Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.136115421A>C | CA348658708 | CXCR4 | c.495T>G (p.Ile165Met) c.462T>G (p.Ile154Met) c.507T>G (p.Ile169Met) c.519T>G (p.Ile173Met) n.701T>G c.720T>G (p.Ile240Met) c.606T>G (p.Ile202Met) | |
2 | g.136115421A>G | CA429206394 | CXCR4 | c.495T>C (p.Ile165=) c.462T>C (p.Ile154=) c.507T>C (p.Ile169=) c.519T>C (p.Ile173=) n.701T>C c.720T>C (p.Ile240=) c.606T>C (p.Ile202=) | dbSNP |
2 | g.136115421A>T | CA429206396 | CXCR4 | c.495T>A (p.Ile165=) c.462T>A (p.Ile154=) c.507T>A (p.Ile169=) c.519T>A (p.Ile173=) n.701T>A c.720T>A (p.Ile240=) c.606T>A (p.Ile202=) | |
2 | g.136115422A= | CA1290966045 | CXCR4 | c.494T= (p.Ile165=) c.461T= (p.Ile154=) c.506T= (p.Ile169=) c.518T= (p.Ile173=) n.700T= c.719T= (p.Ile240=) c.605T= (p.Ile202=) | |
2 | g.136115422A>C | CA348658711 | CXCR4 | c.494T>G (p.Ile165Ser) c.461T>G (p.Ile154Ser) c.506T>G (p.Ile169Ser) c.518T>G (p.Ile173Ser) n.700T>G c.719T>G (p.Ile240Ser) c.605T>G (p.Ile202Ser) | |
2 | g.136115422A>G | CA1890112 | CXCR4 | c.494T>C (p.Ile165Thr) c.461T>C (p.Ile154Thr) c.506T>C (p.Ile169Thr) c.518T>C (p.Ile173Thr) n.700T>C c.719T>C (p.Ile240Thr) c.605T>C (p.Ile202Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115422A>T | CA348658714 | CXCR4 | c.494T>A (p.Ile165Asn) c.461T>A (p.Ile154Asn) c.506T>A (p.Ile169Asn) c.518T>A (p.Ile173Asn) n.700T>A c.719T>A (p.Ile240Asn) c.605T>A (p.Ile202Asn) | |
2 | g.136115423T>A | CA348658715 | CXCR4 | c.493A>T (p.Ile165Phe) c.460A>T (p.Ile154Phe) c.505A>T (p.Ile169Phe) c.517A>T (p.Ile173Phe) n.699A>T c.718A>T (p.Ile240Phe) c.604A>T (p.Ile202Phe) | dbSNP |
2 | g.136115423T>C | CA348658718 | CXCR4 | c.493A>G (p.Ile165Val) c.460A>G (p.Ile154Val) c.505A>G (p.Ile169Val) c.517A>G (p.Ile173Val) n.699A>G c.718A>G (p.Ile240Val) c.604A>G (p.Ile202Val) | dbSNP gnomAD v4 |
2 | g.136115423T>G | CA348658720 | CXCR4 | c.493A>C (p.Ile165Leu) c.460A>C (p.Ile154Leu) c.505A>C (p.Ile169Leu) c.517A>C (p.Ile173Leu) n.699A>C c.718A>C (p.Ile240Leu) c.604A>C (p.Ile202Leu) | dbSNP |
2 | g.136115423T= | CA1290966046 | CXCR4 | c.493A= (p.Ile165=) c.460A= (p.Ile154=) c.505A= (p.Ile169=) c.517A= (p.Ile173=) n.699A= c.718A= (p.Ile240=) c.604A= (p.Ile202=) | |
2 | g.136115424A>C | CA429206397 | CXCR4 | c.492T>G (p.Thr164=) c.459T>G (p.Thr153=) c.504T>G (p.Thr168=) c.516T>G (p.Thr172=) n.698T>G c.717T>G (p.Thr239=) c.603T>G (p.Thr201=) | |
2 | g.136115424A>G | CA429206398 | CXCR4 | c.492T>C (p.Thr164=) c.459T>C (p.Thr153=) c.504T>C (p.Thr168=) c.516T>C (p.Thr172=) n.698T>C c.717T>C (p.Thr239=) c.603T>C (p.Thr201=) | |
2 | g.136115424A>T | CA429206400 | CXCR4 | c.492T>A (p.Thr164=) c.459T>A (p.Thr153=) c.504T>A (p.Thr168=) c.516T>A (p.Thr172=) n.698T>A c.717T>A (p.Thr239=) c.603T>A (p.Thr201=) | ClinVar dbSNP gnomAD v4 |
2 | g.136115425G>A | CA348658727 | CXCR4 | c.491C>T (p.Thr164Ile) c.458C>T (p.Thr153Ile) c.503C>T (p.Thr168Ile) c.515C>T (p.Thr172Ile) n.697C>T c.716C>T (p.Thr239Ile) c.602C>T (p.Thr201Ile) | |
2 | g.136115425G>C | CA348658725 | CXCR4 | c.491C>G (p.Thr164Ser) c.458C>G (p.Thr153Ser) c.503C>G (p.Thr168Ser) c.515C>G (p.Thr172Ser) n.697C>G c.716C>G (p.Thr239Ser) c.602C>G (p.Thr201Ser) | dbSNP |
2 | g.136115425G>T | CA348658723 | CXCR4 | c.491C>A (p.Thr164Asn) c.458C>A (p.Thr153Asn) c.503C>A (p.Thr168Asn) c.515C>A (p.Thr172Asn) n.697C>A c.716C>A (p.Thr239Asn) c.602C>A (p.Thr201Asn) | dbSNP |
2 | g.136115426T>A | CA348658732 | CXCR4 | c.490A>T (p.Thr164Ser) c.457A>T (p.Thr153Ser) c.502A>T (p.Thr168Ser) c.514A>T (p.Thr172Ser) n.696A>T c.715A>T (p.Thr239Ser) c.601A>T (p.Thr201Ser) | dbSNP |
2 | g.136115426T>C | CA348658730 | CXCR4 | c.490A>G (p.Thr164Ala) c.457A>G (p.Thr153Ala) c.502A>G (p.Thr168Ala) c.514A>G (p.Thr172Ala) n.696A>G c.715A>G (p.Thr239Ala) c.601A>G (p.Thr201Ala) | dbSNP |
2 | g.136115426T>G | CA348658734 | CXCR4 | c.490A>C (p.Thr164Pro) c.457A>C (p.Thr153Pro) c.502A>C (p.Thr168Pro) c.514A>C (p.Thr172Pro) n.696A>C c.715A>C (p.Thr239Pro) c.601A>C (p.Thr201Pro) | dbSNP |
2 | g.136115427C>A | CA429206403 | CXCR4 | c.489G>T (p.Leu163=) c.456G>T (p.Leu152=) c.501G>T (p.Leu167=) c.513G>T (p.Leu171=) n.695G>T c.714G>T (p.Leu238=) c.600G>T (p.Leu200=) | dbSNP |
2 | g.136115427C= | CA1290966047 | CXCR4 | c.489G= (p.Leu163=) c.456G= (p.Leu152=) c.501G= (p.Leu167=) c.513G= (p.Leu171=) n.695G= c.714G= (p.Leu238=) c.600G= (p.Leu200=) | |
2 | g.136115427C>G | CA429206404 | CXCR4 | c.489G>C (p.Leu163=) c.456G>C (p.Leu152=) c.501G>C (p.Leu167=) c.513G>C (p.Leu171=) n.695G>C c.714G>C (p.Leu238=) c.600G>C (p.Leu200=) | dbSNP |
2 | g.136115427C>T | CA1890113 | CXCR4 | c.489G>A (p.Leu163=) c.456G>A (p.Leu152=) c.501G>A (p.Leu167=) c.513G>A (p.Leu171=) n.695G>A c.714G>A (p.Leu238=) c.600G>A (p.Leu200=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.136115428A>C | CA348658737 | CXCR4 | c.488T>G (p.Leu163Arg) c.455T>G (p.Leu152Arg) c.500T>G (p.Leu167Arg) c.512T>G (p.Leu171Arg) n.694T>G c.713T>G (p.Leu238Arg) c.599T>G (p.Leu200Arg) | |
2 | g.136115428A>G | CA348658739 | CXCR4 | c.488T>C (p.Leu163Pro) c.455T>C (p.Leu152Pro) c.500T>C (p.Leu167Pro) c.512T>C (p.Leu171Pro) n.694T>C c.713T>C (p.Leu238Pro) c.599T>C (p.Leu200Pro) | gnomAD v4 |
2 | g.136115428A>T | CA348658741 | CXCR4 | c.488T>A (p.Leu163Gln) c.455T>A (p.Leu152Gln) c.500T>A (p.Leu167Gln) c.512T>A (p.Leu171Gln) n.694T>A c.713T>A (p.Leu238Gln) c.599T>A (p.Leu200Gln) | |
2 | g.136115429G>A | CA429206408 | CXCR4 | c.487C>T (p.Leu163=) c.454C>T (p.Leu152=) c.499C>T (p.Leu167=) c.511C>T (p.Leu171=) n.693C>T c.712C>T (p.Leu238=) c.598C>T (p.Leu200=) | |
2 | g.136115429G>C | CA348658744 | CXCR4 | c.487C>G (p.Leu163Val) c.454C>G (p.Leu152Val) c.499C>G (p.Leu167Val) c.511C>G (p.Leu171Val) n.693C>G c.712C>G (p.Leu238Val) c.598C>G (p.Leu200Val) | dbSNP |
2 | g.136115429G= | CA1290966048 | CXCR4 | c.487C= (p.Leu163=) c.454C= (p.Leu152=) c.499C= (p.Leu167=) c.511C= (p.Leu171=) n.693C= c.712C= (p.Leu238=) c.598C= (p.Leu200=) | |
2 | g.136115429G>T | CA348658746 | CXCR4 | c.487C>A (p.Leu163Met) c.454C>A (p.Leu152Met) c.499C>A (p.Leu167Met) c.511C>A (p.Leu171Met) n.693C>A c.712C>A (p.Leu238Met) c.598C>A (p.Leu200Met) | dbSNP |
2 | g.136115430C>A | CA429206411 | CXCR4 | c.486G>T (p.Leu162=) c.453G>T (p.Leu151=) c.498G>T (p.Leu166=) c.510G>T (p.Leu170=) n.692G>T c.711G>T (p.Leu237=) c.597G>T (p.Leu199=) | dbSNP |
2 | g.136115430C= | CA1290966049 | CXCR4 | c.486G= (p.Leu162=) c.453G= (p.Leu151=) c.498G= (p.Leu166=) c.510G= (p.Leu170=) n.692G= c.711G= (p.Leu237=) c.597G= (p.Leu199=) | |
2 | g.136115430C>G | CA429206412 | CXCR4 | c.486G>C (p.Leu162=) c.453G>C (p.Leu151=) c.498G>C (p.Leu166=) c.510G>C (p.Leu170=) n.692G>C c.711G>C (p.Leu237=) c.597G>C (p.Leu199=) | dbSNP |
2 | g.136115430C>T | CA429206413 | CXCR4 | c.486G>A (p.Leu162=) c.453G>A (p.Leu151=) c.498G>A (p.Leu166=) c.510G>A (p.Leu170=) n.692G>A c.711G>A (p.Leu237=) c.597G>A (p.Leu199=) | dbSNP |
2 | g.136115431A>C | CA348658751 | CXCR4 | c.485T>G (p.Leu162Arg) c.452T>G (p.Leu151Arg) c.497T>G (p.Leu166Arg) c.509T>G (p.Leu170Arg) n.691T>G c.710T>G (p.Leu237Arg) c.596T>G (p.Leu199Arg) | |
2 | g.136115431A>G | CA348658747 | CXCR4 | c.485T>C (p.Leu162Pro) c.452T>C (p.Leu151Pro) c.497T>C (p.Leu166Pro) c.509T>C (p.Leu170Pro) n.691T>C c.710T>C (p.Leu237Pro) c.596T>C (p.Leu199Pro) | dbSNP |
2 | g.136115431A>T | CA348658749 | CXCR4 | c.485T>A (p.Leu162Gln) c.452T>A (p.Leu151Gln) c.497T>A (p.Leu166Gln) c.509T>A (p.Leu170Gln) n.691T>A c.710T>A (p.Leu237Gln) c.596T>A (p.Leu199Gln) | dbSNP |
2 | g.136115432G>A | CA429206420 | CXCR4 | c.484C>T (p.Leu162=) c.451C>T (p.Leu151=) c.496C>T (p.Leu166=) c.508C>T (p.Leu170=) n.690C>T c.709C>T (p.Leu237=) c.595C>T (p.Leu199=) | |
2 | g.136115432G>C | CA348658753 | CXCR4 | c.484C>G (p.Leu162Val) c.451C>G (p.Leu151Val) c.496C>G (p.Leu166Val) c.508C>G (p.Leu170Val) n.690C>G c.709C>G (p.Leu237Val) c.595C>G (p.Leu199Val) | |
2 | g.136115432G>T | CA348658754 | CXCR4 | c.484C>A (p.Leu162Met) c.451C>A (p.Leu151Met) c.496C>A (p.Leu166Met) c.508C>A (p.Leu170Met) n.690C>A c.709C>A (p.Leu237Met) c.595C>A (p.Leu199Met) | |
2 | g.136115433del | CA2661289449 | CXCR4 | c.484del (p.Leu162CysfsTer2) c.451del (p.Leu151CysfsTer2) c.496del (p.Leu166CysfsTer2) c.508del (p.Leu170CysfsTer2) n.690del c.709del (p.Leu237CysfsTer2) c.595del (p.Leu199CysfsTer2) | gnomAD v4 |
2 | g.136115433G>A | CA429206423 | CXCR4 | c.483C>T (p.Leu161=) c.450C>T (p.Leu150=) c.495C>T (p.Leu165=) c.507C>T (p.Leu169=) n.689C>T c.708C>T (p.Leu236=) c.594C>T (p.Leu198=) | dbSNP |
2 | g.136115433G>C | CA429206422 | CXCR4 | c.483C>G (p.Leu161=) c.450C>G (p.Leu150=) c.495C>G (p.Leu165=) c.507C>G (p.Leu169=) n.689C>G c.708C>G (p.Leu236=) c.594C>G (p.Leu198=) | dbSNP |
