SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs551470451 | in-del | -/GACCTTGCCTAACCCAGGGGAG | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634089 | AAGACAGAGACAACA[-/GACCTTGCCTAACCCAGGGGAG]GACCTTGCCTAACCC | 3059 |
rs551481350 | snp | G/T | 0.000374301 | 0.0136752 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644719 | AGCATCCACTGTCCT[G/T]TCTTTCAACAAAGAA | 3059 |
rs551542745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651723 | CTGCACCCAGCTAAA[C/T]TTAAAAATACTAACA | 3059 |
rs551752642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658496 | TGAAGCAAAGCAAAT[A/G]GGAGTTGTAGGAAGG | 3059 |
rs551780747 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631101 | GGCATGGTGGTGCAC[A/G]CCTGTAGTTGCAGGT | 3059 |
rs551943989 | in-del | -/TCTCTCTCTCTCTC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635262 | CTCTCTCTCTCTCTC[-/TCTCTCTCTCTCTC]CTCTCTCTCCTCTCT | 3059 |
rs551947430 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639363 | CTGAAATATCAGAGA[C/T]CATATTCTGATCACA | 3059 |
rs552005252 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650816 | ATCAGGATTAAGATC[A/T]TTTGCTCTTAAAAAG | 3059 |
rs552087597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655911 | TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTG | 3059 |
rs552320336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641872 | AGATCACGAGGTCAG[A/G]AGATCGAGACCATCC | 3059 |
rs552350458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647816 | TCAATTAGAGGATGT[A/G]TCTCAAAAAGCAGAA | 3059 |
rs552353012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652791 | CAACTTATCAAGTAC[C/T]TTGTCACTGTAAACA | 3059 |
rs552366008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639611 | CAAAATGTAGTGGCA[C/G]AATCATGGCTTGCTG | 3059 |
rs552411696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655132 | TTCAGTTAGGTTAAC[A/G]AGGAAATGTGCAGGG | 3059 |
rs552489208 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645769 | AACTCATGAACCAAT[A/C/G]AATGAGTCAAAAAAT | 3059 |
rs552545732 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637085 | CCGGGTGAGCTTCCA[A/G]AAAGGAAGGAAGGAG | 3059 |
rs552604549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660263 | AAAATAATGAAGGGG[C/T]TAACGTAGCTCATCT | 3059 |
rs552633362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654062 | ACAATCCCACTACTG[A/T]TCAGCACTGGAGTTT | 3059 |
rs552726823 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651406 | TAACTTAAAAGAGTG[A/G]TTAAGTTGGTTTTGT | 3059 |
rs552924570 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659982 | TTGACCAGAAACCAG[A/C]AAGGTAAGAAGTGCT | 3059 |
rs553018853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650875 | AGGTGTGGTGGCTCA[C/T]GCCTGTAATCTCAGC | 3059 |
rs553021510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660689 | CCACTCACAACCAGG[C/T]CTTCTGGCCATAAAA | 3059 |
rs553080328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658632 | CACTAGGTAACCCAC[A/G]AGTCAAAATTGCTGG | 3059 |
rs553096996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644415 | TAACTTGATTATCTG[C/T]TGCTATGGCAATAAT | 3059 |
rs553269586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653728 | CTTTATTTCCACTTG[C/T]TATAAAATGTCAGGG | 3059 |
rs553356310 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648746 | CTTCTCAGCTTTAGC[C/T]GCAGTTAATTTTAGA | 3059 |
rs553415602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648039 | CTACCTTTCACTAGT[A/G]TACTAGGAAGTCATT | 3059 |
rs553563399 | snp | A/T | 1.67846e-05 | 0.0028969 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632191 | CTGATGATCCTGCAT[A/T]ATGAGAAACACAAAC | 3059 |
rs553609092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637861 | GAGTCACTTGAACAT[A/G]GGGGGTGGAGGTTGC | 3059 |
rs553776916 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641579 | TAAGATGGAATAAGA[-/T]GGAACCAATATACTG | 3059 |
rs553824145 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641691 | AATTTTAAATTTAAG[G/T]CAAAGATGCATGTTA | 3059 |
rs553874090 | in-del | -/T | 0.00278338 | 0.0372014 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637291 | CATGAGAGCCCACCC[-/T]TAGGCTCCAGCACAC | 3059 |
rs553935181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654718 | TTTCCTGCTTTTAGT[C/T]GTCTCAGCTCTACAG | 3059 |
rs554056505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662745 | GTCTCAAAAAAAACC[C/T]AACAAAACAAAACAA | 3059 |
rs554072348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634598 | TGGCATAGCCCTGAA[A/G]CCTGGATTTTTATAA | 3059 |
rs554214553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654515 | AAAAGAAGGTGGAGA[C/G]AAGGGTGATAGTTCT | 3059 |
rs554284623 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639415 | ATACCAATAAAATTA[A/T]CTAGAAAATTTCCCT | 3059 |
rs554568270 | snp | A/G/T | 1.67891e-05 | 0.00289729 | missense | HCLS1 | GRCh38.p7 | 3:121632551 | GGGGCAGAGCTGGGG[A/G/T]CTCCTCATTGTCCTG | 3059 |
rs554614735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647947 | ATGATACTCATTGAA[A/G]CATCGTATATAATAG | 3059 |
rs554620248 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660488 | GGGCAGACACTGTTT[C/T]CGTCTCCTGTGGTCC | 3059 |
rs554736189 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660872 | CCTCGCGTCCACACC[A/G]ACTCCCTCTCTGGCT | 3059 |
rs554751479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645850 | AAATATACTTAAATA[C/T]TATATACTATATATT | 3059 |
rs554823495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634540 | ATTTGTGGGACAGGA[C/T]GGTAAAGAGGTATCG | 3059 |
rs554862039 | snp | A/G | 6.6096e-05 | 0.00574836 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644751 | CATGTGCCTCCATCC[A/G]GGGGTGATCGTGGGC | 3059 |
rs554893908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640091 | GCATTTCATATCACT[A/G]GAAATCTTACAGAAG | 3059 |
rs555134847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657972 | CTTGAATCCTGGATC[A/G]TGGGCCAGGGGAGAC | 3059 |
rs555217292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642410 | GGACACAGAGCTTGC[A/G]GTGAGCCAATATAGT | 3059 |
rs555362883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636186 | ATTTCCAGTCCAATA[C/T]GACCTTTCCCGGCGG | 3059 |
rs555701091 | snp | C/G | 1.64795e-05 | 0.00287045 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635724 | ATGGAGAGTGAATCA[C/G]TAAGCCTCACCGGCT | 3059 |
rs555762513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642329 | AAAAAATTAGCCAGG[C/T]GTGCTGGCAGTCGCC | 3059 |
rs555993107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648943 | CCCAATATCTTCCAA[C/T]TGAAGTATTCAGATG | 3059 |
rs556126880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656331 | GGAGCTTAAAACTGT[A/G]TTAATCTTGCCATTT | 3059 |
rs556608997 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649646 | GTTTTATGTATGGAG[A/G]TAGAGGACAGCTAGA | 3059 |
rs556734389 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640665 | TGTGGTGGCTCATGC[C/G/T]TGTAATCCCAGCACT | 3059 |
rs556789273 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655439 | TTTTAAGTTATTTCA[C/T]TTTTTTATGAGGGTT | 3059 |
rs556916579 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634520 | TTAAATATCCGGGAG[G/T]AGGGATTTGTGGGAC | 3059 |
rs556946064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658545 | AGATGAGAGATGGGA[C/T]TTTAATCAAGACGAA | 3059 |
rs556947495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652274 | TAATAGATATATTCT[A/C]TATCTTGATTGCATT | 3059 |
rs557007474 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657846 | AACAAACAAGAAAAC[A/G]CAAAGAATTAAACTA | 3059 |
rs557087793 | snp | C/G | 3.31131e-05 | 0.00406884 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631822 | ACATGGGAAATCACA[C/G]TTGCAGTAGACAGTG | 3059 |
rs557088196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650232 | CTCAATATCATTAAG[A/G]TGTCAGTTCTCCCTA | 3059 |
rs557100685 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645099 | CAAGATGACTTTTTC[C/T]GGAGACCTGCTCATC | 3059 |
rs557265134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659893 | CTGAGGCCTCAGCCT[A/G]ACTCTCCCATTCACC | 3059 |
rs557417361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643180 | CTGGACACAGACAGT[G/T]TTAGGTTCAAACCCT | 3059 |
rs557546563 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631468 | AGGTTCAGATATTTC[C/T]TCAGGGAAGGAAAGT | 3059 |
rs557548129 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121630920 | CTGATCTGTTTTGGA[A/C]TGGGTTTAAAATGCA | 3059 |
rs557550651 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637657 | AGAGTGAAGCTCAGG[C/T]CGAGCACGGTGCTCA | 3059 |
rs557606670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636218 | TTACCTGTCTCTCTG[A/T]ATGCCTCTCCCACTG | 3059 |
rs557611861 | snp | A/C/T | 3.30187e-05 | 0.00406306 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637136 | CTTCCCCCTTCCAAC[A/C/T]CCAACTCACCTCTCT | 3059 |
rs557614009 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637483 | ATGCCAAGATGAGAA[A/G]AACATTCCCATTTTC | 3059 |
rs557619755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644196 | TGAGTTCAAAGAATC[C/T]GACCTAATAAGGCGT | 3059 |
rs557668199 | in-del | -/AGGGC | 0.373799 | 0.217195 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640838 | AGGGGAGGGGACGGG[-/AGGGC]AGGGCAGGGCAGGGC | 3059 |
rs557742298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658698 | TGGCTGGAGGTGGTT[A/G]GCAATGAGCGGTGCT | 3059 |
rs557753710 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631319 | GAGAAAGTTTCCTGG[A/G]TATGCCTGGAAGAGG | 3059 |
rs557809299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636987 | TCCTCTCTCCCCTCA[C/T]TACCACCACCTGTCC | 3059 |
rs557846639 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656064 | ATGTTGCCCATGCTG[G/T]TCTTGAACTCCTGAC | 3059 |
rs557856417 | snp | C/T | 0.000399281 | 0.0141238 | missense | HCLS1 | GRCh38.p7 | 3:121657346 | GCTCCTTTTCAGAGA[C/T]GTCATTCTGCAAACG | 3059 |
rs557947216 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648298 | TAAGAGAAAGTACCA[-/C]CAAAAAAGGCATTAT | 3059 |
rs558174183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659083 | AGTTGACAATTTACC[A/G]TAGAAAAGAAAAAAG | 3059 |
rs558455819 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642511 | CGGTGGGTGTGGTGG[C/T]TCATGCCTGTAATCC | 3059 |
rs558502926 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640993 | TAACCTAGAGCTAAA[C/G]GAATAACCCAGAATG | 3059 |
rs558513797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649555 | AGGTCTTAATCACAT[A/C]ATTCCTTCATTTTAT | 3059 |
rs558532035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645322 | ACCGGACGCCATAGC[C/T]GGGATGGAATATTTC | 3059 |
rs558534679 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653776 | GCCACTGAGGCAGAC[A/G]TCCTATGGTTATAGC | 3059 |
rs558594626 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660835 | CTCCACCTGTGCAAG[C/T]CTCTGTTCTAAGCGC | 3059 |
rs558621097 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659241 | TCCCAGTGTTCTAGA[C/T]GGCCTTCCGGACTGT | 3059 |
rs559028635 | snp | C/G/T | 4.9429e-05 | 0.00497116 | missense | HCLS1 | GRCh38.p7 | 3:121631920 | CCCGCCACCAGCCCT[C/G/T]GTCCACCATCTCAAT | 3059 |
rs559137693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659404 | TTCCCTCCTCAGACA[A/C]CTCATCCCATTGGAG | 3059 |
rs559143446 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634764 | AGCCTCTGGAGTAGT[A/T]GGGACCACAGATGTG | 3059 |
rs559154276 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652608 | GAGGTTTCAGTGAGC[C/T]GAGATCGTACCACTG | 3059 |
rs559182818 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | HCLS1 | GRCh38.p7 | 3:121632389 | CCTCCTCATAGTCCC[C/T]CTCTGGTTCATCCTC | 3059 |
rs559380859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652391 | GGCAATGGTGGCTTA[C/T]ACCTGTAATCCCAGC | 3059 |
rs559449331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650267 | GATCTATAGATTCAA[C/T]GCAATCCCAATCAAA | 3059 |
rs559464709 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649741 | ACATATTAACTCTCA[G/T]ATATCCAATTTAAGT | 3059 |
rs559505624 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658895 | GCTGTCCCACCTCCA[A/C]CCTGAGTCTGGTCAC | 3059 |
rs559556572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636038 | TTAGAATCTCACATC[A/T]CCAAGCCCAGTTGCC | 3059 |
rs559565943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638082 | GCATTTTTGGGGGAT[G/T]TTTTGTTTTTAGAGG | 3059 |
rs559622913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642746 | GTGTCACTGCACTCC[C/T]GCCTGGGTGACAGTG | 3059 |
rs559702325 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636414 | ACTCTTCTTAAGACA[C/T]TGGTGTTCCGGTGCT | 3059 |
rs559713316 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645095 | AGAGCAAGATGACTT[C/T]TTCTGGAGACCTGCT | 3059 |
rs559843272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647593 | TAGTGATGGGTCTGG[A/C]AGTAAAAGATCAGTC | 3059 |
rs559956316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640269 | AGGAAAAAAAATGTC[C/T]GTTACTATTAAGACC | 3059 |
rs559985743 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661569 | ATGGAAGAAGGTCTT[C/T]GTGGTATCCTGTTTT | 3059 |
rs560128135 | snp | A/G | 0 | 0 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631066 | AACCCCATCTCTACT[A/G]AAAATACAAAAATTA | 3059 |
rs560159908 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633317 | GCCTCCCAGGTTCAA[A/G]CGATTCTCCTGCCTC | 3059 |
rs560218669 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639563 | GTTGTTGTTGTTGTT[G/T]TTTGAGACAGGGTCT | 3059 |
rs560358820 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662280 | GACACCAAGAAGTCC[C/T]ATCTTTCCTTAGCAA | 3059 |
rs560419805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632642 | ATAAGATCCCCCGCC[C/T]TTCACCACCCTGCCT | 3059 |
rs560426840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653206 | GGGACGCTGAAAAAA[C/T]TGTTGTGCACCTGTA | 3059 |
rs560513980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660196 | AGGCGATTAAGAAAT[A/T]CTAACTTTAATAATT | 3059 |
rs561092015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638000 | CTCCAGAAACCAGAG[A/T]CAAAGAGATGAATCA | 3059 |
rs561139234 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653084 | GAGATATCTTGGGGA[C/T]GAGACCCATGTGTAA | 3059 |
rs561202548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660155 | GGCATCAACAGAGTA[A/G]GTACTCATTTGCCAG | 3059 |
rs561214025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633205 | CTCTCAAGTAAGCAA[A/G]CCTCCATCTTCACTC | 3059 |
rs561486428 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635303 | TCTCTCTCTTTCTTT[C/T]GTCTCACTCTGTCAC | 3059 |
rs561603110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657464 | CCACTGCCTTCTTCA[G/T]TCTGGGTCTTTATTC | 3059 |
rs562107254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647643 | TGATTTAAACTCTCC[A/G]TAGGCCAATAATATT | 3059 |
rs562117961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654984 | TGAGAATCAGAGAGG[A/G]AAAGGGACTTGTCTA | 3059 |
rs562123124 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635701 | TGAGGGAGAAGGAAG[G/T]GAGGTGCATGGAGAG | 3059 |
rs562171159 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662082 | GAGCTTTATTTATTC[C/T]TTCTACTTTATTACC | 3059 |
rs562210349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641253 | TACTCAGGAATGATA[A/G]TCTGACACAAGAGAG | 3059 |
rs562231596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634639 | TACGACCTAAGACTC[A/G]TGTCTTTTTTTTTTC | 3059 |
rs562274423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648276 | TTTGAAGGGACACCT[C/G]TATCCCTAAGAGAAA | 3059 |
rs562291771 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641206 | AGAAAATCTTTAATT[A/T]AAAAAAACCCGGAGA | 3059 |
rs562311639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641875 | TCACGAGGTCAGAAG[A/G]TCGAGACCATCCTGG | 3059 |
rs562410902 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633952 | GCCCCTTCCTCATAG[A/T]TCCTACAGCAATAAT | 3059 |
rs562474150 | in-del | -/TCTG | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635165 | CTTCCCCGACGTCAC[-/TCTG]TCTATCCACTTGACT | 3059 |
rs562534577 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644460 | ATCTGTTTTCCTAAA[C/T]GGCATGAGTATTTAT | 3059 |
rs562538015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656758 | TAAAAGTTATTTGGG[C/T]CAGTTATGGGAGCTG | 3059 |
rs562754075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640413 | TTATAAACAAGATTA[A/C]AAACCATCAAGGAAA | 3059 |
rs562759263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655943 | AACCTGTGCCTCCTG[A/G]GTTCAAGAGACTCTC | 3059 |
rs562804371 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660363 | CAATCATGCCTTCTC[C/T]TGGGCTCCATCAGCA | 3059 |
rs562847713 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661780 | AGACTGGGTCCCTGA[C/G]TGAGAAAGAACACAA | 3059 |
rs562897449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654106 | TTCTGACCTGGGCAA[A/G]TTCACCCCTTCTTAG | 3059 |
