Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.17027750_17028737delCA645509076SDHBc.117_369+1del
c.246_498+1del
c.288_540+1del
n.205_458del
n.276_474+1del
1g.17028615T>ACA416087507SDHBc.237A>T (p.Ile79=)
c.366A>T (p.Ile122=)
c.408A>T (p.Ile136=)
n.325A>T
n.357+39A>T
1g.17028615T>CCA338274008SDHBc.237A>G (p.Ile79Met)
c.366A>G (p.Ile122Met)
c.408A>G (p.Ile136Met)
n.325A>G
n.357+39A>G
1g.17028615T>GCA416087510SDHBc.237A>C (p.Ile79=)
c.366A>C (p.Ile122=)
c.408A>C (p.Ile136=)
n.325A>C
n.357+39A>C
 ClinVar gnomAD v4
1g.17028616A=CA1156080484SDHBc.236T= (p.Ile79=)
c.365T= (p.Ile122=)
c.407T= (p.Ile136=)
n.324T=
n.357+38T=
1g.17028616A>CCA338274013SDHBc.236T>G (p.Ile79Arg)
c.365T>G (p.Ile122Arg)
c.407T>G (p.Ile136Arg)
n.324T>G
n.357+38T>G
 ClinVar dbSNP
1g.17028616A>GCA338274009SDHBc.236T>C (p.Ile79Thr)
c.365T>C (p.Ile122Thr)
c.407T>C (p.Ile136Thr)
n.324T>C
n.357+38T>C
1g.17028616A>TCA338274010SDHBc.236T>A (p.Ile79Lys)
c.365T>A (p.Ile122Lys)
c.407T>A (p.Ile136Lys)
n.324T>A
n.357+38T>A
1g.17028617delCA1139768295SDHBc.235del (p.Ile79Ter)
c.364del (p.Ile122Ter)
c.406del (p.Ile136Ter)
n.323del
n.357+37del
1g.17028617T>ACA338274015SDHBc.235A>T (p.Ile79Leu)
c.364A>T (p.Ile122Leu)
c.406A>T (p.Ile136Leu)
n.323A>T
n.357+37A>T
 ClinVar
1g.17028617T>CCA338274037SDHBc.235A>G (p.Ile79Val)
c.364A>G (p.Ile122Val)
c.406A>G (p.Ile136Val)
n.323A>G
n.357+37A>G
 ClinVar dbSNP gnomAD v4
1g.17028617T>GCA338274043SDHBc.235A>C (p.Ile79Leu)
c.364A>C (p.Ile122Leu)
c.406A>C (p.Ile136Leu)
n.323A>C
n.357+37A>C
1g.17028617T=CA1156080485SDHBc.235A= (p.Ile79=)
c.364A= (p.Ile122=)
c.406A= (p.Ile136=)
n.323A=
n.357+37A=
1g.17028618C>ACA416087521SDHBc.234G>T (p.Val78=)
c.363G>T (p.Val121=)
c.405G>T (p.Val135=)
n.322G>T
n.357+36G>T
1g.17028618C>GCA416087522SDHBc.234G>C (p.Val78=)
c.363G>C (p.Val121=)
c.405G>C (p.Val135=)
n.322G>C
n.357+36G>C
1g.17028618C>TCA416087523SDHBc.234G>A (p.Val78=)
c.363G>A (p.Val121=)
c.405G>A (p.Val135=)
n.322G>A
n.357+36G>A
 ClinVar dbSNP gnomAD v4
1g.17028619A>CCA338274044SDHBc.233T>G (p.Val78Gly)
c.362T>G (p.Val121Gly)
c.404T>G (p.Val135Gly)
n.321T>G
n.357+35T>G
1g.17028619A>GCA338274046SDHBc.233T>C (p.Val78Ala)
c.362T>C (p.Val121Ala)
c.404T>C (p.Val135Ala)
n.321T>C
n.357+35T>C
 ClinVar
1g.17028619A>TCA338274050SDHBc.233T>A (p.Val78Glu)
c.362T>A (p.Val121Glu)
c.404T>A (p.Val135Glu)
n.321T>A
n.357+35T>A
1g.17028620C>ACA338274052SDHBc.232G>T (p.Val78Leu)
c.361G>T (p.Val121Leu)
c.403G>T (p.Val135Leu)
n.320G>T
n.357+34G>T
 dbSNP
1g.17028620C=CA1143492238SDHBc.232G= (p.Val78=)
c.361G= (p.Val121=)
c.403G= (p.Val135=)
n.320G=
n.357+34G=
1g.17028620C>GCA338274073SDHBc.232G>C (p.Val78Leu)
c.361G>C (p.Val121Leu)
c.403G>C (p.Val135Leu)
n.320G>C
n.357+34G>C
1g.17028620C>TCA015827SDHBc.232G>A (p.Val78Met)
c.361G>A (p.Val121Met)
c.403G>A (p.Val135Met)
n.320G>A
n.357+34G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.17028621A>CCA338274080SDHBc.231T>G (p.Tyr77Ter)
c.360T>G (p.Tyr120Ter)
c.402T>G (p.Tyr134Ter)
n.319T>G
n.357+33T>G
1g.17028621A>GCA416087534SDHBc.231T>C (p.Tyr77=)
c.360T>C (p.Tyr120=)
c.402T>C (p.Tyr134=)
n.319T>C
n.357+33T>C
 ClinVar dbSNP gnomAD v4
1g.17028621A>TCA338274082SDHBc.231T>A (p.Tyr77Ter)
c.360T>A (p.Tyr120Ter)
c.402T>A (p.Tyr134Ter)
n.319T>A
n.357+33T>A
1g.17028622T>ACA338274087SDHBc.230A>T (p.Tyr77Phe)
c.359A>T (p.Tyr120Phe)
c.401A>T (p.Tyr134Phe)
n.318A>T
n.357+32A>T
1g.17028622T>CCA18666569SDHBc.230A>G (p.Tyr77Cys)
c.359A>G (p.Tyr120Cys)
c.401A>G (p.Tyr134Cys)
n.318A>G
n.357+32A>G
 ClinVar dbSNP gnomAD v4
1g.17028622T>GCA338274086SDHBc.230A>C (p.Tyr77Ser)
c.359A>C (p.Tyr120Ser)
c.401A>C (p.Tyr134Ser)
n.318A>C
n.357+32A>C
1g.17028622T=CA1143446877SDHBc.230A= (p.Tyr77=)
c.359A= (p.Tyr120=)
c.401A= (p.Tyr134=)
n.318A=
n.357+32A=
1g.17028622dupCA2573334464SDHBc.230dup (p.Tyr77Ter)
c.359dup (p.Tyr120Ter)
c.401dup (p.Tyr134Ter)
n.318dup
n.357+32dup
1g.17028623A=CA1156080486SDHBc.229T= (p.Tyr77=)
c.358T= (p.Tyr120=)
c.400T= (p.Tyr134=)
n.317T=
n.357+31T=
1g.17028623A>CCA338274088SDHBc.229T>G (p.Tyr77Asp)
c.358T>G (p.Tyr120Asp)
c.400T>G (p.Tyr134Asp)
n.317T>G
n.357+31T>G
1g.17028623A>GCA089606SDHBc.229T>C (p.Tyr77His)
c.358T>C (p.Tyr120His)
c.400T>C (p.Tyr134His)
n.317T>C
n.357+31T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17028623A>TCA338274095SDHBc.229T>A (p.Tyr77Asn)
c.358T>A (p.Tyr120Asn)
c.400T>A (p.Tyr134Asn)
n.317T>A
n.357+31T>A
1g.17028624C>ACA18666577SDHBc.228G>T (p.Met76Ile)
c.357G>T (p.Met119Ile)
c.399G>T (p.Met133Ile)
n.316G>T
n.357+30G>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17028624C=CA1143479976SDHBc.228G= (p.Met76=)
c.357G= (p.Met119=)
c.399G= (p.Met133=)
n.316G=
n.357+30G=
1g.17028624C>GCA338274099SDHBc.228G>C (p.Met76Ile)
c.357G>C (p.Met119Ile)
c.399G>C (p.Met133Ile)
n.316G>C
n.357+30G>C
1g.17028624C>TCA338274119SDHBc.228G>A (p.Met76Ile)
c.357G>A (p.Met119Ile)
c.399G>A (p.Met133Ile)
n.316G>A
n.357+30G>A
 ClinVar dbSNP
1g.17028624dupCA891842432SDHBc.228dup (p.Tyr77ValfsTer21)
c.357dup (p.Tyr120ValfsTer21)
c.399dup (p.Tyr134ValfsTer21)
n.316dup
n.357+30dup
 ClinVar dbSNP
1g.17028625A=CA1146226690SDHBc.227T= (p.Met76=)
c.356T= (p.Met119=)
c.398T= (p.Met133=)
n.315T=
n.357+29T=
1g.17028625A>CCA338274123SDHBc.227T>G (p.Met76Arg)
c.356T>G (p.Met119Arg)
c.398T>G (p.Met133Arg)
n.315T>G
n.357+29T>G
1g.17028625A>GCA089604SDHBc.227T>C (p.Met76Thr)
c.356T>C (p.Met119Thr)
c.398T>C (p.Met133Thr)
n.315T>C
n.357+29T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17028625A>TCA338274126SDHBc.227T>A (p.Met76Lys)
c.356T>A (p.Met119Lys)
c.398T>A (p.Met133Lys)
n.315T>A
n.357+29T>A
 gnomAD v4
1g.17028626T>ACA338274128SDHBc.226A>T (p.Met76Leu)
c.355A>T (p.Met119Leu)
c.397A>T (p.Met133Leu)
n.314A>T
n.357+28A>T
1g.17028626T>CCA338274130SDHBc.226A>G (p.Met76Val)
c.355A>G (p.Met119Val)
c.397A>G (p.Met133Val)
n.314A>G
n.357+28A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17028626T>GCA338274132SDHBc.226A>C (p.Met76Leu)
c.355A>C (p.Met119Leu)
c.397A>C (p.Met133Leu)
n.314A>C
n.357+28A>C
 dbSNP
1g.17028626T=CA1156080487SDHBc.226A= (p.Met76=)
c.355A= (p.Met119=)
c.397A= (p.Met133=)
n.314A=