2 | g.136115433G>T | CA429206421 | CXCR4 | c.483C>A (p.Leu161=) c.450C>A (p.Leu150=) c.495C>A (p.Leu165=) c.507C>A (p.Leu169=) n.689C>A c.708C>A (p.Leu236=) c.594C>A (p.Leu198=) | |
2 | g.136115434A= | CA1290966050 | CXCR4 | c.482T= (p.Leu161=) c.449T= (p.Leu150=) c.494T= (p.Leu165=) c.506T= (p.Leu169=) n.688T= c.707T= (p.Leu236=) c.593T= (p.Leu198=) | |
2 | g.136115434A>C | CA348658757 | CXCR4 | c.482T>G (p.Leu161Arg) c.449T>G (p.Leu150Arg) c.494T>G (p.Leu165Arg) c.506T>G (p.Leu169Arg) n.688T>G c.707T>G (p.Leu236Arg) c.593T>G (p.Leu198Arg) | |
2 | g.136115434A>G | CA348658759 | CXCR4 | c.482T>C (p.Leu161Pro) c.449T>C (p.Leu150Pro) c.494T>C (p.Leu165Pro) c.506T>C (p.Leu169Pro) n.688T>C c.707T>C (p.Leu236Pro) c.593T>C (p.Leu198Pro) | dbSNP |
2 | g.136115434A>T | CA348658762 | CXCR4 | c.482T>A (p.Leu161His) c.449T>A (p.Leu150His) c.494T>A (p.Leu165His) c.506T>A (p.Leu169His) n.688T>A c.707T>A (p.Leu236His) c.593T>A (p.Leu198His) | dbSNP gnomAD v4 |
2 | g.136115435G>A | CA348658765 | CXCR4 | c.481C>T (p.Leu161Phe) c.448C>T (p.Leu150Phe) c.493C>T (p.Leu165Phe) c.505C>T (p.Leu169Phe) n.687C>T c.706C>T (p.Leu236Phe) c.592C>T (p.Leu198Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115435G>C | CA348658769 | CXCR4 | c.481C>G (p.Leu161Val) c.448C>G (p.Leu150Val) c.493C>G (p.Leu165Val) c.505C>G (p.Leu169Val) n.687C>G c.706C>G (p.Leu236Val) c.592C>G (p.Leu198Val) | |
2 | g.136115435G= | CA1290966051 | CXCR4 | c.481C= (p.Leu161=) c.448C= (p.Leu150=) c.493C= (p.Leu165=) c.505C= (p.Leu169=) n.687C= c.706C= (p.Leu236=) c.592C= (p.Leu198=) | |
2 | g.136115435G>T | CA348658767 | CXCR4 | c.481C>A (p.Leu161Ile) c.448C>A (p.Leu150Ile) c.493C>A (p.Leu165Ile) c.505C>A (p.Leu169Ile) n.687C>A c.706C>A (p.Leu236Ile) c.592C>A (p.Leu198Ile) | |
2 | g.136115436G>A | CA1890114 | CXCR4 | c.480C>T (p.Ala160=) c.447C>T (p.Ala149=) c.492C>T (p.Ala164=) c.504C>T (p.Ala168=) n.686C>T c.705C>T (p.Ala235=) c.591C>T (p.Ala197=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.136115436G>C | CA429206431 | CXCR4 | c.480C>G (p.Ala160=) c.447C>G (p.Ala149=) c.492C>G (p.Ala164=) c.504C>G (p.Ala168=) n.686C>G c.705C>G (p.Ala235=) c.591C>G (p.Ala197=) | dbSNP |
2 | g.136115436G= | CA1290966052 | CXCR4 | c.480C= (p.Ala160=) c.447C= (p.Ala149=) c.492C= (p.Ala164=) c.504C= (p.Ala168=) n.686C= c.705C= (p.Ala235=) c.591C= (p.Ala197=) | |
2 | g.136115436G>T | CA429206430 | CXCR4 | c.480C>A (p.Ala160=) c.447C>A (p.Ala149=) c.492C>A (p.Ala164=) c.504C>A (p.Ala168=) n.686C>A c.705C>A (p.Ala235=) c.591C>A (p.Ala197=) | dbSNP |
2 | g.136115437G>A | CA348658774 | CXCR4 | c.479C>T (p.Ala160Val) c.446C>T (p.Ala149Val) c.491C>T (p.Ala164Val) c.503C>T (p.Ala168Val) n.685C>T c.704C>T (p.Ala235Val) c.590C>T (p.Ala197Val) | dbSNP |
2 | g.136115437G>C | CA348658776 | CXCR4 | c.479C>G (p.Ala160Gly) c.446C>G (p.Ala149Gly) c.491C>G (p.Ala164Gly) c.503C>G (p.Ala168Gly) n.685C>G c.704C>G (p.Ala235Gly) c.590C>G (p.Ala197Gly) | dbSNP |
2 | g.136115437G>T | CA348658779 | CXCR4 | c.479C>A (p.Ala160Asp) c.446C>A (p.Ala149Asp) c.491C>A (p.Ala164Asp) c.503C>A (p.Ala168Asp) n.685C>A c.704C>A (p.Ala235Asp) c.590C>A (p.Ala197Asp) | |
2 | g.136115438C>A | CA348658781 | CXCR4 | c.478G>T (p.Ala160Ser) c.445G>T (p.Ala149Ser) c.490G>T (p.Ala164Ser) c.502G>T (p.Ala168Ser) n.684G>T c.703G>T (p.Ala235Ser) c.589G>T (p.Ala197Ser) | dbSNP |
2 | g.136115438C>G | CA348658784 | CXCR4 | c.478G>C (p.Ala160Pro) c.445G>C (p.Ala149Pro) c.490G>C (p.Ala164Pro) c.502G>C (p.Ala168Pro) n.684G>C c.703G>C (p.Ala235Pro) c.589G>C (p.Ala197Pro) | dbSNP |
2 | g.136115438C>T | CA348658786 | CXCR4 | c.478G>A (p.Ala160Thr) c.445G>A (p.Ala149Thr) c.490G>A (p.Ala164Thr) c.502G>A (p.Ala168Thr) n.684G>A c.703G>A (p.Ala235Thr) c.589G>A (p.Ala197Thr) | dbSNP gnomAD v4 |
2 | g.136115439A>C | CA429206433 | CXCR4 | c.477T>G (p.Pro159=) c.444T>G (p.Pro148=) c.489T>G (p.Pro163=) c.501T>G (p.Pro167=) n.683T>G c.702T>G (p.Pro234=) c.588T>G (p.Pro196=) | |
2 | g.136115439A>G | CA429206434 | CXCR4 | c.477T>C (p.Pro159=) c.444T>C (p.Pro148=) c.489T>C (p.Pro163=) c.501T>C (p.Pro167=) n.683T>C c.702T>C (p.Pro234=) c.588T>C (p.Pro196=) | |
2 | g.136115439A>T | CA429206436 | CXCR4 | c.477T>A (p.Pro159=) c.444T>A (p.Pro148=) c.489T>A (p.Pro163=) c.501T>A (p.Pro167=) n.683T>A c.702T>A (p.Pro234=) c.588T>A (p.Pro196=) | |
2 | g.136115440G>A | CA348658787 | CXCR4 | c.476C>T (p.Pro159Leu) c.443C>T (p.Pro148Leu) c.488C>T (p.Pro163Leu) c.500C>T (p.Pro167Leu) n.682C>T c.701C>T (p.Pro234Leu) c.587C>T (p.Pro196Leu) | dbSNP |
2 | g.136115440G>C | CA348658788 | CXCR4 | c.476C>G (p.Pro159Arg) c.443C>G (p.Pro148Arg) c.488C>G (p.Pro163Arg) c.500C>G (p.Pro167Arg) n.682C>G c.701C>G (p.Pro234Arg) c.587C>G (p.Pro196Arg) | dbSNP |
2 | g.136115440G>T | CA348658789 | CXCR4 | c.476C>A (p.Pro159His) c.443C>A (p.Pro148His) c.488C>A (p.Pro163His) c.500C>A (p.Pro167His) n.682C>A c.701C>A (p.Pro234His) c.587C>A (p.Pro196His) | dbSNP |
2 | g.136115441G>A | CA348658794 | CXCR4 | c.475C>T (p.Pro159Ser) c.442C>T (p.Pro148Ser) c.487C>T (p.Pro163Ser) c.499C>T (p.Pro167Ser) n.681C>T c.700C>T (p.Pro234Ser) c.586C>T (p.Pro196Ser) | dbSNP gnomAD v4 |
2 | g.136115441G>C | CA348658791 | CXCR4 | c.475C>G (p.Pro159Ala) c.442C>G (p.Pro148Ala) c.487C>G (p.Pro163Ala) c.499C>G (p.Pro167Ala) n.681C>G c.700C>G (p.Pro234Ala) c.586C>G (p.Pro196Ala) | dbSNP |
2 | g.136115441G>T | CA348658790 | CXCR4 | c.475C>A (p.Pro159Thr) c.442C>A (p.Pro148Thr) c.487C>A (p.Pro163Thr) c.499C>A (p.Pro167Thr) n.681C>A c.700C>A (p.Pro234Thr) c.586C>A (p.Pro196Thr) | dbSNP |
2 | g.136115442G>A | CA429206437 | CXCR4 | c.474C>T (p.Ile158=) c.441C>T (p.Ile147=) c.486C>T (p.Ile162=) c.498C>T (p.Ile166=) n.680C>T c.699C>T (p.Ile233=) c.585C>T (p.Ile195=) | dbSNP |
2 | g.136115442G>C | CA348658795 | CXCR4 | c.474C>G (p.Ile158Met) c.441C>G (p.Ile147Met) c.486C>G (p.Ile162Met) c.498C>G (p.Ile166Met) n.680C>G c.699C>G (p.Ile233Met) c.585C>G (p.Ile195Met) | dbSNP |
2 | g.136115442G>T | CA429206438 | CXCR4 | c.474C>A (p.Ile158=) c.441C>A (p.Ile147=) c.486C>A (p.Ile162=) c.498C>A (p.Ile166=) n.680C>A c.699C>A (p.Ile233=) c.585C>A (p.Ile195=) | |
2 | g.136115443A>C | CA348658798 | CXCR4 | c.473T>G (p.Ile158Ser) c.440T>G (p.Ile147Ser) c.485T>G (p.Ile162Ser) c.497T>G (p.Ile166Ser) n.679T>G c.698T>G (p.Ile233Ser) c.584T>G (p.Ile195Ser) | dbSNP |
2 | g.136115443A>G | CA348658799 | CXCR4 | c.473T>C (p.Ile158Thr) c.440T>C (p.Ile147Thr) c.485T>C (p.Ile162Thr) c.497T>C (p.Ile166Thr) n.679T>C c.698T>C (p.Ile233Thr) c.584T>C (p.Ile195Thr) | |
2 | g.136115443A>T | CA348658801 | CXCR4 | c.473T>A (p.Ile158Asn) c.440T>A (p.Ile147Asn) c.485T>A (p.Ile162Asn) c.497T>A (p.Ile166Asn) n.679T>A c.698T>A (p.Ile233Asn) c.584T>A (p.Ile195Asn) | dbSNP |
2 | g.136115444T>A | CA348658804 | CXCR4 | c.472A>T (p.Ile158Phe) c.439A>T (p.Ile147Phe) c.484A>T (p.Ile162Phe) c.496A>T (p.Ile166Phe) n.678A>T c.697A>T (p.Ile233Phe) c.583A>T (p.Ile195Phe) | |
2 | g.136115444T>C | CA348658806 | CXCR4 | c.472A>G (p.Ile158Val) c.439A>G (p.Ile147Val) c.484A>G (p.Ile162Val) c.496A>G (p.Ile166Val) n.678A>G c.697A>G (p.Ile233Val) c.583A>G (p.Ile195Val) | |
2 | g.136115444T>G | CA348658808 | CXCR4 | c.472A>C (p.Ile158Leu) c.439A>C (p.Ile147Leu) c.484A>C (p.Ile162Leu) c.496A>C (p.Ile166Leu) n.678A>C c.697A>C (p.Ile233Leu) c.583A>C (p.Ile195Leu) | |
2 | g.136115445C>A | CA348658810 | CXCR4 | c.471G>T (p.Trp157Cys) c.438G>T (p.Trp146Cys) c.483G>T (p.Trp161Cys) c.495G>T (p.Trp165Cys) n.677G>T c.696G>T (p.Trp232Cys) c.582G>T (p.Trp194Cys) | dbSNP |
2 | g.136115445C= | CA1290966053 | CXCR4 | c.471G= (p.Trp157=) c.438G= (p.Trp146=) c.483G= (p.Trp161=) c.495G= (p.Trp165=) n.677G= c.696G= (p.Trp232=) c.582G= (p.Trp194=) | |
2 | g.136115445C>G | CA348658813 | CXCR4 | c.471G>C (p.Trp157Cys) c.438G>C (p.Trp146Cys) c.483G>C (p.Trp161Cys) c.495G>C (p.Trp165Cys) n.677G>C c.696G>C (p.Trp232Cys) c.582G>C (p.Trp194Cys) | dbSNP |
2 | g.136115445C>T | CA348658815 | CXCR4 | c.471G>A (p.Trp157Ter) c.438G>A (p.Trp146Ter) c.483G>A (p.Trp161Ter) c.495G>A (p.Trp165Ter) n.677G>A c.696G>A (p.Trp232Ter) c.582G>A (p.Trp194Ter) | dbSNP |
2 | g.136115446C>A | CA348658818 | CXCR4 | c.470G>T (p.Trp157Leu) c.437G>T (p.Trp146Leu) c.482G>T (p.Trp161Leu) c.494G>T (p.Trp165Leu) n.676G>T c.695G>T (p.Trp232Leu) c.581G>T (p.Trp194Leu) | |
2 | g.136115446C>G | CA348658821 | CXCR4 | c.470G>C (p.Trp157Ser) c.437G>C (p.Trp146Ser) c.482G>C (p.Trp161Ser) c.494G>C (p.Trp165Ser) n.676G>C c.695G>C (p.Trp232Ser) c.581G>C (p.Trp194Ser) | dbSNP |
2 | g.136115446C>T | CA348658822 | CXCR4 | c.470G>A (p.Trp157Ter) c.437G>A (p.Trp146Ter) c.482G>A (p.Trp161Ter) c.494G>A (p.Trp165Ter) n.676G>A c.695G>A (p.Trp232Ter) c.581G>A (p.Trp194Ter) | dbSNP |