rs562928952 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661104 | TCATAGAAAATGCTG[A/C]TTTGACTCTGAGTTT | 3059 |
rs563014515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647626 | GCCTGCATACCATAG[C/T]CTGATTTAAACTCTC | 3059 |
rs563133031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650622 | AACCTCAATCTTGAC[C/G]TCACACTGCACAGAA | 3059 |
rs563150310 | snp | A/C/T | 3.30154e-05 | 0.00406286 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637302 | ACCCTTAGGCTCCAG[A/C/T]ACACAGGGAAGCGCT | 3059 |
rs563571390 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644556 | GTATAATAAAAACCA[C/G]TGGCTTGAGGAATTA | 3059 |
rs563665597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649034 | ATGAATATAATAATT[A/G]TTAAATGGGTTATAA | 3059 |
rs563680377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642651 | CATGGTGGTGCACAC[C/T]TGTAGTCACAGCTAC | 3059 |
rs563741730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642077 | AGAGCCAGACTCCGT[C/T]GCAAAAAAAAAAAAA | 3059 |
rs563773621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649694 | CAAAAAATTCCAATT[C/T]AATATGCTGTGTTGT | 3059 |
rs563839441 | snp | C/T | 0.000115604 | 0.00760189 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657368 | CTGCAAACGACAGCA[C/T]GCAGTAATACATGAC | 3059 |
rs563925638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657573 | GTAATCCTAGCATTT[C/T]AGGAGGCCGAGGCGG | 3059 |
rs563926705 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121630999 | TGGGAGGCTAAGCGG[G/T]GGGCGATCATCTGAG | 3059 |
rs563950670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643633 | TGGGACTGGATATGT[C/T]GCCCAGATACCCAAC | 3059 |
rs563959824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636302 | GTGGGGACTGCAGGA[C/T]GCCAGCAGGACAGGC | 3059 |
rs563975918 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638792 | GAGACAAGAAAGACA[G/T]GCTCCAATGATAAAA | 3059 |
rs564012853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650488 | AATAGATCAACAGAA[C/T]AGAATAGAGTCCAGA | 3059 |
rs564015097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635912 | AGGTATCCCTAACCA[C/T]TGGATGCTCAACAGC | 3059 |
rs564076127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649900 | TGACTCAGAATATAA[C/G]GTTTTTATTCACAGA | 3059 |
rs564350192 | in-del | -/TATAA | 0.0174175 | 0.0916809 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645914 | GTTATATCATATAAT[-/TATAA]TATATTAAAATATAC | 3059 |
rs564435448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655861 | TTATTTATTTATTTA[C/T]TTATTGAGACTGAGT | 3059 |
rs564442343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658144 | AATTAGTCCCAGTAT[A/G]AGGGCTGTCTCAGTC | 3059 |
rs564523171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648343 | ACCCACTTCCATCTT[C/T]ACCATGAAGGTGACT | 3059 |
rs564556252 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656392 | CACTATTTATTGTGT[A/C]TACCTTGCTACTAAT | 3059 |
rs564588266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635334 | CCAGGCTGGAGTTGA[A/G]TGGCATGATCTCAGC | 3059 |
rs564666342 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658828 | AACATCTACATCCCT[-/C]TTTACAACCTGCTGA | 3059 |
rs564704418 | snp | C/T | 4.94988e-05 | 0.00497463 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635834 | ACAGCATGTGTGTTG[C/T]GGGAGAGGGGCAAGG | 3059 |
rs564765440 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652805 | CTTTGTCACTGTAAA[C/T]AGAATAGCAAGCAGC | 3059 |
rs564797722 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641985 | CTCGGGAGGCTGAGG[C/G]AGGAGAATGGCGTGA | 3059 |
rs564883421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645513 | TAGACATAATACATA[A/G]ACATTTAAATGCAGC | 3059 |
rs565135639 | snp | A/G | 3.30049e-05 | 0.00406219 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635842 | TGTGTTGCGGGAGAG[A/G]GGCAAGGGTAGTGGT | 3059 |
rs565218959 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631105 | TGGTGGTGCACGCCT[G/T]TAGTTGCAGGTACTC | 3059 |
rs565227242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638908 | AATGTAAAAAACCAG[A/G]TGTGGTGAATGCCTG | 3059 |
rs565284987 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631627 | GGAGTCAGGAACACA[A/G]GAGAAATGTTCATGA | 3059 |
rs565398681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658942 | GTCAGCAGCGACAGT[C/T]GGCTGAAATTTCCAC | 3059 |
rs565473886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659441 | CCCATGCTCTCCATC[A/G]TCTCCAAAGAGTCCC | 3059 |
rs565653779 | snp | C/T | 0.000757488 | 0.0194466 | missense | HCLS1 | GRCh38.p7 | 3:121642972 | CTTTATAATCAAAGC[C/T]GACTGCTGACTACAG | 3059 |
rs565668141 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631249 | AAAAAAAGTTCAGCC[G/T]AAGGAAAAGGCCTAG | 3059 |
rs565795476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650741 | CTTTGGGGTAGGTAA[A/G]TATTTCTTAGACACA | 3059 |
rs566195326 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635409 | CAGCCTCCCAAGTAG[C/T]TGGGATTATAGGTGT | 3059 |
rs566315595 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657661 | TCTCTACCAAAAAAA[A/T]ACAAAAATTAGCCAG | 3059 |
rs566327207 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654828 | TCCTCTCCAATTTCC[A/C]TCTCCTTTCCAAGGA | 3059 |
rs566335864 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657877 | GTGAGCTCTGAAACC[G/T]CCGTTCCTCCTCTGC | 3059 |
rs566449059 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660762 | CTAAGAGCCAGGTAG[G/T]TTCCTCCTCAACTCT | 3059 |
rs566505179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652654 | GACAGAGCGAAACTC[C/T]GTCTCAAAAAAAACA | 3059 |
rs566549155 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639184 | ATCAGTAAAATTATA[-/G]AAGATCCAAACATTA | 3059 |
rs566659880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655072 | AAATGGGAGATGAGC[A/G]AGATTTTTTTGTCAA | 3059 |
rs566736031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654370 | TGTTATTTTTAACCA[C/T]TTATTTTTCCAGAAA | 3059 |
rs566776576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645678 | CTTATGTGTTGAGAT[A/C]AGAAAAATTTGATAC | 3059 |
rs566790468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659621 | CTAAGGGGACACCGG[A/G]GAGATATTGACTGAG | 3059 |
rs566980862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659106 | GAAAAAAGAATAATA[C/T]GTAATAAATCTGATT | 3059 |
rs567045866 | snp | C/T | 6.61507e-05 | 0.00575074 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632283 | TCTTCTTCCTCTTAC[C/T]CTCCCCTGGACATGA | 3059 |
rs567106685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638717 | ATTTTGGAAAGAGTA[A/G]GCATAAGAAAGATGG | 3059 |
rs567279980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632795 | GGAAGAGAATGTAAA[A/G]GGTGTGAGGGGAGGG | 3059 |
rs567289764 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647639 | AGCCTGATTTAAACT[C/G/T]TCCATAGGCCAATAA | 3059 |
rs567363805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658576 | TTGATGTGGGCTGGG[C/T]CCACCTGGGGCTAGA | 3059 |
rs567397939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638467 | AAGCCAGAAACGAAG[C/T]TCTGTCCACTCCTAT | 3059 |
rs567421463 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654210 | TCAGCATAGAGCACT[A/G]TAGCCCAGAACTACT | 3059 |
rs567447173 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661329 | TTAAAAAGAAACTCA[C/T]CCCTATATTACCCAC | 3059 |
rs567447245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653657 | TTTACAGCAGAGCTG[C/G]AATCAGTCCCTAGAG | 3059 |
rs567696751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655998 | GGATTACAGGTGCCC[A/G]CCACCACGCCCATCT | 3059 |
rs567734042 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636271 | AGACATGCCCCTTAG[A/G]TGCTGAGGGCAGTCA | 3059 |
rs567757742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655272 | TCTGTTTACATGTTT[C/G]TTAGATTTTAGAAAG | 3059 |
rs567851639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637698 | CCCAGCACTTCAGGG[A/G]CCGAGGCAGGTGGAT | 3059 |
rs567966815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651927 | ATATGTCAACAAAAA[C/G]ATTTGTACCCAAATG | 3059 |
rs568056137 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650083 | GTTAAATATAAATAC[A/G]TGAAATAACATGAAA | 3059 |
rs568150171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634947 | GACTTGTGTCCTTTC[C/T]AAATTGTAAACTTTG | 3059 |
rs568215497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641626 | TTGGTTAAAAAGAAT[G/T]TAGTTAAAATATTCT | 3059 |
rs568308031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640226 | AAAACCAGAAAGACT[C/T]GAACTCCATGGGAAA | 3059 |
rs568320350 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642238 | GCCGAGTCGGGTGGA[C/T]CACGAGGTCAGGAGA | 3059 |
rs568356444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639801 | TGTATAGCTTTTCAA[A/G]TGCCCATATAGTAAA | 3059 |
rs568394751 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647183 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 3059 |
rs568440531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633513 | AGGCATGAGCCACCA[C/T]GCTCGGCCCATCTTC | 3059 |
rs568506272 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662666 | CTTGAAACTGGAAGG[C/T]GGAAGGTGCAGTGAG | 3059 |
rs568543327 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661601 | CTGCGTGTCAAGACT[G/T]GCTGCCCCTCCCTTC | 3059 |
rs568584159 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654188 | AGAATTCAGCGTGGA[C/G]ACCCAATCAGCATAG | 3059 |
rs568764762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640454 | TGAGGAACGCAGATT[A/G]GTCAGAAGAAATGGC | 3059 |
rs568809189 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637387 | GCAGGGCTTGAATAC[A/C]GGGGAATTAAAGAGA | 3059 |
rs568984183 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645757 | TGAATGAGTTTTAAC[C/T]CATGAACCAATGAAT | 3059 |
rs569013828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647831 | GTCTCAAAAAGCAGA[A/G]AAATATTCACATACC | 3059 |
rs569027548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648486 | GATCCGGGGATTCTT[A/G]GAAACATTTGGGCAA | 3059 |
rs569138301 | snp | A/G | 0.000214145 | 0.0103454 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637233 | TCTCCACCCCGTACC[A/G]GCCACCAAAGCCACG | 3059 |
rs569177780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639647 | TCAACCTCCTGGGCT[C/G]AAGTGATCCTCCCAC | 3059 |
rs569355100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652830 | AGCAGCCTTAGGGAA[C/T]TGGCAATAGCTTAGT | 3059 |
rs569364213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633369 | TACAGGCACACGCCA[C/T]TATGCCTGGCTAATT | 3059 |
rs569584317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636851 | TCCCTCTAAGACTCA[C/T]GGCAAACCATCTTCT | 3059 |
rs569648675 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636159 | GTTAAGCAATGCCAA[G/T]AAATCAATACAATTT | 3059 |
rs569669357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649391 | CAGGCATGCATGTCA[C/T]GCCCCGCTAGATTTT | 3059 |
rs569679474 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642849 | TAAAAAGCTGATGAC[A/C]ACTGCTGGAAGATAA | 3059 |
rs569786266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657603 | GGTGGATCTCTTTAG[A/G]TCAGGAGCTCAAGAC | 3059 |
rs569917277 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662852 | GGGGCCTAATGTTTT[C/T]ACTATGTGCCAGACA | 3059 |
rs570111190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649322 | CTCACTGTAATCTCC[A/G]CCTCCCGGGTTCAAG | 3059 |
rs570194857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641489 | ATAGGTAAATACCTT[C/G]GTCAATTTAAATAAG | 3059 |
rs570196736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634519 | GTTAAATATCCGGGA[A/G]GAGGGATTTGTGGGA | 3059 |
rs570243411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657214 | CACCTTCCCCCAAGT[C/T]TCCGAGTTTTCTTTG | 3059 |
rs570325206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652405 | ACACCTGTAATCCCA[A/G]CACTGTAGGAGGCCG | 3059 |
rs570386198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642773 | AGTGCAAGACCCTGT[A/C]TCAAAAACAAACAAA | 3059 |
rs570766248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634473 | TGGAGAGTGGGGAAG[C/G]GCATGGCACTTGAAG | 3059 |
rs570807495 | in-del | -/CCTGGGA | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637360 | ACAGAGTGTTAGGGG[-/CCTGGGA]AAAGAGCAGGGCTTG | 3059 |
rs570960627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639875 | TAGGAAAAGAACAAA[A/C]TAAATTAATACTAAG | 3059 |
rs571402684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644756 | GCCTCCATCCAGGGG[G/T]GATCGTGGGCAATTT | 3059 |
rs571402854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636994 | TCCCCTCACTACCAC[C/T]ACCTGTCCCCACACA | 3059 |
rs571403233 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659848 | GAAGCAATGAGGACT[A/G]ATGGTCCCATCCTCC | 3059 |
rs571444745 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641573 | CAATAATAAGATGGA[A/G]TAAGATGGAACCAAT | 3059 |
rs571491713 | in-del | -/TTA | 0.0322114 | 0.122752 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649233 | ATTCTAAACAGGTCT[-/TTA]TTATTATTATTATTA | 3059 |
rs571535864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657809 | TCCAGCCTGGGTGAC[A/G]GAGTGAGACTCTGTC | 3059 |
rs571550416 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659149 | AGGTACTCAGTTTTT[A/G]TCAACTAAATAAATG | 3059 |
rs571867959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644116 | ATCTCAGCTAACTGT[G/T]AAGGAGCTGTCCTCT | 3059 |
rs571868256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650823 | TTAAGATCTTTTGCT[C/G]TTAAAAAGATGCCAT | 3059 |
rs571896492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650341 | AATTTATGTGAAAAT[A/G]TAAAGTCCTGGAATA | 3059 |
rs571929722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658511 | GGGAGTTGTAGGAAG[A/G]CTTTTCTGCTCAGTT | 3059 |
rs571997659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636196 | CAATACGACCTTTCC[C/T]GGCGGTTTACCTGTC | 3059 |
rs572133970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658633 | ACTAGGTAACCCACG[A/G]GTCAAAATTGCTGGA | 3059 |
rs572175844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652628 | TCGTACCACTGCACT[C/T]CAGCCTGGATGACAG | 3059 |
rs572283313 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641100 | GTCACATCTGAGGTT[C/G]AAAAAGGGCAGTAAG | 3059 |
rs572434226 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656372 | TGTTGAATTTTTGCT[A/T]GTTACACTATTTATT | 3059 |
rs572716066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649526 | AGGCGTGAGCCACCA[C/T]GCCTGGCCTAAACAG | 3059 |
rs572776910 | snp | C/T | 1.64814e-05 | 0.00287061 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121657296 | GATGTGTTCTGTGCG[C/T]CCAGACCCCTCGATG | 3059 |
rs572778724 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648965 | ATTCAGATGAAAGAT[C/G]AAGAAAATGGGGCCA | 3059 |
rs572798770 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659983 | TGACCAGAAACCAGA[A/C]AGGTAAGAAGTGCTA | 3059 |
rs572899966 | snp | A/T | 0.000757551 | 0.0194474 | missense | HCLS1 | GRCh38.p7 | 3:121644894 | TGAGAAGAGTGCTTC[A/T]CCACCTCGGCAACAT | 3059 |
rs572922480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647952 | ACTCATTGAAGCATC[A/G]TATATAATAGCAATA | 3059 |
rs573134499 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646597 | TATATATAATATATA[A/C/T]TAATATATATACTTA | 3059 |
rs573197754 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653730 | TTATTTCCACTTGCT[A/T]TAAAATGTCAGGGCA | 3059 |
rs573199755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645486 | ATAAAATAATAAAGA[A/G]AAGTTGCAACATAGA | 3059 |
rs573319387 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635191 | ACTTGACTTTCTCTC[G/T]TTCTTTCTTTTCTTT | 3059 |
rs573707112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658749 | GCCTTATTTCACTCA[A/G]GTTTCTATATATGAT | 3059 |
rs573799745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657863 | AAAGAATTAAACTAG[C/T]GAGCTCTGAAACCTC | 3059 |
rs573808335 | snp | C/T | 1.64963e-05 | 0.00287192 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631843 | GTAGACAGTGAGCTC[C/T]AGTCACTCCAGAAGC | 3059 |
rs573817339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645072 | GGTGCCAAGGAATAC[A/G]CGATGGGAGAGCAAG | 3059 |
rs573921840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652893 | AATTACGGACATGAC[A/G]ATATTATGTTTATTA | 3059 |
rs573929995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650865 | AAAAGTGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 3059 |
rs573957827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643230 | GTTGAAGTTTAAGCA[C/T]GTTCCTTTATATTAC | 3059 |
rs574019748 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650239 | TCATTAAGATGTCAG[A/T]TCTCCCTAAAATGAT | 3059 |
rs574026638 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650815 | CATCAGGATTAAGAT[-/C]TTTTGCTCTTAAAAA | 3059 |
rs574051865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649699 | AATTCCAATTCAATA[G/T]GCTGTGTTGTGCCTA | 3059 |
rs574270892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644197 | GAGTTCAAAGAATCC[A/G]ACCTAATAAGGCGTG | 3059 |
