Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.17027728C>GCA2522359720SDHBc.369+21G>C (n.369+21G>C)
c.498+21G>C (n.498+21G>C)
c.540+21G>C (n.540+21G>C)
n.478G>C
n.474+21G>C
 gnomAD v4
1g.17027730A>GCA2643677598SDHBc.369+19T>C (n.369+19T>C)
c.498+19T>C (n.498+19T>C)
c.540+19T>C (n.540+19T>C)
n.476T>C
n.474+19T>C
 gnomAD v4
1g.17027731T>CCA521039116SDHBc.369+18A>G (n.369+18A>G)
c.498+18A>G (n.498+18A>G)
c.540+18A>G (n.540+18A>G)
n.475A>G
n.474+18A>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17027731T=CA1156080142SDHBc.369+18A= (n.369+18A=)
c.498+18A= (n.498+18A=)
c.540+18A= (n.540+18A=)
n.475A=
n.474+18A=
1g.17027734delCA2574235677SDHBc.369+17del (n.369+17del)
c.498+17del (n.498+17del)
c.540+17del (n.540+17del)
n.474del
n.474+17del
1g.17027733A>GCA2580060645SDHBc.369+16T>C (n.369+16T>C)
c.498+16T>C (n.498+16T>C)
c.540+16T>C (n.540+16T>C)
n.473T>C
n.474+16T>C
 ClinVar gnomAD v4
1g.17027734A=CA1156080143SDHBc.369+15T= (n.369+15T=)
c.498+15T= (n.498+15T=)
c.540+15T= (n.540+15T=)
n.472T=
n.474+15T=
1g.17027734A>GCA089642SDHBc.369+15T>C (n.369+15T>C)
c.498+15T>C (n.498+15T>C)
c.540+15T>C (n.540+15T>C)
n.472T>C
n.474+15T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17027735T>CCA645671466SDHBc.369+14A>G (n.369+14A>G)
c.498+14A>G (n.498+14A>G)
c.540+14A>G (n.540+14A>G)
n.471A>G
n.474+14A>G
 COSMIC
1g.17027735_17027749delinsTAGGGACTAATGACCCA1156080144SDHBc.369_369+14delinsGGTCATTAGTCCCTA
c.498_498+14delinsGGTCATTAGTCCCTA
c.540_540+14delinsGGTCATTAGTCCCTA
n.457_471delinsGGTCATTAGTCCCTA
n.474_474+14delinsGGTCATTAGTCCCTA
1g.17027736A>GCA2573130463SDHBc.369+13T>C (n.369+13T>C)
c.498+13T>C (n.498+13T>C)
c.540+13T>C (n.540+13T>C)
n.470T>C
n.474+13T>C
 ClinVar dbSNP gnomAD v4
1g.17027738_17027751delCA658656888SDHBc.369_369+13del
c.498_498+13del
c.540_540+13del
n.457_470del
n.474_474+13del
 ClinVar dbSNP
1g.17027737G>ACA1156080146SDHBc.369+12C>T (n.369+12C>T)
c.498+12C>T (n.498+12C>T)
c.540+12C>T (n.540+12C>T)
n.469C>T
n.474+12C>T
 ClinVar dbSNP gnomAD v4
1g.17027737G>CCA1156080147SDHBc.369+12C>G (n.369+12C>G)
c.498+12C>G (n.498+12C>G)
c.540+12C>G (n.540+12C>G)
n.469C>G
n.474+12C>G
 ClinVar dbSNP
1g.17027737G=CA1156080145SDHBc.369+12C= (n.369+12C=)
c.498+12C= (n.498+12C=)
c.540+12C= (n.540+12C=)
n.469C=
n.474+12C=
1g.17027737G>TCA2643677626SDHBc.369+12C>A (n.369+12C>A)
c.498+12C>A (n.498+12C>A)
c.540+12C>A (n.540+12C>A)
n.469C>A
n.474+12C>A
 dbSNP gnomAD v4
1g.17027739delCA2643677621SDHBc.369+12del (n.369+12del)
c.498+12del (n.498+12del)
c.540+12del (n.540+12del)
n.469del
n.474+12del
 gnomAD v4
1g.17027738G>ACA891842429SDHBc.369+11C>T (n.369+11C>T)
c.498+11C>T (n.498+11C>T)
c.540+11C>T (n.540+11C>T)
n.468C>T
n.474+11C>T
 ClinVar dbSNP
1g.17027738G>CCA521039120SDHBc.369+11C>G (n.369+11C>G)
c.498+11C>G (n.498+11C>G)
c.540+11C>G (n.540+11C>G)
n.468C>G
n.474+11C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17027738G=CA1156080149SDHBc.369+11C= (n.369+11C=)
c.498+11C= (n.498+11C=)
c.540+11C= (n.540+11C=)
n.468C=
n.474+11C=
1g.17027738G>TCA2643677631SDHBc.369+11C>A (n.369+11C>A)
c.498+11C>A (n.498+11C>A)
c.540+11C>A (n.540+11C>A)
n.468C>A
n.474+11C>A
 gnomAD v4
1g.17027738_17027745delinsGGACTAATCA1156080148SDHBc.369+4_369+11delinsATTAGTCC (n.369+4_369+11delinsATTAGTCC)
c.498+4_498+11delinsATTAGTCC (n.498+4_498+11delinsATTAGTCC)
c.540+4_540+11delinsATTAGTCC (n.540+4_540+11delinsATTAGTCC)
n.461_468delinsATTAGTCC
n.474+4_474+11delinsATTAGTCC
1g.17027739G>ACA2643677635SDHBc.369+10C>T (n.369+10C>T)
c.498+10C>T (n.498+10C>T)
c.540+10C>T (n.540+10C>T)
n.467C>T
n.474+10C>T
 gnomAD v4
1g.17027739G>TCA2643677636SDHBc.369+10C>A (n.369+10C>A)
c.498+10C>A (n.498+10C>A)
c.540+10C>A (n.540+10C>A)
n.467C>A
n.474+10C>A
 gnomAD v4
1g.17027742_17027748delCA10577674SDHBc.369+4_369+10del (n.369+4_369+10del)
c.498+4_498+10del (n.498+4_498+10del)
c.540+4_540+10del (n.540+4_540+10del)
n.461_467del
n.474+4_474+10del
 ClinVar dbSNP
1g.17027740A>GCA2643677640SDHBc.369+9T>C (n.369+9T>C)
c.498+9T>C (n.498+9T>C)
c.540+9T>C (n.540+9T>C)
n.466T>C
n.474+9T>C
 gnomAD v4
1g.17027741C>ACA1139655465SDHBc.369+8G>T (n.369+8G>T)
c.498+8G>T (n.498+8G>T)
c.540+8G>T (n.540+8G>T)
n.465G>T
n.474+8G>T
 ClinVar dbSNP
1g.17027741C=CA1156080150SDHBc.369+8G= (n.369+8G=)
c.498+8G= (n.498+8G=)
c.540+8G= (n.540+8G=)
n.465G=
n.474+8G=
1g.17027741C>TCA2499214299SDHBc.369+8G>A (n.369+8G>A)
c.498+8G>A (n.498+8G>A)
c.540+8G>A (n.540+8G>A)
n.465G>A
n.474+8G>A
 ClinVar dbSNP gnomAD v4
1g.17027743A=CA1156080151SDHBc.369+6T= (n.369+6T=)
c.498+6T= (n.498+6T=)
c.540+6T= (n.540+6T=)
n.463T=
n.474+6T=
1g.17027743A>CCA521039123SDHBc.369+6T>G (n.369+6T>G)
c.498+6T>G (n.498+6T>G)
c.540+6T>G (n.540+6T>G)
n.463T>G
n.474+6T>G
 dbSNP gnomAD v2 gnomAD v4
1g.17027744delCA2643677648SDHBc.369+6del (n.369+6del)
c.498+6del (n.498+6del)
c.540+6del (n.540+6del)
n.463del
n.474+6del
 gnomAD v4
1g.17027744A=CA1156080152SDHBc.369+5T= (n.369+5T=)
c.498+5T= (n.498+5T=)
c.540+5T= (n.540+5T=)
n.462T=
n.474+5T=
1g.17027744A>CCA2580060646SDHBc.369+5T>G (n.369+5T>G)
c.498+5T>G (n.498+5T>G)
c.540+5T>G (n.540+5T>G)
n.462T>G
n.474+5T>G
 ClinVar
1g.17027744A>GCA891842430SDHBc.369+5T>C (n.369+5T>C)
c.498+5T>C (n.498+5T>C)
c.540+5T>C (n.540+5T>C)
n.462T>C
n.474+5T>C
 ClinVar dbSNP gnomAD v4
1g.17027745T>CCA891842431SDHBc.369+4A>G (n.369+4A>G)
c.498+4A>G (n.498+4A>G)
c.540+4A>G (n.540+4A>G)
n.461A>G
n.474+4A>G
 ClinVar dbSNP gnomAD v4
1g.17027745T=CA1156080153SDHBc.369+4A= (n.369+4A=)
c.498+4A= (n.498+4A=)
c.540+4A= (n.540+4A=)
n.461A=
n.474+4A=