n.357+28A=
1g.17028627G>ACA416087565SDHBc.225C>T (p.His75=)
c.354C>T (p.His118=)
c.396C>T (p.His132=)
n.313C>T
n.357+27C>T
 ClinVar gnomAD v4
1g.17028627G>CCA338274146SDHBc.225C>G (p.His75Gln)
c.354C>G (p.His118Gln)
c.396C>G (p.His132Gln)
n.313C>G
n.357+27C>G
1g.17028627G=CA1156080488SDHBc.225C= (p.His75=)
c.354C= (p.His118=)
c.396C= (p.His132=)
n.313C=
n.357+27C=
1g.17028627G>TCA338274133SDHBc.225C>A (p.His75Gln)
c.354C>A (p.His118Gln)
c.396C>A (p.His132Gln)
n.313C>A
n.357+27C>A
 dbSNP gnomAD v3 gnomAD v4
1g.17028628T>ACA338274150SDHBc.224A>T (p.His75Leu)
c.353A>T (p.His118Leu)
c.395A>T (p.His132Leu)
n.312A>T
n.357+26A>T
 gnomAD v4
1g.17028628T>CCA16609937SDHBc.224A>G (p.His75Arg)
c.353A>G (p.His118Arg)
c.395A>G (p.His132Arg)
n.312A>G
n.357+26A>G
 ClinVar dbSNP gnomAD v4
1g.17028628T>GCA015817SDHBc.224A>C (p.His75Pro)
c.353A>C (p.His118Pro)
c.395A>C (p.His132Pro)
n.312A>C
n.357+26A>C
 ClinVar dbSNP
1g.17028628T=CA1140886355SDHBc.224A= (p.His75=)
c.353A= (p.His118=)
c.395A= (p.His132=)
n.312A=
n.357+26A=
1g.17028629G>ACA338274207SDHBc.223C>T (p.His75Tyr)
c.352C>T (p.His118Tyr)
c.394C>T (p.His132Tyr)
n.311C>T
n.357+25C>T
1g.17028629G>CCA338274209SDHBc.223C>G (p.His75Asp)
c.352C>G (p.His118Asp)
c.394C>G (p.His132Asp)
n.311C>G
n.357+25C>G
1g.17028629G>TCA338274211SDHBc.223C>A (p.His75Asn)
c.352C>A (p.His118Asn)
c.394C>A (p.His132Asn)
n.311C>A
n.357+25C>A
1g.17028630delCA2586966131SDHBc.222del (p.His75ThrfsTer4)
c.351del (p.His118ThrfsTer4)
c.393del (p.His132ThrfsTer4)
n.310del
n.357+24del
1g.17028630T>ACA416087581SDHBc.222A>T (p.Pro74=)
c.351A>T (p.Pro117=)
c.393A>T (p.Pro131=)
n.310A>T
n.357+24A>T
1g.17028630T>CCA416087582SDHBc.222A>G (p.Pro74=)
c.351A>G (p.Pro117=)
c.393A>G (p.Pro131=)
n.310A>G
n.357+24A>G
 ClinVar gnomAD v4
1g.17028630T>GCA416087583SDHBc.222A>C (p.Pro74=)
c.351A>C (p.Pro117=)
c.393A>C (p.Pro131=)
n.310A>C
n.357+24A>C
1g.17028630_17028631delinsTGCA1156080489SDHBc.221_222delinsCA (p.Pro74=)
c.350_351delinsCA (p.Pro117=)
c.392_393delinsCA (p.Pro131=)
n.309_310delinsCA
n.357+23_357+24delinsCA
1g.17028631G>ACA338274230SDHBc.221C>T (p.Pro74Leu)
c.350C>T (p.Pro117Leu)
c.392C>T (p.Pro131Leu)
n.309C>T
n.357+23C>T
 ClinVar dbSNP
1g.17028631G>CCA338274223SDHBc.221C>G (p.Pro74Arg)
c.350C>G (p.Pro117Arg)
c.392C>G (p.Pro131Arg)
n.309C>G
n.357+23C>G
1g.17028631G>TCA338274215SDHBc.221C>A (p.Pro74Gln)
c.350C>A (p.Pro117Gln)
c.392C>A (p.Pro131Gln)
n.309C>A
n.357+23C>A
1g.17028632delCA645509069SDHBc.221del (p.Pro74HisfsTer5)
c.350del (p.Pro117HisfsTer5)
c.392del (p.Pro131HisfsTer5)
n.309del
n.357+23del
 ClinVar dbSNP
1g.17028632G>ACA338274233SDHBc.220C>T (p.Pro74Ser)
c.349C>T (p.Pro117Ser)
c.391C>T (p.Pro131Ser)
n.308C>T
n.357+22C>T
 COSMIC
1g.17028632G>CCA338274234SDHBc.220C>G (p.Pro74Ala)
c.349C>G (p.Pro117Ala)
c.391C>G (p.Pro131Ala)
n.308C>G
n.357+22C>G
1g.17028632G>TCA338274235SDHBc.220C>A (p.Pro74Thr)
c.349C>A (p.Pro117Thr)
c.391C>A (p.Pro131Thr)
n.308C>A
n.357+22C>A
1g.17028633A>CCA416087592SDHBc.219T>G (p.Leu73=)
c.348T>G (p.Leu116=)
c.390T>G (p.Leu130=)
n.307T>G
n.357+21T>G
1g.17028633A>GCA416087594SDHBc.219T>C (p.Leu73=)
c.348T>C (p.Leu116=)
c.390T>C (p.Leu130=)
n.307T>C
n.357+21T>C
1g.17028633A>TCA416087601SDHBc.219T>A (p.Leu73=)
c.348T>A (p.Leu116=)
c.390T>A (p.Leu130=)
n.307T>A
n.357+21T>A
1g.17028634A=CA1148278848SDHBc.218T= (p.Leu73=)
c.347T= (p.Leu116=)
c.389T= (p.Leu130=)
n.306T=
n.357+20T=
1g.17028634A>CCA338274236SDHBc.218T>G (p.Leu73Arg)
c.347T>G (p.Leu116Arg)
c.389T>G (p.Leu130Arg)
n.306T>G
n.357+20T>G
1g.17028634A>GCA089602SDHBc.218T>C (p.Leu73Pro)
c.347T>C (p.Leu116Pro)
c.389T>C (p.Leu130Pro)
n.306T>C
n.357+20T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.17028634A>TCA338274255SDHBc.218T>A (p.Leu73His)
c.347T>A (p.Leu116His)
c.389T>A (p.Leu130His)
n.306T>A
n.357+20T>A
1g.17028635G>ACA338274262SDHBc.217C>T (p.Leu73Phe)
c.346C>T (p.Leu116Phe)
c.388C>T (p.Leu130Phe)
n.305C>T
n.357+19C>T
 ClinVar dbSNP
1g.17028635G>CCA338274269SDHBc.217C>G (p.Leu73Val)
c.346C>G (p.Leu116Val)
c.388C>G (p.Leu130Val)
n.305C>G
n.357+19C>G
1g.17028635G>TCA338274266SDHBc.217C>A (p.Leu73Ile)
c.346C>A (p.Leu116Ile)
c.388C>A (p.Leu130Ile)
n.305C>A
n.357+19C>A
1g.17028636A>CCA416087615SDHBc.216T>G (p.Pro72=)
c.345T>G (p.Pro115=)
c.387T>G (p.Pro129=)
n.304T>G
n.357+18T>G
1g.17028636A>GCA416087613SDHBc.216T>C (p.Pro72=)
c.345T>C (p.Pro115=)
c.387T>C (p.Pro129=)
n.304T>C
n.357+18T>C
1g.17028636A>TCA416087614SDHBc.216T>A (p.Pro72=)
c.345T>A (p.Pro115=)
c.387T>A (p.Pro129=)
n.304T>A
n.357+18T>A
1g.17028637G>ACA338274280SDHBc.215C>T (p.Pro72Leu)
c.344C>T (p.Pro115Leu)
c.386C>T (p.Pro129Leu)
n.303C>T
n.357+17C>T
 gnomAD v4
1g.17028637G>CCA015807SDHBc.215C>G (p.Pro72Arg)
c.344C>G (p.Pro115Arg)
c.386C>G (p.Pro129Arg)
n.303C>G
n.357+17C>G
 ClinVar dbSNP COSMIC
1g.17028637G=CA1148224198SDHBc.215C= (p.Pro72=)
c.344C= (p.Pro115=)
c.386C= (p.Pro129=)
n.303C=
n.357+17C=
1g.17028637G>TCA338274287SDHBc.215C>A (p.Pro72His)
c.344C>A (p.Pro115His)
c.386C>A (p.Pro129His)
n.303C>A
n.357+17C>A
1g.17028638G>ACA338274290SDHBc.214C>T (p.Pro72Ser)
c.343C>T (p.Pro115Ser)
c.385C>T (p.Pro129Ser)
n.302C>T
n.357+16C>T
 ClinVar dbSNP gnomAD v4
1g.17028638G>CCA338274293SDHBc.214C>G (p.Pro72Ala)
c.343C>G (p.Pro115Ala)
c.385C>G (p.Pro129Ala)
n.302C>G
n.357+16C>G
 ClinVar dbSNP
1g.17028638G=CA1156080490SDHBc.214C= (p.Pro72=)
c.343C= (p.Pro115=)
c.385C= (p.Pro129=)
n.302C=
n.357+16C=
1g.17028638G>TCA338274306SDHBc.214C>A (p.Pro72Thr)
c.343C>A (p.Pro115Thr)
c.385C>A (p.Pro129Thr)
n.302C>A
n.357+16C>A
 ClinVar
1g.17028639G>ACA416087632SDHBc.213C>T (p.Tyr71=)
c.342C>T (p.Tyr114=)
c.384C>T (p.Tyr128=)
n.301C>T
n.357+15C>T
 dbSNP gnomAD v4
1g.17028639G>CCA338274311SDHBc.213C>G (p.Tyr71Ter)
c.342C>G (p.Tyr114Ter)
c.384C>G (p.Tyr128Ter)
n.301C>G
n.357+15C>G
 COSMIC
1g.17028639G>TCA338274313SDHBc.213C>A (p.Tyr71Ter)
c.342C>A (p.Tyr114Ter)
c.384C>A (p.Tyr128Ter)
n.301C>A
n.357+15C>A
 ClinVar
1g.17028640T>ACA338274314SDHBc.212A>T (p.Tyr71Phe)
c.341A>T (p.Tyr114Phe)
c.383A>T (p.Tyr128Phe)
n.300A>T
n.357+14A>T
 ClinVar gnomAD v4
1g.17028640T>CCA089601SDHBc.212A>G (p.Tyr71Cys)
