTGTTGTTGTTGTTG | 51191 |
rs765297504 | snp | C/T | 1.82234e-05 | 0.0030185 | intron-variant | HERC5 | GRCh38.p7 | 4:88479315 | AAAGCACAATAAAAC[C/T]CATTTTTTAAAAAAT | 51191 |
rs765316062 | snp | A/G | 1.69821e-05 | 0.00291389 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468451 | TCCAGGTGTTCTATA[A/G]CCTGGTATTTTAAGC | 51191 |
rs765341196 | snp | C/G | 1.6498e-05 | 0.00287206 | missense | HERC5 | GRCh38.p7 | 4:88479402 | CAGCAAACTGGTCCA[C/G]ATGTTTAAAACAGCC | 51191 |
rs765343827 | in-del | -/TG | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461673 | ACTCGTTCAAGAAAC[-/TG]TAATTTGAAATTAAT | 51191 |
rs765415066 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474893 | CATAAATACTAGCTT[A/G]TCTTCATAGTGGGAT | 51191 |
rs765428022 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490481 | TTTTTTATTGGGGAC[C/T]TTAGTTTATCACTTC | 51191 |
rs765464469 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497097 | AACCGTGAGCAATAA[A/C]TTTCTATTTATAGAT | 51191 |
rs765480719 | snp | A/C | | | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459452 | TTGAGTATGACAACT[A/C]TAGCATGAAACATCT | 51191 |
rs765482104 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473143 | GCGATCTCGGCTTAC[C/T]GCATGCTTCGTTTAT | 51191 |
rs765484104 | snp | A/G/T | 4.95743e-05 | 0.00497847 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504310 | AGAATTTCGGAGAGG[A/G/T]TTTTATAAAATGTGC | 51191 |
rs765547419 | snp | A/T | | | upstream-variant-2KB, missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457042 | ACAACAACAAACATT[A/T]TGTTTCGTTTTCCAC | 51191 |
rs765560114 | snp | A/G | 0.000149899 | 0.00865604 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504406 | TTATGATTGGAAAAC[A/G]TTTGAAAAGGTACAT | 51191 |
rs765577797 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460072 | TTATGGTGATTAACA[C/T]AAAGTGTATTTTCCT | 51191 |
rs765656820 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483641 | TCAAGCTATCGTCGT[A/G]CCTCAGCTTCCTGAG | 51191 |
rs765659917 | snp | C/G | | | upstream-variant-2KB, synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457116 | GCGTCCCGGCAGGGG[C/G]TCAGTAGCTGAGGCT | 51191 |
rs765766860 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498758 | GTATTTTTAGTAAAG[A/G]TGAGGTTTTGTCATG | 51191 |
rs765808863 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483422 | TATGTTGCTCAGGCT[A/G]GTCTTGAGCTCCTGG | 51191 |
rs765839982 | snp | A/G | 1.65784e-05 | 0.00287905 | intron-variant | HERC5 | GRCh38.p7 | 4:88472541 | GAAAGAAAATACACC[A/G]GAATATTTCTTAAAA | 51191 |
rs765936332 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466852 | ACCATTTGCCAAAGT[A/G]TGACATCATGGTCTT | 51191 |
rs765951859 | snp | C/G | 1.64977e-05 | 0.00287203 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463832 | ATTTTTCTAGCATCT[C/G]ATATGACATTCCCTT | 51191 |
rs765985959 | snp | C/G | 0.00183366 | 0.0302236 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457416 | CGCGCTGCTCCGGAG[C/G]GTGGAGGTGACGCGC | 51191 |
rs765993319 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491612 | AAGGAGATGAGATAT[G/T]AGAAAAAGTCCTTGG | 51191 |
rs765999459 | in-del | -/TG | 3.45758e-05 | 0.00415773 | intron-variant | HERC5 | GRCh38.p7 | 4:88479531 | TCCTTTAGAAACCTC[-/TG]TGTTTTTATCTAGCT | 51191 |
rs766005172 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484876 | ACCTGATTATTCCAT[A/G]TCTACCTAAAAAATC | 51191 |
rs766033795 | snp | C/T | 1.65583e-05 | 0.00287731 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88499980 | TGAGGAAGTATTTTA[C/T]ATCCATTTTAATGTG | 51191 |
rs766048976 | snp | C/G/T | 3.31286e-05 | 0.00406982 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463638 | GGTGGGTGTACCCTT[C/G/T]TCTCTTTTTGGCTGT | 51191 |
rs766060643 | snp | A/G | | | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467806 | AGAGTCTGAGCTCTG[A/G]AACACTCCATTGTAG | 51191 |
rs766161276 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88505273 | TGTTGCCTTTCTAAA[C/T]CTTTCCATCCTTAAA | 51191 |
rs766171077 | snp | C/T | 1.67385e-05 | 0.00289292 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469244 | GTGGAGACTAAACGG[C/T]GGCAGAGCACAAAAA | 51191 |
rs766173838 | snp | A/G | 0.000131922 | 0.00812056 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462281 | GAAGCCCACAGCATG[A/G]CCTTATCCATGTCTG | 51191 |
rs766219664 | snp | C/G | | | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506611 | TGTAAATTACACTTT[C/G]ATAATGTAAAATACA | 51191 |
rs766253979 | snp | G/T | 1.64953e-05 | 0.00287182 | intron-variant | HERC5 | GRCh38.p7 | 4:88470569 | GAGGCTGTATGTATG[G/T]ATACCATGTGATTTG | 51191 |
rs766338419 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88475780 | TTGTTTTATTACCAT[C/G]AGTTGCACCCTGCTT | 51191 |
rs766373374 | snp | C/T | 1.87236e-05 | 0.00305965 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462148 | AGGTGGTGAGCTTTT[C/T]GCCTGGGGACAGAAC | 51191 |
rs766394501 | snp | C/T | 3.30033e-05 | 0.00406209 | missense | HERC5 | GRCh38.p7 | 4:88476019 | TGAGTGACCAGTCTT[C/T]ACTGGTTCTGGGTAA | 51191 |
rs766422605 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88504472 | CCTATTTCCTCAATA[A/G]CTTTTTTTTGTATTT | 51191 |
rs766527120 | in-del | -/AAATTA | 1.65108e-05 | 0.00287317 | cds-indel | HERC5 | GRCh38.p7 | 4:88504340 | GACGAAGACATTATC[-/AAATTA]AAATTATTCCACCCC | 51191 |
rs766560840 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489033 | CATTTATCTTCAGTG[A/G]TGCATATAAGGTTCT | 51191 |
rs766613864 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473089 | TTATTTTTTTGGAAA[C/T]GGAGTCTCGCTTTGT | 51191 |
rs766782420 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482516 | AGACTGGAGGATCTC[A/T]GTTGTGACATAGTTC | 51191 |
rs766800883 | snp | A/G | | | upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455197 | AAATCCATAAGGAAA[A/G]AAAAGAACCTTTATT | 51191 |
rs766807084 | snp | A/G | 1.65353e-05 | 0.00287531 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504295 | AAAGGCGGTTTATGA[A/G]GAATTTCGGAGAGGA | 51191 |
rs766854985 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456248 | ATCTCAAAGCATTGT[C/G]CTAAGTTAAAAAAGC | 51191 |
rs766935541 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497012 | GAAAAGGAATGGGTC[A/G]TCACCTATTCCCTTT | 51191 |
rs766958727 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495675 | GCTCAAGGCCCCATA[A/G]TGGCAGAACGATGAT | 51191 |
rs767002391 | snp | A/T | 1.65488e-05 | 0.00287647 | missense | HERC5 | GRCh38.p7 | 4:88504385 | TGTGATTGTTGGAAA[A/T]ACAGATTATGATTGG | 51191 |
rs767091304 | snp | G/T | 1.648e-05 | 0.0028705 | missense | HERC5 | GRCh38.p7 | 4:88494233 | CCTGTTCAATTGCAA[G/T]GTTGCCAACCTTCCT | 51191 |
rs767107833 | snp | G/T | 1.65323e-05 | 0.00287505 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463629 | ACTCACACAGGTGGG[G/T]GTACCCTTGTCTCTT | 51191 |
rs767121181 | snp | A/T | 1.65091e-05 | 0.00287303 | missense | HERC5 | GRCh38.p7 | 4:88472420 | ACAGAAGAACTACAG[A/T]AATGATGCCTGTTTA | 51191 |
rs767128162 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465545 | CAAAGAAGCGTTCTC[G/T]TCAATATTTATACCT | 51191 |
rs767143770 | snp | C/T | 3.31367e-05 | 0.00407029 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463809 | AGTGAATACTACTTT[C/T]TTATTTTATTTTTCT | 51191 |
rs767232170 | in-del | -/TTGT | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464566 | TTTTGGTTTTCTTGT[-/TTGT]TTGTTTGTTTGTTTT | 51191 |
rs767252050 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483144 | ATTTTAAAGGAAATT[C/T]TTTTTCATGGACTAT | 51191 |
rs767284841 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503584 | TTACCTTCCTGGTAT[A/G]TGACTCGGTTGTCAT | 51191 |
rs767292949 | snp | A/C/T | 3.71142e-05 | 0.00430766 | intron-variant | HERC5 | GRCh38.p7 | 4:88486064 | TTAACAGCTATTAAG[A/C/T]AAAATTGTCTTTAAA | 51191 |
rs767307325 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466532 | TGAATAATAAAGACT[C/G]TCCTCTATCACTTGG | 51191 |
rs767360987 | snp | A/G | 0.00013187 | 0.00811895 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88486176 | ACGAACTCTTGCACC[A/G]TCTCAATTTTTTTGT | 51191 |
rs767383075 | snp | A/G | 1.71062e-05 | 0.00292451 | intron-variant | HERC5 | GRCh38.p7 | 4:88494358 | GAGTTCCTGAGAAAG[A/G]ACCCTTTCTAACATA | 51191 |
rs767401883 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490613 | CTTTAGGAGACTGAG[A/G]TGGGCAGATCACCTG | 51191 |
rs767484869 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466897 | TTCCAAAGTCTTTTC[A/G]GGTACATGTTGATTT | 51191 |
rs767537567 | snp | C/G/T | 4.99316e-05 | 0.00499637 | intron-variant | HERC5 | GRCh38.p7 | 4:88492977 | TAGCAATATAGAGCC[C/G/T]TGGAAGTGATGTATT | 51191 |
rs767538717 | snp | A/G | 1.75545e-05 | 0.00296259 | missense | HERC5 | GRCh38.p7 | 4:88504570 | GCTTTCCACAAATTG[A/G]CTCTGGAAGAAAAGA | 51191 |
rs767566742 | snp | A/G | 1.98367e-05 | 0.00314928 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469127 | TGATGTGTCTAAATT[A/G]TTGTATTTTACTTTC | 51191 |
rs767587592 | snp | A/C | 3.72953e-05 | 0.00431813 | missense | HERC5 | GRCh38.p7 | 4:88505699 | GGAACTGACAGACTA[A/C]AAATGAAAGATTTAA | 51191 |
rs767588301 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463232 | AGTAATTCTAGATGG[C/G]TGTTGGAAATATCTA | 51191 |
rs767595813 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478802 | GTTCTGGTAGAGACC[A/G]AGTTTCTCTATGTTG | 51191 |
