Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.151186427dupCA2685657514ASB10c.553dup (p.Leu185ProfsTer11)
c.508dup (p.Leu170ProfsTer11)
c.688dup (p.Leu230ProfsTer11)
 gnomAD v4
7g.151186427delCA2685657515ASB10c.553del (p.Leu185CysfsTer?)
c.508del (p.Leu170CysfsTer?)
c.688del (p.Leu230CysfsTer?)
 gnomAD v4
7g.151186425G>ACA370035738ASB10c.551C>T (p.Pro184Leu)
c.506C>T (p.Pro169Leu)
c.686C>T (p.Pro229Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.151186425G>CCA169125157ASB10c.551C>G (p.Pro184Arg)
c.506C>G (p.Pro169Arg)
c.686C>G (p.Pro229Arg)
 dbSNP
7g.151186425G=CA1752544830ASB10c.551C= (p.Pro184=)
c.506C= (p.Pro169=)
c.686C= (p.Pro229=)
7g.151186425G>TCA370035739ASB10c.551C>A (p.Pro184His)
c.506C>A (p.Pro169His)
c.686C>A (p.Pro229His)
 gnomAD v4
7g.151186426G>ACA370035741ASB10c.550C>T (p.Pro184Ser)
c.505C>T (p.Pro169Ser)
c.685C>T (p.Pro229Ser)
7g.151186426G>CCA370035743ASB10c.550C>G (p.Pro184Ala)
c.505C>G (p.Pro169Ala)
c.685C>G (p.Pro229Ala)
7g.151186426G>TCA370035744ASB10c.550C>A (p.Pro184Thr)
c.505C>A (p.Pro169Thr)
c.685C>A (p.Pro229Thr)
7g.151186427G>ACA169125158ASB10c.549C>T (p.Arg183=)
c.504C>T (p.Arg168=)
c.684C>T (p.Arg228=)
 dbSNP gnomAD v4
7g.151186427G>CCA458881476ASB10c.549C>G (p.Arg183=)
c.504C>G (p.Arg168=)
c.684C>G (p.Arg228=)
7g.151186427G=CA1752544832ASB10c.549C= (p.Arg183=)
c.504C= (p.Arg168=)
c.684C= (p.Arg228=)
7g.151186427G>TCA458881477ASB10c.549C>A (p.Arg183=)
c.504C>A (p.Arg168=)
c.684C>A (p.Arg228=)
 gnomAD v4
7g.151186428C>ACA370035746ASB10c.548G>T (p.Arg183Leu)
c.503G>T (p.Arg168Leu)
c.683G>T (p.Arg228Leu)
 gnomAD v4
7g.151186428C=CA1752544834ASB10c.548G= (p.Arg183=)
c.503G= (p.Arg168=)
c.683G= (p.Arg228=)
7g.151186428C>GCA370035748ASB10c.548G>C (p.Arg183Pro)
c.503G>C (p.Arg168Pro)
c.683G>C (p.Arg228Pro)
 gnomAD v4
7g.151186428C>TCA370035750ASB10c.548G>A (p.Arg183His)
c.503G>A (p.Arg168His)
c.683G>A (p.Arg228His)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.151186429G>ACA150543ASB10c.547C>T (p.Arg183Cys)
c.502C>T (p.Arg168Cys)
c.682C>T (p.Arg228Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186429G>CCA370035753ASB10c.547C>G (p.Arg183Gly)
c.502C>G (p.Arg168Gly)
c.682C>G (p.Arg228Gly)
7g.151186429G=CA1752544836ASB10c.547C= (p.Arg183=)
c.502C= (p.Arg168=)
c.682C= (p.Arg228=)
7g.151186429G>TCA370035755ASB10c.547C>A (p.Arg183Ser)
c.502C>A (p.Arg168Ser)
c.682C>A (p.Arg228Ser)
 gnomAD v4
7g.151186430T>ACA370035757ASB10c.546A>T (p.Lys182Asn)
c.501A>T (p.Lys167Asn)
c.681A>T (p.Lys227Asn)
 ClinVar
7g.151186430T>CCA458881481ASB10c.546A>G (p.Lys182=)
c.501A>G (p.Lys167=)
c.681A>G (p.Lys227=)
 dbSNP gnomAD v3 gnomAD v4
7g.151186430T>GCA370035758ASB10c.546A>C (p.Lys182Asn)
c.501A>C (p.Lys167Asn)
c.681A>C (p.Lys227Asn)
7g.151186430T=CA1752544842ASB10c.546A= (p.Lys182=)
c.501A= (p.Lys167=)
c.681A= (p.Lys227=)
7g.151186432delCA2685657516ASB10c.546del (p.Lys182AsnfsTer?)
c.501del (p.Lys167AsnfsTer?)
c.681del (p.Lys227AsnfsTer?)
 gnomAD v4
7g.151186431T>ACA370035764ASB10c.545A>T (p.Lys182Ile)
c.500A>T (p.Lys167Ile)
c.680A>T (p.Lys227Ile)
7g.151186431T>CCA370035762ASB10c.545A>G (p.Lys182Arg)
c.500A>G (p.Lys167Arg)
c.680A>G (p.Lys227Arg)
 gnomAD v4
7g.151186431T>GCA370035761ASB10c.545A>C (p.Lys182Thr)
c.500A>C (p.Lys167Thr)
c.680A>C (p.Lys227Thr)
7g.151186432T>ACA370035766ASB10c.544A>T (p.Lys182Ter)
c.499A>T (p.Lys167Ter)
c.679A>T (p.Lys227Ter)
 dbSNP gnomAD v2 gnomAD v4
7g.151186432T>CCA370035767ASB10c.544A>G (p.Lys182Glu)
c.499A>G (p.Lys167Glu)
c.679A>G (p.Lys227Glu)
 gnomAD v4
7g.151186432T>GCA370035769ASB10c.544A>C (p.Lys182Gln)
c.499A>C (p.Lys167Gln)
c.679A>C (p.Lys227Gln)
7g.151186432T=CA1752544846ASB10c.544A= (p.Lys182=)
c.499A= (p.Lys167=)
c.679A= (p.Lys227=)
7g.151186433C>ACA458881485ASB10c.543G>T (p.Gly181=)
c.498G>T (p.Gly166=)
c.678G>T (p.Gly226=)
 gnomAD v4
7g.151186433C=CA1752544847ASB10c.543G= (p.Gly181=)
c.498G= (p.Gly166=)
c.678G= (p.Gly226=)
7g.151186433C>GCA458881486ASB10c.543G>C (p.Gly181=)
c.498G>C (p.Gly166=)
c.678G>C (p.Gly226=)
7g.151186433C>TCA458881487ASB10c.543G>A (p.Gly181=)
c.498G>A (p.Gly166=)
c.678G>A (p.Gly226=)
 dbSNP gnomAD v4
7g.151186434C>ACA370035770ASB10c.542G>T (p.Gly181Val)
c.497G>T (p.Gly166Val)
c.677G>T (p.Gly226Val)
 gnomAD v4
7g.151186434C=CA1752544850ASB10c.542G= (p.Gly181=)
c.497G= (p.Gly166=)
c.677G= (p.Gly226=)
7g.151186434C>GCA370035771ASB10c.542G>C (p.Gly181Ala)
c.497G>C (p.Gly166Ala)
c.677G>C (p.Gly226Ala)
 dbSNP
7g.151186434C>TCA370035773ASB10c.542G>A (p.Gly181Glu)
c.497G>A (p.Gly166Glu)
c.677G>A (p.Gly226Glu)
7g.151186435C>ACA370035775ASB10c.541G>T (p.Gly181Trp)
c.496G>T (p.Gly166Trp)
c.676G>T (p.Gly226Trp)
 gnomAD v4
7g.151186435C=CA1752544853ASB10c.541G= (p.Gly181=)
c.496G= (p.Gly166=)
c.676G= (p.Gly226=)
7g.151186435C>GCA370035777ASB10c.541G>C (p.Gly181Arg)
c.496G>C (p.Gly166Arg)
c.676G>C (p.Gly226Arg)
7g.151186435C>TCA169125160ASB10c.541G>A (p.Gly181Arg)