c.341A>G (p.Tyr114Cys)
c.383A>G (p.Tyr128Cys)
n.300A>G
n.357+14A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17028640T>GCA338274317SDHBc.212A>C (p.Tyr71Ser)
c.341A>C (p.Tyr114Ser)
c.383A>C (p.Tyr128Ser)
n.300A>C
n.357+14A>C
 ClinVar
1g.17028640T=CA1156080491SDHBc.212A= (p.Tyr71=)
c.341A= (p.Tyr114=)
c.383A= (p.Tyr128=)
n.300A=
n.357+14A=
1g.17028641A>CCA338274328SDHBc.211T>G (p.Tyr71Asp)
c.340T>G (p.Tyr114Asp)
c.382T>G (p.Tyr128Asp)
n.299T>G
n.357+13T>G
1g.17028641A>GCA338274321SDHBc.211T>C (p.Tyr71His)
c.340T>C (p.Tyr114His)
c.382T>C (p.Tyr128His)
n.299T>C
n.357+13T>C
1g.17028641A>TCA338274327SDHBc.211T>A (p.Tyr71Asn)
c.340T>A (p.Tyr114Asn)
c.382T>A (p.Tyr128Asn)
n.299T>A
n.357+13T>A
1g.17028642G>ACA416087646SDHBc.210C>T (p.Ile70=)
c.339C>T (p.Ile113=)
c.381C>T (p.Ile127=)
n.298C>T
n.357+12C>T
 gnomAD v4
1g.17028642G>CCA338274330SDHBc.210C>G (p.Ile70Met)
c.339C>G (p.Ile113Met)
c.381C>G (p.Ile127Met)
n.298C>G
n.357+12C>G
1g.17028642G>TCA416087649SDHBc.210C>A (p.Ile70=)
c.339C>A (p.Ile113=)
c.381C>A (p.Ile127=)
n.298C>A
n.357+12C>A
1g.17028643A=CA1156080492SDHBc.209T= (p.Ile70=)
c.338T= (p.Ile113=)
c.380T= (p.Ile127=)
n.297T=
n.357+11T=
1g.17028643A>CCA015797SDHBc.209T>G (p.Ile70Ser)
c.338T>G (p.Ile113Ser)
c.380T>G (p.Ile127Ser)
n.297T>G
n.357+11T>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17028643A>GCA338274344SDHBc.209T>C (p.Ile70Thr)
c.338T>C (p.Ile113Thr)
c.380T>C (p.Ile127Thr)
n.297T>C
n.357+11T>C
1g.17028643A>TCA338274352SDHBc.209T>A (p.Ile70Asn)
c.338T>A (p.Ile113Asn)
c.380T>A (p.Ile127Asn)
n.297T>A
n.357+11T>A
1g.17028644T>ACA338274354SDHBc.208A>T (p.Ile70Phe)
c.337A>T (p.Ile113Phe)
c.379A>T (p.Ile127Phe)
n.296A>T
n.357+10A>T
1g.17028644T>CCA338274355SDHBc.208A>G (p.Ile70Val)
c.337A>G (p.Ile113Val)
c.379A>G (p.Ile127Val)
n.296A>G
n.357+10A>G
 ClinVar dbSNP gnomAD v4
1g.17028644T>GCA16609924SDHBc.208A>C (p.Ile70Leu)
c.337A>C (p.Ile113Leu)
c.379A>C (p.Ile127Leu)
n.296A>C
n.357+10A>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17028644T=CA1143478094SDHBc.208A= (p.Ile70=)
c.337A= (p.Ile113=)
c.379A= (p.Ile127=)
n.296A=
n.357+10A=
1g.17028648dupCA658655535SDHBc.208dup (p.Ile70AsnfsTer28)
c.337dup (p.Ile113AsnfsTer28)
c.379dup (p.Ile127AsnfsTer28)
n.296dup
n.357+10dup
 ClinVar dbSNP
1g.17028645T>ACA338274369SDHBc.207A>T (p.Lys69Asn)
c.336A>T (p.Lys112Asn)
c.378A>T (p.Lys126Asn)
n.295A>T
n.357+9A>T
1g.17028645T>CCA416087659SDHBc.207A>G (p.Lys69=)
c.336A>G (p.Lys112=)
c.378A>G (p.Lys126=)
n.295A>G
n.357+9A>G
1g.17028645T>GCA338274360SDHBc.207A>C (p.Lys69Asn)
c.336A>C (p.Lys112Asn)
c.378A>C (p.Lys126Asn)
n.295A>C
n.357+9A>C
1g.17028646T>ACA338274372SDHBc.206A>T (p.Lys69Ile)
c.335A>T (p.Lys112Ile)
c.377A>T (p.Lys126Ile)
n.294A>T
n.357+8A>T
1g.17028646T>CCA338274377SDHBc.206A>G (p.Lys69Arg)
c.335A>G (p.Lys112Arg)
c.377A>G (p.Lys126Arg)
n.294A>G
n.357+8A>G
1g.17028646T>GCA338274386SDHBc.206A>C (p.Lys69Thr)
c.335A>C (p.Lys112Thr)
c.377A>C (p.Lys126Thr)
n.294A>C
n.357+8A>C
1g.17028647T>ACA338274390SDHBc.205A>T (p.Lys69Ter)
c.334A>T (p.Lys112Ter)
c.376A>T (p.Lys126Ter)
n.293A>T
n.357+7A>T
1g.17028647T>CCA18666643SDHBc.205A>G (p.Lys69Glu)
c.334A>G (p.Lys112Glu)
c.376A>G (p.Lys126Glu)
n.293A>G
n.357+7A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17028647T>GCA338274397SDHBc.205A>C (p.Lys69Gln)
c.334A>C (p.Lys112Gln)
c.376A>C (p.Lys126Gln)
n.293A>C
n.357+7A>C
1g.17028647T=CA1143525359SDHBc.205A= (p.Lys69=)
c.334A= (p.Lys112=)
c.376A= (p.Lys126=)
n.293A=
n.357+7A=
1g.17028648T>ACA416087675SDHBc.204A>T (p.Ser68=)
c.333A>T (p.Ser111=)
c.375A>T (p.Ser125=)
n.292A>T
n.357+6A>T
1g.17028648T>CCA416087677SDHBc.204A>G (p.Ser68=)
c.333A>G (p.Ser111=)
c.375A>G (p.Ser125=)
n.292A>G
n.357+6A>G
 ClinVar dbSNP
1g.17028648T>GCA416087679SDHBc.204A>C (p.Ser68=)
c.333A>C (p.Ser111=)
c.375A>C (p.Ser125=)
n.292A>C
n.357+6A>C
1g.17028649G>ACA338274404SDHBc.203C>T (p.Ser68Leu)
c.332C>T (p.Ser111Leu)
c.374C>T (p.Ser125Leu)
n.291C>T
n.357+5C>T
 ClinVar dbSNP gnomAD v4
1g.17028649G>CCA16609939SDHBc.203C>G (p.Ser68Ter)
c.332C>G (p.Ser111Ter)
c.374C>G (p.Ser125Ter)
n.291C>G
n.357+5C>G
 ClinVar dbSNP gnomAD v4
1g.17028649G=CA1156080493SDHBc.203C= (p.Ser68=)
c.332C= (p.Ser111=)
c.374C= (p.Ser125=)
n.291C=
n.357+5C=
1g.17028649G>TCA015788SDHBc.203C>A (p.Ser68Ter)
c.332C>A (p.Ser111Ter)
c.374C>A (p.Ser125Ter)
n.291C>A
n.357+5C>A
 ClinVar dbSNP
1g.17028650A>CCA338274405SDHBc.202T>G (p.Ser68Ala)
c.331T>G (p.Ser111Ala)
c.373T>G (p.Ser125Ala)
n.290T>G
n.357+4T>G
1g.17028650A>GCA338274406SDHBc.202T>C (p.Ser68Pro)
c.331T>C (p.Ser111Pro)
c.373T>C (p.Ser125Pro)
n.290T>C
n.357+4T>C
1g.17028650A>TCA338274407SDHBc.202T>A (p.Ser68Thr)
c.331T>A (p.Ser111Thr)
c.373T>A (p.Ser125Thr)
n.290T>A
n.357+4T>A
 dbSNP
1g.17028651G>ACA416087702SDHBc.201C>T (p.Val67=)
c.330C>T (p.Val110=)
c.372C>T (p.Val124=)
n.289C>T
n.357+3C>T
1g.17028651G>CCA416087707SDHBc.201C>G (p.Val67=)
c.330C>G (p.Val110=)
c.372C>G (p.Val124=)
n.289C>G
n.357+3C>G
1g.17028651G>TCA416087705SDHBc.201C>A (p.Val67=)
c.330C>A (p.Val110=)
c.372C>A (p.Val124=)
n.289C>A
n.357+3C>A
1g.17028652A=CA1156080494SDHBc.200T= (p.Val67=)
c.329T= (p.Val110=)
c.371T= (p.Val124=)
n.288T=
n.357+2T=
1g.17028652A>CCA338274410SDHBc.200T>G (p.Val67Gly)
c.329T>G (p.Val110Gly)
c.371T>G (p.Val124Gly)
n.288T>G
n.357+2T>G
1g.17028652A>GCA338274420SDHBc.200T>C (p.Val67Ala)
c.329T>C (p.Val110Ala)
c.371T>C (p.Val124Ala)
n.288T>C
n.357+2T>C
 ClinVar dbSNP
1g.17028652A>TCA338274423SDHBc.200T>A (p.Val67Asp)
c.329T>A (p.Val110Asp)
c.371T>A (p.Val124Asp)
n.288T>A
n.357+2T>A
1g.17028653C>ACA18666648SDHBc.199G>T (p.Val67Phe)
c.328G>T (p.Val110Phe)
c.370G>T (p.Val124Phe)
n.287G>T
n.357+1G>T
 dbSNP
1g.17028653C=CA1156080495SDHBc.199G= (p.Val67=)
c.328G= (p.Val110=)
c.370G= (p.Val124=)
n.287G=
n.357+1G=
1g.17028653C>GCA338274429SDHBc.199G>C (p.Val67Leu)
c.328G>C (p.Val110Leu)
c.370G>C (p.Val124Leu)
n.287G>C
n.357+1G>C
1g.17028653C>TCA338274431SDHBc.199G>A (p.Val67Ile)
c.328G>A (p.Val110Ile)
c.370G>A (p.Val124Ile)
n.287G>A
n.357+1G>A
 ClinVar dbSNP
1g.17028653_17028654insTCA645509070SDHBc.198_199insA (p.Val67SerfsTer?)