rs767657240 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501793 | ATCACAGTTTATTTA[A/T]CTGTAGAATTTTTTT | 51191 |
rs767731297 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466912 | AGGTACATGTTGATT[C/T]CTTGGTTTCCAGATG | 51191 |
rs767733410 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | HERC5 | GRCh38.p7 | 4:88493082 | TCTACTGTCTGTTTG[C/T]AGAGATGATCCAGCC | 51191 |
rs767749090 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500382 | CTTTTGAAGCAAGAC[A/T]GCAGTCTTTATTCTT | 51191 |
rs767764944 | snp | G/T | 1.82503e-05 | 0.00302073 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460107 | CAGGTTTGAAAGCAT[G/T]TTACAAGAAAAAAAA | 51191 |
rs767846290 | snp | A/G | 0.000804783 | 0.0200435 | intron-variant | HERC5 | GRCh38.p7 | 4:88479303 | AAAAAAAAAAAAAAA[A/G]CACAATAAAACTCAT | 51191 |
rs767921967 | in-del | -/G | 3.29658e-05 | 0.00405978 | splice-acceptor-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467057 | TGCTTTTATTTAATA[-/G]GGTGGCACACACTTG | 51191 |
rs767942194 | snp | C/T | 1.96435e-05 | 0.0031339 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457485 | ACGCGGCGGGGCGGG[C/T]GTCCAGGTTCACCAG | 51191 |
rs768012914 | snp | A/G | 1.72755e-05 | 0.00293895 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459307 | ATACAGTGGGTAATA[A/G]TCAAAGTGACAATAG | 51191 |
rs768032301 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494530 | TATTCCCATAACTAG[A/G]CTTCAATGTTTGCAT | 51191 |
rs768034556 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458662 | TTTTTACACGAATAG[A/G]TTCTATTTCATTAGC | 51191 |
rs768048195 | snp | A/G | 1.65165e-05 | 0.00287367 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459401 | TGGACCAAGGAGCAG[A/G]GCACATGCTGATTCT | 51191 |
rs768052825 | in-del | -/CA | | | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506268 | TTAAGCTGTGTCTCT[-/CA]CACAATGTTTGCATG | 51191 |
rs768101045 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467117 | TCCTTTGGTTCTGGA[A/G]AAGATGGACAACTGG | 51191 |
rs768127110 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470984 | TTTTTTCTTTTTTTT[A/T]TTGAGACAGGGTCTT | 51191 |
rs768158904 | in-del | -/TT | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466475 | CTCCTGTAGGTCTGA[-/TT]TTTACATCACAGGCC | 51191 |
rs768211170 | snp | A/G | 1.65064e-05 | 0.00287279 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468396 | GCTGGAGGGAATCAA[A/G]GCATTTTGCTCTGGA | 51191 |
rs768279196 | in-del | -/T | 0.000115845 | 0.00760981 | intron-variant | HERC5 | GRCh38.p7 | 4:88472531 | TTATGTGGAGAAAGA[-/T]AAATACACCAGAATA | 51191 |
rs768293753 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496440 | ACAGTATGATGTATG[A/T]TATTGGTGCAGGTTT | 51191 |
rs768346798 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482997 | TAGTATTTACTTATA[A/G]ATTCTTTTGAATTAT | 51191 |
rs768358426 | snp | A/C | 1.65192e-05 | 0.00287391 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489190 | CATAAAGCTTATCTT[A/C]GGTCGGCAGCAATTG | 51191 |
rs768391922 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | HERC5 | GRCh38.p7 | 4:88489254 | CCACGTTTGATCTAA[C/T]AGTCAGAAGGAATCA | 51191 |
rs768409546 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455699 | TAACAAATGAGGAAA[C/T]CTTATAATCTTGAAT | 51191 |
rs768425475 | snp | C/T | 3.42126e-05 | 0.00413583 | intron-variant | HERC5 | GRCh38.p7 | 4:88504476 | TTTCCTCAATAACTT[C/T]TTTTTGTATTTTCTC | 51191 |
rs768448022 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503242 | CTGATTATACTGAAC[C/T]TATAGATCAATTTTT | 51191 |
rs768515516 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463935 | TGAGCTAAGACCCTG[C/T]TTGGTGGCTGAGCTT | 51191 |
rs768593007 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481615 | CCCTAAATCAGGGGT[C/T]GGCAGCTTTTTTCTG | 51191 |
rs768594012 | snp | G/T | 1.6566e-05 | 0.00287797 | intron-variant | HERC5 | GRCh38.p7 | 4:88500867 | TATTGATGATAGATT[G/T]TTCAGAATTATGTTG | 51191 |
rs768605228 | snp | A/G | 1.66377e-05 | 0.00288419 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463662 | TGGCTGTATTTTTAG[A/G]AGAACAGTTTGTATG | 51191 |
rs768636416 | in-del | -/A | 1.65674e-05 | 0.00287809 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463812 | GAATACTACTTTTTT[-/A]TTTTATTTTTCTAGC | 51191 |
rs768659089 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | HERC5 | GRCh38.p7 | 4:88475947 | AATGTCCTATGATGC[A/G]TATTTCCAACAACTG | 51191 |
rs768681721 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484439 | TTCTGCCAGGCTCCT[A/G]GAGATACCACCAGTT | 51191 |
rs768709704 | snp | G/T | 2.1414e-05 | 0.00327208 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457365 | GTCTCCGGGCGCACA[G/T]CTCTGGCTCTTTCCC | 51191 |
rs768751400 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88493641 | AGACAGAATCTCACT[C/G]TGTCACCCAGGCTGG | 51191 |
rs768776629 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466497 | TCACAGGCCAGGAGA[C/G]CTCTCCCAGGATCCT | 51191 |
rs768791439 | snp | A/T | | | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462250 | AGGAGTACCCTTGGC[A/T]CAGATTTCTGCCGGA | 51191 |
rs768827469 | snp | A/G | 3.29717e-05 | 0.00406015 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486165 | TTTCCAAGTAGACGA[A/G]CTCTTGCACCGTCTC | 51191 |
rs768926766 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462732 | CCTTTAAAGCCTTTG[C/T]ACTTAAAGTCTGTTA | 51191 |
rs768940314 | snp | A/G | 5.32817e-05 | 0.0051612 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469293 | ACTCTCTGCTTATAT[A/G]TCACTCTCAAGTATC | 51191 |
rs768959858 | snp | G/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458638 | TGTAATATGGTTTGT[G/T]CTTTGAGATTTTTAC | 51191 |
rs768966920 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463098 | GCGGCCATTAAACTA[C/T]TTTGGCTGAATCTCT | 51191 |
rs768986757 | snp | A/C | 1.6804e-05 | 0.00289858 | intron-variant | HERC5 | GRCh38.p7 | 4:88476076 | TGTCTTCTCAGTGGA[A/C]AGACATGTCTAGTAA | 51191 |
rs768989886 | snp | C/T | 1.69496e-05 | 0.0029111 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88505777 | GACCCTATAAGAGCA[C/T]TGACATGTTTCAGTG | 51191 |
rs769029912 | snp | A/G | 1.66139e-05 | 0.00288213 | intron-variant | HERC5 | GRCh38.p7 | 4:88486256 | TGTTTAAAGGGGGAA[A/G]TTGATAATCAGTGAG | 51191 |
rs769061530 | snp | C/G | 3.30486e-05 | 0.00406487 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462244 | CCTCGCAGGAGTACC[C/G]TTGGCTCAGATTTCT | 51191 |
rs769067289 | in-del | -/A | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497653 | GGAATTTATCATTAG[-/A]AAAAAAAGCCAAACT | 51191 |
rs769079576 | snp | A/T | 8.54324e-05 | 0.0065352 | intron-variant | HERC5 | GRCh38.p7 | 4:88505646 | CTCCATGTAAAACAG[A/T]TTGCCTAATTTTATT | 51191 |
rs769094768 | snp | A/T | 0.000124112 | 0.0078766 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462384 | TTCTCAGATTCCTAT[A/T]ACCAACAGATATACT | 51191 |
rs769095920 | snp | C/G/T | 1.80912e-05 | 0.00300754 | intron-variant | HERC5 | GRCh38.p7 | 4:88494133 | ACTGGTAAAAACTCA[C/G/T]AATACTTTAAGATTT | 51191 |
rs769122250 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495305 | GTAATCCCAGCACTG[C/T]GGGGAGGCTGAGGCA | 51191 |
rs769145906 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486467 | AAATCTGTCTATACT[A/G]TAATTAGAGAAGGAC | 51191 |
rs769183808 | snp | A/G | 9.91424e-05 | 0.00703998 | intron-variant | HERC5 | GRCh38.p7 | 4:88493159 | TTTCCTGTCAAGGTA[A/G]GTTCCCTCTTCTTTG | 51191 |
rs769271117 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501717 | AAACATGCCTATGTA[A/G]TTACTGCCAGATCAA | 51191 |
rs769307063 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501584 | AGCGTGCTGGCCTAC[A/G]TCACATCTTTTTCCA | 51191 |
rs769324266 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487360 | TTTGAATCATCTTCA[A/C]CTTAAGGCAAATTAG | 51191 |
rs769372424 | in-del | -/TCCCTT | 3.29859e-05 | 0.00406102 | intron-variant | HERC5 | GRCh38.p7 | 4:88475811 | CTACTGAGTTTTGAA[-/TCCCTT]TTCCCTGTTCCTTTC | 51191 |
rs769444549 | snp | C/T | 1.65504e-05 | 0.00287662 | missense | HERC5 | GRCh38.p7 | 4:88489184 | AAAAAACATAAAGCT[C/T]ATCTTAGGTCGGCAG | 51191 |
rs769492725 | snp | A/G | 1.65762e-05 | 0.00287886 | missense | HERC5 | GRCh38.p7 | 4:88504263 | AAGTATATCAATTAC[A/G]TTTTCAACGACTCTG | 51191 |
rs769540253 | snp | A/G | 1.65116e-05 | 0.00287324 | missense | HERC5 | GRCh38.p7 | 4:88504333 | AAATGTGCGACGAAG[A/G]CATTATCAAATTATT | 51191 |
rs769632243 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481036 | TCCTTGTGTCTTGTT[C/T]TAAACTTCTTTTCTC | 51191 |
rs769638670 | snp | G/T | 1.96759e-05 | 0.00313649 | intron-variant | HERC5 | GRCh38.p7 | 4:88487194 | GGTATGTATGCCTAT[G/T]TGTCTTCATTAGCAT | 51191 |
rs769653111 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | HERC5 | GRCh38.p7 | 4:88475828 | CCTTTTCCCTGTTCC[C/T]TTCTGACCACAGATA | 51191 |
rs769691668 | in-del | -/T | 0.000149374 | 0.00864087 | intron-variant | HERC5 | GRCh38.p7 | 4:88493176 | TTCCCTCTTCTTTGC[-/T]TAAGGTATTTTGCGA | 51191 |
rs769701017 | snp | A/C | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459514 | TTAATTTTAATCAAA[A/C]GACAATAATAATTTC | 51191 |
rs769850557 | snp | G/T | 1.66134e-05 | 0.00288208 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463655 | CTCTTTTTGGCTGTA[G/T]TTTTAGAAGAACAGT | 51191 |
