Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.136115428A>CCA348658737CXCR4c.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)
2g.136115428A>GCA348658739CXCR4c.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
2g.136115428A>TCA348658741CXCR4c.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)
2g.136115429G>ACA429206408CXCR4c.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=)
2g.136115429G>CCA348658744CXCR4c.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
2g.136115429G=CA1290966048CXCR4c.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=)
2g.136115429G>TCA348658746CXCR4c.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
2g.136115430C>ACA429206411CXCR4c.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
2g.136115430C=CA1290966049CXCR4c.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=)
2g.136115430C>GCA429206412CXCR4c.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
2g.136115430C>TCA429206413CXCR4c.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
2g.136115431A>CCA348658751CXCR4c.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)
2g.136115431A>GCA348658747CXCR4c.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
2g.136115431A>TCA348658749CXCR4c.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
2g.136115432G>ACA429206420CXCR4c.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=)
2g.136115432G>CCA348658753CXCR4c.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)
2g.136115432G>TCA348658754CXCR4c.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)
2g.136115433delCA2661289449CXCR4c.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
2g.136115433G>ACA429206423CXCR4c.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
2g.136115433G>CCA429206422CXCR4c.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
2g.136115433G>TCA429206421CXCR4c.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=)
2g.136115434A=CA1290966050CXCR4c.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=)
2g.136115434A>CCA348658757CXCR4c.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)
2g.136115434A>GCA348658759CXCR4c.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
2g.136115434A>TCA348658762CXCR4c.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
2g.136115435G>ACA348658765CXCR4c.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
2g.136115435G>CCA348658769CXCR4c.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)
2g.136115435G=CA1290966051CXCR4c.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=)
2g.136115435G>TCA348658767CXCR4c.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)
2g.136115436G>ACA1890114CXCR4c.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
2g.136115436G>CCA429206431CXCR4c.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
2g.136115436G=CA1290966052CXCR4c.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=)
2g.136115436G>TCA429206430CXCR4c.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
2g.136115437G>ACA348658774CXCR4c.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
2g.136115437G>CCA348658776CXCR4c.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
2g.136115437G>TCA348658779CXCR4c.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)
2g.136115438C>ACA348658781CXCR4c.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
2g.136115438C>GCA348658784CXCR4c.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
2g.136115438C>TCA348658786CXCR4c.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
2g.136115439A>CCA429206433CXCR4c.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=)
2g.136115439A>GCA429206434CXCR4c.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=)
2g.136115439A>TCA429206436CXCR4c.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=)
2g.136115440G>ACA348658787CXCR4c.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
2g.136115440G>CCA348658788CXCR4c.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
2g.136115440G>TCA348658789CXCR4c.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
2g.136115441G>ACA348658794CXCR4c.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
2g.136115441G>CCA348658791CXCR4c.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
2g.136115441G>TCA348658790CXCR4c.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
2g.136115442G>ACA429206437CXCR4c.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
2g.136115442G>CCA348658795CXCR4c.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
2g.136115442G>TCA429206438CXCR4c.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=)
2g.136115443A>CCA348658798CXCR4c.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