c.327_328insA (p.Val110SerfsTer?)
c.369_370insA (p.Val124SerfsTer?)
n.286_287insA
n.357_357+1insA
 ClinVar dbSNP
1g.17028654C>ACA338274434SDHBc.198G>T (p.Lys66Asn)
c.327G>T (p.Lys109Asn)
c.369G>T (p.Lys123Asn)
n.286G>T
n.357G>T
 dbSNP
1g.17028654C>GCA338274440SDHBc.198G>C (p.Lys66Asn)
c.327G>C (p.Lys109Asn)
c.369G>C (p.Lys123Asn)
n.286G>C
n.357G>C
1g.17028654C>TCA416087738SDHBc.198G>A (p.Lys66=)
c.327G>A (p.Lys109=)
c.369G>A (p.Lys123=)
n.286G>A
n.357G>A
 ClinVar dbSNP
1g.17028655T>ACA338274447SDHBc.197A>T (p.Lys66Met)
c.326A>T (p.Lys109Met)
c.368A>T (p.Lys123Met)
n.285A>T
n.356A>T
1g.17028655T>CCA338274443SDHBc.197A>G (p.Lys66Arg)
c.326A>G (p.Lys109Arg)
c.368A>G (p.Lys123Arg)
n.285A>G
n.356A>G
 ClinVar dbSNP
1g.17028655T>GCA338274445SDHBc.197A>C (p.Lys66Thr)
c.326A>C (p.Lys109Thr)
c.368A>C (p.Lys123Thr)
n.285A>C
n.356A>C
 ClinVar dbSNP gnomAD v4
1g.17028655T=CA1156080496SDHBc.197A= (p.Lys66=)
c.326A= (p.Lys109=)
c.368A= (p.Lys123=)
n.285A=
n.356A=
1g.17028656T>ACA338274450SDHBc.196A>T (p.Lys66Ter)
c.325A>T (p.Lys109Ter)
c.367A>T (p.Lys123Ter)
n.284A>T
n.355A>T
1g.17028656T>CCA338274454SDHBc.196A>G (p.Lys66Glu)
c.325A>G (p.Lys109Glu)
c.367A>G (p.Lys123Glu)
n.284A>G
n.355A>G
 ClinVar dbSNP
1g.17028656T>GCA338274459SDHBc.196A>C (p.Lys66Gln)
c.325A>C (p.Lys109Gln)
c.367A>C (p.Lys123Gln)
n.284A>C
n.355A>C
1g.17028656T=CA1156080497SDHBc.196A= (p.Lys66=)
c.325A= (p.Lys109=)
c.367A= (p.Lys123=)
n.284A=
n.355A=
1g.17028657A=CA1156080498SDHBc.195T= (p.Asn65=)
c.324T= (p.Asn108=)
c.366T= (p.Asn122=)
n.283T=
n.354T=
1g.17028657A>CCA338274461SDHBc.195T>G (p.Asn65Lys)
c.324T>G (p.Asn108Lys)
c.366T>G (p.Asn122Lys)
n.283T>G
n.354T>G
 dbSNP gnomAD v2 gnomAD v4
1g.17028657A>GCA416087756SDHBc.195T>C (p.Asn65=)
c.324T>C (p.Asn108=)
c.366T>C (p.Asn122=)
n.283T>C
n.354T>C
1g.17028657A>TCA338274466SDHBc.195T>A (p.Asn65Lys)
c.324T>A (p.Asn108Lys)
c.366T>A (p.Asn122Lys)
n.283T>A
n.354T>A
1g.17028658T>ACA338274472SDHBc.194A>T (p.Asn65Ile)
c.323A>T (p.Asn108Ile)
c.365A>T (p.Asn122Ile)
n.282A>T
n.353A>T
1g.17028658T>CCA338274471SDHBc.194A>G (p.Asn65Ser)
c.323A>G (p.Asn108Ser)
c.365A>G (p.Asn122Ser)
n.282A>G
n.353A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17028658T>GCA338274470SDHBc.194A>C (p.Asn65Thr)
c.323A>C (p.Asn108Thr)
c.365A>C (p.Asn122Thr)
n.282A>C
n.353A>C
1g.17028658T=CA1156080499SDHBc.194A= (p.Asn65=)
c.323A= (p.Asn108=)
c.365A= (p.Asn122=)
n.282A=
n.353A=
1g.17028659T>ACA338274473SDHBc.193A>T (p.Asn65Tyr)
c.322A>T (p.Asn108Tyr)
c.364A>T (p.Asn122Tyr)
n.281A>T
n.352A>T
1g.17028659T>CCA338274474SDHBc.193A>G (p.Asn65Asp)
c.322A>G (p.Asn108Asp)
c.364A>G (p.Asn122Asp)
n.281A>G
n.352A>G
1g.17028659T>GCA338274475SDHBc.193A>C (p.Asn65His)
c.322A>C (p.Asn108His)
c.364A>C (p.Asn122His)
n.281A>C
n.352A>C
1g.17028660G>ACA18666653SDHBc.192C>T (p.Leu64=)
c.321C>T (p.Leu107=)
c.363C>T (p.Leu121=)
n.280C>T
n.351C>T
 ClinVar dbSNP
1g.17028660G>CCA416087770SDHBc.192C>G (p.Leu64=)
c.321C>G (p.Leu107=)
c.363C>G (p.Leu121=)
n.280C>G
n.351C>G
1g.17028660G=CA1156080500SDHBc.192C= (p.Leu64=)
c.321C= (p.Leu107=)
c.363C= (p.Leu121=)
n.280C=
n.351C=
1g.17028660G>TCA416087774SDHBc.192C>A (p.Leu64=)
c.321C>A (p.Leu107=)
c.363C>A (p.Leu121=)
n.280C>A
n.351C>A
1g.17028661A=CA1156080501SDHBc.191T= (p.Leu64=)
c.320T= (p.Leu107=)
c.362T= (p.Leu121=)
n.279T=
n.350T=
1g.17028661A>CCA338274477SDHBc.191T>G (p.Leu64Arg)
c.320T>G (p.Leu107Arg)
c.362T>G (p.Leu121Arg)
n.279T>G
n.350T>G
1g.17028661A>GCA089597SDHBc.191T>C (p.Leu64Pro)
c.320T>C (p.Leu107Pro)
c.362T>C (p.Leu121Pro)
n.279T>C
n.350T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17028661A>TCA338274491SDHBc.191T>A (p.Leu64His)
c.320T>A (p.Leu107His)
c.362T>A (p.Leu121His)
n.279T>A
n.350T>A
1g.17028662G>ACA338274493SDHBc.190C>T (p.Leu64Phe)
c.319C>T (p.Leu107Phe)
c.361C>T (p.Leu121Phe)
n.278C>T
n.349C>T
 ClinVar dbSNP gnomAD v4
1g.17028662G>CCA338274500SDHBc.190C>G (p.Leu64Val)
c.319C>G (p.Leu107Val)
c.361C>G (p.Leu121Val)
n.278C>G
n.349C>G
1g.17028662G=CA1156080502SDHBc.190C= (p.Leu64=)
c.319C= (p.Leu107=)
c.361C= (p.Leu121=)
n.278C=
n.349C=
1g.17028662G>TCA338274497SDHBc.190C>A (p.Leu64Ile)
c.319C>A (p.Leu107Ile)
c.361C>A (p.Leu121Ile)
n.278C>A
n.349C>A
1g.17028663G>ACA416087790SDHBc.189C>T (p.Asn63=)
c.318C>T (p.Asn106=)
c.360C>T (p.Asn120=)
n.277C>T
n.348C>T
 dbSNP
1g.17028663G>CCA338274503SDHBc.189C>G (p.Asn63Lys)
c.318C>G (p.Asn106Lys)
c.360C>G (p.Asn120Lys)
n.277C>G
n.348C>G
1g.17028663G>TCA338274504SDHBc.189C>A (p.Asn63Lys)
c.318C>A (p.Asn106Lys)
c.360C>A (p.Asn120Lys)
n.277C>A
n.348C>A
1g.17028664T>ACA338274508SDHBc.188A>T (p.Asn63Ile)
c.317A>T (p.Asn106Ile)
c.359A>T (p.Asn120Ile)
n.276A>T
n.347A>T
 ClinVar
1g.17028664T>CCA338274512SDHBc.188A>G (p.Asn63Ser)
c.317A>G (p.Asn106Ser)
c.359A>G (p.Asn120Ser)
n.276A>G
n.347A>G
 ClinVar dbSNP
1g.17028664T>GCA338274515SDHBc.188A>C (p.Asn63Thr)
c.317A>C (p.Asn106Thr)
c.359A>C (p.Asn120Thr)
n.276A>C
n.347A>C
 ClinVar gnomAD v4
1g.17028664T=CA1156080503SDHBc.188A= (p.Asn63=)
c.317A= (p.Asn106=)
c.359A= (p.Asn120=)
n.276A=
n.347A=
1g.17028665T>ACA338274520SDHBc.187A>T (p.Asn63Tyr)
c.316A>T (p.Asn106Tyr)
c.358A>T (p.Asn120Tyr)
n.275A>T
n.346A>T
1g.17028665T>CCA338274521SDHBc.187A>G (p.Asn63Asp)
c.316A>G (p.Asn106Asp)
c.358A>G (p.Asn120Asp)
n.275A>G
n.346A>G
1g.17028665T>GCA338274522SDHBc.187A>C (p.Asn63His)
c.316A>C (p.Asn106His)
c.358A>C (p.Asn120His)
n.275A>C
n.346A>C
1g.17028666G>ACA416087806SDHBc.186C>T (p.Thr62=)
c.315C>T (p.Thr105=)
c.357C>T (p.Thr119=)
n.274C>T
n.345C>T
 ClinVar dbSNP gnomAD v4
1g.17028666G>CCA416087809SDHBc.186C>G (p.Thr62=)
c.315C>G (p.Thr105=)
c.357C>G (p.Thr119=)
n.274C>G
n.345C>G
1g.17028666G=CA1156080504SDHBc.186C= (p.Thr62=)
c.315C= (p.Thr105=)
c.357C= (p.Thr119=)
n.274C=
n.345C=
1g.17028666G>TCA416087807SDHBc.186C>A (p.Thr62=)
c.315C>A (p.Thr105=)
c.357C>A (p.Thr119=)
n.274C>A
n.345C>A
1g.17028667G>ACA18666654SDHBc.185C>T (p.Thr62Ile)
c.314C>T (p.Thr105Ile)
c.356C>T (p.Thr119Ile)
n.273C>T
n.344C>T
 dbSNP