rs574274296 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631520 | AAACCACACAATCTA[A/G]ACGTACTTTCCCGGG | 3059 |
rs574300981 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659307 | TGGATTTGGTGTGAA[A/G]AAGTAACAACAGACA | 3059 |
rs574328450 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640106 | AGAAATCTTACAGAA[G/T]TTAAAAAGAAGAGAA | 3059 |
rs574383695 | snp | A/G | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662190 | GTAGTGTCAAAATAC[A/G]ATTTAGACTAGATGA | 3059 |
rs574636417 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641404 | TTATCAATGGAATAT[C/T]TTAGCAAGAAGGAAA | 3059 |
rs574653999 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661686 | CTTTCTGGCGGAGGC[C/T]GTAAGACCACTGCAA | 3059 |
rs574701904 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644780 | GCAATTTTCACAGGA[C/T]TGGAGGTGGGTGGTT | 3059 |
rs574717691 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660910 | CTTCGGAGTGAGAAA[C/T]TGAGCTGCTGCTTCA | 3059 |
rs574736108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634556 | GGTAAAGAGGTATCG[A/G]TAGAGGAACAAGGGA | 3059 |
rs574832114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639317 | AGTCCATAAGTCTCT[A/G]AGACAGTAAGTCTCA | 3059 |
rs575000842 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660860 | AAGCGCCCGGCTCCT[C/T]GCGTCCACACCGACT | 3059 |
rs575337370 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659641 | TATTGACTGAGTCAG[C/T]CGGGAGTCATGGCTG | 3059 |
rs575354000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645047 | GGTCAGATCTATAGC[C/T]TCTGACAGTGGTGCC | 3059 |
rs575507865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633775 | GAACTCCTGGCTTCA[A/G]GTGATCCTCTCACCT | 3059 |
rs575563664 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655975 | TGCTTCGGCCTCCTG[A/G]GTAGCTGGGATTACA | 3059 |
rs575569331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640019 | ATTGATAAACTTCTA[C/G]TAAGAATAATTAAAA | 3059 |
rs575685638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635161 | ATTCCTTCCCCGACG[C/T]CACTCTGTCTATCCA | 3059 |
rs576209881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641213 | CTTTAATTAAAAAAA[A/C]CCCGGAGATATAAGA | 3059 |
rs576430793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641790 | AGGGATTCAAAAACT[C/T]GATCAATATGGCCAG | 3059 |
rs576463605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662887 | TTCTCCCAGGACCAT[A/G]CATGGACCTGCATCA | 3059 |
rs576491700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641135 | ATATAGGATAATAAA[A/G]GTAGATCTAACATTC | 3059 |
rs576553135 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648040 | TACCTTTCACTAGTG[G/T]ACTAGGAAGTCATTA | 3059 |
rs576560584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648910 | AAGCTACTAGTACCA[A/C]GGACATGTAAATGCC | 3059 |
rs576762966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634626 | TAAAGCCAGGCTATA[C/T]GACCTAAGACTCGTG | 3059 |
rs577240147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633629 | TGTAGCCTCAAACTC[C/T]TGGGCTCAAACAATC | 3059 |
rs577300471 | snp | C/T | 0.000399281 | 0.0141238 | missense | HCLS1 | GRCh38.p7 | 3:121633126 | CCCTGCTGGTTCTCA[C/T]AGGCTCAGACTCTGA | 3059 |
rs577396053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662766 | AACAAAACAAAACAT[A/G]ATAATGCCTATCTAA | 3059 |
rs577410678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654770 | TTGTTTTTTGTTTTT[C/T]CATTTTGGGATCTGT | 3059 |
rs577433573 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639227 | CCTAATTGACTCTTA[C/T]ACAACACTATACCCC | 3059 |
rs577634314 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631328 | TCCTGGATATGCCTG[A/G]AAGAGGAAAGGTTGG | 3059 |
rs577700259 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632679 | CCCTCTACCCTTGCC[G/T]CCATCTAACAGCCTC | 3059 |
rs577704540 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121630973 | GGCTTATGCCTGTCA[A/T]CCCAGCACTTTGGGA | 3059 |
rs577744618 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652237 | GTATTGACTGCAAAG[A/C]GGTGCAGGGAAATTT | 3059 |
rs577875510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658708 | TGGTTGGCAATGAGC[A/G]GTGCTATAATATCCC | 3059 |
rs578059102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649593 | AACTAAACAACTTTT[A/C]AGTGTGAGGTACTGT | 3059 |
rs578124979 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652850 | AATAGCTTAGTTCAT[A/G]GGAATTTGCATTTCA | 3059 |
rs578151403 | snp | A/G | 8.24953e-05 | 0.0064219 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635835 | CAGCATGTGTGTTGC[A/G]GGAGAGGGGCAAGGG | 3059 |
rs578239334 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643072 | CAGCCAGCCCCAGAG[A/G]TAGTTTGTAGGGGCT | 3059 |
rs578254775 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642513 | GTGGGTGTGGTGGCT[C/T]ATGCCTGTAATCCCA | 3059 |
rs745340086 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | HCLS1 | GRCh38.p7 | 3:121634241 | GGCAGTGGGGCCGGT[A/G]CTGCTGGCTCTTCCA | 3059 |
rs745357376 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637030 | TTACTGCCCTGGCAC[A/C]CCCTGCTCTGCACAT | 3059 |
rs745424007 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | HCLS1 | GRCh38.p7 | 3:121634319 | TTTCGCTCCTGTTGC[C/T]TCCTGGCCACCTGCT | 3059 |
rs745526763 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638186 | GTCAAGCAATCCTCC[G/T]GAGTAACTGGGACCA | 3059 |
rs745551801 | snp | C/G | 1.6489e-05 | 0.00287128 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632016 | GGATATTAGAATGGT[C/G]AGACATGAATCTCTT | 3059 |
rs745556331 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651156 | AATCAATCAATCAAT[A/C]AAGTGAAAAAGCAAG | 3059 |
rs745626617 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636387 | CTCTGCACACTTTCC[C/T]AAACTTAGGGAACTC | 3059 |
rs745714416 | snp | C/T | 8.25866e-05 | 0.00642546 | missense | HCLS1 | GRCh38.p7 | 3:121632439 | TCCTCAACGTCCTCA[C/T]AGTCATTCTCAGGCT | 3059 |
rs745746479 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643013 | ACAGAATTGGTTAGA[A/G]TCAGAGCTGACAGGT | 3059 |
rs745757477 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657012 | GAGGCAGTTAATCCA[A/G]TAGACCCACTTGGGG | 3059 |
rs745772271 | in-del | -/ATTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655827 | TAATTGAAACCATTT[-/ATTT]ATTTATTTATTTATT | 3059 |
rs745845290 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642650 | GCATGGTGGTGCACA[A/C]TTGTAGTCACAGCTA | 3059 |
rs745951144 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | HCLS1 | GRCh38.p7 | 3:121644901 | AGTGCTTCTCCACCT[C/T]GGCAACATACTCATG | 3059 |
rs746029899 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647738 | TTAAATATTAGAGGA[A/C]AATGGTACCTATATT | 3059 |
rs746051653 | snp | A/G | 1.65408e-05 | 0.00287578 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647299 | ATTTTTTTAAAGCAA[A/G]TCTTTCCCTTTCAAC | 3059 |
rs746143911 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654504 | CAAGAGTGGAGAAAA[C/G]AAGGTGGAGAGAAGG | 3059 |
rs746153956 | in-del | -/ACCAGAA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659970 | ATCCTTGACCTATTG[-/ACCAGAA]ACCAGAAAGGTAAGA | 3059 |
rs746222681 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | HCLS1 | GRCh38.p7 | 3:121657334 | CTCCCCATCGTTGCT[C/T]CTTTTCAGAGATGTC | 3059 |
rs746254607 | snp | C/G | 1.66034e-05 | 0.00288122 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637116 | ATCCCTGTGCTATCT[C/G]TGACCTTCCCCCTTC | 3059 |
rs746316979 | snp | C/T | 3.29468e-05 | 0.00405861 | intron-variant, synonymous-codon | HCLS1 | GRCh38.p7 | 3:121637222 | CCATTTATCCTTCTC[C/T]ACCCCGTACCGGCCA | 3059 |
rs746323611 | snp | A/T | 0.000460025 | 0.0151592 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632583 | GAAGAGACAGTGTGG[A/T]GCACTGTGACTTCCA | 3059 |
rs746346533 | snp | A/C | 1.65304e-05 | 0.00287488 | missense | HCLS1 | GRCh38.p7 | 3:121632512 | CTGGCTCTTCCTCCA[A/C]CTGGAGGCCTTCCAG | 3059 |
rs746418691 | snp | G/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662645 | GAGACTGAGGCAGGA[G/T]AATCGCTTGAAACTG | 3059 |
rs746451673 | in-del | -/CT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636249 | TCCTCAAAGCTCAGG[-/CT]TTGGCAGACATGCCC | 3059 |
rs746489442 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642893 | GAGCCTGCCGGTCAG[A/G]TTGCTGAGGCTGAGT | 3059 |
rs746545796 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640461 | CGCAGATTAGTCAGA[A/C]GAAATGGCACAGCCA | 3059 |
rs746573749 | in-del | -/CTC | 3.29712e-05 | 0.00406011 | cds-indel | HCLS1 | GRCh38.p7 | 3:121634366 | CTCTCGCTTCCTCTT[-/CTC]CTCAGCCATGGACTC | 3059 |
rs746579032 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642986 | CCGACTGCTGACTAC[A/G]GAGAAGAGGAGACAG | 3059 |
rs746601311 | in-del | -/G | 1.64931e-05 | 0.00287163 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658236 | CCCACCCTCTGCACT[-/G]TCCAAGCAAAGCTAC | 3059 |
rs746622181 | snp | C/T | 0.00036242 | 0.0134566 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637247 | CGGCCACCAAAGCCA[C/T]GAGAGTAATCTGTGG | 3059 |
rs746628961 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652765 | TGAAGTGATTGTAGT[A/G]TTATTAAGGCCAACT | 3059 |
rs746685469 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643654 | GATACCCAACATTAC[C/T]GCAGAGTTTTGGAGC | 3059 |
rs746706081 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638060 | TGACACCACAGAAAA[C/T]CCAAGGGCATTTTTG | 3059 |
rs746774251 | snp | C/T | 1.64743e-05 | 0.00287 | missense | HCLS1 | GRCh38.p7 | 3:121635740 | TAAGCCTCACCGGCT[C/T]CTATGGGCGTCGTCT | 3059 |
rs746850639 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643930 | TTGCCTTCTACATCT[G/T]CCCTTAGCTTTGCAG | 3059 |
rs746880601 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | HCLS1 | GRCh38.p7 | 3:121632356 | CAGAAGAAAAAGAAG[A/G]ATCTTCAGGCTCGAG | 3059 |
rs747040676 | snp | A/G | 0.000250557 | 0.01119 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637096 | TCCAGAAAGGAAGGA[A/G]GGAGATCCCTGTGCT | 3059 |
rs747063631 | snp | A/G | 3.2969e-05 | 0.00405998 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632456 | GTCATTCTCAGGCTC[A/G]GGCTCAGGCTCGGGC | 3059 |
rs747095287 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642783 | CCTGTCTCAAAAACA[A/G]ACAAATGAACAAAAA | 3059 |
rs747144844 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654085 | TGGAGTTTTGACCTG[C/T]TCCATTTCTGACCTG | 3059 |
rs747153736 | snp | C/T | 1.64966e-05 | 0.00287194 | missense | HCLS1 | GRCh38.p7 | 3:121632502 | GCTTCGTACACTGGC[C/T]CTTCCTCCACCTGGA | 3059 |
rs747289675 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651246 | ATATATAAAGAACTT[C/T]CAGCAACTTAATAAA | 3059 |
rs747312612 | snp | C/T | 1.66225e-05 | 0.00288287 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631801 | GTGGAGGCAGAGCCA[C/T]TTTGGACATGGGAAA | 3059 |
rs747364877 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635613 | CTGGGAATATGAGGA[C/T]AGGGATCAGGTCTAA | 3059 |
rs747416232 | snp | C/T | 3.31137e-05 | 0.00406887 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657251 | TCCCATAACCCCCTT[C/T]CTTTTCTCCAGTCCT | 3059 |
rs747439010 | snp | C/T | 3.29565e-05 | 0.00405921 | missense | HCLS1 | GRCh38.p7 | 3:121657322 | CGATGGTCTTGGCTC[C/T]CCATCGTTGCTCCTT | 3059 |
rs747446838 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121632672 | TCTTCTCCCCTCTAC[C/T]CTTGCCTCCATCTAA | 3059 |
rs747471200 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648603 | GACTTTACCAGCGCA[A/G]GACAACCAGACACAT | 3059 |
rs747473070 | snp | A/G | 3.29554e-05 | 0.00405914 | missense | HCLS1 | GRCh38.p7 | 3:121631908 | CATGGCAACGTCCCC[A/G]CCACCAGCCCTCGTC | 3059 |
rs747551514 | in-del | -/TTA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649234 | ATTCTAAACAGGTCT[-/TTA]TTATTATTATTATTA | 3059 |
rs747563378 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649735 | CTTTTGACATATTAA[C/T]TCTCAGATATCCAAT | 3059 |
rs747623002 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662919 | TTTCATGCCCTAAGG[C/T]CCAGCTTATTTGGTT | 3059 |
rs747709357 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637227 | TATCCTTCTCCACCC[C/T]GTACCGGCCACCAAA | 3059 |
rs747714866 | snp | C/G | 1.6476e-05 | 0.00287014 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642881 | GTCTTAGCAGAAGAG[C/G]CTGCCGGTCAGATTG | 3059 |
rs747787833 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660618 | CTCCTGAAACACTTG[C/T]CTTGGGTTTAAGCCC | 3059 |
rs747882233 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638276 | CTGTGTTGCCCAGGC[C/T]AGCCTTAAACTCCTG | 3059 |
rs747897789 | snp | A/C | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661380 | TCATATAGATGTTCA[A/C]ATAAACGTCGACCAA | 3059 |
rs748051655 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | HCLS1 | GRCh38.p7 | 3:121635735 | ATCACTAAGCCTCAC[C/T]GGCTTCTATGGGCGT | 3059 |
rs748139355 | snp | A/C | 3.32044e-05 | 0.00407444 | missense | HCLS1 | GRCh38.p7 | 3:121632151 | CCCAGAGCCACAGCC[A/C]CAGCCCCAGCCCCAG | 3059 |
rs748428896 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643993 | TGGTTTTACCCCCCA[A/T]GATGCAAACAATTAA | 3059 |
rs748579183 | snp | A/G | 0.000559966 | 0.0167233 | missense | HCLS1 | GRCh38.p7 | 3:121634214 | GCGCTCACCTCTGAG[A/G]AGATTTTCTTGGGCA | 3059 |
rs748618787 | in-del | -/CTC | 1.64836e-05 | 0.0028708 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632423 | CTCATGCCTGTCCAT[-/CTC]CTCAACGTCCTCATA | 3059 |
rs748650183 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650968 | TGGTGAAACCCCGTC[C/T]CTACCAAAAATACAA | 3059 |
rs748811899 | snp | C/T | 0.000280433 | 0.011838 | missense | HCLS1 | GRCh38.p7 | 3:121634403 | TTCGCCTTCAGCCCA[C/T]GGGTACCACTAGAAG | 3059 |
rs748843375 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | HCLS1 | GRCh38.p7 | 3:121658266 | CTTCCAAACTCACCA[C/T]AAAGTCAGGATCTGT | 3059 |
rs748878546 | snp | C/T | 1.65583e-05 | 0.00287731 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632062 | GTCTTATATCAGGGG[C/T]CTCCATGTACCAGGC | 3059 |
rs748880168 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121632927 | CCCAGGACAGAGGAG[A/T]TTCCCAGAAGGCAAG | 3059 |
rs748894989 | snp | C/T | 1.65446e-05 | 0.00287612 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632135 | AGCCACAGCTGAGAT[C/T]CCCAGAGCCACAGCC | 3059 |
rs749048106 | snp | A/G | 4.94425e-05 | 0.0049718 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644768 | GGGTGATCGTGGGCA[A/G]TTTTCACAGGACTGG | 3059 |
rs749077930 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645108 | TTTTTCTGGAGACCT[A/G]CTCATCCCTGTTCTT | 3059 |
rs749137005 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634330 | TTGCCTCCTGGCCAC[C/T]TGCTGTGCCTTCTCC | 3059 |
rs749176945 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654305 | GCCTGACAACATCGT[A/G]ATTTTATATCTGTTG | 3059 |
rs749211027 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | HCLS1 | GRCh38.p7 | 3:121644876 | CCTTTGGCAGCATCC[A/G]TCTGAGAAGAGTGCT | 3059 |
rs749213640 | in-del | -/TCTCTCTCTCTCT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635262 | CTCTCTCTCTCTCTC[-/TCTCTCTCTCTCT]CCTCTCTCTCCTCTC | 3059 |
rs749264832 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655561 | GCAATAATCACACCT[C/T]GGATAAACCTCATTG | 3059 |
rs749269961 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647278 | GAGCCACCGCACCCG[A/G]CTTGTATTTTTTTAA | 3059 |
rs749303750 | in-del | CAGAAAAGGAAAAGGGTCTTGTGGTT/TTG | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655657 | TGAGTGGCCTTTATT[CAGAAAAGGAAAAGGGTCTTGTGGTT/TTG]TTTTTTTTTTTTTTT | 3059 |
rs749319943 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | HCLS1 | GRCh38.p7 | 3:121647333 | CCTTGTCCATTCGGT[C/T]TCTTTCTACTCCAAA | 3059 |
rs749397845 | snp | G/T | 1.64947e-05 | 0.00287177 | missense | HCLS1 | GRCh38.p7 | 3:121647429 | GCTCCTCTGATACTT[G/T]GTTCCTCAGCTGGTG | 3059 |
rs749629955 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660813 | TCCCATGGCTCAGAG[C/T]ACCCACCTCCACCTG | 3059 |
rs749678727 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644292 | ACGGTACTTTTTTTT[C/G]TCTTTAAAACAACAT | 3059 |
rs749708136 | snp | A/G/T | 3.75152e-05 | 0.00433087 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633061 | AATCTTTGGGGGTTT[A/G/T]CTTACCTCCGGGAGA | 3059 |
rs749943719 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652549 | ATCCCAGCTACTCGG[G/T]AAGCTGAGGTAGGAG | 3059 |
rs750009180 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | HCLS1 | GRCh38.p7 | 3:121644856 | CTCCGTACTTGCCCC[C/T]AAAGCCTTTGGCAGC | 3059 |
rs750023906 | snp | A/C/T | 4.96852e-05 | 0.00498403 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644955 | CAAGGATGGAGTGAG[A/C/T]GAAAAGATAAAAATG | 3059 |
rs750027205 | snp | C/T | 0.000115442 | 0.00759656 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634390 | CATGGACTCAAATTT[C/T]GCCTTCAGCCCACGG | 3059 |
rs750121257 | snp | A/C | 9.88989e-05 | 0.00703134 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635708 | GAAGGAAGTGAGGTG[A/C]ATGGAGAGTGAATCA | 3059 |