rs769975868 | snp | A/T | 1.65712e-05 | 0.00287843 | missense | HERC5 | GRCh38.p7 | 4:88494322 | AAGAACTCAGTCCTG[A/T]TTTGGGAAAGTAAGT | 51191 |
rs770001081 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88486157 | GAAAGTATTTTCCAA[A/G]TAGACGAACTCTTGC | 51191 |
rs770026200 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460237 | TATGTGGAGCCAGTA[A/G]AATGTCTATATTTCA | 51191 |
rs770097624 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458081 | ATTTTGCGTTTAACT[A/G]CTGGACGTTTGCGTT | 51191 |
rs770127170 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490115 | TTGACCATGTTCGGA[A/G]GATCTTTAACTGATT | 51191 |
rs770144086 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476656 | CCGGGCACGGTGGCT[C/T]ATGCCTGTAATCTCA | 51191 |
rs770144945 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478429 | AAAATAGTGGTTACT[A/G]GTGGATGGGGGTGGA | 51191 |
rs770145855 | snp | C/T | 1.70834e-05 | 0.00292257 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504521 | TGAACCAGGATATAA[C/T]AGTTCACATCCCACC | 51191 |
rs770175372 | snp | A/G | 3.32071e-05 | 0.00407461 | intron-variant | HERC5 | GRCh38.p7 | 4:88499908 | ACCTTTTTAAAAGCA[A/G]GATTATTTTTTCCTT | 51191 |
rs770204911 | snp | A/G | 3.29946e-05 | 0.00406155 | missense | HERC5 | GRCh38.p7 | 4:88472435 | AAATGATGCCTGTTT[A/G]TTTGGACTTAAATAA | 51191 |
rs770208974 | snp | G/T | 1.65266e-05 | 0.00287455 | intron-variant | HERC5 | GRCh38.p7 | 4:88505630 | GTAAAGAGATTTTGG[G/T]CTCCATGTAAAACAG | 51191 |
rs770211501 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460760 | TTGGGAGGCTGAGGT[G/T]GGAGGATCACTTGTA | 51191 |
rs770218246 | in-del | -/GTTGTTGTTGTT | 0.000121256 | 0.00778546 | cds-indel | HERC5 | GRCh38.p7 | 4:88505920 | TTTGTTGTTGTTATC[-/GTTGTTGTTGTT]GTTGTTGTTGTTGTT | 51191 |
rs770245337 | snp | C/T | 9.94398e-05 | 0.00705053 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462232 | GATTGTGGAGCACCT[C/T]GCAGGAGTACCCTTG | 51191 |
rs770247942 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500104 | CTGAATAAATTAGTG[A/G]AAAAGGTATTGTTCT | 51191 |
rs770276177 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462863 | AACATGTAATTTCCA[G/T]TATTGAACAAAGCTG | 51191 |
rs770357692 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494138 | AAAAACTCATAATAC[-/T]TTTAAGATTTTTTTT | 51191 |
rs770409063 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | HERC5 | GRCh38.p7 | 4:88493042 | GAAATTGGGTATGAC[C/T]TCGGAGGAGTCAAGA | 51191 |
rs770445695 | in-del | -/ATC | 2.98726e-05 | 0.00386464 | cds-indel | HERC5 | GRCh38.p7 | 4:88505917 | TATTTTGTTGTTGTT[-/ATC]GTTGTTGTTGTTGTT | 51191 |
rs770536750 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460557 | TCCCCTTTTGTGGCC[A/G]GGCTGCAGACCTCTG | 51191 |
rs770538756 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | HERC5 | GRCh38.p7 | 4:88475971 | ACAACTGGGAGAGCC[C/T]TGTGGTTCCATTTGC | 51191 |
rs770609007 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486395 | CAGCAGAAAAGTGAT[G/T]GGCACCTTGGGAGAT | 51191 |
rs770615525 | snp | C/T | 0.000519615 | 0.0161102 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457532 | GCGGCGCCCGGACGC[C/T]GAGTGAGTGGGGCTG | 51191 |
rs770639048 | snp | A/G | 3.3036e-05 | 0.0040641 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467020 | ACTCTCATCATTGTG[A/G]ATAATTAAGAATTGA | 51191 |
rs770663990 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469086 | TTTACTCTCTAGAGT[A/G]TACCTAAAAGTTGGG | 51191 |
rs770717214 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470298 | GGACTTGCATAGTTG[A/G]TGGGGTGGGAGTATT | 51191 |
rs770733084 | snp | C/T | 3.33985e-05 | 0.00408633 | intron-variant | HERC5 | GRCh38.p7 | 4:88476059 | TTTGAAGATACTTTA[C/T]CTGTCTTCTCAGTGG | 51191 |
rs770778460 | snp | A/G | 1.65105e-05 | 0.00287315 | intron-variant | HERC5 | GRCh38.p7 | 4:88500907 | TCTGAGTTCATTTGC[A/G]GTTACAGGTGCACTG | 51191 |
rs770801159 | snp | A/G | 1.66604e-05 | 0.00288616 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489174 | TTCCTAGAGTAAAAA[A/G]CATAAAGCTTATCTT | 51191 |
rs770828609 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473551 | ACAGCCCCACTGGGG[A/G]TCCGAGGTGAAATGG | 51191 |
rs770854785 | in-del | -/A | 0.00236459 | 0.0343031 | frameshift-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460115 | AAAGCATTTTACAAG[-/A]AAAAAAAATAATTCA | 51191 |
rs770889224 | snp | A/C | 1.76655e-05 | 0.00297194 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88487163 | TACTACATACAGACA[A/C]ACTTTTAAAAATAGA | 51191 |
rs770914155 | snp | A/C | 1.6495e-05 | 0.0028718 | missense | HERC5 | GRCh38.p7 | 4:88472453 | TGGACTTAAATAAAG[A/C]AAGAAACATCTTCAA | 51191 |
rs770941110 | snp | A/G | 4.95896e-05 | 0.00497919 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459385 | ATGAAGATACATTCC[A/G]TGGACCAAGGAGCAG | 51191 |
rs771035202 | snp | C/T | 1.70142e-05 | 0.00291664 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463496 | GAAACTCAGCATTTC[C/T]TTTTGGTCACTTCAG | 51191 |
rs771041844 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494027 | TAATATAAACCCTAA[A/G]CATTCTTATCTCAGG | 51191 |
rs771059308 | snp | A/G | 1.66474e-05 | 0.00288503 | intron-variant | HERC5 | GRCh38.p7 | 4:88494156 | TAAGATTTTTTTTTC[A/G]CTTTTCAGCCTAAAT | 51191 |
rs771086529 | snp | C/T | 2.69931e-05 | 0.00367367 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505910 | ACAGCCTTATTTTGT[C/T]GTTGTTATCGTTGTT | 51191 |
rs771104355 | snp | C/T | 1.64966e-05 | 0.00287194 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463593 | TGAATTTGTCGCTTG[C/T]GGTGGCTCTCACAGT | 51191 |
rs771140568 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503005 | CCAAAATTTGTAATT[A/G]TAATGTAGTCTACTT | 51191 |
rs771189296 | snp | C/T | 0.000363144 | 0.01347 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88504355 | CAAATTATTCCACCC[C/T]GAAGAACTGAAGGAT | 51191 |
rs771212662 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491701 | GGTTTGGAAGTTGGC[A/G]TATATCTCTGAAGTT | 51191 |
rs771244102 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489795 | AGGTGGATCACCTGA[G/T]GTCAGGAGTTCGAGA | 51191 |
rs771253481 | snp | C/G | 1.67902e-05 | 0.00289738 | missense | HERC5 | GRCh38.p7 | 4:88479362 | CCTCAGAAGAGTATT[C/G]GGCAACTCTGCAAGA | 51191 |
rs771286381 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490302 | TTCTGTTTTTCCCTC[A/G]TTTTACAGATGGGGA | 51191 |
rs771292692 | snp | C/G | 1.72588e-05 | 0.00293753 | intron-variant | HERC5 | GRCh38.p7 | 4:88479528 | AGTTCCTTTAGAAAC[C/G]TCTGTGTTTTTATCT | 51191 |
rs771297515 | in-del | -/GT | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486016 | CTGGTCATTATAAGA[-/GT]GTTTCATTTATAATT | 51191 |
rs771339874 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474359 | GGAAGGATATTCGAG[A/G]CAGCTAGAAAAGCGT | 51191 |
rs771382559 | snp | A/G | 1.64988e-05 | 0.00287213 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88494290 | TTTGGACCAAATGCC[A/G]TCATTGGAAGACTTG | 51191 |
rs771455089 | snp | A/T | 1.67052e-05 | 0.00289004 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468433 | AAGAGGTAAAAATAG[A/T]TCTCCAGGTGTTCTA | 51191 |
rs771486868 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466367 | GATTACAGGCATGAG[C/T]CACCACACCCCACCT | 51191 |
rs771547733 | snp | A/C/G | 6.83707e-05 | 0.00584648 | missense | HERC5 | GRCh38.p7 | 4:88504513 | GCACGTTATGAACCA[A/C/G]GATATAACAGTTCAC | 51191 |
rs771553293 | snp | A/G | 3.55556e-05 | 0.00421622 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460159 | GATTACCATTCTCTT[A/G]CACTCTCAAAAGGTA | 51191 |
rs771587034 | snp | A/G | 6.86083e-05 | 0.00585657 | intron-variant | HERC5 | GRCh38.p7 | 4:88504633 | TAGATCTGTAATCGT[A/G]TGTCTTTTTAATGGG | 51191 |
rs771621205 | in-del | -/AA | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499843 | ACCTTCAGAATAGCT[-/AA]ATACACTTGACATTT | 51191 |
rs771624467 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459160 | AATTAAAAAAAATCT[A/G]TGTCAAGACCGTTGT | 51191 |
rs771659218 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474160 | CAGATACATACATGC[A/G]TACATCAGTGCAAAG | 51191 |
rs771762470 | snp | C/T | 4.94181e-05 | 0.00497057 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463948 | TGTTTGGTGGCTGAG[C/T]TTGTTGGGTATAGAG | 51191 |
rs771785396 | snp | C/G | 1.64792e-05 | 0.00287042 | missense | HERC5 | GRCh38.p7 | 4:88475853 | CAGATAACCACCTGC[C/G]TCAAAGATAATCTGC | 51191 |
rs771818919 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88499808 | AGAGAAAGAGGTGCT[C/G]TGAACTATACCTGAC | 51191 |
rs771863718 | snp | A/T | | | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468373 | CAGAAAAGGAGTTAA[A/T]AATGATTGCTGGAGG | 51191 |
rs771879750 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | HERC5 | GRCh38.p7 | 4:88493033 | TTTAGTGGAGAAATT[A/G]GGTATGACCTCGGAG | 51191 |
rs771916773 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460411 | TTATTTTTCAAGTAC[A/G]AAACAGTGAAAATTT | 51191 |
rs771954498 | snp | C/G/T | 0.00226336 | 0.0335734 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457387 | CTCTTTCCCAGCGCC[C/G/T]CGGGCCTCCACCGCG | 51191 |
rs772002168 | snp | C/T | 0.000200783 | 0.0100175 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457518 | GCTCGCCGGGAGCGG[C/T]GGCGCCCGGACGCCG | 51191 |