c.496G>A (p.Gly166Arg)
c.676G>A (p.Gly226Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.151186436A>CCA370035779ASB10c.540T>G (p.Asp180Glu)
c.495T>G (p.Asp165Glu)
c.675T>G (p.Asp225Glu)
7g.151186436A>GCA458881492ASB10c.540T>C (p.Asp180=)
c.495T>C (p.Asp165=)
c.675T>C (p.Asp225=)
7g.151186436A>TCA370035781ASB10c.540T>A (p.Asp180Glu)
c.495T>A (p.Asp165Glu)
c.675T>A (p.Asp225Glu)
 gnomAD v4
7g.151186437T>ACA370035787ASB10c.539A>T (p.Asp180Val)
c.494A>T (p.Asp165Val)
c.674A>T (p.Asp225Val)
7g.151186437T>CCA370035785ASB10c.539A>G (p.Asp180Gly)
c.494A>G (p.Asp165Gly)
c.674A>G (p.Asp225Gly)
7g.151186437T>GCA370035783ASB10c.539A>C (p.Asp180Ala)
c.494A>C (p.Asp165Ala)
c.674A>C (p.Asp225Ala)
7g.151186438C>ACA370035789ASB10c.538G>T (p.Asp180Tyr)
c.493G>T (p.Asp165Tyr)
c.673G>T (p.Asp225Tyr)
 gnomAD v4
7g.151186438C>GCA370035791ASB10c.538G>C (p.Asp180His)
c.493G>C (p.Asp165His)
c.673G>C (p.Asp225His)
7g.151186438C>TCA370035792ASB10c.538G>A (p.Asp180Asn)
c.493G>A (p.Asp165Asn)
c.673G>A (p.Asp225Asn)
 gnomAD v4
7g.151186439C>ACA370035794ASB10c.537G>T (p.Gln179His)
c.492G>T (p.Gln164His)
c.672G>T (p.Gln224His)
 gnomAD v4
7g.151186439C=CA1752544854ASB10c.537G= (p.Gln179=)
c.492G= (p.Gln164=)
c.672G= (p.Gln224=)
7g.151186439C>GCA370035796ASB10c.537G>C (p.Gln179His)
c.492G>C (p.Gln164His)
c.672G>C (p.Gln224His)
7g.151186439C>TCA458881496ASB10c.537G>A (p.Gln179=)
c.492G>A (p.Gln164=)
c.672G>A (p.Gln224=)
 dbSNP gnomAD v2 gnomAD v4
7g.151186440T>ACA370035798ASB10c.536A>T (p.Gln179Leu)
c.491A>T (p.Gln164Leu)
c.671A>T (p.Gln224Leu)
7g.151186440T>CCA370035800ASB10c.536A>G (p.Gln179Arg)
c.491A>G (p.Gln164Arg)
c.671A>G (p.Gln224Arg)
 gnomAD v4
7g.151186440T>GCA370035801ASB10c.536A>C (p.Gln179Pro)
c.491A>C (p.Gln164Pro)
c.671A>C (p.Gln224Pro)
7g.151186441G>ACA370035803ASB10c.535C>T (p.Gln179Ter)
c.490C>T (p.Gln164Ter)
c.670C>T (p.Gln224Ter)
 gnomAD v4
7g.151186441G>CCA370035804ASB10c.535C>G (p.Gln179Glu)
c.490C>G (p.Gln164Glu)
c.670C>G (p.Gln224Glu)
7g.151186441G>TCA370035806ASB10c.535C>A (p.Gln179Lys)
c.490C>A (p.Gln164Lys)
c.670C>A (p.Gln224Lys)
 gnomAD v4
7g.151186442G>ACA458881497ASB10c.534C>T (p.Asp178=)
c.489C>T (p.Asp163=)
c.669C>T (p.Asp223=)
 dbSNP gnomAD v4
7g.151186442G>CCA370035808ASB10c.534C>G (p.Asp178Glu)
c.489C>G (p.Asp163Glu)
c.669C>G (p.Asp223Glu)
7g.151186442G=CA1752544856ASB10c.534C= (p.Asp178=)
c.489C= (p.Asp163=)
c.669C= (p.Asp223=)
7g.151186442G>TCA370035810ASB10c.534C>A (p.Asp178Glu)
c.489C>A (p.Asp163Glu)
c.669C>A (p.Asp223Glu)
7g.151186443T>ACA370035816ASB10c.533A>T (p.Asp178Val)
c.488A>T (p.Asp163Val)
c.668A>T (p.Asp223Val)
7g.151186443T>CCA370035812ASB10c.533A>G (p.Asp178Gly)
c.488A>G (p.Asp163Gly)
c.668A>G (p.Asp223Gly)
7g.151186443T>GCA370035814ASB10c.533A>C (p.Asp178Ala)
c.488A>C (p.Asp163Ala)
c.668A>C (p.Asp223Ala)
7g.151186444C>ACA370035817ASB10c.532G>T (p.Asp178Tyr)
c.487G>T (p.Asp163Tyr)
c.667G>T (p.Asp223Tyr)
 gnomAD v4
7g.151186444C=CA1752544859ASB10c.532G= (p.Asp178=)
c.487G= (p.Asp163=)
c.667G= (p.Asp223=)
7g.151186444C>GCA370035819ASB10c.532G>C (p.Asp178His)
c.487G>C (p.Asp163His)
c.667G>C (p.Asp223His)
7g.151186444C>TCA370035820ASB10c.532G>A (p.Asp178Asn)
c.487G>A (p.Asp163Asn)
c.667G>A (p.Asp223Asn)
 dbSNP
7g.151186445A=CA1752544861ASB10c.531T= (p.Ala177=)
c.486T= (p.Ala162=)
c.666T= (p.Ala222=)
7g.151186445A>CCA458881500ASB10c.531T>G (p.Ala177=)
c.486T>G (p.Ala162=)
c.666T>G (p.Ala222=)
7g.151186445A>GCA458881501ASB10c.531T>C (p.Ala177=)
c.486T>C (p.Ala162=)
c.666T>C (p.Ala222=)
 dbSNP gnomAD v2 gnomAD v4
7g.151186445A>TCA458881503ASB10c.531T>A (p.Ala177=)
c.486T>A (p.Ala162=)
c.666T>A (p.Ala222=)
7g.151186446G>ACA370035822ASB10c.530C>T (p.Ala177Val)
c.485C>T (p.Ala162Val)
c.665C>T (p.Ala222Val)
 gnomAD v4
7g.151186446G>CCA370035823ASB10c.530C>G (p.Ala177Gly)
c.485C>G (p.Ala162Gly)
c.665C>G (p.Ala222Gly)
7g.151186446G>TCA370035825ASB10c.530C>A (p.Ala177Asp)
c.485C>A (p.Ala162Asp)
c.665C>A (p.Ala222Asp)
7g.151186447C>ACA370035827ASB10c.529G>T (p.Ala177Ser)
c.484G>T (p.Ala162Ser)
c.664G>T (p.Ala222Ser)
 dbSNP gnomAD v2 gnomAD v4
7g.151186447C=CA1752544866ASB10c.529G= (p.Ala177=)
c.484G= (p.Ala162=)
c.664G= (p.Ala222=)
7g.151186447C>GCA370035829ASB10c.529G>C (p.Ala177Pro)
c.484G>C (p.Ala162Pro)
c.664G>C (p.Ala222Pro)
7g.151186447C>TCA4573859ASB10c.529G>A (p.Ala177Thr)
c.484G>A (p.Ala162Thr)
c.664G>A (p.Ala222Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186448G>ACA4573860ASB10c.528C>T (p.Ile176=)
c.483C>T (p.Ile161=)
c.663C>T (p.Ile221=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186448G>CCA370035833ASB10c.528C>G (p.Ile176Met)
c.483C>G (p.Ile161Met)
c.663C>G (p.Ile221Met)
7g.151186448G=CA1752544868ASB10c.528C= (p.Ile176=)
c.483C= (p.Ile161=)
c.663C= (p.Ile221=)
7g.151186448G>TCA458881505ASB10c.528C>A (p.Ile176=)
c.483C>A (p.Ile161=)
c.663C>A (p.Ile221=)
 dbSNP gnomAD v3 gnomAD v4
7g.151186449A>CCA370035839ASB10c.527T>G (p.Ile176Ser)
