SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs765829 | snp | A/G | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654127 | gagcaggggaccata[A/G]gttgcctaagaaggg | 3059 |
rs1128154 | snp | A/C | 0.357877 | 0.225527 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631769 | CCCTCCCTATTCCTG[A/C]TGCAAATGTCTAACC | 3059 |
rs1128158 | snp | G/T | 0.357238 | 0.225832 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631746 | GTCTAACCAGATGAG[G/T]TTCTGGACAGACTTC | 3059 |
rs1128159 | snp | A/G | 0.484701 | 0.0861117 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631736 | ATGAGGTTCTGGACA[A/G]ACTTCCCTCTCCTGC | 3059 |
rs1128163 | snp | C/T | 0.372995 | 0.217652 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631726 | GGACAGACTTCCCTC[C/T]CCTGCTTCATTAAGG | 3059 |
rs1814668 | snp | C/T | 0.213635 | 0.247341 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662625 | CTGTAATCCCAGCTA[C/T]TTGGGAGACTGAGGC | 3059 |
rs1919550 | snp | A/T | 0.164546 | 0.234942 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645326 | GACGCCATAGCCGGG[A/T]TGGAATATTTCACTA | 3059 |
rs1986874 | snp | C/T | 0.453209 | 0.145623 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654028 | TGTGAGTAGCCACTG[C/T]ACTCCAGCCTGGGCA | 3059 |
rs2070178 | snp | C/T | 0.36044 | 0.224283 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121642940 | AGAAGTGGAGAAGCA[C/T]ACATCTCAGAAAGGC | 3059 |
rs2070179 | snp | A/G | 0.42026 | 0.183076 | missense | HCLS1 | GRCh38.p7 | 3:121634407 | GCAGCTTCTAGTGGT[A/G]CCCGTGGGCTGAAGG | 3059 |
rs2070180 | snp | A/G | 0.339008 | 0.233618 | missense | HCLS1 | GRCh38.p7 | 3:121632491 | GAAGAGCCAGTGTAC[A/G]AAGCAGAGCCTGAGC | 3059 |
rs3772126 | snp | A/G | 0.354548 | 0.22709 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121635736 | TCACTAAGCCTCACC[A/G]GCTTCTATGGGCGTC | 3059 |
rs3772127 | snp | C/T | 0.4628 | 0.13121 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636078 | GCAGGGCCCCCTGGC[C/T]CATGCATGAGGAGGA | 3059 |
rs3966067 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653675 | TCAGTCCCTAGAGCT[C/G]CAGAATTCTATTTCT | 3059 |
rs3966068 | snp | A/G | 0.355096 | 0.226837 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653882 | GTGTGTGGTCCACAA[A/G]CTGAACTGTTTCTGT | 3059 |
rs4048703 | snp | A/G | 0.343254 | 0.231956 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655514 | ACTATATTGCAAGTC[A/G]TCATGGCGGAGTGTT | 3059 |
rs4048704 | in-del | -/TTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655698 | ttttttttttttttt[-/TTT]ttatCTATGAGTCTA | 3059 |
rs4048711 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635270 | CTCTCTCTCTCTCTC[-/T]CTCTCCTCTCTCTCC | 3059 |
rs6438644 | snp | A/G | 0.35809 | 0.225425 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631129 | ggtactcgggaggct[A/G]aggcaggagaatctc | 3059 |
rs6438645 | snp | C/T | 0.453697 | 0.14494 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635041 | CACTCATCCTCAACC[C/T]CATCCGAAACTCCTG | 3059 |
rs6438648 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660322 | gattctgtgatCTAC[A/G]AACACAGAAACTAGC | 3059 |
rs6770842 | snp | A/C | 0.356597 | 0.226135 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634481 | GGGGAAGGGCATGGC[A/C]CTTGAAGGAAGAAGG | 3059 |
rs6779102 | snp | A/G | 0 | 0 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631716 | TGCCCCAAGCCCTTA[A/G]TGAAGCAGGAGAGGG | 3059 |
rs6782837 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646693 | ataatatataaaata[A/T]aatatacattatatt | 3059 |
rs6791882 | snp | C/T | 0.343477 | 0.231866 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654211 | CAGCATAGAGCACTA[C/T]AGCCCAGAACTACTG | 3059 |
rs6791896 | snp | C/T | 0.452842 | 0.146134 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654264 | CAGCCTCCTGAGTAG[C/T]TGGGTCTATAGGCAC | 3059 |
rs6792659 | snp | A/G | 0.453453 | 0.145282 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658016 | CTTCTCACCTTCAGT[A/G]TAGCCTGCCATGGCC | 3059 |
rs6802033 | snp | A/C | 0.4628 | 0.13121 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636255 | AAGCTCAGGCTTTGG[A/C]AGACATGCCCCTTAG | 3059 |
rs6804322 | snp | A/G | 0.355954 | 0.226437 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649536 | CACCACGCCTGGCCT[A/G]AACAGGTCTTAATCA | 3059 |
rs7356043 | snp | A/G | 0.363392 | 0.222805 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647530 | AAATGGAAGCCTTGA[A/G]GTCTGTCCTGTTTAC | 3059 |
rs7427165 | snp | C/T | 0.251859 | 0.249993 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645777 | AACCAATGAATGAGT[C/T]AAAAAATATATATTT | 3059 |
rs7428192 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647145 | caccacgacgcacgg[C/G]taattttttgtattt | 3059 |
rs7428749 | snp | A/G | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653939 | gagaatatgtgttta[A/G]aaacttttatagcaa | 3059 |
rs7428752 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653995 | tctttttctttttta[A/G]aaatggggtctcact | 3059 |
rs7429247 | snp | C/T | 0.453087 | 0.145793 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645640 | GTTCTAATATCTTGG[C/T]TCTTATTTTCTGCCA | 3059 |
rs7611913 | snp | A/C | 0.461813 | 0.132798 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632903 | AGGATAATCATCTAT[A/C]CTAGTTTGCCCAGGA | 3059 |
rs7620842 | snp | A/T | 0.453818 | 0.144769 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635534 | CCTCCCACTTTAGCC[A/T]CCAAAGTGCTGGGAT | 3059 |
rs7628179 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646372 | cattatattacatat[A/T]attactatgtaatat | 3059 |
rs7628761 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646990 | tattttatttatttt[A/T]tttttttttgagaca | 3059 |
rs7648708 | snp | G/T | 0.030278 | 0.119257 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642747 | tgtcactgcactccc[G/T]cctgggtgacagtgc | 3059 |
rs9289172 | snp | A/C | 0.462691 | 0.131387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637521 | TTCTTCAAGAAGGGG[A/C]AAGTATAGAGAGTGA | 3059 |
rs9289173 | snp | C/T | 0.453697 | 0.14494 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639850 | tatctaagtttctac[C/T]ttaagaggctaggaa | 3059 |
rs9289174 | snp | A/T | 0.477853 | 0.102875 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646985 | TTATTTATTTTATTT[A/T]TTTTTTTTTTTTTTG | 3059 |
rs9289175 | snp | A/T | 0.369958 | 0.21934 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646991 | ATTTTATTTATTTTT[A/T]TTTTTTTTGAGACAG | 3059 |
rs9809114 | snp | C/T | 0.453697 | 0.14494 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636876 | TCTTCTGACCATCAC[C/T]CAGCTTGTCTGTCCT | 3059 |
rs9815500 | snp | C/T | 0.5 | 0.00019968 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632633 | GGAGGACTGATAAGA[C/T]CCCCCGCCCTTCACC | 3059 |
rs9818073 | snp | C/T | 0.373598 | 0.21731 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647082 | TGCCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 3059 |
rs9818194 | snp | A/T | 0.355525 | 0.226637 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654446 | TGAAAATAAACAAAC[A/T]GGTCAAGGGAAAAGA | 3059 |
rs9818402 | snp | C/T | 0.362097 | 0.22346 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647276 | GTGAGCCACCGCACC[C/T]GGCTTGTATTTTTTT | 3059 |
rs9820511 | snp | A/G | 0.372592 | 0.217879 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642498 | GTATGTAAAATAGCG[A/G]TGGGTGTGGTGGCTC | 3059 |
rs9838301 | snp | G/T | 0.3742 | 0.216966 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656297 | CTGCTTTTAGGGTGC[G/T]GTAGGGGGAGTTAAA | 3059 |
rs9844611 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657790 | tgagattgcaccacc[A/G]tactccagcctgggt | 3059 |
rs9846174 | snp | C/T | 0.365232 | 0.22186 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643792 | ACTGGGTGATTCCAT[C/T]TGTGGCTTGTGAGCA | 3059 |
rs9849847 | snp | A/T | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649759 | ATCCAATTTAAGTTT[A/T]AAAAGACTTTGTATT | 3059 |
rs9859116 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656899 | ATTTATCTGAAGAGA[C/T]AGATAGGAGATAGAT | 3059 |
rs9859243 | snp | G/T | 0.354881 | 0.226936 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656955 | GACCTTAGTATTTGG[G/T]CCACTTCCTCTATGA | 3059 |
rs9864907 | snp | C/T | 0.453331 | 0.145452 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652216 | acaaaaagatcagta[C/T]ggggtgtattgactg | 3059 |
rs9869984 | snp | C/G | 0.00254008 | 0.0355478 | missense | HCLS1 | GRCh38.p7 | 3:121632119 | CTTGGTAATCATATA[C/G]AGCCACAGCTGAGAT | 3059 |
rs9873644 | snp | A/G | 0.355525 | 0.226637 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645389 | TCCTGTATGGCCATC[A/G]AAGTTCAGAAGTGAA | 3059 |
rs9873648 | snp | A/T | 0.355525 | 0.226637 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645404 | AAAGTTCAGAAGTGA[A/T]CTCTGAGCTTTATAC | 3059 |
rs9883663 | snp | A/T | 0.354881 | 0.226936 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652916 | GTTTATTAGACAAAA[A/T]CAATATATTGGTTAA | 3059 |
rs10049060 | snp | C/T | 0.372391 | 0.217992 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639601 | ttgcccaggccaaaa[C/T]gtagtggcacaatca | 3059 |
rs10212342 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639045 | cacacacacacacac[A/G]cacacacacacaAat | 3059 |
rs10677529 | in-del | -/ATATA | 0.440746 | 0.161604 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646151 | ACTATATATAAGTAT[-/ATATA]ATATATAATATATCT | 3059 |
rs10934555 | snp | A/C | 0.355311 | 0.226737 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641807 | ATCAATATGGCCAGG[A/C]GCGGTGACTCAAGCC | 3059 |
rs11382500 | in-del | -/A | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642098 | AAAAAAAAAAAAAAA[-/A]CTTGATCAATATTAT | 3059 |
rs11425636 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642304 | TCTACTAAAAATACA[-/A]AAAAAAAAAAAAAAA | 3059 |
rs11541877 | snp | A/G | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631744 | GGGAAGTCTGTCCAG[A/G]AACTCATCTGGTTAG | 3059 |
rs11707716 | snp | A/G | 0.252421 | 0.249988 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647139 | GGCACCCACCACGAC[A/G]CACGGCTAATTTTTT | 3059 |
rs11714406 | snp | C/T | 0.25045 | 0.25 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653666 | GAGCTGGAATCAGTC[C/T]CTAGAGCTCCAGAAT | 3059 |
rs11716984 | snp | A/T | 0.250168 | 0.25 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643560 | AATAATGGAAACACA[A/T]ATATGTGGATTTTGG | 3059 |
rs11720859 | snp | A/T | 0.251578 | 0.249995 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657660 | ATCTCTACCAAAAAA[A/T]TACAAAAATTAGCCA | 3059 |
rs12487377 | snp | A/G | 0.355311 | 0.226737 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642799 | ACAAATGAACAAAAA[A/G]TAAATAAAATAGTGG | 3059 |
rs12491714 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653001 | atccctcatcccaaa[C/T]gcttgggaccagaag | 3059 |
rs12493927 | snp | A/G | 0.175897 | 0.238765 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660080 | GTACACAGACTGGGA[A/G]TCAGAAGCCCTGGCT | 3059 |
rs12494379 | snp | A/G | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655659 | AGTGGCCTTTATTCA[A/G]AAAAGGAAAAGGGTC | 3059 |
rs12494408 | snp | A/G | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655774 | TTCAATCTTTTTCCA[A/G]AATGGCATGGTTTAA | 3059 |
rs12629986 | snp | A/G | 0.487241 | 0.0788465 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641874 | ATCACGAGGTCAGAA[A/G]ATCGAGACCATCCTG | 3059 |
rs12635865 | snp | A/C | 0.34303 | 0.232046 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642045 | AGATCCAGCCACTGC[A/C]CTCCAGCCTGGGCGA | 3059 |
rs12637092 | snp | A/G | 0 | 0 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661902 | ATTGTATCTGACCTA[A/G]CCTTTCCTAATCTTG | 3059 |
rs13067629 | snp | C/T | 0.454061 | 0.144427 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659440 | CCCCATGCTCTCCAT[C/T]GTCTCCAAAGAGTCC | 3059 |
rs13071671 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642379 | gaggctgaggcagga[A/G]aatggcgtgaaccca | 3059 |
rs13087578 | snp | A/C | 0.224116 | 0.248656 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650360 | agtcctggaatagta[A/C]aatcttttgtttctt | 3059 |
rs13090660 | snp | C/T | 0.249603 | 0.25 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645933 | atatattaaaatata[C/T]ataatataaATTTAT | 3059 |
rs17691170 | snp | C/G | 0.249603 | 0.25 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638779 | AAGTGCATTCTAAGA[C/G]ACAAGAAAGACATGC | 3059 |
rs28407082 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639041 | CACACACACACACAC[A/G]CACACACACACACAC | 3059 |
rs28575449 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640792 | AAGGGAAGGGGAGGG[A/G]AGGGGAGGGGAGGGG | 3059 |
rs34065758 | snp | C/T | 0.0112374 | 0.074111 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121658309 | TGATGTGTCTGTTTC[C/T]GTGGAGACCCAGGGT | 3059 |
rs34086988 | snp | C/G | 0.262985 | 0.249663 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633898 | CTGCCAATTCAAATG[C/G]AACTCATCCCTCAAG | 3059 |
rs34089682 | in-del | -/T | 0.445064 | 0.156365 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639522 | TTTTTAACTGAATGA[-/T]TTTATTTTTTGTTGT | 3059 |
rs34223359 | in-del | -/A/AAA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642319 | AAAAAAAAAAAAAAA[-/A/AAA]TTAGCCAGGCGTGCT | 3059 |
rs34254619 | in-del | -/T | | | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121632427 | GCCTGTCCATCTCCT[-/T]CAACGTCCTCATAGT | 3059 |
rs34277781 | in-del | -/G | | | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121632487 | CAGGCTCAGGCTCTG[-/G]CTTCGTACACTGGCT | 3059 |
rs34388296 | in-del | -/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642829 | TGCGCTGGGTCATGG[-/G]AAGTTAAAAAGCTGA | 3059 |
rs34440810 | snp | A/G | 0.177996 | 0.23942 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121644833 | GTACGGAGTTGAGAG[A/G]GACAGGGCAGACAAG | 3059 |
rs34623011 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655189 | ACCCGTCAGAGTGAT[-/A]CTGTGTATAGGAGTT | 3059 |
rs34667636 | snp | A/G | 0.340587 | 0.233011 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634444 | AGGCAAGAAAAATTA[A/G]GGTTGTCTTGGATTG | 3059 |
rs34730875 | in-del | -/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121644227 | GAACTAAAAACATCG[-/C]ATGAGTTATCAATCT | 3059 |
rs34767273 | snp | A/G | 0.0154471 | 0.0865253 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637215 | TACGGGGTGGAGAAG[A/G]ATAAATGGGACAAAG | 3059 |
rs34798973 | in-del | -/CA | 0.452842 | 0.146134 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631457 | AACAGAAAGAAGGTT[-/CA]CAGATATTTCTTCAG | 3059 |
rs34804866 | in-del | -/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660452 | GTGGGTTTGTTTCCC[-/C]TGAGACCATATGCTC | 3059 |
rs34917887 | snp | A/C | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645464 | AAAATCACTAAATAC[A/C]CAGTAAATAAAATAA | 3059 |
rs34931050 | in-del | -/G | | | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121631873 | TTGACATAATTTGCA[-/G]GGGAAGAGTCCAAAG | 3059 |
rs35077759 | in-del | -/GTTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656588 | TTTGTTTGTTTGTTT[-/GTTT]CTGGTAAAATGCATA | 3059 |
rs35252445 | in-del | -/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642717 | GAAGTCGAAGCTGCA[-/C]GTGACCCATGATTGT | 3059 |
rs35488369 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655776 | AATCTTTTTCCAGAA[-/A]TGGCATGGTTTAAGA | 3059 |
rs35691635 | in-del | -/ATATA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646152 | CTATATATAAGTATA[-/ATATA]TATATAATATATCTT | 3059 |
rs35745057 | multinucleotide-polymorphism | AC/GT | | | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637237 | CACCCCGTACCGGCC[AC/GT]CAAAGCCACGAGAGT | 3059 |
rs35997908 | in-del | -/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639242 | ACAACACTATACCCC[-/C]AAACTACAGAATATA | 3059 |
rs36104070 | snp | C/T | 0.0259695 | 0.110952 | missense | HCLS1 | GRCh38.p7 | 3:121636456 | GTGGCCAGTATGGAA[C/T]CCAGAAGGACCGAGT | 3059 |
rs41271407 | snp | A/C | 0.175897 | 0.238765 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631604 | GGCAGAGAGGTGTTC[A/C]TTGGGAAGGAGTCAG | 3059 |
rs41271409 | snp | A/C | 0.0100852 | 0.0702915 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632123 | GTAATCATATACAGC[A/C]ACAGCTGAGATCCCC | 3059 |
rs55964830 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641380 | TCTTTCATAGACTCA[C/T]TGAAAGAATTATCAA | 3059 |
rs56054727 | in-del | -/AC | 0.463343 | 0.130326 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639011 | CATCGCAAGACTCCA[-/AC]ACACACACACACGCA | 3059 |
rs56198567 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649611 | TGTGAGGTACTGTTA[A/G]GCTCTGAGGACACAA | 3059 |