rs772009697 | snp | C/T | 3.41653e-05 | 0.00413297 | missense, intron-variant | HERC5 | GRCh38.p7 | 4:88487136 | TCTTTAATAATCTGT[C/T]GAAAATTAAACTACT | 51191 |
rs772014584 | in-del | -/A | 1.80837e-05 | 0.00300691 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462394 | CTATTACCAACAGAT[-/A]ATACTTGTTAGATGA | 51191 |
rs772058726 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480679 | AATTCCCATTGCTCC[A/G]TGTCTGACTTTAACA | 51191 |
rs772071323 | snp | G/T | | | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506312 | GGGATACTCTTTACC[G/T]TAGAAGTTTTTTTAA | 51191 |
rs772091890 | snp | C/T | 1.65329e-05 | 0.0028751 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467008 | GTATTGCTAAACACT[C/T]TCATCATTGTGGATA | 51191 |
rs772116287 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468798 | AAAAGTCCATAACTT[C/T]CCTGCCCTACTTCAC | 51191 |
rs772197086 | snp | G/T | 1.76328e-05 | 0.00296919 | intron-variant | HERC5 | GRCh38.p7 | 4:88504197 | TTTGTTCAGGATATT[G/T]CAGTAAGTGGAAATA | 51191 |
rs772251327 | snp | A/G | 6.67947e-05 | 0.00577866 | intron-variant | HERC5 | GRCh38.p7 | 4:88486275 | ATAATCAGTGAGTTA[A/G]TACAGGCATTTCTTG | 51191 |
rs772316595 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482010 | TTCTTAAAATTCTAC[A/G]TTGAAAAATGGTGGC | 51191 |
rs772390045 | in-del | -/TCTT | 1.65712e-05 | 0.00287843 | intron-variant | HERC5 | GRCh38.p7 | 4:88472395 | AAAATACTTAATTTA[-/TCTT]TCTTCTACAGAAGAA | 51191 |
rs772402846 | snp | C/G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88482666 | GAAAATAGACAGGTC[C/G/T]CCCTGGCCCTGCAGA | 51191 |
rs772403500 | snp | C/T | 1.65119e-05 | 0.00287327 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467223 | AATTCTATAGGAACA[C/T]AGGGTTTGGCATAGT | 51191 |
rs772448672 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88504124 | GACAGTCCATGGCAC[A/G]TGGTAGGTACTCAAT | 51191 |
rs772486307 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465674 | AGTTGGAGATCTGTC[G/T]TAATGCACATCAGGG | 51191 |
rs772490597 | snp | A/C | 1.66032e-05 | 0.0028812 | intron-variant | HERC5 | GRCh38.p7 | 4:88493178 | CCCTCTTCTTTGCTT[A/C]AGGTATTTTGCGACA | 51191 |
rs772497191 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490070 | TTTTCTCTTTAAATC[C/G]TACAGTTATTTTGGG | 51191 |
rs772506916 | snp | A/G | 1.68029e-05 | 0.00289848 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88479498 | AGAAATGTTGAAGAA[A/G]CTGCACAGGGTAAGA | 51191 |
rs772539472 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462787 | AAATTATATTTAAGA[A/G]CTCACATATCCTGAT | 51191 |
rs772551100 | snp | A/G | 2.39003e-05 | 0.00345682 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505898 | CTTGCTTGTCCAACA[A/G]CCTTATTTTGTTGTT | 51191 |
rs772554974 | snp | C/T | 3.2993e-05 | 0.00406145 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463587 | GAAAGTTGAATTTGT[C/T]GCTTGTGGTGGCTCT | 51191 |
rs772588598 | in-del | -/AAG | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498426 | TGGGACATTGAGTCA[-/AAG]ATTATTCTCAAGCCT | 51191 |
rs772596875 | snp | C/T | 0.000153352 | 0.00875514 | intron-variant | HERC5 | GRCh38.p7 | 4:88479346 | TTGCTTTCCTTGTGT[C/T]CCTCAGAAGAGTATT | 51191 |
rs772670364 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491364 | CTGAAGGTTAAATAC[A/G]TATGGGTGGTAAACA | 51191 |
rs772690760 | in-del | -/C | 3.29473e-05 | 0.00405864 | frameshift-variant | HERC5 | GRCh38.p7 | 4:88475937 | CTTCTCCCAGAATGT[-/C]CTATGATGCATATTT | 51191 |
rs772693096 | in-del | -/TTTATT | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473061 | TCCAAACATGCTTCC[-/TTTATT]TTTATTTTTATTTTT | 51191 |
rs772693828 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488886 | GCATTAATAATTGTG[C/T]GTATAGGAGAAAGTG | 51191 |
rs772730181 | snp | C/T | 3.31329e-05 | 0.00407005 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463814 | ATACTACTTTTTTAT[C/T]TTATTTTTCTAGCAT | 51191 |
rs772750082 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496934 | GAATTCATTCCCCTA[C/T]GAAAGAGGCCCAAGG | 51191 |
rs772774362 | snp | A/G | 3.71168e-05 | 0.00430778 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460174 | GCACTCTCAAAAGGT[A/G]ATTTTTCTGTAATAT | 51191 |
rs772778692 | in-del | -/A | 1.69795e-05 | 0.00291367 | intron-variant | HERC5 | GRCh38.p7 | 4:88493206 | CAGAAAAAGTACACC[-/A]ATATACCATAGAAAA | 51191 |
rs772779620 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | HERC5 | GRCh38.p7 | 4:88493034 | TTAGTGGAGAAATTG[A/G]GTATGACCTCGGAGG | 51191 |
rs772781731 | snp | A/C | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458698 | AGATGAAACAAGGTC[A/C]CAAAACTATCCTAGT | 51191 |
rs772807134 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88483268 | GGCTGGAGTGCAGTG[A/G]TGCAGTCATGGCTCA | 51191 |
rs772807264 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498435 | GAGTCAAAGATTATT[C/T]TCAAGCCTTAAGATT | 51191 |
rs772867587 | snp | A/G | 3.34409e-05 | 0.00408893 | intron-variant | HERC5 | GRCh38.p7 | 4:88489347 | TATGGGTAAGGTGTA[A/G]TTCTCACTTAATGTT | 51191 |
rs772933076 | snp | A/G | 3.30852e-05 | 0.00406712 | intron-variant | HERC5 | GRCh38.p7 | 4:88500891 | TATGTTGGAGATATT[A/G]TCTGAGTTCATTTGC | 51191 |
rs772985220 | snp | A/T | | | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506325 | CCTTAGAAGTTTTTT[A/T]AAAAAACTTGTAATT | 51191 |
rs772993183 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468937 | GCTGAGTGTTGAGTC[C/T]TCAAAGAAATTTACT | 51191 |
rs773015678 | snp | C/G | 2.51746e-05 | 0.00354777 | intron-variant | HERC5 | GRCh38.p7 | 4:88487024 | TAAAGTGTAAGGTTT[C/G]TCTGTCCTTTAACTT | 51191 |
rs773018703 | snp | A/G | 1.65296e-05 | 0.00287481 | missense | HERC5 | GRCh38.p7 | 4:88499955 | TTCTGGATGATGAAG[A/G]TGATAACTTTGAGGA | 51191 |
rs773048252 | in-del | -/TTCC | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473276 | TGGGTCGCACTGTAG[-/TTCC]TTCTTTCTTTCTCTC | 51191 |
rs773051393 | snp | C/T | 3.30502e-05 | 0.00406497 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486132 | AAACCAGGTGAAATG[C/T]CAACTACCTGAAAGT | 51191 |
rs773104002 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463955 | TGGCTGAGCTTGTTG[A/G]GTATAGAGTGACTCA | 51191 |
rs773211796 | snp | A/G | 3.61559e-05 | 0.00425166 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469302 | TTATATATCACTCTC[A/G]AGTATCATTTCCCAA | 51191 |
rs773230600 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463246 | GCTGTTGGAAATATC[G/T]AATGTGCTGCAATTA | 51191 |
rs773271841 | snp | C/G | 2.39197e-05 | 0.00345822 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505899 | TTGCTTGTCCAACAG[C/G]CTTATTTTGTTGTTG | 51191 |
rs773324771 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502879 | CTTTTTTTTTTCTTG[G/T]CAGTTTATGAGAGTT | 51191 |
rs773345669 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485594 | ACTAACAGTCACTAA[C/T]GTCTGAAGTGTCTAG | 51191 |
rs773388047 | snp | A/G | 6.59652e-05 | 0.00574267 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462273 | CTGCCGGAGAAGCCC[A/G]CAGCATGGCCTTATC | 51191 |
rs773398871 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480690 | CTCCATGTCTGACTT[C/T]AACATTTTGAAAATA | 51191 |
rs773452090 | snp | A/G | 1.66427e-05 | 0.00288462 | intron-variant | HERC5 | GRCh38.p7 | 4:88493188 | TGCTTAAGGTATTTT[A/G]CGACAGAAAAAGTAC | 51191 |
rs773471925 | snp | C/T | 1.67108e-05 | 0.00289052 | intron-variant | HERC5 | GRCh38.p7 | 4:88494154 | TTTAAGATTTTTTTT[C/T]CGCTTTTCAGCCTAA | 51191 |
rs773497703 | snp | A/G | 1.69295e-05 | 0.00290937 | splice-acceptor-variant | HERC5 | GRCh38.p7 | 4:88479351 | TTCCTTGTGTTCCTC[A/G]GAAGAGTATTGGGCA | 51191 |
rs773517012 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488892 | ATAATTGTGTGTATA[A/G]GAGAAAGTGGTCCTT | 51191 |
rs773536254 | snp | A/G | 1.74048e-05 | 0.00294993 | missense | HERC5 | GRCh38.p7 | 4:88505819 | CCTAAATATTCTACA[A/G]TGGAAACAGTTGAAG | 51191 |
rs773586105 | snp | A/C | 3.41087e-05 | 0.00412955 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463488 | TCCACTGTGAAACTC[A/C]GCATTTCCTTTTGGT | 51191 |
rs773587494 | snp | A/C | 0.000333692 | 0.0129126 | intron-variant | HERC5 | GRCh38.p7 | 4:88479304 | AAAAAAAAAAAAAAG[A/C]ACAATAAAACTCATT | 51191 |
rs773698058 | snp | A/G | 1.65138e-05 | 0.00287343 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467224 | ATTCTATAGGAACAT[A/G]GGGTTTGGCATAGTA | 51191 |
rs773711416 | in-del | -/TCG | 0.000464965 | 0.0152403 | cds-indel | HERC5 | GRCh38.p7 | 4:88505918 | ATTTTGTTGTTGTTA[-/TCG]TTGTTGTTGTTGTTG | 51191 |
rs773716751 | in-del | -/ATT | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501082 | TAATTTTTCATTCTC[-/ATT]AATCATTTTTCACTA | 51191 |
rs773748688 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490196 | AATCATAATGACCAG[A/T]AGATCTTTTGAGTGC | 51191 |
rs773759273 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463097 | AGCGGCCATTAAACT[A/G]CTTTGGCTGAATCTC | 51191 |
rs773825610 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495538 | GCACTCCAGCCTGGG[C/T]GACAGTAGAAGACCC | 51191 |
rs773827213 | snp | C/T | 1.65438e-05 | 0.00287605 | missense | HERC5 | GRCh38.p7 | 4:88504285 | ACGACTCTGTAAAGG[C/T]GGTTTATGAAGAATT | 51191 |
rs773835373 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472846 | ATAAGAACATTTTAT[A/G]TGCAAAGCATAAATG | 51191 |
rs773850214 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455827 | AAGACACTTAAAATG[A/C]AGAGGCAAGCCACAG | 51191 |