1g.17027746G>ACA2580060647SDHBc.369+3C>T (n.369+3C>T)
c.498+3C>T (n.498+3C>T)
c.540+3C>T (n.540+3C>T)
n.460C>T
n.474+3C>T
 ClinVar
1g.17027746G>TCA2574235678SDHBc.369+3C>A (n.369+3C>A)
c.498+3C>A (n.498+3C>A)
c.540+3C>A (n.540+3C>A)
n.460C>A
n.474+3C>A
 gnomAD v4
1g.17027747A>CCA338272382SDHBc.369+2T>G (n.369+2T>G)
c.498+2T>G (n.498+2T>G)
c.540+2T>G (n.540+2T>G)
n.459T>G
n.474+2T>G
1g.17027747A>GCA338272384SDHBc.369+2T>C (n.369+2T>C)
c.498+2T>C (n.498+2T>C)
c.540+2T>C (n.540+2T>C)
n.459T>C
n.474+2T>C
 gnomAD v4
1g.17027747A>TCA338272387SDHBc.369+2T>A (n.369+2T>A)
c.498+2T>A (n.498+2T>A)
c.540+2T>A (n.540+2T>A)
n.459T>A
n.474+2T>A
1g.17027748C>ACA338272389SDHBc.369+1G>T (n.369+1G>T)
c.498+1G>T (n.498+1G>T)
c.540+1G>T (n.540+1G>T)
n.458G>T
n.474+1G>T
1g.17027748C=CA1156080154SDHBc.369+1G= (n.369+1G=)
c.498+1G= (n.498+1G=)
c.540+1G= (n.540+1G=)
n.458G=
n.474+1G=
1g.17027748C>GCA338272391SDHBc.369+1G>C (n.369+1G>C)
c.498+1G>C (n.498+1G>C)
c.540+1G>C (n.540+1G>C)
n.458G>C
n.474+1G>C
1g.17027748C>TCA338272394SDHBc.369+1G>A (n.369+1G>A)
c.498+1G>A (n.498+1G>A)
c.540+1G>A (n.540+1G>A)
n.458G>A
n.474+1G>A
 ClinVar dbSNP gnomAD v4
1g.17027750_17028737delCA645509076SDHBc.117_369+1del
c.246_498+1del
c.288_540+1del
n.205_458del
n.276_474+1del
 ClinVar
1g.17027749C>ACA416085614SDHBc.369G>T (p.Leu123=)
c.498G>T (p.Leu166=)
c.540G>T (p.Leu180=)
n.457G>T
n.474G>T
1g.17027749C=CA1144324514SDHBc.369G= (p.Leu123=)
c.498G= (p.Leu166=)
c.540G= (p.Leu180=)
n.457G=
n.474G=
1g.17027749C>GCA416085618SDHBc.369G>C (p.Leu123=)
c.498G>C (p.Leu166=)
c.540G>C (p.Leu180=)
n.457G>C
n.474G>C
1g.17027749C>TCA089647SDHBc.369G>A (p.Leu123=)
c.498G>A (p.Leu166=)
c.540G>A (p.Leu180=)
n.457G>A
n.474G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17027750A=CA1156080155SDHBc.368T= (p.Leu123=)
c.497T= (p.Leu166=)
c.539T= (p.Leu180=)
n.456T=
n.473T=
1g.17027750A>CCA338272397SDHBc.368T>G (p.Leu123Arg)
c.497T>G (p.Leu166Arg)
c.539T>G (p.Leu180Arg)
n.456T>G
n.473T>G
1g.17027750A>GCA338272400SDHBc.368T>C (p.Leu123Pro)
c.497T>C (p.Leu166Pro)
c.539T>C (p.Leu180Pro)
n.456T>C
n.473T>C
 ClinVar dbSNP
1g.17027750A>TCA338272404SDHBc.368T>A (p.Leu123Gln)
c.497T>A (p.Leu166Gln)
c.539T>A (p.Leu180Gln)
n.456T>A
n.473T>A
1g.17027751G>ACA416085630SDHBc.367C>T (p.Leu123=)
c.496C>T (p.Leu166=)
c.538C>T (p.Leu180=)
n.455C>T
n.472C>T
1g.17027751G>CCA338272407SDHBc.367C>G (p.Leu123Val)
c.496C>G (p.Leu166Val)
c.538C>G (p.Leu180Val)
n.455C>G
n.472C>G
1g.17027751G=CA1156080156SDHBc.367C= (p.Leu123=)
c.496C= (p.Leu166=)
c.538C= (p.Leu180=)
n.455C=
n.472C=
1g.17027751G>TCA338272409SDHBc.367C>A (p.Leu123Met)
c.496C>A (p.Leu166Met)
c.538C>A (p.Leu180Met)
n.455C>A
n.472C>A
 gnomAD v4
1g.17027752T>ACA338272412SDHBc.366A>T (p.Lys122Asn)
c.495A>T (p.Lys165Asn)
c.537A>T (p.Lys179Asn)
n.454A>T
n.471A>T
1g.17027752T>CCA416085645SDHBc.366A>G (p.Lys122=)
c.495A>G (p.Lys165=)
c.537A>G (p.Lys179=)
n.454A>G
n.471A>G
 ClinVar gnomAD v4
1g.17027752T>GCA338272415SDHBc.366A>C (p.Lys122Asn)
c.495A>C (p.Lys165Asn)
c.537A>C (p.Lys179Asn)
n.454A>C
n.471A>C
1g.17027754dupCA658820982SDHBc.366dup (p.Leu123ThrfsTer14)
c.495dup (p.Leu166ThrfsTer14)
c.537dup (p.Leu180ThrfsTer14)
c.366dup (p.Leu123ThrfsTer?)
n.454dup
n.471dup
 ClinVar dbSNP
1g.17027753T>ACA338272421SDHBc.365A>T (p.Lys122Ile)
c.494A>T (p.Lys165Ile)
c.536A>T (p.Lys179Ile)
n.453A>T
n.470A>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17027753T>CCA338272419SDHBc.365A>G (p.Lys122Arg)
c.494A>G (p.Lys165Arg)
c.536A>G (p.Lys179Arg)
n.453A>G
n.470A>G
1g.17027753T>GCA338272416SDHBc.365A>C (p.Lys122Thr)
c.494A>C (p.Lys165Thr)
c.536A>C (p.Lys179Thr)
n.453A>C
n.470A>C
1g.17027753T=CA1156080157SDHBc.365A= (p.Lys122=)
c.494A= (p.Lys165=)
c.536A= (p.Lys179=)
n.453A=
n.470A=
1g.17027754T>ACA338272424SDHBc.364A>T (p.Lys122Ter)
c.493A>T (p.Lys165Ter)
c.535A>T (p.Lys179Ter)
n.452A>T
n.469A>T
1g.17027754T>CCA338272429SDHBc.364A>G (p.Lys122Glu)
c.493A>G (p.Lys165Glu)
c.535A>G (p.Lys179Glu)
n.452A>G
n.469A>G
1g.17027754T>GCA338272427SDHBc.364A>C (p.Lys122Gln)
c.493A>C (p.Lys165Gln)
c.535A>C (p.Lys179Gln)
n.452A>C
n.469A>C
1g.17027755C>ACA338272431SDHBc.363G>T (p.Glu121Asp)
c.492G>T (p.Glu164Asp)
c.534G>T (p.Glu178Asp)
n.451G>T
n.468G>T
 ClinVar dbSNP
1g.17027755C=CA1156080158SDHBc.363G= (p.Glu121=)
c.492G= (p.Glu164=)
c.534G= (p.Glu178=)
n.451G=
n.468G=
1g.17027755C>GCA338272433SDHBc.363G>C (p.Glu121Asp)
c.492G>C (p.Glu164Asp)
c.534G>C (p.Glu178Asp)
n.451G>C
n.468G>C
1g.17027755C>TCA416085665SDHBc.363G>A (p.Glu121=)
c.492G>A (p.Glu164=)
c.534G>A (p.Glu178=)
n.451G>A
n.468G>A
 ClinVar dbSNP gnomAD v4
1g.17027756T>ACA338272434SDHBc.362A>T (p.Glu121Val)
c.491A>T (p.Glu164Val)
c.533A>T (p.Glu178Val)
n.450A>T
n.467A>T
 ClinVar dbSNP
1g.17027756T>CCA338272439SDHBc.362A>G (p.Glu121Gly)
c.491A>G (p.Glu164Gly)
c.533A>G (p.Glu178Gly)
n.450A>G
n.467A>G
1g.17027756T>GCA338272436SDHBc.362A>C (p.Glu121Ala)
c.491A>C (p.Glu164Ala)
c.533A>C (p.Glu178Ala)
n.450A>C
n.467A>C
1g.17027757C>ACA338272447SDHBc.361G>T (p.Glu121Ter)
c.490G>T (p.Glu164Ter)
c.532G>T (p.Glu178Ter)
n.449G>T
n.466G>T
1g.17027757C=CA1156080159SDHBc.361G= (p.Glu121=)
c.490G= (p.Glu164=)
c.532G= (p.Glu178=)
n.449G=
n.466G=
1g.17027757C>GCA338272453SDHBc.361G>C (p.Glu121Gln)
c.490G>C (p.Glu164Gln)
c.532G>C (p.Glu178Gln)
n.449G>C
n.466G>C
 ClinVar dbSNP gnomAD v4
1g.17027757C>TCA338272450SDHBc.361G>A (p.Glu121Lys)
c.490G>A (p.Glu164Lys)
c.532G>A (p.Glu178Lys)
n.449G>A
n.466G>A
1g.17027758A>CCA416085678SDHBc.360T>G (p.Arg120=)
c.489T>G (p.Arg163=)