rs750301674 | snp | A/C/G | 3.2948e-05 | 0.00405871 | missense | HCLS1 | GRCh38.p7 | 3:121636472 | TTCCATACTGGCCAC[A/C/G]AAAGCCCTTGGCATA | 3059 |
rs750320223 | snp | C/T | 2.46418e-05 | 0.00351003 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632489 | AGGCTCAGGCTCTGC[C/T]TCGTACACTGGCTCT | 3059 |
rs750394706 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647534 | GGAAGCCTTGAAGTC[-/T]GTCCTGTTTACTTTC | 3059 |
rs750428338 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121658389 | TTAGGGACAAAAAAG[C/G]ATCAAGAGGAGGGAA | 3059 |
rs750435280 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636947 | TAGGCCCTGCTCTTA[A/G]TCCTTCTGTTTTCCT | 3059 |
rs750533010 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | HCLS1 | GRCh38.p7 | 3:121642930 | CAGTGTCCTTGCCTT[C/T]CTGAGATGTGTGCTT | 3059 |
rs750578811 | snp | A/G | 3.74855e-05 | 0.00432913 | missense | HCLS1 | GRCh38.p7 | 3:121633108 | GCAAGGGCACTGGGT[A/G]TTCCCTGCTGGTTCT | 3059 |
rs750680290 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635464 | TGTATTTTTTATAGA[A/G]ATGAGGTTTCCCCAT | 3059 |
rs750854323 | in-del | -/A | 0.000217761 | 0.0104323 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647272 | GGCGTGAGCCACCGC[-/A]ACCCGGCTTGTATTT | 3059 |
rs750877815 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649328 | GTAATCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 3059 |
rs750898200 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640966 | TACAGCTAAAGGAAG[A/G]ATTAGTGAACTTAAC | 3059 |
rs750997470 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641828 | GACTCAAGCCTGTAA[A/T]CCCAGCACTTTGGGA | 3059 |
rs751215274 | snp | A/G | 1.70673e-05 | 0.00292119 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644732 | CTGTCTTTCAACAAA[A/G]AAGCATGTGCCTCCA | 3059 |
rs751338615 | in-del | -/TTTG | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656570 | CTGGTATCGGAGGGT[-/TTTG]TTTGTTTGTTTGTTT | 3059 |
rs751425180 | snp | C/T | 1.8256e-05 | 0.0030212 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647526 | AGAAAAATGGAAGCC[C/T]TGAAGTCTGTCCTGT | 3059 |
rs751432457 | snp | A/G | 8.25784e-05 | 0.00642514 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635849 | CGGGAGAGGGGCAAG[A/G]GTAGTGGTGACCTGG | 3059 |
rs751516554 | snp | A/G | 1.64931e-05 | 0.00287163 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632429 | CCTGTCCATCTCCTC[A/G]ACGTCCTCATAGTCA | 3059 |
rs751518676 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | HCLS1 | GRCh38.p7 | 3:121636450 | TTATCCACTCGGTCC[C/T]TCTGGATTCCATACT | 3059 |
rs751537571 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645056 | TATAGCCTCTGACAG[C/T]GGTGCCAAGGAATAC | 3059 |
rs751663139 | snp | A/G/T | 0.00013184 | 0.00811813 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637265 | GAGTAATCTGTGGTC[A/G/T]AAGGAGCAGTCATGA | 3059 |
rs751673959 | in-del | -/TCTCTCTCTCTCTCT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635260 | CTCTCTCTCTCTCTC[-/TCTCTCTCTCTCTCT]CCTCTCTCTCCTCTC | 3059 |
rs751715922 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637185 | TCTCTCCCTTGTAGT[C/T]ATATCCCAGAGCTGC | 3059 |
rs751719344 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636672 | AAAAAATCTGGGAGC[A/G]AATGGAGAAGACAAA | 3059 |
rs751746202 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651917 | AGAAATAAGGATATG[C/T]CAACAAAAAGATTTG | 3059 |
rs751763823 | snp | G/T | 4.04604e-05 | 0.00449762 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633032 | AGACTCGAGAAGATG[G/T]GGTGGGGGCAGAGAA | 3059 |
rs751796699 | in-del | -/CCCAGA | 1.66056e-05 | 0.00288141 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632149 | CCCCAGAGCCACAGC[-/CCCAGA]CCCAGCCCCAGCCCC | 3059 |
rs751809062 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637535 | GAAAGTATAGAGAGT[A/G]AGGAGATTGCAGAAA | 3059 |
rs751853579 | snp | A/G | 9.15072e-05 | 0.00676352 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121633096 | GCCTAATGGGCAGCA[A/G]GGGCACTGGGTGTTC | 3059 |
rs751935482 | snp | C/T | 9.89136e-05 | 0.00703186 | missense | HCLS1 | GRCh38.p7 | 3:121634368 | CTCGCTTCCTCTTCT[C/T]CTCAGCCATGGACTC | 3059 |
rs751951891 | snp | A/G | 1.64825e-05 | 0.00287071 | intron-variant | HCLS1 | GRCh38.p7 | 3:121631991 | CTTCCCTCTGGGGAG[A/G]AAGTTGAGGGGATAT | 3059 |
rs752040032 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637601 | CTACTCCCATATAAG[A/C]ACATAGAAATGTCAG | 3059 |
rs752041854 | snp | C/T | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631540 | ACTTTCCCGGGTAAA[C/T]AAACTGGGAAGCCCA | 3059 |
rs752177587 | snp | A/C | 3.45614e-05 | 0.00415686 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647505 | GATCAAGAAACCCAT[A/C]TTCCCAGAAAAATGG | 3059 |
rs752233386 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649602 | ACTTTTAAGTGTGAG[A/G]TACTGTTAGGCTCTG | 3059 |
rs752267901 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635841 | GTGTGTTGCGGGAGA[A/G]GGGCAAGGGTAGTGG | 3059 |
rs752279862 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655354 | GAGCTGCTCAGAAGT[A/G]CTAAGTACTGCATTA | 3059 |
rs752334664 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | HCLS1 | GRCh38.p7 | 3:121632420 | CTGCTCATGCCTGTC[C/T]ATCTCCTCAACGTCC | 3059 |
rs752357950 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652541 | TGCCTGTAATCCCAG[C/T]TACTCGGGAAGCTGA | 3059 |
rs752655948 | snp | G/T | 1.64765e-05 | 0.00287019 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121635793 | CTCCATTTCATTGAA[G/T]CCGACAGCGCTCTGC | 3059 |
rs752707412 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633977 | AATAATTGGCTGTGC[A/T]GGCTGGTGACTTGCT | 3059 |
rs752840934 | in-del | -/T | 1.6473e-05 | 0.00286988 | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121642937 | CTTGCCTTTCTGAGA[-/T]GTGTGCTTCTCCACT | 3059 |
rs752892564 | in-del | -/A | 2.03415e-05 | 0.0031891 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633028 | CTAAGACTCGAGAAG[-/A]ATGGGGTGGGGGCAG | 3059 |
rs752899993 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121636479 | CTGGCCACCAAAGCC[C/T]TTGGCATAATCTGCA | 3059 |
rs752903669 | snp | A/G | 1.6537e-05 | 0.00287545 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658219 | CCAGATGCCCTCCTC[A/G]CCCCACCCTCTGCAC | 3059 |
rs753002605 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637707 | TCAGGGGCCGAGGCA[G/T]GTGGATCACCTGAGG | 3059 |
rs753007937 | in-del | -/TTA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649236 | CTAAACAGGTCTTTA[-/TTA]TTATTATTATTATTA | 3059 |
rs753072223 | snp | C/G | 2.06264e-05 | 0.00321135 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644712 | TCCTCACAGCATCCA[C/G]TGTCCTGTCTTTCAA | 3059 |
rs753086881 | snp | A/G | 8.23621e-05 | 0.00641672 | missense | HCLS1 | GRCh38.p7 | 3:121642963 | CCACTTCTCCTTTAT[A/G]ATCAAAGCCGACTGC | 3059 |
rs753102988 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653449 | TGATATAGGATTGTT[C/T]TTAAAAAGTACTCTG | 3059 |
rs753160799 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642666 | TTGTAGTCACAGCTA[C/G]TCAGAACGCTGAGGT | 3059 |
rs753193137 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644814 | AGAGAGAGTGGTCAC[C/T]TACCTTGTCTGCCCT | 3059 |
rs753236130 | snp | C/T | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631517 | GGCAAACCACACAAT[C/T]TAGACGTACTTTCCC | 3059 |
rs753268549 | snp | C/G | 1.64855e-05 | 0.00287097 | missense | HCLS1 | GRCh38.p7 | 3:121634361 | TCTTCCTCTCGCTTC[C/G]TCTTCTCCTCAGCCA | 3059 |
rs753360195 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635716 | TGAGGTGCATGGAGA[A/G]TGAATCACTAAGCCT | 3059 |
rs753422914 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642409 | AGGACACAGAGCTTG[C/T]GGTGAGCCAATATAG | 3059 |
rs753425148 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121658124 | TGACAGCCAATTGTC[C/T]TACCAATTAGTCCCA | 3059 |
rs753458716 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | HCLS1 | GRCh38.p7 | 3:121647390 | TGGGCCCTGACTCCA[C/T]CTCTTTCTTCCTGAG | 3059 |
rs753473025 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121635778 | AGCTGTGGTCGGGGC[C/T]TCCATTTCATTGAAG | 3059 |
rs753515153 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643518 | ATTCCCAGTTGATAA[C/T]GCTGTGCCTCTTCTC | 3059 |
rs753577860 | snp | A/C | 1.65105e-05 | 0.00287315 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632300 | TCCCCTGGACATGAG[A/C]AAATTCTCCTGCTTC | 3059 |
rs753619544 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656790 | AGTGGCCTCTTTTTA[C/T]AGCATTTATTCTGAG | 3059 |
rs753752592 | in-del | -/AGCCAC | 0.000166021 | 0.00910948 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632140 | AGCTGAGATCCCCAG[-/AGCCAC]AGCCACAGCCCCAGC | 3059 |
rs753862912 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649397 | TGCATGTCATGCCCC[A/G]CTAGATTTTGTATTT | 3059 |
rs753962859 | snp | A/C | 1.64754e-05 | 0.00287009 | missense | HCLS1 | GRCh38.p7 | 3:121634286 | TGTGGAGCCTCAGGG[A/C]TCCTCTTTGTCACAG | 3059 |
rs754053756 | snp | G/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662331 | ATGAGGTAGTGAGGT[G/T]TATCACACAGAAAAA | 3059 |
rs754073020 | snp | C/T | 1.66106e-05 | 0.00288184 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657232 | CGAGTTTTCTTTGGG[C/T]TCTTCCCATAACCCC | 3059 |
rs754143382 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648293 | ATCCCTAAGAGAAAG[C/T]ACCACCAAAAAAGGC | 3059 |
rs754198823 | snp | G/T | 1.65026e-05 | 0.00287246 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658377 | AGATGGGAATAATTA[G/T]GGACAAAAAAGGATC | 3059 |
rs754209481 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643098 | GGGCTTCAGGCTGAG[C/T]ATAGGTGTTTAATGT | 3059 |
rs754222081 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640393 | TCTCCTTCACTAAAA[G/T]AAGTTTATAAACAAG | 3059 |
rs754365872 | snp | C/T | 3.0859e-05 | 0.00392792 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644693 | TCCCTGTGACGGTGT[C/T]AGGTCCTCACAGCAT | 3059 |
rs754367904 | in-del | -/GAGA | 1.64754e-05 | 0.00287009 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644798 | GAGGTGGGTGGTTGG[-/GAGA]GAGAGTGGTCACTTA | 3059 |
rs754420540 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638822 | AGAACAATACCTTAC[A/C]TCAGGAGTATGTATG | 3059 |
rs754450913 | snp | C/T | 3.295e-05 | 0.00405881 | missense | HCLS1 | GRCh38.p7 | 3:121635780 | CTGTGGTCGGGGCCT[C/T]CATTTCATTGAAGCC | 3059 |
rs754501479 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635722 | GCATGGAGAGTGAAT[C/T]ACTAAGCCTCACCGG | 3059 |
rs754540495 | snp | C/T | 3.29968e-05 | 0.00406169 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632306 | GGACATGAGCAAATT[C/T]TCCTGCTTCTCCTCC | 3059 |
rs754541179 | snp | C/T | 3.30934e-05 | 0.00406763 | missense | HCLS1 | GRCh38.p7 | 3:121632136 | GCCACAGCTGAGATC[C/T]CCAGAGCCACAGCCC | 3059 |
rs754579197 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649137 | ACAGAAAAACTAGTC[-/A]GGGGATCATACCAAT | 3059 |
rs754643029 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655150 | GAAATGTGCAGGGTC[A/T]CCATGTTGTACCACT | 3059 |
rs754655049 | snp | C/G | 3.30502e-05 | 0.00406497 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658392 | GGGACAAAAAAGGAT[C/G]AAGAGGAGGGAAAAT | 3059 |
rs754692527 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647016 | AGACAGAGTCTCGCT[C/G]TGTCTCCCAGGCTGG | 3059 |
rs754751278 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | HCLS1 | GRCh38.p7 | 3:121644879 | TTGGCAGCATCCGTC[C/T]GAGAAGAGTGCTTCT | 3059 |
rs754813274 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633936 | CCAGCCTGAAGTGAC[A/G]GCCCCTTCCTCATAG | 3059 |
rs754818917 | snp | A/T | 2.02784e-05 | 0.00318415 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633030 | TAAGACTCGAGAAGA[A/T]GGGGTGGGGGCAGAG | 3059 |
rs754933976 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121632924 | TTGCCCAGGACAGAG[C/G]AGTTTCCCAGAAGGC | 3059 |
rs755040563 | in-del | -/AG | 3.39582e-05 | 0.00412043 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632236 | ATGAAGAAGGCAAAC[-/AG]AGAAAGATCCTACTG | 3059 |
rs755046173 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | HCLS1 | GRCh38.p7 | 3:121634296 | CAGGGCTCCTCTTTG[C/T]CACAGCCTTTCGCTC | 3059 |
rs755049159 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121658935 | GTGTAAGGTCAGCAG[C/T]GACAGTCGGCTGAAA | 3059 |
rs755067513 | in-del | -/ACACAC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639011 | CATCGCAAGACTCCA[-/ACACAC]ACACACACGCACACA | 3059 |
rs755100532 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121631888 | AGGGAAGAGTCCAAA[A/G]TGGCCATGGCAACGT | 3059 |
rs755126270 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656181 | ATTAAACAATGTGGT[A/G]TTGTCATCCAGTTGT | 3059 |
rs755138778 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660106 | TGGCTGTCACCCCAG[A/C]TCTGTGACTAAGCCT | 3059 |
rs755139135 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643957 | GCAGTATGTTTTAAA[C/T]TTTCCTGATTTTGTT | 3059 |
rs755270317 | snp | A/G | 4.94548e-05 | 0.00497242 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636394 | CACTTTCCTAAACTT[A/G]GGGAACTCTTCTTAA | 3059 |
rs755330806 | in-del | -/AC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639015 | GCAAGACTCCAACAC[-/AC]ACACACACGCACACA | 3059 |
rs755338082 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636786 | TCAGCCATCCGTATG[C/G]GTTCCAGGGAAGCAG | 3059 |
rs755366947 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121642952 | TGTGTGCTTCTCCAC[C/T]TCTCCTTTATAATCA | 3059 |
rs755408383 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649766 | TTAAGTTTTAAAAGA[A/C]TTTGTATTGATAAAG | 3059 |
rs755455142 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637700 | CAGCACTTCAGGGGC[C/T]GAGGCAGGTGGATCA | 3059 |
rs755527595 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121658044 | GCCTGTCAATCACAC[-/T]GTCAAACTCACCCAC | 3059 |
rs755529606 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649679 | AGATAGAGAGGAAAA[C/G]AAAAAATTCCAATTC | 3059 |
rs755531827 | snp | C/T | 6.59065e-05 | 0.00574012 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634200 | TCCCAGAGGGCCAGG[C/T]GCTCACCTCTGAGGA | 3059 |
rs755591638 | snp | G/T | 0.000131776 | 0.00811608 | missense | HCLS1 | GRCh38.p7 | 3:121644865 | TGCCCCCAAAGCCTT[G/T]GGCAGCATCCGTCTG | 3059 |
rs755732373 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656750 | CTGTATTTTAAAAGT[A/T]ATTTGGGCCAGTTAT | 3059 |
rs755883294 | snp | A/G | 1.64825e-05 | 0.00287071 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635711 | GGAAGTGAGGTGCAT[A/G]GAGAGTGAATCACTA | 3059 |
rs755927429 | snp | A/C | 1.64732e-05 | 0.0028699 | missense | HCLS1 | GRCh38.p7 | 3:121632443 | CAACGTCCTCATAGT[A/C]ATTCTCAGGCTCGGG | 3059 |
rs755933127 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655397 | CCCATTGACCTGTAA[C/G]TATACATCTTCAGGG | 3059 |
rs756033634 | snp | A/G | 1.71923e-05 | 0.00293187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632598 | AGCACTGTGACTTCC[A/G]CTTTCCAGGAGGAAT | 3059 |
rs756103142 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634039 | TTTCTAACATTCTGA[C/T]AGGAGGTCCAATTAC | 3059 |
rs756138985 | in-del | -/AAGCATCTCTCAAGTAAGC | 3.3077e-05 | 0.00406662 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633184 | GGCCTGTGGAAAATG[-/AAGCATCTCTCAAGTAAGC]AAGCCTCCATCTTCA | 3059 |
rs756162960 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662189 | TGTAGTGTCAAAATA[C/T]GATTTAGACTAGATG | 3059 |
rs756172136 | snp | A/G | 8.23635e-05 | 0.00641677 | missense | HCLS1 | GRCh38.p7 | 3:121642938 | TTGCCTTTCTGAGAT[A/G]TGTGCTTCTCCACTT | 3059 |
rs756220255 | snp | G/T | 1.64931e-05 | 0.00287163 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634175 | CTGGGCAAGAGATCC[G/T]GGATGTGGATCCCAG | 3059 |
rs756278135 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121632082 | ATGTACCAGGCTCCT[C/T]GGGCCACTCCCAACC | 3059 |
rs756286326 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660589 | ACACTTTGCTTGATG[C/T]TGGTGCTAGATGGCT | 3059 |
rs756389789 | snp | C/T | 1.88571e-05 | 0.00307053 | missense | HCLS1 | GRCh38.p7 | 3:121633111 | AGGGCACTGGGTGTT[C/T]CCTGCTGGTTCTCAC | 3059 |
rs756403060 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658253 | CCAAGCAAAGCTACT[C/T]CCAAACTCACCACAA | 3059 |
rs756418046 | snp | A/G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659251 | CTAGACGGCCTTCCG[A/G/T]ACTGTGCAGAAGGAA | 3059 |
rs756439704 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638783 | GCATTCTAAGAGACA[A/T]GAAAGACATGCTCCA | 3059 |
rs756580210 | in-del | -/CTCAGGCTCGGG | 0.000165695 | 0.00910054 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632447 | GTCCTCATAGTCATT[-/CTCAGGCTCGGG]CTCAGGCTCGGGCTC | 3059 |
rs756659066 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652343 | ACTATTTGCTTATAA[C/T]GATTAGGTATCAATA | 3059 |