2 | g.136115447A>C | CA348658828 | CXCR4 | c.469T>G (p.Trp157Gly) c.436T>G (p.Trp146Gly) c.481T>G (p.Trp161Gly) c.493T>G (p.Trp165Gly) n.675T>G c.694T>G (p.Trp232Gly) c.580T>G (p.Trp194Gly) | |
2 | g.136115447A>G | CA348658824 | CXCR4 | c.469T>C (p.Trp157Arg) c.436T>C (p.Trp146Arg) c.481T>C (p.Trp161Arg) c.493T>C (p.Trp165Arg) n.675T>C c.694T>C (p.Trp232Arg) c.580T>C (p.Trp194Arg) | dbSNP |
2 | g.136115447A>T | CA348658825 | CXCR4 | c.469T>A (p.Trp157Arg) c.436T>A (p.Trp146Arg) c.481T>A (p.Trp161Arg) c.493T>A (p.Trp165Arg) n.675T>A c.694T>A (p.Trp232Arg) c.580T>A (p.Trp194Arg) | |
2 | g.136115448G>A | CA429206446 | CXCR4 | c.468C>T (p.Val156=) c.435C>T (p.Val145=) c.480C>T (p.Val160=) c.492C>T (p.Val164=) n.674C>T c.693C>T (p.Val231=) c.579C>T (p.Val193=) | dbSNP COSMIC COSMIC |
2 | g.136115448G>C | CA429206448 | CXCR4 | c.468C>G (p.Val156=) c.435C>G (p.Val145=) c.480C>G (p.Val160=) c.492C>G (p.Val164=) n.674C>G c.693C>G (p.Val231=) c.579C>G (p.Val193=) | dbSNP COSMIC COSMIC |
2 | g.136115448G>T | CA429206449 | CXCR4 | c.468C>A (p.Val156=) c.435C>A (p.Val145=) c.480C>A (p.Val160=) c.492C>A (p.Val164=) n.674C>A c.693C>A (p.Val231=) c.579C>A (p.Val193=) | dbSNP |
2 | g.136115449A>C | CA348658830 | CXCR4 | c.467T>G (p.Val156Gly) c.434T>G (p.Val145Gly) c.479T>G (p.Val160Gly) c.491T>G (p.Val164Gly) n.673T>G c.692T>G (p.Val231Gly) c.578T>G (p.Val193Gly) | |
2 | g.136115449A>G | CA348658832 | CXCR4 | c.467T>C (p.Val156Ala) c.434T>C (p.Val145Ala) c.479T>C (p.Val160Ala) c.491T>C (p.Val164Ala) n.673T>C c.692T>C (p.Val231Ala) c.578T>C (p.Val193Ala) | dbSNP |
2 | g.136115449A>T | CA348658833 | CXCR4 | c.467T>A (p.Val156Asp) c.434T>A (p.Val145Asp) c.479T>A (p.Val160Asp) c.491T>A (p.Val164Asp) n.673T>A c.692T>A (p.Val231Asp) c.578T>A (p.Val193Asp) | |
2 | g.136115449dup | CA2577108867 | CXCR4 | c.467dup (p.Trp157LeufsTer19) c.434dup (p.Trp146LeufsTer19) c.479dup (p.Trp161LeufsTer19) c.491dup (p.Trp165LeufsTer19) n.673dup c.692dup (p.Trp232LeufsTer19) c.578dup (p.Trp194LeufsTer19) | |
2 | g.136115450C>A | CA348658835 | CXCR4 | c.466G>T (p.Val156Phe) c.433G>T (p.Val145Phe) c.478G>T (p.Val160Phe) c.490G>T (p.Val164Phe) n.672G>T c.691G>T (p.Val231Phe) c.577G>T (p.Val193Phe) | dbSNP |
2 | g.136115450C= | CA1290966054 | CXCR4 | c.466G= (p.Val156=) c.433G= (p.Val145=) c.478G= (p.Val160=) c.490G= (p.Val164=) n.672G= c.691G= (p.Val231=) c.577G= (p.Val193=) | |
2 | g.136115450C>G | CA348658838 | CXCR4 | c.466G>C (p.Val156Leu) c.433G>C (p.Val145Leu) c.478G>C (p.Val160Leu) c.490G>C (p.Val164Leu) n.672G>C c.691G>C (p.Val231Leu) c.577G>C (p.Val193Leu) | dbSNP |
2 | g.136115450C>T | CA1890115 | CXCR4 | c.466G>A (p.Val156Ile) c.433G>A (p.Val145Ile) c.478G>A (p.Val160Ile) c.490G>A (p.Val164Ile) n.672G>A c.691G>A (p.Val231Ile) c.577G>A (p.Val193Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115451G>A | CA429206452 | CXCR4 | c.465C>T (p.Gly155=) c.432C>T (p.Gly144=) c.477C>T (p.Gly159=) c.489C>T (p.Gly163=) n.671C>T c.690C>T (p.Gly230=) c.576C>T (p.Gly192=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115451G>C | CA429206454 | CXCR4 | c.465C>G (p.Gly155=) c.432C>G (p.Gly144=) c.477C>G (p.Gly159=) c.489C>G (p.Gly163=) n.671C>G c.690C>G (p.Gly230=) c.576C>G (p.Gly192=) | dbSNP |
2 | g.136115451G= | CA1290966055 | CXCR4 | c.465C= (p.Gly155=) c.432C= (p.Gly144=) c.477C= (p.Gly159=) c.489C= (p.Gly163=) n.671C= c.690C= (p.Gly230=) c.576C= (p.Gly192=) | |
2 | g.136115451G>T | CA429206453 | CXCR4 | c.465C>A (p.Gly155=) c.432C>A (p.Gly144=) c.477C>A (p.Gly159=) c.489C>A (p.Gly163=) n.671C>A c.690C>A (p.Gly230=) c.576C>A (p.Gly192=) | dbSNP |
2 | g.136115452C>A | CA348658841 | CXCR4 | c.464G>T (p.Gly155Val) c.431G>T (p.Gly144Val) c.476G>T (p.Gly159Val) c.488G>T (p.Gly163Val) n.670G>T c.689G>T (p.Gly230Val) c.575G>T (p.Gly192Val) | dbSNP |
2 | g.136115452C>G | CA348658843 | CXCR4 | c.464G>C (p.Gly155Ala) c.431G>C (p.Gly144Ala) c.476G>C (p.Gly159Ala) c.488G>C (p.Gly163Ala) n.670G>C c.689G>C (p.Gly230Ala) c.575G>C (p.Gly192Ala) | dbSNP |
2 | g.136115452C>T | CA348658844 | CXCR4 | c.464G>A (p.Gly155Asp) c.431G>A (p.Gly144Asp) c.476G>A (p.Gly159Asp) c.488G>A (p.Gly163Asp) n.670G>A c.689G>A (p.Gly230Asp) c.575G>A (p.Gly192Asp) | dbSNP |
2 | g.136115453C>A | CA56886523 | CXCR4 | c.463G>T (p.Gly155Cys) c.430G>T (p.Gly144Cys) c.475G>T (p.Gly159Cys) c.487G>T (p.Gly163Cys) n.669G>T c.688G>T (p.Gly230Cys) c.574G>T (p.Gly192Cys) | dbSNP gnomAD v4 |
2 | g.136115453C= | CA1290966056 | CXCR4 | c.463G= (p.Gly155=) c.430G= (p.Gly144=) c.475G= (p.Gly159=) c.487G= (p.Gly163=) n.669G= c.688G= (p.Gly230=) c.574G= (p.Gly192=) | |
2 | g.136115453C>G | CA348658845 | CXCR4 | c.463G>C (p.Gly155Arg) c.430G>C (p.Gly144Arg) c.475G>C (p.Gly159Arg) c.487G>C (p.Gly163Arg) n.669G>C c.688G>C (p.Gly230Arg) c.574G>C (p.Gly192Arg) | dbSNP |
2 | g.136115453C>T | CA348658847 | CXCR4 | c.463G>A (p.Gly155Ser) c.430G>A (p.Gly144Ser) c.475G>A (p.Gly159Ser) c.487G>A (p.Gly163Ser) n.669G>A c.688G>A (p.Gly230Ser) c.574G>A (p.Gly192Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.136115454A= | CA1290966057 | CXCR4 | c.462T= (p.Val154=) c.429T= (p.Val143=) c.474T= (p.Val158=) c.486T= (p.Val162=) n.668T= c.687T= (p.Val229=) c.573T= (p.Val191=) | |
2 | g.136115454A>C | CA429206457 | CXCR4 | c.462T>G (p.Val154=) c.429T>G (p.Val143=) c.474T>G (p.Val158=) c.486T>G (p.Val162=) n.668T>G c.687T>G (p.Val229=) c.573T>G (p.Val191=) | |
2 | g.136115454A>G | CA56886525 | CXCR4 | c.462T>C (p.Val154=) c.429T>C (p.Val143=) c.474T>C (p.Val158=) c.486T>C (p.Val162=) n.668T>C c.687T>C (p.Val229=) c.573T>C (p.Val191=) | dbSNP |
2 | g.136115454A>T | CA429206459 | CXCR4 | c.462T>A (p.Val154=) c.429T>A (p.Val143=) c.474T>A (p.Val158=) c.486T>A (p.Val162=) n.668T>A c.687T>A (p.Val229=) c.573T>A (p.Val191=) | dbSNP |
2 | g.136115455A= | CA1290966058 | CXCR4 | c.461T= (p.Val154=) c.428T= (p.Val143=) c.473T= (p.Val158=) c.485T= (p.Val162=) n.667T= c.686T= (p.Val229=) c.572T= (p.Val191=) | |
2 | g.136115455A>C | CA348658852 | CXCR4 | c.461T>G (p.Val154Gly) c.428T>G (p.Val143Gly) c.473T>G (p.Val158Gly) c.485T>G (p.Val162Gly) n.667T>G c.686T>G (p.Val229Gly) c.572T>G (p.Val191Gly) | |
2 | g.136115455A>G | CA1890116 | CXCR4 | c.461T>C (p.Val154Ala) c.428T>C (p.Val143Ala) c.473T>C (p.Val158Ala) c.485T>C (p.Val162Ala) n.667T>C c.686T>C (p.Val229Ala) c.572T>C (p.Val191Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.136115455A>T | CA348658850 | CXCR4 | c.461T>A (p.Val154Asp) c.428T>A (p.Val143Asp) c.473T>A (p.Val158Asp) c.485T>A (p.Val162Asp) n.667T>A c.686T>A (p.Val229Asp) c.572T>A (p.Val191Asp) | dbSNP gnomAD v4 |
2 | g.136115455_136115469dup | CA536548296 | CXCR4 | c.447_461dup (p.Val154_Gly155insLysValValTyrVal) c.414_428dup (p.Val143_Gly144insLysValValTyrVal) c.459_473dup (p.Val158_Gly159insLysValValTyrVal) c.471_485dup (p.Val162_Gly163insLysValValTyrVal) n.653_667dup c.672_686dup (p.Val229_Gly230insLysValValTyrVal) c.558_572dup (p.Val191_Gly192insLysValValTyrVal) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.136115456C>A | CA348658856 | CXCR4 | c.460G>T (p.Val154Phe) c.427G>T (p.Val143Phe) c.472G>T (p.Val158Phe) c.484G>T (p.Val162Phe) n.666G>T c.685G>T (p.Val229Phe) c.571G>T (p.Val191Phe) | dbSNP |
2 | g.136115456C>G | CA348658860 | CXCR4 | c.460G>C (p.Val154Leu) c.427G>C (p.Val143Leu) c.472G>C (p.Val158Leu) c.484G>C (p.Val162Leu) n.666G>C c.685G>C (p.Val229Leu) c.571G>C (p.Val191Leu) | dbSNP |
2 | g.136115456C>T | CA348658859 | CXCR4 | c.460G>A (p.Val154Ile) c.427G>A (p.Val143Ile) c.472G>A (p.Val158Ile) c.484G>A (p.Val162Ile) n.666G>A c.685G>A (p.Val229Ile) c.571G>A (p.Val191Ile) | dbSNP |
2 | g.136115457A>C | CA348658861 | CXCR4 | c.459T>G (p.Tyr153Ter) c.426T>G (p.Tyr142Ter) c.471T>G (p.Tyr157Ter) c.483T>G (p.Tyr161Ter) n.665T>G c.684T>G (p.Tyr228Ter) c.570T>G (p.Tyr190Ter) | |
2 | g.136115457A>G | CA429206465 | CXCR4 | c.459T>C (p.Tyr153=) c.426T>C (p.Tyr142=) c.471T>C (p.Tyr157=) c.483T>C (p.Tyr161=) n.665T>C c.684T>C (p.Tyr228=) c.570T>C (p.Tyr190=) | |
2 | g.136115457A>T | CA348658863 | CXCR4 | c.459T>A (p.Tyr153Ter) c.426T>A (p.Tyr142Ter) c.471T>A (p.Tyr157Ter) c.483T>A (p.Tyr161Ter) n.665T>A c.684T>A (p.Tyr228Ter) c.570T>A (p.Tyr190Ter) | dbSNP |
2 | g.136115458T>A | CA348658867 | CXCR4 | c.458A>T (p.Tyr153Phe) c.425A>T (p.Tyr142Phe) c.470A>T (p.Tyr157Phe) c.482A>T (p.Tyr161Phe) n.664A>T c.683A>T (p.Tyr228Phe) c.569A>T (p.Tyr190Phe) | dbSNP |
2 | g.136115458T>C | CA56886527 | CXCR4 | c.458A>G (p.Tyr153Cys) c.425A>G (p.Tyr142Cys) c.470A>G (p.Tyr157Cys) c.482A>G (p.Tyr161Cys) n.664A>G c.683A>G (p.Tyr228Cys) c.569A>G (p.Tyr190Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115458T>G | CA348658871 | CXCR4 | c.458A>C (p.Tyr153Ser) c.425A>C (p.Tyr142Ser) c.470A>C (p.Tyr157Ser) c.482A>C (p.Tyr161Ser) n.664A>C c.683A>C (p.Tyr228Ser) c.569A>C (p.Tyr190Ser) | |