c.482T>G (p.Ile161Ser)
c.662T>G (p.Ile221Ser)
7g.151186449A>GCA370035837ASB10c.527T>C (p.Ile176Thr)
c.482T>C (p.Ile161Thr)
c.662T>C (p.Ile221Thr)
7g.151186449A>TCA370035835ASB10c.527T>A (p.Ile176Asn)
c.482T>A (p.Ile161Asn)
c.662T>A (p.Ile221Asn)
7g.151186450T>ACA370035840ASB10c.526A>T (p.Ile176Phe)
c.481A>T (p.Ile161Phe)
c.661A>T (p.Ile221Phe)
7g.151186450T>CCA370035843ASB10c.526A>G (p.Ile176Val)
c.481A>G (p.Ile161Val)
c.661A>G (p.Ile221Val)
7g.151186450T>GCA370035842ASB10c.526A>C (p.Ile176Leu)
c.481A>C (p.Ile161Leu)
c.661A>C (p.Ile221Leu)
7g.151186451G>ACA458881508ASB10c.525C>T (p.Asn175=)
c.480C>T (p.Asn160=)
c.660C>T (p.Asn220=)
 gnomAD v4
7g.151186451G>CCA370035845ASB10c.525C>G (p.Asn175Lys)
c.480C>G (p.Asn160Lys)
c.660C>G (p.Asn220Lys)
7g.151186451G>TCA370035847ASB10c.525C>A (p.Asn175Lys)
c.480C>A (p.Asn160Lys)
c.660C>A (p.Asn220Lys)
 gnomAD v4
7g.151186452T>ACA370035849ASB10c.524A>T (p.Asn175Ile)
c.479A>T (p.Asn160Ile)
c.659A>T (p.Asn220Ile)
7g.151186452T>CCA370035850ASB10c.524A>G (p.Asn175Ser)
c.479A>G (p.Asn160Ser)
c.659A>G (p.Asn220Ser)
7g.151186452T>GCA150494ASB10c.524A>C (p.Asn175Thr)
c.479A>C (p.Asn160Thr)
c.659A>C (p.Asn220Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186452T=CA1752544874ASB10c.524A= (p.Asn175=)
c.479A= (p.Asn160=)
c.659A= (p.Asn220=)
7g.151186453T>ACA370035852ASB10c.523A>T (p.Asn175Tyr)
c.478A>T (p.Asn160Tyr)
c.658A>T (p.Asn220Tyr)
7g.151186453T>CCA370035854ASB10c.523A>G (p.Asn175Asp)
c.478A>G (p.Asn160Asp)
c.658A>G (p.Asn220Asp)
 gnomAD v4
7g.151186453T>GCA370035856ASB10c.523A>C (p.Asn175His)
c.478A>C (p.Asn160His)
c.658A>C (p.Asn220His)
 dbSNP
7g.151186453T=CA1752544877ASB10c.523A= (p.Asn175=)
c.478A= (p.Asn160=)
c.658A= (p.Asn220=)
7g.151186454G>ACA4573861ASB10c.522C>T (p.Pro174=)
c.477C>T (p.Pro159=)
c.657C>T (p.Pro219=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186454G>CCA458881511ASB10c.522C>G (p.Pro174=)
c.477C>G (p.Pro159=)
c.657C>G (p.Pro219=)
7g.151186454G=CA1752544881ASB10c.522C= (p.Pro174=)
c.477C= (p.Pro159=)
c.657C= (p.Pro219=)
7g.151186454G>TCA458881512ASB10c.522C>A (p.Pro174=)
c.477C>A (p.Pro159=)
c.657C>A (p.Pro219=)
 gnomAD v4
7g.151186455G>ACA370035859ASB10c.521C>T (p.Pro174Leu)
c.476C>T (p.Pro159Leu)
c.656C>T (p.Pro219Leu)
7g.151186455G>CCA370035861ASB10c.521C>G (p.Pro174Arg)
c.476C>G (p.Pro159Arg)
c.656C>G (p.Pro219Arg)
7g.151186455G>TCA370035863ASB10c.521C>A (p.Pro174His)
c.476C>A (p.Pro159His)
c.656C>A (p.Pro219His)
 gnomAD v4
7g.151186456G>ACA370035867ASB10c.520C>T (p.Pro174Ser)
c.475C>T (p.Pro159Ser)
c.655C>T (p.Pro219Ser)
 COSMIC COSMIC COSMIC COSMIC
7g.151186456G>CCA370035865ASB10c.520C>G (p.Pro174Ala)
c.475C>G (p.Pro159Ala)
c.655C>G (p.Pro219Ala)
 gnomAD v4
7g.151186456G>TCA370035866ASB10c.520C>A (p.Pro174Thr)
c.475C>A (p.Pro159Thr)
c.655C>A (p.Pro219Thr)
 gnomAD v4
7g.151186457G>ACA458881515ASB10c.519C>T (p.Asp173=)
c.474C>T (p.Asp158=)
c.654C>T (p.Asp218=)
 gnomAD v4
7g.151186457G>CCA370035869ASB10c.519C>G (p.Asp173Glu)
c.474C>G (p.Asp158Glu)
c.654C>G (p.Asp218Glu)
7g.151186457G=CA1752544886ASB10c.519C= (p.Asp173=)
c.474C= (p.Asp158=)
c.654C= (p.Asp218=)
7g.151186457G>TCA4573862ASB10c.519C>A (p.Asp173Glu)
c.474C>A (p.Asp158Glu)
c.654C>A (p.Asp218Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186458T>ACA370035872ASB10c.518A>T (p.Asp173Val)
c.473A>T (p.Asp158Val)
c.653A>T (p.Asp218Val)
7g.151186458T>CCA370035873ASB10c.518A>G (p.Asp173Gly)
c.473A>G (p.Asp158Gly)
c.653A>G (p.Asp218Gly)
7g.151186458T>GCA370035875ASB10c.518A>C (p.Asp173Ala)
c.473A>C (p.Asp158Ala)
c.653A>C (p.Asp218Ala)
7g.151186459C>ACA370035878ASB10c.517G>T (p.Asp173Tyr)
c.472G>T (p.Asp158Tyr)
c.652G>T (p.Asp218Tyr)
 gnomAD v4
7g.151186459C=CA1752544889ASB10c.517G= (p.Asp173=)
c.472G= (p.Asp158=)
c.652G= (p.Asp218=)
7g.151186459C>GCA370035879ASB10c.517G>C (p.Asp173His)
c.472G>C (p.Asp158His)
c.652G>C (p.Asp218His)
 dbSNP gnomAD v2 gnomAD v4
7g.151186459C>TCA4573863ASB10c.517G>A (p.Asp173Asn)
c.472G>A (p.Asp158Asn)
c.652G>A (p.Asp218Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
7g.151186460G>ACA150492ASB10c.516C>T (p.Ala172=)
c.471C>T (p.Ala157=)
c.651C>T (p.Ala217=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186460G>CCA4573864ASB10c.516C>G (p.Ala172=)
c.471C>G (p.Ala157=)
c.651C>G (p.Ala217=)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.151186460G=CA1752544897ASB10c.516C= (p.Ala172=)
c.471C= (p.Ala157=)
c.651C= (p.Ala217=)
7g.151186460G>TCA458881518ASB10c.516C>A (p.Ala172=)
c.471C>A (p.Ala157=)
c.651C>A (p.Ala217=)
 gnomAD v4
7g.151186461G>ACA150541ASB10c.515C>T (p.Ala172Val)
c.470C>T (p.Ala157Val)
c.650C>T (p.Ala217Val)
 ClinVar dbSNP gnomAD v4
7g.151186461G>CCA4573865ASB10c.515C>G (p.Ala172Gly)
c.470C>G (p.Ala157Gly)
c.650C>G (p.Ala217Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
7g.151186461G=CA1752544904ASB10c.515C= (p.Ala172=)
c.470C= (p.Ala157=)