rs56314138 | snp | A/G | 0.249886 | 0.25 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637809 | GGCATGGTGATGTGC[A/G]TCTGTAGCCCCAGCT | 3059 |
rs56404875 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636645 | GATGGGAAGAGAGGG[A/G]AACAGATGGGGAAAA | 3059 |
rs56651751 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646367 | TATTACATTATATTA[C/T]ATATTATTACTATGT | 3059 |
rs56676179 | snp | A/G | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639023 | CCAACACACACACAC[A/G]CGCACACACACACAC | 3059 |
rs56877030 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661697 | AGGCCGTAAGACCAC[C/T]GCAAGCTTTGCCATG | 3059 |
rs57154480 | in-del | -/ATATA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646695 | AATATATAAAATATA[-/ATATA]CATTATATTATATTT | 3059 |
rs58527943 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633227 | CTTCACTCCTTTTTT[-/T]TTTTTTGAGATAGAC | 3059 |
rs58817111 | in-del | -/TATT | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655866 | ATTTATTTATTTATT[-/TATT]GAGACTGAGTCTCGC | 3059 |
rs59288284 | snp | A/T | 0.202959 | 0.245534 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659020 | TATTACTCAATTTTT[A/T]AAAAATGGTTCAATT | 3059 |
rs59424510 | in-del | -/ATATA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646156 | ATATAAGTATATATA[-/ATATA]TAATATATCTTATAA | 3059 |
rs61617145 | snp | A/G | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639025 | AACACACACACACAC[A/G]CACACACACACACAC | 3059 |
rs61720711 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646351 | ATTATAGTATATAAT[-/A]TATTACATTATATTA | 3059 |
rs61720712 | in-del | -/TTAC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646354 | ATAGTATATAATATA[-/TTAC]ATTATATTACATATT | 3059 |
rs61720713 | in-del | -/TT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646371 | ACATTATATTACATA[-/TT]ATTACTATGTAATAT | 3059 |
rs61720714 | in-del | -/TATGTA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646378 | ATTACATATTATTAC[-/TATGTA]ATATATTACTATGTA | 3059 |
rs61720715 | in-del | -/TATTACTAT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646387 | TATTACTATGTAATA[-/TATTACTAT]GTAATATATTACATA | 3059 |
rs61724320 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646364 | ATATATTACATTATA[G/T]TACATATTATTACTA | 3059 |
rs61749596 | snp | A/G | 0.0013994 | 0.0264148 | missense | HCLS1 | GRCh38.p7 | 3:121635773 | TTATAAGCTGTGGTC[A/G]GGGCCTCCATTTCAT | 3059 |
rs62268723 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635217 | TCTTTCTTTCTCTCT[C/T]TCTCTCTCTTCTCTC | 3059 |
rs62268724 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635221 | TCTTTCTCTCTCTCT[C/T]TCTCTTCTCTCCCTT | 3059 |
rs62268725 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635233 | TCTCTCTCTTCTCTC[C/T]CTTTTCTCTCTCTCT | 3059 |
rs62268726 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635236 | CTCTCTTCTCTCCCT[C/T]TTCTCTCTCTCTCTC | 3059 |
rs62268727 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635251 | TTTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 3059 |
rs62268728 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638774 | AGACAAAGTGCATTC[C/T]AAGAGACAAGAAAGA | 3059 |
rs62268729 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641440 | GACACAAAGGTGAAA[C/T]AATGAAATACAATAA | 3059 |
rs62268730 | snp | A/G | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650388 | CTTTTTTTTTTTTTA[A/G]GGAGAGCAAAGTTGA | 3059 |
rs62268731 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650390 | TTTTTTTTTTTTAAG[G/T]AGAGCAAAGTTGAGG | 3059 |
rs62268732 | snp | G/T | 0.252702 | 0.249985 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651608 | AATTTTTTTGTAGAC[G/T]CTGAATCTCTCCACA | 3059 |
rs63029362 | in-del | -/A | 0.180383 | 0.240111 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637547 | TTGCAGAAAAAAAAA[-/A]GGCAGATACATGAAA | 3059 |
rs66527345 | in-del | -/CAA | 0.17654 | 0.238964 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659764 | TCCTGGGCTGCTGTG[-/CAA]CAACAAAAGGACTGT | 3059 |
rs66683706 | in-del | -/A | 0.375 | 0.216506 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655699 | ATAGACTCATAGATC[-/A]AAAAAAAAAAAAAAA | 3059 |
rs71329229 | snp | C/T | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632315 | CAAATTCTCCTGCTT[C/T]TCCTCCCATCACTCA | 3059 |
rs71329230 | snp | C/G | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640804 | GGGGAGGGGAGGGGA[C/G]GGGAGGGCAGGGCAG | 3059 |
rs71632699 | in-del | -/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639533 | CAACAACAACAACAA[-/C]AAAAAATAAAATCAT | 3059 |
rs71766880 | in-del | -/CA | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631458 | ACAGAAAGAAGGTTC[-/CA]AGATATTTCTTCAGG | 3059 |
rs72955370 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633759 | TGCCCAGGTTGGTCT[A/G]GAACTCCTGGCTTCA | 3059 |
rs73179962 | snp | A/C | 0.356169 | 0.226336 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634710 | AGTCATGGGACACTG[A/C]AGCCTCAACCTCCCA | 3059 |
rs73179967 | snp | A/T | 0.355311 | 0.226737 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642103 | AAAAAAAAAAACTTG[A/T]TCAATATTATAGAAA | 3059 |
rs74509467 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634938 | TGCCCAGCTGACTTG[A/T]GTCCTTTCTAAATTG | 3059 |
rs74746356 | snp | A/G | 0.356597 | 0.226135 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637872 | ACATGGGGGGTGGAG[A/G]TTGCAGTGAGCCAAG | 3059 |
rs75598081 | snp | C/G | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636601 | AATGTAGGAGGAAAT[C/G]TGAGAATCAGAGGAT | 3059 |
rs75679992 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652884 | CAACAAAAGAATTAC[A/G]GACATGACGATATTA | 3059 |
rs75865465 | snp | A/G | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655732 | AGGGGTATCACAGAA[A/G]CTTCCTGAATGACCC | 3059 |
rs75917506 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634935 | CCATGCCCAGCTGAC[C/T]TGTGTCCTTTCTAAA | 3059 |
rs76043066 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640702 | GGCCAAGGCAGAAGG[A/G]TCACTTCAGCCCAGG | 3059 |
rs76253170 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660174 | CTCATTTGCCAGGTA[G/T]CAGACCAGGCGATTA | 3059 |
rs77060751 | snp | A/G | 0.0248432 | 0.108648 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631600 | GGGTGGCAGAGAGGT[A/G]TTCATTGGGAAGGAG | 3059 |
rs77244471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641006 | AAGGAATAACCCAGA[A/G]TGCGGCACAAGGACA | 3059 |
rs77378626 | snp | G/T | 0.228842 | 0.249103 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639533 | ATGATTTTATTTTTT[G/T]TTGTTGTTGTTGTTG | 3059 |
rs77693733 | snp | C/T | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634644 | CCTAAGACTCGTGTC[C/T]TTTTTTTTTCTTGAG | 3059 |
rs77776399 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631611 | AGGTGTTCATTGGGA[A/G]GGAGTCAGGAACACA | 3059 |
rs77796550 | snp | G/T | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655488 | TTTTTTTTTTTTTTT[G/T]GCCAATGCCTACTAT | 3059 |
rs77852202 | snp | C/T | 0.0861326 | 0.188805 | missense | HCLS1 | GRCh38.p7 | 3:121632410 | GTTCATCCTCCTGCT[C/T]ATGCCTGTCCATCTC | 3059 |
rs77952416 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639230 | AATTGACTCTTATAC[A/C]ACACTATACCCCAAA | 3059 |
rs77953723 | snp | A/G | 0.000856644 | 0.0206782 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121631864 | CTCCAGAAGCTTGAC[A/G]TAATTTGCAGGGAAG | 3059 |
rs78571288 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643862 | AGTGGTGCCAAGATG[C/G]AACAGGGAATTCCAT | 3059 |
rs78618042 | snp | C/T | 3.29538e-05 | 0.00405904 | missense | HCLS1 | GRCh38.p7 | 3:121631907 | CCATGGCAACGTCCC[C/T]GCCACCAGCCCTCGT | 3059 |
rs78654812 | snp | A/C | 0.0865458 | 0.189163 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659058 | AAAGTCAAAAAATAG[A/C]ATGTTTTCAAGTTGA | 3059 |
rs78740052 | snp | A/G | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637548 | GTGAGGAGATTGCAG[A/G]AAAAAAAAGGCAGAT | 3059 |
rs78781147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640619 | GATATGCAATAGAAC[C/G]AAAAGAAACTCCAGA | 3059 |
rs78827834 | snp | C/T | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655457 | TTTTATGAGGGTTGC[C/T]TGCTCTTTTTTTTTT | 3059 |
rs78907191 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635070 | TGTCCCTGTGTGTTC[G/T]TCCCAAGTGGTTCCT | 3059 |
rs79173165 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658727 | CTATAATATCCCTAG[A/G]ATTATGGCCTTATTT | 3059 |
rs79565052 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634937 | ATGCCCAGCTGACTT[A/G]TGTCCTTTCTAAATT | 3059 |
rs79579040 | snp | A/T | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650386 | TTCTTTTTTTTTTTT[A/T]AAGGAGAGCAAAGTT | 3059 |
rs79788081 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650025 | ATTATATCAAAATCA[A/G]TTGTATTTTTACATA | 3059 |
rs79916774 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644539 | TATCTTCATGCATAT[A/G]AGTATAATAAAAACC | 3059 |
rs80082211 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653195 | TTTTTCCCTTGGGGA[C/T]GCTGAAAAAACTGTT | 3059 |
rs80289672 | snp | A/G | 0.11935 | 0.213144 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632468 | CTCGGGCTCAGGCTC[A/G]GGCTCAGGCTCAGGC | 3059 |
rs111215344 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646480 | ATATAATATATAATA[G/T]AGATATATTATATAT | 3059 |
rs111215436 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646489 | ATAATATAGATATAT[A/T]ATATATTATATATAC | 3059 |
rs111215437 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646773 | TTATATAATTATATA[A/C]TTACATATAATTGGC | 3059 |
rs111317205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643932 | GCCTTCTACATCTTC[C/T]CTTAGCTTTGCAGTA | 3059 |
rs111338398 | in-del | -/TTTG | 0.3512 | 0.228601 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656569 | CTGGTATCGGAGGGT[-/TTTG]TTTTGTTTGTTTGTT | 3059 |
rs111371802 | snp | C/T | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636916 | CTCAACGCCCCCTTC[C/T]CTCTCACCTCCCTCC | 3059 |
rs111509389 | in-del | -/A | 0.5 | 0 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631228 | GCAAAACTCCTTCTC[-/A]AAAAAAAAAAAAGTT | 3059 |
rs111618238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634054 | TAGGAGGTCCAATTA[C/T]AGTCAGACTGAAGTC | 3059 |
rs111759137 | snp | C/T | 4.94181e-05 | 0.00497057 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121642943 | TTTCTGAGATGTGTG[C/T]TTCTCCACTTCTCCT | 3059 |
rs111780489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636140 | GGAAGAGACTTAAGA[C/T]TGGGTTAAGCAATGC | 3059 |
rs111914785 | snp | C/T | 0.00744973 | 0.0605753 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631803 | GGAGGCAGAGCCACT[C/T]TGGACATGGGAAATC | 3059 |
rs112043027 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634892 | CTACTTCAGCATCCC[A/G]AAGTGCTGGGATTAC | 3059 |
rs112102372 | snp | A/G | 0.357024 | 0.225933 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637885 | AGGTTGCAGTGAGCC[A/G]AGATTGCACCATTGC | 3059 |
rs112339997 | snp | C/T | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636925 | CCCTTCTCTCTCACC[C/T]CCCTCCTAGGCCCTG | 3059 |
rs112494135 | in-del | -/AGCCAC | 0.000166021 | 0.00910948 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632141 | AGCTGAGATCCCCAG[-/AGCCAC]AGCCCCAGCCCCAGC | 3059 |
rs112503052 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662822 | TTCTCCCATTCCCAC[A/C]CAGAGGGATCCCTAG | 3059 |
rs112649175 | in-del | -/T | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632633 | GGAGGACTGATAAGA[-/T]CCCCCGCCCTTCACC | 3059 |
rs112707298 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635304 | CTCTCTCTTTCTTTC[A/G]TCTCACTCTGTCACC | 3059 |
rs112823146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641926 | CTCCACTAAAAATAC[A/G]AAAATTAGCCCGGCG | 3059 |
rs112834269 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641808 | TCAATATGGCCAGGC[G/T]CGGTGACTCAAGCCT | 3059 |
rs112931947 | snp | C/T | 0.5 | 0 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121642979 | ATCAAAGCCGACTGC[C/T]GACTACAGAGAAGAG | 3059 |
rs113194478 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635149 | TCTCTGCCTCCGATT[C/G]CTTCCCCGACGTCAC | 3059 |
rs113234078 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662716 | CTCCAGCCTGAGCGA[A/G]AGAGTGAAACTCGGT | 3059 |
rs113380849 | snp | A/G | 0.000199302 | 0.00998056 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633038 | GAGAAGATGGGGTGG[A/G]GGCAGAGAATCTTTG | 3059 |
rs113581023 | snp | C/T | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639024 | CAACACACACACACA[C/T]GCACACACACACACA | 3059 |
rs113897197 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648600 | TGGGACTTTACCAGC[A/G]CAGGACAACCAGACA | 3059 |
rs114010868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645378 | TAGATCTTTGCTCCT[A/G]TATGGCCATCAAAGT | 3059 |
rs114157000 | snp | A/G | 0.0154997 | 0.0866579 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633174 | CTGGAGGCCAGGCCT[A/G]TGGAAAATGAAGCAT | 3059 |
rs114208868 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659940 | AGTTTCTGAAATAGA[C/G]ACAATTTATCTAATA | 3059 |
rs114644585 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654524 | TGGAGAGAAGGGTGA[G/T]AGTTCTTGAAAACCA | 3059 |
rs114739036 | snp | C/T | 0.00184426 | 0.0303105 | missense | HCLS1 | GRCh38.p7 | 3:121657294 | TTGATGTGTTCTGTG[C/T]GTCCAGACCCCTCGA | 3059 |
rs114950876 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651009 | GGCTTGGTGGTGGGC[A/G]CCTGAGTCCCAGCTA | 3059 |
rs115045663 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662685 | AGGTGCAGTGAGTTG[A/G]GATTGTGCCACTGCA | 3059 |
rs115063595 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656451 | GATGGTCCTGGTTAG[A/G]TGATCCTGAATCATC | 3059 |
rs115532770 | snp | C/T | 0.030665 | 0.119967 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651545 | GGGCTCAAGTGCTTC[C/T]CCTGCCTCAGCCTCC | 3059 |
rs115596040 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656100 | GTGATCTTCCTCGCT[C/T]GGCCTTCCAAAGTTT | 3059 |
rs115940921 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659410 | CCTCAGACACCTCAT[C/T]CCATTGGAGACCTTC | 3059 |
rs115945856 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633521 | GCCACCACGCTCGGC[C/T]CATCTTCATTCTTTT | 3059 |
rs116012752 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639270 | ATACTTTTTTCATGC[A/T]TATAGAACATTGACC | 3059 |
rs116067712 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655030 | TTACCAGCAGATACC[A/G]GGCTTTCACTCCTTG | 3059 |
rs116352732 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644103 | AAACAAAGAAAAAAT[A/C]TCAGCTAACTGTGAA | 3059 |
rs116381221 | snp | A/C | 0.00386275 | 0.0437773 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631808 | CAGAGCCACTTTGGA[A/C]ATGGGAAATCACAGT | 3059 |
rs116408096 | snp | C/T | 0.00637239 | 0.0560856 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633209 | CAAGTAAGCAAGCCT[C/T]CATCTTCACTCCTTT | 3059 |
rs116446291 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647790 | TCTTTTCTGAATGGA[A/T]CTGCTTTCTATCAAT | 3059 |
rs116536179 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654916 | ATCCCCAAATAGTGG[A/G]GACTTACTACTGGAA | 3059 |
rs116691276 | snp | C/G | 0.00501168 | 0.0498069 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633023 | ACATTCCTAAGACTC[C/G]AGAAGATGGGGTGGG | 3059 |
rs116761773 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650762 | CTTAGACACATAAAG[C/T]ATTAGCCCCATAAAT | 3059 |
rs117353371 | snp | C/T | 6.65724e-05 | 0.00576903 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634432 | AGCTGCAGACACAGG[C/T]AAGAAAAATTAGGGT | 3059 |
rs117550164 | snp | A/G | 0.000966618 | 0.021963 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644968 | AGTGAAAAGATAAAA[A/G]TGACCTTAAAAAAAT | 3059 |
rs137976245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649737 | TTTGACATATTAACT[C/G]TCAGATATCCAATTT | 3059 |
rs138082949 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654838 | TTTCCCTCTCCTTTC[C/T]AAGGACCATGGTGAT | 3059 |
rs138115518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659326 | TAACAACAGACAATG[C/T]TCATCTGCTGTGGTC | 3059 |
rs138329587 | snp | C/T | 3.29957e-05 | 0.00406162 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634399 | AAATTTCGCCTTCAG[C/T]CCACGGGTACCACTA | 3059 |
rs138443230 | snp | C/T | 0.000287003 | 0.0119758 | missense | HCLS1 | GRCh38.p7 | 3:121633132 | TGGTTCTCACAGGCT[C/T]AGACTCTGATGATGG | 3059 |
rs138536890 | snp | C/G | 0.00258315 | 0.0358455 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644802 | TGGGTGGTTGGGAGA[C/G]AGAGTGGTCACTTAC | 3059 |