2g.136115443A>GCA348658799CXCR4c.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)
2g.136115443A>TCA348658801CXCR4c.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
2g.136115444T>ACA348658804CXCR4c.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)
2g.136115444T>CCA348658806CXCR4c.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)
2g.136115444T>GCA348658808CXCR4c.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)
2g.136115445C>ACA348658810CXCR4c.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
2g.136115445C=CA1290966053CXCR4c.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=)
2g.136115445C>GCA348658813CXCR4c.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
2g.136115445C>TCA348658815CXCR4c.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
2g.136115446C>ACA348658818CXCR4c.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)
2g.136115446C>GCA348658821CXCR4c.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
2g.136115446C>TCA348658822CXCR4c.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
2g.136115447A>CCA348658828CXCR4c.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)
2g.136115447A>GCA348658824CXCR4c.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
2g.136115447A>TCA348658825CXCR4c.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)
2g.136115448G>ACA429206446CXCR4c.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
2g.136115448G>CCA429206448CXCR4c.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
2g.136115448G>TCA429206449CXCR4c.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
2g.136115449A>CCA348658830CXCR4c.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)
2g.136115449A>GCA348658832CXCR4c.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
2g.136115449A>TCA348658833CXCR4c.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)
2g.136115449dupCA2577108867CXCR4c.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)
2g.136115450C>ACA348658835CXCR4c.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
2g.136115450C=CA1290966054CXCR4c.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=)
2g.136115450C>GCA348658838CXCR4c.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
2g.136115450C>TCA1890115CXCR4c.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
2g.136115451G>ACA429206452CXCR4c.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
2g.136115451G>CCA429206454CXCR4c.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
2g.136115451G=CA1290966055CXCR4c.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=)
2g.136115451G>TCA429206453CXCR4c.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
2g.136115452C>ACA348658841CXCR4c.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
2g.136115452C>GCA348658843CXCR4c.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
2g.136115452C>TCA348658844CXCR4c.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
2g.136115453C>ACA56886523CXCR4c.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
2g.136115453C=CA1290966056CXCR4c.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=)
2g.136115453C>GCA348658845CXCR4c.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
2g.136115453C>TCA348658847CXCR4c.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
2g.136115454A=CA1290966057CXCR4c.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=)
2g.136115454A>CCA429206457CXCR4c.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=)
2g.136115454A>GCA56886525CXCR4c.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
2g.136115454A>TCA429206459CXCR4c.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
2g.136115455A=CA1290966058CXCR4c.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=)
2g.136115455A>CCA348658852CXCR4c.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)
2g.136115455A>GCA1890116CXCR4c.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
2g.136115455A>TCA348658850CXCR4c.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
2g.136115455_136115469dupCA536548296CXCR4c.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
2g.136115456C>ACA348658856CXCR4c.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
2g.136115456C>GCA348658860CXCR4c.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
2g.136115456C>TCA348658859CXCR4c.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
2g.136115457A>CCA348658861CXCR4c.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)
2g.136115457A>GCA429206465CXCR4c.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=)
2g.136115457A>TCA348658863CXCR4c.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
2g.136115458T>ACA348658867CXCR4c.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
2g.136115458T>CCA56886527CXCR4c.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