c.531T>G (p.Arg177=)
n.448T>G
n.465T>G
 gnomAD v4
1g.17027758A>GCA416085681SDHBc.360T>C (p.Arg120=)
c.489T>C (p.Arg163=)
c.531T>C (p.Arg177=)
n.448T>C
n.465T>C
1g.17027758A>TCA416085682SDHBc.360T>A (p.Arg120=)
c.489T>A (p.Arg163=)
c.531T>A (p.Arg177=)
n.448T>A
n.465T>A
1g.17027759C>ACA338272456SDHBc.359G>T (p.Arg120Leu)
c.488G>T (p.Arg163Leu)
c.530G>T (p.Arg177Leu)
n.447G>T
n.464G>T
 ClinVar dbSNP
1g.17027759C=CA1142363913SDHBc.359G= (p.Arg120=)
c.488G= (p.Arg163=)
c.530G= (p.Arg177=)
n.447G=
n.464G=
1g.17027759C>GCA338272458SDHBc.359G>C (p.Arg120Pro)
c.488G>C (p.Arg163Pro)
c.530G>C (p.Arg177Pro)
n.447G>C
n.464G>C
1g.17027759C>TCA089641SDHBc.359G>A (p.Arg120His)
c.488G>A (p.Arg163His)
c.530G>A (p.Arg177His)
n.447G>A
n.464G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17027760G>ACA089640SDHBc.358C>T (p.Arg120Cys)
c.487C>T (p.Arg163Cys)
c.529C>T (p.Arg177Cys)
n.446C>T
n.463C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17027760G>CCA338272485SDHBc.358C>G (p.Arg120Gly)
c.487C>G (p.Arg163Gly)
c.529C>G (p.Arg177Gly)
n.446C>G
n.463C>G
 ClinVar gnomAD v4
1g.17027760G=CA1142280515SDHBc.358C= (p.Arg120=)
c.487C= (p.Arg163=)
c.529C= (p.Arg177=)
n.446C=
n.463C=
1g.17027760G>TCA10581746SDHBc.358C>A (p.Arg120Ser)
c.487C>A (p.Arg163Ser)
c.529C>A (p.Arg177Ser)
n.446C>A
n.463C>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17027761C>ACA338272490SDHBc.357G>T (p.Glu119Asp)
c.486G>T (p.Glu162Asp)
c.528G>T (p.Glu176Asp)
n.445G>T
n.462G>T
1g.17027761C>GCA338272492SDHBc.357G>C (p.Glu119Asp)
c.486G>C (p.Glu162Asp)
c.528G>C (p.Glu176Asp)
n.445G>C
n.462G>C
1g.17027761C>TCA416085696SDHBc.357G>A (p.Glu119=)
c.486G>A (p.Glu162=)
c.528G>A (p.Glu176=)
n.445G>A
n.462G>A
 ClinVar
1g.17027761_17027766delinsCTCTTCCA1156080160SDHBc.352_357delinsGAAGAG (p.Glu118=)
c.481_486delinsGAAGAG (p.Glu161=)
c.523_528delinsGAAGAG (p.Glu175=)
n.440_445delinsGAAGAG
n.457_462delinsGAAGAG
1g.17027762T>ACA338272496SDHBc.356A>T (p.Glu119Val)
c.485A>T (p.Glu162Val)
c.527A>T (p.Glu176Val)
n.444A>T
n.461A>T
1g.17027762T>CCA089639SDHBc.356A>G (p.Glu119Gly)
c.485A>G (p.Glu162Gly)
c.527A>G (p.Glu176Gly)
n.444A>G
n.461A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17027762T>GCA338272500SDHBc.356A>C (p.Glu119Ala)
c.485A>C (p.Glu162Ala)
c.527A>C (p.Glu176Ala)
n.444A>C
n.461A>C
1g.17027762T=CA1143459197SDHBc.356A= (p.Glu119=)
c.485A= (p.Glu162=)
c.527A= (p.Glu176=)
n.444A=
n.461A=
1g.17027762_17027766delinsCCTTCA645509077SDHBc.352_356delinsAAGG (p.Glu118LysfsTer?)
c.481_485delinsAAGG (p.Glu161LysfsTer?)
c.523_527delinsAAGG (p.Glu175LysfsTer?)
n.440_444delinsAAGG
n.457_461delinsAAGG
 ClinVar dbSNP
1g.17027763C>ACA015940SDHBc.355G>T (p.Glu119Ter)
c.484G>T (p.Glu162Ter)
c.526G>T (p.Glu176Ter)
n.443G>T
n.460G>T
 ClinVar dbSNP gnomAD v4
1g.17027763C=CA1156080161SDHBc.355G= (p.Glu119=)
c.484G= (p.Glu162=)
c.526G= (p.Glu176=)
n.443G=
n.460G=
1g.17027763C>GCA338272505SDHBc.355G>C (p.Glu119Gln)
c.484G>C (p.Glu162Gln)
c.526G>C (p.Glu176Gln)
n.443G>C
n.460G>C
 dbSNP
1g.17027763C>TCA338272503SDHBc.355G>A (p.Glu119Lys)
c.484G>A (p.Glu162Lys)
c.526G>A (p.Glu176Lys)
n.443G>A
n.460G>A
 ClinVar
1g.17027764T>ACA338272508SDHBc.354A>T (p.Glu118Asp)
c.483A>T (p.Glu161Asp)
c.525A>T (p.Glu175Asp)
n.442A>T
n.459A>T
1g.17027764T>CCA416085716SDHBc.354A>G (p.Glu118=)
c.483A>G (p.Glu161=)
c.525A>G (p.Glu175=)
n.442A>G
n.459A>G
1g.17027764T>GCA338272509SDHBc.354A>C (p.Glu118Asp)
c.483A>C (p.Glu161Asp)
c.525A>C (p.Glu175Asp)
n.442A>C
n.459A>C
1g.17027765T>ACA338272510SDHBc.353A>T (p.Glu118Val)
c.482A>T (p.Glu161Val)
c.524A>T (p.Glu175Val)
n.441A>T
n.458A>T
1g.17027765T>CCA089638SDHBc.353A>G (p.Glu118Gly)
c.482A>G (p.Glu161Gly)
c.524A>G (p.Glu175Gly)
n.441A>G
n.458A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17027765T>GCA338272511SDHBc.353A>C (p.Glu118Ala)
c.482A>C (p.Glu161Ala)
c.524A>C (p.Glu175Ala)
n.441A>C
n.458A>C
1g.17027765T=CA1148402004SDHBc.353A= (p.Glu118=)
c.482A= (p.Glu161=)
c.524A= (p.Glu175=)
n.441A=
n.458A=
1g.17027766C>ACA338272512SDHBc.352G>T (p.Glu118Ter)
c.481G>T (p.Glu161Ter)
c.523G>T (p.Glu175Ter)
n.440G>T
n.457G>T
1g.17027766C=CA1143531997SDHBc.352G= (p.Glu118=)
c.481G= (p.Glu161=)
c.523G= (p.Glu175=)
n.440G=
n.457G=
1g.17027766C>GCA18665895SDHBc.352G>C (p.Glu118Gln)
c.481G>C (p.Glu161Gln)
c.523G>C (p.Glu175Gln)
n.440G>C
n.457G>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17027766C>TCA338272514SDHBc.352G>A (p.Glu118Lys)
c.481G>A (p.Glu161Lys)
c.523G>A (p.Glu175Lys)
n.440G>A
n.457G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17027766dupCA1139655466SDHBc.352dup (p.Glu118GlyfsTer4)
c.481dup (p.Glu161GlyfsTer4)
c.523dup (p.Glu175GlyfsTer4)
n.440dup
n.457dup
 ClinVar dbSNP
1g.17027767T>ACA416085738SDHBc.351A>T (p.Ile117=)
c.480A>T (p.Ile160=)
c.522A>T (p.Ile174=)
n.439A>T
n.456A>T
1g.17027767T>CCA338272516SDHBc.351A>G (p.Ile117Met)
c.480A>G (p.Ile160Met)
c.522A>G (p.Ile174Met)
n.439A>G
n.456A>G
 ClinVar dbSNP
1g.17027767T>GCA416085739SDHBc.351A>C (p.Ile117=)
c.480A>C (p.Ile160=)
c.522A>C (p.Ile174=)
n.439A>C
n.456A>C
1g.17027768A=CA1143408092SDHBc.350T= (p.Ile117=)
c.479T= (p.Ile160=)
c.521T= (p.Ile174=)
n.438T=
n.455T=
1g.17027768A>CCA338272526SDHBc.350T>G (p.Ile117Arg)
c.479T>G (p.Ile160Arg)
c.521T>G (p.Ile174Arg)
n.438T>G
n.455T>G
1g.17027768A>GCA16609935SDHBc.350T>C (p.Ile117Thr)
c.479T>C (p.Ile160Thr)
c.521T>C (p.Ile174Thr)
n.438T>C
n.455T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17027768A>TCA338272520SDHBc.350T>A (p.Ile117Lys)
c.479T>A (p.Ile160Lys)