c.650C= (p.Ala217=)
7g.151186461G>TCA370035882ASB10c.515C>A (p.Ala172Asp)
c.470C>A (p.Ala157Asp)
c.650C>A (p.Ala217Asp)
 gnomAD v4
7g.151186462C>ACA370035885ASB10c.514G>T (p.Ala172Ser)
c.469G>T (p.Ala157Ser)
c.649G>T (p.Ala217Ser)
 gnomAD v4
7g.151186462C=CA1752544909ASB10c.514G= (p.Ala172=)
c.469G= (p.Ala157=)
c.649G= (p.Ala217=)
7g.151186462C>GCA370035887ASB10c.514G>C (p.Ala172Pro)
c.469G>C (p.Ala157Pro)
c.649G>C (p.Ala217Pro)
7g.151186462C>TCA370035888ASB10c.514G>A (p.Ala172Thr)
c.469G>A (p.Ala157Thr)
c.649G>A (p.Ala217Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.151186463T>ACA458881522ASB10c.513A>T (p.Gly171=)
c.468A>T (p.Gly156=)
c.648A>T (p.Gly216=)
7g.151186463T>CCA458881523ASB10c.513A>G (p.Gly171=)
c.468A>G (p.Gly156=)
c.648A>G (p.Gly216=)
 dbSNP gnomAD v4
7g.151186463T>GCA458881524ASB10c.513A>C (p.Gly171=)
c.468A>C (p.Gly156=)
c.648A>C (p.Gly216=)
7g.151186463T=CA1752544913ASB10c.513A= (p.Gly171=)
c.468A= (p.Gly156=)
c.648A= (p.Gly216=)
7g.151186464C>ACA370035889ASB10c.512G>T (p.Gly171Val)
c.467G>T (p.Gly156Val)
c.647G>T (p.Gly216Val)
 gnomAD v4
7g.151186464C=CA1752544917ASB10c.512G= (p.Gly171=)
c.467G= (p.Gly156=)
c.647G= (p.Gly216=)
7g.151186464C>GCA370035891ASB10c.512G>C (p.Gly171Ala)
c.467G>C (p.Gly156Ala)
c.647G>C (p.Gly216Ala)
7g.151186464C>TCA169125197ASB10c.512G>A (p.Gly171Glu)
c.467G>A (p.Gly156Glu)
c.647G>A (p.Gly216Glu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.151186465C>ACA370035894ASB10c.511G>T (p.Gly171Ter)
c.466G>T (p.Gly156Ter)
c.646G>T (p.Gly216Ter)
 dbSNP gnomAD v2 gnomAD v4
7g.151186465C=CA1752544919ASB10c.511G= (p.Gly171=)
c.466G= (p.Gly156=)
c.646G= (p.Gly216=)
7g.151186465C>GCA370035896ASB10c.511G>C (p.Gly171Arg)
c.466G>C (p.Gly156Arg)
c.646G>C (p.Gly216Arg)
7g.151186465C>TCA4573866ASB10c.511G>A (p.Gly171Arg)
c.466G>A (p.Gly156Arg)
c.646G>A (p.Gly216Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.151186466T>ACA458881527ASB10c.510A>T (p.Ala170=)
c.465A>T (p.Ala155=)
c.645A>T (p.Ala215=)
7g.151186466T>CCA458881529ASB10c.510A>G (p.Ala170=)
c.465A>G (p.Ala155=)
c.645A>G (p.Ala215=)
 gnomAD v4
7g.151186466T>GCA458881530ASB10c.510A>C (p.Ala170=)
c.465A>C (p.Ala155=)
c.645A>C (p.Ala215=)
7g.151186467G>ACA370035899ASB10c.509C>T (p.Ala170Val)
c.464C>T (p.Ala155Val)
c.644C>T (p.Ala215Val)
 gnomAD v4
7g.151186467G>CCA370035901ASB10c.509C>G (p.Ala170Gly)
c.464C>G (p.Ala155Gly)
c.644C>G (p.Ala215Gly)
7g.151186467G>TCA370035903ASB10c.509C>A (p.Ala170Glu)
c.464C>A (p.Ala155Glu)
c.644C>A (p.Ala215Glu)
7g.151186468C>ACA370035909ASB10c.508G>T (p.Ala170Ser)
c.463G>T (p.Ala155Ser)
c.643G>T (p.Ala215Ser)
 gnomAD v4
7g.151186468C>GCA370035907ASB10c.508G>C (p.Ala170Pro)
c.463G>C (p.Ala155Pro)
c.643G>C (p.Ala215Pro)
7g.151186468C>TCA370035905ASB10c.508G>A (p.Ala170Thr)
c.463G>A (p.Ala155Thr)
c.643G>A (p.Ala215Thr)
7g.151186469C>ACA458881532ASB10c.507G>T (p.Val169=)
c.462G>T (p.Val154=)
c.642G>T (p.Val214=)
 gnomAD v4
7g.151186469C>GCA458881533ASB10c.507G>C (p.Val169=)
c.462G>C (p.Val154=)
c.642G>C (p.Val214=)
7g.151186469C>TCA458881534ASB10c.507G>A (p.Val169=)
c.462G>A (p.Val154=)
c.642G>A (p.Val214=)
7g.151186470A>CCA370035910ASB10c.506T>G (p.Val169Gly)
c.461T>G (p.Val154Gly)
c.641T>G (p.Val214Gly)
7g.151186470A>GCA370035912ASB10c.506T>C (p.Val169Ala)
c.461T>C (p.Val154Ala)
c.641T>C (p.Val214Ala)
7g.151186470A>TCA370035914ASB10c.506T>A (p.Val169Glu)
c.461T>A (p.Val154Glu)
c.641T>A (p.Val214Glu)
7g.151186471C>ACA370035916ASB10c.505G>T (p.Val169Leu)
c.460G>T (p.Val154Leu)
c.640G>T (p.Val214Leu)
 gnomAD v4
7g.151186471C=CA1752544921ASB10c.505G= (p.Val169=)
c.460G= (p.Val154=)
c.640G= (p.Val214=)
7g.151186471C>GCA370035917ASB10c.505G>C (p.Val169Leu)
c.460G>C (p.Val154Leu)
c.640G>C (p.Val214Leu)
 gnomAD v4
7g.151186471C>TCA169125236ASB10c.505G>A (p.Val169Met)
c.460G>A (p.Val154Met)
c.640G>A (p.Val214Met)
 dbSNP gnomAD v2 gnomAD v4
7g.151186472C>ACA458881537ASB10c.504G>T (p.Leu168=)
c.459G>T (p.Leu153=)
c.639G>T (p.Leu213=)
 gnomAD v4
7g.151186472C>GCA458881539ASB10c.504G>C (p.Leu168=)
c.459G>C (p.Leu153=)
c.639G>C (p.Leu213=)
7g.151186472C>TCA458881538ASB10c.504G>A (p.Leu168=)
c.459G>A (p.Leu153=)
c.639G>A (p.Leu213=)
7g.151186473A>CCA370035920ASB10c.503T>G (p.Leu168Arg)
c.458T>G (p.Leu153Arg)
c.638T>G (p.Leu213Arg)
7g.151186473A>GCA370035922ASB10c.503T>C (p.Leu168Pro)
c.458T>C (p.Leu153Pro)
c.638T>C (p.Leu213Pro)
7g.151186473A>TCA370035924ASB10c.503T>A (p.Leu168Gln)
c.458T>A (p.Leu153Gln)
c.638T>A (p.Leu213Gln)
7g.151186474G>ACA458881540ASB10c.502C>T (p.Leu168=)
c.457C>T (p.Leu153=)
c.637C>T (p.Leu213=)
 gnomAD v4
7g.151186474G>CCA370035926ASB10c.502C>G (p.Leu168Val)
c.457C>G (p.Leu153Val)
c.637C>G (p.Leu213Val)
7g.151186474G>TCA370035927ASB10c.502C>A (p.Leu168Met)
c.457C>A (p.Leu153Met)
c.637C>A (p.Leu213Met)
 gnomAD v4
7g.151186475C>ACA458881541ASB10c.501G>T (p.Leu167=)
c.456G>T (p.Leu152=)
c.636G>T (p.Leu212=)