rs773876355 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456039 | GGCTGGGGTTACAGG[A/C]AGGAGCCCAGGCCCA | 51191 |
rs773905045 | in-del | -/ATG | | | intron-variant | HERC5 | GRCh38.p7 | 4:88492864 | ATGTAGAGATTAAAT[-/ATG]ATAATATAAGTAGGA | 51191 |
rs773932844 | in-del | -/A | 3.51924e-05 | 0.00419463 | intron-variant | HERC5 | GRCh38.p7 | 4:88479549 | TTTTTATCTAGCTGT[-/A]AAAAATTCCCTTCCT | 51191 |
rs773951218 | snp | A/C | 6.59152e-05 | 0.00574049 | missense | HERC5 | GRCh38.p7 | 4:88494247 | ATGTTGCCAACCTTC[A/C]TTTCCCACTGGCACT | 51191 |
rs773955130 | snp | A/G | 3.30376e-05 | 0.0040642 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459402 | GGACCAAGGAGCAGA[A/G]CACATGCTGATTCTC | 51191 |
rs774036443 | in-del | -/TTTC | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473971 | AGAAGACCTGTAATG[-/TTTC]TTTCTATCTTGAGGT | 51191 |
rs774055958 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496784 | CATTTAATTGCAATA[A/C]GATTAAAGAACTTCT | 51191 |
rs774093968 | snp | C/T | 1.66001e-05 | 0.00288094 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463805 | CATCAGTGAATACTA[C/T]TTTTTTATTTTATTT | 51191 |
rs774141429 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468186 | TTTACTCCAAAGGAT[A/G]TGTATTTCAGCTGCT | 51191 |
rs774181723 | snp | G/T | 1.65225e-05 | 0.00287419 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463627 | CTACTCACACAGGTG[G/T]GTGTACCCTTGTCTC | 51191 |
rs774194456 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466682 | AGGAAAATCAGTGTG[C/G]TAAAGGTCTTTGAGA | 51191 |
rs774249953 | snp | G/T | 1.64792e-05 | 0.00287042 | missense | HERC5 | GRCh38.p7 | 4:88475850 | CCACAGATAACCACC[G/T]GCCTCAAAGATAATC | 51191 |
rs774250565 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503245 | ATTATACTGAACCTA[C/T]AGATCAATTTTTTGA | 51191 |
rs774287927 | in-del | -/AGAGTAGTCTAC | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501392 | GTATATTCAGTACCT[-/AGAGTAGTCTAC]AGTGGTGCCTGATAC | 51191 |
rs774297795 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478529 | CTACTAGATAAGACA[A/G]CAGGAGGACTGTAGT | 51191 |
rs774483809 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476899 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 51191 |
rs774484061 | snp | A/C/T | 0.000506714 | 0.0159091 | missense, synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457383 | CTGGCTCTTTCCCAG[A/C/T]GCCGCGGGCCTCCAC | 51191 |
rs774503918 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486265 | GGGGAAATTGATAAT[A/C]AGTGAGTTAATACAG | 51191 |
rs774505847 | snp | C/G | 1.65803e-05 | 0.00287922 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469213 | TGAAGGGACTGTAAA[C/G]AGATGGATTGCTGAT | 51191 |
rs774593839 | snp | A/C | 1.64855e-05 | 0.00287097 | synonymous-codon, intron-variant | HERC5 | GRCh38.p7 | 4:88486168 | CCAAGTAGACGAACT[A/C]TTGCACCGTCTCAAT | 51191 |
rs774613324 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478768 | GACATGTGCCACCAC[A/G]CCCTGCTAATTTTTT | 51191 |
rs774621119 | snp | A/G | 2.23202e-05 | 0.0033406 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460219 | AAGTAATACCTGTGT[A/G]TATATGTGGAGCCAG | 51191 |
rs774629285 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464812 | GTCTCGCTCTGCTGC[A/G]AAGGCTGGAGTGCGG | 51191 |
rs774633208 | snp | A/C/T | 3.34707e-05 | 0.00409078 | intron-variant | HERC5 | GRCh38.p7 | 4:88493167 | CAAGGTAAGTTCCCT[A/C/T]TTCTTTGCTTAAGGT | 51191 |
rs774700186 | snp | A/C | 5.35117e-05 | 0.00517233 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469295 | TCTCTGCTTATATAT[A/C]ACTCTCAAGTATCAT | 51191 |
rs774721012 | snp | A/G | 1.64743e-05 | 0.00287 | missense | HERC5 | GRCh38.p7 | 4:88493070 | AGAAAGAGTTCTTCT[A/G]CTGTCTGTTTGCAGA | 51191 |
rs774723010 | snp | A/G | 1.70371e-05 | 0.0029186 | missense | HERC5 | GRCh38.p7 | 4:88505790 | CACTGACATGTTTCA[A/G]TGTCCTCTTCCTCCC | 51191 |
rs774726426 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88500353 | TCTTTCATTCTCCAA[G/T]AGGCTAGCTGAGGCT | 51191 |
rs774824003 | snp | C/T | 3.29951e-05 | 0.00406159 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467213 | AAACTTGGTAAATTC[C/T]ATAGGAACATAGGGT | 51191 |
rs774829254 | in-del | -/C | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455494 | TCCTGGTGCAGTGGG[-/C]CCCCAAGTCCCTTGT | 51191 |
rs774882435 | in-del | -/CTTT | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501195 | CTTTCTCAGAGAGAC[-/CTTT]CTATTTCCTCCTGTC | 51191 |
rs774898357 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501765 | GCTATATAGTTGTGT[A/G]TTGTATGAATATATC | 51191 |
rs774911914 | snp | C/G/T | 3.41473e-05 | 0.00413191 | intron-variant | HERC5 | GRCh38.p7 | 4:88479344 | ATTTGCTTTCCTTGT[C/G/T]TTCCTCAGAAGAGTA | 51191 |
rs774915950 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458639 | GTAATATGGTTTGTG[C/T]TTTGAGATTTTTACA | 51191 |
rs774916422 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487193 | AGGTATGTATGCCTA[C/T]TTGTCTTCATTAGCA | 51191 |
rs774953486 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487370 | CTTCACCTTAAGGCA[A/G]ATTAGGGCCTTGGTA | 51191 |
rs775002121 | snp | A/G | 4.13155e-05 | 0.00454489 | intron-variant | HERC5 | GRCh38.p7 | 4:88487208 | TTTGTCTTCATTAGC[A/G]TAAATCACATGCTAA | 51191 |
rs775006753 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488594 | ATGGACATTCTGTCT[C/G]TCTGTCTGTCTCTCC | 51191 |
rs775090313 | snp | C/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457577 | TGAGGGCTGTGAGGG[C/G]TGAGGGCTGAGGGCT | 51191 |
rs775105692 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467093 | GTTTCTGATTTGGGA[A/G]AGGTCTTTTCCTTTG | 51191 |
rs775226010 | snp | C/G | 0.000214417 | 0.0103519 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88472478 | CTTCAAGGAGTTAAC[C/G]CAAAAGGACTGGATT | 51191 |
rs775267765 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498981 | CACAATGAATAAAAC[A/G]TGGTCTGTTACTTCA | 51191 |
rs775314533 | snp | C/T | 6.66567e-05 | 0.00577268 | intron-variant | HERC5 | GRCh38.p7 | 4:88472371 | TTGCATCTAGGGAGA[C/T]AATCTAACAAAATAC | 51191 |
rs775401675 | in-del | -/CT | 1.70699e-05 | 0.00292142 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463485 | AACTCCACTGTGAAA[-/CT]CAGCATTTCCTTTTG | 51191 |
rs775406639 | snp | C/T | 1.65405e-05 | 0.00287576 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88489186 | AAAACATAAAGCTTA[C/T]CTTAGGTCGGCAGCA | 51191 |
rs775418915 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88495321 | GGGGAGGCTGAGGCA[A/G]GTGGCTTGCTTGAGC | 51191 |
rs775544939 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481061 | TTTCTCCCATAAAGG[A/G]TTTTGATTCGAGACA | 51191 |
rs775558041 | snp | G/T | 1.68218e-05 | 0.00290011 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505925 | TGTTGTTATCGTTGT[G/T]GTTGTTGTTGTTGTT | 51191 |
rs775592002 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465189 | CAGAGTGTTGGGATT[A/G]CAGGGGTGAGCCACC | 51191 |
rs775610583 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490538 | CTTTACCAAGTCTCA[A/G]GATACCAATTTAAAA | 51191 |
rs775630233 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88472922 | GGACTGCCTGGATTC[-/T]TTTTTTTTTTTTTTT | 51191 |
rs775647188 | snp | C/T | 1.75965e-05 | 0.00296613 | intron-variant | HERC5 | GRCh38.p7 | 4:88479549 | GTTTTTATCTAGCTG[C/T]AAAAATTCCCTTCCT | 51191 |
rs775648873 | snp | A/T | 1.65583e-05 | 0.00287731 | intron-variant | HERC5 | GRCh38.p7 | 4:88499923 | AGATTATTTTTTCCT[A/T]AGGAATTTGCAAACA | 51191 |
rs775654623 | snp | A/C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460850 | TAAAAATTAGCTGGG[A/C/T]ATGGTGGCTTCCACC | 51191 |
rs775662778 | snp | A/C | 1.70793e-05 | 0.00292222 | intron-variant | HERC5 | GRCh38.p7 | 4:88489383 | TGCTGAGAAAAGAAA[A/C]ACATAAAAGAATGTG | 51191 |
rs775716888 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476708 | GGCAGATCACCTGAG[A/G]TCAGGAGTTCAAGAC | 51191 |
rs775738831 | snp | C/G | 1.68644e-05 | 0.00290378 | intron-variant | HERC5 | GRCh38.p7 | 4:88494343 | GAAAGTAAGTAAACA[C/G]AGTTCCTGAGAAAGG | 51191 |
rs775750496 | snp | C/G | 1.70813e-05 | 0.00292239 | stop-gained | HERC5 | GRCh38.p7 | 4:88504526 | CAGGATATAACAGTT[C/G]ACATCCCACCATAGT | 51191 |
rs775758969 | snp | A/C/T | 3.31742e-05 | 0.00407262 | missense, synonymous-codon, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469198 | AATTCCTACTCTGAA[A/C/T]GAAGGGACTGTAAAG | 51191 |
rs775766328 | snp | C/G | 1.70287e-05 | 0.00291788 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468453 | CAGGTGTTCTATAAC[C/G]TGGTATTTTAAGCAA | 51191 |
rs775774341 | snp | A/G | 2.97801e-05 | 0.00385865 | intron-variant | HERC5 | GRCh38.p7 | 4:88505635 | GAGATTTTGGTCTCC[A/G]TGTAAAACAGATTGC | 51191 |
rs775930263 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490531 | AGATTGACTTTACCA[A/G]GTCTCAAGATACCAA | 51191 |
rs775961448 | in-del | -/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498497 | AGTTGGGACCTATTA[-/C]CCCCTTTCTTATTTC | 51191 |
rs775962643 | snp | C/G | 6.32958e-05 | 0.00562529 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460078 | TGATTAACACAAAGT[C/G]TATTTTCCTTCATCA | 51191 |
rs775965383 | snp | C/T | 1.67005e-05 | 0.00288963 | intron-variant | HERC5 | GRCh38.p7 | 4:88476061 | TGAAGATACTTTACC[C/T]GTCTTCTCAGTGGAA | 51191 |