c.521T>A (p.Ile174Lys)
n.438T>A
n.455T>A
1g.17027769T>ACA338272532SDHBc.349A>T (p.Ile117Leu)
c.478A>T (p.Ile160Leu)
c.520A>T (p.Ile174Leu)
n.437A>T
n.454A>T
1g.17027769T>CCA18665905SDHBc.349A>G (p.Ile117Val)
c.478A>G (p.Ile160Val)
c.520A>G (p.Ile174Val)
n.437A>G
n.454A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17027769T>GCA338272537SDHBc.349A>C (p.Ile117Leu)
c.478A>C (p.Ile160Leu)
c.520A>C (p.Ile174Leu)
n.437A>C
n.454A>C
1g.17027769T=CA1156080162SDHBc.349A= (p.Ile117=)
c.478A= (p.Ile160=)
c.520A= (p.Ile174=)
n.437A=
n.454A=
1g.17027770G>ACA089637SDHBc.348C>T (p.Ser116=)
c.477C>T (p.Ser159=)
c.519C>T (p.Ser173=)
n.436C>T
n.453C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17027770G>CCA416085776SDHBc.348C>G (p.Ser116=)
c.477C>G (p.Ser159=)
c.519C>G (p.Ser173=)
n.436C>G
n.453C>G
1g.17027770G=CA1156080163SDHBc.348C= (p.Ser116=)
c.477C= (p.Ser159=)
c.519C= (p.Ser173=)
n.436C=
n.453C=
1g.17027770G>TCA416085779SDHBc.348C>A (p.Ser116=)
c.477C>A (p.Ser159=)
c.519C>A (p.Ser173=)
n.436C>A
n.453C>A
 gnomAD v4
1g.17027771G>ACA18665918SDHBc.347C>T (p.Ser116Phe)
c.476C>T (p.Ser159Phe)
c.518C>T (p.Ser173Phe)
n.435C>T
n.452C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17027771G>CCA338272542SDHBc.347C>G (p.Ser116Cys)
c.476C>G (p.Ser159Cys)
c.518C>G (p.Ser173Cys)
n.435C>G
n.452C>G
1g.17027771G=CA1156080164SDHBc.347C= (p.Ser116=)
c.476C= (p.Ser159=)
c.518C= (p.Ser173=)
n.435C=
n.452C=
1g.17027771G>TCA338272541SDHBc.347C>A (p.Ser116Tyr)
c.476C>A (p.Ser159Tyr)
c.518C>A (p.Ser173Tyr)
n.435C>A
n.452C>A
 gnomAD v4
1g.17027772A=CA1156080165SDHBc.346T= (p.Ser116=)
c.475T= (p.Ser159=)
c.517T= (p.Ser173=)
n.434T=
n.451T=
1g.17027772A>CCA338272543SDHBc.346T>G (p.Ser116Ala)
c.475T>G (p.Ser159Ala)
c.517T>G (p.Ser173Ala)
n.434T>G
n.451T>G
1g.17027772A>GCA338272544SDHBc.346T>C (p.Ser116Pro)
c.475T>C (p.Ser159Pro)
c.517T>C (p.Ser173Pro)
n.434T>C
n.451T>C
 ClinVar dbSNP gnomAD v4
1g.17027772A>TCA338272545SDHBc.346T>A (p.Ser116Thr)
c.475T>A (p.Ser159Thr)
c.517T>A (p.Ser173Thr)
n.434T>A
n.451T>A
1g.17027773C>ACA338272546SDHBc.345G>T (p.Gln115His)
c.474G>T (p.Gln158His)
c.516G>T (p.Gln172His)
n.433G>T
n.450G>T
 gnomAD v4
1g.17027773C=CA1141648122SDHBc.345G= (p.Gln115=)
c.474G= (p.Gln158=)
c.516G= (p.Gln172=)
n.433G=
n.450G=
1g.17027773C>GCA338272547SDHBc.345G>C (p.Gln115His)
c.474G>C (p.Gln158His)
c.516G>C (p.Gln172His)
n.433G>C
n.450G>C
1g.17027773C>TCA18665926SDHBc.345G>A (p.Gln115=)
c.474G>A (p.Gln158=)
c.516G>A (p.Gln172=)
n.433G>A
n.450G>A
 ClinVar dbSNP
1g.17027774T>ACA338272551SDHBc.344A>T (p.Gln115Leu)
c.473A>T (p.Gln158Leu)
c.515A>T (p.Gln172Leu)
n.432A>T
n.449A>T
1g.17027774T>CCA338272556SDHBc.344A>G (p.Gln115Arg)
c.473A>G (p.Gln158Arg)
c.515A>G (p.Gln172Arg)
n.432A>G
n.449A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17027774T>GCA338272554SDHBc.344A>C (p.Gln115Pro)
c.473A>C (p.Gln158Pro)
c.515A>C (p.Gln172Pro)
n.432A>C
n.449A>C
1g.17027774T=CA1156080166SDHBc.344A= (p.Gln115=)
c.473A= (p.Gln158=)
c.515A= (p.Gln172=)
n.432A=
n.449A=
1g.17027775G>ACA338272564SDHBc.343C>T (p.Gln115Ter)
c.472C>T (p.Gln158Ter)
c.514C>T (p.Gln172Ter)
n.431C>T
n.448C>T
 gnomAD v4
1g.17027775G>CCA338272565SDHBc.343C>G (p.Gln115Glu)
c.472C>G (p.Gln158Glu)
c.514C>G (p.Gln172Glu)
n.431C>G
n.448C>G
1g.17027775G>TCA338272567SDHBc.343C>A (p.Gln115Lys)
c.472C>A (p.Gln158Lys)
c.514C>A (p.Gln172Lys)
n.431C>A
n.448C>A
 gnomAD v4
1g.17027776C>ACA416085824SDHBc.342G>T (p.Leu114=)
c.471G>T (p.Leu157=)
c.513G>T (p.Leu171=)
n.430G>T
n.447G>T
1g.17027776C>GCA416085827SDHBc.342G>C (p.Leu114=)
c.471G>C (p.Leu157=)
c.513G>C (p.Leu171=)
n.430G>C
n.447G>C
1g.17027776C>TCA416085826SDHBc.342G>A (p.Leu114=)
c.471G>A (p.Leu157=)
c.513G>A (p.Leu171=)
n.430G>A
n.447G>A
 ClinVar dbSNP
1g.17027777A>CCA338272570SDHBc.341T>G (p.Leu114Arg)
c.470T>G (p.Leu157Arg)
c.512T>G (p.Leu171Arg)
n.429T>G
n.446T>G
1g.17027777A>GCA338272578SDHBc.341T>C (p.Leu114Pro)
c.470T>C (p.Leu157Pro)
c.512T>C (p.Leu171Pro)
n.429T>C
n.446T>C
 gnomAD v4
1g.17027777A>TCA338272579SDHBc.341T>A (p.Leu114Gln)
c.470T>A (p.Leu157Gln)
c.512T>A (p.Leu171Gln)
n.429T>A
n.446T>A
1g.17027778delCA2573051409SDHBc.340del (p.Leu114CysfsTer4)
c.469del (p.Leu157CysfsTer4)
c.511del (p.Leu171CysfsTer4)
n.428del
n.445del
 dbSNP
1g.17027778G>ACA089636SDHBc.340C>T (p.Leu114=)
c.469C>T (p.Leu157=)
c.511C>T (p.Leu171=)
n.428C>T
n.445C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17027778G>CCA338272583SDHBc.340C>G (p.Leu114Val)
c.469C>G (p.Leu157Val)
c.511C>G (p.Leu171Val)
n.428C>G
n.445C>G
1g.17027778G=CA1156080167SDHBc.340C= (p.Leu114=)
c.469C= (p.Leu157=)
c.511C= (p.Leu171=)
n.428C=
n.445C=
1g.17027778G>TCA338272585SDHBc.340C>A (p.Leu114Met)
c.469C>A (p.Leu157Met)
c.511C>A (p.Leu171Met)
n.428C>A
n.445C>A
 gnomAD v4
1g.17027779A>CCA338272587SDHBc.339T>G (p.Tyr113Ter)
c.468T>G (p.Tyr156Ter)
c.510T>G (p.Tyr170Ter)
n.427T>G
n.444T>G
1g.17027779A>GCA416085845SDHBc.339T>C (p.Tyr113=)
c.468T>C (p.Tyr156=)
c.510T>C (p.Tyr170=)
n.427T>C
n.444T>C
1g.17027779A>TCA338272589SDHBc.339T>A (p.Tyr113Ter)
c.468T>A (p.Tyr156Ter)
c.510T>A (p.Tyr170Ter)
n.427T>A
n.444T>A
1g.17027780T>ACA338272593SDHBc.338A>T (p.Tyr113Phe)
c.467A>T (p.Tyr156Phe)
c.509A>T (p.Tyr170Phe)
n.426A>T
n.443A>T
1g.17027780T>CCA338272595SDHBc.338A>G (p.Tyr113Cys)
c.467A>G (p.Tyr156Cys)
c.509A>G (p.Tyr170Cys)
n.426A>G
n.443A>G
1g.17027780T>GCA338272591SDHBc.338A>C (p.Tyr113Ser)
c.467A>C (p.Tyr156Ser)
c.509A>C (p.Tyr170Ser)
n.426A>C
n.443A>C
1g.17027781A>CCA338272596SDHBc.337T>G (p.Tyr113Asp)