 gnomAD v4
7g.151186475C=CA1752544925ASB10c.501G= (p.Leu167=)
c.456G= (p.Leu152=)
c.636G= (p.Leu212=)
7g.151186475C>GCA458881542ASB10c.501G>C (p.Leu167=)
c.456G>C (p.Leu152=)
c.636G>C (p.Leu212=)
 dbSNP
7g.151186475C>TCA4573867ASB10c.501G>A (p.Leu167=)
c.456G>A (p.Leu152=)
c.636G>A (p.Leu212=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186476A>CCA370035934ASB10c.500T>G (p.Leu167Arg)
c.455T>G (p.Leu152Arg)
c.635T>G (p.Leu212Arg)
7g.151186476A>GCA370035932ASB10c.500T>C (p.Leu167Pro)
c.455T>C (p.Leu152Pro)
c.635T>C (p.Leu212Pro)
 gnomAD v4
7g.151186476A>TCA370035930ASB10c.500T>A (p.Leu167Gln)
c.455T>A (p.Leu152Gln)
c.635T>A (p.Leu212Gln)
7g.151186477G>ACA4573868ASB10c.499C>T (p.Leu167=)
c.454C>T (p.Leu152=)
c.634C>T (p.Leu212=)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.151186477G>CCA370035938ASB10c.499C>G (p.Leu167Val)
c.454C>G (p.Leu152Val)
c.634C>G (p.Leu212Val)
7g.151186477G=CA1752544930ASB10c.499C= (p.Leu167=)
c.454C= (p.Leu152=)
c.634C= (p.Leu212=)
7g.151186477G>TCA370035936ASB10c.499C>A (p.Leu167Met)
c.454C>A (p.Leu152Met)
c.634C>A (p.Leu212Met)
 gnomAD v4
7g.151186478C>ACA458881545ASB10c.498G>T (p.Val166=)
c.453G>T (p.Val151=)
c.633G>T (p.Val211=)
 gnomAD v4
7g.151186478C>GCA458881544ASB10c.498G>C (p.Val166=)
c.453G>C (p.Val151=)
c.633G>C (p.Val211=)
7g.151186478C>TCA458881543ASB10c.498G>A (p.Val166=)
c.453G>A (p.Val151=)
c.633G>A (p.Val211=)
7g.151186479A=CA1752544933ASB10c.497T= (p.Val166=)
c.452T= (p.Val151=)
c.632T= (p.Val211=)
7g.151186479A>CCA370035940ASB10c.497T>G (p.Val166Gly)
c.452T>G (p.Val151Gly)
c.632T>G (p.Val211Gly)
7g.151186479A>GCA370035942ASB10c.497T>C (p.Val166Ala)
c.452T>C (p.Val151Ala)
c.632T>C (p.Val211Ala)
7g.151186479A>TCA370035944ASB10c.497T>A (p.Val166Glu)
c.452T>A (p.Val151Glu)
c.632T>A (p.Val211Glu)
 dbSNP gnomAD v2 gnomAD v4
7g.151186480C>ACA370035946ASB10c.496G>T (p.Val166Leu)
c.451G>T (p.Val151Leu)
c.631G>T (p.Val211Leu)
7g.151186480C>GCA370035947ASB10c.496G>C (p.Val166Leu)
c.451G>C (p.Val151Leu)
c.631G>C (p.Val211Leu)
7g.151186480C>TCA370035949ASB10c.496G>A (p.Val166Met)
c.451G>A (p.Val151Met)
c.631G>A (p.Val211Met)
 gnomAD v4
7g.151186481A=CA1752544935ASB10c.495T= (p.His165=)
c.450T= (p.His150=)
c.630T= (p.His210=)
7g.151186481A>CCA370035953ASB10c.495T>G (p.His165Gln)
c.450T>G (p.His150Gln)
c.630T>G (p.His210Gln)
7g.151186481A>GCA458881546ASB10c.495T>C (p.His165=)
c.450T>C (p.His150=)
c.630T>C (p.His210=)
 dbSNP gnomAD v3 gnomAD v4
7g.151186481A>TCA370035951ASB10c.495T>A (p.His165Gln)
c.450T>A (p.His150Gln)
c.630T>A (p.His210Gln)
7g.151186482T>ACA370035955ASB10c.494A>T (p.His165Leu)
c.449A>T (p.His150Leu)
c.629A>T (p.His210Leu)
 gnomAD v4
7g.151186482T>CCA370035957ASB10c.494A>G (p.His165Arg)
c.449A>G (p.His150Arg)
c.629A>G (p.His210Arg)
 gnomAD v4
7g.151186482T>GCA370035958ASB10c.494A>C (p.His165Pro)
c.449A>C (p.His150Pro)
c.629A>C (p.His210Pro)
7g.151186483G>ACA370035960ASB10c.493C>T (p.His165Tyr)
c.448C>T (p.His150Tyr)
c.628C>T (p.His210Tyr)
 dbSNP gnomAD v4
7g.151186483G>CCA370035961ASB10c.493C>G (p.His165Asp)
c.448C>G (p.His150Asp)
c.628C>G (p.His210Asp)
 dbSNP
7g.151186483G=CA1752544938ASB10c.493C= (p.His165=)
c.448C= (p.His150=)
c.628C= (p.His210=)
7g.151186483G>TCA370035963ASB10c.493C>A (p.His165Asn)
c.448C>A (p.His150Asn)
c.628C>A (p.His210Asn)
 dbSNP gnomAD v2 gnomAD v4
7g.151186484A>CCA458881547ASB10c.492T>G (p.Val164=)
c.447T>G (p.Val149=)
c.627T>G (p.Val209=)
7g.151186484A>GCA458881548ASB10c.492T>C (p.Val164=)
c.447T>C (p.Val149=)
c.627T>C (p.Val209=)
7g.151186484A>TCA458881549ASB10c.492T>A (p.Val164=)
c.447T>A (p.Val149=)
c.627T>A (p.Val209=)
7g.151186485A=CA1752544943ASB10c.491T= (p.Val164=)
c.446T= (p.Val149=)
c.626T= (p.Val209=)
7g.151186485A>CCA370035965ASB10c.491T>G (p.Val164Gly)
c.446T>G (p.Val149Gly)
c.626T>G (p.Val209Gly)
7g.151186485A>GCA370035969ASB10c.491T>C (p.Val164Ala)
c.446T>C (p.Val149Ala)
c.626T>C (p.Val209Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.151186485A>TCA370035967ASB10c.491T>A (p.Val164Asp)
c.446T>A (p.Val149Asp)
c.626T>A (p.Val209Asp)
7g.151186485_151186506delinsACACAGGCAGTGTGGCCTGCAGCA1752544946ASB10c.470_491delinsCTGCAGGCCACACTGCCTGTGT (p.Ala157=)
c.425_446delinsCTGCAGGCCACACTGCCTGTGT (p.Ala142=)
c.605_626delinsCTGCAGGCCACACTGCCTGTGT (p.Ala202=)
7g.151186486C>ACA370035971ASB10c.490G>T (p.Val164Phe)
c.445G>T (p.Val149Phe)
c.625G>T (p.Val209Phe)
 gnomAD v4
7g.151186486C=CA1752544951ASB10c.490G= (p.Val164=)
c.445G= (p.Val149=)
c.625G= (p.Val209=)
7g.151186486C>GCA370035973ASB10c.490G>C (p.Val164Leu)
c.445G>C (p.Val149Leu)
c.625G>C (p.Val209Leu)
7g.151186486C>TCA4573869ASB10c.490G>A (p.Val164Ile)
c.445G>A (p.Val149Ile)
c.625G>A (p.Val209Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.151186493_151186513delCA579077210ASB10c.470_490del (p.Ala157_Cys163del)
c.425_445del (p.Ala142_Cys148del)
c.605_625del (p.Ala202_Cys208del)
 dbSNP gnomAD v2 gnomAD v4