1g.17028667G>CCA338274530SDHBc.185C>G (p.Thr62Ser)
c.314C>G (p.Thr105Ser)
c.356C>G (p.Thr119Ser)
n.273C>G
n.344C>G
 dbSNP
1g.17028667G=CA1140263947SDHBc.185C= (p.Thr62=)
c.314C= (p.Thr105=)
c.356C= (p.Thr119=)
n.273C=
n.344C=
1g.17028667G>TCA089596SDHBc.185C>A (p.Thr62Asn)
c.314C>A (p.Thr105Asn)
c.356C>A (p.Thr119Asn)
n.273C>A
n.344C>A
 ClinVar dbSNP ExAC gnomAD v2
1g.17028668T>ACA338274534SDHBc.184A>T (p.Thr62Ser)
c.313A>T (p.Thr105Ser)
c.355A>T (p.Thr119Ser)
n.272A>T
n.343A>T
1g.17028668T>CCA338274541SDHBc.184A>G (p.Thr62Ala)
c.313A>G (p.Thr105Ala)
c.355A>G (p.Thr119Ala)
n.272A>G
n.343A>G
1g.17028668T>GCA338274538SDHBc.184A>C (p.Thr62Pro)
c.313A>C (p.Thr105Pro)
c.355A>C (p.Thr119Pro)
n.272A>C
n.343A>C
1g.17028669G>ACA416087828SDHBc.183C>T (p.Asp61=)
c.312C>T (p.Asp104=)
c.354C>T (p.Asp118=)
n.271C>T
n.342C>T
 dbSNP gnomAD v4
1g.17028669G>CCA338274546SDHBc.183C>G (p.Asp61Glu)
c.312C>G (p.Asp104Glu)
c.354C>G (p.Asp118Glu)
n.271C>G
n.342C>G
1g.17028669G>TCA338274548SDHBc.183C>A (p.Asp61Glu)
c.312C>A (p.Asp104Glu)
c.354C>A (p.Asp118Glu)
n.271C>A
n.342C>A
1g.17028670T>ACA338274551SDHBc.182A>T (p.Asp61Val)
c.311A>T (p.Asp104Val)
c.353A>T (p.Asp118Val)
n.270A>T
n.341A>T
1g.17028670T>CCA338274559SDHBc.182A>G (p.Asp61Gly)
c.311A>G (p.Asp104Gly)
c.353A>G (p.Asp118Gly)
n.270A>G
n.341A>G
 dbSNP
1g.17028670T>GCA338274556SDHBc.182A>C (p.Asp61Ala)
c.311A>C (p.Asp104Ala)
c.353A>C (p.Asp118Ala)
n.270A>C
n.341A>C
 gnomAD v4
1g.17028670_17028675delinsTCAATCCA1156080505SDHBc.177_182delinsGATTGA (p.Arg59=)
c.306_311delinsGATTGA (p.Arg102=)
c.348_353delinsGATTGA (p.Arg116=)
n.265_270delinsGATTGA
n.336_341delinsGATTGA
1g.17028671C>ACA015778SDHBc.181G>T (p.Asp61Tyr)
c.310G>T (p.Asp104Tyr)
c.352G>T (p.Asp118Tyr)
n.269G>T
n.340G>T
 ClinVar dbSNP
1g.17028671C=CA1143390144SDHBc.181G= (p.Asp61=)
c.310G= (p.Asp104=)
c.352G= (p.Asp118=)
n.269G=
n.340G=
1g.17028671C>GCA338274577SDHBc.181G>C (p.Asp61His)
c.310G>C (p.Asp104His)
c.352G>C (p.Asp118His)
n.269G>C
n.340G>C
1g.17028671C>TCA089595SDHBc.181G>A (p.Asp61Asn)
c.310G>A (p.Asp104Asn)
c.352G>A (p.Asp118Asn)
n.269G>A
n.340G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17028672_17028676delCA521039524SDHBc.177_181del (p.Ile60HisfsTer5)
c.306_310del (p.Ile103HisfsTer5)
c.348_352del (p.Ile117HisfsTer5)
n.265_269del
n.336_340del
 ClinVar dbSNP gnomAD v2
1g.17028674_17028687delCA658655534SDHBc.168_181del (p.Cys56Ter)
c.297_310del (p.Cys99Ter)
c.339_352del (p.Cys113Ter)
n.256_269del
n.327_340del
1g.17028672A>CCA338274580SDHBc.180T>G (p.Ile60Met)
c.309T>G (p.Ile103Met)
c.351T>G (p.Ile117Met)
n.268T>G
n.339T>G
1g.17028672A>GCA416087847SDHBc.180T>C (p.Ile60=)
c.309T>C (p.Ile103=)
c.351T>C (p.Ile117=)
n.268T>C
n.339T>C
1g.17028672A>TCA416087849SDHBc.180T>A (p.Ile60=)
c.309T>A (p.Ile103=)
c.351T>A (p.Ile117=)
n.268T>A
n.339T>A
 ClinVar dbSNP
1g.17028673A=CA1156080506SDHBc.179T= (p.Ile60=)
c.308T= (p.Ile103=)
c.350T= (p.Ile117=)
n.267T=
n.338T=
1g.17028673A>CCA338274592SDHBc.179T>G (p.Ile60Ser)
c.308T>G (p.Ile103Ser)
c.350T>G (p.Ile117Ser)
n.267T>G
n.338T>G
1g.17028673A>GCA338274586SDHBc.179T>C (p.Ile60Thr)
c.308T>C (p.Ile103Thr)
c.350T>C (p.Ile117Thr)
n.267T>C
n.338T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17028673A>TCA338274593SDHBc.179T>A (p.Ile60Asn)
c.308T>A (p.Ile103Asn)
c.350T>A (p.Ile117Asn)
n.267T>A
n.338T>A
1g.17028674T>ACA338274597SDHBc.178A>T (p.Ile60Phe)
c.307A>T (p.Ile103Phe)
c.349A>T (p.Ile117Phe)
n.266A>T
n.337A>T
1g.17028674T>CCA338274611SDHBc.178A>G (p.Ile60Val)
c.307A>G (p.Ile103Val)
c.349A>G (p.Ile117Val)
n.266A>G
n.337A>G
 ClinVar
1g.17028674T>GCA338274616SDHBc.178A>C (p.Ile60Leu)
c.307A>C (p.Ile103Leu)
c.349A>C (p.Ile117Leu)
n.266A>C
n.337A>C
1g.17028675C>ACA338274621SDHBc.177G>T (p.Arg59Ser)
c.306G>T (p.Arg102Ser)
c.348G>T (p.Arg116Ser)
n.265G>T
n.336G>T
 ClinVar dbSNP
1g.17028675C=CA1156080507SDHBc.177G= (p.Arg59=)
c.306G= (p.Arg102=)
c.348G= (p.Arg116=)
n.265G=
n.336G=
1g.17028675C>GCA338274626SDHBc.177G>C (p.Arg59Ser)
c.306G>C (p.Arg102Ser)
c.348G>C (p.Arg116Ser)
n.265G>C
n.336G>C
 dbSNP
1g.17028675C>TCA416087861SDHBc.177G>A (p.Arg59=)
c.306G>A (p.Arg102=)
c.348G>A (p.Arg116=)
n.265G>A
n.336G>A
 gnomAD v4
1g.17028676C>ACA338274628SDHBc.176G>T (p.Arg59Met)
c.305G>T (p.Arg102Met)
c.347G>T (p.Arg116Met)
n.264G>T
n.335G>T
 ClinVar dbSNP
1g.17028676C=CA1156080508SDHBc.176G= (p.Arg59=)
c.305G= (p.Arg102=)
c.347G= (p.Arg116=)
n.264G=
n.335G=
1g.17028676C>GCA089593SDHBc.176G>C (p.Arg59Thr)
c.305G>C (p.Arg102Thr)
c.347G>C (p.Arg116Thr)
n.264G>C
n.335G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17028676C>TCA338274648SDHBc.176G>A (p.Arg59Lys)
c.305G>A (p.Arg102Lys)
c.347G>A (p.Arg116Lys)
n.264G>A
n.335G>A
 ClinVar
1g.17028677T>ACA338274668SDHBc.175A>T (p.Arg59Trp)
c.304A>T (p.Arg102Trp)
c.346A>T (p.Arg116Trp)
n.263A>T
n.334A>T
1g.17028677T>CCA338274673SDHBc.175A>G (p.Arg59Gly)
c.304A>G (p.Arg102Gly)
c.346A>G (p.Arg116Gly)
n.263A>G
n.334A>G
1g.17028677T>GCA416087879SDHBc.175A>C (p.Arg59=)
c.304A>C (p.Arg102=)
c.346A>C (p.Arg116=)
n.263A>C
n.334A>C
 ClinVar
1g.17028678T>ACA416087883SDHBc.174A>T (p.Arg58=)
c.303A>T (p.Arg101=)
c.345A>T (p.Arg115=)
n.262A>T
n.333A>T
1g.17028678T>CCA416087884SDHBc.174A>G (p.Arg58=)
c.303A>G (p.Arg101=)
c.345A>G (p.Arg115=)
n.262A>G
n.333A>G
1g.17028678T>GCA416087885SDHBc.174A>C (p.Arg58=)
c.303A>C (p.Arg101=)
c.345A>C (p.Arg115=)
n.262A>C
n.333A>C
1g.17028679C>ACA089592SDHBc.173G>T (p.Arg58Leu)
c.302G>T (p.Arg101Leu)
c.344G>T (p.Arg115Leu)
n.261G>T
n.332G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17028679C=CA1143451603SDHBc.173G= (p.Arg58=)
c.302G= (p.Arg101=)
c.344G= (p.Arg115=)
n.261G=
n.332G=
1g.17028679C>GCA338274685SDHBc.173G>C (p.Arg58Pro)
c.302G>C (p.Arg101Pro)
c.344G>C (p.Arg115Pro)
n.261G>C
n.332G>C
 dbSNP
1g.17028679C>TCA015769SDHBc.173G>A (p.Arg58Gln)
c.302G>A (p.Arg101Gln)
c.344G>A (p.Arg115Gln)
n.261G>A
n.332G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17028680G>ACA015763SDHBc.172C>T (p.Arg58Ter)
c.301C>T (p.Arg101Ter)