rs138568093 | snp | C/T | 8.23689e-05 | 0.00641698 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121635748 | ACCGGCTTCTATGGG[C/T]GTCGTCTTCTTATAA | 3059 |
rs138720682 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658451 | CCAATATTTCCTGCC[A/G]TTTTTTTTTTCTTAG | 3059 |
rs138785861 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654183 | GATTCAGAATTCAGC[A/G]TGGAGACCCAATCAG | 3059 |
rs138907395 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637863 | GTCACTTGAACATGG[G/T]GGGTGGAGGTTGCAG | 3059 |
rs139020299 | snp | C/T | 3.74714e-05 | 0.00432831 | missense | HCLS1 | GRCh38.p7 | 3:121633107 | AGCAAGGGCACTGGG[C/T]GTTCCCTGCTGGTTC | 3059 |
rs139051946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634480 | TGGGGAAGGGCATGG[C/G]ACTTGAAGGAAGAAG | 3059 |
rs139715069 | snp | A/T | 0.477853 | 0.102875 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646986 | TATTTATTTTATTTA[A/T]TTTTTTTTTTTTTGA | 3059 |
rs139834889 | snp | A/G | 0.000214184 | 0.0103463 | missense | HCLS1 | GRCh38.p7 | 3:121631902 | AGTGGCCATGGCAAC[A/G]TCCCCGCCACCAGCC | 3059 |
rs139857201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639279 | TCATGCATATAGAAC[A/G]TTGACCAAATAGACC | 3059 |
rs139861864 | snp | A/C/T | 0.00019767 | 0.00993982 | intron-variant, synonymous-codon | HCLS1 | GRCh38.p7 | 3:121637225 | TTTATCCTTCTCCAC[A/C/T]CCGTACCGGCCACCA | 3059 |
rs139890624 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634914 | TGGGATTACAGGTGT[A/G]AGCCACCATGCCCAG | 3059 |
rs139983736 | in-del | -/TGTACATCA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660396 | GGTACTCAGTGCTAG[-/TGTACATCA]TGTACATCAGTGACT | 3059 |
rs140067695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659547 | GCTCCATCTTCTCCA[C/T]TGAGCAACCTCTTAA | 3059 |
rs140101359 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656059 | TCATCATGTTGCCCA[C/T]GCTGGTCTTGAACTC | 3059 |
rs140124715 | snp | A/C/G | 0.000398778 | 0.0141151 | missense | HCLS1 | GRCh38.p7 | 3:121633158 | GATGGAGGAGTCCCA[A/C/G]CTGGAGGCCAGGCCT | 3059 |
rs140445778 | snp | C/T | 0.000247245 | 0.0111158 | missense | HCLS1 | GRCh38.p7 | 3:121634355 | TTCTCCTCTTCCTCT[C/T]GCTTCCTCTTCTCCT | 3059 |
rs140462442 | in-del | -/AGAT | 0.0185938 | 0.0946107 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641266 | AGTCTGACACAAGAG[-/AGAT]AGATGTCAGAGACGA | 3059 |
rs140529957 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650186 | AGATCTAAATAAATG[G/T]AGAGATATCCCATGT | 3059 |
rs140555971 | snp | A/G/T | 0.000115315 | 0.00759247 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642994 | TGACTACAGAGAAGA[A/G/T]GAGACAGAATTGGTT | 3059 |
rs140593710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656992 | CATGCCTTACTAAAG[A/G]AAGGGAGGCAGTTAA | 3059 |
rs140664841 | snp | A/C/G | 0.0103295 | 0.0711199 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650909 | TTGGGAGGTCAAGGC[A/C/G]GGTGGATCACAAGGT | 3059 |
rs140730999 | snp | C/T | 0 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647754 | AATGGTACCTATATT[C/T]TGATAACTGGAAAGT | 3059 |
rs140763344 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653787 | AGACATCCTATGGTT[A/G]TAGCTCAGTAAAGAT | 3059 |
rs141027261 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631279 | GTCTTTGACATCTAG[A/G]GTACAGGGGAATTGG | 3059 |
rs141075247 | snp | A/C | 0.00072465 | 0.019021 | missense | HCLS1 | GRCh38.p7 | 3:121632357 | AGAAGAAAAAGAAGA[A/C]TCTTCAGGCTCGAGC | 3059 |
rs141123695 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661458 | AAGGAGAGTTTCCTA[G/T]CTTGTTTGGGGCACT | 3059 |
rs141199732 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661832 | GGGGGAATTGGAGTC[A/T]TTCACTAAAAAATAG | 3059 |
rs141271409 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658735 | TCCCTAGAATTATGG[A/C]CTTATTTCACTCAGG | 3059 |
rs141320665 | snp | C/T | 1.84018e-05 | 0.00303324 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121633070 | GGGTTTGCTTACCTC[C/T]GGGAGAGTCTGCCTA | 3059 |
rs141353721 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652110 | GATAAATCTGGAAAA[C/T]ATTATGCTGAAAGAA | 3059 |
rs141396640 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648986 | AATGGGGCCAAAATT[C/T]ACTTTCAAATGGAAA | 3059 |
rs141510428 | in-del | -/GTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639542 | TTTTTGTTGTTGTTG[-/GTT]TTGTTGTTGTTGTTG | 3059 |
rs141551761 | snp | A/C/T | 8.23898e-05 | 0.00641786 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636423 | AAGACATTGGTGTTC[A/C/T]GGTGCTTTACCTTAT | 3059 |
rs141595315 | snp | A/T | 0.00379824 | 0.043413 | missense | HCLS1 | GRCh38.p7 | 3:121634263 | GCTCTTCCATAGCTA[A/T]CACTGGCTGTGGAGC | 3059 |
rs141597699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645071 | TGGTGCCAAGGAATA[C/T]GCGATGGGAGAGCAA | 3059 |
rs141768077 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659003 | GCTGGGAATAAGTCA[G/T]TTATTACTCAATTTT | 3059 |
rs142271721 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650964 | ACTATGGTGAAACCC[C/T]GTCTCTACCAAAAAT | 3059 |
rs142355953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638833 | TTACATCAGGAGTAT[A/G]TATGCTGGCATAAAC | 3059 |
rs142411170 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642397 | TGGCGTGAACCCAGG[A/T]CACAGAGCTTGCGGT | 3059 |
rs142437444 | snp | G/T | 0.000263609 | 0.0114776 | missense | HCLS1 | GRCh38.p7 | 3:121634305 | TCTTTGTCACAGCCT[G/T]TCGCTCCTGTTGCCT | 3059 |
rs142478875 | snp | C/T | 0.000691688 | 0.018584 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637232 | TTCTCCACCCCGTAC[C/T]GGCCACCAAAGCCAC | 3059 |
rs142545513 | snp | C/T | 0.000263591 | 0.0114772 | missense | HCLS1 | GRCh38.p7 | 3:121631950 | TGTCAGTGATTACGT[C/T]GTCCGGATCAAAGGA | 3059 |
rs142693789 | snp | G/T | 0.000153988 | 0.00877328 | missense | HCLS1 | GRCh38.p7 | 3:121631871 | AGCTTGACATAATTT[G/T]CAGGGAAGAGTCCAA | 3059 |
rs142712112 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636303 | TGGGGACTGCAGGAC[A/G]CCAGCAGGACAGGCT | 3059 |
rs142758913 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659350 | TGTGGTCACCACTGA[C/G]ACTTCTTGACCCTGG | 3059 |
rs142833657 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656589 | TTTGTTTGTTTGTTT[C/G]TGGTAAAATGCATAT | 3059 |
rs142849490 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655670 | TTCAGAAAAGGAAAA[C/G]GGTCTTGTGGTTTTT | 3059 |
rs142857431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650833 | TTGCTCTTAAAAAGA[C/T]GCCATTAATAAAATG | 3059 |
rs142955418 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660945 | CGTATTCAGGTTTTC[A/G]TCATTTCCTGCCACC | 3059 |
rs143095062 | in-del | -/TC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635210 | TTTCTTTTCTTTCTT[-/TC]TCTCTCTCTCTCTCT | 3059 |
rs143155499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662728 | CGAAAGAGTGAAACT[C/T]GGTCTCAAAAAAAAC | 3059 |
rs143297542 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640076 | CAGAAATGAAAATAG[A/G]CATTTCATATCACTA | 3059 |
rs143408084 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | HCLS1 | GRCh38.p7 | 3:121636446 | TACCTTATCCACTCG[C/G]TCCTTCTGGATTCCA | 3059 |
rs143728343 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659801 | CAGAAAACTGGAATG[C/G]AGAAGTTTCTGAAAT | 3059 |
rs143755492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648614 | CGCAGGACAACCAGA[C/T]ACATTGGTTATACGT | 3059 |
rs143784915 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656096 | TCAAGTGATCTTCCT[C/T]GCTCGGCCTTCCAAA | 3059 |
rs143992317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633365 | GGATTACAGGCACAC[A/G]CCACTATGCCTGGCT | 3059 |
rs144024377 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634862 | ATCTTGAACTCCTGG[A/G]TTCAAGTGATTATCC | 3059 |
rs144060043 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631003 | AGGCTAAGCGGGGGG[C/T]GATCATCTGAGGTCA | 3059 |
rs144192602 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661590 | ATCCTGTTTTACTGC[A/G]TGTCAAGACTTGCTG | 3059 |
rs144205157 | snp | A/G | 6.60208e-05 | 0.00574509 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121647442 | TTTGTTCCTCAGCTG[A/G]TGGATGCTGGAAGAA | 3059 |
rs144275149 | snp | A/G | 0.00032944 | 0.0128301 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637169 | GACTCGTGTTTCTCC[A/G]TCTCTCCCTTGTAGT | 3059 |
rs144499613 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645372 | TTGTTCTAGATCTTT[C/G]CTCCTGTATGGCCAT | 3059 |
rs144548256 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647254 | CCAAAGTGCTGGGAT[C/T]ACAGGCGTGAGCCAC | 3059 |
rs144589441 | snp | A/G | 0.000131785 | 0.00811635 | missense | HCLS1 | GRCh38.p7 | 3:121635752 | GCTTCTATGGGCGTC[A/G]TCTTCTTATAAGCTG | 3059 |
rs144663219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655328 | TAACAGGAAACAAAA[C/T]TAACATCACTGAGCT | 3059 |
rs144773022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659880 | TCCTGTGGCTCCTCT[A/G]AGGCCTCAGCCTGAC | 3059 |
rs144841158 | snp | C/T | 0.00478085 | 0.0486577 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631364 | TAAGATTTGAGGCCA[C/T]GAGGGCCACACAAAA | 3059 |
rs145046503 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121657299 | GTGTTCTGTGCGTCC[A/G]GACCCCTCGATGGTC | 3059 |
rs145136463 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652174 | GTTTGCATGAAATTC[A/T]ATGCCAGACAAAACT | 3059 |
rs145170176 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649022 | TGCAATTTTTTAATG[A/G]ATATAATAATTGTTA | 3059 |
rs145436824 | snp | C/T | 3.29511e-05 | 0.00405887 | missense | HCLS1 | GRCh38.p7 | 3:121631935 | CGTCCACCATCTCAA[C/T]GTCAGTGATTACGTC | 3059 |
rs145562548 | snp | A/G | 0.000461141 | 0.0151775 | missense | HCLS1 | GRCh38.p7 | 3:121634238 | TTGGGCAGTGGGGCC[A/G]GTACTGCTGGCTCTT | 3059 |
rs145703341 | in-del | -/AAC | 0.0298908 | 0.118541 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641595 | GGAACCAATATACTG[-/AAC]AACAACAATATGGTT | 3059 |
rs145735987 | snp | A/C | 4.94572e-05 | 0.00497254 | missense | HCLS1 | GRCh38.p7 | 3:121634363 | TTCCTCTCGCTTCCT[A/C]TTCTCCTCAGCCATG | 3059 |
rs145763698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648166 | CCTTCCCCCCAGGCT[G/T]ATAATACCTGAGAAA | 3059 |
rs145800601 | in-del | -/GGGGGGGGTG | | | frameshift-variant | HCLS1 | GRCh38.p7 | 3:121634271 | TAGCTATCACTGGCT[-/GGGGGGGGTG]GTGGAGCCTCAGGGC | 3059 |
rs145823873 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657859 | ACACAAAGAATTAAA[C/T]TAGTGAGCTCTGAAA | 3059 |
rs145890638 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653949 | GTTTAGAAACTTTTA[C/T]AGCAATTTGACATAG | 3059 |
rs145932746 | snp | C/T | 0.00118447 | 0.0243071 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644687 | GAGGTATCCCTGTGA[C/T]GGTGTCAGGTCCTCA | 3059 |
rs145951531 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639168 | TTTTAGGCAAAAACG[A/T]ATCAGTAAAATTATA | 3059 |
rs145987912 | snp | C/T | 0.000153988 | 0.00877328 | missense | HCLS1 | GRCh38.p7 | 3:121632556 | AGAGCTGGGGGCTCC[C/T]CATTGTCCTGAGAAG | 3059 |
rs146030198 | snp | C/T | 0.000362456 | 0.0134572 | missense | HCLS1 | GRCh38.p7 | 3:121631901 | AAGTGGCCATGGCAA[C/T]GTCCCCGCCACCAGC | 3059 |
rs146073274 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659518 | ATTCTCCAGTTTTCT[A/G]TTTCCACTTGAAAGC | 3059 |
rs146092130 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655880 | TTGAGACTGAGTCTC[A/G]CTCTATCACCCTGGC | 3059 |
rs146486774 | in-del | -/A | 0.0372196 | 0.131242 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639903 | AAGTAGAAGAAAAAC[-/A]TAATAAAGATAAGAG | 3059 |
rs146539124 | snp | A/G | 0.000181562 | 0.00952617 | missense | HCLS1 | GRCh38.p7 | 3:121647446 | TTCCTCAGCTGGTGG[A/G]TGCTGGAAGAAACCA | 3059 |
rs146596173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651761 | ATGTTGACAAAAATG[G/T]GGAGCATCTGAAACC | 3059 |
rs146614877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648810 | GTGCTGGAAGAACCC[C/T]CTGTTCCCATGCCTC | 3059 |
rs146857381 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656129 | TTTGGGATTACAAGC[A/G]TGAGCCACCACGCCC | 3059 |
rs146876634 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652515 | ACAAATTAGCTGGGC[A/G]AGGTGGCACATGCCT | 3059 |
rs146961422 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662397 | TAAACCACTTATTGT[A/T]CTTTGAGAAAGTGAG | 3059 |
rs146977752 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658799 | TACAAATTGGTTCTG[A/C]TTCTCACAAAGTGAA | 3059 |
rs147065779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632931 | GGACAGAGGAGTTTC[C/T]CAGAAGGCAAGGTCT | 3059 |
rs147125943 | snp | C/T | 1.65378e-05 | 0.00287552 | missense | HCLS1 | GRCh38.p7 | 3:121632125 | AATCATATACAGCCA[C/T]AGCTGAGATCCCCAG | 3059 |
rs147129061 | snp | A/G | 3.29533e-05 | 0.00405901 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637161 | CTCTCTGGGACTCGT[A/G]TTTCTCCGTCTCTCC | 3059 |
rs147187746 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650142 | TGCAAGACCTAAACA[C/G]TAAAAAATATTTCTG | 3059 |
rs147312346 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633477 | TCTGTCTGCCTTGAC[C/T]TCCCAAAGTGCTGGG | 3059 |
rs147417267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654416 | TTTTACAAAAGTATC[A/T]GTCTGTGACAGATTT | 3059 |
rs147418754 | in-del | -/ACTG | 0.00874735 | 0.0655527 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643773 | TGATTTACATGACAC[-/ACTG]ACTGGGTGATTCCAT | 3059 |
rs147433907 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650867 | AAGTGGCCAGGTGTG[C/G]TGGCTCACGCCTGTA | 3059 |
rs147577795 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639286 | TATAGAACATTGACC[-/A]AATAGACCATGTGCC | 3059 |
rs147587662 | snp | C/T | 0.00037621 | 0.01371 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121633145 | CTCAGACTCTGATGA[C/T]GGAGGAGTCCCAACT | 3059 |
rs147660624 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647634 | ACCATAGCCTGATTT[A/G]AACTCTCCATAGGCC | 3059 |
rs147676942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642135 | CGATCACGGAGAAAA[A/G]GAGAAGCAAGTGCAC | 3059 |
rs147706872 | snp | A/G | 0.000741027 | 0.0192345 | missense | HCLS1 | GRCh38.p7 | 3:121634239 | TGGGCAGTGGGGCCG[A/G]TACTGCTGGCTCTTC | 3059 |
rs147742489 | snp | A/C/G | 0.00184635 | 0.0303284 | missense | HCLS1 | GRCh38.p7 | 3:121632169 | GCCCCAGCCCCAGCC[A/C/G]GGCAGCCTGATGATC | 3059 |
rs147780745 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661692 | GGCGGAGGCCGTAAG[A/T]CCACTGCAAGCTTTG | 3059 |
rs147970530 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638745 | TGGCATGAATATGAG[A/C]TAAAGTGATCTCAAG | 3059 |
rs147989532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653417 | TTTCTGTGAAATCAG[G/T]ATGCCAACGTCATCT | 3059 |
rs148039922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658908 | CACCCTGAGTCTGGT[C/T]ACCTCACAGCTGTGT | 3059 |
rs148254045 | snp | C/G | 1.64751e-05 | 0.00287007 | missense | HCLS1 | GRCh38.p7 | 3:121658285 | GTCAGGATCTGTGTC[C/G]CAATCATCACCCTGG | 3059 |
rs148270026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662870 | TATGTGCCAGACAAG[A/G]GTTCTCCCAGGACCA | 3059 |
rs148342297 | snp | A/G | 0.00115254 | 0.0239779 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642912 | CTGAGGCTGAGTGAA[A/G]TACAGTGTCCTTGCC | 3059 |
rs148435056 | snp | A/G | 8.23784e-05 | 0.00641735 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121631948 | AATGTCAGTGATTAC[A/G]TCGTCCGGATCAAAG | 3059 |
rs148442474 | snp | C/G/T | 0.0123036 | 0.0774623 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645489 | AAATAATAAAGAGAA[C/G/T]TTGCAACATAGACAT | 3059 |
rs148511790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655339 | AAAACTAACATCACT[A/G]AGCTGCTCAGAAGTG | 3059 |
rs148564503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660119 | AGCTCTGTGACTAAG[C/T]CTCTGAGGGACCATC | 3059 |
rs148896911 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636199 | TACGACCTTTCCCGG[C/T]GGTTTACCTGTCTCT | 3059 |
rs148967407 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648312 | ACCAAAAAAGGCATT[A/G]TCTTTCTTACTTCAC | 3059 |
rs148997047 | snp | A/G | 3.29527e-05 | 0.00405898 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121644917 | GGCAACATACTCATG[A/G]CCCACTGCACTCTGA | 3059 |
rs149016931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653054 | CAGGTTTTGGAATAT[C/T]TGCATATACATAATG | 3059 |
rs149333073 | snp | C/T | 0.000280022 | 0.0118293 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121635751 | GGCTTCTATGGGCGT[C/T]GTCTTCTTATAAGCT | 3059 |
rs149387044 | snp | C/T | 6.59261e-05 | 0.00574097 | missense | HCLS1 | GRCh38.p7 | 3:121632455 | AGTCATTCTCAGGCT[C/T]GGGCTCAGGCTCGGG | 3059 |