2 | g.136115458T= | CA1290966059 | CXCR4 | c.458A= (p.Tyr153=) c.425A= (p.Tyr142=) c.470A= (p.Tyr157=) c.482A= (p.Tyr161=) n.664A= c.683A= (p.Tyr228=) c.569A= (p.Tyr190=) | |
2 | g.136115459A>C | CA348658872 | CXCR4 | c.457T>G (p.Tyr153Asp) c.424T>G (p.Tyr142Asp) c.469T>G (p.Tyr157Asp) c.481T>G (p.Tyr161Asp) n.663T>G c.682T>G (p.Tyr228Asp) c.568T>G (p.Tyr190Asp) | |
2 | g.136115459A>G | CA348658874 | CXCR4 | c.457T>C (p.Tyr153His) c.424T>C (p.Tyr142His) c.469T>C (p.Tyr157His) c.481T>C (p.Tyr161His) n.663T>C c.682T>C (p.Tyr228His) c.568T>C (p.Tyr190His) | dbSNP |
2 | g.136115459A>T | CA348658875 | CXCR4 | c.457T>A (p.Tyr153Asn) c.424T>A (p.Tyr142Asn) c.469T>A (p.Tyr157Asn) c.481T>A (p.Tyr161Asn) n.663T>A c.682T>A (p.Tyr228Asn) c.568T>A (p.Tyr190Asn) | |
2 | g.136115459_136115461del | CA2661289450 | CXCR4 | c.455_457del (p.Val152_Tyr153delinsAsp) c.422_424del (p.Val141_Tyr142delinsAsp) c.467_469del (p.Val156_Tyr157delinsAsp) c.479_481del (p.Val160_Tyr161delinsAsp) n.661_663del c.680_682del (p.Val227_Tyr228delinsAsp) c.566_568del (p.Val189_Tyr190delinsAsp) | gnomAD v4 |
2 | g.136115460G>A | CA429206470 | CXCR4 | c.456C>T (p.Val152=) c.423C>T (p.Val141=) c.468C>T (p.Val156=) c.480C>T (p.Val160=) n.662C>T c.681C>T (p.Val227=) c.567C>T (p.Val189=) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.136115460G>C | CA429206471 | CXCR4 | c.456C>G (p.Val152=) c.423C>G (p.Val141=) c.468C>G (p.Val156=) c.480C>G (p.Val160=) n.662C>G c.681C>G (p.Val227=) c.567C>G (p.Val189=) | dbSNP |
2 | g.136115460G= | CA1290966060 | CXCR4 | c.456C= (p.Val152=) c.423C= (p.Val141=) c.468C= (p.Val156=) c.480C= (p.Val160=) n.662C= c.681C= (p.Val227=) c.567C= (p.Val189=) | |
2 | g.136115460G>T | CA429206473 | CXCR4 | c.456C>A (p.Val152=) c.423C>A (p.Val141=) c.468C>A (p.Val156=) c.480C>A (p.Val160=) n.662C>A c.681C>A (p.Val227=) c.567C>A (p.Val189=) | dbSNP COSMIC COSMIC |
2 | g.136115461A>C | CA348658876 | CXCR4 | c.455T>G (p.Val152Gly) c.422T>G (p.Val141Gly) c.467T>G (p.Val156Gly) c.479T>G (p.Val160Gly) n.661T>G c.680T>G (p.Val227Gly) c.566T>G (p.Val189Gly) | |
2 | g.136115461A>G | CA348658877 | CXCR4 | c.455T>C (p.Val152Ala) c.422T>C (p.Val141Ala) c.467T>C (p.Val156Ala) c.479T>C (p.Val160Ala) n.661T>C c.680T>C (p.Val227Ala) c.566T>C (p.Val189Ala) | |
2 | g.136115461A>T | CA348658880 | CXCR4 | c.455T>A (p.Val152Asp) c.422T>A (p.Val141Asp) c.467T>A (p.Val156Asp) c.479T>A (p.Val160Asp) n.661T>A c.680T>A (p.Val227Asp) c.566T>A (p.Val189Asp) | gnomAD v4 |
2 | g.136115462C>A | CA348658882 | CXCR4 | c.454G>T (p.Val152Phe) c.421G>T (p.Val141Phe) c.466G>T (p.Val156Phe) c.478G>T (p.Val160Phe) n.660G>T c.679G>T (p.Val227Phe) c.565G>T (p.Val189Phe) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.136115462C= | CA1290966061 | CXCR4 | c.454G= (p.Val152=) c.421G= (p.Val141=) c.466G= (p.Val156=) c.478G= (p.Val160=) n.660G= c.679G= (p.Val227=) c.565G= (p.Val189=) | |
2 | g.136115462C>G | CA348658884 | CXCR4 | c.454G>C (p.Val152Leu) c.421G>C (p.Val141Leu) c.466G>C (p.Val156Leu) c.478G>C (p.Val160Leu) n.660G>C c.679G>C (p.Val227Leu) c.565G>C (p.Val189Leu) | |
2 | g.136115462C>T | CA348658886 | CXCR4 | c.454G>A (p.Val152Ile) c.421G>A (p.Val141Ile) c.466G>A (p.Val156Ile) c.478G>A (p.Val160Ile) n.660G>A c.679G>A (p.Val227Ile) c.565G>A (p.Val189Ile) | COSMIC COSMIC |
2 | g.136115463C>A | CA429206474 | CXCR4 | c.453G>T (p.Val151=) c.420G>T (p.Val140=) c.465G>T (p.Val155=) c.477G>T (p.Val159=) n.659G>T c.678G>T (p.Val226=) c.564G>T (p.Val188=) | |
2 | g.136115463C>G | CA429206475 | CXCR4 | c.453G>C (p.Val151=) c.420G>C (p.Val140=) c.465G>C (p.Val155=) c.477G>C (p.Val159=) n.659G>C c.678G>C (p.Val226=) c.564G>C (p.Val188=) | |
2 | g.136115463C>T | CA429206476 | CXCR4 | c.453G>A (p.Val151=) c.420G>A (p.Val140=) c.465G>A (p.Val155=) c.477G>A (p.Val159=) n.659G>A c.678G>A (p.Val226=) c.564G>A (p.Val188=) | |
2 | g.136115463_136115464delinsCA | CA1290966062 | CXCR4 | c.452_453delinsTG (p.Val151=) c.419_420delinsTG (p.Val140=) c.464_465delinsTG (p.Val155=) c.476_477delinsTG (p.Val159=) n.658_659delinsTG c.677_678delinsTG (p.Val226=) c.563_564delinsTG (p.Val188=) | |
2 | g.136115464del | CA1036829506 | CXCR4 | c.452del (p.Val151GlyfsTer13) c.419del (p.Val140GlyfsTer13) c.464del (p.Val155GlyfsTer13) c.476del (p.Val159GlyfsTer13) n.658del c.677del (p.Val226GlyfsTer13) c.563del (p.Val188GlyfsTer13) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.136115464A>C | CA348658892 | CXCR4 | c.452T>G (p.Val151Gly) c.419T>G (p.Val140Gly) c.464T>G (p.Val155Gly) c.476T>G (p.Val159Gly) n.658T>G c.677T>G (p.Val226Gly) c.563T>G (p.Val188Gly) | |
2 | g.136115464A>G | CA348658891 | CXCR4 | c.452T>C (p.Val151Ala) c.419T>C (p.Val140Ala) c.464T>C (p.Val155Ala) c.476T>C (p.Val159Ala) n.658T>C c.677T>C (p.Val226Ala) c.563T>C (p.Val188Ala) | gnomAD v4 |
2 | g.136115464A>T | CA348658889 | CXCR4 | c.452T>A (p.Val151Glu) c.419T>A (p.Val140Glu) c.464T>A (p.Val155Glu) c.476T>A (p.Val159Glu) n.658T>A c.677T>A (p.Val226Glu) c.563T>A (p.Val188Glu) | |
2 | g.136115465C>A | CA348658895 | CXCR4 | c.451G>T (p.Val151Leu) c.418G>T (p.Val140Leu) c.463G>T (p.Val155Leu) c.475G>T (p.Val159Leu) n.657G>T c.676G>T (p.Val226Leu) c.562G>T (p.Val188Leu) | gnomAD v4 |
2 | g.136115465C>G | CA348658897 | CXCR4 | c.451G>C (p.Val151Leu) c.418G>C (p.Val140Leu) c.463G>C (p.Val155Leu) c.475G>C (p.Val159Leu) n.657G>C c.676G>C (p.Val226Leu) c.562G>C (p.Val188Leu) | dbSNP gnomAD v4 |
2 | g.136115465C>T | CA348658900 | CXCR4 | c.451G>A (p.Val151Met) c.418G>A (p.Val140Met) c.463G>A (p.Val155Met) c.475G>A (p.Val159Met) n.657G>A c.676G>A (p.Val226Met) c.562G>A (p.Val188Met) | dbSNP COSMIC COSMIC |
2 | g.136115466C>A | CA348658902 | CXCR4 | c.450G>T (p.Lys150Asn) c.417G>T (p.Lys139Asn) c.462G>T (p.Lys154Asn) c.474G>T (p.Lys158Asn) n.656G>T c.675G>T (p.Lys225Asn) c.561G>T (p.Lys187Asn) | |
2 | g.136115466C>G | CA348658905 | CXCR4 | c.450G>C (p.Lys150Asn) c.417G>C (p.Lys139Asn) c.462G>C (p.Lys154Asn) c.474G>C (p.Lys158Asn) n.656G>C c.675G>C (p.Lys225Asn) c.561G>C (p.Lys187Asn) | |
2 | g.136115466C>T | CA429206479 | CXCR4 | c.450G>A (p.Lys150=) c.417G>A (p.Lys139=) c.462G>A (p.Lys154=) c.474G>A (p.Lys158=) n.656G>A c.675G>A (p.Lys225=) c.561G>A (p.Lys187=) | |
2 | g.136115466_136115467delinsCT | CA1290966063 | CXCR4 | c.449_450delinsAG (p.Lys150=) c.416_417delinsAG (p.Lys139=) c.461_462delinsAG (p.Lys154=) c.473_474delinsAG (p.Lys158=) n.655_656delinsAG c.674_675delinsAG (p.Lys225=) c.560_561delinsAG (p.Lys187=) | |
2 | g.136115467T>A | CA348658907 | CXCR4 | c.449A>T (p.Lys150Met) c.416A>T (p.Lys139Met) c.461A>T (p.Lys154Met) c.473A>T (p.Lys158Met) n.655A>T c.674A>T (p.Lys225Met) c.560A>T (p.Lys187Met) | |
2 | g.136115467T>C | CA348658909 | CXCR4 | c.449A>G (p.Lys150Arg) c.416A>G (p.Lys139Arg) c.461A>G (p.Lys154Arg) c.473A>G (p.Lys158Arg) n.655A>G c.674A>G (p.Lys225Arg) c.560A>G (p.Lys187Arg) | |
2 | g.136115467T>G | CA348658911 | CXCR4 | c.449A>C (p.Lys150Thr) c.416A>C (p.Lys139Thr) c.461A>C (p.Lys154Thr) c.473A>C (p.Lys158Thr) n.655A>C c.674A>C (p.Lys225Thr) c.560A>C (p.Lys187Thr) | |
2 | g.136115470dup | CA2842108662 | CXCR4 | c.449dup (p.Val151GlyfsTer25) c.416dup (p.Val140GlyfsTer25) c.461dup (p.Val155GlyfsTer25) c.473dup (p.Val159GlyfsTer25) n.655dup c.674dup (p.Val226GlyfsTer25) c.560dup (p.Val188GlyfsTer25) | |
2 | g.136115470del | CA56886529 | CXCR4 | c.449del (p.Lys150ArgfsTer14) c.416del (p.Lys139ArgfsTer14) c.461del (p.Lys154ArgfsTer14) c.473del (p.Lys158ArgfsTer14) n.655del c.674del (p.Lys225ArgfsTer14) c.560del (p.Lys187ArgfsTer14) | dbSNP |
2 | g.136115468T>A | CA348658913 | CXCR4 | c.448A>T (p.Lys150Ter) c.415A>T (p.Lys139Ter) c.460A>T (p.Lys154Ter) c.472A>T (p.Lys158Ter) n.654A>T c.673A>T (p.Lys225Ter) c.559A>T (p.Lys187Ter) | |
2 | g.136115468T>C | CA348658916 | CXCR4 | c.448A>G (p.Lys150Glu) c.415A>G (p.Lys139Glu) c.460A>G (p.Lys154Glu) c.472A>G (p.Lys158Glu) n.654A>G c.673A>G (p.Lys225Glu) c.559A>G (p.Lys187Glu) | dbSNP |
2 | g.136115468T>G | CA348658918 | CXCR4 | c.448A>C (p.Lys150Gln) c.415A>C (p.Lys139Gln) c.460A>C (p.Lys154Gln) c.472A>C (p.Lys158Gln) n.654A>C c.673A>C (p.Lys225Gln) c.559A>C (p.Lys187Gln) | |
2 | g.136115469T>A | CA348658920 | CXCR4 | c.447A>T (p.Glu149Asp) c.414A>T (p.Glu138Asp) c.459A>T (p.Glu153Asp) c.471A>T (p.Glu157Asp) n.653A>T c.672A>T (p.Glu224Asp) c.558A>T (p.Glu186Asp) | |
2 | g.136115469T>C | CA429206487 | CXCR4 | c.447A>G (p.Glu149=) c.414A>G (p.Glu138=) c.459A>G (p.Glu153=) c.471A>G (p.Glu157=) n.653A>G c.672A>G (p.Glu224=) c.558A>G (p.Glu186=) | |