rs756707069 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637708 | CAGGGGCCGAGGCAG[A/G]TGGATCACCTGAGGT | 3059 |
rs756752441 | snp | A/G | 1.64743e-05 | 0.00287 | missense | HCLS1 | GRCh38.p7 | 3:121632487 | TCAGGCTCAGGCTCT[A/G]CTTCGTACACTGGCT | 3059 |
rs756883265 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643543 | CTTCTCTTTCATTAC[A/T]CAATAATGGAAACAC | 3059 |
rs756898922 | snp | A/G | 3.2956e-05 | 0.00405918 | stop-gained | HCLS1 | GRCh38.p7 | 3:121634308 | TTGTCACAGCCTTTC[A/G]CTCCTGTTGCCTCCT | 3059 |
rs756983398 | snp | C/G | 3.2956e-05 | 0.00405918 | missense | HCLS1 | GRCh38.p7 | 3:121635798 | TTTCATTGAAGCCGA[C/G]AGCGCTCTGCAGGCA | 3059 |
rs757006680 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | HCLS1 | GRCh38.p7 | 3:121644844 | TGTCCCTCTCAACTC[C/T]GTACTTGCCCCCAAA | 3059 |
rs757033672 | snp | G/T | 1.6486e-05 | 0.00287102 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636384 | CTTCTCTGCACACTT[G/T]CCTAAACTTAGGGAA | 3059 |
rs757079321 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642493 | AAAAAGTATGTAAAA[C/T]AGCGGTGGGTGTGGT | 3059 |
rs757104479 | in-del | -/CAGCCC/CAGCCCCAGCCC | 4.96811e-05 | 0.00498382 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632145 | AGATCCCCAGAGCCA[-/CAGCCC/CAGCCCCAGCCC]CAGCCCCAGCCCCAG | 3059 |
rs757135736 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653459 | TTGTTTTTAAAAAGT[A/T]CTCTGTGTTTTGCAA | 3059 |
rs757215425 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655997 | GGGATTACAGGTGCC[C/T]GCCACCACGCCCATC | 3059 |
rs757231296 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650692 | CTAAAACTGTCAGTC[C/T]TTTAGGACAAAACAT | 3059 |
rs757442924 | snp | A/G | 2.01656e-05 | 0.00317528 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633033 | GACTCGAGAAGATGG[A/G]GTGGGGGCAGAGAAT | 3059 |
rs757535540 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636831 | CTCTGTGAGGACAGC[A/C]GAGATCCCTCTAAGA | 3059 |
rs757559288 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649421 | TGTATTTTTAGTAGA[G/T]ACAGGGTTTCACCAT | 3059 |
rs757601050 | snp | C/G | 1.83687e-05 | 0.00303051 | missense | HCLS1 | GRCh38.p7 | 3:121633099 | TAATGGGCAGCAAGG[C/G]CACTGGGTGTTCCCT | 3059 |
rs757624390 | snp | A/G | 1.64887e-05 | 0.00287125 | missense | HCLS1 | GRCh38.p7 | 3:121634373 | TTCCTCTTCTCCTCA[A/G]CCATGGACTCAAATT | 3059 |
rs757642882 | snp | C/G | 3.29696e-05 | 0.00406001 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632000 | GGGGAGAAAGTTGAG[C/G]GGATATTAGAATGGT | 3059 |
rs757643613 | snp | A/C | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662474 | GGGCACGGTGGCTCA[A/C]ACCTCTAATCCCAGC | 3059 |
rs757651482 | in-del | -/TTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633222 | CTCCATCTTCACTCC[-/TTT]TTTTTTTTTGAGATA | 3059 |
rs757667210 | snp | A/C | 3.29571e-05 | 0.00405924 | missense | HCLS1 | GRCh38.p7 | 3:121657325 | TGGTCTTGGCTCCCC[A/C]TCGTTGCTCCTTTTC | 3059 |
rs757692384 | in-del | -/TG | 1.64827e-05 | 0.00287073 | splice-acceptor-variant | HCLS1 | GRCh38.p7 | 3:121644930 | TGGCCCACTGCACTC[-/TG]AGAAAAATCAAGGAT | 3059 |
rs757767048 | snp | A/G | 1.64999e-05 | 0.00287222 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658231 | CTCACCCCACCCTCT[A/G]CACTGTCCAAGCAAA | 3059 |
rs757823701 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | HCLS1 | GRCh38.p7 | 3:121632395 | CATAGTCCCCCTCTG[A/G]TTCATCCTCCTGCTC | 3059 |
rs757912463 | snp | C/G | 1.64751e-05 | 0.00287007 | missense | HCLS1 | GRCh38.p7 | 3:121632352 | AGAGCAGAAGAAAAA[C/G]AAGAATCTTCAGGCT | 3059 |
rs757926053 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652625 | AGATCGTACCACTGC[A/C]CTCCAGCCTGGATGA | 3059 |
rs758060088 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643522 | CCAGTTGATAATGCT[G/T]TGCCTCTTCTCTTTC | 3059 |
rs758152517 | in-del | -/TTCTTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653973 | GACATAGTGATTTTA[-/TTCTTT]TTCTTTTTCTTTTTT | 3059 |
rs758207778 | snp | C/T | 4.9467e-05 | 0.00497303 | missense | HCLS1 | GRCh38.p7 | 3:121647408 | CTTTCTTCCTGAGAA[C/T]ATCATGCTCCTCTGA | 3059 |
rs758214954 | snp | A/C/G | 3.29501e-05 | 0.00405884 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121644905 | CTTCTCCACCTCGGC[A/C/G]ACATACTCATGGCCC | 3059 |
rs758322891 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643778 | TACATGACACACTGA[C/T]TGGGTGATTCCATTT | 3059 |
rs758355551 | snp | A/G | 0.000131826 | 0.00811762 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121657308 | GCGTCCAGACCCCTC[A/G]ATGGTCTTGGCTCCC | 3059 |
rs758467846 | snp | G/T | 1.64784e-05 | 0.00287035 | missense | HCLS1 | GRCh38.p7 | 3:121631968 | CCGGATCAAAGGAAA[G/T]CTCATCACTTCCCTC | 3059 |
rs758540758 | snp | C/T | 1.65151e-05 | 0.00287355 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658223 | ATGCCCTCCTCACCC[C/T]ACCCTCTGCACTGTC | 3059 |
rs758585835 | snp | A/T | 1.6477e-05 | 0.00287024 | missense | HCLS1 | GRCh38.p7 | 3:121636489 | AAGCCCTTGGCATAA[A/T]CTGCAGGACAGAAAG | 3059 |
rs758593267 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650911 | GGGAGGTCAAGGCGG[A/G]TGGATCACAAGGTCA | 3059 |
rs758664331 | in-del | -/C | 1.73186e-05 | 0.00294261 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647508 | CAAGAAACCCATCTT[-/C]CCAGAAAAATGGAAG | 3059 |
rs758676885 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | HCLS1 | GRCh38.p7 | 3:121634220 | ACCTCTGAGGAGATT[C/T]TCTTGGGCAGTGGGG | 3059 |
rs758685533 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636643 | TGGATGGGAAGAGAG[A/G]GAAACAGATGGGGAA | 3059 |
rs758743103 | snp | A/T | 2.41257e-05 | 0.00347308 | missense | HCLS1 | GRCh38.p7 | 3:121632494 | CAGGCTCTGCTTCGT[A/T]CACTGGCTCTTCCTC | 3059 |
rs758780348 | snp | A/T | 1.96748e-05 | 0.0031364 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644715 | TCACAGCATCCACTG[A/T]CCTGTCTTTCAACAA | 3059 |
rs758897981 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662649 | CTGAGGCAGGAGAAT[C/T]GCTTGAAACTGGAAG | 3059 |
rs759037096 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121647391 | GGGCCCTGACTCCAT[C/T]TCTTTCTTCCTGAGA | 3059 |
rs759055415 | snp | A/G | 1.70907e-05 | 0.00292319 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647498 | CTAGGGAGATCAAGA[A/G]ACCCATCTTCCCAGA | 3059 |
rs759064368 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634717 | GGACACTGCAGCCTC[A/C]ACCTCCCAGGCTCAA | 3059 |
rs759090532 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656414 | GCTACTAATGTTTGA[C/T]ATTCTGATACTATCC | 3059 |
rs759132094 | in-del | -/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635117 | CCACCCCACCCCTGT[-/C]CCAAGCCACACTGTG | 3059 |
rs759276978 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636066 | GCCTAGAATGTAGCA[A/G]GGCCCCCTGGCTCAT | 3059 |
rs759395954 | snp | A/G | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662592 | GTGCAAAGATTAGCC[A/G]GGCATGGTGGCAGGT | 3059 |
rs759403341 | snp | A/G | 1.64798e-05 | 0.00287047 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637262 | CGAGAGTAATCTGTG[A/G]TCGAAGGAGCAGTCA | 3059 |
rs759407320 | snp | A/G | 0.000428251 | 0.0146268 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642902 | GGTCAGATTGCTGAG[A/G]CTGAGTGAAGTACAG | 3059 |
rs759407542 | snp | A/G | 3.63921e-05 | 0.00426553 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121633085 | CGGGAGAGTCTGCCT[A/G]ATGGGCAGCAAGGGC | 3059 |
rs759495448 | snp | C/T | 3.86361e-05 | 0.00439506 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633189 | GTGGAAAATGAAGCA[C/T]CTCTCAAGTAAGCAA | 3059 |
rs759661285 | snp | G/T | 1.64741e-05 | 0.00286998 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644804 | GGTGGTTGGGAGAGA[G/T]AGTGGTCACTTACCT | 3059 |
rs759748703 | in-del | -/G | 1.67452e-05 | 0.0028935 | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121632547 | CTAGGGGGCAGAGCT[-/G]GGGGCTCCTCATTGT | 3059 |
rs759783676 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653425 | AAATCAGGATGCCAA[C/T]GTCATCTATGATATA | 3059 |
rs759812697 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | HCLS1 | GRCh38.p7 | 3:121636439 | GGTGCTTTACCTTAT[C/T]CACTCGGTCCTTCTG | 3059 |
rs759823962 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638638 | TACACATTTTTTTTC[C/T]ACTTATGTGATGCAG | 3059 |
rs759830049 | snp | A/G | 0.000181883 | 0.00953459 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632474 | CTCAGGCTCGGGCTC[A/G]GGCTCAGGCTCTGCT | 3059 |
rs759916155 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | HCLS1 | GRCh38.p7 | 3:121632415 | TCCTCCTGCTCATGC[C/T]TGTCCATCTCCTCAA | 3059 |
rs759991425 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644585 | TATTCATTCAAACAC[A/G]CAGTTTGAGAGTCTT | 3059 |
rs760002949 | snp | C/T | | | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632390 | CTCCTCATAGTCCCC[C/T]TCTGGTTCATCCTCC | 3059 |
rs760037235 | in-del | -/GAGAAGA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653746 | AAAATGTCAGGGCAC[-/GAGAAGA]GAGAAGAGGACAGGG | 3059 |
rs760089351 | snp | A/C | 2.51102e-05 | 0.00354323 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644702 | CGGTGTCAGGTCCTC[A/C]CAGCATCCACTGTCC | 3059 |
rs760099006 | in-del | -/GGCTCGGGCTCG | | | cds-indel | HCLS1 | GRCh38.p7 | 3:121632450 | TCATAGTCATTCTCA[-/GGCTCGGGCTCG]GGCTCGGGCTCAGGC | 3059 |
rs760230001 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655051 | TCACTCCTTGATAAC[C/G]TGGGTAAATGGGAGA | 3059 |
rs760378199 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652659 | GCGAAACTCCGTCTC[-/A]AAAAAAAACAAAGTT | 3059 |
rs760425153 | snp | A/G | 1.64827e-05 | 0.00287073 | missense | HCLS1 | GRCh38.p7 | 3:121647378 | CATGGGATGCTTTGG[A/G]CCCTGACTCCATCTC | 3059 |
rs760508122 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649383 | TGGGATTACAGGCAT[G/T]CATGTCATGCCCCGC | 3059 |
rs760534243 | snp | C/T | 3.30967e-05 | 0.00406783 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658213 | AGTGGCCCAGATGCC[C/T]TCCTCACCCCACCCT | 3059 |
rs760554492 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | HCLS1 | GRCh38.p7 | 3:121658295 | GTGTCCCAATCATCA[C/T]CCTGGGTCTCCACGG | 3059 |
rs760560653 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636209 | CCCGGCGGTTTACCT[C/G]TCTCTCTGTATGCCT | 3059 |
rs760599135 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638746 | GGCATGAATATGAGA[C/T]AAAGTGATCTCAAGA | 3059 |
rs760601153 | in-del | -/C | 1.64798e-05 | 0.00287047 | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121631978 | GAAAGCTCATCACTT[-/C]CCCTCTGGGGAGAAA | 3059 |
rs760837782 | snp | G/T | 1.64741e-05 | 0.00286998 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644800 | GGTGGGTGGTTGGGA[G/T]AGAGAGTGGTCACTT | 3059 |
rs760844408 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641619 | AATATGGTTGGTTAA[A/C]AAGAATGTAGTTAAA | 3059 |
rs760944527 | snp | A/G | 1.66255e-05 | 0.00288314 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647476 | ACATGACCAAGGCTC[A/G]TCTATCCTAGGGAGA | 3059 |
rs761129522 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654773 | TTTTTTGTTTTTTCA[C/T]TTTGGGATCTGTCAG | 3059 |
rs761129707 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633688 | GACTATAGGCACACA[C/T]CACCATGCCCAGCTA | 3059 |
rs761135367 | snp | C/T | 3.29712e-05 | 0.00406011 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635820 | CTGCAGGCAGGAGAA[C/T]AGCATGTGTGTTGCG | 3059 |
rs761225411 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | HCLS1 | GRCh38.p7 | 3:121632396 | ATAGTCCCCCTCTGG[G/T]TCATCCTCCTGCTCA | 3059 |
rs761226958 | snp | C/T | 0.000131841 | 0.00811808 | intron-variant, synonymous-codon | HCLS1 | GRCh38.p7 | 3:121637156 | CTCACCTCTCTGGGA[C/T]TCGTGTTTCTCCGTC | 3059 |
rs761228231 | in-del | -/TCTCTCTCTCTCT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635260 | CTCTCTCTCTCTCTC[-/TCTCTCTCTCTCT]CTCCTCTCTCTCCTC | 3059 |
rs761325867 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653619 | GGTAAAATATTATTA[C/T]TCTCCTCAGCATCAT | 3059 |
rs761328084 | snp | C/G/T | 1.66482e-05 | 0.0028851 | synonymous-codon, missense | HCLS1 | GRCh38.p7 | 3:121632533 | GGCCTTCCAGAGTCC[C/G/T]AGGGGGCAGAGCTGG | 3059 |
rs761353621 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659619 | TGCTAAGGGGACACC[C/G]GAGAGATATTGACTG | 3059 |
rs761431137 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655621 | GCATCCTCATCTGGA[A/C]AATTCCCAGAATACC | 3059 |
rs761462653 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657581 | AGCATTTTAGGAGGC[C/T]GAGGCGGGTGGATCT | 3059 |
rs761486488 | snp | A/C/G | 3.29637e-05 | 0.00405968 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121631861 | TCACTCCAGAAGCTT[A/C/G]ACATAATTTGCAGGG | 3059 |
rs761641478 | snp | A/C | 1.64819e-05 | 0.00287066 | missense | HCLS1 | GRCh38.p7 | 3:121634339 | GGCCACCTGCTGTGC[A/C]TTCTCCTCTTCCTCT | 3059 |
rs761698836 | snp | A/T | 1.64857e-05 | 0.00287099 | missense | HCLS1 | GRCh38.p7 | 3:121657287 | CACCTACTTGATGTG[A/T]TCTGTGCGTCCAGAC | 3059 |
rs761702598 | snp | A/G | | | missense | HCLS1 | GRCh38.p7 | 3:121658301 | CAATCATCACCCTGG[A/G]TCTCCACGGAAACAG | 3059 |
rs761736566 | in-del | -/AGGCTCAGGCTT | 6.58979e-05 | 0.00573974 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632479 | CTCGGGCTCAGGCTC[-/AGGCTCAGGCTT]AGGCTCTGCTTCGTA | 3059 |
rs761791701 | in-del | -/G | 1.64751e-05 | 0.00287007 | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121636481 | GCCACCAAAGCCCTT[-/G]GGCATAATCTGCAGG | 3059 |
rs761858013 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121636467 | CTGGATTCCATACTG[A/G]CCACCAAAGCCCTTG | 3059 |
rs761875638 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641569 | GAATCAATAATAAGA[C/T]GGAATAAGATGGAAC | 3059 |
rs761892813 | snp | A/T | 1.64765e-05 | 0.00287019 | missense | HCLS1 | GRCh38.p7 | 3:121658340 | TGGCCCACTACAGAC[A/T]TCCACATCTGAGAGT | 3059 |
rs761917549 | snp | A/G | 1.6832e-05 | 0.00290099 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632203 | CATAATGAGAAACAC[A/G]AACATGGGATCATCA | 3059 |
rs761935101 | in-del | -/AACAA | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662745 | TCTCAAAAAAAACCC[-/AACAA]AACAAAACAAAACAA | 3059 |
rs761989509 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642918 | CTGAGTGAAGTACAG[C/T]GTCCTTGCCTTTCTG | 3059 |
rs762171824 | snp | C/T | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631428 | AGTCTCACTTTATTT[C/T]GAATTTTAGGACTGA | 3059 |
rs762214453 | snp | A/C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651801 | CTGGTAGGAATGAAA[A/C/G]AGGGTAAATTCCCTT | 3059 |
rs762253887 | snp | C/T | 1.65176e-05 | 0.00287376 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644946 | GAGAAAAATCAAGGA[C/T]GGAGTGAGTGAAAAG | 3059 |
rs762271895 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121647361 | AAACCGACCTCCATA[A/G]CCATGGGATGCTTTG | 3059 |
rs762278152 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641760 | ACCTTATTTTCAACC[C/T]ATTAGAGAAAAAAGA | 3059 |
rs762358026 | snp | C/T | 1.64743e-05 | 0.00287 | missense | HCLS1 | GRCh38.p7 | 3:121635761 | GGCGTCGTCTTCTTA[C/T]AAGCTGTGGTCGGGG | 3059 |
rs762389253 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648762 | GCAGTTAATTTTAGA[A/C]AGCTGGCTATGAACC | 3059 |
rs762434372 | snp | A/C/G | 4.9522e-05 | 0.00497584 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657270 | TTCTCCAGTCCTTTC[A/C/G]GCACCTACTTGATGT | 3059 |
rs762450754 | snp | A/G | 4.94246e-05 | 0.0049709 | stop-gained | HCLS1 | GRCh38.p7 | 3:121636445 | TTACCTTATCCACTC[A/G]GTCCTTCTGGATTCC | 3059 |
rs762542912 | snp | C/T | 1.65132e-05 | 0.00287339 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637135 | CCTTCCCCCTTCCAA[C/T]CCCAACTCACCTCTC | 3059 |
rs762602757 | snp | C/T | 0.0006094 | 0.017445 | intron-variant, synonymous-codon | HCLS1 | GRCh38.p7 | 3:121637168 | GGACTCGTGTTTCTC[C/T]GTCTCTCCCTTGTAG | 3059 |
rs762615241 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633057 | AGAGAATCTTTGGGG[G/T]TTTGCTTACCTCCGG | 3059 |
rs762616081 | snp | A/G | 0.000230635 | 0.0107361 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632480 | CTCGGGCTCAGGCTC[A/G]GGCTCTGCTTCGTAC | 3059 |
rs762653127 | in-del | -/GAA | 9.8846e-05 | 0.00702945 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642889 | GAAGAGCCTGCCGGT[-/GAA]CAGATTGCTGAGGCT | 3059 |
rs762816948 | snp | A/G | 3.29473e-05 | 0.00405864 | missense | HCLS1 | GRCh38.p7 | 3:121634262 | GGCTCTTCCATAGCT[A/G]TCACTGGCTGTGGAG | 3059 |
rs762834186 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638492 | TCCTATAAGAGAGTG[C/G]TAGAAAAATTCTACT | 3059 |
rs762850355 | in-del | -/ATTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655824 | TACTTAATTGAAACC[-/ATTT]ATTTATTTATTTATT | 3059 |
rs762877331 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121658138 | CCTACCAATTAGTCC[C/G]AGTATGAGGGCTGTC | 3059 |
rs762914284 | snp | C/G | 1.74211e-05 | 0.00295132 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647510 | AGAAACCCATCTTCC[C/G]AGAAAAATGGAAGCC | 3059 |