c.466T>G (p.Tyr156Asp)
c.508T>G (p.Tyr170Asp)
n.425T>G
n.442T>G
1g.17027781A>GCA338272599SDHBc.337T>C (p.Tyr113His)
c.466T>C (p.Tyr156His)
c.508T>C (p.Tyr170His)
n.425T>C
n.442T>C
 ClinVar
1g.17027781A>TCA338272602SDHBc.337T>A (p.Tyr113Asn)
c.466T>A (p.Tyr156Asn)
c.508T>A (p.Tyr170Asn)
n.425T>A
n.442T>A
1g.17027781dupCA2586964056SDHBc.337dup (p.Tyr113LeufsTer9)
c.466dup (p.Tyr156LeufsTer9)
c.508dup (p.Tyr170LeufsTer9)
n.425dup
n.442dup
 ClinVar
1g.17027782C>ACA338272605SDHBc.336G>T (p.Gln112His)
c.465G>T (p.Gln155His)
c.507G>T (p.Gln169His)
n.424G>T
n.441G>T
1g.17027782C>GCA338272608SDHBc.336G>C (p.Gln112His)
c.465G>C (p.Gln155His)
c.507G>C (p.Gln169His)
n.424G>C
n.441G>C
1g.17027782C>TCA416085864SDHBc.336G>A (p.Gln112=)
c.465G>A (p.Gln155=)
c.507G>A (p.Gln169=)
n.424G>A
n.441G>A
 ClinVar dbSNP
1g.17027783T>ACA338272610SDHBc.335A>T (p.Gln112Leu)
c.464A>T (p.Gln155Leu)
c.506A>T (p.Gln169Leu)
n.423A>T
n.440A>T
1g.17027783T>CCA338272611SDHBc.335A>G (p.Gln112Arg)
c.464A>G (p.Gln155Arg)
c.506A>G (p.Gln169Arg)
n.423A>G
n.440A>G
 ClinVar
1g.17027783T>GCA338272620SDHBc.335A>C (p.Gln112Pro)
c.464A>C (p.Gln155Pro)
c.506A>C (p.Gln169Pro)
n.423A>C
n.440A>C
1g.17027784G>ACA16602226SDHBc.334C>T (p.Gln112Ter)
c.463C>T (p.Gln155Ter)
c.505C>T (p.Gln169Ter)
n.422C>T
n.439C>T
 ClinVar dbSNP gnomAD v4
1g.17027784G>CCA338272629SDHBc.334C>G (p.Gln112Glu)
c.463C>G (p.Gln155Glu)
c.505C>G (p.Gln169Glu)
n.422C>G
n.439C>G
 ClinVar dbSNP gnomAD v4
1g.17027784G=CA1156080168SDHBc.334C= (p.Gln112=)
c.463C= (p.Gln155=)
c.505C= (p.Gln169=)
n.422C=
n.439C=
1g.17027784G>TCA338272631SDHBc.334C>A (p.Gln112Lys)
c.463C>A (p.Gln155Lys)
c.505C>A (p.Gln169Lys)
n.422C>A
n.439C>A
 gnomAD v4
1g.17027785C>ACA338272634SDHBc.333G>T (p.Gln111His)
c.462G>T (p.Gln154His)
c.504G>T (p.Gln168His)
n.421G>T
n.438G>T
1g.17027785C>GCA338272637SDHBc.333G>C (p.Gln111His)
c.462G>C (p.Gln154His)
c.504G>C (p.Gln168His)
n.421G>C
n.438G>C
1g.17027785C>TCA416085874SDHBc.333G>A (p.Gln111=)
c.462G>A (p.Gln154=)
c.504G>A (p.Gln168=)
n.421G>A
n.438G>A
 dbSNP
1g.17027786T>ACA338272659SDHBc.332A>T (p.Gln111Leu)
c.461A>T (p.Gln154Leu)
c.503A>T (p.Gln168Leu)
n.420A>T
n.437A>T
1g.17027786T>CCA338272655SDHBc.332A>G (p.Gln111Arg)
c.461A>G (p.Gln154Arg)
c.503A>G (p.Gln168Arg)
n.420A>G
n.437A>G
 ClinVar
1g.17027786T>GCA338272652SDHBc.332A>C (p.Gln111Pro)
c.461A>C (p.Gln154Pro)
c.503A>C (p.Gln168Pro)
n.420A>C
n.437A>C
1g.17027786dupCA2586964058SDHBc.332dup (p.Gln112AlafsTer10)
c.461dup (p.Gln155AlafsTer10)
c.503dup (p.Gln169AlafsTer10)
n.420dup
n.437dup
1g.17027787G>ACA338272662SDHBc.331C>T (p.Gln111Ter)
c.460C>T (p.Gln154Ter)
c.502C>T (p.Gln168Ter)
n.419C>T
n.436C>T
 ClinVar dbSNP
1g.17027787G>CCA338272676SDHBc.331C>G (p.Gln111Glu)
c.460C>G (p.Gln154Glu)
c.502C>G (p.Gln168Glu)
n.419C>G
n.436C>G
1g.17027787G=CA1156080169SDHBc.331C= (p.Gln111=)
c.460C= (p.Gln154=)
c.502C= (p.Gln168=)
n.419C=
n.436C=
1g.17027787G>TCA338272678SDHBc.331C>A (p.Gln111Lys)
c.460C>A (p.Gln154Lys)
c.502C>A (p.Gln168Lys)
n.419C>A
n.436C>A
 gnomAD v4
1g.17027787dupCA658655542SDHBc.331dup (p.Gln111ProfsTer11)
c.460dup (p.Gln154ProfsTer11)
c.502dup (p.Gln168ProfsTer11)
n.419dup
n.436dup
1g.17027788C>ACA338272680SDHBc.330G>T (p.Lys110Asn)
c.459G>T (p.Lys153Asn)
c.501G>T (p.Lys167Asn)
n.418G>T
n.435G>T
 ClinVar dbSNP gnomAD v4
1g.17027788C=CA1156080170SDHBc.330G= (p.Lys110=)
c.459G= (p.Lys153=)
c.501G= (p.Lys167=)
n.418G=
n.435G=
1g.17027788C>GCA338272684SDHBc.330G>C (p.Lys110Asn)
c.459G>C (p.Lys153Asn)
c.501G>C (p.Lys167Asn)
n.418G>C
n.435G>C
1g.17027788C>TCA416085892SDHBc.330G>A (p.Lys110=)
c.459G>A (p.Lys153=)
c.501G>A (p.Lys167=)
n.418G>A
n.435G>A
 ClinVar dbSNP gnomAD v4
1g.17027788_17027789delinsAGCA1139655468SDHBc.329_330delinsCT (p.Lys110Thr)
c.458_459delinsCT (p.Lys153Thr)
c.500_501delinsCT (p.Lys167Thr)
n.417_418delinsCT
n.434_435delinsCT
 ClinVar
1g.17027789T>ACA338272687SDHBc.329A>T (p.Lys110Met)
c.458A>T (p.Lys153Met)
c.500A>T (p.Lys167Met)
n.417A>T
n.434A>T
1g.17027789T>CCA338272692SDHBc.329A>G (p.Lys110Arg)
c.458A>G (p.Lys153Arg)
c.500A>G (p.Lys167Arg)
n.417A>G
n.434A>G
 ClinVar
1g.17027789T>GCA338272693SDHBc.329A>C (p.Lys110Thr)
c.458A>C (p.Lys153Thr)
c.500A>C (p.Lys167Thr)
n.417A>C
n.434A>C
 gnomAD v4
1g.17027790T>ACA16609934SDHBc.328A>T (p.Lys110Ter)
c.457A>T (p.Lys153Ter)
c.499A>T (p.Lys167Ter)
n.416A>T
n.433A>T
 ClinVar dbSNP
1g.17027790T>CCA338272695SDHBc.328A>G (p.Lys110Glu)
c.457A>G (p.Lys153Glu)
c.499A>G (p.Lys167Glu)
n.416A>G
n.433A>G
1g.17027790T>GCA338272696SDHBc.328A>C (p.Lys110Gln)
c.457A>C (p.Lys153Gln)
c.499A>C (p.Lys167Gln)
n.416A>C
n.433A>C
1g.17027790T=CA1156080171SDHBc.328A= (p.Lys110=)
c.457A= (p.Lys153=)
c.499A= (p.Lys167=)
n.416A=
n.433A=
1g.17027791G>ACA416085918SDHBc.327C>T (p.Gly109=)
c.456C>T (p.Gly152=)
c.498C>T (p.Gly166=)
n.415C>T
n.432C>T
1g.17027791G>CCA416085915SDHBc.327C>G (p.Gly109=)
c.456C>G (p.Gly152=)
c.498C>G (p.Gly166=)
n.415C>G
n.432C>G
1g.17027791G>TCA416085919SDHBc.327C>A (p.Gly109=)
c.456C>A (p.Gly152=)
c.498C>A (p.Gly166=)
n.415C>A
n.432C>A
1g.17027792C>ACA338272697SDHBc.326G>T (p.Gly109Val)
c.455G>T (p.Gly152Val)
c.497G>T (p.Gly166Val)
n.414G>T
n.431G>T
1g.17027792C=CA1156080172SDHBc.326G= (p.Gly109=)
c.455G= (p.Gly152=)
c.497G= (p.Gly166=)
n.414G=
n.431G=
1g.17027792C>GCA338272698SDHBc.326G>C (p.Gly109Ala)
c.455G>C (p.Gly152Ala)
c.497G>C (p.Gly166Ala)
n.414G>C
n.431G>C
1g.17027792C>TCA16609936SDHBc.326G>A (p.Gly109Asp)
c.455G>A (p.Gly152Asp)
c.497G>A (p.Gly166Asp)
n.414G>A
n.431G>A
 ClinVar dbSNP gnomAD v4