rs149493736 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649916 | GTTTTTATTCACAGA[G/T]GACCTGATCATGTAT | 3059 |
rs149543747 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655210 | TATAGGAGTTGTGCA[A/G]TCCAACAGTCCAGGT | 3059 |
rs149669324 | snp | A/G | 0.00225475 | 0.0335006 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121631921 | CCGCCACCAGCCCTC[A/G]TCCACCATCTCAATG | 3059 |
rs149787965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648034 | AAATACTACCTTTCA[C/G]TAGTGTACTAGGAAG | 3059 |
rs150068129 | snp | C/T | 0.0014046 | 0.0264637 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657259 | CCCCCTTCCTTTTCT[C/T]CAGTCCTTTCGGCAC | 3059 |
rs150106978 | in-del | -/GC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655459 | TTATGAGGGTTGCTT[-/GC]TCTTTTTTTTTTTTT | 3059 |
rs150134739 | in-del | -/G | 0.0248432 | 0.108648 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641790 | GGGATTCAAAAACTT[-/G]GATCAATATGGCCAG | 3059 |
rs150241727 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637391 | GGCTTGAATACAGGG[A/G]AATTAAAGAGAAGCC | 3059 |
rs150255804 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647291 | CGGCTTGTATTTTTT[-/T]AAAGCAAATCTTTCC | 3059 |
rs150308839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649725 | GCCTAAGAAACTTTT[A/G]ACATATTAACTCTCA | 3059 |
rs150386736 | snp | C/G | 0.000527079 | 0.0162253 | missense | HCLS1 | GRCh38.p7 | 3:121658328 | ACAGACACATCATGG[C/G]CCACTACAGACTTCC | 3059 |
rs150470413 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643904 | AACACTGCATGCTCC[A/G]TATTTCACTATTGCC | 3059 |
rs150591193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659270 | GTGCAGAAGGAAGAG[C/T]GGCACAGTTGCTCTG | 3059 |
rs150627065 | in-del | -/GGCTCAGGCTCA | 0.36606 | 0.221428 | cds-indel | HCLS1 | GRCh38.p7 | 3:121632468 | TCGGGCTCAGGCTCG[-/GGCTCAGGCTCA]GGCTCAGGCTCAGGC | 3059 |
rs150713543 | snp | A/G | 0.000659543 | 0.0181476 | missense | HCLS1 | GRCh38.p7 | 3:121634391 | ATGGACTCAAATTTC[A/G]CCTTCAGCCCACGGG | 3059 |
rs150723074 | snp | A/G | 0.000679341 | 0.0184176 | missense | HCLS1 | GRCh38.p7 | 3:121633071 | GGTTTGCTTACCTCC[A/G]GGAGAGTCTGCCTAA | 3059 |
rs150763892 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640587 | AACCATAATGTCTTA[C/T]GGAAAATGAATCAGC | 3059 |
rs150795147 | in-del | -/T/TT | 0.043412 | 0.141194 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633221 | CTCCATCTTCACTCC[-/T/TT]CTTTTTTTTTTTTGA | 3059 |
rs151117586 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661238 | AAAGGAATTCAGAGC[A/G]TTTGGTATTGGGTGT | 3059 |
rs151221153 | snp | A/G | 0.0162398 | 0.0886349 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631731 | ATGAAGCAGGAGAGG[A/G]AAGTCTGTCCAGAAC | 3059 |
rs151238598 | snp | C/T | 0.00164747 | 0.0286535 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636386 | TCTCTGCACACTTTC[C/T]TAAACTTAGGGAACT | 3059 |
rs151256233 | snp | C/T | 3.29582e-05 | 0.00405931 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634327 | CTGTTGCCTCCTGGC[C/T]ACCTGCTGTGCCTTC | 3059 |
rs180785124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655497 | TTTTTTTGCCAATGC[C/T]TACTATATTGCAAGT | 3059 |
rs180873811 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638403 | ATAGGGATTAGGATC[A/G]AGGCTCTGTGATTCT | 3059 |
rs181062543 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646414 | ATATATTACATAGTA[A/T]TAATATGTAATATAA | 3059 |
rs181117138 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654503 | GCAAGAGTGGAGAAA[A/G]GAAGGTGGAGAGAAG | 3059 |
rs181117448 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637574 | CAGATACATGAAATG[A/T]ATGCCTTTCCCCTAC | 3059 |
rs181327300 | snp | A/C | | | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660908 | CACTTCGGAGTGAGA[A/C]ACTGAGCTGCTGCTT | 3059 |
rs181335738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650714 | ACAAAACATCAAAGA[A/G]AGTCTTCACAACTTT | 3059 |
rs181388068 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641053 | GAGGTATTATTCCAA[A/G]AGAAAATGCCTGAGA | 3059 |
rs181543689 | snp | A/G/T | 0.0001325 | 0.00813841 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632083 | TGTACCAGGCTCCTC[A/G/T]GGCCACTCCCAACCT | 3059 |
rs181548166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649927 | CAGATGACCTGATCA[C/T]GTATGTAGAAAATCC | 3059 |
rs181648363 | snp | C/G | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661782 | ACTGGGTCCCTGAGT[C/G]AGAAAGAACACAAGT | 3059 |
rs181708910 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642211 | ACACCTATAATCCCA[A/G]CACTTTGGGAGGCCG | 3059 |
rs181944314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641167 | GACACACCCTAATAA[C/T]AGTGAAGAATATCAG | 3059 |
rs182143575 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639427 | TTATCTAGAAAATTT[A/C]CCTGATGCTCAGAAA | 3059 |
rs182157071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657742 | TGAGGTAGGAGAATC[A/G]CTTGAACCTGGGAGG | 3059 |
rs182177699 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645358 | GAGAGCCAATGATTT[C/T]GTTCTAGATCTTTGC | 3059 |
rs182203880 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655948 | GTGCCTCCTGGGTTC[A/C]AGAGACTCTCGTGCT | 3059 |
rs182230946 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661514 | GATTTGGCTCTAGAG[C/T]GTAGGAAGAATTCTG | 3059 |
rs182443712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651135 | GCAATCAATCAATAA[A/G]TAATCAATCAATCAA | 3059 |
rs182472338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638784 | CATTCTAAGAGACAA[C/G]AAAGACATGCTCCAA | 3059 |
rs182612873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642691 | TGAGGTGGGAGGATC[A/G]CTTGAGCCCAGGAAG | 3059 |
rs182614765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662904 | ATGGACCTGCATCAA[C/T]TTCATGCCCTAAGGC | 3059 |
rs182731170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643546 | CTCTTTCATTACTCA[A/G]TAATGGAAACACAAA | 3059 |
rs182748596 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647148 | CACGACGCACGGCTA[A/G]TTTTTTGTATTTTTA | 3059 |
rs182970019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652095 | ATACACAACACCATG[G/T]ATAAATCTGGAAAAC | 3059 |
rs183020118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652514 | CACAAATTAGCTGGG[C/T]AAGGTGGCACATGCC | 3059 |
rs183196403 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648045 | TTCACTAGTGTACTA[C/G]GAAGTCATTAAATAT | 3059 |
rs183249857 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633906 | TCAAATGGAACTCAT[C/T]CCTCAAGATGGGCTC | 3059 |
rs183286566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634890 | TCCTACTTCAGCATC[C/G]CAAAGTGCTGGGATT | 3059 |
rs183343342 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634514 | AATCAGTTAAATATC[C/T]GGGAGGAGGGATTTG | 3059 |
rs183376046 | snp | C/G | 0.000234308 | 0.0108212 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647524 | CCAGAAAAATGGAAG[C/G]CTTGAAGTCTGTCCT | 3059 |
rs183588618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639093 | AAGTAGAAAGAGAAA[C/T]AGACAAATCTGTAAT | 3059 |
rs183680435 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641130 | GTCCCATATAGGATA[A/T]TAAAAGTAGATCTAA | 3059 |
rs183680872 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661014 | CTTCTGCTTTAGACA[C/G]TTAAATTTTAAAAGG | 3059 |
rs183802688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652988 | CTACAGGTTGACTAT[C/T]CCTCATCCCAAACGC | 3059 |
rs183823760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657109 | AAATGGAAATATGCA[A/G]TGACACACAGGTACA | 3059 |
rs184207164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645154 | GAATCCTTCATTCTG[A/T]ACACTCCCATAGGAT | 3059 |
rs184299934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648871 | AGATCTTGTGTTGTC[A/T]GTTCAACACCAACAC | 3059 |
rs184450846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645169 | AACACTCCCATAGGA[C/T]GGGCTGGGAACCAGG | 3059 |
rs184479854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644479 | ATGAGTATTTATAAG[A/G]TTTTGATGTTAAGCC | 3059 |
rs184707027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655179 | CTCCAGGCAGCACCC[A/G]TCAGAGTGATCTGTG | 3059 |
rs184715901 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640817 | GAGGGGAGGGGAGGG[C/G]AGGGGAGGGGAGGGG | 3059 |
rs184749405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649329 | TAATCTCCGCCTCCC[A/G]GGTTCAAGTGATTCT | 3059 |
rs184922984 | snp | A/C/T | 0.0162398 | 0.0886349 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637922 | GCCTGGGTGACAGAG[A/C/T]GAGACTCCATCTCAA | 3059 |
rs185045362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636150 | TAAGATTGGGTTAAG[C/T]AATGCCAAGAAATCA | 3059 |
rs185148835 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653747 | AAAATGTCAGGGCAC[A/G]AGAAGAGGACAGGGC | 3059 |
rs185386105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660042 | GGTGAGGCCTTGTTG[C/T]GATGCTGACCTCCTG | 3059 |
rs185429250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638735 | ATAAGAAAGATGGCA[A/T]GAATATGAGATAAAG | 3059 |
rs185437347 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655543 | TTGGGAAGTTTTCAA[C/T]TAGCAATAATCACAC | 3059 |
rs185446939 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646989 | TTATTTTATTTATTT[A/T]TTTTTTTTTTGAGAC | 3059 |
rs185584348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659221 | AACTTATTCTGCTGG[A/G]GCATTCCCAGTGTTC | 3059 |
rs185708457 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640328 | TATTTCCCTGGATGA[A/G]GTACTTACTAAACCC | 3059 |
rs185763548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645828 | TGGGTGTTTTAGCAA[A/C]ATTTTTAAATATACT | 3059 |
rs185893525 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650951 | GACCAGCCTAGCCAC[C/T]ATGGTGAAACCCCGT | 3059 |
rs185991843 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642263 | AGGAGATCGACACCA[C/T]CCTGGCTAACACAGT | 3059 |
rs186011811 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661942 | TTCTTGATTTGTTCA[A/C/T]AACGGTGCATCCTCC | 3059 |
rs186094297 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647155 | CACGGCTAATTTTTT[G/T]TATTTTTAGTAGAGA | 3059 |
rs186412205 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634086 | TCTAAAGACAGAGAC[A/C]ACAGACCTTGCCTAA | 3059 |
rs186428009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651304 | GAAAAAGATGTGAAC[A/C]GATACTTCATAAAGA | 3059 |
rs186477115 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642713 | CCCAGGAAGTCGAAG[A/C]TGCAGTGACCCATGA | 3059 |
rs186493505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635053 | ACCTCATCCGAAACT[C/T]CTGTCCCTGTGTGTT | 3059 |
rs186545048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638832 | CTTACATCAGGAGTA[C/T]GTATGCTGGCATAAA | 3059 |
rs186714713 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639689 | GAATAGCTGGGACCA[C/T]GGGTTTGTGATGAAT | 3059 |
rs186773294 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656384 | GCTTGTTACACTATT[G/T]ATTGTGTCTACCTTG | 3059 |
rs186890848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650195 | TAAATGGAGAGATAT[C/T]CCATGTTCATGGATT | 3059 |
rs186993766 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639254 | CCCCAAACTACAGAA[C/T]ATACTTTTTTCATGC | 3059 |
rs187074624 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632883 | ATTGTTGAGCTACCA[C/T]AGCTAGGATAATCAT | 3059 |
rs187156502 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661679 | GATACCACTTTCTGG[C/T]GGAGGCCGTAAGACC | 3059 |
rs187347411 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641327 | AAATAAAAATGAAGA[A/C]TGATGCAACATAAAG | 3059 |
rs187380708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647618 | TCAGTCTGGCCTGCA[C/T]ACCATAGCCTGATTT | 3059 |
rs187587938 | snp | A/C | 1.64738e-05 | 0.00286995 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644803 | GGGTGGTTGGGAGAG[A/C]GAGTGGTCACTTACC | 3059 |
rs187680983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653232 | CTGTATTTTGACTGA[A/G]ACCCATCACATGTAG | 3059 |
rs187724683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652856 | TTAGTTCATGGGAAT[C/T]TGCATTTCATTTCAA | 3059 |
rs187969134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657182 | TAGACATGAACTACC[C/T]TATCCTTTTCCTCCC | 3059 |
rs188165693 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648160 | TCTGCCCCTTCCCCC[C/G]AGGCTGATAATACCT | 3059 |
rs188225329 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640807 | GAGGGGAGGGGAGGG[C/G]AGGGGAGGGCAGGGG | 3059 |
rs188292578 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661403 | TCGACCAATTGAATG[C/T]CAGAAGAGAATAACT | 3059 |
rs188294503 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641141 | GATAATAAAAGTAGA[C/T]CTAACATTCAGACAC | 3059 |
rs188427961 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652291 | ATCTTGATTGCATTG[C/G]TGGTTATATTATATA | 3059 |
rs188594899 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640964 | AATACAGCTAAAGGA[A/C]GAATTAGTGAACTTA | 3059 |
rs188615481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660464 | TCCCTGAGACCATAT[G/T]CTCTTCAAGGGCAGA | 3059 |
rs188716744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634752 | TCCTCCTACCTCAGC[C/T]TCTGGAGTAGTTGGG | 3059 |
rs188838794 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638039 | TGTGTGAAGATAATT[A/C]TGAACTGACACCACA | 3059 |
rs188859050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655194 | GTCAGAGTGATCTGT[A/G]TATAGGAGTTGTGCA | 3059 |
rs188960129 | snp | C/T | 0.357664 | 0.225629 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646272 | AATAAAAATATATAA[C/T]ATATATTATATTTTA | 3059 |
rs189045749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643813 | CTTGTGAGCAAAAGA[C/T]GTAAGAATCGGTGAT | 3059 |
rs189212082 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659282 | GAGCGGCACAGTTGC[C/T]CTGCATCTGTGGATT | 3059 |
rs189234521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635357 | ATCTCAGCTCACTCC[G/T]ACTTCCGCCTCCTGG | 3059 |
rs189252068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649230 | AGTCATTCTAAACAG[A/G]TCTTTATTATTATTA | 3059 |
rs189494153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649917 | TTTTTATTCACAGAT[G/T]ACCTGATCATGTATG | 3059 |
rs189516687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632951 | AGGCAAGGTCTTCAG[C/T]GCTAACACCAGAACA | 3059 |
rs189755159 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645161 | TCATTCTGAACACTC[C/G]CATAGGATGGGCTGG | 3059 |
rs189787600 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650506 | AATAGAGTCCAGAAA[C/T]AGACCCACATGTATG | 3059 |
rs189869017 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633514 | GGCATGAGCCACCAC[G/T]CTCGGCCCATCTTCA | 3059 |
rs189964476 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642437 | TAGTGCCACTGCACT[C/G]TAGCCTGGGTGACAG | 3059 |
rs189983058 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661996 | GAAACTGGCCCATGA[C/T]ACAGGCACTTTTCTG | 3059 |
rs190080539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654004 | TTTTTAGAAATGGGG[A/T]CTCACTGTTGCCCAG | 3059 |
rs190206780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639258 | AAACTACAGAATATA[C/T]TTTTTTCATGCATAT | 3059 |
rs190215034 | snp | C/T | 6.6012e-05 | 0.00574471 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657360 | ATGTCATTCTGCAAA[C/T]GACAGCACGCAGTAA | 3059 |
rs190335024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637315 | AGCACACAGGGAAGC[A/G]CTGGAGAAGAGAGGT | 3059 |
rs190565336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645314 | GGGGACTGACCGGAC[A/G]CCATAGCCGGGATGG | 3059 |
rs190814060 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650965 | CTATGGTGAAACCCC[A/G]TCTCTACCAAAAATA | 3059 |
rs190885954 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655700 | TTTTTTTTTTTTTTT[G/T]ATCTATGAGTCTATA | 3059 |
rs190891735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638742 | AGATGGCATGAATAT[A/G]AGATAAAGTGATCTC | 3059 |
rs191005107 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642626 | TACAAAGAATAAAAA[A/T]TTAGCCAGGCATGGT | 3059 |
rs191078379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643504 | AGAGACATTACCCTA[C/T]TCCCAGTTGATAATG | 3059 |
rs191133665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651828 | CCTTTGGAAAAGAGT[C/T]TGAGAGTCTCTCAAA | 3059 |
rs191221886 | snp | C/T | 6.58913e-05 | 0.00573945 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634237 | CTTGGGCAGTGGGGC[C/T]GGTACTGCTGGCTCT | 3059 |
rs191253792 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652900 | GACATGACGATATTA[C/T]GTTTATTAGACAAAA | 3059 |
rs191371575 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647135 | TACAGGCACCCACCA[C/T]GACGCACGGCTAATT | 3059 |