c.343C>T (p.Arg115Ter)
n.260C>T
n.331C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
1g.17028680G>CCA338274697SDHBc.172C>G (p.Arg58Gly)
c.301C>G (p.Arg101Gly)
c.343C>G (p.Arg115Gly)
n.260C>G
n.331C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17028680G=CA1156080509SDHBc.172C= (p.Arg58=)
c.301C= (p.Arg101=)
c.343C= (p.Arg115=)
n.260C=
n.331C=
1g.17028680G>TCA416087896SDHBc.172C>A (p.Arg58=)
c.301C>A (p.Arg101=)
c.343C>A (p.Arg115=)
n.260C>A
n.331C>A
1g.17028681G>ACA18666709SDHBc.171C>T (p.Thr57=)
c.300C>T (p.Thr100=)
c.342C>T (p.Thr114=)
n.259C>T
n.330C>T
 ClinVar dbSNP gnomAD v4
1g.17028681G>CCA416087903SDHBc.171C>G (p.Thr57=)
c.300C>G (p.Thr100=)
c.342C>G (p.Thr114=)
n.259C>G
n.330C>G
 ClinVar
1g.17028681G=CA1144336504SDHBc.171C= (p.Thr57=)
c.300C= (p.Thr100=)
c.342C= (p.Thr114=)
n.259C=
n.330C=
1g.17028681G>TCA416087902SDHBc.171C>A (p.Thr57=)
c.300C>A (p.Thr100=)
c.342C>A (p.Thr114=)
n.259C>A
n.330C>A
 ClinVar
1g.17028682G>ACA338274733SDHBc.170C>T (p.Thr57Ile)
c.299C>T (p.Thr100Ile)
c.341C>T (p.Thr114Ile)
n.258C>T
n.329C>T
 ClinVar
1g.17028682G>CCA338274737SDHBc.170C>G (p.Thr57Ser)
c.299C>G (p.Thr100Ser)
c.341C>G (p.Thr114Ser)
n.258C>G
n.329C>G
1g.17028682G>TCA338274739SDHBc.170C>A (p.Thr57Asn)
c.299C>A (p.Thr100Asn)
c.341C>A (p.Thr114Asn)
n.258C>A
n.329C>A
1g.17028683T>ACA338274743SDHBc.169A>T (p.Thr57Ser)
c.298A>T (p.Thr100Ser)
c.340A>T (p.Thr114Ser)
n.257A>T
n.328A>T
 ClinVar dbSNP gnomAD v4
1g.17028683T>CCA338274746SDHBc.169A>G (p.Thr57Ala)
c.298A>G (p.Thr100Ala)
c.340A>G (p.Thr114Ala)
n.257A>G
n.328A>G
 ClinVar dbSNP
1g.17028683T>GCA338274750SDHBc.169A>C (p.Thr57Pro)
c.298A>C (p.Thr100Pro)
c.340A>C (p.Thr114Pro)
n.257A>C
n.328A>C
 dbSNP
1g.17028683T=CA1156080510SDHBc.169A= (p.Thr57=)
c.298A= (p.Thr100=)
c.340A= (p.Thr114=)
n.257A=
n.328A=
1g.17028684G>ACA089590SDHBc.168C>T (p.Cys56=)
c.297C>T (p.Cys99=)
c.339C>T (p.Cys113=)
n.256C>T
n.327C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17028684G>CCA338274759SDHBc.168C>G (p.Cys56Trp)
c.297C>G (p.Cys99Trp)
c.339C>G (p.Cys113Trp)
n.256C>G
n.327C>G
1g.17028684G=CA1156080511SDHBc.168C= (p.Cys56=)
c.297C= (p.Cys99=)
c.339C= (p.Cys113=)
n.256C=
n.327C=
1g.17028684G>TCA338274765SDHBc.168C>A (p.Cys56Ter)
c.297C>A (p.Cys99Ter)
c.339C>A (p.Cys113Ter)
n.256C>A
n.327C>A
1g.17028685C>ACA338274771SDHBc.167G>T (p.Cys56Phe)
c.296G>T (p.Cys99Phe)
c.338G>T (p.Cys113Phe)
n.255G>T
n.326G>T
 dbSNP
1g.17028685C=CA1156080512SDHBc.167G= (p.Cys56=)
c.296G= (p.Cys99=)
c.338G= (p.Cys113=)
n.255G=
n.326G=
1g.17028685C>GCA279931SDHBc.167G>C (p.Cys56Ser)
c.296G>C (p.Cys99Ser)
c.338G>C (p.Cys113Ser)
n.255G>C
n.326G>C
 ClinVar dbSNP
1g.17028685C>TCA338274769SDHBc.167G>A (p.Cys56Tyr)
c.296G>A (p.Cys99Tyr)
c.338G>A (p.Cys113Tyr)
n.255G>A
n.326G>A
 ClinVar dbSNP gnomAD v4
1g.17028686A=CA1156080513SDHBc.166T= (p.Cys56=)
c.295T= (p.Cys99=)
c.337T= (p.Cys113=)
n.254T=
n.325T=
1g.17028686A>CCA338274774SDHBc.166T>G (p.Cys56Gly)
c.295T>G (p.Cys99Gly)
c.337T>G (p.Cys113Gly)
n.254T>G
n.325T>G
 ClinVar dbSNP
1g.17028686A>GCA338274776SDHBc.166T>C (p.Cys56Arg)
c.295T>C (p.Cys99Arg)
c.337T>C (p.Cys113Arg)
n.254T>C
n.325T>C
1g.17028686A>TCA338274780SDHBc.166T>A (p.Cys56Ser)
c.295T>A (p.Cys99Ser)
c.337T>A (p.Cys113Ser)
n.254T>A
n.325T>A
1g.17028687A>CCA416087915SDHBc.165T>G (p.Ala55=)
c.294T>G (p.Ala98=)
c.336T>G (p.Ala112=)
n.253T>G
n.324T>G
 gnomAD v4
1g.17028687A>GCA416087916SDHBc.165T>C (p.Ala55=)
c.294T>C (p.Ala98=)
c.336T>C (p.Ala112=)
n.253T>C
n.324T>C
 ClinVar dbSNP
1g.17028687A>TCA416087918SDHBc.165T>A (p.Ala55=)
c.294T>A (p.Ala98=)
c.336T>A (p.Ala112=)
n.253T>A
n.324T>A
1g.17028688G>ACA338274791SDHBc.164C>T (p.Ala55Val)
c.293C>T (p.Ala98Val)
c.335C>T (p.Ala112Val)
n.252C>T
n.323C>T
 ClinVar dbSNP
1g.17028688G>CCA338274795SDHBc.164C>G (p.Ala55Gly)
c.293C>G (p.Ala98Gly)
c.335C>G (p.Ala112Gly)
n.252C>G
n.323C>G
 ClinVar dbSNP
1g.17028688G=CA1156080514SDHBc.164C= (p.Ala55=)
c.293C= (p.Ala98=)
c.335C= (p.Ala112=)
n.252C=
n.323C=
1g.17028688G>TCA338274814SDHBc.164C>A (p.Ala55Asp)
c.293C>A (p.Ala98Asp)
c.335C>A (p.Ala112Asp)
n.252C>A
n.323C>A
1g.17028690_17028700delCA658655532SDHBc.154_164del (p.Asn52LeufsTer6)
c.283_293del (p.Asn95LeufsTer6)
c.325_335del (p.Asn109LeufsTer6)
n.242_252del
n.313_323del
 ClinVar dbSNP
1g.17028689C>ACA338274817SDHBc.163G>T (p.Ala55Ser)
c.292G>T (p.Ala98Ser)
c.334G>T (p.Ala112Ser)
n.251G>T
n.322G>T
 gnomAD v4
1g.17028689C=CA1156080515SDHBc.163G= (p.Ala55=)
c.292G= (p.Ala98=)
c.334G= (p.Ala112=)
n.251G=
n.322G=
1g.17028689C>GCA338274820SDHBc.163G>C (p.Ala55Pro)
c.292G>C (p.Ala98Pro)
c.334G>C (p.Ala112Pro)
n.251G>C
n.322G>C
1g.17028689C>TCA338274826SDHBc.163G>A (p.Ala55Thr)
c.292G>A (p.Ala98Thr)
c.334G>A (p.Ala112Thr)
n.251G>A
n.322G>A
1g.17028689_17028691delCA658655533SDHBc.161_163del (p.Leu54_Ala55delinsPro)
c.290_292del (p.Leu97_Ala98delinsPro)
c.332_334del (p.Leu111_Ala112delinsPro)
n.249_251del
n.320_322del
1g.17028690T>ACA416087934SDHBc.162A>T (p.Leu54=)
c.291A>T (p.Leu97=)
c.333A>T (p.Leu111=)
n.250A>T
n.321A>T
 dbSNP
1g.17028690T>CCA416087937SDHBc.162A>G (p.Leu54=)
c.291A>G (p.Leu97=)
c.333A>G (p.Leu111=)
n.250A>G
n.321A>G
 ClinVar dbSNP
1g.17028690T>GCA416087940SDHBc.162A>C (p.Leu54=)
c.291A>C (p.Leu97=)
c.333A>C (p.Leu111=)
n.250A>C
n.321A>C
1g.17028690_17028692delinsTAGCA1156080516SDHBc.160_162delinsCTA (p.Leu54=)
c.289_291delinsCTA (p.Leu97=)
c.331_333delinsCTA (p.Leu111=)
n.248_250delinsCTA
n.319_321delinsCTA
1g.17028690_17028693dupCA308155SDHBc.159_162dup (p.Ala55SerfsTer8)
c.288_291dup (p.Ala98SerfsTer8)
c.330_333dup (p.Ala112SerfsTer8)
n.247_250dup
n.318_321dup
 ClinVar dbSNP
1g.17028691A=CA1156080517SDHBc.161T= (p.Leu54=)
c.290T= (p.Leu97=)
c.332T= (p.Leu111=)
n.249T=
n.320T=
1g.17028691A>CCA338274835SDHBc.161T>G (p.Leu54Arg)
c.290T>G (p.Leu97Arg)
c.332T>G (p.Leu111Arg)
n.249T>G
n.320T>G
 gnomAD v4
1g.17028691A>GCA338274838SDHBc.161T>C (p.Leu54Pro)
c.290T>C (p.Leu97Pro)
c.332T>C (p.Leu111Pro)
n.249T>C
n.320T>C
 ClinVar dbSNP
1g.17028691A>TCA338274830SDHBc.161T>A (p.Leu54Gln)
c.290T>A (p.Leu97Gln)
c.332T>A (p.Leu111Gln)
n.249T>A
n.320T>A
1g.17028691_17028692delinsTTCA2580060619SDHBc.160_161delinsAA (p.Leu54Lys)
c.289_290delinsAA (p.Leu97Lys)
c.331_332delinsAA (p.Leu111Lys)
n.248_249delinsAA
n.319_320delinsAA
 ClinVar
1g.17028693_17028694delCA16609938SDHBc.160_161del (p.Leu54SerfsTer7)
c.289_290del (p.Leu97SerfsTer7)
c.331_332del (p.Leu111SerfsTer7)
n.248_249del
n.319_320del
 ClinVar dbSNP
1g.17028692G>ACA416087948SDHBc.160C>T (p.Leu54=)
c.289C>T (p.Leu97=)
c.331C>T (p.Leu111=)
n.248C>T
n.319C>T
 ClinVar gnomAD v4
1g.17028692G>CCA338274842SDHBc.160C>G (p.Leu54Val)
c.289C>G (p.Leu97Val)
c.331C>G (p.Leu111Val)
n.248C>G
n.319C>G
 ClinVar dbSNP gnomAD v4
1g.17028692G=CA1156080518SDHBc.160C= (p.Leu54=)
c.289C= (p.Leu97=)
c.331C= (p.Leu111=)
n.248C=
n.319C=
1g.17028692G>TCA338274843SDHBc.160C>A (p.Leu54Ile)
c.289C>A (p.Leu97Ile)
c.331C>A (p.Leu111Ile)
n.248C>A
n.319C>A
1g.17028693A>CCA416087952SDHBc.159T>G (p.Thr53=)
c.288T>G (p.Thr96=)
c.330T>G (p.Thr110=)
n.247T>G
n.318T>G
1g.17028693A>GCA416087954SDHBc.159T>C (p.Thr53=)
c.288T>C (p.Thr96=)
c.330T>C (p.Thr110=)
n.247T>C
n.318T>C
 ClinVar dbSNP
1g.17028693A>TCA416087958SDHBc.159T>A (p.Thr53=)
c.288T>A (p.Thr96=)
c.330T>A (p.Thr110=)
n.247T>A
n.318T>A
1g.17028694G>ACA338274850SDHBc.158C>T (p.Thr53Ile)
c.287C>T (p.Thr96Ile)
c.329C>T (p.Thr110Ile)
n.246C>T
n.317C>T
 ClinVar gnomAD v4
1g.17028694G>CCA338274853SDHBc.158C>G (p.Thr53Ser)
c.287C>G (p.Thr96Ser)
c.329C>G (p.Thr110Ser)
n.246C>G
n.317C>G
1g.17028694G>TCA338274856SDHBc.158C>A (p.Thr53Asn)
c.287C>A (p.Thr96Asn)
c.329C>A (p.Thr110Asn)
n.246C>A
n.317C>A
1g.17028695T>ACA338274868SDHBc.157A>T (p.Thr53Ser)
c.286A>T (p.Thr96Ser)
c.328A>T (p.Thr110Ser)
n.245A>T
n.316A>T
 ClinVar dbSNP gnomAD v2
1g.17028695T>CCA338274859SDHBc.157A>G (p.Thr53Ala)
c.286A>G (p.Thr96Ala)
c.328A>G (p.Thr110Ala)
n.245A>G
n.316A>G
 COSMIC
1g.17028695T>GCA338274862SDHBc.157A>C (p.Thr53Pro)
c.286A>C (p.Thr96Pro)
c.328A>C (p.Thr110Pro)
n.245A>C
n.316A>C
1g.17028695T=CA1156080519SDHBc.157A= (p.Thr53=)
c.286A= (p.Thr96=)
c.328A= (p.Thr110=)
n.245A=
n.316A=
1g.17028696G>ACA416087970SDHBc.156C>T (p.Asn52=)
c.285C>T (p.Asn95=)
c.327C>T (p.Asn109=)
n.244C>T
n.315C>T
 ClinVar dbSNP
1g.17028696G>CCA338274872SDHBc.156C>G (p.Asn52Lys)
c.285C>G (p.Asn95Lys)
c.327C>G (p.Asn109Lys)
n.244C>G
n.315C>G
1g.17028696G=CA1156080520SDHBc.156C= (p.Asn52=)
c.285C= (p.Asn95=)
c.327C= (p.Asn109=)
n.244C=
n.315C=
1g.17028696G>TCA338274885SDHBc.156C>A (p.Asn52Lys)
c.285C>A (p.Asn95Lys)
c.327C>A (p.Asn109Lys)
n.244C>A
n.315C>A
1g.17028697T>ACA338274889SDHBc.155A>T (p.Asn52Ile)
c.284A>T (p.Asn95Ile)
c.326A>T (p.Asn109Ile)
n.243A>T
n.314A>T
1g.17028697T>CCA338274896SDHBc.155A>G (p.Asn52Ser)
c.284A>G (p.Asn95Ser)
c.326A>G (p.Asn109Ser)
n.243A>G
n.314A>G
 ClinVar dbSNP gnomAD v4
1g.17028697T>GCA338274897SDHBc.155A>C (p.Asn52Thr)
c.284A>C (p.Asn95Thr)
c.326A>C (p.Asn109Thr)
n.243A>C
n.314A>C
1g.17028697T=CA1156080521SDHBc.155A= (p.Asn52=)
c.284A= (p.Asn95=)
c.326A= (p.Asn109=)
n.243A=
n.314A=
1g.17028698T>ACA338274900SDHBc.154A>T (p.Asn52Tyr)
c.283A>T (p.Asn95Tyr)
c.325A>T (p.Asn109Tyr)
n.242A>T
n.313A>T
1g.17028698T>CCA338274899SDHBc.154A>G (p.Asn52Asp)
c.283A>G (p.Asn95Asp)
c.325A>G (p.Asn109Asp)
n.242A>G
n.313A>G
1g.17028698T>GCA338274898SDHBc.154A>C (p.Asn52His)
c.283A>C (p.Asn95His)
c.325A>C (p.Asn109His)
n.242A>C
n.313A>C
 dbSNP gnomAD v2
1g.17028698T=CA1156080522SDHBc.154A= (p.Asn52=)
c.283A= (p.Asn95=)
c.325A= (p.Asn109=)
n.242A=
n.313A=
1g.17028699G>ACA416087982SDHBc.153C>T (p.Gly51=)
c.282C>T (p.Gly94=)
c.324C>T (p.Gly108=)
n.241C>T
n.312C>T
 dbSNP
1g.17028699G>CCA416087985SDHBc.153C>G (p.Gly51=)
c.282C>G (p.Gly94=)
c.324C>G (p.Gly108=)
n.241C>G
n.312C>G
 dbSNP
1g.17028699G>TCA416087987SDHBc.153C>A (p.Gly51=)
c.282C>A (p.Gly94=)
c.324C>A (p.Gly108=)
n.241C>A
n.312C>A
 dbSNP
1g.17028700C>ACA338274903SDHBc.152G>T (p.Gly51Val)
c.281G>T (p.Gly94Val)
c.323G>T (p.Gly108Val)
n.240G>T
n.311G>T
1g.17028700C=CA1156080523SDHBc.152G= (p.Gly51=)
c.281G= (p.Gly94=)
c.323G= (p.Gly108=)
n.240G=
n.311G=
1g.17028700C>GCA338274918SDHBc.152G>C (p.Gly51Ala)
c.281G>C (p.Gly94Ala)
c.323G>C (p.Gly108Ala)
n.240G>C
n.311G>C
1g.17028700C>TCA089588SDHBc.152G>A (p.Gly51Asp)
c.281G>A (p.Gly94Asp)
c.323G>A (p.Gly108Asp)
n.240G>A
n.311G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17028701C>ACA338274921SDHBc.151G>T (p.Gly51Cys)
c.280G>T (p.Gly94Cys)
c.322G>T (p.Gly108Cys)
n.239G>T
n.310G>T
1g.17028701C>GCA338274922SDHBc.151G>C (p.Gly51Arg)
c.280G>C (p.Gly94Arg)
c.322G>C (p.Gly108Arg)
n.239G>C
n.310G>C
1g.17028701C>TCA338274923SDHBc.151G>A (p.Gly51Ser)
c.280G>A (p.Gly94Ser)
c.322G>A (p.Gly108Ser)
n.239G>A
n.310G>A
1g.17028702T>ACA416087998SDHBc.150A>T (p.Gly50=)
c.279A>T (p.Gly93=)
c.321A>T (p.Gly107=)
n.238A>T
n.309A>T
 dbSNP
1g.17028702T>CCA416088002SDHBc.150A>G (p.Gly50=)
c.279A>G (p.Gly93=)
c.321A>G (p.Gly107=)
n.238A>G
n.309A>G
 dbSNP
1g.17028702T>GCA416088000SDHBc.150A>C (p.Gly50=)
c.279A>C (p.Gly93=)
c.321A>C (p.Gly107=)
n.238A>C
n.309A>C
1g.17028703C>ACA338274924SDHBc.149G>T (p.Gly50Val)
c.278G>T (p.Gly93Val)
c.320G>T (p.Gly107Val)
n.237G>T
n.308G>T
1g.17028703C>GCA338274925SDHBc.149G>C (p.Gly50Ala)
c.278G>C (p.Gly93Ala)
c.320G>C (p.Gly107Ala)
n.237G>C
n.308G>C
1g.17028703C>TCA338274926SDHBc.149G>A (p.Gly50Glu)
c.278G>A (p.Gly93Glu)
c.320G>A (p.Gly107Glu)
n.237G>A
n.308G>A
 ClinVar
1g.17028704C>ACA338274927SDHBc.148G>T (p.Gly50Ter)
c.277G>T (p.Gly93Ter)
c.319G>T (p.Gly107Ter)
n.236G>T
n.307G>T
 dbSNP
1g.17028704C=CA1156080524SDHBc.148G= (p.Gly50=)
c.277G= (p.Gly93=)
c.319G= (p.Gly107=)
n.236G=
n.307G=
1g.17028704C>GCA338274929SDHBc.148G>C (p.Gly50Arg)
c.277G>C (p.Gly93Arg)
c.319G>C (p.Gly107Arg)
n.236G>C
n.307G>C
1g.17028704C>TCA089586SDHBc.148G>A (p.Gly50Arg)
c.277G>A (p.Gly93Arg)
c.319G>A (p.Gly107Arg)
n.236G>A
n.307G>A
 dbSNP ExAC gnomAD v2
1g.17028705A>CCA338274936SDHBc.147T>G (p.Asn49Lys)
c.276T>G (p.Asn92Lys)