rs776038551 | snp | A/C | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462873 | TTCCATTATTGAACA[A/C]AGCTGATGGTGAAAT | 51191 |
rs776063521 | in-del | -/T | 3.31581e-05 | 0.00407161 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463813 | AATACTACTTTTTTA[-/T]TTTATTTTTCTAGCA | 51191 |
rs776065071 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486474 | TCTATACTGTAATTA[C/G]AGAAGGACTAGTGGA | 51191 |
rs776068909 | snp | G/T | 4.96899e-05 | 0.00498422 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462233 | ATTGTGGAGCACCTC[G/T]CAGGAGTACCCTTGG | 51191 |
rs776080863 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88458699 | GATGAAACAAGGTCC[C/T]AAAACTATCCTAGTT | 51191 |
rs776143845 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501600 | TCACATCTTTTTCCA[C/T]GATTTCTTAATCTTT | 51191 |
rs776157603 | snp | C/T | 0.000180131 | 0.00948859 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457427 | GGAGGGTGGAGGTGA[C/T]GCGCCAACTCTGCTG | 51191 |
rs776233049 | snp | C/T | 4.94621e-05 | 0.00497279 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88500932 | GCACTGGGACAGAAA[C/T]GACACAAACTTAATT | 51191 |
rs776241435 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486405 | GTGATTGGCACCTTG[A/G]GAGATGACTATGGGA | 51191 |
rs776297063 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473675 | ATTTGTTAGAGCTCA[C/T]TTTCTTTTGTTTTCT | 51191 |
rs776434342 | snp | A/G | 1.67363e-05 | 0.00289272 | missense | HERC5 | GRCh38.p7 | 4:88504242 | TAAAGGAGAGACTAT[A/G]TTTCTAAGTATATCA | 51191 |
rs776435312 | snp | A/G | 1.65121e-05 | 0.00287329 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467034 | GGATAATTAAGAATT[A/G]ACCATATGTGCTTTT | 51191 |
rs776436327 | snp | A/C/T | 0.000143197 | 0.00846061 | intron-variant | HERC5 | GRCh38.p7 | 4:88487041 | CTGTCCTTTAACTTA[A/C/T]CAGAATTATTGTCAT | 51191 |
rs776437160 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478903 | AGGTGTGAGCCACCA[C/T]GCCTGGCCTACCAAA | 51191 |
rs776473687 | in-del | -/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88456214 | CAAATGAATTACTAA[-/T]TTAAACACAATAGTA | 51191 |
rs776610206 | snp | C/T | 1.68806e-05 | 0.00290517 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463507 | TTTCCTTTTGGTCAC[C/T]TCAGCTATTTTTTTC | 51191 |
rs776635331 | in-del | -/TTAAGTATTTTGT/TTAAGTATTTTGTTAGATTATC | 8.27597e-05 | 0.00643228 | intron-variant | HERC5 | GRCh38.p7 | 4:88472534 | TGTGGAGAAAGAAAA[lengthTooLong]TACACCAGAATATTT | 51191 |
rs776662423 | snp | C/T | 3.74525e-05 | 0.00432722 | intron-variant | HERC5 | GRCh38.p7 | 4:88494114 | AATATAAATATTTCA[C/T]TGTACTGGTAAAAAC | 51191 |
rs776688113 | snp | A/G | 1.74949e-05 | 0.00295756 | missense | HERC5 | GRCh38.p7 | 4:88505823 | AATATTCTACAATGG[A/G]AACAGTTGAAGAAGC | 51191 |
rs776713187 | snp | C/T | 1.6543e-05 | 0.00287597 | missense | HERC5 | GRCh38.p7 | 4:88494166 | TTTTCGCTTTTCAGC[C/T]TAAATTTGAGAAGAA | 51191 |
rs776721345 | snp | C/T | 1.64988e-05 | 0.00287213 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463603 | GCTTGTGGTGGCTCT[C/T]ACAGTGCCCTACTCA | 51191 |
rs776722418 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490424 | TTTCTGCTTAATGAA[C/G]ACGGATAAAGATTGG | 51191 |
rs776728430 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503136 | GAAGCTTATCATTTT[A/T]TTTCTCACATTTAGA | 51191 |
rs776734416 | snp | A/C | 1.64947e-05 | 0.00287177 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88472454 | GGACTTAAATAAAGC[A/C]AGAAACATCTTCAAG | 51191 |
rs776828833 | in-del | -/GTGA | 3.31906e-05 | 0.0040736 | splice-donor-variant | HERC5 | GRCh38.p7 | 4:88499993 | TACATCCATTTTAAT[-/GTGA]GTAACAATAAAAGCA | 51191 |
rs776849640 | in-del | -/TGTA | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489137 | AATGGTAAAATGAAG[-/TGTA]TGTAATATTTCTGTT | 51191 |
rs776861326 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489037 | TATCTTCAGTGGTGC[A/G]TATAAGGTTCTTTTC | 51191 |
rs776880796 | snp | A/G | 0.000180429 | 0.00949643 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505914 | CCTTATTTTGTTGTT[A/G]TTATCGTTGTTGTTG | 51191 |
rs776904053 | snp | A/C | 1.67652e-05 | 0.00289522 | missense | HERC5 | GRCh38.p7 | 4:88479365 | CAGAAGAGTATTGGG[A/C]AACTCTGCAAGAATC | 51191 |
rs776913155 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479530 | TTCCTTTAGAAACCT[A/C]TGTGTTTTTATCTAG | 51191 |
rs776917078 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474381 | GAAAAGCGTATGCCA[A/G]AGCACAGTGTGTCAG | 51191 |
rs776937170 | snp | C/T | 1.67804e-05 | 0.00289653 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468438 | GTAAAAATAGATCTC[C/T]AGGTGTTCTATAACC | 51191 |
rs777062367 | snp | G/T | 3.31785e-05 | 0.00407286 | missense | HERC5 | GRCh38.p7 | 4:88504395 | GGAAATACAGATTAT[G/T]ATTGGAAAACATTTG | 51191 |
rs777168804 | snp | A/T | 4.64846e-05 | 0.0048208 | intron-variant | HERC5 | GRCh38.p7 | 4:88504636 | ATCTGTAATCGTATG[A/T]CTTTTTAATGGGATA | 51191 |
rs777210662 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498666 | ACCTCCACCTCCCAG[G/T]TTCAAGCGATTCTCG | 51191 |
rs777241725 | snp | A/G | 1.66551e-05 | 0.00288571 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462216 | CAACCACCACACCAC[A/G]GATTGTGGAGCACCT | 51191 |
rs777271920 | snp | C/G | 3.40084e-05 | 0.00412347 | missense | HERC5 | GRCh38.p7 | 4:88505762 | AGTTGGAATGAAAGA[C/G]ACCCTATAAGAGCAC | 51191 |
rs777282253 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479936 | GCTGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 51191 |
rs777312133 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460599 | CATTGCTTTTGAATT[C/G]AAGGATCTCCCTAGC | 51191 |
rs777333784 | snp | A/C | 1.7184e-05 | 0.00293117 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469268 | ACAAAAAGGTACACC[A/C]CACAGTCTGACTCTC | 51191 |
rs777359798 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88476173 | TCTAAAGGTACTATA[A/T]CAATTACCATGGTCA | 51191 |
rs777379231 | snp | A/C | 1.65334e-05 | 0.00287514 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467010 | ATTGCTAAACACTCT[A/C]ATCATTGTGGATAAT | 51191 |
rs777432412 | snp | A/T | 1.65111e-05 | 0.0028732 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462318 | TTTATTCATGGGGAA[A/T]AAATGAATGTGGACA | 51191 |
rs777555407 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460498 | TCCAGAAACTGCTTC[C/T]CTTTTCCTAACACCT | 51191 |
rs777605129 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501160 | CATGGAGTTTATATT[A/G]TGGTAAGGAATGGAA | 51191 |
rs777610558 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462641 | AGTTTACTAACTGCA[A/G]GCCTTGCCCAGTCAC | 51191 |
rs777658162 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486955 | CCAGTAATTTGGATT[A/G]CTTTTGTTGGAAGTA | 51191 |
rs777677298 | snp | A/G | 0.000352731 | 0.0132756 | missense | HERC5 | GRCh38.p7 | 4:88489166 | TTTCTGTTTTCCTAG[A/G]GTAAAAAACATAAAG | 51191 |
rs777688987 | in-del | -/CAA | 5.60648e-05 | 0.00529427 | cds-indel | HERC5 | GRCh38.p7 | 4:88505854 | GCTTCAAGAAGCCAT[-/CAA]CAACAACAGAGGATT | 51191 |
rs777709268 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487793 | AAGTAGTAAAATTGG[A/G]CAATTGAAAATTCCC | 51191 |
rs777725471 | in-del | -/TAAT | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486046 | TTTAATCTGATAATC[-/TAAT]TAACAGCTATTAAGC | 51191 |
rs777755774 | snp | A/G | 1.66109e-05 | 0.00288187 | intron-variant | HERC5 | GRCh38.p7 | 4:88476043 | TGGGTAAGTTTGATC[A/G]TTTGAAGATACTTTA | 51191 |
rs777767660 | snp | G/T | 3.29533e-05 | 0.00405901 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467180 | CTTCCAGTGAAAGTA[G/T]CATCAAGTGAAGAAC | 51191 |
rs777779463 | in-del | -/AAT | 2.52605e-05 | 0.00355382 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459518 | TTTTAATCAAAAGAC[-/AAT]AATAATTTCTGTAGG | 51191 |
rs777785079 | snp | A/G | 0.00218228 | 0.0329602 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457459 | TCGCCGGGGCGCCTC[A/G]CGGTCTTGGAACGCG | 51191 |
rs777789865 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470236 | TACTCCTTCCCCCAT[G/T]TAATTTCTGGTAATT | 51191 |
rs777948130 | snp | C/G | 3.29576e-05 | 0.00405928 | missense | HERC5 | GRCh38.p7 | 4:88489217 | ATTGAGGAAGAAAGA[C/G]AGTCTGAATTCGCTT | 51191 |
rs777962939 | snp | A/G | 1.66615e-05 | 0.00288626 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459363 | ATGCATTAAATTAGG[A/G]AAAAACATGAAGATA | 51191 |
rs777998119 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471187 | GTTGGCCAGGCTGGT[C/G]TCGAACTCCTGAGCT | 51191 |
rs778053461 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496243 | GAACCAGTGATCTCT[G/T]TGTTCAGTAAAACTC | 51191 |
rs778057734 | snp | G/T | | | intron-variant, nc-transcript-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467762 | GTAAGTGGTTTGTCT[G/T]GAGTTGAACCCGTGC | 51191 |
rs778106332 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497438 | ATTGGAAATTGGAGG[A/G]GAGGTGCTCCTTGTT | 51191 |
rs778126053 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468038 | AACATGGTTTTTAGT[A/G]ATGGGAGTTGAATTA | 51191 |
rs778127848 | snp | A/G | 3.34024e-05 | 0.00408657 | intron-variant | HERC5 | GRCh38.p7 | 4:88499877 | TTAGATGCTGTGTCT[A/G]GTGATCATGGTTATT | 51191 |
rs778130580 | snp | A/T | 1.65449e-05 | 0.00287614 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467240 | GGGTTTGGCATAGTA[A/T]CTTTTTAGAGAAAAT | 51191 |