2 | g.136115469T>G | CA348658922 | CXCR4 | c.447A>C (p.Glu149Asp) c.414A>C (p.Glu138Asp) c.459A>C (p.Glu153Asp) c.471A>C (p.Glu157Asp) n.653A>C c.672A>C (p.Glu224Asp) c.558A>C (p.Glu186Asp) | gnomAD v4 |
2 | g.136115469_136115470insGGAAAAATATCCATG | CA2700535354 | CXCR4 | c.446_447insCATGGATATTTTTCC (p.Glu149delinsAspMetAspIlePhePro) c.413_414insCATGGATATTTTTCC (p.Glu138delinsAspMetAspIlePhePro) c.458_459insCATGGATATTTTTCC (p.Glu153delinsAspMetAspIlePhePro) c.470_471insCATGGATATTTTTCC (p.Glu157delinsAspMetAspIlePhePro) n.652_653insCATGGATATTTTTCC c.671_672insCATGGATATTTTTCC (p.Glu224delinsAspMetAspIlePhePro) c.557_558insCATGGATATTTTTCC (p.Glu186delinsAspMetAspIlePhePro) | dbSNP |
2 | g.136115470T>A | CA348658927 | CXCR4 | c.446A>T (p.Glu149Val) c.413A>T (p.Glu138Val) c.458A>T (p.Glu153Val) c.470A>T (p.Glu157Val) n.652A>T c.671A>T (p.Glu224Val) c.557A>T (p.Glu186Val) | |
2 | g.136115470T>C | CA348658930 | CXCR4 | c.446A>G (p.Glu149Gly) c.413A>G (p.Glu138Gly) c.458A>G (p.Glu153Gly) c.470A>G (p.Glu157Gly) n.652A>G c.671A>G (p.Glu224Gly) c.557A>G (p.Glu186Gly) | |
2 | g.136115470T>G | CA348658924 | CXCR4 | c.446A>C (p.Glu149Ala) c.413A>C (p.Glu138Ala) c.458A>C (p.Glu153Ala) c.470A>C (p.Glu157Ala) n.652A>C c.671A>C (p.Glu224Ala) c.557A>C (p.Glu186Ala) | ClinVar dbSNP |
2 | g.136115470T= | CA1290966064 | CXCR4 | c.446A= (p.Glu149=) c.413A= (p.Glu138=) c.458A= (p.Glu153=) c.470A= (p.Glu157=) n.652A= c.671A= (p.Glu224=) c.557A= (p.Glu186=) | |
2 | g.136115471C>A | CA348658933 | CXCR4 | c.445G>T (p.Glu149Ter) c.412G>T (p.Glu138Ter) c.457G>T (p.Glu153Ter) c.469G>T (p.Glu157Ter) n.651G>T c.670G>T (p.Glu224Ter) c.556G>T (p.Glu186Ter) | dbSNP |
2 | g.136115471C>G | CA348658935 | CXCR4 | c.445G>C (p.Glu149Gln) c.412G>C (p.Glu138Gln) c.457G>C (p.Glu153Gln) c.469G>C (p.Glu157Gln) n.651G>C c.670G>C (p.Glu224Gln) c.556G>C (p.Glu186Gln) | |
2 | g.136115471C>T | CA348658937 | CXCR4 | c.445G>A (p.Glu149Lys) c.412G>A (p.Glu138Lys) c.457G>A (p.Glu153Lys) c.469G>A (p.Glu157Lys) n.651G>A c.670G>A (p.Glu224Lys) c.556G>A (p.Glu186Lys) | dbSNP COSMIC COSMIC |
2 | g.136115472A>C | CA429206490 | CXCR4 | c.444T>G (p.Ala148=) c.411T>G (p.Ala137=) c.456T>G (p.Ala152=) c.468T>G (p.Ala156=) n.650T>G c.669T>G (p.Ala223=) c.555T>G (p.Ala185=) | |
2 | g.136115472A>G | CA429206494 | CXCR4 | c.444T>C (p.Ala148=) c.411T>C (p.Ala137=) c.456T>C (p.Ala152=) c.468T>C (p.Ala156=) n.650T>C c.669T>C (p.Ala223=) c.555T>C (p.Ala185=) | dbSNP |
2 | g.136115472A>T | CA429206496 | CXCR4 | c.444T>A (p.Ala148=) c.411T>A (p.Ala137=) c.456T>A (p.Ala152=) c.468T>A (p.Ala156=) n.650T>A c.669T>A (p.Ala223=) c.555T>A (p.Ala185=) | |
2 | g.136115473G>A | CA348658939 | CXCR4 | c.443C>T (p.Ala148Val) c.410C>T (p.Ala137Val) c.455C>T (p.Ala152Val) c.467C>T (p.Ala156Val) n.649C>T c.668C>T (p.Ala223Val) c.554C>T (p.Ala185Val) | dbSNP |
2 | g.136115473G>C | CA348658942 | CXCR4 | c.443C>G (p.Ala148Gly) c.410C>G (p.Ala137Gly) c.455C>G (p.Ala152Gly) c.467C>G (p.Ala156Gly) n.649C>G c.668C>G (p.Ala223Gly) c.554C>G (p.Ala185Gly) | |
2 | g.136115473G>T | CA348658944 | CXCR4 | c.443C>A (p.Ala148Asp) c.410C>A (p.Ala137Asp) c.455C>A (p.Ala152Asp) c.467C>A (p.Ala156Asp) n.649C>A c.668C>A (p.Ala223Asp) c.554C>A (p.Ala185Asp) | |
2 | g.136115474C>A | CA348658951 | CXCR4 | c.442G>T (p.Ala148Ser) c.409G>T (p.Ala137Ser) c.454G>T (p.Ala152Ser) c.466G>T (p.Ala156Ser) n.648G>T c.667G>T (p.Ala223Ser) c.553G>T (p.Ala185Ser) | |
2 | g.136115474C>G | CA348658947 | CXCR4 | c.442G>C (p.Ala148Pro) c.409G>C (p.Ala137Pro) c.454G>C (p.Ala152Pro) c.466G>C (p.Ala156Pro) n.648G>C c.667G>C (p.Ala223Pro) c.553G>C (p.Ala185Pro) | |
2 | g.136115474C>T | CA348658949 | CXCR4 | c.442G>A (p.Ala148Thr) c.409G>A (p.Ala137Thr) c.454G>A (p.Ala152Thr) c.466G>A (p.Ala156Thr) n.648G>A c.667G>A (p.Ala223Thr) c.553G>A (p.Ala185Thr) | |
2 | g.136115475C>A | CA348658954 | CXCR4 | c.441G>T (p.Leu147Phe) c.408G>T (p.Leu136Phe) c.453G>T (p.Leu151Phe) c.465G>T (p.Leu155Phe) n.647G>T c.666G>T (p.Leu222Phe) c.552G>T (p.Leu184Phe) | dbSNP |
2 | g.136115475C= | CA1290966065 | CXCR4 | c.441G= (p.Leu147=) c.408G= (p.Leu136=) c.453G= (p.Leu151=) c.465G= (p.Leu155=) n.647G= c.666G= (p.Leu222=) c.552G= (p.Leu184=) | |
2 | g.136115475C>G | CA348658956 | CXCR4 | c.441G>C (p.Leu147Phe) c.408G>C (p.Leu136Phe) c.453G>C (p.Leu151Phe) c.465G>C (p.Leu155Phe) n.647G>C c.666G>C (p.Leu222Phe) c.552G>C (p.Leu184Phe) | |
2 | g.136115475C>T | CA429206503 | CXCR4 | c.441G>A (p.Leu147=) c.408G>A (p.Leu136=) c.453G>A (p.Leu151=) c.465G>A (p.Leu155=) n.647G>A c.666G>A (p.Leu222=) c.552G>A (p.Leu184=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115476A>C | CA348658959 | CXCR4 | c.440T>G (p.Leu147Trp) c.407T>G (p.Leu136Trp) c.452T>G (p.Leu151Trp) c.464T>G (p.Leu155Trp) n.646T>G c.665T>G (p.Leu222Trp) c.551T>G (p.Leu184Trp) | |
2 | g.136115476A>G | CA348658961 | CXCR4 | c.440T>C (p.Leu147Ser) c.407T>C (p.Leu136Ser) c.452T>C (p.Leu151Ser) c.464T>C (p.Leu155Ser) n.646T>C c.665T>C (p.Leu222Ser) c.551T>C (p.Leu184Ser) | |
2 | g.136115476A>T | CA348658963 | CXCR4 | c.440T>A (p.Leu147Ter) c.407T>A (p.Leu136Ter) c.452T>A (p.Leu151Ter) c.464T>A (p.Leu155Ter) n.646T>A c.665T>A (p.Leu222Ter) c.551T>A (p.Leu184Ter) | |
2 | g.136115477A= | CA1290966066 | CXCR4 | c.439T= (p.Leu147=) c.406T= (p.Leu136=) c.451T= (p.Leu151=) c.463T= (p.Leu155=) n.645T= c.664T= (p.Leu222=) c.550T= (p.Leu184=) | |
2 | g.136115477A>C | CA348658965 | CXCR4 | c.439T>G (p.Leu147Val) c.406T>G (p.Leu136Val) c.451T>G (p.Leu151Val) c.463T>G (p.Leu155Val) n.645T>G c.664T>G (p.Leu222Val) c.550T>G (p.Leu184Val) | dbSNP |
2 | g.136115477A>G | CA1890117 | CXCR4 | c.439T>C (p.Leu147=) c.406T>C (p.Leu136=) c.451T>C (p.Leu151=) c.463T>C (p.Leu155=) n.645T>C c.664T>C (p.Leu222=) c.550T>C (p.Leu184=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115477A>T | CA348658967 | CXCR4 | c.439T>A (p.Leu147Met) c.406T>A (p.Leu136Met) c.451T>A (p.Leu151Met) c.463T>A (p.Leu155Met) n.645T>A c.664T>A (p.Leu222Met) c.550T>A (p.Leu184Met) | dbSNP |
2 | g.136115478C>A | CA429206510 | CXCR4 | c.438G>T (p.Leu146=) c.405G>T (p.Leu135=) c.450G>T (p.Leu150=) c.462G>T (p.Leu154=) n.644G>T c.663G>T (p.Leu221=) c.549G>T (p.Leu183=) | |
2 | g.136115478C= | CA1290966067 | CXCR4 | c.438G= (p.Leu146=) c.405G= (p.Leu135=) c.450G= (p.Leu150=) c.462G= (p.Leu154=) n.644G= c.663G= (p.Leu221=) c.549G= (p.Leu183=) | |
2 | g.136115478C>G | CA429206511 | CXCR4 | c.438G>C (p.Leu146=) c.405G>C (p.Leu135=) c.450G>C (p.Leu150=) c.462G>C (p.Leu154=) n.644G>C c.663G>C (p.Leu221=) c.549G>C (p.Leu183=) | dbSNP |
2 | g.136115478C>T | CA429206512 | CXCR4 | c.438G>A (p.Leu146=) c.405G>A (p.Leu135=) c.450G>A (p.Leu150=) c.462G>A (p.Leu154=) n.644G>A c.663G>A (p.Leu221=) c.549G>A (p.Leu183=) | dbSNP gnomAD v4 |
2 | g.136115479A>C | CA348658969 | CXCR4 | c.437T>G (p.Leu146Arg) c.404T>G (p.Leu135Arg) c.449T>G (p.Leu150Arg) c.461T>G (p.Leu154Arg) n.643T>G c.662T>G (p.Leu221Arg) c.548T>G (p.Leu183Arg) | |
2 | g.136115479A>G | CA348658972 | CXCR4 | c.437T>C (p.Leu146Pro) c.404T>C (p.Leu135Pro) c.449T>C (p.Leu150Pro) c.461T>C (p.Leu154Pro) n.643T>C c.662T>C (p.Leu221Pro) c.548T>C (p.Leu183Pro) | |
2 | g.136115479A>T | CA348658974 | CXCR4 | c.437T>A (p.Leu146Gln) c.404T>A (p.Leu135Gln) c.449T>A (p.Leu150Gln) c.461T>A (p.Leu154Gln) n.643T>A c.662T>A (p.Leu221Gln) c.548T>A (p.Leu183Gln) | |
2 | g.136115480G>A | CA429206513 | CXCR4 | c.436C>T (p.Leu146=) c.403C>T (p.Leu135=) c.448C>T (p.Leu150=) c.460C>T (p.Leu154=) n.642C>T c.661C>T (p.Leu221=) c.547C>T (p.Leu183=) | dbSNP |
2 | g.136115480G>C | CA1890118 | CXCR4 | c.436C>G (p.Leu146Val) c.403C>G (p.Leu135Val) c.448C>G (p.Leu150Val) c.460C>G (p.Leu154Val) n.642C>G c.661C>G (p.Leu221Val) c.547C>G (p.Leu183Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.136115480G= | CA1290966068 | CXCR4 | c.436C= (p.Leu146=) c.403C= (p.Leu135=) c.448C= (p.Leu150=) c.460C= (p.Leu154=) n.642C= c.661C= (p.Leu221=) c.547C= (p.Leu183=) | |
2 | g.136115480G>T | CA348658979 | CXCR4 | c.436C>A (p.Leu146Met) c.403C>A (p.Leu135Met) c.448C>A (p.Leu150Met) c.460C>A (p.Leu154Met) n.642C>A c.661C>A (p.Leu221Met) c.547C>A (p.Leu183Met) | dbSNP |
2 | g.136115481C>A | CA348658986 | CXCR4 | c.435G>T (p.Lys145Asn) c.402G>T (p.Lys134Asn) c.447G>T (p.Lys149Asn) c.459G>T (p.Lys153Asn) n.641G>T c.660G>T (p.Lys220Asn) c.546G>T (p.Lys182Asn) | dbSNP |
2 | g.136115481C>G | CA348658988 | CXCR4 | c.435G>C (p.Lys145Asn) c.402G>C (p.Lys134Asn) c.447G>C (p.Lys149Asn) c.459G>C (p.Lys153Asn) n.641G>C c.660G>C (p.Lys220Asn) c.546G>C (p.Lys182Asn) | |
2 | g.136115481C>T | CA429206517 | CXCR4 | c.435G>A (p.Lys145=) c.402G>A (p.Lys134=) c.447G>A (p.Lys149=) c.459G>A (p.Lys153=) n.641G>A c.660G>A (p.Lys220=) c.546G>A (p.Lys182=) | dbSNP COSMIC |