2g.136115458T>GCA348658871CXCR4c.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)
2g.136115458T=CA1290966059CXCR4c.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=)
2g.136115459A>CCA348658872CXCR4c.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)
2g.136115459A>GCA348658874CXCR4c.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
2g.136115459A>TCA348658875CXCR4c.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)
2g.136115459_136115461delCA2661289450CXCR4c.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
2g.136115460G>ACA429206470CXCR4c.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
2g.136115460G>CCA429206471CXCR4c.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
2g.136115460G=CA1290966060CXCR4c.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=)
2g.136115460G>TCA429206473CXCR4c.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
2g.136115461A>CCA348658876CXCR4c.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)
2g.136115461A>GCA348658877CXCR4c.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)
2g.136115461A>TCA348658880CXCR4c.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
2g.136115462C>ACA348658882CXCR4c.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
2g.136115462C=CA1290966061CXCR4c.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=)
2g.136115462C>GCA348658884CXCR4c.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)
2g.136115462C>TCA348658886CXCR4c.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
2g.136115463C>ACA429206474CXCR4c.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=)
2g.136115463C>GCA429206475CXCR4c.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=)
2g.136115463C>TCA429206476CXCR4c.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=)
2g.136115463_136115464delinsCACA1290966062CXCR4c.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=)
2g.136115464delCA1036829506CXCR4c.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
2g.136115464A>CCA348658892CXCR4c.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)
2g.136115464A>GCA348658891CXCR4c.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
2g.136115464A>TCA348658889CXCR4c.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)
2g.136115465C>ACA348658895CXCR4c.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
2g.136115465C>GCA348658897CXCR4c.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
2g.136115465C>TCA348658900CXCR4c.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
2g.136115466C>ACA348658902CXCR4c.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)
2g.136115466C>GCA348658905CXCR4c.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)
2g.136115466C>TCA429206479CXCR4c.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=)
2g.136115466_136115467delinsCTCA1290966063CXCR4c.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=)
2g.136115467T>ACA348658907CXCR4c.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)
2g.136115467T>CCA348658909CXCR4c.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)
2g.136115467T>GCA348658911CXCR4c.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)
2g.136115470delCA56886529CXCR4c.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
2g.136115468T>ACA348658913CXCR4c.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)
2g.136115468T>CCA348658916CXCR4c.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
2g.136115468T>GCA348658918CXCR4c.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)
2g.136115469T>ACA348658920CXCR4c.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)
2g.136115469T>CCA429206487CXCR4c.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=)
2g.136115469T>GCA348658922CXCR4c.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
2g.136115469_136115470insGGAAAAATATCCATGCA2700535354CXCR4c.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
2g.136115470T>ACA348658927CXCR4c.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)
2g.136115470T>CCA348658930CXCR4c.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)
2g.136115470T>GCA348658924CXCR4c.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
2g.136115470T=CA1290966064CXCR4c.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=)
2g.136115471C>ACA348658933CXCR4c.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
2g.136115471C>GCA348658935CXCR4c.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)
2g.136115471C>TCA348658937CXCR4c.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
2g.136115472A>CCA429206490CXCR4c.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=)
2g.136115472A>GCA429206494CXCR4c.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