1g.17027795_17027798delCA2573334482SDHBc.323_326del (p.Glu108AlafsTer9)
c.452_455del (p.Glu151AlafsTer9)
c.494_497del (p.Glu165AlafsTer9)
n.411_414del
n.428_431del
1g.17027793C>ACA338272705SDHBc.325G>T (p.Gly109Cys)
c.454G>T (p.Gly152Cys)
c.496G>T (p.Gly166Cys)
n.413G>T
n.430G>T
1g.17027793C>GCA338272706SDHBc.325G>C (p.Gly109Arg)
c.454G>C (p.Gly152Arg)
c.496G>C (p.Gly166Arg)
n.413G>C
n.430G>C
 ClinVar
1g.17027793C>TCA338272701SDHBc.325G>A (p.Gly109Ser)
c.454G>A (p.Gly152Ser)
c.496G>A (p.Gly166Ser)
n.413G>A
n.430G>A
 gnomAD v4
1g.17027794T>ACA338272708SDHBc.324A>T (p.Glu108Asp)
c.453A>T (p.Glu151Asp)
c.495A>T (p.Glu165Asp)
n.412A>T
n.429A>T
1g.17027794T>CCA416085942SDHBc.324A>G (p.Glu108=)
c.453A>G (p.Glu151=)
c.495A>G (p.Glu165=)
n.412A>G
n.429A>G
 gnomAD v4
1g.17027794T>GCA338272710SDHBc.324A>C (p.Glu108Asp)
c.453A>C (p.Glu151Asp)
c.495A>C (p.Glu165Asp)
n.412A>C
n.429A>C
1g.17027795T>ACA338272712SDHBc.323A>T (p.Glu108Val)
c.452A>T (p.Glu151Val)
c.494A>T (p.Glu165Val)
n.411A>T
n.428A>T
1g.17027795T>CCA338272716SDHBc.323A>G (p.Glu108Gly)
c.452A>G (p.Glu151Gly)
c.494A>G (p.Glu165Gly)
n.411A>G
n.428A>G
1g.17027795T>GCA338272718SDHBc.323A>C (p.Glu108Ala)
c.452A>C (p.Glu151Ala)
c.494A>C (p.Glu165Ala)
n.411A>C
n.428A>C
1g.17027796C>ACA338272720SDHBc.322G>T (p.Glu108Ter)
c.451G>T (p.Glu151Ter)
c.493G>T (p.Glu165Ter)
n.410G>T
n.427G>T
1g.17027796C>GCA338272721SDHBc.322G>C (p.Glu108Gln)
c.451G>C (p.Glu151Gln)
c.493G>C (p.Glu165Gln)
n.410G>C
n.427G>C
1g.17027796C>TCA338272724SDHBc.322G>A (p.Glu108Lys)
c.451G>A (p.Glu151Lys)
c.493G>A (p.Glu165Lys)
n.410G>A
n.427G>A
 ClinVar dbSNP
1g.17027797delCA658655541SDHBc.322del (p.Glu108LysfsTer10)
c.451del (p.Glu151LysfsTer10)
c.493del (p.Glu165LysfsTer10)
n.410del
n.427del
1g.17027797C>ACA338272726SDHBc.321G>T (p.Gln107His)
c.450G>T (p.Gln150His)
c.492G>T (p.Gln164His)
n.409G>T
n.426G>T
1g.17027797C>GCA338272734SDHBc.321G>C (p.Gln107His)
c.450G>C (p.Gln150His)
c.492G>C (p.Gln164His)
n.409G>C
n.426G>C
1g.17027797C>TCA416085962SDHBc.321G>A (p.Gln107=)
c.450G>A (p.Gln150=)
c.492G>A (p.Gln164=)
n.409G>A
n.426G>A
 ClinVar dbSNP gnomAD v4
1g.17027797_17027798delinsCTCA1156080173SDHBc.320_321delinsAG (p.Gln107=)
c.449_450delinsAG (p.Gln150=)
c.491_492delinsAG (p.Gln164=)
n.408_409delinsAG
n.425_426delinsAG
1g.17027798delCA658795404SDHBc.320del (p.Gln107ArgfsTer11)
c.449del (p.Gln150ArgfsTer11)
c.491del (p.Gln164ArgfsTer11)
n.408del
n.425del
 ClinVar dbSNP
1g.17027798T>ACA338272736SDHBc.320A>T (p.Gln107Leu)
c.449A>T (p.Gln150Leu)
c.491A>T (p.Gln164Leu)
n.408A>T
n.425A>T
1g.17027798T>CCA089634SDHBc.320A>G (p.Gln107Arg)
c.449A>G (p.Gln150Arg)
c.491A>G (p.Gln164Arg)
n.408A>G
n.425A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17027798T>GCA338272743SDHBc.320A>C (p.Gln107Pro)
c.449A>C (p.Gln150Pro)
c.491A>C (p.Gln164Pro)
n.408A>C
n.425A>C
1g.17027798T=CA1148714518SDHBc.320A= (p.Gln107=)
c.449A= (p.Gln150=)
c.491A= (p.Gln164=)
n.408A=
n.425A=
1g.17027799G>ACA338272750SDHBc.319C>T (p.Gln107Ter)
c.448C>T (p.Gln150Ter)
c.490C>T (p.Gln164Ter)
n.407C>T
n.424C>T
 ClinVar dbSNP
1g.17027799G>CCA338272746SDHBc.319C>G (p.Gln107Glu)
c.448C>G (p.Gln150Glu)
c.490C>G (p.Gln164Glu)
n.407C>G
n.424C>G
1g.17027799G=CA1156080174SDHBc.319C= (p.Gln107=)
c.448C= (p.Gln150=)
c.490C= (p.Gln164=)
n.407C=
n.424C=
1g.17027799G>TCA338272748SDHBc.319C>A (p.Gln107Lys)
c.448C>A (p.Gln150Lys)
c.490C>A (p.Gln164Lys)
n.407C>A
n.424C>A
1g.17027800A>CCA416085976SDHBc.318T>G (p.Ser106=)
c.447T>G (p.Ser149=)
c.489T>G (p.Ser163=)
n.406T>G
n.423T>G
1g.17027800A>GCA416085979SDHBc.318T>C (p.Ser106=)
c.447T>C (p.Ser149=)
c.489T>C (p.Ser163=)
n.406T>C
n.423T>C
1g.17027800A>TCA416085981SDHBc.318T>A (p.Ser106=)
c.447T>A (p.Ser149=)
c.489T>A (p.Ser163=)
n.406T>A
n.423T>A
1g.17027801G>ACA089633SDHBc.317C>T (p.Ser106Phe)
c.446C>T (p.Ser149Phe)
c.488C>T (p.Ser163Phe)
n.405C>T
n.422C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
1g.17027801G>CCA338272752SDHBc.317C>G (p.Ser106Cys)
c.446C>G (p.Ser149Cys)
c.488C>G (p.Ser163Cys)
n.405C>G
n.422C>G
 dbSNP
1g.17027801G=CA1156080175SDHBc.317C= (p.Ser106=)
c.446C= (p.Ser149=)
c.488C= (p.Ser163=)
n.405C=
n.422C=
1g.17027801G>TCA338272755SDHBc.317C>A (p.Ser106Tyr)
c.446C>A (p.Ser149Tyr)
c.488C>A (p.Ser163Tyr)
n.405C>A
n.422C>A
 ClinVar dbSNP gnomAD v4 COSMIC
1g.17027802A=CA1140495524SDHBc.316T= (p.Ser106=)
c.445T= (p.Ser149=)
c.487T= (p.Ser163=)
n.404T=
n.421T=
1g.17027802A>CCA338272759SDHBc.316T>G (p.Ser106Ala)
c.445T>G (p.Ser149Ala)
c.487T>G (p.Ser163Ala)
n.404T>G
n.421T>G
1g.17027802A>GCA015910SDHBc.316T>C (p.Ser106Pro)
c.445T>C (p.Ser149Pro)
c.487T>C (p.Ser163Pro)
n.404T>C
n.421T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17027802A>TCA338272762SDHBc.316T>A (p.Ser106Thr)
c.445T>A (p.Ser149Thr)
c.487T>A (p.Ser163Thr)
n.404T>A
n.421T>A
1g.17027803T>ACA338272766SDHBc.315A>T (p.Glu105Asp)
c.444A>T (p.Glu148Asp)
c.486A>T (p.Glu162Asp)
n.403A>T
n.420A>T
1g.17027803T>CCA416085998SDHBc.315A>G (p.Glu105=)
c.444A>G (p.Glu148=)
c.486A>G (p.Glu162=)
n.403A>G
n.420A>G
 ClinVar dbSNP
1g.17027803T>GCA338272767SDHBc.315A>C (p.Glu105Asp)
c.444A>C (p.Glu148Asp)
c.486A>C (p.Glu162Asp)
n.403A>C
n.420A>C
1g.17027803T=CA1156080176SDHBc.315A= (p.Glu105=)
c.444A= (p.Glu148=)
c.486A= (p.Glu162=)
n.403A=
n.420A=
1g.17027804T>ACA338272770SDHBc.314A>T (p.Glu105Val)
c.443A>T (p.Glu148Val)
c.485A>T (p.Glu162Val)
n.402A>T
n.419A>T
 ClinVar
1g.17027804T>CCA338272772SDHBc.314A>G (p.Glu105Gly)
c.443A>G (p.Glu148Gly)
c.485A>G (p.Glu162Gly)
n.402A>G
n.419A>G
 ClinVar
1g.17027804T>GCA338272773SDHBc.314A>C (p.Glu105Ala)
c.443A>C (p.Glu148Ala)
c.485A>C (p.Glu162Ala)
n.402A>C
n.419A>C
1g.17027805C>ACA338272779SDHBc.313G>T (p.Glu105Ter)
c.442G>T (p.Glu148Ter)
c.484G>T (p.Glu162Ter)
n.401G>T
n.418G>T
 ClinVar dbSNP
1g.17027805C>GCA338272777SDHBc.313G>C (p.Glu105Gln)
c.442G>C (p.Glu148Gln)
c.484G>C (p.Glu162Gln)
n.401G>C
n.418G>C
1g.17027805C>TCA338272775SDHBc.313G>A (p.Glu105Lys)
c.442G>A (p.Glu148Lys)
c.484G>A (p.Glu162Lys)
n.401G>A
n.418G>A
1g.17027806A>CCA338272781SDHBc.312T>G (p.Asp104Glu)
c.441T>G (p.Asp147Glu)
c.483T>G (p.Asp161Glu)
n.400T>G
n.417T>G
1g.17027806A>GCA416086012SDHBc.312T>C (p.Asp104=)
c.441T>C (p.Asp147=)
c.483T>C (p.Asp161=)
n.400T>C
n.417T>C
1g.17027806A>TCA338272787SDHBc.312T>A (p.Asp104Glu)
c.441T>A (p.Asp147Glu)
c.483T>A (p.Asp161Glu)
n.400T>A
n.417T>A
 gnomAD v4
1g.17027807T>ACA338272790SDHBc.311A>T (p.Asp104Val)
c.440A>T (p.Asp147Val)
c.482A>T (p.Asp161Val)
n.399A>T
n.416A>T
 ClinVar dbSNP
1g.17027807T>CCA18665939SDHBc.311A>G (p.Asp104Gly)
c.440A>G (p.Asp147Gly)
c.482A>G (p.Asp161Gly)
n.399A>G
n.416A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.17027807T>GCA338272795SDHBc.311A>C (p.Asp104Ala)
c.440A>C (p.Asp147Ala)
c.482A>C (p.Asp161Ala)
n.399A>C
n.416A>C
1g.17027807T=CA1156080178SDHBc.311A= (p.Asp104=)
c.440A= (p.Asp147=)
c.482A= (p.Asp161=)
n.399A=
n.416A=
1g.17027807_17027808delinsTCCA1156080177SDHBc.310_311delinsGA (p.Asp104=)
c.439_440delinsGA (p.Asp147=)
c.481_482delinsGA (p.Asp161=)
n.398_399delinsGA
n.415_416delinsGA
1g.17027809_17027812delCA2499214300SDHBc.308_311del (p.Lys103MetfsTer14)
c.437_440del (p.Lys146MetfsTer14)
c.479_482del (p.Lys160MetfsTer14)
n.396_399del
n.413_416del
 ClinVar dbSNP
1g.17027809_17027829delCA658655540SDHBc.291_311del (p.Glu97_Lys103del)
c.420_440del (p.Glu140_Lys146del)
c.462_482del (p.Glu154_Lys160del)
n.379_399del
n.396_416del
1g.17027808C>ACA338272803SDHBc.310G>T (p.Asp104Tyr)
c.439G>T (p.Asp147Tyr)
c.481G>T (p.Asp161Tyr)
n.398G>T
n.415G>T
 dbSNP
1g.17027808C=CA1156080180SDHBc.310G= (p.Asp104=)
c.439G= (p.Asp147=)
c.481G= (p.Asp161=)
n.398G=
n.415G=
1g.17027808C>GCA338272806SDHBc.310G>C (p.Asp104His)
c.439G>C (p.Asp147His)
c.481G>C (p.Asp161His)
n.398G>C
n.415G>C
1g.17027808C>TCA338272813SDHBc.310G>A (p.Asp104Asn)
c.439G>A (p.Asp147Asn)
c.481G>A (p.Asp161Asn)
n.398G>A
n.415G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17027809delCA015897SDHBc.310del (p.Asp104MetfsTer14)
c.439del (p.Asp147MetfsTer14)
c.481del (p.Asp161MetfsTer14)
n.398del
n.415del
 ClinVar dbSNP
1g.17027808_17027811delinsCCTTCA1156080179SDHBc.307_310delinsAAGG (p.Lys103=)
c.436_439delinsAAGG (p.Lys146=)
c.478_481delinsAAGG (p.Lys160=)
n.395_398delinsAAGG
n.412_415delinsAAGG
1g.17027809C>ACA338272822SDHBc.309G>T (p.Lys103Asn)
c.438G>T (p.Lys146Asn)
c.480G>T (p.Lys160Asn)
n.397G>T
n.414G>T
1g.17027809C=CA1156080181SDHBc.309G= (p.Lys103=)
c.438G= (p.Lys146=)
c.480G= (p.Lys160=)
n.397G=
n.414G=
1g.17027809C>GCA338272824SDHBc.309G>C (p.Lys103Asn)
c.438G>C (p.Lys146Asn)
c.480G>C (p.Lys160Asn)
n.397G>C
n.414G>C
 gnomAD v4
1g.17027809C>TCA416086043SDHBc.309G>A (p.Lys103=)
c.438G>A (p.Lys146=)
c.480G>A (p.Lys160=)
n.397G>A
n.414G>A
 ClinVar dbSNP
1g.17027816_17027818delCA521039145SDHBc.307_309del (p.Lys103del)
c.436_438del (p.Lys146del)
c.478_480del (p.Lys160del)
n.395_397del
n.412_414del
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17027810T>ACA338272826SDHBc.308A>T (p.Lys103Met)
c.437A>T (p.Lys146Met)
c.479A>T (p.Lys160Met)
n.396A>T
n.413A>T
1g.17027810T>CCA338272829SDHBc.308A>G (p.Lys103Arg)
c.437A>G (p.Lys146Arg)
c.479A>G (p.Lys160Arg)
n.396A>G
n.413A>G
1g.17027810T>GCA338272838SDHBc.308A>C (p.Lys103Thr)
c.437A>C (p.Lys146Thr)
c.479A>C (p.Lys160Thr)
n.396A>C
n.413A>C
 ClinVar dbSNP
1g.17027810T=CA1156080182SDHBc.308A= (p.Lys103=)
c.437A= (p.Lys146=)
c.479A= (p.Lys160=)
n.396A=
n.413A=
1g.17027811T>ACA338272842SDHBc.307A>T (p.Lys103Ter)
c.436A>T (p.Lys146Ter)
c.478A>T (p.Lys160Ter)
n.395A>T
n.412A>T
1g.17027811T>CCA338272846SDHBc.307A>G (p.Lys103Glu)
c.436A>G (p.Lys146Glu)
c.478A>G (p.Lys160Glu)
n.395A>G
n.412A>G
 ClinVar
1g.17027811T>GCA338272853SDHBc.307A>C (p.Lys103Gln)
c.436A>C (p.Lys146Gln)
c.478A>C (p.Lys160Gln)
n.395A>C
n.412A>C
1g.17027812C>ACA338272865SDHBc.306G>T (p.Lys102Asn)
c.435G>T (p.Lys145Asn)
c.477G>T (p.Lys159Asn)
n.394G>T
n.411G>T
1g.17027812C>GCA338272858SDHBc.306G>C (p.Lys102Asn)
c.435G>C (p.Lys145Asn)
c.477G>C (p.Lys159Asn)
n.394G>C
n.411G>C
 ClinVar
1g.17027812C>TCA416086063SDHBc.306G>A (p.Lys102=)
c.435G>A (p.Lys145=)
c.477G>A (p.Lys159=)
n.394G>A
n.411G>A
 ClinVar dbSNP gnomAD v4
1g.17027813T>ACA338272867SDHBc.305A>T (p.Lys102Met)
c.434A>T (p.Lys145Met)
c.476A>T (p.Lys159Met)
n.393A>T
n.410A>T
1g.17027813T>CCA338272869SDHBc.305A>G (p.Lys102Arg)
c.434A>G (p.Lys145Arg)
c.476A>G (p.Lys159Arg)
n.393A>G
n.410A>G
 gnomAD v4
1g.17027813T>GCA338272871SDHBc.305A>C (p.Lys102Thr)
c.434A>C (p.Lys145Thr)
c.476A>C (p.Lys159Thr)
n.393A>C
n.410A>C
1g.17027814T>ACA338272873SDHBc.304A>T (p.Lys102Ter)
c.433A>T (p.Lys145Ter)
c.475A>T (p.Lys159Ter)
n.392A>T
n.409A>T
1g.17027814T>CCA338272876SDHBc.304A>G (p.Lys102Glu)
c.433A>G (p.Lys145Glu)
c.475A>G (p.Lys159Glu)
n.392A>G
n.409A>G
1g.17027814T>GCA338272897SDHBc.304A>C (p.Lys102Gln)
c.433A>C (p.Lys145Gln)
c.475A>C (p.Lys159Gln)
n.392A>C
n.409A>C
1g.17027815C>ACA338272900SDHBc.303G>T (p.Lys101Asn)
c.432G>T (p.Lys144Asn)
c.474G>T (p.Lys158Asn)
n.391G>T
n.408G>T
1g.17027815C>GCA338272908SDHBc.303G>C (p.Lys101Asn)