rs191622358 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645069 | AGTGGTGCCAAGGAA[A/T]ACGCGATGGGAGAGC | 3059 |
rs191626789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656476 | ATCATCCGTGGAAGA[C/G]AGAAGGGGATCTCTC | 3059 |
rs191912449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638905 | AAAAATGTAAAAAAC[C/G]AGGTGTGGTGAATGC | 3059 |
rs192111436 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641970 | CTGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 3059 |
rs192118746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647625 | GGCCTGCATACCATA[A/G]CCTGATTTAAACTCT | 3059 |
rs192154116 | snp | A/C | 0.000529942 | 0.0162693 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647468 | AAGAAACCACATGAC[A/C]AAGGCTCATCTATCC | 3059 |
rs192307506 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121630985 | TCATCCCAGCACTTT[A/G]GGAGGCTAAGCGGGG | 3059 |
rs192316764 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649326 | CTGTAATCTCCGCCT[C/T]CCGGGTTCAAGTGAT | 3059 |
rs192393102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659182 | GCAGAAATATTTAGA[C/G]AACCCTAGCTTGGAA | 3059 |
rs192604388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634858 | CCTCATCTTGAACTC[C/T]TGGGTTCAAGTGATT | 3059 |
rs192634949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636149 | TTAAGATTGGGTTAA[A/G]CAATGCCAAGAAATC | 3059 |
rs192643161 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653351 | AGGGATGCTCAACCT[A/G]TATCTCTGTATCCTC | 3059 |
rs192702532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645167 | TGAACACTCCCATAG[A/G]ATGGGCTGGGAACCA | 3059 |
rs192768632 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648747 | TTCTCAGCTTTAGCC[A/G]CAGTTAATTTTAGAA | 3059 |
rs192853802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652416 | CCCAGCACTGTAGGA[A/G]GCCGAGGCAGGCGGA | 3059 |
rs192892129 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659352 | TGGTCACCACTGAGA[C/G]TTCTTGACCCTGGCA | 3059 |
rs193050001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639989 | AAAAGCTTGTTCTTT[A/G]GAAAGAGTAATAAAA | 3059 |
rs193090812 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640812 | GAGGGGAGGGGAGGG[C/G]AGGGCAGGGGAGGGG | 3059 |
rs193129501 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643966 | TTTAAACTTTCCTGA[G/T]TTTGTTTTTCATGGT | 3059 |
rs199530034 | snp | C/T | 0.000528926 | 0.0162537 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647462 | TGCTGGAAGAAACCA[C/T]ATGACCAAGGCTCAT | 3059 |
rs199584417 | snp | A/C | 0.00119737 | 0.0244387 | missense | HCLS1 | GRCh38.p7 | 3:121632145 | GAGATCCCCAGAGCC[A/C]CAGCCCCAGCCCCAG | 3059 |
rs199599138 | in-del | -/CACACG | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639020 | ACTCCAACACACACA[-/CACACG]CACACACACACACAC | 3059 |
rs199653719 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639477 | TAATACATGTGTCAA[A/G]GAAGAAATTACAAGG | 3059 |
rs199750662 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655687 | GTCTTGTGGTTTTTT[C/T]TTTTTTTTTTTTGAT | 3059 |
rs199784536 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646985 | TTATTTATTTTATTT[-/A]TTTTTTTTTTTTTTG | 3059 |
rs199890405 | snp | A/T | | | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632450 | CTCATAGTCATTCTC[A/T]GGCTCGGGCTCAGGC | 3059 |
rs199916491 | snp | A/C | 9.2626e-05 | 0.00680474 | splice-donor-variant | HCLS1 | GRCh38.p7 | 3:121633066 | TTGGGGGTTTGCTTA[A/C]CTCCGGGAGAGTCTG | 3059 |
rs199972787 | snp | A/C/G | 0.000807222 | 0.0200741 | missense | HCLS1 | GRCh38.p7 | 3:121647369 | CTCCATAGCCATGGG[A/C/G]TGCTTTGGGCCCTGA | 3059 |
rs200000017 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645452 | TGTATACAAAAAAAA[-/A]TCACTAAATACACAG | 3059 |
rs200112290 | snp | A/G | 0.00533698 | 0.051381 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657369 | TGCAAACGACAGCAC[A/G]CAGTAATACATGACG | 3059 |
rs200119312 | snp | C/T | 0.0178054 | 0.092659 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634276 | TATCACTGGCTGTGG[C/T]GCCTCAGGGCTCCTC | 3059 |
rs200143933 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643801 | TTCCATTTGTGGCTT[A/C]TGAGCAAAAGATGTA | 3059 |
rs200292060 | in-del | -/TG | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655699 | TTTTTTTTTTTTTTT[-/TG]ATCTATGAGTCTATA | 3059 |
rs200301832 | in-del | -/CG | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639021 | TCCAACACACACACA[-/CG]CACGCACACACACAC | 3059 |
rs200350490 | in-del | -/A | 0.162909 | 0.23434 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646416 | ATATTACATAGTAAT[-/A]ATATGTAATATAATG | 3059 |
rs200380365 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655867 | ATTTATTTATTTATT[G/T]AGACTGAGTCTCGCT | 3059 |
rs200528198 | snp | C/T | 9.88533e-05 | 0.00702971 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121631954 | AGTGATTACGTCGTC[C/T]GGATCAAAGGAAAGC | 3059 |
rs200567383 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639525 | TTAACTGAATGATTT[A/T]ATTTTTTGTTGTTGT | 3059 |
rs200686618 | in-del | -/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642799 | ACAAATGAACAAAAA[-/G]TAAATAAAATAGTGG | 3059 |
rs200688886 | in-del | -/ATA | 0.0248432 | 0.108648 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662764 | AAAACAAAACAAAAC[-/ATA]ATAATGCCTATCTAA | 3059 |
rs200768827 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647743 | TATTAGAGGACAATG[C/G]TACCTATATTCTGAT | 3059 |
rs200827424 | snp | A/G | 0.000692898 | 0.0186002 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657361 | TGTCATTCTGCAAAC[A/G]ACAGCACGCAGTAAT | 3059 |
rs200847413 | snp | A/C/G | 0.000297533 | 0.0121935 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632120 | TTGGTAATCATATAC[A/C/G]GCCACAGCTGAGATC | 3059 |
rs200851857 | snp | C/G | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631460 | CAGAAAGAAGGTTCA[C/G]ATATTTCTTCAGGGA | 3059 |
rs201049344 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646981 | TATTTATTTATTTTA[-/T]TTTATTTTTTTTTTT | 3059 |
rs201168614 | in-del | -/GA | 0.0944967 | 0.195752 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647107 | CTGCCTCAGCCTCCT[-/GA]GTAGCTGGGACTACA | 3059 |
rs201252242 | snp | A/G | 0.00060944 | 0.0174456 | missense | HCLS1 | GRCh38.p7 | 3:121631955 | GTGATTACGTCGTCC[A/G]GATCAAAGGAAAGCT | 3059 |
rs201263672 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652895 | TTACGGACATGACGA[C/T]ATTATGTTTATTAGA | 3059 |
rs201290743 | in-del | -/TCTC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635238 | CTCTTCTCTCCCTTT[-/TCTC]TCTCTCTCTCTCTCT | 3059 |
rs201300213 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659684 | CTTTCCCTGATGCGG[C/T]TGGAGACAGCAAAAC | 3059 |
rs201357234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635873 | GACCTGGAGGTAGTA[C/T]TGGGGGTTGGGGGCC | 3059 |
rs201382649 | snp | A/G | 1.66255e-05 | 0.00288314 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121632165 | CCCAGCCCCAGCCCC[A/G]GCCGGGCAGCCTGAT | 3059 |
rs201392507 | in-del | -/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655700 | TTTTTTTTTTTTTTT[-/G]ATCTATGAGTCTATA | 3059 |
rs201508325 | in-del | -/CG | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639024 | CAACACACACACACA[-/CG]CACACACACACACAC | 3059 |
rs201534688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657589 | AGGAGGCCGAGGCGG[A/G]TGGATCTCTTTAGGT | 3059 |
rs201700737 | in-del | -/T | 0.243633 | 0.249919 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650374 | AAAATCTTTTGTTTC[-/T]TTTTTTTTTTTTAAG | 3059 |
rs201726811 | in-del | -/TCTCTC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635238 | CTCTTCTCTCCCTTT[-/TCTCTC]TCTCTCTCTCTCTCT | 3059 |
rs201729356 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639029 | CACACACACACGCAC[A/G]CACACACACACACAC | 3059 |
rs201757606 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639526 | TAACTGAATGATTTT[A/T]TTTTTTGTTGTTGTT | 3059 |
rs201978006 | snp | C/T | 3.29576e-05 | 0.00405928 | missense | HCLS1 | GRCh38.p7 | 3:121657307 | TGCGTCCAGACCCCT[C/T]GATGGTCTTGGCTCC | 3059 |
rs202020296 | snp | C/T | 0.00268209 | 0.0365219 | missense | HCLS1 | GRCh38.p7 | 3:121635795 | CCATTTCATTGAAGC[C/T]GACAGCGCTCTGCAG | 3059 |
rs202153247 | in-del | -/T | 0.15879 | 0.232768 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633222 | CTCCATCTTCACTCC[-/T]TTTTTTTTTTTGAGA | 3059 |
rs202153876 | in-del | -/TTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639526 | AACTGAATGATTTTA[-/TTT]TTTTTTGTTGTTGTT | 3059 |
rs202175021 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | HCLS1 | GRCh38.p7 | 3:121631953 | CAGTGATTACGTCGT[C/T]CGGATCAAAGGAAAG | 3059 |
rs202222919 | in-del | -/TGTT | 0.030665 | 0.119967 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649845 | TCATTCCTCAATCTG[-/TGTT]TGTTTTTTATTACAA | 3059 |
rs267599567 | snp | C/T | 8.23635e-05 | 0.00641677 | HCLS1 | 3 | allele_origin=T(somatic)/C(germline) | 3:121632423 | CTCATGCCTGTCCAT[C/T]TCCTCAACGTCCTCA | 3059 |
rs267599568 | snp | A/C/T | 3.29876e-05 | 0.00406115 | HCLS1 | 3 | allele_origin=T(germline)/C(somatic) | 3:121647424 | ATCATGCTCCTCTGA[A/C/T]ACTTTGTTCCTCAGC | 3059 |
rs367573404 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660489 | GGCAGACACTGTTTT[C/T]GTCTCCTGTGGTCCT | 3059 |
rs367590458 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641670 | ACTCAGGAAGAGATT[G/T]TGATTAATTTTAAAT | 3059 |
rs367896416 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | HCLS1 | GRCh38.p7 | 3:121632431 | TGTCCATCTCCTCAA[C/T]GTCCTCATAGTCATT | 3059 |
rs367959517 | in-del | -/AA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650249 | GTCAGTTCTCCCTAA[-/AA]TGATCTATAGATTCA | 3059 |
rs367979047 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660023 | GAGAACCAGAGAGTA[A/G]TCTGGTGAGGCCTTG | 3059 |
rs368121558 | in-del | -/CACA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639026 | ACACACACACACACG[-/CACA]CACACACACACACAC | 3059 |
rs368236790 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | HCLS1 | GRCh38.p7 | 3:121632368 | AAGAATCTTCAGGCT[C/T]GAGCACCTCCTCATA | 3059 |
rs368261834 | snp | A/G | 0.000247078 | 0.0111121 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121644884 | AGCATCCGTCTGAGA[A/G]GAGTGCTTCTCCACC | 3059 |
rs368270663 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632003 | GAGAAAGTTGAGGGG[A/G]TATTAGAATGGTCAG | 3059 |
rs368298643 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651385 | GGTCATCAGAGAAAT[A/T]CAAATTAACTTAAAA | 3059 |
rs368300982 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655636 | CAATTCCCAGAATAC[C/T]AGCGTTGAGTGGCCT | 3059 |
rs368357196 | snp | C/G/T | 0.000116146 | 0.00761975 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657234 | AGTTTTCTTTGGGCT[C/G/T]TTCCCATAACCCCCT | 3059 |
rs368506277 | snp | A/C | | | missense | HCLS1 | GRCh38.p7 | 3:121632137 | CCACAGCTGAGATCC[A/C]CAGAGCCACAGCCCC | 3059 |
rs368538744 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645278 | AGAGTGTAGTGTGGG[A/G]TAGTGTGGAGGAGAG | 3059 |
rs368592702 | snp | A/G | 1.65173e-05 | 0.00287374 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631832 | TCACAGTTGCAGTAG[A/G]CAGTGAGCTCTAGTC | 3059 |
rs368633246 | in-del | -/A/AA | 0.474363 | 0.110278 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642303 | CTCTACTAAAAATAC[-/A/AA]AAAAAAAAAAAAAAA | 3059 |
rs368720242 | snp | G/T | 0.000153988 | 0.00877328 | missense | HCLS1 | GRCh38.p7 | 3:121647432 | CCTCTGATACTTTGT[G/T]CCTCAGCTGGTGGAT | 3059 |
rs368774232 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644944 | CTGAGAAAAATCAAG[C/G]ATGGAGTGAGTGAAA | 3059 |
rs368834635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633279 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCATTGC | 3059 |
rs368885768 | snp | C/G | 8.23798e-05 | 0.00641741 | missense | HCLS1 | GRCh38.p7 | 3:121635794 | TCCATTTCATTGAAG[C/G]CGACAGCGCTCTGCA | 3059 |
rs368893881 | snp | A/C/G | 9.88609e-05 | 0.0070301 | intron-variant, missense, synonymous-codon | HCLS1 | GRCh38.p7 | 3:121637159 | ACCTCTCTGGGACTC[A/C/G]TGTTTCTCCGTCTCT | 3059 |
rs369094417 | snp | A/G | 8.23771e-05 | 0.0064173 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642880 | AGTCTTAGCAGAAGA[A/G]CCTGCCGGTCAGATT | 3059 |
rs369219547 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651846 | AGAGTCTCTCAAAAT[G/T]TTTAACATACACTTA | 3059 |
rs369323617 | snp | A/G | 0.000164861 | 0.00907764 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658247 | CACTGTCCAAGCAAA[A/G]CTACTTCCAAACTCA | 3059 |
rs369453761 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645809 | GATCTAGAACAAAAG[C/T]ATCTGGGTGTTTTAG | 3059 |
rs369488633 | snp | C/T | | | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660852 | TCTGTTCTAAGCGCC[C/T]GGCTCCTCGCGTCCA | 3059 |
rs369492582 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634196 | TGGATCCCAGAGGGC[C/T]AGGCGCTCACCTCTG | 3059 |
rs369513627 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121634351 | TGCCTTCTCCTCTTC[C/T]TCTCGCTTCCTCTTC | 3059 |
rs369551744 | snp | C/T | 5.04953e-05 | 0.00502445 | missense | HCLS1 | GRCh38.p7 | 3:121632557 | GAGCTGGGGGCTCCT[C/T]ATTGTCCTGAGAAGA | 3059 |
rs369652294 | in-del | -/TACC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655633 | GGACAATTCCCAGAA[-/TACC]AGCGTTGAGTGGCCT | 3059 |
rs369726540 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662507 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACAAGG | 3059 |
rs369880530 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646392 | TATGTAATATATTAC[-/A]TATGTAATATATTAC | 3059 |
rs369909604 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653034 | TTTTGGATTCAGGAT[G/T]TTTTCAGGTTTTGGA | 3059 |
rs369933696 | in-del | -/CTCTC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635271 | TCTCTCTCTCTCTCT[-/CTCTC]CTCTCTCTCCTCTCT | 3059 |
rs369963309 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657586 | TTTAGGAGGCCGAGG[C/T]GGGTGGATCTCTTTA | 3059 |
rs369984427 | snp | A/C/G | 3.29723e-05 | 0.00406018 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635691 | AGAAAAAGAATGAGG[A/C/G]AGAAGGAAGTGAGGT | 3059 |
rs370169975 | snp | C/T | 8.23784e-05 | 0.00641735 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121631924 | CCACCAGCCCTCGTC[C/T]ACCATCTCAATGTCA | 3059 |
rs370193754 | snp | A/G | 0.000280059 | 0.0118301 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643027 | AGTCAGAGCTGACAG[A/G]TTTTCCTCTTCCTAA | 3059 |
rs370295803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654032 | CAGGCTGGAGTACAG[A/T]GGCTACTCACAGACA | 3059 |
rs370406484 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | HCLS1 | GRCh38.p7 | 3:121632364 | AAAGAAGAATCTTCA[C/G]GCTCGAGCACCTCCT | 3059 |
rs370417463 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121638487 | TCCACTCCTATAAGA[C/G]AGTGCTAGAAAAATT | 3059 |
rs370437286 | snp | A/G | 6.59022e-05 | 0.00573993 | missense | HCLS1 | GRCh38.p7 | 3:121632347 | CAGCCAGAGCAGAAG[A/G]AAAAGAAGAATCTTC | 3059 |
rs370446441 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646157 | ATATAAGTATATATA[A/T]AATATATCTTATAAT | 3059 |
rs370499173 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648143 | GTCATGAATTAAGAT[A/C]TTCTGCCCCTTCCCC | 3059 |
rs370544185 | snp | A/G | 8.32438e-05 | 0.00645097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647277 | TGAGCCACCGCACCC[A/G]GCTTGTATTTTTTTA | 3059 |
rs370553020 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653754 | CAGGGCACGAGAAGA[A/G]GACAGGGCCACTGAG | 3059 |
rs370618550 | snp | A/C | 0.00175047 | 0.0295325 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657217 | CTTCCCCCAAGTCTC[A/C]GAGTTTTCTTTGGGC | 3059 |
rs370624675 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646352 | TTATAGTATATAATA[A/T]ATTACATTATATTAC | 3059 |
rs370678684 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636365 | TCCCAGCCTTCTTCA[C/T]GCTCTTCTCTGCACA | 3059 |
rs370731062 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639970 | AGAGAAAATTAGCAA[A/G]GCCAAAAGCTTGTTC | 3059 |
rs370839716 | snp | A/G | 0.000181328 | 0.00952004 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658360 | CATCTGAGAGTGACC[A/G]GAGATGGGAATAATT | 3059 |
rs370856378 | snp | A/G | 0.000280064 | 0.0118302 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121635796 | CATTTCATTGAAGCC[A/G]ACAGCGCTCTGCAGG | 3059 |
rs370934839 | snp | A/G | | | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631568 | CCAGAGCTCACAGAG[A/G]AGGAGAGCAGAGCTT | 3059 |
rs370943100 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649225 | GTGGAAGTCATTCTA[A/G]ACAGGTCTTTATTAT | 3059 |