7g.151186487A=CA1752544954ASB10c.489T= (p.Cys163=)
c.444T= (p.Cys148=)
c.624T= (p.Cys208=)
7g.151186487A>CCA169125254ASB10c.489T>G (p.Cys163Trp)
c.444T>G (p.Cys148Trp)
c.624T>G (p.Cys208Trp)
 dbSNP
7g.151186487A>GCA458881550ASB10c.489T>C (p.Cys163=)
c.444T>C (p.Cys148=)
c.624T>C (p.Cys208=)
 COSMIC COSMIC COSMIC COSMIC
7g.151186487A>TCA370035976ASB10c.489T>A (p.Cys163Ter)
c.444T>A (p.Cys148Ter)
c.624T>A (p.Cys208Ter)
7g.151186488C>ACA370035978ASB10c.488G>T (p.Cys163Phe)
c.443G>T (p.Cys148Phe)
c.623G>T (p.Cys208Phe)
7g.151186488C>GCA370035980ASB10c.488G>C (p.Cys163Ser)
c.443G>C (p.Cys148Ser)
c.623G>C (p.Cys208Ser)
7g.151186488C>TCA370035982ASB10c.488G>A (p.Cys163Tyr)
c.443G>A (p.Cys148Tyr)
c.623G>A (p.Cys208Tyr)
7g.151186489A=CA1752544959ASB10c.487T= (p.Cys163=)
c.442T= (p.Cys148=)
c.622T= (p.Cys208=)
7g.151186489A>CCA370035984ASB10c.487T>G (p.Cys163Gly)
c.442T>G (p.Cys148Gly)
c.622T>G (p.Cys208Gly)
7g.151186489A>GCA370035986ASB10c.487T>C (p.Cys163Arg)
c.442T>C (p.Cys148Arg)
c.622T>C (p.Cys208Arg)
 gnomAD v4
7g.151186489A>TCA150490ASB10c.487T>A (p.Cys163Ser)
c.442T>A (p.Cys148Ser)
c.622T>A (p.Cys208Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186490G>ACA4573870ASB10c.486C>T (p.Ala162=)
c.441C>T (p.Ala147=)
c.621C>T (p.Ala207=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186490G>CCA458881551ASB10c.486C>G (p.Ala162=)
c.441C>G (p.Ala147=)
c.621C>G (p.Ala207=)
7g.151186490G=CA1752544963ASB10c.486C= (p.Ala162=)
c.441C= (p.Ala147=)
c.621C= (p.Ala207=)
7g.151186490G>TCA458881552ASB10c.486C>A (p.Ala162=)
c.441C>A (p.Ala147=)
c.621C>A (p.Ala207=)
 gnomAD v4
7g.151186491G>ACA370035993ASB10c.485C>T (p.Ala162Val)
c.440C>T (p.Ala147Val)
c.620C>T (p.Ala207Val)
 gnomAD v4
7g.151186491G>CCA370035990ASB10c.485C>G (p.Ala162Gly)
c.440C>G (p.Ala147Gly)
c.620C>G (p.Ala207Gly)
7g.151186491G>TCA370035992ASB10c.485C>A (p.Ala162Asp)
c.440C>A (p.Ala147Asp)
c.620C>A (p.Ala207Asp)
 gnomAD v4
7g.151186492C>ACA370035995ASB10c.484G>T (p.Ala162Ser)
c.439G>T (p.Ala147Ser)
c.619G>T (p.Ala207Ser)
7g.151186492C=CA1752544965ASB10c.484G= (p.Ala162=)
c.439G= (p.Ala147=)
c.619G= (p.Ala207=)
7g.151186492C>GCA370035997ASB10c.484G>C (p.Ala162Pro)
c.439G>C (p.Ala147Pro)
c.619G>C (p.Ala207Pro)
7g.151186492C>TCA4573871ASB10c.484G>A (p.Ala162Thr)
c.439G>A (p.Ala147Thr)
c.619G>A (p.Ala207Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186493A=CA1752544969ASB10c.483T= (p.Thr161=)
c.438T= (p.Thr146=)
c.618T= (p.Thr206=)
7g.151186493A>CCA458881553ASB10c.483T>G (p.Thr161=)
c.438T>G (p.Thr146=)
c.618T>G (p.Thr206=)
7g.151186493A>GCA458881554ASB10c.483T>C (p.Thr161=)
c.438T>C (p.Thr146=)
c.618T>C (p.Thr206=)
 dbSNP
7g.151186493A>TCA458881555ASB10c.483T>A (p.Thr161=)
c.438T>A (p.Thr146=)
c.618T>A (p.Thr206=)
7g.151186494G>ACA370035999ASB10c.482C>T (p.Thr161Ile)
c.437C>T (p.Thr146Ile)
c.617C>T (p.Thr206Ile)
 dbSNP
7g.151186494G>CCA370036000ASB10c.482C>G (p.Thr161Ser)
c.437C>G (p.Thr146Ser)
c.617C>G (p.Thr206Ser)
7g.151186494G=CA1752544970ASB10c.482C= (p.Thr161=)
c.437C= (p.Thr146=)
c.617C= (p.Thr206=)
7g.151186494G>TCA370036002ASB10c.482C>A (p.Thr161Asn)
c.437C>A (p.Thr146Asn)
c.617C>A (p.Thr206Asn)
 gnomAD v4
7g.151186495T>ACA370036004ASB10c.481A>T (p.Thr161Ser)
c.436A>T (p.Thr146Ser)
c.616A>T (p.Thr206Ser)
7g.151186495T>CCA4573872ASB10c.481A>G (p.Thr161Ala)
c.436A>G (p.Thr146Ala)
c.616A>G (p.Thr206Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186495T>GCA370036005ASB10c.481A>C (p.Thr161Pro)
c.436A>C (p.Thr146Pro)
c.616A>C (p.Thr206Pro)
7g.151186495T=CA1752544975ASB10c.481A= (p.Thr161=)
c.436A= (p.Thr146=)
c.616A= (p.Thr206=)
7g.151186496G>ACA458881556ASB10c.480C>T (p.His160=)
c.435C>T (p.His145=)
c.615C>T (p.His205=)
 gnomAD v4
7g.151186496G>CCA370036007ASB10c.480C>G (p.His160Gln)
c.435C>G (p.His145Gln)
c.615C>G (p.His205Gln)
7g.151186496G>TCA370036009ASB10c.480C>A (p.His160Gln)
c.435C>A (p.His145Gln)
c.615C>A (p.His205Gln)
7g.151186497T>ACA370036014ASB10c.479A>T (p.His160Leu)
c.434A>T (p.His145Leu)
c.614A>T (p.His205Leu)
7g.151186497T>CCA370036011ASB10c.479A>G (p.His160Arg)
c.434A>G (p.His145Arg)
c.614A>G (p.His205Arg)
7g.151186497T>GCA370036013ASB10c.479A>C (p.His160Pro)
c.434A>C (p.His145Pro)
c.614A>C (p.His205Pro)
7g.151186498G>ACA370036017ASB10c.478C>T (p.His160Tyr)
c.433C>T (p.His145Tyr)
c.613C>T (p.His205Tyr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.151186498G>CCA370036018ASB10c.478C>G (p.His160Asp)
c.433C>G (p.His145Asp)
c.613C>G (p.His205Asp)
7g.151186498G=CA1752544978ASB10c.478C= (p.His160=)
c.433C= (p.His145=)
c.613C= (p.His205=)
7g.151186498G>TCA370036020ASB10c.478C>A (p.His160Asn)
c.433C>A (p.His145Asn)
c.613C>A (p.His205Asn)
7g.151186499G>ACA458881557ASB10c.477C>T (p.Gly159=)
c.432C>T (p.Gly144=)
c.612C>T (p.Gly204=)
7g.151186499G>CCA458881558ASB10c.477C>G (p.Gly159=)
c.432C>G (p.Gly144=)
c.612C>G (p.Gly204=)