2 | g.136115482T>A | CA348658991 | CXCR4 | c.434A>T (p.Lys145Met) c.401A>T (p.Lys134Met) c.446A>T (p.Lys149Met) c.458A>T (p.Lys153Met) n.640A>T c.659A>T (p.Lys220Met) c.545A>T (p.Lys182Met) | dbSNP |
2 | g.136115482T>C | CA348658992 | CXCR4 | c.434A>G (p.Lys145Arg) c.401A>G (p.Lys134Arg) c.446A>G (p.Lys149Arg) c.458A>G (p.Lys153Arg) n.640A>G c.659A>G (p.Lys220Arg) c.545A>G (p.Lys182Arg) | |
2 | g.136115482T>G | CA348658995 | CXCR4 | c.434A>C (p.Lys145Thr) c.401A>C (p.Lys134Thr) c.446A>C (p.Lys149Thr) c.458A>C (p.Lys153Thr) n.640A>C c.659A>C (p.Lys220Thr) c.545A>C (p.Lys182Thr) | |
2 | g.136115483T>A | CA348658997 | CXCR4 | c.433A>T (p.Lys145Ter) c.400A>T (p.Lys134Ter) c.445A>T (p.Lys149Ter) c.457A>T (p.Lys153Ter) n.639A>T c.658A>T (p.Lys220Ter) c.544A>T (p.Lys182Ter) | dbSNP |
2 | g.136115483T>C | CA348659000 | CXCR4 | c.433A>G (p.Lys145Glu) c.400A>G (p.Lys134Glu) c.445A>G (p.Lys149Glu) c.457A>G (p.Lys153Glu) n.639A>G c.658A>G (p.Lys220Glu) c.544A>G (p.Lys182Glu) | |
2 | g.136115483T>G | CA348658999 | CXCR4 | c.433A>C (p.Lys145Gln) c.400A>C (p.Lys134Gln) c.445A>C (p.Lys149Gln) c.457A>C (p.Lys153Gln) n.639A>C c.658A>C (p.Lys220Gln) c.544A>C (p.Lys182Gln) | |
2 | g.136115484C>A | CA348659003 | CXCR4 | c.432G>T (p.Arg144Ser) c.399G>T (p.Arg133Ser) c.444G>T (p.Arg148Ser) c.456G>T (p.Arg152Ser) n.638G>T c.657G>T (p.Arg219Ser) c.543G>T (p.Arg181Ser) | |
2 | g.136115484C= | CA1290966069 | CXCR4 | c.432G= (p.Arg144=) c.399G= (p.Arg133=) c.444G= (p.Arg148=) c.456G= (p.Arg152=) n.638G= c.657G= (p.Arg219=) c.543G= (p.Arg181=) | |
2 | g.136115484C>G | CA348659007 | CXCR4 | c.432G>C (p.Arg144Ser) c.399G>C (p.Arg133Ser) c.444G>C (p.Arg148Ser) c.456G>C (p.Arg152Ser) n.638G>C c.657G>C (p.Arg219Ser) c.543G>C (p.Arg181Ser) | dbSNP |
2 | g.136115484C>T | CA56886532 | CXCR4 | c.432G>A (p.Arg144=) c.399G>A (p.Arg133=) c.444G>A (p.Arg148=) c.456G>A (p.Arg152=) n.638G>A c.657G>A (p.Arg219=) c.543G>A (p.Arg181=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115485C>A | CA348659010 | CXCR4 | c.431G>T (p.Arg144Met) c.398G>T (p.Arg133Met) c.443G>T (p.Arg148Met) c.455G>T (p.Arg152Met) n.637G>T c.656G>T (p.Arg219Met) c.542G>T (p.Arg181Met) | dbSNP |
2 | g.136115485C>G | CA348659011 | CXCR4 | c.431G>C (p.Arg144Thr) c.398G>C (p.Arg133Thr) c.443G>C (p.Arg148Thr) c.455G>C (p.Arg152Thr) n.637G>C c.656G>C (p.Arg219Thr) c.542G>C (p.Arg181Thr) | dbSNP |
2 | g.136115485C>T | CA348659012 | CXCR4 | c.431G>A (p.Arg144Lys) c.398G>A (p.Arg133Lys) c.443G>A (p.Arg148Lys) c.455G>A (p.Arg152Lys) n.637G>A c.656G>A (p.Arg219Lys) c.542G>A (p.Arg181Lys) | COSMIC COSMIC |
2 | g.136115486T>A | CA348659014 | CXCR4 | c.430A>T (p.Arg144Trp) c.397A>T (p.Arg133Trp) c.442A>T (p.Arg148Trp) c.454A>T (p.Arg152Trp) n.636A>T c.655A>T (p.Arg219Trp) c.541A>T (p.Arg181Trp) | dbSNP |
2 | g.136115486T>C | CA348659016 | CXCR4 | c.430A>G (p.Arg144Gly) c.397A>G (p.Arg133Gly) c.442A>G (p.Arg148Gly) c.454A>G (p.Arg152Gly) n.636A>G c.655A>G (p.Arg219Gly) c.541A>G (p.Arg181Gly) | dbSNP |
2 | g.136115486T>G | CA429206524 | CXCR4 | c.430A>C (p.Arg144=) c.397A>C (p.Arg133=) c.442A>C (p.Arg148=) c.454A>C (p.Arg152=) n.636A>C c.655A>C (p.Arg219=) c.541A>C (p.Arg181=) | |
2 | g.136115487T>A | CA429206525 | CXCR4 | c.429A>T (p.Pro143=) c.396A>T (p.Pro132=) c.441A>T (p.Pro147=) c.453A>T (p.Pro151=) n.635A>T c.654A>T (p.Pro218=) c.540A>T (p.Pro180=) | dbSNP |
2 | g.136115487T>C | CA429206526 | CXCR4 | c.429A>G (p.Pro143=) c.396A>G (p.Pro132=) c.441A>G (p.Pro147=) c.453A>G (p.Pro151=) n.635A>G c.654A>G (p.Pro218=) c.540A>G (p.Pro180=) | |
2 | g.136115487T>G | CA429206527 | CXCR4 | c.429A>C (p.Pro143=) c.396A>C (p.Pro132=) c.441A>C (p.Pro147=) c.453A>C (p.Pro151=) n.635A>C c.654A>C (p.Pro218=) c.540A>C (p.Pro180=) | |
2 | g.136115487_136115488delinsTG | CA1290966070 | CXCR4 | c.428_429delinsCA (p.Pro143=) c.395_396delinsCA (p.Pro132=) c.440_441delinsCA (p.Pro147=) c.452_453delinsCA (p.Pro151=) n.634_635delinsCA c.653_654delinsCA (p.Pro218=) c.539_540delinsCA (p.Pro180=) | |
2 | g.136115488G>A | CA348659018 | CXCR4 | c.428C>T (p.Pro143Leu) c.395C>T (p.Pro132Leu) c.440C>T (p.Pro147Leu) c.452C>T (p.Pro151Leu) n.634C>T c.653C>T (p.Pro218Leu) c.539C>T (p.Pro180Leu) | dbSNP |
2 | g.136115488G>C | CA348659019 | CXCR4 | c.428C>G (p.Pro143Arg) c.395C>G (p.Pro132Arg) c.440C>G (p.Pro147Arg) c.452C>G (p.Pro151Arg) n.634C>G c.653C>G (p.Pro218Arg) c.539C>G (p.Pro180Arg) | |
2 | g.136115488G>T | CA348659022 | CXCR4 | c.428C>A (p.Pro143Gln) c.395C>A (p.Pro132Gln) c.440C>A (p.Pro147Gln) c.452C>A (p.Pro151Gln) n.634C>A c.653C>A (p.Pro218Gln) c.539C>A (p.Pro180Gln) | |
2 | g.136115489del | CA1290966071 | CXCR4 | c.428del (p.Pro143GlnfsTer21) c.395del (p.Pro132GlnfsTer21) c.440del (p.Pro147GlnfsTer21) c.452del (p.Pro151GlnfsTer21) n.634del c.653del (p.Pro218GlnfsTer21) c.539del (p.Pro180GlnfsTer21) | dbSNP |
2 | g.136115489G>A | CA348659026 | CXCR4 | c.427C>T (p.Pro143Ser) c.394C>T (p.Pro132Ser) c.439C>T (p.Pro147Ser) c.451C>T (p.Pro151Ser) n.633C>T c.652C>T (p.Pro218Ser) c.538C>T (p.Pro180Ser) | dbSNP |
2 | g.136115489G>C | CA348659027 | CXCR4 | c.427C>G (p.Pro143Ala) c.394C>G (p.Pro132Ala) c.439C>G (p.Pro147Ala) c.451C>G (p.Pro151Ala) n.633C>G c.652C>G (p.Pro218Ala) c.538C>G (p.Pro180Ala) | dbSNP |
2 | g.136115489G>T | CA348659029 | CXCR4 | c.427C>A (p.Pro143Thr) c.394C>A (p.Pro132Thr) c.439C>A (p.Pro147Thr) c.451C>A (p.Pro151Thr) n.633C>A c.652C>A (p.Pro218Thr) c.538C>A (p.Pro180Thr) | |
2 | g.136115490C>A | CA348659032 | CXCR4 | c.426G>T (p.Arg142Ser) c.393G>T (p.Arg131Ser) c.438G>T (p.Arg146Ser) c.450G>T (p.Arg150Ser) n.632G>T c.651G>T (p.Arg217Ser) c.537G>T (p.Arg179Ser) | dbSNP |
2 | g.136115490C>G | CA348659034 | CXCR4 | c.426G>C (p.Arg142Ser) c.393G>C (p.Arg131Ser) c.438G>C (p.Arg146Ser) c.450G>C (p.Arg150Ser) n.632G>C c.651G>C (p.Arg217Ser) c.537G>C (p.Arg179Ser) | dbSNP |
2 | g.136115490C>T | CA429206534 | CXCR4 | c.426G>A (p.Arg142=) c.393G>A (p.Arg131=) c.438G>A (p.Arg146=) c.450G>A (p.Arg150=) n.632G>A c.651G>A (p.Arg217=) c.537G>A (p.Arg179=) | ClinVar gnomAD v4 |
2 | g.136115491C>A | CA348659037 | CXCR4 | c.425G>T (p.Arg142Met) c.392G>T (p.Arg131Met) c.437G>T (p.Arg146Met) c.449G>T (p.Arg150Met) n.631G>T c.650G>T (p.Arg217Met) c.536G>T (p.Arg179Met) | dbSNP gnomAD v4 |
2 | g.136115491C= | CA1290966072 | CXCR4 | c.425G= (p.Arg142=) c.392G= (p.Arg131=) c.437G= (p.Arg146=) c.449G= (p.Arg150=) n.631G= c.650G= (p.Arg217=) c.536G= (p.Arg179=) | |
2 | g.136115491C>G | CA348659040 | CXCR4 | c.425G>C (p.Arg142Thr) c.392G>C (p.Arg131Thr) c.437G>C (p.Arg146Thr) c.449G>C (p.Arg150Thr) n.631G>C c.650G>C (p.Arg217Thr) c.536G>C (p.Arg179Thr) | |
2 | g.136115491C>T | CA1890119 | CXCR4 | c.425G>A (p.Arg142Lys) c.392G>A (p.Arg131Lys) c.437G>A (p.Arg146Lys) c.449G>A (p.Arg150Lys) n.631G>A c.650G>A (p.Arg217Lys) c.536G>A (p.Arg179Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115492T>A | CA348659047 | CXCR4 | c.424A>T (p.Arg142Trp) c.391A>T (p.Arg131Trp) c.436A>T (p.Arg146Trp) c.448A>T (p.Arg150Trp) n.630A>T c.649A>T (p.Arg217Trp) c.535A>T (p.Arg179Trp) | |
2 | g.136115492T>C | CA348659050 | CXCR4 | c.424A>G (p.Arg142Gly) c.391A>G (p.Arg131Gly) c.436A>G (p.Arg146Gly) c.448A>G (p.Arg150Gly) n.630A>G c.649A>G (p.Arg217Gly) c.535A>G (p.Arg179Gly) | dbSNP |
2 | g.136115492T>G | CA429206540 | CXCR4 | c.424A>C (p.Arg142=) c.391A>C (p.Arg131=) c.436A>C (p.Arg146=) c.448A>C (p.Arg150=) n.630A>C c.649A>C (p.Arg217=) c.535A>C (p.Arg179=) | |
2 | g.136115493C>A | CA348659052 | CXCR4 | c.423G>T (p.Gln141His) c.390G>T (p.Gln130His) c.435G>T (p.Gln145His) c.447G>T (p.Gln149His) n.629G>T c.648G>T (p.Gln216His) c.534G>T (p.Gln178His) | |
2 | g.136115493C>G | CA348659054 | CXCR4 | c.423G>C (p.Gln141His) c.390G>C (p.Gln130His) c.435G>C (p.Gln145His) c.447G>C (p.Gln149His) n.629G>C c.648G>C (p.Gln216His) c.534G>C (p.Gln178His) | |
2 | g.136115493C>T | CA429206545 | CXCR4 | c.423G>A (p.Gln141=) c.390G>A (p.Gln130=) c.435G>A (p.Gln145=) c.447G>A (p.Gln149=) n.629G>A c.648G>A (p.Gln216=) c.534G>A (p.Gln178=) | |
2 | g.136115494T>A | CA348659057 | CXCR4 | c.422A>T (p.Gln141Leu) c.389A>T (p.Gln130Leu) c.434A>T (p.Gln145Leu) c.446A>T (p.Gln149Leu) n.628A>T c.647A>T (p.Gln216Leu) c.533A>T (p.Gln178Leu) | |
2 | g.136115494T>C | CA348659059 | CXCR4 | c.422A>G (p.Gln141Arg) c.389A>G (p.Gln130Arg) c.434A>G (p.Gln145Arg) c.446A>G (p.Gln149Arg) n.628A>G c.647A>G (p.Gln216Arg) c.533A>G (p.Gln178Arg) | |
2 | g.136115494T>G | CA348659060 | CXCR4 | c.422A>C (p.Gln141Pro) c.389A>C (p.Gln130Pro) c.434A>C (p.Gln145Pro) c.446A>C (p.Gln149Pro) n.628A>C c.647A>C (p.Gln216Pro) c.533A>C (p.Gln178Pro) | |
2 | g.136115495G>A | CA348659063 | CXCR4 | c.421C>T (p.Gln141Ter) c.388C>T (p.Gln130Ter) c.433C>T (p.Gln145Ter) c.445C>T (p.Gln149Ter) n.627C>T c.646C>T (p.Gln216Ter) c.532C>T (p.Gln178Ter) | |