rs370995398 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | HCLS1 | GRCh38.p7 | 3:121636442 | GCTTTACCTTATCCA[C/T]TCGGTCCTTCTGGAT | 3059 |
rs371041353 | snp | C/T | 1.65509e-05 | 0.00287666 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632055 | TCCCCCTGTCTTATA[C/T]CAGGGGCCTCCATGT | 3059 |
rs371050025 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646987 | ATTTATTTTATTTAT[A/T]TTTTTTTTTTTTGAG | 3059 |
rs371393467 | snp | C/T | 0.000397338 | 0.0140894 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632096 | TCGGGCCACTCCCAA[C/T]CTACCTCCTTGGTAA | 3059 |
rs371546371 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121632891 | GCTACCACAGCTAGG[A/C]TAATCATCTATACTA | 3059 |
rs371555603 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639289 | AGAACATTGACCAAA[C/T]AGACCATGTGCCAGT | 3059 |
rs371572740 | snp | A/C/T | 8.23885e-05 | 0.00641781 | missense | HCLS1 | GRCh38.p7 | 3:121634307 | TTTGTCACAGCCTTT[A/C/T]GCTCCTGTTGCCTCC | 3059 |
rs371577841 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121647409 | TTTCTTCCTGAGAAC[A/G]TCATGCTCCTCTGAT | 3059 |
rs371660641 | in-del | -/ATGAGGGTTGCTTGCTC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655446 | TTATTTCATTTTTTT[-/ATGAGGGTTGCTTGCTC]TTTTTTTTTTTTTTT | 3059 |
rs371726106 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654845 | CTCCTTTCCAAGGAC[C/G]ATGGTGATTCCCATC | 3059 |
rs371735546 | in-del | -/CAA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641603 | TATACTGAACAACAA[-/CAA]TATGGTTGGTTAAAA | 3059 |
rs371758156 | snp | A/G | 4.94279e-05 | 0.00497107 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637248 | GGCCACCAAAGCCAC[A/G]AGAGTAATCTGTGGT | 3059 |
rs371805159 | snp | A/G | 3.87274e-05 | 0.00440025 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121633118 | TGGGTGTTCCCTGCT[A/G]GTTCTCACAGGCTCA | 3059 |
rs371935774 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637290 | TCATGAGAGCCCACC[A/C]TTAGGCTCCAGCACA | 3059 |
rs372001545 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651974 | TTGTAATAGATCCAA[A/G]TTGTCAATAATCCAA | 3059 |
rs372065267 | in-del | -/ATA | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646362 | AATATATTACATTAT[-/ATA]ATTACATATTATTAC | 3059 |
rs372080261 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647013 | TTGAGACAGAGTCTC[A/G]CTCTGTCTCCCAGGC | 3059 |
rs372081397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635364 | CTCACTCCGACTTCC[A/G]CCTCCTGGGTTCAAG | 3059 |
rs372129934 | snp | A/G | 8.25198e-05 | 0.00642286 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631837 | GTTGCAGTAGACAGT[A/G]AGCTCTAGTCACTCC | 3059 |
rs372191150 | snp | C/G/T | 9.88381e-05 | 0.00702929 | intron-variant, missense | HCLS1 | GRCh38.p7 | 3:121637224 | ATTTATCCTTCTCCA[C/G/T]CCCGTACCGGCCACC | 3059 |
rs372219717 | in-del | -/CAAT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121651152 | AATCAATCAATCAAT[-/CAAT]AAAGTGAAAAAGCAA | 3059 |
rs372238865 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659414 | AGACACCTCATCCCA[C/T]TGGAGACCTTCCCCA | 3059 |
rs372267588 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641287 | CAGAGACGATGAAAT[-/T]AAGATCTTCAAAGTG | 3059 |
rs372312755 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660826 | AGTACCCACCTCCAC[A/C]TGTGCAAGCCTCTGT | 3059 |
rs372470597 | in-del | -/AAT | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662769 | AAAACAAAACATAAT[-/AAT]GCCTATCTAACCTGC | 3059 |
rs372518070 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661269 | ATTCATCAAGAAAGG[C/T]TTTATGGGAAAAGTG | 3059 |
rs372553631 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647078 | GCTCTGCCTCCCAGG[C/T]TCACGCCATTCTCCT | 3059 |
rs372720825 | in-del | -/A/AGGCTCAGGCTC/G | 0.000131791 | 0.00811673 | frameshift-variant, cds-indel | HCLS1 | GRCh38.p7 | 3:121632485 | CTCAGGCTCAGGCTC[-/A/AGGCTCAGGCTC/G]TGCTTCGTACACTGG | 3059 |
rs372783966 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646158 | TATAAGTATATATAT[A/T]ATATATCTTATAATT | 3059 |
rs372788622 | snp | A/G | 7.94407e-05 | 0.00630191 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633039 | AGAAGATGGGGTGGG[A/G]GCAGAGAATCTTTGG | 3059 |
rs372790259 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649964 | ATTCACACAAAAAAA[G/T]CTACTAAAGCATTGT | 3059 |
rs372797954 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | HCLS1 | GRCh38.p7 | 3:121658291 | ATCTGTGTCCCAATC[A/C]TCACCCTGGGTCTCC | 3059 |
rs372909816 | snp | C/T | 1.65677e-05 | 0.00287812 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657246 | GCTCTTCCCATAACC[C/T]CCTTCCTTTTCTCCA | 3059 |
rs373015540 | snp | A/C/G | 6.59408e-05 | 0.00574168 | missense, stop-gained | HCLS1 | GRCh38.p7 | 3:121634356 | TCTCCTCTTCCTCTC[A/C/G]CTTCCTCTTCTCCTC | 3059 |
rs373038271 | snp | C/G/T | 3.35306e-05 | 0.00409441 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647270 | ACAGGCGTGAGCCAC[C/G/T]GCACCCGGCTTGTAT | 3059 |
rs373082154 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653638 | CCTCAGCATCATAAG[C/T]CTTTTTACAGCAGAG | 3059 |
rs373119014 | snp | A/G | 9.88403e-05 | 0.00702925 | missense | HCLS1 | GRCh38.p7 | 3:121635749 | CCGGCTTCTATGGGC[A/G]TCGTCTTCTTATAAG | 3059 |
rs373331701 | snp | C/T | | | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631016 | GGCGATCATCTGAGG[C/T]CAGGAGTTCAAGATC | 3059 |
rs373336851 | snp | C/T | 0.00039697 | 0.0140829 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657383 | CGCAGTAATACATGA[C/T]GGCAAGAAATGTGCC | 3059 |
rs373343888 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637596 | TTCCCCTACTCCCAT[A/T]TAAGCACATAGAAAT | 3059 |
rs373397783 | snp | A/G | 4.94882e-05 | 0.0049741 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634158 | ACCCCTTAGGCTCCT[A/G]TCTGGGCAAGAGATC | 3059 |
rs373440778 | snp | A/G/T | 0.0123036 | 0.0774623 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633504 | TGGGATTACAGGCAT[A/G/T]AGCCACCACGCTCGG | 3059 |
rs373472447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638815 | TGATAAAAGAACAAT[A/G]CCTTACATCAGGAGT | 3059 |
rs373474739 | snp | A/G | 0.000263587 | 0.0114771 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121631951 | GTCAGTGATTACGTC[A/G]TCCGGATCAAAGGAA | 3059 |
rs373588841 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634161 | CCTTAGGCTCCTGTC[A/T]GGGCAAGAGATCCTG | 3059 |
rs373654542 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650902 | CAGCACTTTGGGAGG[C/T]CAAGGCGGGTGGATC | 3059 |
rs373752878 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648627 | GACACATTGGTTATA[C/T]GTAGAATGGCTGTCT | 3059 |
rs373818113 | in-del | -/TTG | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639530 | GAATGATTTTATTTT[-/TTG]TTGTTGTTGTTGTTG | 3059 |
rs374104805 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640446 | AATAACCATGAGGAA[C/T]GCAGATTAGTCAGAA | 3059 |
rs374110570 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659876 | TCCTTCCTGTGGCTC[C/T]TCTGAGGCCTCAGCC | 3059 |
rs374119909 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640090 | GGCATTTCATATCAC[C/T]AGAAATCTTACAGAA | 3059 |
rs374263565 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646359 | ATATAATATATTACA[G/T]TATATTACATATTAT | 3059 |
rs374286282 | snp | A/G | 0.000153988 | 0.00877328 | missense | HCLS1 | GRCh38.p7 | 3:121631880 | TAATTTGCAGGGAAG[A/G]GTCCAAAGTGGCCAT | 3059 |
rs374314261 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646395 | TGTAATATATTACTA[-/T]GTAATATATTACATA | 3059 |
rs374456259 | snp | C/G | 1.65611e-05 | 0.00287755 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632079 | TCCATGTACCAGGCT[C/G]CTCGGGCCACTCCCA | 3059 |
rs374503954 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645240 | ACAAAAAGAGCTGAA[A/T]CAAGAGCATTGTGCA | 3059 |
rs374566386 | snp | C/T | 6.59783e-05 | 0.00574324 | missense | HCLS1 | GRCh38.p7 | 3:121647426 | CATGCTCCTCTGATA[C/T]TTTGTTCCTCAGCTG | 3059 |
rs374599371 | snp | G/T | 0.000153988 | 0.00877328 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631813 | CCACTTTGGACATGG[G/T]AAATCACAGTTGCAG | 3059 |
rs374775044 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660442 | ACATTTCCTGTGTGG[A/G]TTTGTTTCCCTGAGA | 3059 |
rs374973259 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648002 | GACCAATGGTTGGAT[A/T]ATAGTTAAATAAATT | 3059 |
rs374974934 | snp | C/G/T | 1.64803e-05 | 0.00287052 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637264 | AGAGTAATCTGTGGT[C/G/T]GAAGGAGCAGTCATG | 3059 |
rs374989824 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636234 | ATGCCTCTCCCACTG[A/T]CCTCAAAGCTCAGGC | 3059 |
rs375072179 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637363 | GAGTGTTAGGGGCCT[C/G]GGAAAAGAGCAGGGC | 3059 |
rs375238578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632049 | CACATGTCCCCCTGT[A/C]TTATATCAGGGGCCT | 3059 |
rs375257082 | snp | A/G | 0.000807402 | 0.0200761 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635815 | GCGCTCTGCAGGCAG[A/G]AGAACAGCATGTGTG | 3059 |
rs375272596 | snp | A/C | 1.64811e-05 | 0.00287059 | missense | HCLS1 | GRCh38.p7 | 3:121634338 | TGGCCACCTGCTGTG[A/C]CTTCTCCTCTTCCTC | 3059 |
rs375453462 | snp | C/T | 4.94189e-05 | 0.00497062 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642985 | GCCGACTGCTGACTA[C/T]AGAGAAGAGGAGACA | 3059 |
rs375463846 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121655521 | TGCAAGTCGTCATGG[C/T]GGAGTGTTGGGAAGT | 3059 |
rs375467328 | snp | C/T | 3.31263e-05 | 0.00406965 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637122 | GTGCTATCTGTGACC[C/T]TCCCCCTTCCAACCC | 3059 |
rs375508297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657013 | AGGCAGTTAATCCAA[C/T]AGACCCACTTGGGGA | 3059 |
rs375575405 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657880 | AGCTCTGAAACCTCC[A/G]TTCCTCCTCTGCCTA | 3059 |
rs375578562 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646992 | TTTTATTTATTTTTT[A/T]TTTTTTTGAGACAGA | 3059 |
rs375796675 | snp | C/G | 3.29489e-05 | 0.00405874 | missense | HCLS1 | GRCh38.p7 | 3:121632365 | AAGAAGAATCTTCAG[C/G]CTCGAGCACCTCCTC | 3059 |
rs375804712 | snp | G/T | 8.44174e-05 | 0.00649627 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632211 | GAAACACAAACATGG[G/T]ATCATCAACATGAAG | 3059 |
rs375905525 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641433 | AATAGAAGACACAAA[A/G]GTGAAACAATGAAAT | 3059 |
rs375913343 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650148 | ACCTAAACACTAAAA[A/C]ATATTTCTGAAAATA | 3059 |
rs375941647 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653860 | TATTCCAGAGCAGTG[C/T]CACTCAGTGTGTGGT | 3059 |
rs375950186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637072 | TATTCTGGGGCACCC[A/G]GGTGAGCTTCCAGAA | 3059 |
rs375971571 | snp | A/G | 9.88468e-05 | 0.00702948 | synonymous-codon | HCLS1 | GRCh38.p7 | 3:121644902 | GTGCTTCTCCACCTC[A/G]GCAACATACTCATGG | 3059 |
rs375975877 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646166 | TATATATAATATATC[A/T]TATAATTAATATATA | 3059 |
rs376015693 | in-del | -/AC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646366 | ATATTACATTATATT[-/AC]ATATTATTACTATGT | 3059 |
rs376067908 | snp | C/T | | | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631084 | AATACAAAAATTAGC[C/T]GGGCATGGTGGTGCA | 3059 |
rs376081921 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639108 | TAGACAAATCTGTAA[A/T]AGTAGTTGAACATTT | 3059 |
rs376083217 | snp | A/C/G | 3.29588e-05 | 0.00405938 | missense | HCLS1 | GRCh38.p7 | 3:121632452 | CATAGTCATTCTCAG[A/C/G]CTCGGGCTCAGGCTC | 3059 |
rs376116048 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121645007 | ATATGGAGTGGGATG[A/T]AGGCATGTAAGAAAT | 3059 |
rs376225701 | in-del | -/TCTCT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121635262 | CTCTCTCTCTCTCTC[-/TCTCT]CTCTCTCTCCTCTCT | 3059 |
rs376237878 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121647282 | CACCGCACCCGGCTT[A/G]TATTTTTTTAAAGCA | 3059 |
rs376238054 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651834 | GAAAAGAGTTTGAGA[A/G]TCTCTCAAAATGTTT | 3059 |
rs376245237 | snp | A/C | 1.65562e-05 | 0.00287712 | missense | HCLS1 | GRCh38.p7 | 3:121632103 | ACTCCCAACCTACCT[A/C]CTTGGTAATCATATA | 3059 |
rs376300042 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661687 | TTTCTGGCGGAGGCC[A/G]TAAGACCACTGCAAG | 3059 |
rs376377325 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646901 | AGAGGTATATAATTA[C/T]ATATAAGTATATAAT | 3059 |
rs376424833 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633597 | CCTGGCTGGAGCACA[A/G]TGAGATCATAGCTCA | 3059 |
rs376456839 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648109 | ATGTAAACATTAGTG[G/T]TATTTTTTATGCTTT | 3059 |
rs376657206 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658841 | CTCTTTACAACCTGC[-/T]GAACTACACTGAGAA | 3059 |
rs376669270 | in-del | -/GTTT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649850 | CCTCAATCTGTGTTT[-/GTTT]TTTATTACAAAACTA | 3059 |
rs376707994 | snp | G/T | 0.000362689 | 0.0134615 | missense | HCLS1 | GRCh38.p7 | 3:121647405 | TCTCTTTCTTCCTGA[G/T]AACATCATGCTCCTC | 3059 |
rs376722959 | snp | C/G | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661372 | TGGAGTTTTCATATA[C/G]ATGTTCAAATAAACG | 3059 |
rs376854611 | in-del | -/TT | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653177 | TAAATGAAGGTAACT[-/TT]ATTTTTCCCTTGGGG | 3059 |
rs376907022 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659271 | TGCAGAAGGAAGAGC[A/G]GCACAGTTGCTCTGC | 3059 |
rs376913911 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642394 | GAATGGCGTGAACCC[A/G]GGACACAGAGCTTGC | 3059 |
rs376931694 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121643965 | TTTTAAACTTTCCTG[A/G]TTTTGTTTTTCATGG | 3059 |
rs376961306 | in-del | -/AATAT | 0.17461 | 0.238362 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646689 | ATATATAATATATAA[-/AATAT]AATATACATTATATT | 3059 |
rs377000996 | snp | A/C/G | 1.64762e-05 | 0.00287016 | missense | HCLS1 | GRCh38.p7 | 3:121631916 | CGTCCCCGCCACCAG[A/C/G]CCTCGTCCACCATCT | 3059 |
rs377029672 | snp | A/G | 0.000101568 | 0.00712555 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634464 | GTCTTGGATTGGAGA[A/G]TGGGGAAGGGCATGG | 3059 |
rs377068706 | snp | A/G | 0.000281199 | 0.0118541 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657384 | GCAGTAATACATGAC[A/G]GCAAGAAATGTGCCA | 3059 |
rs377321539 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648913 | CTACTAGTACCAAGG[A/C]CATGTAAATGCCTGC | 3059 |
rs377344402 | snp | C/T | 1.64871e-05 | 0.00287111 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634186 | ATCCTGGATGTGGAT[C/T]CCAGAGGGCCAGGCG | 3059 |
rs377408617 | snp | C/G | 1.64833e-05 | 0.00287078 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658356 | TCCACATCTGAGAGT[C/G]ACCGGAGATGGGAAT | 3059 |
rs377411573 | snp | A/C | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634623 | TTATAAAGCCAGGCT[A/C]TACGACCTAAGACTC | 3059 |
rs377471422 | in-del | -/A | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121646387 | ATTACTATGTAATAT[-/A]ATTACTATGTAATAT | 3059 |
rs377475481 | in-del | -/ATTT/ATTTATTT | 0.481087 | 0.0953875 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655823 | TACTTAATTGAAACC[-/ATTT/ATTTATTT]ATTTATTTATTTATT | 3059 |
rs377507551 | snp | A/G | 0.000516129 | 0.0160561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634433 | GCTGCAGACACAGGC[A/G]AGAAAAATTAGGGTT | 3059 |
rs377542775 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638240 | CTAATTTAAAAAAAA[A/T]TCTGTAGTGATAGGA | 3059 |
rs377546522 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121658036 | CTGCCATGGCCTGTC[A/G]ATCACACTGTCAAAC | 3059 |
rs377644536 | snp | G/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662090 | TTTATTCCTTCTACT[G/T]TATTACCTATTTATC | 3059 |
rs377752378 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642782 | CCCTGTCTCAAAAAC[A/T]AACAAATGAACAAAA | 3059 |
rs377759752 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633188 | TGTGGAAAATGAAGC[A/G]TCTCTCAAGTAAGCA | 3059 |
rs386665209 | multinucleotide-polymorphism | CT/TC | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639849 | TTATCTAAGTTTCTA[CT/TC]TTAAGAGGCTAGGAA | 3059 |
rs397876429 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639525 | TTAACTGAATGATTT[-/T]ATTTTTTGTTGTTGT | 3059 |
rs397957356 | in-del | -/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633233 | TCCTTTTTTTTTTTT[-/T]GAGATAGACTCTCGC | 3059 |
rs398052237 | in-del | -/AC/CG | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639023 | CCAACACACACACAC[-/AC/CG]GCACACACACACACA | 3059 |