7g.151186499G>TCA458881559ASB10c.477C>A (p.Gly159=)
c.432C>A (p.Gly144=)
c.612C>A (p.Gly204=)
 gnomAD v4
7g.151186500C>ACA370036022ASB10c.476G>T (p.Gly159Val)
c.431G>T (p.Gly144Val)
c.611G>T (p.Gly204Val)
 gnomAD v4
7g.151186500C>GCA370036024ASB10c.476G>C (p.Gly159Ala)
c.431G>C (p.Gly144Ala)
c.611G>C (p.Gly204Ala)
7g.151186500C>TCA370036026ASB10c.476G>A (p.Gly159Asp)
c.431G>A (p.Gly144Asp)
c.611G>A (p.Gly204Asp)
 gnomAD v4
7g.151186501C>ACA370036028ASB10c.475G>T (p.Gly159Cys)
c.430G>T (p.Gly144Cys)
c.610G>T (p.Gly204Cys)
7g.151186501C>GCA370036029ASB10c.475G>C (p.Gly159Arg)
c.430G>C (p.Gly144Arg)
c.610G>C (p.Gly204Arg)
7g.151186501C>TCA370036031ASB10c.475G>A (p.Gly159Ser)
c.430G>A (p.Gly144Ser)
c.610G>A (p.Gly204Ser)
7g.151186502T>ACA458881560ASB10c.474A>T (p.Ala158=)
c.429A>T (p.Ala143=)
c.609A>T (p.Ala203=)
7g.151186502T>CCA458881562ASB10c.474A>G (p.Ala158=)
c.429A>G (p.Ala143=)
c.609A>G (p.Ala203=)
7g.151186502T>GCA458881561ASB10c.474A>C (p.Ala158=)
c.429A>C (p.Ala143=)
c.609A>C (p.Ala203=)
7g.151186502_151186515delCA2685657517ASB10c.461_474del (p.Glu154GlyfsTer20)
c.416_429del (p.Glu139GlyfsTer20)
c.596_609del (p.Glu199GlyfsTer20)
 gnomAD v4
7g.151186503G>ACA370036033ASB10c.473C>T (p.Ala158Val)
c.428C>T (p.Ala143Val)
c.608C>T (p.Ala203Val)
 dbSNP gnomAD v2 gnomAD v4
7g.151186503G>CCA370036035ASB10c.473C>G (p.Ala158Gly)
c.428C>G (p.Ala143Gly)
c.608C>G (p.Ala203Gly)
 dbSNP gnomAD v3 gnomAD v4
7g.151186503G=CA1752544980ASB10c.473C= (p.Ala158=)
c.428C= (p.Ala143=)
c.608C= (p.Ala203=)
7g.151186503G>TCA370036037ASB10c.473C>A (p.Ala158Glu)
c.428C>A (p.Ala143Glu)
c.608C>A (p.Ala203Glu)
7g.151186504C>ACA370036039ASB10c.472G>T (p.Ala158Ser)
c.427G>T (p.Ala143Ser)
c.607G>T (p.Ala203Ser)
 dbSNP gnomAD v2 gnomAD v4
7g.151186504C=CA1752544982ASB10c.472G= (p.Ala158=)
c.427G= (p.Ala143=)
c.607G= (p.Ala203=)
7g.151186504C>GCA370036041ASB10c.472G>C (p.Ala158Pro)
c.427G>C (p.Ala143Pro)
c.607G>C (p.Ala203Pro)
7g.151186504C>TCA4573873ASB10c.472G>A (p.Ala158Thr)
c.427G>A (p.Ala143Thr)
c.607G>A (p.Ala203Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186505A>CCA458881563ASB10c.471T>G (p.Ala157=)
c.426T>G (p.Ala142=)
c.606T>G (p.Ala202=)
7g.151186505A>GCA458881564ASB10c.471T>C (p.Ala157=)
c.426T>C (p.Ala142=)
c.606T>C (p.Ala202=)
7g.151186505A>TCA458881565ASB10c.471T>A (p.Ala157=)
c.426T>A (p.Ala142=)
c.606T>A (p.Ala202=)
7g.151186506G>ACA150488ASB10c.470C>T (p.Ala157Val)
c.425C>T (p.Ala142Val)
c.605C>T (p.Ala202Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186506G>CCA370036046ASB10c.470C>G (p.Ala157Gly)
c.425C>G (p.Ala142Gly)
c.605C>G (p.Ala202Gly)
7g.151186506G=CA1752544989ASB10c.470C= (p.Ala157=)
c.425C= (p.Ala142=)
c.605C= (p.Ala202=)
7g.151186506G>TCA370036044ASB10c.470C>A (p.Ala157Asp)
c.425C>A (p.Ala142Asp)
c.605C>A (p.Ala202Asp)
 gnomAD v4
7g.151186507C>ACA370036048ASB10c.469G>T (p.Ala157Ser)
c.424G>T (p.Ala142Ser)
c.604G>T (p.Ala202Ser)
 gnomAD v4
7g.151186507C>GCA370036050ASB10c.469G>C (p.Ala157Pro)
c.424G>C (p.Ala142Pro)
c.604G>C (p.Ala202Pro)
7g.151186507C>TCA370036051ASB10c.469G>A (p.Ala157Thr)
c.424G>A (p.Ala142Thr)
c.604G>A (p.Ala202Thr)
 gnomAD v4
7g.151186508A=CA1752545000ASB10c.468T= (p.Cys156=)
c.423T= (p.Cys141=)
c.603T= (p.Cys201=)
7g.151186508A>CCA370036053ASB10c.468T>G (p.Cys156Trp)
c.423T>G (p.Cys141Trp)
c.603T>G (p.Cys201Trp)
 dbSNP
7g.151186508A>GCA458881566ASB10c.468T>C (p.Cys156=)
c.423T>C (p.Cys141=)
c.603T>C (p.Cys201=)
7g.151186508A>TCA370036055ASB10c.468T>A (p.Cys156Ter)
c.423T>A (p.Cys141Ter)
c.603T>A (p.Cys201Ter)
7g.151186509C>ACA370036057ASB10c.467G>T (p.Cys156Phe)
c.422G>T (p.Cys141Phe)
c.602G>T (p.Cys201Phe)
 gnomAD v4
7g.151186509C=CA1752545008ASB10c.467G= (p.Cys156=)
c.422G= (p.Cys141=)
c.602G= (p.Cys201=)
7g.151186509C>GCA370036059ASB10c.467G>C (p.Cys156Ser)
c.422G>C (p.Cys141Ser)
c.602G>C (p.Cys201Ser)
7g.151186509C>TCA169125268ASB10c.467G>A (p.Cys156Tyr)
c.422G>A (p.Cys141Tyr)
c.602G>A (p.Cys201Tyr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.151186510A=CA1752545012ASB10c.466T= (p.Cys156=)
c.421T= (p.Cys141=)
c.601T= (p.Cys201=)
7g.151186510A>CCA370036062ASB10c.466T>G (p.Cys156Gly)
c.421T>G (p.Cys141Gly)
c.601T>G (p.Cys201Gly)
7g.151186510A>GCA370036063ASB10c.466T>C (p.Cys156Arg)
c.421T>C (p.Cys141Arg)
c.601T>C (p.Cys201Arg)
 dbSNP gnomAD v2 gnomAD v4
7g.151186510A>TCA370036065ASB10c.466T>A (p.Cys156Ser)
c.421T>A (p.Cys141Ser)
c.601T>A (p.Cys201Ser)
7g.151186511G>ACA458881569ASB10c.465C>T (p.Ala155=)
c.420C>T (p.Ala140=)
c.600C>T (p.Ala200=)
 gnomAD v4
7g.151186511G>CCA458881567ASB10c.465C>G (p.Ala155=)
c.420C>G (p.Ala140=)
c.600C>G (p.Ala200=)
 dbSNP gnomAD v2
7g.151186511G=CA1752545014ASB10c.465C= (p.Ala155=)
c.420C= (p.Ala140=)
c.600C= (p.Ala200=)
7g.151186511G>TCA458881568ASB10c.465C>A (p.Ala155=)
c.420C>A (p.Ala140=)
c.600C>A (p.Ala200=)
 gnomAD v4
7g.151186512G>ACA370036070ASB10c.464C>T (p.Ala155Val)
c.419C>T (p.Ala140Val)