rs778134075 | snp | C/T | | | downstream-variant-500B | HERC5 | GRCh38.p7 | 4:88506465 | AGGGACAGGTGGCAG[C/T]GGTGACAGTTATTGG | 51191 |
rs778237632 | snp | G/T | 1.70327e-05 | 0.00291823 | intron-variant | HERC5 | GRCh38.p7 | 4:88479514 | CTGCACAGGGTAAGA[G/T]TTCCTTTAGAAACCT | 51191 |
rs778257480 | snp | A/C | 1.65726e-05 | 0.00287855 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463642 | GGTGTACCCTTGTCT[A/C]TTTTTGGCTGTATTT | 51191 |
rs778271374 | snp | C/T | 1.65004e-05 | 0.00287227 | intron-variant | HERC5 | GRCh38.p7 | 4:88475793 | ATCAGTTGCACCCTG[C/T]TTCTACTGAGTTTTG | 51191 |
rs778341896 | snp | C/T | 1.69571e-05 | 0.00291174 | synonymous-codon, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469165 | TTTACAGAATTCATA[C/T]GTTAATCTGAAGAGG | 51191 |
rs778345432 | snp | A/G | 6.5987e-05 | 0.00574362 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463588 | AAAGTTGAATTTGTC[A/G]CTTGTGGTGGCTCTC | 51191 |
rs778353353 | in-del | -/T | 3.31375e-05 | 0.00407034 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468310 | TTTGTGCCAAATGAC[-/T]TTTCTAAAACTCTTA | 51191 |
rs778391826 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502146 | TCAAGTTTTGGACTA[C/T]TATGAATAATGCTCT | 51191 |
rs778431912 | snp | A/G | 3.38015e-05 | 0.00411091 | intron-variant | HERC5 | GRCh38.p7 | 4:88486101 | ACTTTTTCACAAGTC[A/G]TATTTTATTTAAGGT | 51191 |
rs778504834 | snp | C/T | 5.13545e-05 | 0.00506701 | intron-variant | HERC5 | GRCh38.p7 | 4:88504485 | TAACTTTTTTTTGTA[C/T]TTTCTCTAGAATGCA | 51191 |
rs778512358 | snp | C/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460273 | AACAGGACAGAAATA[C/G]AGTTTTGAATTTGAT | 51191 |
rs778546106 | snp | A/T | 1.70936e-05 | 0.00292344 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469265 | AGCACAAAAAGGTAC[A/T]CCCCACAGTCTGACT | 51191 |
rs778547365 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88505361 | TCTCCTTATTCTCAA[A/G]CATAGCATTGACTCA | 51191 |
rs778626830 | snp | A/C | 1.72499e-05 | 0.00293677 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462173 | CAGAACCTGCATGGG[A/C]AGCTTGGAGTTGGAA | 51191 |
rs778627713 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490048 | AATTGCTTTGTAGAA[A/G]AGAGAATTTTCTCTT | 51191 |
rs778635414 | snp | C/T | 1.74458e-05 | 0.0029534 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460146 | GATCACATGTGGAGA[C/T]TACCATTCTCTTGCA | 51191 |
rs778678797 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88474070 | CTGTGTGCTGGGCAC[C/T]GTAATGATGACTCGA | 51191 |
rs778731078 | snp | G/T | 1.64727e-05 | 0.00286986 | | | GRCh38.p7 | 4:88463942 | AGACCCTGTTTGGTG[G/T]CTGAGCTTGTTGGGT | 51191 |
rs778731969 | snp | A/G | 1.64923e-05 | 0.00287156 | | | GRCh38.p7 | 4:88476013 | GTAAAATGAGTGACC[A/G]GTCTTCACTGGTTCT | 51191 |
rs778755577 | snp | A/C | | | | | GRCh38.p7 | 4:88485270 | TTTGTCAGGCTCCCC[A/C]CCTCAGCAGGAGGCC | 51191 |
rs778787986 | snp | A/G | 1.76939e-05 | 0.00297433 | intron-variant | HERC5 | GRCh38.p7 | 4:88504185 | GCCCCTCACCATTTT[A/G]TTCAGGATATTGCAG | 51191 |
rs778790322 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471700 | CATGAGAAGATACTT[A/C]AACATTTCATTAATA | 51191 |
rs778807481 | snp | C/T | 3.29511e-05 | 0.00405887 | missense | HERC5 | GRCh38.p7 | 4:88493115 | AATATGGGATGTTCA[C/T]GTATCCTGAAGGGGC | 51191 |
rs778841083 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467164 | TGACCAGCTGATGCC[A/G]CTTCCAGTGAAAGTA | 51191 |
rs778899694 | snp | C/T | 1.74732e-05 | 0.00295572 | missense | HERC5 | GRCh38.p7 | 4:88505730 | ATAATATGAAAATAA[C/T]ATTTTGCTGTCCTGA | 51191 |
rs778905069 | snp | A/G | 1.6498e-05 | 0.00287206 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462263 | GCTCAGATTTCTGCC[A/G]GAGAAGCCCACAGCA | 51191 |
rs778919356 | snp | A/G | 1.65403e-05 | 0.00287574 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88476029 | GTCTTCACTGGTTCT[A/G]GGTAAGTTTGATCAT | 51191 |
rs778944857 | snp | C/G | 0.000168734 | 0.00918359 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457512 | CCAGCTGCTCGCCGG[C/G]AGCGGCGGCGCCCGG | 51191 |
rs778945773 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485844 | GCATTGTTTTTTTTT[C/T]TCTTCCTATTGAAAG | 51191 |
rs778998710 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455379 | CCTGCCAACAGGCTC[C/T]CAGCTCACAGACTGA | 51191 |
rs779085653 | in-del | -/AG | 0.000282378 | 0.0118789 | intron-variant | HERC5 | GRCh38.p7 | 4:88470726 | TAAGAGTACCGTGAA[-/AG]AGGATAAAAAAATGA | 51191 |
rs779119741 | snp | A/G | 1.65397e-05 | 0.00287569 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464030 | TAAAATGAGTGCAGC[A/G]AACTAGATAGTAATT | 51191 |
rs779139866 | snp | G/T | 1.71097e-05 | 0.00292481 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459333 | AATAGTTCCTGGTTG[G/T]ATTTGCTCTGTAGAA | 51191 |
rs779188555 | snp | A/C | 2.09304e-05 | 0.00323492 | utr-variant-3-prime | HERC5 | GRCh38.p7 | 4:88505881 | AGGATTTGGCTGACC[A/C]GCTTGCTTGTCCAAC | 51191 |
rs779229291 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496041 | TAAACACAGGAATAC[A/G]CAAATATCTGTTAGC | 51191 |
rs779237328 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465583 | TATCTCTTAACCAAA[A/G]CAGTCTTATCACCTC | 51191 |
rs779254040 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497961 | CATTTGATGTCCAGC[A/G]CTGCCTCAAGTCCCT | 51191 |
rs779277763 | in-del | -/A | 0.00236459 | 0.0343031 | frameshift-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460114 | AAAGCATTTTACAAG[-/A]AAAAAAAAATAATTC | 51191 |
rs779288540 | snp | C/T | 1.78074e-05 | 0.00298385 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462387 | TCAGATTCCTATTAC[C/T]AACAGATATACTTGT | 51191 |
rs779372004 | snp | A/G | 3.46524e-05 | 0.00416233 | intron-variant | HERC5 | GRCh38.p7 | 4:88489139 | ATGGTAAAATGAAGT[A/G]TAATATTTCTGTTTC | 51191 |
rs779388983 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88465795 | GGATACAAACTAGTA[C/T]CAGTCAAAGGAAGAC | 51191 |
rs779445657 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88466998 | GCAATTTACTGTATT[G/T]CTAAACACTCTCATC | 51191 |
rs779458539 | snp | A/T | 1.65392e-05 | 0.00287564 | stop-gained | HERC5 | GRCh38.p7 | 4:88470664 | TAACTGGAAGTTTTT[A/T]AAGGAAAAGGTAATA | 51191 |
rs779569050 | snp | C/G | 1.65007e-05 | 0.00287229 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463572 | AGGACTAGACAATCA[C/G]AAAGTTGAATTTGTC | 51191 |
rs779575284 | snp | A/G | 3.29712e-05 | 0.00406011 | missense | HERC5 | GRCh38.p7 | 4:88479442 | CAGTTGGATTACTGG[A/G]ATGAAAGTGCTGAGG | 51191 |
rs779586956 | snp | C/T | 3.2962e-05 | 0.00405954 | missense | HERC5 | GRCh38.p7 | 4:88494253 | CCAACCTTCCTTTCC[C/T]ACTGGCACTGTTTAA | 51191 |
rs779606716 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88489825 | ACCAGCCTGGTCAAC[A/G]TGGTAAAACCCTGTC | 51191 |
rs779674897 | snp | A/C | 1.64746e-05 | 0.00287002 | missense | HERC5 | GRCh38.p7 | 4:88489248 | TGAGGCCCACGTTTG[A/C]TCTAACAGTCAGAAG | 51191 |
rs779693650 | snp | A/T | 0.000164532 | 0.00906858 | intron-variant | HERC5 | GRCh38.p7 | 4:88486078 | GCAAAATTGTCTTTA[A/T]ATATAAAACTTTTTC | 51191 |
rs779713889 | in-del | -/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88487650 | GATGGTGCCATAAAA[-/G]AGGTTTGTACAGATT | 51191 |
rs779764808 | snp | C/T | 1.70391e-05 | 0.00291878 | intron-variant | HERC5 | GRCh38.p7 | 4:88504464 | TTTTCCTTCCTATTT[C/T]CTCAATAACTTTTTT | 51191 |
rs779772070 | snp | A/G | 1.64969e-05 | 0.00287196 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468374 | AGAAAAGGAGTTAAT[A/G]ATGATTGCTGGAGGG | 51191 |
rs779774530 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88471911 | TCGAAAAACCTTTAT[C/G]TTTTTTCTATGGCCC | 51191 |
rs779777033 | snp | C/G | 1.88642e-05 | 0.00307111 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469138 | AATTATTGTATTTTA[C/G]TTTCCTGTTTGTTTA | 51191 |
rs779831212 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88503690 | GTTTGCATAGTGTAT[C/T]TTTTTCCCTTCTTTG | 51191 |
rs779940515 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88486847 | CATCCAAAGTTTATA[A/G]TTAATTGCTAAATTA | 51191 |
rs779950907 | snp | G/T | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88458278 | TTTTAGTGCATTTTT[G/T]GGGGGGTAGTCTGTC | 51191 |
rs779976280 | snp | A/T | 6.988e-05 | 0.00591059 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460121 | TTTTACAAGAAAAAA[A/T]AATAATTCAGATCAC | 51191 |
rs780000759 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469302 | TTATATATCACTCTC[-/AAG]TATCATTTCCCAAAC | 51191 |
rs780004169 | snp | C/T | | | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460097 | TTTCCTTCATCAGGT[C/T]TGAAAGCATTTTACA | 51191 |
rs780025943 | snp | C/T | 1.6596e-05 | 0.00288058 | intron-variant | HERC5 | GRCh38.p7 | 4:88492987 | GAGCCCTGGAAGTGA[C/T]GTATTATTTGCTCTG | 51191 |
rs780061270 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463919 | ATAATTCAACACAGA[A/G]TGAGCTAAGACCCTG | 51191 |
rs780061991 | snp | A/G | 2.49479e-05 | 0.00353176 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459515 | TAATTTTAATCAAAA[A/G]ACAATAATAATTTCT | 51191 |
rs780063902 | in-del | -/TTC | 0.000198692 | 0.00996526 | intron-variant | HERC5 | GRCh38.p7 | 4:88472397 | ATACTTAATTTATCT[-/TTC]TTCTTCTACAGAAGA | 51191 |