rs398052596 | in-del | AAAAAAAT/CAAAAAATA | 0.5 | 0 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639525 | CAACAACAACAACAA[AAAAAAAT/CAAAAAATA]AAATCATTCAGTTAA | 3059 |
rs527265244 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656972 | CACTTCCTCTATGAA[A/T]CTCTCATGCCTTACT | 3059 |
rs527590755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649288 | TCGCCCAGGCTGGAG[C/T]GCAGTGGTATGATCT | 3059 |
rs527592462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657495 | ACATCCCCTCTATAT[G/T]TATCCCATCCTGACC | 3059 |
rs527671085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640539 | TTAAAATAATTAAAC[A/G]GCTTAAAGAAGTGGC | 3059 |
rs527672435 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648286 | CACCTCTATCCCTAA[G/T]AGAAAGTACCACCAA | 3059 |
rs527735362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647663 | CCAATAATATTTCCT[C/G]TAGTCTGTTATTTGC | 3059 |
rs527736854 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644547 | TGCATATGAGTATAA[C/T]AAAAACCAGTGGCTT | 3059 |
rs527945459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634763 | CAGCCTCTGGAGTAG[C/T]TGGGACCACAGATGT | 3059 |
rs528071847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637429 | AAGTAGTCTTTTAAT[G/T]GAATATTGCTTACTT | 3059 |
rs528078835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645143 | AATACCATTAGGAAT[A/C]CTTCATTCTGAACAC | 3059 |
rs528137850 | snp | A/G | 0.000313234 | 0.0125108 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644711 | GTCCTCACAGCATCC[A/G]CTGTCCTGTCTTTCA | 3059 |
rs528174645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649815 | CCAAGCAAAATGTAG[C/T]ACCTCAAAGATGACT | 3059 |
rs528239107 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653480 | TGTTTTGCAAGACAT[A/G]TAATAGCTTAATAAA | 3059 |
rs528284007 | snp | A/C | 0.0622301 | 0.165053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632646 | GATCCCCCGCCCTTC[A/C]CCACCCTGCCTCTTC | 3059 |
rs528332003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632089 | AGGCTCCTCGGGCCA[C/T]TCCCAACCTACCTCC | 3059 |
rs528400966 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638134 | AAGCTATAGTGCAGA[A/G]TACAATCATGGCTCA | 3059 |
rs528489566 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631071 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCGG | 3059 |
rs528649497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658902 | CACCTCCACCCTGAG[G/T]CTGGTCACCTCACAG | 3059 |
rs528717768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658465 | CATTTTTTTTTTCTT[A/G]GAAGAAAATAGAAAA | 3059 |
rs528815327 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121633419 | CAGGGTTTCACTATG[C/T]TGGTCAGGCTGGTCT | 3059 |
rs528847864 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121651179 | AAAGCAAGTTATGTT[C/G]TGGGAGAATACACTT | 3059 |
rs528908033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650627 | CAATCTTGACCTCAC[A/G]CTGCACAGAAAAGTC | 3059 |
rs528985293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658429 | GCTGAAGTCAAAATA[C/T]AGCAGCCCAATATTT | 3059 |
rs529128300 | snp | A/G | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661680 | ATACCACTTTCTGGC[A/G]GAGGCCGTAAGACCA | 3059 |
rs529151908 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636875 | ATCTTCTGACCATCA[C/T]TCAGCTTGTCTGTCC | 3059 |
rs529174672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644638 | TCAGCTCAGCATGTG[G/T]CTTCCAACATTGGCA | 3059 |
rs529286147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635944 | GGACAGCATGTTCCA[A/G]TGTTGTTTTGTGGTA | 3059 |
rs529390721 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642092 | CGCAAAAAAAAAAAA[A/C]AAAAAACTTGATCAA | 3059 |
rs529459211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657626 | CTCAAGACTAGCTTG[A/G]CCAACATGGTGAAAC | 3059 |
rs529734083 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639536 | ATTTTATTTTTTGTT[G/T]TTGTTGTTGTTGTTG | 3059 |
rs529754687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639229 | TAATTGACTCTTATA[C/T]AACACTATACCCCAA | 3059 |
rs529756288 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632826 | AAGTAGAAAACAAGT[C/G/T]AGATTCTTTGGGAGA | 3059 |
rs529798702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647077 | AGCTCTGCCTCCCAG[A/G]TTCACGCCATTCTCC | 3059 |
rs529847821 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662138 | ATGATAAGGAAGAGT[A/G]CGTTTGTACAAGAGA | 3059 |
rs529886632 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661395 | AATAAACGTCGACCA[A/G]TTGAATGCCAGAAGA | 3059 |
rs530012013 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659577 | AAAACCAGCCCAGGG[G/T]AAGTCTGGGTAAATC | 3059 |
rs530023319 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636261 | AGGCTTTGGCAGACA[C/T]GCCCCTTAGATGCTG | 3059 |
rs530056228 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662169 | AAAATCACTTGGAAT[C/T]CTCATGTAGTGTCAA | 3059 |
rs530195536 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636590 | TGTGGAAAACAAATG[C/T]AGGAGGAAATGTGAG | 3059 |
rs530198200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645616 | GGTTGGGGCTACAAC[A/G]GGCCAGCAGTTCTAA | 3059 |
rs530256913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653085 | AGATATCTTGGGGAC[A/G]AGACCCATGTGTAAA | 3059 |
rs530316493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660158 | ATCAACAGAGTAGGT[A/C]CTCATTTGCCAGGTA | 3059 |
rs530367709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645217 | ACAGAGCAGTGTTTA[A/C]ACCAGAAACAAAAAG | 3059 |
rs530498586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639009 | AACATCGCAAGACTC[C/T]AACACACACACACAC | 3059 |
rs530562658 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638269 | GATCTCACTGTGTTG[A/C]CCAGGCTAGCCTTAA | 3059 |
rs530569246 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645597 | GGTCTAGGAGTTACA[A/G]TGTGGTTGGGGCTAC | 3059 |
rs530677368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660372 | CTTCTCTTGGGCTCC[A/G]TCAGCACTTGGTACT | 3059 |
rs530842399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632704 | AGCCTCTCCTGGGGA[A/G]CACAGCCTTTCATCC | 3059 |
rs530870011 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631680 | TCTTGGGGAAGGGGA[C/T]CTCCTTCCCCATGCT | 3059 |
rs530978173 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652420 | GCACTGTAGGAGGCC[A/G]AGGCAGGCGGATCAC | 3059 |
rs531056290 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631108 | TGGTGCACGCCTGTA[C/G]TTGCAGGTACTCGGG | 3059 |
rs531119590 | in-del | -/TCTCTCTCTCTCTC | 0.489259 | 0.0724914 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635238 | CTCTTCTCTCCCTTT[-/TCTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 3059 |
rs531227944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658973 | ATGGAACAATGCATT[G/T]GGAGAGCATTATTTG | 3059 |
rs531322529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634667 | TTCTTGAGACAGGGT[A/C]TCAGCCCAGGCTAGA | 3059 |
rs531424820 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634115 | AACCCAGGGGAGGAC[C/T]TTGCCTTATTTTCTG | 3059 |
rs531430680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656844 | AATTGTTCTTAGTTC[A/T]TCTGAAGGAAGTCAC | 3059 |
rs531433788 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648547 | GCAGCAAGCAATGAG[A/G]GTTTAGGGTATTAAG | 3059 |
rs531498247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649051 | TAAATGGGTTATAAC[C/T]ATATTATAGTTAAAA | 3059 |
rs531575208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647202 | TAGCCAGGATGGTCT[C/T]GATCTCCTAACCTCA | 3059 |
rs531638081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654115 | GGGCAAGTTCACCCC[G/T]TCTTAGGCAACCTAT | 3059 |
rs531674935 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121653151 | AAGGAAGGTATTAAA[A/G]AAGAACTAAATAAAT | 3059 |
rs531697352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654871 | CCATCAGATGTTAAA[A/G]ACTGACTTAGCCCAC | 3059 |
rs531769897 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | HCLS1 | GRCh38.p7 | 3:121634362 | CTTCCTCTCGCTTCC[C/T]CTTCTCCTCAGCCAT | 3059 |
rs531828983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640439 | GGAAATAAATAACCA[G/T]GAGGAACGCAGATTA | 3059 |
rs531883518 | snp | C/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662486 | TCACACCTCTAATCC[C/T]AGCACTTTGGGAGGC | 3059 |
rs532131577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633329 | CAAGCGATTCTCCTG[C/T]CTCAGCCCCCTGAGT | 3059 |
rs532234612 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638481 | GCTCTGTCCACTCCT[A/G]TAAGAGAGTGCTAGA | 3059 |
rs532238663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655108 | CCATCGTTTATTCTA[C/T]CTGATAGATTCAGTT | 3059 |
rs532433044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660211 | ACTAACTTTAATAAT[C/T]TGGCAAATCAGCAAT | 3059 |
rs532508346 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121660986 | AGCTACTTCCTGAAA[G/T]TTGAGTCAGTTCCTT | 3059 |
rs532611734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647143 | CCCACCACGACGCAC[A/G]GCTAATTTTTTGTAT | 3059 |
rs532675527 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645765 | TTTTAACTCATGAAC[A/C]AATGAATGAGTCAAA | 3059 |
rs532760081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658145 | ATTAGTCCCAGTATG[A/T]GGGCTGTCTCAGTCC | 3059 |
rs532809849 | snp | C/G | | | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631142 | CTGAGGCAGGAGAAT[C/G]TCTTGAACCCAGGAA | 3059 |
rs532893696 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121636609 | AGGAAATGTGAGAAT[C/T]AGAGGATAGAGGGAG | 3059 |
rs532945349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636679 | CTGGGAGCGAATGGA[A/G]AAGACAAAGATGGAA | 3059 |
rs533409437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649017 | AAATCTGCAATTTTT[A/T]AATGAATATAATAAT | 3059 |
rs533411347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641445 | AAAGGTGAAACAATG[A/G]AATACAATAAGCAAT | 3059 |
rs533472674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648345 | CCACTTCCATCTTTA[A/C]CATGAAGGTGACTGC | 3059 |
rs533516416 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648629 | CACATTGGTTATACG[C/T]AGAATGGCTGTCTCA | 3059 |
rs533525178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641009 | GAATAACCCAGAATG[C/T]GGCACAAGGACATAA | 3059 |
rs533526095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649515 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCT | 3059 |
rs533576036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656002 | TACAGGTGCCCGCCA[C/T]CACGCCCATCTAATT | 3059 |
rs533638293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655295 | TTAGAAAGGAAATCT[A/G]ATTAAACTAACCTAT | 3059 |
rs533699074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635347 | GAGTGGCATGATCTC[A/G]GCTCACTCCGACTTC | 3059 |
rs533734895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635428 | GATTATAGGTGTGCA[C/T]CTCCATGCCTGGCTA | 3059 |
rs533795272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642188 | AATAGGGCCGGGCAC[A/G]GTGGCTCACACCTAT | 3059 |
rs533975196 | snp | A/T | 0.000345338 | 0.0131358 | missense | HCLS1 | GRCh38.p7 | 3:121633078 | TTACCTCCGGGAGAG[A/T]CTGCCTAATGGGCAG | 3059 |
rs534044746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639407 | AGAAGTCAATACCAA[G/T]AAAATTATCTAGAAA | 3059 |
rs534248229 | snp | C/T | 0.030278 | 0.119257 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639849 | TTATCTAAGTTTCTA[C/T]TTTAAGAGGCTAGGA | 3059 |
rs534312451 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647260 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 3059 |
rs534365333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636976 | CTCTCCATCTCTCCT[C/T]TCTCCCCTCACTACC | 3059 |
rs534369840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662736 | TGAAACTCGGTCTCA[A/G]AAAAAACCCAACAAA | 3059 |
rs534502654 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659247 | TGTTCTAGACGGCCT[C/T]CCGGACTGTGCAGAA | 3059 |
rs534715017 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643980 | ATTTTGTTTTTCATG[A/G]TTTTACCCCCCATGA | 3059 |
rs534874861 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637454 | TTACTTTTTCCCTCT[C/T]TTCTCTCATTTCCAT | 3059 |
rs535047827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636166 | AATGCCAAGAAATCA[A/G]TACAATTTCCAGTCC | 3059 |
rs535188757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650005 | AGGTCACAGGATACA[A/G]GGTCATTATATCAAA | 3059 |
rs535306858 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631227 | AGCAAAACTCCTTCT[C/T]AAAAAAAAAAAAAGT | 3059 |
rs535942437 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641973 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 3059 |
rs536021963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649434 | GAGACAGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 3059 |
rs536213782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659970 | ATCCTTGACCTATTG[A/C]CCAGAAACCAGAAAG | 3059 |
rs536220836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652050 | TACAATGGGACACTA[C/T]ATGACAATATAAAAG | 3059 |
rs536344656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658608 | AGAAGTCATCATGGG[A/T]GTGGGTAACACTAGG | 3059 |
rs536547608 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660656 | TTGTTTCTATCTCCA[C/G]ATGCTGATTTGCTAC | 3059 |
rs536613784 | snp | C/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121634513 | GAATCAGTTAAATAT[C/G]CGGGAGGAGGGATTT | 3059 |
rs536621131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644385 | TTCTGTAAATAGTAA[C/T]CCTAATTAGTTGTTT | 3059 |
rs536636012 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121649204 | AACAGACTTCTTTAG[G/T]TTATAGTGGAAGTCA | 3059 |
rs536998308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658535 | CTCAGTTACAAGATG[A/G]GAGATGGGACTTTAA | 3059 |
rs537335523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650829 | TCTTTTGCTCTTAAA[A/C]AGATGCCATTAATAA | 3059 |
rs537403540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650216 | TTCATGGATTGGAAA[A/G]CTCAATATCATTAAG | 3059 |
rs537456726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654507 | GAGTGGAGAAAAGAA[A/G]GTGGAGAGAAGGGTG | 3059 |
rs537467847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657837 | GTCTCAAAAAACAAA[A/C]AAGAAAACACAAAGA | 3059 |
rs537548227 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661648 | TTACTCAGGTGACTT[C/G]TTTTGGCCAGTGACA | 3059 |
rs537607496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641495 | AAATACCTTGGTCAA[A/T]TTAAATAAGCATTTA | 3059 |
rs537609500 | snp | A/G | 8.24545e-05 | 0.00642032 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644761 | CATCCAGGGGTGATC[A/G]TGGGCAATTTTCACA | 3059 |
rs537672170 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644139 | TGTCCTCTCTCTGTG[G/T]GCAGCTGCAGGGCAG | 3059 |
rs537735781 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121637469 | CTTCTCTCATTTCCA[G/T]GCCAAGATGAGAAGA | 3059 |
rs537810771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639281 | ATGCATATAGAACAT[G/T]GACCAAATAGACCAT | 3059 |
rs537816523 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121642684 | AGAACGCTGAGGTGG[A/G]AGGATCGCTTGAGCC | 3059 |
rs538002443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634535 | GAGGGATTTGTGGGA[C/G]AGGATGGTAAAGAGG | 3059 |
rs538039894 | in-del | -/AAGT | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640048 | AAAGAGAAAAAACAC[-/AAGT]AAGTAAGATCAGAAA | 3059 |
rs538065654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640927 | AAGTTTAAAATGCAA[C/T]GGACAGCTTAAACAA | 3059 |
rs538130665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647854 | CACATACCATTGGAC[A/C]TACACATTCTAGTTT | 3059 |
rs538227729 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121640835 | GGGAGGGGAGGGGAC[A/G]GGAGGGCAGGGCAGG | 3059 |
rs538325895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653439 | ACGTCATCTATGATA[C/T]AGGATTGTTTTTAAA | 3059 |
rs538598476 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661519 | GGCTCTAGAGCGTAG[G/T]AAGAATTCTGAAAGA | 3059 |
rs538678325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652655 | ACAGAGCGAAACTCC[A/G]TCTCAAAAAAAACAA | 3059 |
rs538795919 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121659059 | AAGTCAAAAAATAGC[A/G]TGTTTTCAAGTTGAC | 3059 |
rs538803456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639971 | GAGAAAATTAGCAAA[A/G]CCAAAAGCTTGTTCT | 3059 |
rs538807082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647808 | GCTTTCTATCAATTA[A/G]AGGATGTGTCTCAAA | 3059 |
rs538856304 | snp | C/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662932 | GGCCCAGCTTATTTG[C/G]TTCAGTATTAGGATA | 3059 |