rs763032767 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653002 | TCCCTCATCCCAAAC[A/G]CTTGGGACCAGAAGT | 3059 |
rs763032774 | snp | A/T | 1.65526e-05 | 0.00287681 | stop-gained | HCLS1 | GRCh38.p7 | 3:121632114 | ACCTCCTTGGTAATC[A/T]TATACAGCCACAGCT | 3059 |
rs763119132 | snp | C/T | 1.67511e-05 | 0.00289401 | splice-acceptor-variant | HCLS1 | GRCh38.p7 | 3:121632185 | GGCAGCCTGATGATC[C/T]TGCATAATGAGAAAC | 3059 |
rs763136883 | snp | A/G | 1.64743e-05 | 0.00287 | missense | HCLS1 | GRCh38.p7 | 3:121658311 | CCTGGGTCTCCACGG[A/G]AACAGACACATCATG | 3059 |
rs763254851 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121644821 | GTGGTCACTTACCTT[A/G]TCTGCCCTGTCCCTC | 3059 |
rs763426551 | snp | C/T | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631508 | GCACAATGAGGCAAA[C/T]CACACAATCTAGACG | 3059 |
rs763467588 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641831 | TCAAGCCTGTAATCC[C/T]AGCACTTTGGGAAGC | 3059 |
rs763554816 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643289 | CAGGAGAGGCATGCC[C/T]GCCTTATCTACCTCG | 3059 |
rs763585150 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654736 | CTCAGCTCTACAGCT[A/G]CTGTTTTGTTTTGTT | 3059 |
rs763637840 | in-del | -/TC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635250 | TTTTCTCTCTCTCTC[-/TC]TCTCTCTCTCTCTCT | 3059 |
rs763646245 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644633 | GTCTTTCAGCTCAGC[A/G]TGTGGCTTCCAACAT | 3059 |
rs763709694 | snp | A/G/T | 0.000243634 | 0.0110347 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632486 | CTCAGGCTCAGGCTC[A/G/T]GCTTCGTACACTGGC | 3059 |
rs763750462 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121658082 | TCTTTTCATCCCTGA[C/T]ACCAGGTATCGTGCA | 3059 |
rs763799656 | snp | A/G | 1.67055e-05 | 0.00289006 | missense | HCLS1 | GRCh38.p7 | 3:121632539 | CCAGAGTCCTAGGGG[A/G]CAGAGCTGGGGGCTC | 3059 |
rs763927682 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650642 | ACTGCACAGAAAAGT[C/T]TACTTGAAATGGGTC | 3059 |
rs764000529 | snp | C/T | 1.6498e-05 | 0.00287206 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631841 | CAGTAGACAGTGAGC[C/T]CTAGTCACTCCAGAA | 3059 |
rs764011681 | snp | C/T | 1.65537e-05 | 0.0028769 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632117 | TCCTTGGTAATCATA[C/T]ACAGCCACAGCTGAG | 3059 |
rs764028328 | snp | G/T | 1.651e-05 | 0.0028731 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635844 | TGTTGCGGGAGAGGG[G/T]CAAGGGTAGTGGTGA | 3059 |
rs764035763 | snp | A/C/T | 4.95187e-05 | 0.00497567 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658225 | GCCCTCCTCACCCCA[A/C/T]CCTCTGCACTGTCCA | 3059 |
rs764122793 | in-del | -/AA | 1.64792e-05 | 0.00287042 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644775 | GTGGGCAATTTTCAC[-/AA]AGGACTGGAGGTGGG | 3059 |
rs764228542 | snp | G/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662276 | AGATGACACCAAGAA[G/T]TCCCATCTTTCCTTA | 3059 |
rs764258954 | in-del | -/TT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655681 | AAAAGGGTCTTGTGG[-/TT]TTTTTTTTTTTTTTT | 3059 |
rs764260871 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648691 | AGATCCATCTGGTGG[C/T]CTTTAGTGGATAATT | 3059 |
rs764277420 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649396 | ATGCATGTCATGCCC[C/T]GCTAGATTTTGTATT | 3059 |
rs764369232 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | HCLS1 | GRCh38.p7 | 3:121658314 | GGGTCTCCACGGAAA[C/G]AGACACATCATGGCC | 3059 |
rs764517744 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654815 | ACAGCTACTGTTCTC[C/T]TCTCCAATTTCCCTC | 3059 |
rs764529452 | in-del | -/TTTCTCTCTCTCTC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635236 | CTCTCTTCTCTCCCT[-/TTTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 3059 |
rs764567754 | snp | A/G | 8.42098e-05 | 0.00648828 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634454 | AATTAGGGTTGTCTT[A/G]GATTGGAGAGTGGGG | 3059 |
rs764571987 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645736 | ACCAAATGACTACTG[C/T]ACTTTTGAATGAGTT | 3059 |
rs764641872 | snp | A/G | 3.29641e-05 | 0.00405968 | intron-variant | HCLS1 | GRCh38.p7 | 3:121631987 | ATCACTTCCCTCTGG[A/G]GAGAAAGTTGAGGGG | 3059 |
rs764672415 | in-del | -/GG | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657720 | CTGCAGGGACTACTT[-/GG]GAGGCTGAGGTAGGA | 3059 |
rs764690543 | snp | A/T | 1.72505e-05 | 0.00293682 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647503 | GAGATCAAGAAACCC[A/T]TCTTCCCAGAAAAAT | 3059 |
rs764716021 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653654 | CTTTTTACAGCAGAG[C/T]TGGAATCAGTCCCTA | 3059 |
rs764749650 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633694 | AGGCACACACCACCA[C/T]GCCCAGCTAATTTTT | 3059 |
rs764766490 | snp | C/T | 3.29527e-05 | 0.00405898 | missense | HCLS1 | GRCh38.p7 | 3:121635788 | GGGGCCTCCATTTCA[C/T]TGAAGCCGACAGCGC | 3059 |
rs764855451 | snp | A/C | 3.29457e-05 | 0.00405854 | missense | HCLS1 | GRCh38.p7 | 3:121632419 | CCTGCTCATGCCTGT[A/C]CATCTCCTCAACGTC | 3059 |
rs764896607 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642905 | CAGATTGCTGAGGCT[A/G]AGTGAAGTACAGTGT | 3059 |
rs764944832 | snp | A/G | | | missense | HCLS1 | GRCh38.p7 | 3:121634275 | CTATCACTGGCTGTG[A/G]AGCCTCAGGGCTCCT | 3059 |
rs765059889 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643556 | ACTCAATAATGGAAA[C/T]ACAAATATGTGGATT | 3059 |
rs765081040 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637405 | GGAATTAAAGAGAAG[A/C]CATGTCTTAAGTAGT | 3059 |
rs765082128 | snp | A/G | 3.65143e-05 | 0.00427268 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121633093 | TCTGCCTAATGGGCA[A/G]CAAGGGCACTGGGTG | 3059 |
rs765116397 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659823 | TTCTGAAATAGTCAT[A/G]AGCAATAAGGAAGCA | 3059 |
rs765174683 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121647400 | CTCCATCTCTTTCTT[C/T]CTGAGAACATCATGC | 3059 |
rs765243652 | snp | C/T | 4.26085e-05 | 0.00461546 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633192 | GAAAATGAAGCATCT[C/T]TCAAGTAAGCAAGCC | 3059 |
rs765406330 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636361 | CCTCTCCCAGCCTTC[C/T]TCACGCTCTTCTCTG | 3059 |
rs765464497 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648947 | ATATCTTCCAACTGA[A/C]GTATTCAGATGAAAG | 3059 |
rs765569784 | snp | A/G | 1.64743e-05 | 0.00287 | missense | HCLS1 | GRCh38.p7 | 3:121632475 | TCAGGCTCGGGCTCA[A/G]GCTCAGGCTCTGCTT | 3059 |
rs765573046 | snp | C/T | 1.65359e-05 | 0.00287536 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658217 | GCCCAGATGCCCTCC[C/T]CACCCCACCCTCTGC | 3059 |
rs765668569 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646881 | ATATAGTTGGCTCTT[A/C]TTATAGAGGTATATA | 3059 |
rs765724379 | snp | C/G | 1.64732e-05 | 0.0028699 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644808 | GTTGGGAGAGAGAGT[C/G]GTCACTTACCTTGTC | 3059 |
rs765792319 | snp | C/G | 1.64773e-05 | 0.00287026 | missense | HCLS1 | GRCh38.p7 | 3:121634299 | GGCTCCTCTTTGTCA[C/G]AGCCTTTCGCTCCTG | 3059 |
rs765844895 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655060 | GATAACCTGGGTAAA[C/T]GGGAGATGAGCGAGA | 3059 |
rs765866751 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644956 | AAGGATGGAGTGAGT[A/G]AAAAGATAAAAATGA | 3059 |
rs765917819 | snp | C/G | 3.29696e-05 | 0.00406001 | missense | HCLS1 | GRCh38.p7 | 3:121647388 | TTTGGGCCCTGACTC[C/G]ATCTCTTTCTTCCTG | 3059 |
rs766009848 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121635775 | ATAAGCTGTGGTCGG[A/G]GCCTCCATTTCATTG | 3059 |
rs766043455 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645001 | ATACAGATATGGAGT[A/G]GGATGTAGGCATGTA | 3059 |
rs766045875 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633789 | AAGTGATCCTCTCAC[C/T]TTGGCCACCTCAAGT | 3059 |
rs766204843 | snp | C/T | 1.73715e-05 | 0.00294711 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632613 | ACTTTCCAGGAGGAA[C/T]CAATGGAGGACTGAT | 3059 |
rs766381488 | snp | C/T | 0.00014835 | 0.0086112 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658359 | ACATCTGAGAGTGAC[C/T]GGAGATGGGAATAAT | 3059 |
rs766406575 | snp | A/G | 3.42977e-05 | 0.00414097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644688 | AGGTATCCCTGTGAC[A/G]GTGTCAGGTCCTCAC | 3059 |
rs766408141 | snp | A/G | 1.82317e-05 | 0.00301919 | missense | HCLS1 | GRCh38.p7 | 3:121633075 | TGCTTACCTCCGGGA[A/G]AGTCTGCCTAATGGG | 3059 |
rs766424630 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639519 | ATATTTTTAACTGAA[C/T]GATTTTATTTTTTGT | 3059 |
rs766429965 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660066 | CCTCCTGCATCAAAG[C/T]ACACAGACTGGGAGT | 3059 |
rs766467679 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638527 | TACTCAGGAAAATCA[G/T]GAAGGGGGCTTGTAA | 3059 |
rs766604540 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634285 | CTGTGGAGCCTCAGG[A/G]CTCCTCTTTGTCACA | 3059 |
rs766658539 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | HCLS1 | GRCh38.p7 | 3:121634344 | CCTGCTGTGCCTTCT[C/T]CTCTTCCTCTCGCTT | 3059 |
rs766704248 | snp | C/T | 1.64882e-05 | 0.00287121 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635825 | GGCAGGAGAACAGCA[C/T]GTGTGTTGCGGGAGA | 3059 |
rs766768907 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650949 | AAGACCAGCCTAGCC[A/G]CTATGGTGAAACCCC | 3059 |
rs766786519 | snp | C/G | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631511 | CAATGAGGCAAACCA[C/G]ACAATCTAGACGTAC | 3059 |
rs766786654 | snp | A/G | 1.65195e-05 | 0.00287393 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632293 | CTTACCCTCCCCTGG[A/G]CATGAGCAAATTCTC | 3059 |
rs766871649 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652327 | AGTCAAAACTCATTG[A/C]ACTATTTGCTTATAA | 3059 |
rs766873481 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | HCLS1 | GRCh38.p7 | 3:121632401 | CCCCCTCTGGTTCAT[C/T]CTCCTGCTCATGCCT | 3059 |
rs766896968 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656468 | GATCCTGAATCATCC[A/G]TGGAAGAGAGAAGGG | 3059 |
rs766948902 | snp | C/T | 1.68618e-05 | 0.00290356 | missense | HCLS1 | GRCh38.p7 | 3:121632562 | GGGGGCTCCTCATTG[C/T]CCTGAGAAGAGACAG | 3059 |
rs766983050 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641859 | AGCCGAGGCAGGCAG[A/T]TCACGAGGTCAGAAG | 3059 |
rs767167038 | snp | C/G | 1.64833e-05 | 0.00287078 | missense | HCLS1 | GRCh38.p7 | 3:121657291 | TACTTGATGTGTTCT[C/G]TGCGTCCAGACCCCT | 3059 |
rs767248555 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121658932 | GCTGTGTAAGGTCAG[C/T]AGCGACAGTCGGCTG | 3059 |
rs767274055 | snp | A/G | 6.58913e-05 | 0.00573945 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121644845 | GTCCCTCTCAACTCC[A/G]TACTTGCCCCCAAAG | 3059 |
rs767290391 | snp | C/G | 1.65531e-05 | 0.00287686 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644954 | TCAAGGATGGAGTGA[C/G]TGAAAAGATAAAAAT | 3059 |
rs767319336 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649541 | CGCCTGGCCTAAACA[A/G]GTCTTAATCACATCA | 3059 |
rs767324275 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | HCLS1 | GRCh38.p7 | 3:121636471 | ATTCCATACTGGCCA[C/T]CAAAGCCCTTGGCAT | 3059 |
rs767328288 | snp | A/G | 4.9436e-05 | 0.00497148 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121635802 | ATTGAAGCCGACAGC[A/G]CTCTGCAGGCAGGAG | 3059 |
rs767382603 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648903 | GTGTCATAAGCTACT[A/T]GTACCAAGGACATGT | 3059 |
rs767446803 | snp | A/G | 3.29734e-05 | 0.00406025 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637281 | AAGGAGCAGTCATGA[A/G]AGCCCACCCTTAGGC | 3059 |
rs767472628 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634720 | CACTGCAGCCTCAAC[C/T]TCCCAGGCTCAAGCA | 3059 |
rs767498346 | snp | C/G | 2.46121e-05 | 0.00350791 | missense | HCLS1 | GRCh38.p7 | 3:121632488 | CAGGCTCAGGCTCTG[C/G]TTCGTACACTGGCTC | 3059 |
rs767502116 | in-del | -/C | 1.68196e-05 | 0.00289992 | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121632554 | GCAGAGCTGGGGGCT[-/C]CTCATTGTCCTGAGA | 3059 |
rs767550556 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637158 | CACCTCTCTGGGACT[C/T]GTGTTTCTCCGTCTC | 3059 |
rs767604983 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642551 | GAGAGGGTGAGAGGG[C/G]AGAATCACTTGAGCC | 3059 |
rs767703929 | snp | A/G | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662140 | GATAAGGAAGAGTAC[A/G]TTTGTACAAGAGAAA | 3059 |
rs767748750 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642920 | GAGTGAAGTACAGTG[C/T]CCTTGCCTTTCTGAG | 3059 |
rs767812773 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653426 | AATCAGGATGCCAAC[A/G]TCATCTATGATATAG | 3059 |
rs767833433 | snp | C/T | 0.00037154 | 0.0136247 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633220 | GCCTCCATCTTCACT[C/T]CTTTTTTTTTTTTGA | 3059 |
rs767839146 | in-del | -/TACA | 1.64836e-05 | 0.0028708 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642912 | TGAGGCTGAGTGAAG[-/TACA]TACAGTGTCCTTGCC | 3059 |
rs767847553 | in-del | -/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643446 | AAGTGAAATGTGATA[-/C]CTAGAAAAGTGCCTT | 3059 |
rs767951175 | snp | C/G | 1.6483e-05 | 0.00287076 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635707 | AGAAGGAAGTGAGGT[C/G]CATGGAGAGTGAATC | 3059 |
rs767968075 | snp | C/G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637683 | GCTCATGCCTGTAAT[C/G/T]CCAGCACTTCAGGGG | 3059 |
rs767979007 | snp | A/G | 1.68513e-05 | 0.00290265 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632207 | ATGAGAAACACAAAC[A/G]TGGGATCATCAACAT | 3059 |
rs768116498 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659469 | CCCTTTACAACCACT[C/G]CTCGGGTTCTCCTGT | 3059 |
rs768118694 | snp | A/G | 1.64743e-05 | 0.00287 | missense | HCLS1 | GRCh38.p7 | 3:121635770 | TTCTTATAAGCTGTG[A/G]TCGGGGCCTCCATTT | 3059 |
rs768166977 | snp | A/G | | | missense | HCLS1 | GRCh38.p7 | 3:121657295 | TGATGTGTTCTGTGC[A/G]TCCAGACCCCTCGAT | 3059 |
rs768208368 | snp | C/G | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661083 | ACAATGGGGGTCATA[C/G]AGCAGTCATAGAAAA | 3059 |
rs768249755 | in-del | -/G | 1.65814e-05 | 0.00287931 | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121634418 | CGGGTACCACTAGAA[-/G]CTGCAGACACAGGCA | 3059 |
rs768270380 | snp | A/G | 1.65578e-05 | 0.00287726 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632069 | ATCAGGGGCCTCCAT[A/G]TACCAGGCTCCTCGG | 3059 |
rs768331903 | snp | C/G | 1.64751e-05 | 0.00287007 | missense | HCLS1 | GRCh38.p7 | 3:121658278 | CCACAAAGTCAGGAT[C/G]TGTGTCCCAATCATC | 3059 |
rs768356781 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652859 | GTTCATGGGAATTTG[C/T]ATTTCATTTCAACAA | 3059 |
rs768390845 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638163 | CACTGTAACCTTGAA[C/T]TCCTGGGGTCAAGCA | 3059 |
rs768432176 | snp | G/T | 3.29592e-05 | 0.00405938 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644771 | TGATCGTGGGCAATT[G/T]TCACAGGACTGGAGG | 3059 |
rs768520224 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634336 | CCTGGCCACCTGCTG[C/T]GCCTTCTCCTCTTCC | 3059 |
rs768520291 | snp | A/G | 6.59924e-05 | 0.00574385 | missense | HCLS1 | GRCh38.p7 | 3:121634404 | TCGCCTTCAGCCCAC[A/G]GGTACCACTAGAAGC | 3059 |
rs768592550 | snp | C/T | | | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637256 | AAGCCACGAGAGTAA[C/T]CTGTGGTCGAAGGAG | 3059 |
rs768608716 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121632056 | CCCCCTGTCTTATAT[A/C]AGGGGCCTCCATGTA | 3059 |
rs768639173 | snp | A/C | 3.29625e-05 | 0.00405958 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635808 | GCCGACAGCGCTCTG[A/C]AGGCAGGAGAACAGC | 3059 |
rs768695965 | in-del | -/GGCTCA | 0.000164823 | 0.00907659 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632456 | TCATTCTCAGGCTCG[-/GGCTCA]GGCTCAGGCTCGGGC | 3059 |
rs768758074 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | HCLS1 | GRCh38.p7 | 3:121631927 | CCAGCCCTCGTCCAC[C/T]ATCTCAATGTCAGTG | 3059 |
rs768804530 | in-del | -/TTTA | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662071 | TATGCCTGGGGGAGC[-/TTTA]TTTATTCCTTCTACT | 3059 |
rs768916414 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641634 | AAAGAATGTAGTTAA[A/T]ATATTCTATGTTTCC | 3059 |
rs768983935 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654141 | CCTATGGTCCCCTGC[C/T]CCTGGGAGGTGGGAG | 3059 |
rs769014624 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635156 | CTCCGATTCCTTCCC[C/T]GACGTCACTCTGTCT | 3059 |
rs769115324 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647147 | CCACGACGCACGGCT[A/G]ATTTTTTGTATTTTT | 3059 |
rs769189210 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656135 | ATTACAAGCGTGAGC[A/C]ACCACGCCCGGCCGA | 3059 |