c.599C>T (p.Ala200Val)
 gnomAD v4
7g.151186512G>CCA370036069ASB10c.464C>G (p.Ala155Gly)
c.419C>G (p.Ala140Gly)
c.599C>G (p.Ala200Gly)
7g.151186512G>TCA370036067ASB10c.464C>A (p.Ala155Asp)
c.419C>A (p.Ala140Asp)
c.599C>A (p.Ala200Asp)
 dbSNP gnomAD v4
7g.151186513C>ACA4573874ASB10c.463G>T (p.Ala155Ser)
c.418G>T (p.Ala140Ser)
c.598G>T (p.Ala200Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.151186513C=CA1752545017ASB10c.463G= (p.Ala155=)
c.418G= (p.Ala140=)
c.598G= (p.Ala200=)
7g.151186513C>GCA370036073ASB10c.463G>C (p.Ala155Pro)
c.418G>C (p.Ala140Pro)
c.598G>C (p.Ala200Pro)
7g.151186513C>TCA370036074ASB10c.463G>A (p.Ala155Thr)
c.418G>A (p.Ala140Thr)
c.598G>A (p.Ala200Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.151186514C>ACA370036075ASB10c.462G>T (p.Glu154Asp)
c.417G>T (p.Glu139Asp)
c.597G>T (p.Glu199Asp)
7g.151186514C>GCA370036077ASB10c.462G>C (p.Glu154Asp)
c.417G>C (p.Glu139Asp)
c.597G>C (p.Glu199Asp)
7g.151186514C>TCA458881570ASB10c.462G>A (p.Glu154=)
c.417G>A (p.Glu139=)
c.597G>A (p.Glu199=)
 gnomAD v4
7g.151186515T>ACA370036079ASB10c.461A>T (p.Glu154Val)
c.416A>T (p.Glu139Val)
c.596A>T (p.Glu199Val)
7g.151186515T>CCA370036080ASB10c.461A>G (p.Glu154Gly)
c.416A>G (p.Glu139Gly)
c.596A>G (p.Glu199Gly)
7g.151186515T>GCA370036081ASB10c.461A>C (p.Glu154Ala)
c.416A>C (p.Glu139Ala)
c.596A>C (p.Glu199Ala)
7g.151186516C>ACA370036083ASB10c.460G>T (p.Glu154Ter)
c.415G>T (p.Glu139Ter)
c.595G>T (p.Glu199Ter)
 gnomAD v4
7g.151186516C=CA1752545022ASB10c.460G= (p.Glu154=)
c.415G= (p.Glu139=)
c.595G= (p.Glu199=)
7g.151186516C>GCA370036084ASB10c.460G>C (p.Glu154Gln)
c.415G>C (p.Glu139Gln)
c.595G>C (p.Glu199Gln)
 dbSNP gnomAD v3 gnomAD v4
7g.151186516C>TCA4573875ASB10c.460G>A (p.Glu154Lys)
c.415G>A (p.Glu139Lys)
c.595G>A (p.Glu199Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186517G>ACA4573876ASB10c.459C>T (p.His153=)
c.414C>T (p.His138=)
c.594C>T (p.His198=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.151186517G>CCA370036089ASB10c.459C>G (p.His153Gln)
c.414C>G (p.His138Gln)
c.594C>G (p.His198Gln)
7g.151186517G=CA1752545027ASB10c.459C= (p.His153=)
c.414C= (p.His138=)
c.594C= (p.His198=)
7g.151186517G>TCA370036087ASB10c.459C>A (p.His153Gln)
c.414C>A (p.His138Gln)
c.594C>A (p.His198Gln)
7g.151186518T>ACA370036091ASB10c.458A>T (p.His153Leu)
c.413A>T (p.His138Leu)
c.593A>T (p.His198Leu)
7g.151186518T>CCA370036093ASB10c.458A>G (p.His153Arg)
c.413A>G (p.His138Arg)
c.593A>G (p.His198Arg)
7g.151186518T>GCA370036095ASB10c.458A>C (p.His153Pro)
c.413A>C (p.His138Pro)
c.593A>C (p.His198Pro)
7g.151186519G>ACA370036097ASB10c.457C>T (p.His153Tyr)
c.412C>T (p.His138Tyr)
c.592C>T (p.His198Tyr)
7g.151186519G>CCA370036098ASB10c.457C>G (p.His153Asp)
c.412C>G (p.His138Asp)
c.592C>G (p.His198Asp)
7g.151186519G>TCA370036100ASB10c.457C>A (p.His153Asn)
c.412C>A (p.His138Asn)
c.592C>A (p.His198Asn)
 gnomAD v4
7g.151186520C>ACA458881571ASB10c.456G>T (p.Leu152=)
c.411G>T (p.Leu137=)
c.591G>T (p.Leu197=)
 gnomAD v4
7g.151186520C>GCA458881572ASB10c.456G>C (p.Leu152=)
c.411G>C (p.Leu137=)
c.591G>C (p.Leu197=)
7g.151186520C>TCA458881573ASB10c.456G>A (p.Leu152=)
c.411G>A (p.Leu137=)
c.591G>A (p.Leu197=)
 gnomAD v4
7g.151186521A>CCA370036106ASB10c.455T>G (p.Leu152Arg)
c.410T>G (p.Leu137Arg)
c.590T>G (p.Leu197Arg)
7g.151186521A>GCA370036103ASB10c.455T>C (p.Leu152Pro)
c.410T>C (p.Leu137Pro)
c.590T>C (p.Leu197Pro)
 gnomAD v4
7g.151186521A>TCA370036104ASB10c.455T>A (p.Leu152Gln)
c.410T>A (p.Leu137Gln)
c.590T>A (p.Leu197Gln)
 gnomAD v4
7g.151186522G>ACA458881574ASB10c.454C>T (p.Leu152=)
c.409C>T (p.Leu137=)
c.589C>T (p.Leu197=)
7g.151186522G>CCA370036108ASB10c.454C>G (p.Leu152Val)
c.409C>G (p.Leu137Val)
c.589C>G (p.Leu197Val)
7g.151186522G>TCA370036110ASB10c.454C>A (p.Leu152Met)
c.409C>A (p.Leu137Met)
c.589C>A (p.Leu197Met)
7g.151186523G>ACA458881575ASB10c.453C>T (p.Ala151=)
c.408C>T (p.Ala136=)
c.588C>T (p.Ala196=)
 COSMIC COSMIC COSMIC COSMIC
7g.151186523G>CCA458881577ASB10c.453C>G (p.Ala151=)
c.408C>G (p.Ala136=)
c.588C>G (p.Ala196=)
7g.151186523G>TCA458881576ASB10c.453C>A (p.Ala151=)
c.408C>A (p.Ala136=)
c.588C>A (p.Ala196=)
7g.151186524G>ACA370036111ASB10c.452C>T (p.Ala151Val)
c.407C>T (p.Ala136Val)
c.587C>T (p.Ala196Val)
7g.151186524G>CCA370036113ASB10c.452C>G (p.Ala151Gly)
c.407C>G (p.Ala136Gly)
c.587C>G (p.Ala196Gly)
7g.151186524G>TCA370036114ASB10c.452C>A (p.Ala151Asp)
c.407C>A (p.Ala136Asp)
c.587C>A (p.Ala196Asp)
7g.151186525C>ACA370036117ASB10c.451G>T (p.Ala151Ser)
c.406G>T (p.Ala136Ser)
c.586G>T (p.Ala196Ser)
 gnomAD v4
7g.151186525C=CA1752545031ASB10c.451G= (p.Ala151=)
c.406G= (p.Ala136=)
c.586G= (p.Ala196=)
7g.151186525C>GCA370036118ASB10c.451G>C (p.Ala151Pro)
c.406G>C (p.Ala136Pro)
c.586G>C (p.Ala196Pro)
7g.151186525C>TCA4573877ASB10c.451G>A (p.Ala151Thr)
c.406G>A (p.Ala136Thr)
c.586G>A (p.Ala196Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched