Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.17024009_17024013dupCA645369142SDHBc.434_438dup (p.Asp147ThrfsTer18)
c.563_567dup (p.Asp190ThrfsTer18)
c.605_609dup (p.Asp204ThrfsTer18)
n.539_543dup
c.563_567dup (p.Asp190ThrfsTer?)
 ClinVar dbSNP
1g.17024010T>ACA338271029SDHBc.434A>T (p.Asn145Ile)
c.563A>T (p.Asn188Ile)
c.605A>T (p.Asn202Ile)
n.539A>T
1g.17024010T>CCA338271033SDHBc.434A>G (p.Asn145Ser)
c.563A>G (p.Asn188Ser)
c.605A>G (p.Asn202Ser)
n.539A>G
1g.17024010T>GCA338271034SDHBc.434A>C (p.Asn145Thr)
c.563A>C (p.Asn188Thr)
c.605A>C (p.Asn202Thr)
n.539A>C
1g.17024011dupCA645369143SDHBc.434dup (p.Asn145LysfsTer20)
c.563dup (p.Asn188LysfsTer20)
c.605dup (p.Asn202LysfsTer20)
n.539dup
c.563dup (p.Asn188LysfsTer?)
 ClinVar dbSNP
1g.17024010_17024020delinsTTCCACCAGTACA1156078636SDHBc.424_434delinsTACTGGTGGAA (p.Tyr142=)
c.553_563delinsTACTGGTGGAA (p.Tyr185=)
c.595_605delinsTACTGGTGGAA (p.Tyr199=)
n.529_539delinsTACTGGTGGAA
1g.17024011T>ACA338271035SDHBc.433A>T (p.Asn145Tyr)
c.562A>T (p.Asn188Tyr)
c.604A>T (p.Asn202Tyr)
n.538A>T
1g.17024011T>CCA338271043SDHBc.433A>G (p.Asn145Asp)
c.562A>G (p.Asn188Asp)
c.604A>G (p.Asn202Asp)
n.538A>G
1g.17024011T>GCA338271037SDHBc.433A>C (p.Asn145His)
c.562A>C (p.Asn188His)
c.604A>C (p.Asn202His)
n.538A>C
1g.17024011_17024020delinsCCCA645369144SDHBc.424_433delinsGG (p.Tyr142GlyfsTer20)
c.553_562delinsGG (p.Tyr185GlyfsTer20)
c.595_604delinsGG (p.Tyr199GlyfsTer20)
n.529_538delinsGG
c.553_562delinsGG (p.Tyr185GlyfsTer?)
 ClinVar dbSNP
1g.17024012C>ACA338271045SDHBc.432G>T (p.Trp144Cys)
c.561G>T (p.Trp187Cys)
c.603G>T (p.Trp201Cys)
n.537G>T
1g.17024012C=CA1156078637SDHBc.432G= (p.Trp144=)
c.561G= (p.Trp187=)
c.603G= (p.Trp201=)
n.537G=
1g.17024012C>GCA338271048SDHBc.432G>C (p.Trp144Cys)
c.561G>C (p.Trp187Cys)
c.603G>C (p.Trp201Cys)
n.537G>C
 ClinVar dbSNP
1g.17024012C>TCA338271046SDHBc.432G>A (p.Trp144Ter)
c.561G>A (p.Trp187Ter)
c.603G>A (p.Trp201Ter)
n.537G>A
 ClinVar dbSNP
1g.17024012_17024017delinsTCACCTCA658655549SDHBc.427_432delinsAGGTGA (p.Trp143ArgfsTer2)
c.556_561delinsAGGTGA (p.Trp186ArgfsTer2)
c.598_603delinsAGGTGA (p.Trp200ArgfsTer2)
n.532_537delinsAGGTGA
1g.17024013C>ACA338271050SDHBc.431G>T (p.Trp144Leu)
c.560G>T (p.Trp187Leu)
c.602G>T (p.Trp201Leu)
n.536G>T
 gnomAD v4
1g.17024013C=CA1156078638SDHBc.431G= (p.Trp144=)
c.560G= (p.Trp187=)
c.602G= (p.Trp201=)
n.536G=
1g.17024013C>GCA338271053SDHBc.431G>C (p.Trp144Ser)
c.560G>C (p.Trp187Ser)
c.602G>C (p.Trp201Ser)
n.536G>C
1g.17024013C>TCA16609931SDHBc.431G>A (p.Trp144Ter)
c.560G>A (p.Trp187Ter)
c.602G>A (p.Trp201Ter)
n.536G>A
 ClinVar dbSNP gnomAD v2
1g.17024014A>CCA338271056SDHBc.430T>G (p.Trp144Gly)
c.559T>G (p.Trp187Gly)
c.601T>G (p.Trp201Gly)
n.535T>G
1g.17024014A>GCA338271058SDHBc.430T>C (p.Trp144Arg)
c.559T>C (p.Trp187Arg)
c.601T>C (p.Trp201Arg)
n.535T>C
 ClinVar dbSNP
1g.17024014A>TCA338271060SDHBc.430T>A (p.Trp144Arg)
c.559T>A (p.Trp187Arg)
c.601T>A (p.Trp201Arg)
n.535T>A
 gnomAD v4
1g.17024014_17024020delCA658655548SDHBc.424_430del (p.Tyr142GlyfsTer19)
c.553_559del (p.Tyr185GlyfsTer19)
c.595_601del (p.Tyr199GlyfsTer19)
n.529_535del
c.553_559del (p.Tyr185GlyfsTer?)