rs769278469 | snp | C/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662923 | ATGCCCTAAGGCCCA[C/G]CTTATTTGGTTCAGT | 3059 |
rs769313787 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661396 | ATAAACGTCGACCAA[C/T]TGAATGCCAGAAGAG | 3059 |
rs769344632 | snp | A/C/G | 3.2961e-05 | 0.00405951 | missense | HCLS1 | GRCh38.p7 | 3:121647351 | TTTCTACTCCAAACC[A/C/G]ACCTCCATAGCCATG | 3059 |
rs769367326 | snp | A/G | 9.88712e-05 | 0.00703035 | missense | HCLS1 | GRCh38.p7 | 3:121634325 | TCCTGTTGCCTCCTG[A/G]CCACCTGCTGTGCCT | 3059 |
rs769492256 | snp | A/G | 1.64966e-05 | 0.00287194 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657355 | CAGAGATGTCATTCT[A/G]CAAACGACAGCACGC | 3059 |
rs769506604 | snp | C/G | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661005 | AGTCAGTTCCTTCTG[C/G]TTTAGACACTTAAAT | 3059 |
rs769745318 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643014 | CAGAATTGGTTAGAG[C/T]CAGAGCTGACAGGTT | 3059 |
rs769882900 | snp | A/C | 1.64944e-05 | 0.00287175 | splice-donor-variant | HCLS1 | GRCh38.p7 | 3:121647317 | TTTCCCTTTCAACTT[A/C]CCTTGTCCATTCGGT | 3059 |
rs769907706 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651793 | ACACATTACTGGTAG[A/G]AATGAAAGAGGGTAA | 3059 |
rs769914693 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | HCLS1 | GRCh38.p7 | 3:121634244 | AGTGGGGCCGGTACT[C/G]CTGGCTCTTCCATAG | 3059 |
rs769983687 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657789 | CTGAGATTGCACCAC[C/T]GTACTCCAGCCTGGG | 3059 |
rs770014971 | in-del | -/TCTCTCCTCTCTCT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635279 | TCTCTCTCTCTCCTC[-/TCTCTCCTCTCTCT]CTCTTTCTTTCGTCT | 3059 |
rs770067402 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | HCLS1 | GRCh38.p7 | 3:121635744 | CCTCACCGGCTTCTA[C/T]GGGCGTCGTCTTCTT | 3059 |
rs770076130 | snp | G/T | 4.96298e-05 | 0.00498121 | missense | HCLS1 | GRCh38.p7 | 3:121632515 | GCTCTTCCTCCACCT[G/T]GAGGCCTTCCAGAGT | 3059 |
rs770105631 | snp | A/G | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631443 | CGAATTTTAGGACTG[A/G]ACAGAAAGAAGGTTC | 3059 |
rs770107699 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644107 | AAAGAAAAAATCTCA[C/G]CTAACTGTGAAGGAG | 3059 |
rs770370402 | snp | G/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661980 | TTAAGCAGGACTGGA[G/T]GAAACTGGCCCATGA | 3059 |
rs770370681 | snp | C/T | 1.97658e-05 | 0.00314364 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633041 | AAGATGGGGTGGGGG[C/T]AGAGAATCTTTGGGG | 3059 |
rs770491973 | in-del | -/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651838 | AGAGTTTGAGAGTCT[-/C]TCAAAATGTTTAACA | 3059 |
rs770590908 | snp | C/G | | | missense | HCLS1 | GRCh38.p7 | 3:121647420 | GAACATCATGCTCCT[C/G]TGATACTTTGTTCCT | 3059 |
rs770634229 | in-del | -/TCT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634848 | TGTTGCCCAGCCTCA[-/TCT]TGAACTCCTGGGTTC | 3059 |
rs770634522 | snp | C/T | 3.29728e-05 | 0.00406021 | missense | HCLS1 | GRCh38.p7 | 3:121647329 | CTTACCTTGTCCATT[C/T]GGTCTCTTTCTACTC | 3059 |
rs770677587 | snp | C/T | 1.6701e-05 | 0.00288968 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647481 | ACCAAGGCTCATCTA[C/T]CCTAGGGAGATCAAG | 3059 |
rs770812723 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121658297 | GTCCCAATCATCACC[C/T]TGGGTCTCCACGGAA | 3059 |
rs770929849 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653092 | TTGGGGACGAGACCC[A/G]TGTGTAAACAGGAAA | 3059 |
rs770973831 | in-del | -/TTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655682 | AAGGGTCTTGTGGTT[-/TTT]TTTTTTTTTTTTTTT | 3059 |
rs771060465 | snp | A/G | 8.23689e-05 | 0.00641698 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642899 | GCCGGTCAGATTGCT[A/G]AGGCTGAGTGAAGTA | 3059 |
rs771074712 | snp | C/T | 1.65512e-05 | 0.00287669 | missense | HCLS1 | GRCh38.p7 | 3:121632506 | CGTACACTGGCTCTT[C/T]CTCCACCTGGAGGCC | 3059 |
rs771134810 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644420 | TGATTATCTGCTGCT[A/G]TGGCAATAATATTTA | 3059 |
rs771138789 | snp | C/T | 1.65405e-05 | 0.00287576 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657257 | AACCCCCTTCCTTTT[C/T]TCCAGTCCTTTCGGC | 3059 |
rs771153850 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633406 | TTTTTAATAGAGACA[A/G]GGTTTCACTATGTTG | 3059 |
rs771162014 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645130 | CCTGTTCTTCTCTAA[G/T]ACCATTAGGAATCCT | 3059 |
rs771213997 | snp | A/G/T | 3.29496e-05 | 0.00405881 | missense | HCLS1 | GRCh38.p7 | 3:121644897 | GAAGAGTGCTTCTCC[A/G/T]CCTCGGCAACATACT | 3059 |
rs771494413 | in-del | -/G | | | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121632451 | TCATAGTCATTCTCA[-/G]GCTCGGGCTCAGGCT | 3059 |
rs771511453 | snp | C/T | 1.66654e-05 | 0.00288659 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637104 | GGAAGGAAGGAGATC[C/T]CTGTGCTATCTGTGA | 3059 |
rs771551016 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659887 | CTCCTCTGAGGCCTC[-/A]AGCCTGACTCTCCCA | 3059 |
rs771555323 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647575 | TGGGCCCCCAAAATA[A/T]ACTAGTGATGGGTCT | 3059 |
rs771568622 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638262 | GTGATAGGATCTCAC[C/T]GTGTTGCCCAGGCTA | 3059 |
rs771596457 | snp | C/T | 1.84899e-05 | 0.0030405 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121633067 | TGGGGGTTTGCTTAC[C/T]TCCGGGAGAGTCTGC | 3059 |
rs771601832 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640042 | AATTAAAAAGAGAAA[A/G]AACACAAGTAAGTAA | 3059 |
rs771607958 | snp | C/T | 8.25389e-05 | 0.0064236 | missense | HCLS1 | GRCh38.p7 | 3:121632467 | GCTCGGGCTCAGGCT[C/T]GGGCTCAGGCTCAGG | 3059 |
rs771614069 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650584 | TATTGTTGAACAACT[-/A]AATAATCACATGGAG | 3059 |
rs771638275 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642886 | AGCAGAAGAGCCTGC[C/T]GGTCAGATTGCTGAG | 3059 |
rs771650999 | snp | C/T | | | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637151 | CCCAACTCACCTCTC[C/T]GGGACTCGTGTTTCT | 3059 |
rs771796785 | snp | C/G | 1.66346e-05 | 0.00288393 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634430 | GAAGCTGCAGACACA[C/G]GCAAGAAAAATTAGG | 3059 |
rs771797629 | snp | A/G | 4.59834e-05 | 0.00479474 | missense | HCLS1 | GRCh38.p7 | 3:121633150 | ACTCTGATGATGGAG[A/G]AGTCCCAACTGGAGG | 3059 |
rs771820311 | in-del | -/AGCCTCA | 0.00088924 | 0.0210673 | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121634276 | TATCACTGGCTGTGG[-/AGCCTCA]GGGCTCCTCTTTGTC | 3059 |
rs771849371 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651427 | TTGGTTTTGTTGTTG[C/T]TGTTGTTGTTTTGTT | 3059 |
rs771851023 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636070 | AGAATGTAGCAGGGC[C/T]CCCTGGCTCATGCAT | 3059 |
rs771981069 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656033 | TTTGTATTTTTAGTA[A/G]ACACAGGGTTTCATC | 3059 |
rs772043240 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650200 | GGAGAGATATCCCAT[A/G]TTCATGGATTGGAAA | 3059 |
rs772134906 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | HCLS1 | GRCh38.p7 | 3:121632391 | TCCTCATAGTCCCCC[C/T]CTGGTTCATCCTCCT | 3059 |
rs772196565 | snp | A/G | 6.58946e-05 | 0.0057396 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121658288 | AGGATCTGTGTCCCA[A/G]TCATCACCCTGGGTC | 3059 |
rs772221339 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636420 | CTTAAGACATTGGTG[C/T]TCCGGTGCTTTACCT | 3059 |
rs772240449 | snp | C/T | 1.66399e-05 | 0.00288438 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644662 | ATTGGCACCAAGGAA[C/T]TTGCTGAGGGAGGTA | 3059 |
rs772279410 | snp | C/G | | | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631086 | TACAAAAATTAGCCG[C/G]GCATGGTGGTGCACG | 3059 |
rs772336014 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647942 | TCTAAATGATACTCA[C/T]TGAAGCATCGTATAT | 3059 |
rs772574562 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648700 | TGGTGGCCTTTAGTG[G/T]ATAATTCTACCAAAG | 3059 |
rs772650407 | snp | G/T | 1.64757e-05 | 0.00287012 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642889 | AGAAGAGCCTGCCGG[G/T]CAGATTGCTGAGGCT | 3059 |
rs772685507 | snp | A/C | 1.65504e-05 | 0.00287662 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647466 | GGAAGAAACCACATG[A/C]CCAAGGCTCATCTAT | 3059 |
rs772686654 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633728 | TTGTTTTTATAGCGA[C/T]AGGTTCTTACTATGT | 3059 |
rs772704569 | snp | C/G/T | 4.96926e-05 | 0.0049844 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657247 | CTCTTCCCATAACCC[C/G/T]CTTCCTTTTCTCCAG | 3059 |
rs772769017 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662943 | TTTGGTTCAGTATTA[A/G]GATAGAATTTCCTCA | 3059 |
rs772772393 | snp | C/T | 0.000117597 | 0.00766711 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634448 | AAGAAAAATTAGGGT[C/T]GTCTTGGATTGGAGA | 3059 |
rs772773713 | snp | A/T | 1.64844e-05 | 0.00287087 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635816 | CGCTCTGCAGGCAGG[A/T]GAACAGCATGTGTGT | 3059 |
rs772934763 | in-del | -/CACACA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639026 | ACACACACACACACG[-/CACACA]CACACACACACACAC | 3059 |
rs772944682 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647182 | GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 3059 |
rs773024093 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638478 | GAAGCTCTGTCCACT[A/C]CTATAAGAGAGTGCT | 3059 |
rs773076666 | in-del | -/GG | 9.88484e-05 | 0.00702954 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642887 | GCAGAAGAGCCTGCC[-/GG]TCAGATTGCTGAGGC | 3059 |
rs773209591 | snp | C/T | 0.000265274 | 0.0115138 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657402 | AAGAAATGTGCCACA[C/T]TGAGAAGGGCCACCC | 3059 |
rs773366860 | snp | G/T | 4.72981e-05 | 0.0048628 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644667 | CACCAAGGAACTTGC[G/T]GAGGGAGGTATCCCT | 3059 |
rs773394969 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637406 | GAATTAAAGAGAAGC[C/T]ATGTCTTAAGTAGTC | 3059 |
rs773441425 | in-del | -/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637388 | CAGGGCTTGAATACA[-/G]GGGAATTAAAGAGAA | 3059 |
rs773456612 | snp | A/G | 6.58979e-05 | 0.00573974 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644792 | GGACTGGAGGTGGGT[A/G]GTTGGGAGAGAGAGT | 3059 |
rs773508944 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644141 | TCCTCTCTCTGTGTG[C/T]AGCTGCAGGGCAGGA | 3059 |
rs773517485 | snp | G/T | 0.0206528 | 0.099498 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634273 | AGCTATCACTGGCTG[G/T]GGAGCCTCAGGGCTC | 3059 |
rs773603244 | snp | C/T | | | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121642928 | TACAGTGTCCTTGCC[C/T]TTCTGAGATGTGTGC | 3059 |
rs773715321 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635887 | ATTGGGGGTTGGGGG[A/C]CACTATAAGAGGTAT | 3059 |
rs773755604 | snp | C/T | 3.29484e-05 | 0.00405871 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121635772 | CTTATAAGCTGTGGT[C/T]GGGGCCTCCATTTCA | 3059 |
rs773774670 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | HCLS1 | GRCh38.p7 | 3:121658283 | AAGTCAGGATCTGTG[C/T]CCCAATCATCACCCT | 3059 |
rs773776388 | snp | A/G | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631477 | TATTTCTTCAGGGAA[A/G]GAAAGTGGGCAAATA | 3059 |
rs773806929 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654462 | GGTCAAGGGAAAAGA[C/G]ACCCTTGAGTCTTGA | 3059 |
rs773843483 | snp | A/G | 1.64852e-05 | 0.00287094 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635817 | GCTCTGCAGGCAGGA[A/G]AACAGCATGTGTGTT | 3059 |
rs773855388 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633470 | CTCGTGATCTGTCTG[C/T]CTTGACCTCCCAAAG | 3059 |
rs773864484 | snp | C/G | 1.64738e-05 | 0.00286995 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637226 | TTATCCTTCTCCACC[C/G]CGTACCGGCCACCAA | 3059 |
rs773999994 | snp | A/C/G | 1.85596e-05 | 0.00304622 | splice-donor-variant | HCLS1 | GRCh38.p7 | 3:121633065 | TTTGGGGGTTTGCTT[A/C/G]CCTCCGGGAGAGTCT | 3059 |
rs774180393 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649958 | TAAAGAATTCACACA[A/C]AAAAAGCTACTAAAG | 3059 |
rs774338969 | snp | C/G | 1.68077e-05 | 0.00289889 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632196 | GATCCTGCATAATGA[C/G]AAACACAAACATGGG | 3059 |
rs774362322 | snp | A/C | 1.65605e-05 | 0.0028775 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632073 | GGGGCCTCCATGTAC[A/C]AGGCTCCTCGGGCCA | 3059 |
rs774386250 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638568 | ATTTGATAGGGGGAA[A/C]ATTTGCTTATGAGAC | 3059 |
rs774452543 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661916 | AGCCTTTCCTAATCT[C/T]GATTGTGGACTTCTT | 3059 |
rs774459630 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653143 | ACTATATTAAGGAAG[G/T]TATTAAAGAAGAACT | 3059 |
rs774572669 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656929 | TGATTGCCAGGTAGA[C/T]AGATAGAGAGGACCT | 3059 |
rs774625408 | snp | A/G | 6.58935e-05 | 0.00573955 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632369 | AGAATCTTCAGGCTC[A/G]AGCACCTCCTCATAG | 3059 |
rs774664740 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643039 | CAGGTTTTCCTCTTC[C/T]TAACCTCCCCTTACT | 3059 |
rs774665416 | in-del | -/CTC | 3.29457e-05 | 0.00405854 | cds-indel | HCLS1 | GRCh38.p7 | 3:121642954 | TGTGCTTCTCCACTT[-/CTC]CTTTATAATCAAAGC | 3059 |
rs774760183 | snp | A/G | 0.000181212 | 0.00951698 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632354 | AGCAGAAGAAAAAGA[A/G]GAATCTTCAGGCTCG | 3059 |
rs774789210 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654957 | AGGTCTTTTTGATCC[A/C]GATGGGCAAAATGAG | 3059 |
rs774922667 | snp | A/C | 1.64768e-05 | 0.00287021 | missense | HCLS1 | GRCh38.p7 | 3:121644918 | GCAACATACTCATGG[A/C]CCACTGCACTCTGAG | 3059 |
rs774976590 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657975 | GAATCCTGGATCATG[A/G]GCCAGGGGAGACCCA | 3059 |
rs774976646 | in-del | -/TT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635208 | TCTTTCTTTTCTTTC[-/TT]TCTCTCTCTCTCTCT | 3059 |
rs774997333 | in-del | -/GGCTCG | 6.59283e-05 | 0.00574106 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632451 | TCATAGTCATTCTCA[-/GGCTCG]GGCTCAGGCTCGGGC | 3059 |
rs775030525 | in-del | -/TTCT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635237 | TCTCTTCTCTCCCTT[-/TTCT]CTCTCTCTCTCTCTC | 3059 |
rs775036654 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | HCLS1 | GRCh38.p7 | 3:121632476 | CAGGCTCGGGCTCAG[A/G]CTCAGGCTCTGCTTC | 3059 |
rs775045944 | snp | C/T | 3.303e-05 | 0.00406373 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657269 | TTTCTCCAGTCCTTT[C/T]GGCACCTACTTGATG | 3059 |
rs775062262 | snp | C/T | 0.00011532 | 0.00759255 | missense | HCLS1 | GRCh38.p7 | 3:121636444 | TTTACCTTATCCACT[C/T]GGTCCTTCTGGATTC | 3059 |
rs775154424 | snp | C/T | 1.65444e-05 | 0.00287609 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637126 | TATCTGTGACCTTCC[C/T]CCTTCCAACCCCAAC | 3059 |
rs775238204 | in-del | -/TTTG | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656573 | TATCGGAGGGTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 3059 |
rs775397728 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650315 | TGTAGGAATTGACTA[G/T]TGAATTATAAAATTT | 3059 |
rs775470849 | snp | A/G | 3.35537e-05 | 0.00409582 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634446 | GCAAGAAAAATTAGG[A/G]TTGTCTTGGATTGGA | 3059 |
rs775487605 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651503 | GTGCAGTGGGGCAAA[C/T]ATGGCTCACTGCAGC | 3059 |
rs775521636 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654588 | TAGGACCATTTGAAT[G/T]ATTCACTGAATTACC | 3059 |
rs775528068 | in-del | -/CT | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661776 | CAGCAGACTGGGTCC[-/CT]GAGTGAGAAAGAACA | 3059 |
rs775551103 | snp | A/C | 1.64732e-05 | 0.0028699 | missense | HCLS1 | GRCh38.p7 | 3:121634249 | GGCCGGTACTGCTGG[A/C]TCTTCCATAGCTATC | 3059 |
rs775571166 | snp | A/T | 1.65075e-05 | 0.00287289 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631836 | AGTTGCAGTAGACAG[A/T]GAGCTCTAGTCACTC | 3059 |
rs775692474 | snp | C/T | 5.00939e-05 | 0.00500444 | missense | HCLS1 | GRCh38.p7 | 3:121632175 | GCCCCAGCCGGGCAG[C/T]CTGATGATCCTGCAT | 3059 |
rs775699825 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121632671 | CTCTTCTCCCCTCTA[C/T]CCTTGCCTCCATCTA | 3059 |
rs775968916 | snp | A/G | 0.000198672 | 0.00996477 | missense | HCLS1 | GRCh38.p7 | 3:121632518 | CTTCCTCCACCTGGA[A/G]GCCTTCCAGAGTCCT | 3059 |
rs775978803 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633518 | TGAGCCACCACGCTC[A/G]GCCCATCTTCATTCT | 3059 |
rs776091120 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644664 | TGGCACCAAGGAACT[C/T]GCTGAGGGAGGTATC | 3059 |
rs776092123 | snp | A/G | 6.82361e-05 | 0.00584067 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647497 | CCTAGGGAGATCAAG[A/G]AACCCATCTTCCCAG | 3059 |