rs780070684 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88497716 | TGTAAAGAATGCAAA[C/T]GTGTTTGGAAGAGAG | 51191 |
rs780145799 | snp | A/G | 0.000920386 | 0.0214324 | missense, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457349 | CGACCCAGCCCGCGA[A/G]GTCTCCGGGCGCACA | 51191 |
rs780147043 | snp | C/G | 1.64743e-05 | 0.00287 | missense | HERC5 | GRCh38.p7 | 4:88475938 | TTCTCCCAGAATGTC[C/G]TATGATGCATATTTC | 51191 |
rs780262079 | snp | C/T | 3.29843e-05 | 0.00406092 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464005 | GTTGTAAAGTATCAA[C/T]AAGAATTGATAAAAT | 51191 |
rs780262227 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88493343 | TTTCCTGGGTTCCCA[A/T]GTCTGTTCACATCGA | 51191 |
rs780413914 | snp | A/G | 1.69321e-05 | 0.0029096 | intron-variant | HERC5 | GRCh38.p7 | 4:88500038 | AGTTTTAATCTGATT[A/G]ACCCTTTACATATTT | 51191 |
rs780417335 | snp | C/T | 1.73679e-05 | 0.0029468 | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469275 | GGTACACCCCACAGT[C/T]TGACTCTCTGCTTAT | 51191 |
rs780422039 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88470151 | GTAGTTGCACAAAAT[A/G]GTTGCATCATAATTT | 51191 |
rs780439103 | snp | C/T | 1.64999e-05 | 0.00287222 | missense | HERC5 | GRCh38.p7 | 4:88470630 | GAAATCCAAGAGATA[C/T]TTTCATCTCCTGCTT | 51191 |
rs780512927 | snp | A/G | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462774 | CAAAAGAATACTAAA[A/G]TTATATTTAAGAACT | 51191 |
rs780527292 | snp | C/T | 0.000436332 | 0.014764 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457506 | GGTTCACCAGCTGCT[C/T]GCCGGGAGCGGCGGC | 51191 |
rs780608102 | snp | A/G | 1.66109e-05 | 0.00288187 | intron-variant | HERC5 | GRCh38.p7 | 4:88486252 | AGCATGTTTAAAGGG[A/G]GAAATTGATAATCAG | 51191 |
rs780616858 | snp | A/G | 1.65119e-05 | 0.00287327 | missense | HERC5 | GRCh38.p7 | 4:88493153 | ATGTGGTTTCCTGTC[A/G]AGGTAAGTTCCCTCT | 51191 |
rs780635099 | snp | C/G | 1.75603e-05 | 0.00296308 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88462379 | ACACATTCTCAGATT[C/G]CTATTACCAACAGAT | 51191 |
rs780733759 | snp | A/C | 1.65037e-05 | 0.00287256 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463561 | TCCCTTATTGAAGGA[A/C]TAGACAATCAGAAAG | 51191 |
rs780734258 | snp | C/T | 1.90925e-05 | 0.00308964 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88505860 | AGAAGCCATCAACAA[C/T]AACAGAGGATTTGGC | 51191 |
rs780751945 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88480880 | CTTACTGATTATAGA[A/G]TTCTTTTATTTTGGA | 51191 |
rs780788625 | snp | A/C | | | intron-variant | HERC5 | GRCh38.p7 | 4:88488091 | AACAAAGGGAAATCA[A/C]AGATAAAAAGATAAA | 51191 |
rs780790770 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484470 | TGGTAGTACTTTACA[-/T]TTTTGGCTTGAAGCT | 51191 |
rs780805057 | in-del | -/T | 0.000446399 | 0.0149332 | intron-variant | HERC5 | GRCh38.p7 | 4:88493001 | ATGTATTATTTGCTC[-/T]GTTTCCTCAGGTTTC | 51191 |
rs780872737 | snp | G/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501536 | AGAACCTTCCCTTGA[G/T]AGTTGGTCAGAGTGG | 51191 |
rs780897377 | snp | C/T | 4.95626e-05 | 0.00497784 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88464026 | TTGATAAAATGAGTG[C/T]AGCAAACTAGATAGT | 51191 |
rs780913681 | snp | A/G | 1.75256e-05 | 0.00296015 | intron-variant | HERC5 | GRCh38.p7 | 4:88479325 | AAAACTCATTTTTTA[A/G]AAAATTTGCTTTCCT | 51191 |
rs780917266 | snp | A/G | 1.6486e-05 | 0.00287102 | missense | HERC5 | GRCh38.p7 | 4:88479425 | AAACAGCCGTCATAT[A/G]CCAGTTGGATTACTG | 51191 |
rs781071225 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468171 | GTTTGCCAACTAGAC[-/TT]TACTCCAAAGGATAT | 51191 |
rs781083412 | snp | C/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88460014 | GAGCTTCATTTCTAA[C/T]TAAATACTATTAATA | 51191 |
rs781083552 | in-del | -/T | 0.000138836 | 0.00833059 | intron-variant | HERC5 | GRCh38.p7 | 4:88504474 | TATTTCCTCAATAAC[-/T]TTTTTTTGTATTTTC | 51191 |
rs781098163 | snp | C/T | 6.66067e-05 | 0.00577052 | missense | HERC5 | GRCh38.p7 | 4:88489175 | TCCTAGAGTAAAAAA[C/T]ATAAAGCTTATCTTA | 51191 |
rs781110845 | snp | C/T | 3.30513e-05 | 0.00406504 | missense, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459386 | TGAAGATACATTCCG[C/T]GGACCAAGGAGCAGA | 51191 |
rs781112889 | snp | A/G | 1.65034e-05 | 0.00287253 | missense, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468349 | GCATCCTTTCAGAAA[A/G]CCATACCTCAGAAAA | 51191 |
rs781179982 | snp | C/T | 1.70009e-05 | 0.0029155 | intron-variant | HERC5 | GRCh38.p7 | 4:88504457 | AATTCAGTTTTCCTT[C/T]CTATTTCCTCAATAA | 51191 |
rs781199302 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88467200 | AAGTGAAGAACTCAA[A/G]CTTGGTAAATTCTAT | 51191 |
rs781202822 | snp | C/G | 1.64879e-05 | 0.00287118 | intron-variant | HERC5 | GRCh38.p7 | 4:88475826 | TCCCTTTTCCCTGTT[C/G]CTTTCTGACCACAGA | 51191 |
rs781273465 | snp | C/T | 1.66067e-05 | 0.00288151 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88463651 | TTGTCTCTTTTTGGC[C/T]GTATTTTTAGAAGAA | 51191 |
rs781307300 | snp | G/T | | | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88461884 | TTATAATCAAATTTA[G/T]TATGTTGAAGATATT | 51191 |
rs781309083 | snp | C/T | 1.96837e-05 | 0.00313711 | intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88459492 | AACTTTTTTCTTTTA[C/T]TAAAAATTAATTTTA | 51191 |
rs781360548 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88484410 | AGGGCTGGCTTTCTT[C/T]GCAGAGAATTTTCTT | 51191 |
rs781366473 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88496458 | TTGGTGCAGGTTTTC[C/T]GATAGAACAGACGAT | 51191 |
rs781393962 | snp | A/G | 5.08634e-05 | 0.00504273 | missense | HERC5 | GRCh38.p7 | 4:88505774 | AGAGACCCTATAAGA[A/G]CACTGACATGTTTCA | 51191 |
rs781398061 | snp | A/G | 3.295e-05 | 0.00405881 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88475903 | TTCTCCACCCCAAGA[A/G]GCTTTAGAAATTTTC | 51191 |
rs781500392 | in-del | -/TGAGGGC | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88457577 | GAGGGCTGTGAGGGG[-/TGAGGGC]TGAGGGCTGAGGGCT | 51191 |
rs781564823 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88493797 | TTTTGTATTTTTTGT[A/G]GAGATGGGGTTTCAC | 51191 |
rs781566521 | snp | A/G | 1.65523e-05 | 0.00287678 | intron-variant | HERC5 | GRCh38.p7 | 4:88486235 | ATGACTGTGGTAGGT[A/G]TAGCATGTTTAAAGG | 51191 |
rs781570267 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88478214 | CCAGAAAGTTAAATT[C/G]TAAACTTGTAATAGT | 51191 |
rs781587665 | snp | A/G | 9.45582e-05 | 0.00687533 | synonymous-codon, upstream-variant-2KB, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88457314 | GCGCAACGGGCGCTC[A/G]ACCGCGGGCAAGGCC | 51191 |
rs781594552 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88491798 | AAGGTTAAGGGGGAC[C/T]TTAACATGTTTGTGA | 51191 |
rs781638920 | snp | A/G | 4.94222e-05 | 0.00497078 | synonymous-codon | HERC5 | GRCh38.p7 | 4:88493098 | AGAGATGATCCAGCC[A/G]GAATATGGGATGTTC | 51191 |
rs781658713 | snp | C/T | 1.66701e-05 | 0.002887 | intron-variant | HERC5 | GRCh38.p7 | 4:88499888 | GTCTAGTGATCATGG[C/T]TATTACCTTTTTAAA | 51191 |
rs781675848 | snp | A/T | 0.000348771 | 0.0132009 | synonymous-codon, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88469192 | GAGGACAATTCCTAC[A/T]CTGAATGAAGGGACT | 51191 |
rs781741126 | snp | C/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88467985 | GGCTTAAAGTACTTA[C/T]ATTCTTTATAGCCAG | 51191 |
rs796081421 | snp | C/T | | | missense | HERC5 | GRCh38.p7 | 4:88494202 | ACTTCTTTTTTGGGG[C/T]TCTATGTGGACTTTC | 51191 |
rs796206389 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88485834 | TGGGATATTGCATTG[-/T]TTTTTTTTTTTCTTC | 51191 |
rs796353477 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88494607 | AGGTTACACCTTGGT[A/G]CAAAATCTGCTAGTG | 51191 |
rs796378679 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | HERC5, LOC102723458 | GRCh38.p7 | 4:88455378 | TCCTGCCAACAGGCT[A/C]CCAGCTCACAGACTG | 51191 |
rs796550779 | snp | A/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88493711 | TCCCAAGCTCAAGCC[A/G]TTCTCTTGCCTCAGC | 51191 |
rs796553772 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC5, LOC102723458 | GRCh38.p7 | 4:88468957 | AGAAATTTACTTTCA[A/G]TCTAAGCCCCCTTGG | 51191 |
rs796608771 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88502838 | CAGAAATAATTATTC[C/T]TCATCTTTAGTCTAT | 51191 |
rs796613563 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88498938 | TGGAGAACAGTTCAC[C/T]GCCTTCCCCACAAAA | 51191 |
rs796635515 | snp | A/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479277 | GCAACAGGGTGAGAC[A/T]CTGTCTCAAAAAAAA | 51191 |
rs796835983 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481458 | CAGTTATAGCTTGTC[-/T]TTTTGCTTTTATGGT | 51191 |
rs796869839 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88501801 | TATTTATCTGTAGAA[-/T]TTTTTTTTTTCTTTT | 51191 |
rs796873923 | snp | C/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88481423 | CCTTTGTCAATGATA[C/T]GTGTTGCAAATATTT | 51191 |
rs796904226 | in-del | -/A | | | intron-variant | HERC5 | GRCh38.p7 | 4:88490008 | GCGAGACTCTGTCTC[-/A]AAAAAAAACAAAAAT | 51191 |
rs796927408 | snp | C/G | | | intron-variant | HERC5 | GRCh38.p7 | 4:88479849 | AAGGCGGGCGGATCA[C/G]GAGGTCAGGAGATCG | 51191 |
rs797016684 | in-del | -/T | | | intron-variant | HERC5 | GRCh38.p7 | 4:88473890 | AAAAAGAACATATGG[-/T]TATGTAAATGAAATA | 51191 |