rs538865727 | snp | C/G | 0.00115382 | 0.0239912 | missense | HCLS1 | GRCh38.p7 | 3:121647418 | GAGAACATCATGCTC[C/G]TCTGATACTTTGTTC | 3059 |
rs538903227 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652406 | CACCTGTAATCCCAG[A/C]ACTGTAGGAGGCCGA | 3059 |
rs538917911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654391 | TTTCCAGAAACTTAA[C/T]TGTATTTTATTTTAC | 3059 |
rs539118021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659779 | CAACAACAAAAGGAC[G/T]GTCACACAGAAAACT | 3059 |
rs539208764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632917 | TACTAGTTTGCCCAG[A/G]ACAGAGGAGTTTCCC | 3059 |
rs539264636 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639259 | AACTACAGAATATAC[C/T]TTTTTCATGCATATA | 3059 |
rs539352445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635567 | CAGATGTGAGCTCCG[C/T]CTTACCTGGTTTTTC | 3059 |
rs539363398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636905 | CTCATTCCTTCCTCA[A/G]CGCCCCCTTCTCTCT | 3059 |
rs539552696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633690 | CTATAGGCACACACC[A/G]CCATGCCCAGCTAAT | 3059 |
rs539741448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, downstream-variant-500B | GOLGB1, HCLS1 | GRCh38.p7 | 3:121662811 | TTAAGCTTCTCTTCT[C/T]CCATTCCCACCCAGA | 3059 |
rs539936393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647576 | GGGCCCCCAAAATAT[A/G]CTAGTGATGGGTCTG | 3059 |
rs539947720 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639539 | TTATTTTTTGTTGTT[G/T]TTGTTGTTGTTGTTG | 3059 |
rs540163561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634586 | ATAATAGGAGGATGG[C/T]ATAGCCCTGAAGCCT | 3059 |
rs540335181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632638 | ACTGATAAGATCCCC[C/T]GCCCTTCACCACCCT | 3059 |
rs540386449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654586 | CATAGGACCATTTGA[A/G]TTATTCACTGAATTA | 3059 |
rs540397176 | snp | G/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639575 | GTTTTTTGAGACAGG[G/T]TCTCACTCTGTTGCC | 3059 |
rs540552049 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641479 | AGCTAGGAAATAGGT[-/A]AAATACCTTGGTCAA | 3059 |
rs540904478 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660913 | CGGAGTGAGAAACTG[A/G]GCTGCTGCTTCAGTT | 3059 |
rs540948166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658093 | CTGATACCAGGTATC[A/G]TGCATGCCCCACAGG | 3059 |
rs541098308 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656179 | TGATTAAACAATGTG[A/G]TATTGTCATCCAGTT | 3059 |
rs541236419 | snp | C/G | 0.000379059 | 0.0137618 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635814 | AGCGCTCTGCAGGCA[C/G]GAGAACAGCATGTGT | 3059 |
rs541238942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658696 | AGTGGCTGGAGGTGG[C/T]TGGCAATGAGCGGTG | 3059 |
rs541357949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121657503 | TCTATATTTATCCCA[C/T]CCTGACCCCATGTAA | 3059 |
rs541393864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648971 | ATGAAAGATCAAGAA[A/T]ATGGGGCCAAAATTT | 3059 |
rs541518400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655790 | AATGGCATGGTTTAA[A/G]AATAATATTCATTAT | 3059 |
rs541535537 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635215 | TTTCTTTCTTTCTCT[C/G]TCTCTCTCTCTTCTC | 3059 |
rs541644137 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635306 | CTCTCTTTCTTTCGT[C/T]TCACTCTGTCACCCA | 3059 |
rs541848807 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648544 | TCTGCAGCAAGCAAT[A/G]AGGGTTTAGGGTATT | 3059 |
rs541956170 | snp | A/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121656687 | TGTTACATTTCTTCA[A/T]ATTACCATTCATGGC | 3059 |
rs542093971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648932 | GTAAATGCCTGCCCA[A/G]TATCTTCCAACTGAA | 3059 |
rs542266665 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654893 | TTAGCCCACACTAAC[A/G]AGAGGGAATCCCCAA | 3059 |
rs542292036 | in-del | -/TTC | 0.00358779 | 0.0422022 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632267 | GGGGCAATAGAGAAA[-/TTC]TTCTTCCTCTTACCC | 3059 |
rs542445129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641217 | AATTAAAAAAAACCC[A/G]GAGATATAAGACATG | 3059 |
rs542488801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638044 | GAAGATAATTATGAA[C/T]TGACACCACAGAAAA | 3059 |
rs542508843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648256 | TAAGCCTCAAATTAT[C/T]TTGATTTGAAGGGAC | 3059 |
rs542552753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645084 | TACGCGATGGGAGAG[C/T]AAGATGACTTTTTCT | 3059 |
rs542602414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652307 | TGGTTATATTATATA[C/T]ATATAGTCAAAACTC | 3059 |
rs542607149 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654790 | TTGGGATCTGTCAGT[-/G]TTAGCATCTACAGCT | 3059 |
rs542693572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643337 | ATGATCCCTCTTCAT[C/T]TGGGATGTCATGAGA | 3059 |
rs542709272 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650244 | AAGATGTCAGTTCTC[C/T]CTAAAATGATCTATA | 3059 |
rs542844069 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657066 | AAAGATAGATAATAG[A/G]GTTGAGGAGGGTAAG | 3059 |
rs543164479 | snp | C/T | 1.64963e-05 | 0.00287192 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637298 | GCCCACCCTTAGGCT[C/T]CAGCACACAGGGAAG | 3059 |
rs543289840 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631532 | CTAGACGTACTTTCC[C/T]GGGTAAACAAACTGG | 3059 |
rs543316141 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant, synonymous-codon | HCLS1 | GRCh38.p7 | 3:121637180 | CTCCGTCTCTCCCTT[A/G]TAGTCATATCCCAGA | 3059 |
rs543317082 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636680 | TGGGAGCGAATGGAG[A/C]AGACAAAGATGGAAG | 3059 |
rs543351196 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631015 | GGGCGATCATCTGAG[A/G]TCAGGAGTTCAAGAT | 3059 |
rs543616512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121652241 | TGACTGCAAAGAGGT[A/G]CAGGGAAATTTTCAT | 3059 |
rs543791261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642617 | CTCCATCTCTACAAA[A/G]AATAAAAAATTAGCC | 3059 |
rs543935064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656538 | CCCTGGATATGTCTG[C/T]AAGTTCCTTTTATCT | 3059 |
rs543940697 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121641528 | AAGTAATAATAATGA[C/T]TCATTTTTGTGGGGT | 3059 |
rs543970193 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645599 | TCTAGGAGTTACAAT[A/G]TGGTTGGGGCTACAA | 3059 |
rs543975716 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121657362 | GTCATTCTGCAAACG[A/G]CAGCACGCAGTAATA | 3059 |
rs544116769 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HCLS1 | GRCh38.p7 | 3:121643178 | CCCTGGACACAGACA[G/T]TTTTAGGTTCAAACC | 3059 |
rs544180214 | snp | G/T | 0.0898077 | 0.191933 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639530 | TGAATGATTTTATTT[G/T]TTGTTGTTGTTGTTG | 3059 |
rs544228256 | snp | G/T | 1.64855e-05 | 0.00287097 | missense | HCLS1 | GRCh38.p7 | 3:121657286 | GCACCTACTTGATGT[G/T]TTCTGTGCGTCCAGA | 3059 |
rs544271570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653793 | CCTATGGTTATAGCT[C/T]AGTAAAGATTTAATC | 3059 |
rs544288897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637991 | AAATCCTGGCTCCAG[A/C]AACCAGAGACAAAGA | 3059 |
rs544362604 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | HCLS1 | GRCh38.p7 | 3:121660861 | AGCGCCCGGCTCCTC[A/G]CGTCCACACCGACTC | 3059 |
rs544441234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653073 | ATATACATAATGAGA[C/T]ATCTTGGGGACGAGA | 3059 |
rs544509632 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121633196 | ATGAAGCATCTCTCA[A/G/T]GTAAGCAAGCCTCCA | 3059 |
rs544584616 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121652419 | AGCACTGTAGGAGGC[C/T]GAGGCAGGCGGATCA | 3059 |
rs544791573 | in-del | -/TGTC | 0.00636936 | 0.0560724 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656575 | TCGGAGGGTTTTGTT[-/TGTC]TGTTTGTTTGTTTCT | 3059 |
rs544883012 | snp | C/T | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121648829 | TTCCCATGCCTCCTC[C/T]AAACTCTCTGGCAGC | 3059 |
rs544901419 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632663 | CACCCTGCCTCTTCT[A/C]CCCTCTACCCTTGCC | 3059 |
rs545068088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121660006 | AAGTGCTATCTAGAG[A/G]TGAGAACCAGAGAGT | 3059 |
rs545091335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644475 | CGGCATGAGTATTTA[C/T]AAGGTTTTGATGTTA | 3059 |
rs545245513 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121660683 | CTACAACCACTCACA[A/G]CCAGGCCTTCTGGCC | 3059 |
rs545253254 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639493 | GAAGAAATTACAAGG[G/T]AAATAAGAAAATATT | 3059 |
rs545313596 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646868 | TATATATACTTATAT[A/G]TAGTTGGCTCTTATT | 3059 |
rs545449526 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635111 | CCCATGCCACCCCAC[C/T]CCTGTCCCAAGCCAC | 3059 |
rs545475747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636589 | ATGTGGAAAACAAAT[C/G]TAGGAGGAAATGTGA | 3059 |
rs545753929 | in-del | -/CTGT | 0.00279162 | 0.0372561 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644122 | CTAACTGTGAAGGAG[-/CTGT]CTGTCCTCTCTCTGT | 3059 |
rs545814382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634635 | GCTATACGACCTAAG[A/T]CTCGTGTCTTTTTTT | 3059 |
rs545947713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640379 | AAAACAAATATCCCT[C/T]TCCTTCACTAAAATA | 3059 |
rs546097289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655355 | AGCTGCTCAGAAGTG[C/T]TAAGTACTGCATTAG | 3059 |
rs546257971 | snp | G/T | | | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631011 | CGGGGGGCGATCATC[G/T]GAGGTCAGGAGTTCA | 3059 |
rs546269380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645310 | CCAAGGGGACTGACC[A/G]GACGCCATAGCCGGG | 3059 |
rs546429347 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121654525 | GGAGAGAAGGGTGAT[A/G]GTTCTTGAAAACCAG | 3059 |
rs546453383 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HCLS1 | GRCh38.p7 | 3:121654833 | TCCAATTTCCCTCTC[A/C]TTTCCAAGGACCATG | 3059 |
rs546497540 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662161 | ACAAGAGAAAAATCA[C/T]TTGGAATCCTCATGT | 3059 |
rs546510443 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661702 | GTAAGACCACTGCAA[A/G]CTTTGCCATGCTTTC | 3059 |
rs546594848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659584 | GCCCAGGGGAAGTCT[A/G]GGTAAATCAGTTAAA | 3059 |
rs546602141 | snp | G/T | 0.00199481 | 0.0315187 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631241 | TCAAAAAAAAAAAAA[G/T]TTCAGCCTAAGGAAA | 3059 |
rs546867872 | in-del | -/TATTACTATGTAATA | 0.162581 | 0.234218 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646372 | CATTATATTACATAT[-/TATTACTATGTAATA]TATTACTATGTAATA | 3059 |
rs546900122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638655 | CTTATGTGATGCAGG[A/G]ATTCTAAGCTGAGAA | 3059 |
rs546961493 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645243 | AAAAGAGCTGAAACA[A/G]GAGCATTGTGCAGCA | 3059 |
rs547206159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642768 | GTGACAGTGCAAGAC[A/C]CTGTCTCAAAAACAA | 3059 |
rs547229881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636086 | CCCTGGCTCATGCAT[A/G]AGGAGGAACTAGTGT | 3059 |
rs547270801 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649850 | CCTCAATCTGTGTTT[G/T]TTTTTTATTACAAAA | 3059 |
rs547270865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642195 | CCGGGCACGGTGGCT[A/C]ACACCTATAATCCCA | 3059 |
rs547329763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649321 | GCTCACTGTAATCTC[C/T]GCCTCCCGGGTTCAA | 3059 |
rs547389142 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645615 | TGGTTGGGGCTACAA[A/C]AGGCCAGCAGTTCTA | 3059 |
rs547429443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641366 | CAAAGACTGAAAGTT[A/C]TTTCATAGACTCATT | 3059 |
rs547434998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121656005 | AGGTGCCCGCCACCA[C/T]GCCCATCTAATTTTT | 3059 |
rs547586723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635443 | CCTCCATGCCTGGCT[A/C]ATTTTTGTATTTTTT | 3059 |
rs547787307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121640580 | ATAATGAAACCATAA[C/T]GTCTTATGGAAAATG | 3059 |
rs547836359 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121662697 | TTGAGATTGTGCCAC[C/T]GCACTCCAGCCTGAG | 3059 |
rs547951997 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647261 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 3059 |
rs547953831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655071 | TAAATGGGAGATGAG[C/T]GAGATTTTTTTGTCA | 3059 |
rs548105981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121649203 | AAACAGACTTCTTTA[A/G]GTTATAGTGGAAGTC | 3059 |
rs548124064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121655958 | GGTTCAAGAGACTCT[C/T]GTGCTTCGGCCTCCT | 3059 |
rs548140538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121639746 | ATTTGTTGAATGTAG[C/T]AAATGTTTGTAGCAA | 3059 |
rs548439488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121653599 | GCTGGAAATCAAGAT[A/G]GGATGGTAAAATATT | 3059 |
rs548588469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121647251 | CTTCCAAAGTGCTGG[G/T]ATTACAGGCGTGAGC | 3059 |
rs548747232 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121639703 | ACGGGTTTGTGATGA[A/G]TGAAAATTAAAACAC | 3059 |
rs548747509 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661301 | TTTATATGTGGGTTT[C/T]GAAGCATAAGACTTA | 3059 |
rs548800906 | snp | A/T | | | upstream-variant-2KB | HCLS1 | GRCh38.p7 | 3:121661843 | AGTCTTTCACTAAAA[A/T]ATAGTCCTTTGTTTT | 3059 |
rs548920375 | snp | C/T | 5.01895e-05 | 0.00500921 | intron-variant | HCLS1 | GRCh38.p7 | 3:121644652 | GGCTTCCAACATTGG[C/T]ACCAAGGAACTTGCT | 3059 |
rs549143988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650008 | TCACAGGATACAAGG[C/T]CATTATATCAAAATC | 3059 |
rs549144235 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121658449 | GCCCAATATTTCCTG[A/C]CATTTTTTTTTTCTT | 3059 |
rs549153501 | in-del | -/GTA | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121646563 | TATATATTAATATAT[-/GTA]ATTTATTACATATAT | 3059 |
rs549255720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121637384 | AGAGCAGGGCTTGAA[C/T]ACAGGGGAATTAAAG | 3059 |
rs549326506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642829 | GTGCGCTGGGTCATG[G/T]AAGTTAAAAAGCTGA | 3059 |
rs549435468 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121636035 | ACCTTAGAATCTCAC[A/G/T]TCTCCAAGCCCAGTT | 3059 |
rs549492646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635387 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC | 3059 |
rs549663648 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HCLS1 | GRCh38.p7 | 3:121631121 | TAGTTGCAGGTACTC[A/G]GGAGGCTGAGGCAGG | 3059 |
rs550044554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121648447 | CCACGTGACAATCAG[A/G]TCTGTTATTTGGACA | 3059 |
rs550087042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121650599 | AAATAATCACATGGA[A/G]AAAAATGAACCTCAA | 3059 |
rs550150666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121635356 | GATCTCAGCTCACTC[C/T]GACTTCCGCCTCCTG | 3059 |
rs550212064 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HCLS1 | GRCh38.p7 | 3:121642071 | GGCGACAGAGCCAGA[A/C]TCCGTCGCAAAAAAA | 3059 |
rs550212299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HCLS1 | GRCh38.p7 | 3:121634880 | CAAGTGATTATCCTA[C/T]TTCAGCATCCCAAAG | 3059 |
rs550275669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121641483 | TAGGAAATAGGTAAA[C/T]ACCTTGGTCAATTTA | 3059 |
rs550566345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121632792 | ATGGGAAGAGAATGT[A/G]AAAGGTGTGAGGGGA | 3059 |
rs550693596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638458 | GAGGGAAGAAAGCCA[A/G]AAACGAAGCTCTGTC | 3059 |
rs550804867 | snp | A/G | | | intron-variant | HCLS1 | GRCh38.p7 | 3:121650954 | CAGCCTAGCCACTAT[A/G]GTGAAACCCCGTCTC | 3059 |
rs550849153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121659529 | TTCTATTTCCACTTG[A/G]AAGCTCCATCTTCTC | 3059 |
rs551040701 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631773 | AGACATTTGCAGCAG[A/G]AATAGGGAGGGGGTG | 3059 |
rs551044677 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HCLS1 | GRCh38.p7 | 3:121631718 | CCCCAAGCCCTTAAT[A/G]AAGCAGGAGAGGGAA | 3059 |
rs551311411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121638231 | CATGACTTGCTAATT[A/T]AAAAAAAAATCTGTA | 3059 |
rs551348949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HCLS1 | GRCh38.p7 | 3:121645171 | CACTCCCATAGGATG[A/G]GCTGGGAACCAGGGG | 3059 |