rs776181630 | snp | C/T | 1.64906e-05 | 0.00287142 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635827 | CAGGAGAACAGCATG[C/T]GTGTTGCGGGAGAGG | 3059 |
rs776266401 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637286 | GCAGTCATGAGAGCC[C/T]ACCCTTAGGCTCCAG | 3059 |
rs776372895 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659549 | TCCATCTTCTCCATT[A/G]AGCAACCTCTTAAAA | 3059 |
rs776381252 | snp | A/G/T | 3.30738e-05 | 0.00406645 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657258 | ACCCCCTTCCTTTTC[A/G/T]CCAGTCCTTTCGGCA | 3059 |
rs776461642 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651612 | TTTTTGTAGACTCTG[A/C]ATCTCTCCACATTGT | 3059 |
rs776577764 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650659 | ACTTGAAATGGGTCA[C/T]AGACTTAAATGTAAA | 3059 |
rs776611275 | snp | C/G | 1.64798e-05 | 0.00287047 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637261 | ACGAGAGTAATCTGT[C/G]GTCGAAGGAGCAGTC | 3059 |
rs776650016 | snp | A/G | 8.23689e-05 | 0.00641698 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642900 | CCGGTCAGATTGCTG[A/G]GGCTGAGTGAAGTAC | 3059 |
rs776664390 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641403 | ATTATCAATGGAATA[C/T]TTTAGCAAGAAGGAA | 3059 |
rs776684026 | in-del | -/A | 0.00365163 | 0.0425733 | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121632467 | CTCGGGCTCAGGCTC[-/A]GGGCTCAGGCTCAGG | 3059 |
rs776739490 | snp | A/G | 7.30914e-05 | 0.00604486 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633186 | CCTGTGGAAAATGAA[A/G]CATCTCTCAAGTAAG | 3059 |
rs776739600 | in-del | -/AGG | 0.000313208 | 0.0125102 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635694 | AAAGAATGAGGGAGA[-/AGG]AGGAAGTGAGGTGCA | 3059 |
rs776966571 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648739 | AAAAAGCCTTCTCAG[A/C]TTTAGCCGCAGTTAA | 3059 |
rs777007155 | snp | C/T | 3.30508e-05 | 0.00406501 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632510 | CACTGGCTCTTCCTC[C/T]ACCTGGAGGCCTTCC | 3059 |
rs777099951 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656149 | CCACCACGCCCGGCC[A/G]AAACCATTTATTTCT | 3059 |
rs777106113 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636424 | AGACATTGGTGTTCC[A/G]GTGCTTTACCTTATC | 3059 |
rs777189818 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641676 | GAAGAGATTGTGATT[A/T]ATTTTAAATTTAAGT | 3059 |
rs777223626 | snp | C/T | 1.6486e-05 | 0.00287102 | missense | HCLS1 | GRCh38.p7 | 3:121632428 | GCCTGTCCATCTCCT[C/T]AACGTCCTCATAGTC | 3059 |
rs777275307 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | HCLS1 | GRCh38.p7 | 3:121632470 | CGGGCTCAGGCTCGG[A/G]CTCAGGCTCAGGCTC | 3059 |
rs777296061 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654865 | TGATTCCCATCAGAT[A/G]TTAAAGACTGACTTA | 3059 |
rs777398713 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659106 | GAAAAAAGAATAATA[-/T]GTAATAAATCTGATT | 3059 |
rs777497001 | snp | G/T | 1.64743e-05 | 0.00287 | missense | HCLS1 | GRCh38.p7 | 3:121635737 | CACTAAGCCTCACCG[G/T]CTTCTATGGGCGTCG | 3059 |
rs777497606 | snp | C/T | 4.94205e-05 | 0.0049707 | missense | HCLS1 | GRCh38.p7 | 3:121634223 | TCTGAGGAGATTTTC[C/T]TGGGCAGTGGGGCCG | 3059 |
rs777613333 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641201 | CCAAAAGAAAATCTT[C/T]AATTAAAAAAAACCC | 3059 |
rs777666687 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648195 | AAACTAAGGACTAAT[A/G]AAAACTAACTAAGAA | 3059 |
rs777690862 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654302 | CATGCCTGACAACAT[C/T]GTGATTTTATATCTG | 3059 |
rs777761340 | snp | C/T | 4.99023e-05 | 0.00499486 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632168 | AGCCCCAGCCCCAGC[C/T]GGGCAGCCTGATGAT | 3059 |
rs777954273 | snp | A/G | 1.64798e-05 | 0.00287047 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636503 | ATCTGCAGGACAGAA[A/G]GTTCTGAGTTATAGG | 3059 |
rs777969839 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659082 | AAGTTGACAATTTAC[C/T]GTAGAAAAGAAAAAA | 3059 |
rs778005093 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656636 | AGATCCCTGAACATC[A/G]TTGCCAAAATAGTTT | 3059 |
rs778027722 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639983 | AAAGCCAAAAGCTTG[C/T]TCTTTGGAAAGAGTA | 3059 |
rs778043102 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634137 | TATTTTCTGCCAATG[A/G]TTTGGACCCCTTAGG | 3059 |
rs778053234 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655682 | AAAGGGTCTTGTGGT[-/T]TTTTTTTTTTTTTTT | 3059 |
rs778072301 | snp | A/C | 1.66236e-05 | 0.00288297 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631800 | GGTGGAGGCAGAGCC[A/C]CTTTGGACATGGGAA | 3059 |
rs778109194 | in-del | -/TCTCTCTCTCTCTC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635240 | CTTCTCTCCCTTTTC[-/TCTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 3059 |
rs778112497 | snp | G/T | 1.65318e-05 | 0.002875 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632498 | CTCTGCTTCGTACAC[G/T]GGCTCTTCCTCCACC | 3059 |
rs778156560 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637777 | CTGTCTCTACTAAAA[A/G]ATACAAAAATTATCC | 3059 |
rs778200441 | snp | A/G | 2.02645e-05 | 0.00318305 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633031 | AAGACTCGAGAAGAT[A/G]GGGTGGGGGCAGAGA | 3059 |
rs778248397 | snp | A/G | 0.000132437 | 0.0081364 | missense | HCLS1 | GRCh38.p7 | 3:121632142 | GCTGAGATCCCCAGA[A/G]CCACAGCCCCAGCCC | 3059 |
rs778252095 | in-del | -/CTCAGGCGCGGG/CTCAGGCTCAGG/CTCAGGCTCGGA/CTCAGGCTCGGG/CTCAGGCTTGGG | 0.000165695 | 0.00910054 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632446 | GTCCTCATAGTCATT[lengthTooLong]CTCAGGCTCGGGCTC | 3059 |
rs778351044 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | HCLS1 | GRCh38.p7 | 3:121657310 | GTCCAGACCCCTCGA[C/T]GGTCTTGGCTCCCCA | 3059 |
rs778433434 | snp | A/C | 1.64784e-05 | 0.00287035 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636422 | TAAGACATTGGTGTT[A/C]CGGTGCTTTACCTTA | 3059 |
rs778542606 | in-del | -/T/TCTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635275 | CTCTCTCTCTCTCTC[-/T/TCTT]CTCTCTCTCCTCTCT | 3059 |
rs778543941 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651050 | TGAAGCAGCAGAATC[G/T]CTTGAACCCAGGAGG | 3059 |
rs778555796 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636907 | CATTCCTTCCTCAAC[A/G]CCCCCTTCTCTCTCA | 3059 |
rs778606518 | snp | A/G | 4.94425e-05 | 0.0049718 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632323 | CCTGCTTCTCCTCCC[A/G]TCACTCACCAGCCAG | 3059 |
rs778635934 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652429 | GAGGCCGAGGCAGGC[A/G]GATCACTTGAGGTCA | 3059 |
rs778734340 | snp | C/T | | | | | GRCh38.p7 | 3:121660416 | CATCAGTGACTACTT[C/T]CTGATCTGTTACATT | 3059 |
rs778816753 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635093 | TGGTTCCTCACCAAT[G/T]TTCCCATGCCACCCC | 3059 |
rs778822064 | snp | A/G | 3.35272e-05 | 0.0040942 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647271 | CAGGCGTGAGCCACC[A/G]CACCCGGCTTGTATT | 3059 |
rs778826424 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641420 | TTAGCAAGAAGGAAA[C/T]AGAAGACACAAAGGT | 3059 |
rs778899842 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | HCLS1 | GRCh38.p7 | 3:121631895 | AGTCCAAAGTGGCCA[C/T]GGCAACGTCCCCGCC | 3059 |
rs778968400 | in-del | -/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641342 | ATGATGCAACATAAA[-/G]ACATTTTTCAAAGAC | 3059 |
rs779019133 | snp | A/G | 1.65556e-05 | 0.00287707 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632444 | AACGTCCTCATAGTC[A/G]TTCTCAGGCTCGGGC | 3059 |
rs779098862 | snp | A/C | 1.64735e-05 | 0.00286993 | stop-gained | HCLS1 | GRCh38.p7 | 3:121642954 | TGTGCTTCTCCACTT[A/C]TCCTTTATAATCAAA | 3059 |
rs779201124 | in-del | -/TT | 0.0039254 | 0.0441281 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633222 | CTCCATCTTCACTCC[-/TT]TTTTTTTTTTGAGAT | 3059 |
rs779203250 | snp | A/G | 0.000151888 | 0.00871327 | missense | HCLS1 | GRCh38.p7 | 3:121633141 | CAGGCTCAGACTCTG[A/G]TGATGGAGGAGTCCC | 3059 |
rs779275464 | snp | A/G | 1.64817e-05 | 0.00287064 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636410 | GGGAACTCTTCTTAA[A/G]ACATTGGTGTTCCGG | 3059 |
rs779291945 | snp | A/G | 3.29484e-05 | 0.00405871 | missense | HCLS1 | GRCh38.p7 | 3:121636475 | CATACTGGCCACCAA[A/G]GCCCTTGGCATAATC | 3059 |
rs779366301 | snp | A/G | 6.59065e-05 | 0.00574012 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634201 | CCCAGAGGGCCAGGC[A/G]CTCACCTCTGAGGAG | 3059 |
rs779385074 | in-del | -/A | 4.97026e-05 | 0.00498486 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644957 | AGGATGGAGTGAGTG[-/A]AAAGATAAAAATGAC | 3059 |
rs779431304 | snp | A/G | | | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660863 | CGCCCGGCTCCTCGC[A/G]TCCACACCGACTCCC | 3059 |
rs779555694 | in-del | -/CTC | 0.000379022 | 0.0137611 | cds-indel | HCLS1 | GRCh38.p7 | 3:121634342 | CACCTGCTGTGCCTT[-/CTC]CTCTTCCTCTCGCTT | 3059 |
rs779565202 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653867 | GAGCAGTGCCACTCA[C/G]TGTGTGGTCCACAAG | 3059 |
rs779580228 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652643 | CCAGCCTGGATGACA[C/G]AGCGAAACTCCGTCT | 3059 |
rs779598172 | in-del | -/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640255 | AAAAATAATAATAAA[-/G]GAAAAAAAATGTCCG | 3059 |
rs779710044 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121658264 | TACTTCCAAACTCAC[C/T]ACAAAGTCAGGATCT | 3059 |
rs779729181 | snp | A/G | 1.64822e-05 | 0.00287068 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635712 | GAAGTGAGGTGCATG[A/G]AGAGTGAATCACTAA | 3059 |
rs779796706 | in-del | -/GAAGCCTT | 5.31543e-05 | 0.00515503 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647520 | CTTCCCAGAAAAATG[-/GAAGCCTT]GAAGTCTGTCCTGTT | 3059 |
rs779824969 | snp | A/G | 3.31087e-05 | 0.00406857 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632061 | TGTCTTATATCAGGG[A/G]CCTCCATGTACCAGG | 3059 |
rs779858265 | snp | C/G | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631783 | AGCAGGAATAGGGAG[C/G]GGGTGGAGGCAGAGC | 3059 |
rs779862401 | snp | A/G/T | 0.000558964 | 0.0167087 | stop-gained, synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632492 | CTCAGGCTCTGCTTC[A/G/T]TACACTGGCTCTTCC | 3059 |
rs779862509 | snp | A/C | 1.6473e-05 | 0.00286988 | missense | HCLS1 | GRCh38.p7 | 3:121644868 | CCCCAAAGCCTTTGG[A/C]AGCATCCGTCTGAGA | 3059 |
rs780025745 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644765 | CAGGGGTGATCGTGG[A/G]CAATTTTCACAGGAC | 3059 |
rs780090508 | snp | C/T | 3.29549e-05 | 0.00405911 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634303 | CCTCTTTGTCACAGC[C/T]TTTCGCTCCTGTTGC | 3059 |
rs780143738 | snp | C/T | 0.000197716 | 0.00994078 | missense | HCLS1 | GRCh38.p7 | 3:121635801 | CATTGAAGCCGACAG[C/T]GCTCTGCAGGCAGGA | 3059 |
rs780300046 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660435 | ATCTGTTACATTTCC[C/T]GTGTGGGTTTGTTTC | 3059 |
rs780325344 | snp | A/G | 1.87156e-05 | 0.00305899 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647531 | AATGGAAGCCTTGAA[A/G]TCTGTCCTGTTTACT | 3059 |
rs780344105 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649635 | GACACAAAAATGTTT[C/T]ATGTATGGAGATAGA | 3059 |
rs780416658 | snp | C/T | 0.00028816 | 0.0119999 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633051 | GGGGGCAGAGAATCT[C/T]TGGGGGTTTGCTTAC | 3059 |
rs780436169 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635566 | ACAGATGTGAGCTCC[A/G]CCTTACCTGGTTTTT | 3059 |
rs780446159 | snp | C/T | 3.30017e-05 | 0.00406199 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658375 | GGAGATGGGAATAAT[C/T]AGGGACAAAAAAGGA | 3059 |
rs780532205 | snp | A/G | 1.65031e-05 | 0.00287251 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637301 | CACCCTTAGGCTCCA[A/G]CACACAGGGAAGCGC | 3059 |
rs780540505 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648602 | GGACTTTACCAGCGC[A/G]GGACAACCAGACACA | 3059 |
rs780621432 | snp | C/T | 3.79766e-05 | 0.00435739 | missense | HCLS1 | GRCh38.p7 | 3:121633113 | GGCACTGGGTGTTCC[C/T]TGCTGGTTCTCACAG | 3059 |
rs780639478 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657834 | TCTGTCTCAAAAAAC[-/A]AACAAGAAAACACAA | 3059 |
rs780717219 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639200 | AAGATCCAAACATTA[C/T]CAACTAATAAACCTA | 3059 |
rs780784287 | snp | G/T | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631787 | GGAATAGGGAGGGGG[G/T]GGAGGCAGAGCCACT | 3059 |
rs780809422 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662740 | ACTCGGTCTCAAAAA[A/G]AACCCAACAAAACAA | 3059 |
rs780837204 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647044 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 3059 |
rs780855779 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644545 | CATGCATATGAGTAT[A/G]ATAAAAACCAGTGGC | 3059 |
rs780894566 | snp | A/C/T | 0.00018144 | 0.00952309 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644760 | CCATCCAGGGGTGAT[A/C/T]GTGGGCAATTTTCAC | 3059 |
rs780909710 | snp | C/G | 1.64762e-05 | 0.00287016 | missense | HCLS1 | GRCh38.p7 | 3:121631918 | TCCCCGCCACCAGCC[C/G]TCGTCCACCATCTCA | 3059 |
rs780915239 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654040 | AGTACAGTGGCTACT[C/T]ACAGACACAATCCCA | 3059 |
rs780986542 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | HCLS1 | GRCh38.p7 | 3:121634311 | TCACAGCCTTTCGCT[C/G]CTGTTGCCTCCTGGC | 3059 |
rs781000935 | snp | C/T | 1.64898e-05 | 0.00287135 | missense | HCLS1 | GRCh38.p7 | 3:121634382 | TCCTCAGCCATGGAC[C/T]CAAATTTCGCCTTCA | 3059 |
rs781014122 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652872 | TGCATTTCATTTCAA[C/T]AAAAGAATTACGGAC | 3059 |
rs781073897 | snp | A/G | 1.64982e-05 | 0.00287208 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632432 | GTCCATCTCCTCAAC[A/G]TCCTCATAGTCATTC | 3059 |
rs781165290 | snp | C/T | 4.96874e-05 | 0.0049841 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632077 | CCTCCATGTACCAGG[C/T]TCCTCGGGCCACTCC | 3059 |
rs781173840 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121632957 | GGTCTTCAGTGCTAA[C/T]ACCAGAACAGTGCAA | 3059 |
rs781282148 | in-del | -/CTC | 1.64966e-05 | 0.00287194 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632306 | GGACATGAGCAAATT[-/CTC]CTGCTTCTCCTCCCA | 3059 |
rs781368357 | snp | C/G | 1.64885e-05 | 0.00287123 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632014 | GGGGATATTAGAATG[C/G]TCAGACATGAATCTC | 3059 |
rs781370824 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643989 | TTCATGGTTTTACCC[C/G]CCATGATGCAAACAA | 3059 |
rs781372548 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660134 | CCTCTGAGGGACCAT[C/G]ACAAGGGCATCAACA | 3059 |
rs781400355 | snp | A/G | 1.65696e-05 | 0.00287828 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647293 | GCTTGTATTTTTTTA[A/G]AGCAAATCTTTCCCT | 3059 |
rs781400527 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639902 | AAGTAGAAGAAAAAC[-/A]ATAATAAAGATAAGA | 3059 |
rs781494219 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636859 | AGACTCATGGCAAAC[C/G]ATCTTCTGACCATCA | 3059 |
rs781523153 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637767 | TGGGGAAACCCTGTC[A/T]CTACTAAAAAATACA | 3059 |
rs781526507 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656222 | GCCAGGCTTTCACAG[C/T]ATGTTGCTTGTGCAA | 3059 |
rs781535516 | snp | A/C | 0.000698103 | 0.0186699 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637110 | AAGGAGATCCCTGTG[A/C]TATCTGTGACCTTCC | 3059 |
rs781573878 | snp | A/G | 1.64789e-05 | 0.0028704 | stop-gained | HCLS1 | GRCh38.p7 | 3:121657328 | TCTTGGCTCCCCATC[A/G]TTGCTCCTTTTCAGA | 3059 |
rs781652918 | snp | A/T | 3.29723e-05 | 0.00406018 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658246 | GCACTGTCCAAGCAA[A/T]GCTACTTCCAAACTC | 3059 |
rs781671214 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635727 | GAGAGTGAATCACTA[A/C]GCCTCACCGGCTTCT | 3059 |
rs796285307 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656141 | AGCGTGAGCCACCAC[A/G]CCCGGCCGAAACCAT | 3059 |
rs796353173 | in-del | -/AC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639023 | CCAACACACACACAC[-/AC]GCACACACACACACA | 3059 |
rs796371952 | in-del | ATTT/TA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639525 | TAACTGAATGATTTT[ATTT/TA]TTTTTGTTGTTGTTG | 3059 |
rs796664408 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652759 | TGTTTATGAAGTGAT[G/T]GTAGTATTATTAAGG | 3059 |
rs796899450 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656069 | GCCCATGCTGGTCTT[A/G]AACTCCTGACCTCAA | 3059 |
rs796900465 | multinucleotide-polymorphism | CCG/TCA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655177 | ACTCCAGGCAGCACC[CCG/TCA]CAGAGTGATCTGTGT | 3059 |