c.318T>G (p.Asn106Lys)
n.235T>G
n.306T>G
1g.17028705A>GCA416088015SDHBc.147T>C (p.Asn49=)
c.276T>C (p.Asn92=)
c.318T>C (p.Asn106=)
n.235T>C
n.306T>C
 ClinVar dbSNP
1g.17028705A>TCA338274941SDHBc.147T>A (p.Asn49Lys)
c.276T>A (p.Asn92Lys)
c.318T>A (p.Asn106Lys)
n.235T>A
n.306T>A
1g.17028706T>ACA338274955SDHBc.146A>T (p.Asn49Ile)
c.275A>T (p.Asn92Ile)
c.317A>T (p.Asn106Ile)
n.234A>T
n.305A>T
1g.17028706T>CCA16609940SDHBc.146A>G (p.Asn49Ser)
c.275A>G (p.Asn92Ser)
c.317A>G (p.Asn106Ser)
n.234A>G
n.305A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.17028706T>GCA338274945SDHBc.146A>C (p.Asn49Thr)
c.275A>C (p.Asn92Thr)
c.317A>C (p.Asn106Thr)
n.234A>C
n.305A>C
1g.17028706T=CA1156080525SDHBc.146A= (p.Asn49=)
c.275A= (p.Asn92=)
c.317A= (p.Asn106=)
n.234A=
n.305A=
1g.17028707T>ACA338274959SDHBc.145A>T (p.Asn49Tyr)
c.274A>T (p.Asn92Tyr)
c.316A>T (p.Asn106Tyr)
n.233A>T
n.304A>T
1g.17028707T>CCA338274961SDHBc.145A>G (p.Asn49Asp)
c.274A>G (p.Asn92Asp)
c.316A>G (p.Asn106Asp)
n.233A>G
n.304A>G
 ClinVar dbSNP
1g.17028707T>GCA338274965SDHBc.145A>C (p.Asn49His)
c.274A>C (p.Asn92His)
c.316A>C (p.Asn106His)
n.233A>C
n.304A>C
1g.17028707T=CA1156080526SDHBc.145A= (p.Asn49=)
c.274A= (p.Asn92=)
c.316A= (p.Asn106=)
n.233A=
n.304A=
1g.17028709_17028711delCA658655531SDHBc.143_145del (p.Ile48del)
c.272_274del (p.Ile91del)
c.314_316del (p.Ile105del)
n.231_233del
n.302_304del
1g.17028708G>ACA416088029SDHBc.144C>T (p.Ile48=)
c.273C>T (p.Ile91=)
c.315C>T (p.Ile105=)
n.232C>T
n.303C>T
 ClinVar
1g.17028708G>CCA338274968SDHBc.144C>G (p.Ile48Met)
c.273C>G (p.Ile91Met)
c.315C>G (p.Ile105Met)
n.232C>G
n.303C>G
 ClinVar
1g.17028708G>TCA416088031SDHBc.144C>A (p.Ile48=)
c.273C>A (p.Ile91=)
c.315C>A (p.Ile105=)
n.232C>A
n.303C>A
1g.17028708_17028718delCA2580060626SDHBc.134_144del (p.Ala45GlufsTer13)
c.263_273del (p.Ala88GlufsTer13)
c.305_315del (p.Ala102GlufsTer13)
n.222_232del
n.293_303del
 ClinVar
1g.17028709A=CA1156080527SDHBc.143T= (p.Ile48=)
c.272T= (p.Ile91=)
c.314T= (p.Ile105=)
n.231T=
n.302T=
1g.17028709A>CCA338274976SDHBc.143T>G (p.Ile48Ser)
c.272T>G (p.Ile91Ser)
c.314T>G (p.Ile105Ser)
n.231T>G
n.302T>G
 dbSNP gnomAD v3 gnomAD v4
1g.17028709A>GCA338274980SDHBc.143T>C (p.Ile48Thr)
c.272T>C (p.Ile91Thr)
c.314T>C (p.Ile105Thr)
n.231T>C
n.302T>C
1g.17028709A>TCA338274981SDHBc.143T>A (p.Ile48Asn)
c.272T>A (p.Ile91Asn)
c.314T>A (p.Ile105Asn)
n.231T>A
n.302T>A
1g.17028710T>ACA338274990SDHBc.142A>T (p.Ile48Phe)
c.271A>T (p.Ile91Phe)
c.313A>T (p.Ile105Phe)
n.230A>T
n.301A>T
 ClinVar
1g.17028710T>CCA338274995SDHBc.142A>G (p.Ile48Val)
c.271A>G (p.Ile91Val)
c.313A>G (p.Ile105Val)
n.230A>G
n.301A>G
 ClinVar dbSNP gnomAD v4
1g.17028710T>GCA338274997SDHBc.142A>C (p.Ile48Leu)
c.271A>C (p.Ile91Leu)
c.313A>C (p.Ile105Leu)
n.230A>C
n.301A>C
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17028710T=CA1156080528SDHBc.142A= (p.Ile48=)
c.271A= (p.Ile91=)
c.313A= (p.Ile105=)
n.230A=
n.301A=
1g.17028712_17028713insGCAGTGTCA2586966132SDHBc.142_143insCTGCACA (p.Ile48ThrfsTer16)
c.271_272insCTGCACA (p.Ile91ThrfsTer16)
c.313_314insCTGCACA (p.Ile105ThrfsTer16)
n.230_231insCTGCACA
n.301_302insCTGCACA
1g.17028711G>ACA10577677SDHBc.141C>T (p.Asn47=)
c.270C>T (p.Asn90=)
c.312C>T (p.Asn104=)
n.229C>T
n.300C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17028711G>CCA338275011SDHBc.141C>G (p.Asn47Lys)
c.270C>G (p.Asn90Lys)
c.312C>G (p.Asn104Lys)
n.229C>G
n.300C>G
 dbSNP gnomAD v4
1g.17028711G=CA1156080529SDHBc.141C= (p.Asn47=)
c.270C= (p.Asn90=)
c.312C= (p.Asn104=)
n.229C=
n.300C=
1g.17028711G>TCA338275006SDHBc.141C>A (p.Asn47Lys)
c.270C>A (p.Asn90Lys)
c.312C>A (p.Asn104Lys)
n.229C>A
n.300C>A
1g.17028711_17028712delinsGTCA1156080530SDHBc.140_141delinsAC (p.Asn47=)
c.269_270delinsAC (p.Asn90=)
c.311_312delinsAC (p.Asn104=)
n.228_229delinsAC
n.299_300delinsAC
1g.17028711_17028712insCCA338275015SDHBc.140_141insG (p.Asn47LysfsTer15)
c.269_270insG (p.Asn90LysfsTer15)
c.311_312insG (p.Asn104LysfsTer15)
n.228_229insG
n.299_300insG
 dbSNP gnomAD v4
1g.17028712T>ACA338275031SDHBc.140A>T (p.Asn47Ile)
c.269A>T (p.Asn90Ile)
c.311A>T (p.Asn104Ile)
n.228A>T
n.299A>T
1g.17028712T>CCA338275033SDHBc.140A>G (p.Asn47Ser)
c.269A>G (p.Asn90Ser)
c.311A>G (p.Asn104Ser)
n.228A>G
n.299A>G
 dbSNP gnomAD v2 gnomAD v4
1g.17028712T>GCA338275035SDHBc.140A>C (p.Asn47Thr)
c.269A>C (p.Asn90Thr)
c.311A>C (p.Asn104Thr)
n.228A>C
n.299A>C
1g.17028712T=CA1156080531SDHBc.140A= (p.Asn47=)
c.269A= (p.Asn90=)
c.311A= (p.Asn104=)
n.228A=
n.299A=
1g.17028712delinsCCCA188076SDHBc.140delinsGG (p.Asn47ArgfsTer15)
c.269delinsGG (p.Asn90ArgfsTer15)
c.311delinsGG (p.Asn104ArgfsTer15)
n.228delinsGG
n.299delinsGG
 ClinVar dbSNP
1g.17028713T>ACA338275041SDHBc.139A>T (p.Asn47Tyr)
c.268A>T (p.Asn90Tyr)
c.310A>T (p.Asn104Tyr)
n.227A>T
n.298A>T
1g.17028713T>CCA338275040SDHBc.139A>G (p.Asn47Asp)
c.268A>G (p.Asn90Asp)
c.310A>G (p.Asn104Asp)
n.227A>G
n.298A>G
1g.17028713T>GCA338275038SDHBc.139A>C (p.Asn47His)
c.268A>C (p.Asn90His)
c.310A>C (p.Asn104His)
n.227A>C
n.298A>C
1g.17028714C>ACA338275043SDHBc.138G>T (p.Met46Ile)
c.267G>T (p.Met89Ile)
c.309G>T (p.Met103Ile)
n.226G>T
n.297G>T
1g.17028714C=CA1156080532SDHBc.138G= (p.Met46=)
c.267G= (p.Met89=)
c.309G= (p.Met103=)
n.226G=
n.297G=
1g.17028714C>GCA338275045SDHBc.138G>C (p.Met46Ile)
c.267G>C (p.Met89Ile)
c.309G>C (p.Met103Ile)
n.226G>C
n.297G>C
1g.17028714C>TCA338275048SDHBc.138G>A (p.Met46Ile)
c.267G>A (p.Met89Ile)
c.309G>A (p.Met103Ile)
n.226G>A
n.297G>A
 ClinVar dbSNP
1g.17028715A=CA1156080533SDHBc.137T= (p.Met46=)
c.266T= (p.Met89=)
c.308T= (p.Met103=)
n.225T=
n.296T=
1g.17028715A>CCA338275051SDHBc.137T>G (p.Met46Arg)
c.266T>G (p.Met89Arg)
c.308T>G (p.Met103Arg)
n.225T>G
n.296T>G
 ClinVar dbSNP
1g.17028715A>GCA338275056SDHBc.137T>C (p.Met46Thr)
c.266T>C (p.Met89Thr)
c.308T>C (p.Met103Thr)
n.225T>C
n.296T>C
 ClinVar dbSNP gnomAD v4
1g.17028715A>TCA338275065SDHBc.137T>A (p.Met46Lys)
c.266T>A (p.Met89Lys)
c.308T>A (p.Met103Lys)
n.225T>A
n.296T>A

Number of alleles fetched