2g.136115472A>TCA429206496CXCR4c.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=)
2g.136115473G>ACA348658939CXCR4c.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
2g.136115473G>CCA348658942CXCR4c.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)
2g.136115473G>TCA348658944CXCR4c.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)
2g.136115474C>ACA348658951CXCR4c.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)
2g.136115474C>GCA348658947CXCR4c.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)
2g.136115474C>TCA348658949CXCR4c.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)
2g.136115475C>ACA348658954CXCR4c.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
2g.136115475C=CA1290966065CXCR4c.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=)
2g.136115475C>GCA348658956CXCR4c.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)
2g.136115475C>TCA429206503CXCR4c.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
2g.136115476A>CCA348658959CXCR4c.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)
2g.136115476A>GCA348658961CXCR4c.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)
2g.136115476A>TCA348658963CXCR4c.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)
2g.136115477A=CA1290966066CXCR4c.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=)
2g.136115477A>CCA348658965CXCR4c.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
2g.136115477A>GCA1890117CXCR4c.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
2g.136115477A>TCA348658967CXCR4c.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
2g.136115478C>ACA429206510CXCR4c.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=)
2g.136115478C=CA1290966067CXCR4c.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=)
2g.136115478C>GCA429206511CXCR4c.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
2g.136115478C>TCA429206512CXCR4c.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
2g.136115479A>CCA348658969CXCR4c.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)
2g.136115479A>GCA348658972CXCR4c.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)
2g.136115479A>TCA348658974CXCR4c.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)
2g.136115480G>ACA429206513CXCR4c.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
2g.136115480G>CCA1890118CXCR4c.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
2g.136115480G=CA1290966068CXCR4c.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=)
2g.136115480G>TCA348658979CXCR4c.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
2g.136115481C>ACA348658986CXCR4c.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
2g.136115481C>GCA348658988CXCR4c.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)
2g.136115481C>TCA429206517CXCR4c.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
2g.136115482T>ACA348658991CXCR4c.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
2g.136115482T>CCA348658992CXCR4c.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)
2g.136115482T>GCA348658995CXCR4c.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)
2g.136115483T>ACA348658997CXCR4c.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
2g.136115483T>CCA348659000CXCR4c.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)
2g.136115483T>GCA348658999CXCR4c.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)
2g.136115484C>ACA348659003CXCR4c.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)
2g.136115484C=CA1290966069CXCR4c.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=)
2g.136115484C>GCA348659007CXCR4c.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
2g.136115484C>TCA56886532CXCR4c.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
2g.136115485C>ACA348659010CXCR4c.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
2g.136115485C>GCA348659011CXCR4c.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
2g.136115485C>TCA348659012CXCR4c.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
2g.136115486T>ACA348659014CXCR4c.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
2g.136115486T>CCA348659016CXCR4c.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
2g.136115486T>GCA429206524CXCR4c.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=)
2g.136115487T>ACA429206525CXCR4c.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
2g.136115487T>CCA429206526CXCR4c.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=)
2g.136115487T>GCA429206527CXCR4c.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=)
2g.136115487_136115488delinsTGCA1290966070CXCR4c.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=)
2g.136115488G>ACA348659018CXCR4c.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
2g.136115488G>CCA348659019CXCR4c.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)
2g.136115488G>TCA348659022CXCR4c.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)
2g.136115489delCA1290966071CXCR4c.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
2g.136115489G>ACA348659026CXCR4c.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
2g.136115489G>CCA348659027CXCR4c.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
2g.136115489G>TCA348659029CXCR4c.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)
2g.136115490C>ACA348659032CXCR4c.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
2g.136115490C>GCA348659034CXCR4c.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
2g.136115490C>TCA429206534CXCR4c.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
2g.136115491C>ACA348659037CXCR4c.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
2g.136115491C=CA1290966072CXCR4c.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=)
2g.136115491C>GCA348659040CXCR4c.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)
2g.136115491C>TCA1890119CXCR4c.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
2g.136115492T>ACA348659047CXCR4c.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)
2g.136115492T>CCA348659050CXCR4c.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
2g.136115492T>GCA429206540CXCR4c.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=)
2g.136115493C>ACA348659052CXCR4c.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)
2g.136115493C>GCA348659054CXCR4c.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)
2g.136115493C>TCA429206545CXCR4c.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=)
2g.136115494T>ACA348659057CXCR4c.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)
2g.136115494T>CCA348659059CXCR4c.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)
2g.136115494T>GCA348659060CXCR4c.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)
2g.136115495G>ACA348659063CXCR4c.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)
2g.136115495G>CCA348659066CXCR4c.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)
2g.136115495G>TCA348659068CXCR4c.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)
2g.136115496A>CCA348659072CXCR4c.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)
2g.136115496A>GCA429206552CXCR4c.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=)
2g.136115496A>TCA348659073CXCR4c.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
2g.136115497C>ACA348659077CXCR4c.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)
2g.136115497C>GCA348659078CXCR4c.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)
2g.136115497C>TCA348659080CXCR4c.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
2g.136115498T>ACA348659081CXCR4c.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)
2g.136115498T>CCA348659082CXCR4c.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)
2g.136115498T>GCA348659084CXCR4c.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)
2g.136115499G>ACA429206557CXCR4c.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
2g.136115499G>CCA348659086CXCR4c.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
2g.136115499G=CA1290966073CXCR4c.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=)
2g.136115499G>TCA348659087CXCR4c.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)
2g.136115500T>ACA348659090CXCR4c.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)
2g.136115500T>CCA348659092CXCR4c.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
2g.136115500T>GCA348659093CXCR4c.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)
2g.136115501T>ACA348659101CXCR4c.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)
2g.136115501T>CCA348659099CXCR4c.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)
2g.136115501T>GCA348659097CXCR4c.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)
2g.136115502G>ACA429206564CXCR4c.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
2g.136115502G>CCA429206565CXCR4c.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
2g.136115502G=CA1290966074CXCR4c.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=)
2g.136115502G>TCA429206566CXCR4c.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=)
2g.136115503G>ACA348659104CXCR4c.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
2g.136115503G>CCA348659106CXCR4c.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)
2g.136115503G>TCA348659108CXCR4c.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)
2g.136115504T>ACA348659111CXCR4c.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)
2g.136115504T>CCA348659113CXCR4c.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)
2g.136115504T>GCA348659115CXCR4c.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)
2g.136115505G>ACA429206568CXCR4c.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=)
2g.136115505G>CCA429206570CXCR4c.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=)
2g.136115505G>TCA429206572CXCR4c.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=)
2g.136115506G>ACA1890120CXCR4c.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
2g.136115506G>CCA348659118CXCR4c.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)
2g.136115506G=CA1290966075CXCR4c.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=)
2g.136115506G>TCA348659120CXCR4c.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
2g.136115507C>ACA348659123CXCR4c.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)
2g.136115507C=CA1290966076CXCR4c.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=)
2g.136115507C>GCA56886534CXCR4c.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
2g.136115507C>TCA1890121CXCR4c.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
2g.136115508G>ACA1890122CXCR4c.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
2g.136115508G>CCA348659130CXCR4c.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)
2g.136115508G=CA1290966077CXCR4c.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=)
2g.136115508G>TCA348659128CXCR4c.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)
2g.136115509T>ACA348659131CXCR4c.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)
2g.136115509T>CCA348659136CXCR4c.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
2g.136115509T>GCA348659134CXCR4c.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)
2g.136115510G>ACA348659139CXCR4c.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)
2g.136115510G>CCA348659144CXCR4c.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)
2g.136115510G>TCA348659141CXCR4c.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)
2g.136115511G>ACA429206584CXCR4c.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=)
2g.136115511G>CCA429206585CXCR4c.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
2g.136115511G>TCA429206586CXCR4c.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=)
2g.136115512A>CCA348659146CXCR4c.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)
2g.136115512A>GCA348659149CXCR4c.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)
2g.136115512A>TCA348659151CXCR4c.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)
2g.136115513C>ACA348659153CXCR4c.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)
2g.136115513C=CA1290966078CXCR4c.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=)
2g.136115513C>GCA348659156CXCR4c.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
2g.136115513C>TCA348659157CXCR4c.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
2g.136115514G>ACA1890123CXCR4c.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
2g.136115514G>CCA348659160CXCR4c.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)
2g.136115514G=CA1290966079CXCR4c.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=)
2g.136115514G>TCA429206592CXCR4c.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=)
2g.136115515A>CCA348659162CXCR4c.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)
2g.136115515A>GCA348659164CXCR4c.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)
2g.136115515A>TCA348659166CXCR4c.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)
2g.136115516T>ACA348659173CXCR4c.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)
2g.136115516T>CCA348659168CXCR4c.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)
2g.136115516T>GCA348659170CXCR4c.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)
2g.136115517G>ACA429206599CXCR4c.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=)
2g.136115517G>CCA429206601CXCR4c.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=)
2g.136115517G>TCA429206602CXCR4c.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
2g.136115518G>ACA348659175CXCR4c.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)
2g.136115518G>CCA348659177CXCR4c.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)
2g.136115518G>TCA348659178CXCR4c.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)
2g.136115519C>ACA348659179CXCR4c.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)
2g.136115519C>GCA348659181CXCR4c.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)
2g.136115519C>TCA348659184CXCR4c.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)
2g.136115520C>ACA429206609CXCR4c.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=)
2g.136115520C>GCA429206611CXCR4c.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=)
2g.136115520C>TCA429206613CXCR4c.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=)
2g.136115521A>CCA348659188CXCR4c.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)
2g.136115521A>GCA348659190CXCR4c.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)
2g.136115521A>TCA348659192CXCR4c.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)
2g.136115522G>ACA429206620CXCR4c.394C>T (p.Leu132=)
c.361C>T (p.Leu121=)
c.406C>T (p.Leu136=)
c.418C>T (p.Leu140=)
n.600C>T
c.619C>T (p.Leu207=)
c.505C>T (p.Leu169=)
 gnomAD v4
2g.136115522G>CCA348659195CXCR4c.394C>G (p.Leu132Val)
c.361C>G (p.Leu121Val)
c.406C>G (p.Leu136Val)
c.418C>G (p.Leu140Val)
n.600C>G
c.619C>G (p.Leu207Val)
c.505C>G (p.Leu169Val)
2g.136115522G>TCA348659196CXCR4c.394C>A (p.Leu132Met)
c.361C>A (p.Leu121Met)
c.406C>A (p.Leu136Met)
c.418C>A (p.Leu140Met)
n.600C>A
c.619C>A (p.Leu207Met)
c.505C>A (p.Leu169Met)
2g.136115525_136115530delCA2661289451CXCR4c.389_394del (p.Arg130_Tyr131del)
c.356_361del (p.Arg119_Tyr120del)
c.401_406del (p.Arg134_Tyr135del)
c.413_418del (p.Arg138_Tyr139del)
n.595_600del
c.614_619del (p.Arg205_Tyr206del)
c.500_505del (p.Arg167_Tyr168del)
 gnomAD v4
2g.136115523G>ACA429206626CXCR4c.393C>T (p.Tyr131=)
c.360C>T (p.Tyr120=)
c.405C>T (p.Tyr135=)
c.417C>T (p.Tyr139=)
n.599C>T
c.618C>T (p.Tyr206=)
c.504C>T (p.Tyr168=)
2g.136115523G>CCA348659200CXCR4c.393C>G (p.Tyr131Ter)
c.360C>G (p.Tyr120Ter)
c.405C>G (p.Tyr135Ter)
c.417C>G (p.Tyr139Ter)
n.599C>G
c.618C>G (p.Tyr206Ter)
c.504C>G (p.Tyr168Ter)
2g.136115523G>TCA348659197CXCR4c.393C>A (p.Tyr131Ter)
c.360C>A (p.Tyr120Ter)
c.405C>A (p.Tyr135Ter)
c.417C>A (p.Tyr139Ter)
n.599C>A
c.618C>A (p.Tyr206Ter)
c.504C>A (p.Tyr168Ter)
2g.136115524T>ACA348659202CXCR4c.392A>T (p.Tyr131Phe)
c.359A>T (p.Tyr120Phe)
c.404A>T (p.Tyr135Phe)
c.416A>T (p.Tyr139Phe)
n.598A>T
c.617A>T (p.Tyr206Phe)
c.503A>T (p.Tyr168Phe)
2g.136115524T>CCA348659203CXCR4c.392A>G (p.Tyr131Cys)
c.359A>G (p.Tyr120Cys)
c.404A>G (p.Tyr135Cys)
c.416A>G (p.Tyr139Cys)
n.598A>G
c.617A>G (p.Tyr206Cys)
c.503A>G (p.Tyr168Cys)
 dbSNP gnomAD v2 gnomAD v4
2g.136115524T>GCA348659205CXCR4c.392A>C (p.Tyr131Ser)
c.359A>C (p.Tyr120Ser)
c.404A>C (p.Tyr135Ser)
c.416A>C (p.Tyr139Ser)
n.598A>C
c.617A>C (p.Tyr206Ser)
c.503A>C (p.Tyr168Ser)
2g.136115524T=CA1290966080CXCR4c.392A= (p.Tyr131=)
c.359A= (p.Tyr120=)
c.404A= (p.Tyr135=)
c.416A= (p.Tyr139=)
n.598A=
c.617A= (p.Tyr206=)
c.503A= (p.Tyr168=)
2g.136115525A>CCA348659207CXCR4c.391T>G (p.Tyr131Asp)
c.358T>G (p.Tyr120Asp)
c.403T>G (p.Tyr135Asp)
c.415T>G (p.Tyr139Asp)
n.597T>G
c.616T>G (p.Tyr206Asp)
c.502T>G (p.Tyr168Asp)
2g.136115525A>GCA348659210CXCR4c.391T>C (p.Tyr131His)
c.358T>C (p.Tyr120His)
c.403T>C (p.Tyr135His)
c.415T>C (p.Tyr139His)
n.597T>C
c.616T>C (p.Tyr206His)
c.502T>C (p.Tyr168His)
2g.136115525A>TCA348659212CXCR4c.391T>A (p.Tyr131Asn)
c.358T>A (p.Tyr120Asn)
c.403T>A (p.Tyr135Asn)
c.415T>A (p.Tyr139Asn)
n.597T>A
c.616T>A (p.Tyr206Asn)
c.502T>A (p.Tyr168Asn)
2g.136115526G>ACA429206633CXCR4c.390C>T (p.Arg130=)
c.357C>T (p.Arg119=)
c.402C>T (p.Arg134=)
c.414C>T (p.Arg138=)
n.596C>T
c.615C>T (p.Arg205=)
c.501C>T (p.Arg167=)
2g.136115526G>CCA429206636CXCR4c.390C>G (p.Arg130=)
c.357C>G (p.Arg119=)
c.402C>G (p.Arg134=)
c.414C>G (p.Arg138=)
n.596C>G
c.615C>G (p.Arg205=)
c.501C>G (p.Arg167=)
2g.136115526G>TCA429206637CXCR4c.390C>A (p.Arg130=)
c.357C>A (p.Arg119=)
c.402C>A (p.Arg134=)
c.414C>A (p.Arg138=)
n.596C>A
c.615C>A (p.Arg205=)
c.501C>A (p.Arg167=)
 ClinVar dbSNP
2g.136115527C>ACA348659220CXCR4c.389G>T (p.Arg130Leu)
c.356G>T (p.Arg119Leu)
c.401G>T (p.Arg134Leu)
c.413G>T (p.Arg138Leu)
n.595G>T
c.614G>T (p.Arg205Leu)
c.500G>T (p.Arg167Leu)
 COSMIC COSMIC
2g.136115527C>GCA348659216CXCR4c.389G>C (p.Arg130Pro)
c.356G>C (p.Arg119Pro)
c.401G>C (p.Arg134Pro)
c.413G>C (p.Arg138Pro)
n.595G>C
c.614G>C (p.Arg205Pro)
c.500G>C (p.Arg167Pro)
2g.136115527C>TCA348659218CXCR4c.389G>A (p.Arg130His)
c.356G>A (p.Arg119His)
c.401G>A (p.Arg134His)
c.413G>A (p.Arg138His)
n.595G>A
c.614G>A (p.Arg205His)
c.500G>A (p.Arg167His)
 gnomAD v4 COSMIC
2g.136115528G>ACA348659223CXCR4c.388C>T (p.Arg130Cys)
c.355C>T (p.Arg119Cys)
c.400C>T (p.Arg134Cys)
c.412C>T (p.Arg138Cys)
n.594C>T
c.613C>T (p.Arg205Cys)
c.499C>T (p.Arg167Cys)
 gnomAD v4
2g.136115528G>CCA348659225CXCR4c.388C>G (p.Arg130Gly)
c.355C>G (p.Arg119Gly)
c.400C>G (p.Arg134Gly)
c.412C>G (p.Arg138Gly)
n.594C>G
c.613C>G (p.Arg205Gly)
c.499C>G (p.Arg167Gly)
2g.136115528G>TCA348659227CXCR4c.388C>A (p.Arg130Ser)
c.355C>A (p.Arg119Ser)
c.400C>A (p.Arg134Ser)
c.412C>A (p.Arg138Ser)
n.594C>A
c.613C>A (p.Arg205Ser)
c.499C>A (p.Arg167Ser)

Number of alleles fetched