c.432G>C (p.Lys144Asn)
c.474G>C (p.Lys158Asn)
n.391G>C
n.408G>C
1g.17027815C>TCA416086088SDHBc.303G>A (p.Lys101=)
c.432G>A (p.Lys144=)
c.474G>A (p.Lys158=)
n.391G>A
n.408G>A
 gnomAD v4
1g.17027816T>ACA338272912SDHBc.302A>T (p.Lys101Met)
c.431A>T (p.Lys144Met)
c.473A>T (p.Lys158Met)
n.390A>T
n.407A>T
1g.17027816T>CCA338272913SDHBc.302A>G (p.Lys101Arg)
c.431A>G (p.Lys144Arg)
c.473A>G (p.Lys158Arg)
n.390A>G
n.407A>G
1g.17027816T>GCA338272914SDHBc.302A>C (p.Lys101Thr)
c.431A>C (p.Lys144Thr)
c.473A>C (p.Lys158Thr)
n.390A>C
n.407A>C
1g.17027817delCA2580060651SDHBc.302del (p.Lys101ArgfsTer17)
c.431del (p.Lys144ArgfsTer17)
c.473del (p.Lys158ArgfsTer17)
n.390del
n.407del
 ClinVar
1g.17027817T>ACA338272917SDHBc.301A>T (p.Lys101Ter)
c.430A>T (p.Lys144Ter)
c.472A>T (p.Lys158Ter)
n.389A>T
n.406A>T
1g.17027817T>CCA338272916SDHBc.301A>G (p.Lys101Glu)
c.430A>G (p.Lys144Glu)
c.472A>G (p.Lys158Glu)
n.389A>G
n.406A>G
1g.17027817T>GCA338272915SDHBc.301A>C (p.Lys101Gln)
c.430A>C (p.Lys144Gln)
c.472A>C (p.Lys158Gln)
n.389A>C
n.406A>C
1g.17027818C>ACA338272918SDHBc.300G>T (p.Leu100Phe)
c.429G>T (p.Leu143Phe)
c.471G>T (p.Leu157Phe)
n.388G>T
n.405G>T
1g.17027818C>GCA338272920SDHBc.300G>C (p.Leu100Phe)
c.429G>C (p.Leu143Phe)
c.471G>C (p.Leu157Phe)
n.388G>C
n.405G>C
1g.17027818C>TCA416086106SDHBc.300G>A (p.Leu100=)
c.429G>A (p.Leu143=)
c.471G>A (p.Leu157=)
n.388G>A
n.405G>A
1g.17027818_17027819delinsCACA1156080183SDHBc.299_300delinsTG (p.Leu100=)
c.428_429delinsTG (p.Leu143=)
c.470_471delinsTG (p.Leu157=)
n.387_388delinsTG
n.404_405delinsTG
1g.17027819A=CA1156080184SDHBc.299T= (p.Leu100=)
c.428T= (p.Leu143=)
c.470T= (p.Leu157=)
n.387T=
n.404T=
1g.17027819A>CCA338272923SDHBc.299T>G (p.Leu100Trp)
c.428T>G (p.Leu143Trp)
c.470T>G (p.Leu157Trp)
n.387T>G
n.404T>G
1g.17027819A>GCA338272931SDHBc.299T>C (p.Leu100Ser)
c.428T>C (p.Leu143Ser)
c.470T>C (p.Leu157Ser)
n.387T>C
n.404T>C
 ClinVar dbSNP
1g.17027819A>TCA338272932SDHBc.299T>A (p.Leu100Ter)
c.428T>A (p.Leu143Ter)
c.470T>A (p.Leu157Ter)
n.387T>A
n.404T>A
1g.17027821delCA1139655469SDHBc.299del (p.Leu100Ter)
c.428del (p.Leu143Ter)
c.470del (p.Leu157Ter)
n.387del
n.404del
 ClinVar dbSNP gnomAD v4
1g.17027820A>CCA338272935SDHBc.298T>G (p.Leu100Val)
c.427T>G (p.Leu143Val)
c.469T>G (p.Leu157Val)
n.386T>G
n.403T>G
1g.17027820A>GCA416086126SDHBc.298T>C (p.Leu100=)
c.427T>C (p.Leu143=)
c.469T>C (p.Leu157=)
n.386T>C
n.403T>C
 ClinVar gnomAD v4
1g.17027820A>TCA338272936SDHBc.298T>A (p.Leu100Met)
c.427T>A (p.Leu143Met)
c.469T>A (p.Leu157Met)
n.386T>A
n.403T>A
1g.17027821A=CA1143370233SDHBc.297T= (p.Tyr99=)
c.426T= (p.Tyr142=)
c.468T= (p.Tyr156=)
n.385T=
n.402T=
1g.17027821A>CCA338272937SDHBc.297T>G (p.Tyr99Ter)
c.426T>G (p.Tyr142Ter)
c.468T>G (p.Tyr156Ter)
n.385T>G
n.402T>G
1g.17027821A>GCA18665949SDHBc.297T>C (p.Tyr99=)
c.426T>C (p.Tyr142=)
c.468T>C (p.Tyr156=)
n.385T>C
n.402T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17027821A>TCA338272940SDHBc.297T>A (p.Tyr99Ter)
c.426T>A (p.Tyr142Ter)
c.468T>A (p.Tyr156Ter)
n.385T>A
n.402T>A
1g.17027822T>ACA338272942SDHBc.296A>T (p.Tyr99Phe)
c.425A>T (p.Tyr142Phe)
c.467A>T (p.Tyr156Phe)
n.384A>T
n.401A>T
1g.17027822T>CCA338272951SDHBc.296A>G (p.Tyr99Cys)
c.425A>G (p.Tyr142Cys)
c.467A>G (p.Tyr156Cys)
n.384A>G
n.401A>G
1g.17027822T>GCA338272959SDHBc.296A>C (p.Tyr99Ser)
c.425A>C (p.Tyr142Ser)
c.467A>C (p.Tyr156Ser)
n.384A>C
n.401A>C
1g.17027823A=CA1156080185SDHBc.295T= (p.Tyr99=)
c.424T= (p.Tyr142=)
c.466T= (p.Tyr156=)
n.383T=
n.400T=
1g.17027823A>CCA338272980SDHBc.295T>G (p.Tyr99Asp)
c.424T>G (p.Tyr142Asp)
c.466T>G (p.Tyr156Asp)
n.383T>G
n.400T>G
1g.17027823A>GCA338272960SDHBc.295T>C (p.Tyr99His)
c.424T>C (p.Tyr142His)
c.466T>C (p.Tyr156His)
n.383T>C
n.400T>C
 dbSNP gnomAD v4
1g.17027823A>TCA338272965SDHBc.295T>A (p.Tyr99Asn)
c.424T>A (p.Tyr142Asn)
c.466T>A (p.Tyr156Asn)
n.383T>A
n.400T>A
1g.17027824delCA2499214301SDHBc.295del (p.Tyr99IlefsTer2)
c.424del (p.Tyr142IlefsTer2)
c.466del (p.Tyr156IlefsTer2)
n.383del
n.400del
 ClinVar dbSNP
1g.17027824A=CA1156080186SDHBc.294T= (p.Pro98=)
c.423T= (p.Pro141=)
c.465T= (p.Pro155=)
n.382T=
n.399T=
1g.17027824A>CCA416086149SDHBc.294T>G (p.Pro98=)
c.423T>G (p.Pro141=)
c.465T>G (p.Pro155=)
n.382T>G
n.399T>G
 gnomAD v4
1g.17027824A>GCA416086152SDHBc.294T>C (p.Pro98=)
c.423T>C (p.Pro141=)
c.465T>C (p.Pro155=)
n.382T>C
n.399T>C
 ClinVar dbSNP gnomAD v4
1g.17027824A>TCA416086154SDHBc.294T>A (p.Pro98=)
c.423T>A (p.Pro141=)
c.465T>A (p.Pro155=)
n.382T>A
n.399T>A
1g.17027825G>ACA338272998SDHBc.293C>T (p.Pro98Leu)
c.422C>T (p.Pro141Leu)
c.464C>T (p.Pro155Leu)
n.381C>T
n.398C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17027825G>CCA338273002SDHBc.293C>G (p.Pro98Arg)
c.422C>G (p.Pro141Arg)
c.464C>G (p.Pro155Arg)
n.381C>G
n.398C>G
 ClinVar
1g.17027825G=CA1156080187SDHBc.293C= (p.Pro98=)
c.422C= (p.Pro141=)
c.464C= (p.Pro155=)
n.381C=
n.398C=
1g.17027825G>TCA338273013SDHBc.293C>A (p.Pro98His)
c.422C>A (p.Pro141His)
c.464C>A (p.Pro155His)
n.381C>A
n.398C>A
1g.17027826G>ACA089630SDHBc.292C>T (p.Pro98Ser)
c.421C>T (p.Pro141Ser)
c.463C>T (p.Pro155Ser)
n.380C>T
n.397C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17027826G>CCA338273026SDHBc.292C>G (p.Pro98Ala)
c.421C>G (p.Pro141Ala)
c.463C>G (p.Pro155Ala)
n.380C>G
n.397C>G
1g.17027826G=CA1156080188SDHBc.292C= (p.Pro98=)
c.421C= (p.Pro141=)
c.463C= (p.Pro155=)
n.380C=
n.397C=
1g.17027826G>TCA338273035SDHBc.292C>A (p.Pro98Thr)
c.421C>A (p.Pro141Thr)
c.463C>A (p.Pro155Thr)
n.380C>A
n.397C>A

Number of alleles fetched