2 | g.136115495G>C | CA348659066 | CXCR4 | c.421C>G (p.Gln141Glu) c.388C>G (p.Gln130Glu) c.433C>G (p.Gln145Glu) c.445C>G (p.Gln149Glu) n.627C>G c.646C>G (p.Gln216Glu) c.532C>G (p.Gln178Glu) | |
2 | g.136115495G>T | CA348659068 | CXCR4 | c.421C>A (p.Gln141Lys) c.388C>A (p.Gln130Lys) c.433C>A (p.Gln145Lys) c.445C>A (p.Gln149Lys) n.627C>A c.646C>A (p.Gln216Lys) c.532C>A (p.Gln178Lys) | |
2 | g.136115496A>C | CA348659072 | CXCR4 | c.420T>G (p.Ser140Arg) c.387T>G (p.Ser129Arg) c.432T>G (p.Ser144Arg) c.444T>G (p.Ser148Arg) n.626T>G c.645T>G (p.Ser215Arg) c.531T>G (p.Ser177Arg) | |
2 | g.136115496A>G | CA429206552 | CXCR4 | c.420T>C (p.Ser140=) c.387T>C (p.Ser129=) c.432T>C (p.Ser144=) c.444T>C (p.Ser148=) n.626T>C c.645T>C (p.Ser215=) c.531T>C (p.Ser177=) | |
2 | g.136115496A>T | CA348659073 | CXCR4 | c.420T>A (p.Ser140Arg) c.387T>A (p.Ser129Arg) c.432T>A (p.Ser144Arg) c.444T>A (p.Ser148Arg) n.626T>A c.645T>A (p.Ser215Arg) c.531T>A (p.Ser177Arg) | COSMIC COSMIC |
2 | g.136115497C>A | CA348659077 | CXCR4 | c.419G>T (p.Ser140Ile) c.386G>T (p.Ser129Ile) c.431G>T (p.Ser144Ile) c.443G>T (p.Ser148Ile) n.625G>T c.644G>T (p.Ser215Ile) c.530G>T (p.Ser177Ile) | |
2 | g.136115497C>G | CA348659078 | CXCR4 | c.419G>C (p.Ser140Thr) c.386G>C (p.Ser129Thr) c.431G>C (p.Ser144Thr) c.443G>C (p.Ser148Thr) n.625G>C c.644G>C (p.Ser215Thr) c.530G>C (p.Ser177Thr) | |
2 | g.136115497C>T | CA348659080 | CXCR4 | c.419G>A (p.Ser140Asn) c.386G>A (p.Ser129Asn) c.431G>A (p.Ser144Asn) c.443G>A (p.Ser148Asn) n.625G>A c.644G>A (p.Ser215Asn) c.530G>A (p.Ser177Asn) | gnomAD v4 |
2 | g.136115498T>A | CA348659081 | CXCR4 | c.418A>T (p.Ser140Cys) c.385A>T (p.Ser129Cys) c.430A>T (p.Ser144Cys) c.442A>T (p.Ser148Cys) n.624A>T c.643A>T (p.Ser215Cys) c.529A>T (p.Ser177Cys) | |
2 | g.136115498T>C | CA348659082 | CXCR4 | c.418A>G (p.Ser140Gly) c.385A>G (p.Ser129Gly) c.430A>G (p.Ser144Gly) c.442A>G (p.Ser148Gly) n.624A>G c.643A>G (p.Ser215Gly) c.529A>G (p.Ser177Gly) | |
2 | g.136115498T>G | CA348659084 | CXCR4 | c.418A>C (p.Ser140Arg) c.385A>C (p.Ser129Arg) c.430A>C (p.Ser144Arg) c.442A>C (p.Ser148Arg) n.624A>C c.643A>C (p.Ser215Arg) c.529A>C (p.Ser177Arg) | |
2 | g.136115499G>A | CA429206557 | CXCR4 | c.417C>T (p.Asn139=) c.384C>T (p.Asn128=) c.429C>T (p.Asn143=) c.441C>T (p.Asn147=) n.623C>T c.642C>T (p.Asn214=) c.528C>T (p.Asn176=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115499G>C | CA348659086 | CXCR4 | c.417C>G (p.Asn139Lys) c.384C>G (p.Asn128Lys) c.429C>G (p.Asn143Lys) c.441C>G (p.Asn147Lys) n.623C>G c.642C>G (p.Asn214Lys) c.528C>G (p.Asn176Lys) | gnomAD v4 |
2 | g.136115499G= | CA1290966073 | CXCR4 | c.417C= (p.Asn139=) c.384C= (p.Asn128=) c.429C= (p.Asn143=) c.441C= (p.Asn147=) n.623C= c.642C= (p.Asn214=) c.528C= (p.Asn176=) | |
2 | g.136115499G>T | CA348659087 | CXCR4 | c.417C>A (p.Asn139Lys) c.384C>A (p.Asn128Lys) c.429C>A (p.Asn143Lys) c.441C>A (p.Asn147Lys) n.623C>A c.642C>A (p.Asn214Lys) c.528C>A (p.Asn176Lys) | |
2 | g.136115500T>A | CA348659090 | CXCR4 | c.416A>T (p.Asn139Ile) c.383A>T (p.Asn128Ile) c.428A>T (p.Asn143Ile) c.440A>T (p.Asn147Ile) n.622A>T c.641A>T (p.Asn214Ile) c.527A>T (p.Asn176Ile) | |
2 | g.136115500T>C | CA348659092 | CXCR4 | c.416A>G (p.Asn139Ser) c.383A>G (p.Asn128Ser) c.428A>G (p.Asn143Ser) c.440A>G (p.Asn147Ser) n.622A>G c.641A>G (p.Asn214Ser) c.527A>G (p.Asn176Ser) | gnomAD v4 |
2 | g.136115500T>G | CA348659093 | CXCR4 | c.416A>C (p.Asn139Thr) c.383A>C (p.Asn128Thr) c.428A>C (p.Asn143Thr) c.440A>C (p.Asn147Thr) n.622A>C c.641A>C (p.Asn214Thr) c.527A>C (p.Asn176Thr) | |
2 | g.136115501T>A | CA348659101 | CXCR4 | c.415A>T (p.Asn139Tyr) c.382A>T (p.Asn128Tyr) c.427A>T (p.Asn143Tyr) c.439A>T (p.Asn147Tyr) n.621A>T c.640A>T (p.Asn214Tyr) c.526A>T (p.Asn176Tyr) | |
2 | g.136115501T>C | CA348659099 | CXCR4 | c.415A>G (p.Asn139Asp) c.382A>G (p.Asn128Asp) c.427A>G (p.Asn143Asp) c.439A>G (p.Asn147Asp) n.621A>G c.640A>G (p.Asn214Asp) c.526A>G (p.Asn176Asp) | |
2 | g.136115501T>G | CA348659097 | CXCR4 | c.415A>C (p.Asn139His) c.382A>C (p.Asn128His) c.427A>C (p.Asn143His) c.439A>C (p.Asn147His) n.621A>C c.640A>C (p.Asn214His) c.526A>C (p.Asn176His) | |
2 | g.136115502G>A | CA429206564 | CXCR4 | c.414C>T (p.Thr138=) c.381C>T (p.Thr127=) c.426C>T (p.Thr142=) c.438C>T (p.Thr146=) n.620C>T c.639C>T (p.Thr213=) c.525C>T (p.Thr175=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.136115502G>C | CA429206565 | CXCR4 | c.414C>G (p.Thr138=) c.381C>G (p.Thr127=) c.426C>G (p.Thr142=) c.438C>G (p.Thr146=) n.620C>G c.639C>G (p.Thr213=) c.525C>G (p.Thr175=) | gnomAD v4 |
2 | g.136115502G= | CA1290966074 | CXCR4 | c.414C= (p.Thr138=) c.381C= (p.Thr127=) c.426C= (p.Thr142=) c.438C= (p.Thr146=) n.620C= c.639C= (p.Thr213=) c.525C= (p.Thr175=) | |
2 | g.136115502G>T | CA429206566 | CXCR4 | c.414C>A (p.Thr138=) c.381C>A (p.Thr127=) c.426C>A (p.Thr142=) c.438C>A (p.Thr146=) n.620C>A c.639C>A (p.Thr213=) c.525C>A (p.Thr175=) | |
2 | g.136115503G>A | CA348659104 | CXCR4 | c.413C>T (p.Thr138Ile) c.380C>T (p.Thr127Ile) c.425C>T (p.Thr142Ile) c.437C>T (p.Thr146Ile) n.619C>T c.638C>T (p.Thr213Ile) c.524C>T (p.Thr175Ile) | gnomAD v4 |
2 | g.136115503G>C | CA348659106 | CXCR4 | c.413C>G (p.Thr138Ser) c.380C>G (p.Thr127Ser) c.425C>G (p.Thr142Ser) c.437C>G (p.Thr146Ser) n.619C>G c.638C>G (p.Thr213Ser) c.524C>G (p.Thr175Ser) | |
2 | g.136115503G>T | CA348659108 | CXCR4 | c.413C>A (p.Thr138Asn) c.380C>A (p.Thr127Asn) c.425C>A (p.Thr142Asn) c.437C>A (p.Thr146Asn) n.619C>A c.638C>A (p.Thr213Asn) c.524C>A (p.Thr175Asn) | |
2 | g.136115504T>A | CA348659111 | CXCR4 | c.412A>T (p.Thr138Ser) c.379A>T (p.Thr127Ser) c.424A>T (p.Thr142Ser) c.436A>T (p.Thr146Ser) n.618A>T c.637A>T (p.Thr213Ser) c.523A>T (p.Thr175Ser) | |
2 | g.136115504T>C | CA348659113 | CXCR4 | c.412A>G (p.Thr138Ala) c.379A>G (p.Thr127Ala) c.424A>G (p.Thr142Ala) c.436A>G (p.Thr146Ala) n.618A>G c.637A>G (p.Thr213Ala) c.523A>G (p.Thr175Ala) | |
2 | g.136115504T>G | CA348659115 | CXCR4 | c.412A>C (p.Thr138Pro) c.379A>C (p.Thr127Pro) c.424A>C (p.Thr142Pro) c.436A>C (p.Thr146Pro) n.618A>C c.637A>C (p.Thr213Pro) c.523A>C (p.Thr175Pro) | |
2 | g.136115505G>A | CA429206568 | CXCR4 | c.411C>T (p.Ala137=) c.378C>T (p.Ala126=) c.423C>T (p.Ala141=) c.435C>T (p.Ala145=) n.617C>T c.636C>T (p.Ala212=) c.522C>T (p.Ala174=) | |
2 | g.136115505G>C | CA429206570 | CXCR4 | c.411C>G (p.Ala137=) c.378C>G (p.Ala126=) c.423C>G (p.Ala141=) c.435C>G (p.Ala145=) n.617C>G c.636C>G (p.Ala212=) c.522C>G (p.Ala174=) | |
2 | g.136115505G>T | CA429206572 | CXCR4 | c.411C>A (p.Ala137=) c.378C>A (p.Ala126=) c.423C>A (p.Ala141=) c.435C>A (p.Ala145=) n.617C>A c.636C>A (p.Ala212=) c.522C>A (p.Ala174=) | |
2 | g.136115506G>A | CA1890120 | CXCR4 | c.410C>T (p.Ala137Val) c.377C>T (p.Ala126Val) c.422C>T (p.Ala141Val) c.434C>T (p.Ala145Val) n.616C>T c.635C>T (p.Ala212Val) c.521C>T (p.Ala174Val) | ClinVar dbSNP ExAC gnomAD v2 |
2 | g.136115506G>C | CA348659118 | CXCR4 | c.410C>G (p.Ala137Gly) c.377C>G (p.Ala126Gly) c.422C>G (p.Ala141Gly) c.434C>G (p.Ala145Gly) n.616C>G c.635C>G (p.Ala212Gly) c.521C>G (p.Ala174Gly) | |
2 | g.136115506G= | CA1290966075 | CXCR4 | c.410C= (p.Ala137=) c.377C= (p.Ala126=) c.422C= (p.Ala141=) c.434C= (p.Ala145=) n.616C= c.635C= (p.Ala212=) c.521C= (p.Ala174=) | |
2 | g.136115506G>T | CA348659120 | CXCR4 | c.410C>A (p.Ala137Asp) c.377C>A (p.Ala126Asp) c.422C>A (p.Ala141Asp) c.434C>A (p.Ala145Asp) n.616C>A c.635C>A (p.Ala212Asp) c.521C>A (p.Ala174Asp) | dbSNP |
2 | g.136115507C>A | CA348659123 | CXCR4 | c.409G>T (p.Ala137Ser) c.376G>T (p.Ala126Ser) c.421G>T (p.Ala141Ser) c.433G>T (p.Ala145Ser) n.615G>T c.634G>T (p.Ala212Ser) c.520G>T (p.Ala174Ser) | |
2 | g.136115507C= | CA1290966076 | CXCR4 | c.409G= (p.Ala137=) c.376G= (p.Ala126=) c.421G= (p.Ala141=) c.433G= (p.Ala145=) n.615G= c.634G= (p.Ala212=) c.520G= (p.Ala174=) | |
2 | g.136115507C>G | CA56886534 | CXCR4 | c.409G>C (p.Ala137Pro) c.376G>C (p.Ala126Pro) c.421G>C (p.Ala141Pro) c.433G>C (p.Ala145Pro) n.615G>C c.634G>C (p.Ala212Pro) c.520G>C (p.Ala174Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115507C>T | CA1890121 | CXCR4 | c.409G>A (p.Ala137Thr) c.376G>A (p.Ala126Thr) c.421G>A (p.Ala141Thr) c.433G>A (p.Ala145Thr) n.615G>A c.634G>A (p.Ala212Thr) c.520G>A (p.Ala174Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115508G>A | CA1890122 | CXCR4 | c.408C>T (p.His136=) c.375C>T (p.His125=) c.420C>T (p.His140=) c.432C>T (p.His144=) n.614C>T c.633C>T (p.His211=) c.519C>T (p.His173=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
2 | g.136115508G>C | CA348659130 | CXCR4 | c.408C>G (p.His136Gln) c.375C>G (p.His125Gln) c.420C>G (p.His140Gln) c.432C>G (p.His144Gln) n.614C>G c.633C>G (p.His211Gln) c.519C>G (p.His173Gln) | |
2 | g.136115508G= | CA1290966077 | CXCR4 | c.408C= (p.His136=) c.375C= (p.His125=) c.420C= (p.His140=) c.432C= (p.His144=) n.614C= c.633C= (p.His211=) c.519C= (p.His173=) | |
2 | g.136115508G>T | CA348659128 | CXCR4 | c.408C>A (p.His136Gln) c.375C>A (p.His125Gln) c.420C>A (p.His140Gln) c.432C>A (p.His144Gln) n.614C>A c.633C>A (p.His211Gln) c.519C>A (p.His173Gln) | |
2 | g.136115509T>A | CA348659131 | CXCR4 | c.407A>T (p.His136Leu) c.374A>T (p.His125Leu) c.419A>T (p.His140Leu) c.431A>T (p.His144Leu) n.613A>T c.632A>T (p.His211Leu) c.518A>T (p.His173Leu) | |
2 | g.136115509T>C | CA348659136 | CXCR4 | c.407A>G (p.His136Arg) c.374A>G (p.His125Arg) c.419A>G (p.His140Arg) c.431A>G (p.His144Arg) n.613A>G c.632A>G (p.His211Arg) c.518A>G (p.His173Arg) | gnomAD v4 |
2 | g.136115509T>G | CA348659134 | CXCR4 | c.407A>C (p.His136Pro) c.374A>C (p.His125Pro) c.419A>C (p.His140Pro) c.431A>C (p.His144Pro) n.613A>C c.632A>C (p.His211Pro) c.518A>C (p.His173Pro) | |
2 | g.136115510G>A | CA348659139 | CXCR4 | c.406C>T (p.His136Tyr) c.373C>T (p.His125Tyr) c.418C>T (p.His140Tyr) c.430C>T (p.His144Tyr) n.612C>T c.631C>T (p.His211Tyr) c.517C>T (p.His173Tyr) | |
2 | g.136115510G>C | CA348659144 | CXCR4 | c.406C>G (p.His136Asp) c.373C>G (p.His125Asp) c.418C>G (p.His140Asp) c.430C>G (p.His144Asp) n.612C>G c.631C>G (p.His211Asp) c.517C>G (p.His173Asp) | |
2 | g.136115510G>T | CA348659141 | CXCR4 | c.406C>A (p.His136Asn) c.373C>A (p.His125Asn) c.418C>A (p.His140Asn) c.430C>A (p.His144Asn) n.612C>A c.631C>A (p.His211Asn) c.517C>A (p.His173Asn) | |
2 | g.136115511G>A | CA429206584 | CXCR4 | c.405C>T (p.Val135=) c.372C>T (p.Val124=) c.417C>T (p.Val139=) c.429C>T (p.Val143=) n.611C>T c.630C>T (p.Val210=) c.516C>T (p.Val172=) | |
2 | g.136115511G>C | CA429206585 | CXCR4 | c.405C>G (p.Val135=) c.372C>G (p.Val124=) c.417C>G (p.Val139=) c.429C>G (p.Val143=) n.611C>G c.630C>G (p.Val210=) c.516C>G (p.Val172=) | gnomAD v4 |
2 | g.136115511G>T | CA429206586 | CXCR4 | c.405C>A (p.Val135=) c.372C>A (p.Val124=) c.417C>A (p.Val139=) c.429C>A (p.Val143=) n.611C>A c.630C>A (p.Val210=) c.516C>A (p.Val172=) | |
2 | g.136115512A>C | CA348659146 | CXCR4 | c.404T>G (p.Val135Gly) c.371T>G (p.Val124Gly) c.416T>G (p.Val139Gly) c.428T>G (p.Val143Gly) n.610T>G c.629T>G (p.Val210Gly) c.515T>G (p.Val172Gly) | |
2 | g.136115512A>G | CA348659149 | CXCR4 | c.404T>C (p.Val135Ala) c.371T>C (p.Val124Ala) c.416T>C (p.Val139Ala) c.428T>C (p.Val143Ala) n.610T>C c.629T>C (p.Val210Ala) c.515T>C (p.Val172Ala) | |
2 | g.136115512A>T | CA348659151 | CXCR4 | c.404T>A (p.Val135Asp) c.371T>A (p.Val124Asp) c.416T>A (p.Val139Asp) c.428T>A (p.Val143Asp) n.610T>A c.629T>A (p.Val210Asp) c.515T>A (p.Val172Asp) | |
2 | g.136115513C>A | CA348659153 | CXCR4 | c.403G>T (p.Val135Phe) c.370G>T (p.Val124Phe) c.415G>T (p.Val139Phe) c.427G>T (p.Val143Phe) n.609G>T c.628G>T (p.Val210Phe) c.514G>T (p.Val172Phe) | |
2 | g.136115513C= | CA1290966078 | CXCR4 | c.403G= (p.Val135=) c.370G= (p.Val124=) c.415G= (p.Val139=) c.427G= (p.Val143=) n.609G= c.628G= (p.Val210=) c.514G= (p.Val172=) | |
2 | g.136115513C>G | CA348659156 | CXCR4 | c.403G>C (p.Val135Leu) c.370G>C (p.Val124Leu) c.415G>C (p.Val139Leu) c.427G>C (p.Val143Leu) n.609G>C c.628G>C (p.Val210Leu) c.514G>C (p.Val172Leu) | gnomAD v4 |
2 | g.136115513C>T | CA348659157 | CXCR4 | c.403G>A (p.Val135Ile) c.370G>A (p.Val124Ile) c.415G>A (p.Val139Ile) c.427G>A (p.Val143Ile) n.609G>A c.628G>A (p.Val210Ile) c.514G>A (p.Val172Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115514G>A | CA1890123 | CXCR4 | c.402C>T (p.Ile134=) c.369C>T (p.Ile123=) c.414C>T (p.Ile138=) c.426C>T (p.Ile142=) n.608C>T c.627C>T (p.Ile209=) c.513C>T (p.Ile171=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136115514G>C | CA348659160 | CXCR4 | c.402C>G (p.Ile134Met) c.369C>G (p.Ile123Met) c.414C>G (p.Ile138Met) c.426C>G (p.Ile142Met) n.608C>G c.627C>G (p.Ile209Met) c.513C>G (p.Ile171Met) | |
2 | g.136115514G= | CA1290966079 | CXCR4 | c.402C= (p.Ile134=) c.369C= (p.Ile123=) c.414C= (p.Ile138=) c.426C= (p.Ile142=) n.608C= c.627C= (p.Ile209=) c.513C= (p.Ile171=) | |
2 | g.136115514G>T | CA429206592 | CXCR4 | c.402C>A (p.Ile134=) c.369C>A (p.Ile123=) c.414C>A (p.Ile138=) c.426C>A (p.Ile142=) n.608C>A c.627C>A (p.Ile209=) c.513C>A (p.Ile171=) | |
2 | g.136115515A>C | CA348659162 | CXCR4 | c.401T>G (p.Ile134Ser) c.368T>G (p.Ile123Ser) c.413T>G (p.Ile138Ser) c.425T>G (p.Ile142Ser) n.607T>G c.626T>G (p.Ile209Ser) c.512T>G (p.Ile171Ser) | |
2 | g.136115515A>G | CA348659164 | CXCR4 | c.401T>C (p.Ile134Thr) c.368T>C (p.Ile123Thr) c.413T>C (p.Ile138Thr) c.425T>C (p.Ile142Thr) n.607T>C c.626T>C (p.Ile209Thr) c.512T>C (p.Ile171Thr) | |
2 | g.136115515A>T | CA348659166 | CXCR4 | c.401T>A (p.Ile134Asn) c.368T>A (p.Ile123Asn) c.413T>A (p.Ile138Asn) c.425T>A (p.Ile142Asn) n.607T>A c.626T>A (p.Ile209Asn) c.512T>A (p.Ile171Asn) | |
2 | g.136115516T>A | CA348659173 | CXCR4 | c.400A>T (p.Ile134Phe) c.367A>T (p.Ile123Phe) c.412A>T (p.Ile138Phe) c.424A>T (p.Ile142Phe) n.606A>T c.625A>T (p.Ile209Phe) c.511A>T (p.Ile171Phe) | |
2 | g.136115516T>C | CA348659168 | CXCR4 | c.400A>G (p.Ile134Val) c.367A>G (p.Ile123Val) c.412A>G (p.Ile138Val) c.424A>G (p.Ile142Val) n.606A>G c.625A>G (p.Ile209Val) c.511A>G (p.Ile171Val) | |
2 | g.136115516T>G | CA348659170 | CXCR4 | c.400A>C (p.Ile134Leu) c.367A>C (p.Ile123Leu) c.412A>C (p.Ile138Leu) c.424A>C (p.Ile142Leu) n.606A>C c.625A>C (p.Ile209Leu) c.511A>C (p.Ile171Leu) | |
2 | g.136115517G>A | CA429206599 | CXCR4 | c.399C>T (p.Ala133=) c.366C>T (p.Ala122=) c.411C>T (p.Ala137=) c.423C>T (p.Ala141=) n.605C>T c.624C>T (p.Ala208=) c.510C>T (p.Ala170=) | |
2 | g.136115517G>C | CA429206601 | CXCR4 | c.399C>G (p.Ala133=) c.366C>G (p.Ala122=) c.411C>G (p.Ala137=) c.423C>G (p.Ala141=) n.605C>G c.624C>G (p.Ala208=) c.510C>G (p.Ala170=) | |
2 | g.136115517G>T | CA429206602 | CXCR4 | c.399C>A (p.Ala133=) c.366C>A (p.Ala122=) c.411C>A (p.Ala137=) c.423C>A (p.Ala141=) n.605C>A c.624C>A (p.Ala208=) c.510C>A (p.Ala170=) | COSMIC COSMIC |
2 | g.136115518G>A | CA348659175 | CXCR4 | c.398C>T (p.Ala133Val) c.365C>T (p.Ala122Val) c.410C>T (p.Ala137Val) c.422C>T (p.Ala141Val) n.604C>T c.623C>T (p.Ala208Val) c.509C>T (p.Ala170Val) | |
2 | g.136115518G>C | CA348659177 | CXCR4 | c.398C>G (p.Ala133Gly) c.365C>G (p.Ala122Gly) c.410C>G (p.Ala137Gly) c.422C>G (p.Ala141Gly) n.604C>G c.623C>G (p.Ala208Gly) c.509C>G (p.Ala170Gly) | |
2 | g.136115518G>T | CA348659178 | CXCR4 | c.398C>A (p.Ala133Asp) c.365C>A (p.Ala122Asp) c.410C>A (p.Ala137Asp) c.422C>A (p.Ala141Asp) n.604C>A c.623C>A (p.Ala208Asp) c.509C>A (p.Ala170Asp) | |
2 | g.136115519C>A | CA348659179 | CXCR4 | c.397G>T (p.Ala133Ser) c.364G>T (p.Ala122Ser) c.409G>T (p.Ala137Ser) c.421G>T (p.Ala141Ser) n.603G>T c.622G>T (p.Ala208Ser) c.508G>T (p.Ala170Ser) | |
2 | g.136115519C>G | CA348659181 | CXCR4 | c.397G>C (p.Ala133Pro) c.364G>C (p.Ala122Pro) c.409G>C (p.Ala137Pro) c.421G>C (p.Ala141Pro) n.603G>C c.622G>C (p.Ala208Pro) c.508G>C (p.Ala170Pro) | |
2 | g.136115519C>T | CA348659184 | CXCR4 | c.397G>A (p.Ala133Thr) c.364G>A (p.Ala122Thr) c.409G>A (p.Ala137Thr) c.421G>A (p.Ala141Thr) n.603G>A c.622G>A (p.Ala208Thr) c.508G>A (p.Ala170Thr) | |
2 | g.136115520C>A | CA429206609 | CXCR4 | c.396G>T (p.Leu132=) c.363G>T (p.Leu121=) c.408G>T (p.Leu136=) c.420G>T (p.Leu140=) n.602G>T c.621G>T (p.Leu207=) c.507G>T (p.Leu169=) | |
2 | g.136115520C>G | CA429206611 | CXCR4 | c.396G>C (p.Leu132=) c.363G>C (p.Leu121=) c.408G>C (p.Leu136=) c.420G>C (p.Leu140=) n.602G>C c.621G>C (p.Leu207=) c.507G>C (p.Leu169=) | |
2 | g.136115520C>T | CA429206613 | CXCR4 | c.396G>A (p.Leu132=) c.363G>A (p.Leu121=) c.408G>A (p.Leu136=) c.420G>A (p.Leu140=) n.602G>A c.621G>A (p.Leu207=) c.507G>A (p.Leu169=) | |
2 | g.136115521A>C | CA348659188 | CXCR4 | c.395T>G (p.Leu132Arg) c.362T>G (p.Leu121Arg) c.407T>G (p.Leu136Arg) c.419T>G (p.Leu140Arg) n.601T>G c.620T>G (p.Leu207Arg) c.506T>G (p.Leu169Arg) | |
2 | g.136115521A>G | CA348659190 | CXCR4 | c.395T>C (p.Leu132Pro) c.362T>C (p.Leu121Pro) c.407T>C (p.Leu136Pro) c.419T>C (p.Leu140Pro) n.601T>C c.620T>C (p.Leu207Pro) c.506T>C (p.Leu169Pro) | |
2 | g.136115521A>T | CA348659192 | CXCR4 | c.395T>A (p.Leu132Gln) c.362T>A (p.Leu121Gln) c.407T>A (p.Leu136Gln) c.419T>A (p.Leu140Gln) n.601T>A c.620T>A (p.Leu207Gln) c.506T>A (p.Leu169Gln) | |
2 | g.136115521dup | CA2842108663 | CXCR4 | c.395dup (p.Ala133GlyfsTer17) c.362dup (p.Ala122GlyfsTer17) c.407dup (p.Ala137GlyfsTer17) c.419dup (p.Ala141GlyfsTer17) n.601dup c.620dup (p.Ala208GlyfsTer17) c.506dup (p.Ala170GlyfsTer17) |