1g.17024015C>ACA016022SDHBc.429G>T (p.Trp143Cys)
c.558G>T (p.Trp186Cys)
c.600G>T (p.Trp200Cys)
n.534G>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17024015C=CA1144228681SDHBc.429G= (p.Trp143=)
c.558G= (p.Trp186=)
c.600G= (p.Trp200=)
n.534G=
1g.17024015C>GCA338271061SDHBc.429G>C (p.Trp143Cys)
c.558G>C (p.Trp186Cys)
c.600G>C (p.Trp200Cys)
n.534G>C
1g.17024015C>TCA016011SDHBc.429G>A (p.Trp143Ter)
c.558G>A (p.Trp186Ter)
c.600G>A (p.Trp200Ter)
n.534G>A
 ClinVar dbSNP gnomAD v4
1g.17024015_17024026dupCA2586964032SDHBc.418_429dup (p.Trp143_Trp144insProSerTyrTrp)
c.547_558dup (p.Trp186_Trp187insProSerTyrTrp)
c.589_600dup (p.Trp200_Trp201insProSerTyrTrp)
n.523_534dup
1g.17024016C>ACA338271063SDHBc.428G>T (p.Trp143Leu)
c.557G>T (p.Trp186Leu)
c.599G>T (p.Trp200Leu)
n.533G>T
1g.17024016C>GCA338271065SDHBc.428G>C (p.Trp143Ser)
c.557G>C (p.Trp186Ser)
c.599G>C (p.Trp200Ser)
n.533G>C
1g.17024016C>TCA338271069SDHBc.428G>A (p.Trp143Ter)
c.557G>A (p.Trp186Ter)
c.599G>A (p.Trp200Ter)
n.533G>A
1g.17024017delCA2573130773SDHBc.427del (p.Trp143GlyfsTer20)
c.556del (p.Trp186GlyfsTer20)
c.598del (p.Trp200GlyfsTer20)
n.532del
c.556del (p.Trp186GlyfsTer?)
 ClinVar dbSNP
1g.17024017A=CA1156078639SDHBc.427T= (p.Trp143=)
c.556T= (p.Trp186=)
c.598T= (p.Trp200=)
n.532T=
1g.17024017A>CCA338271072SDHBc.427T>G (p.Trp143Gly)
c.556T>G (p.Trp186Gly)
c.598T>G (p.Trp200Gly)
n.532T>G
 ClinVar
1g.17024017A>GCA338271075SDHBc.427T>C (p.Trp143Arg)
c.556T>C (p.Trp186Arg)
c.598T>C (p.Trp200Arg)
n.532T>C
 ClinVar dbSNP gnomAD v4
1g.17024017A>TCA338271076SDHBc.427T>A (p.Trp143Arg)
c.556T>A (p.Trp186Arg)
c.598T>A (p.Trp200Arg)
n.532T>A
1g.17024017dupCA2573130774SDHBc.427dup (p.Trp143LeufsTer22)
c.556dup (p.Trp186LeufsTer22)
c.598dup (p.Trp200LeufsTer22)
n.532dup
c.556dup (p.Trp186LeufsTer?)
 ClinVar dbSNP
1g.17024019_17024021delCA2586964034SDHBc.425_427del (p.Tyr142del)
c.554_556del (p.Tyr185del)
c.596_598del (p.Tyr199del)
n.530_532del
1g.17024018G>ACA416083565SDHBc.426C>T (p.Tyr142=)
c.555C>T (p.Tyr185=)
c.597C>T (p.Tyr199=)
n.531C>T
 ClinVar dbSNP
1g.17024018G>CCA338271081SDHBc.426C>G (p.Tyr142Ter)
c.555C>G (p.Tyr185Ter)
c.597C>G (p.Tyr199Ter)
n.531C>G
 ClinVar
1g.17024018G=CA1156078640SDHBc.426C= (p.Tyr142=)
c.555C= (p.Tyr185=)
c.597C= (p.Tyr199=)
n.531C=
1g.17024018G>TCA338271079SDHBc.426C>A (p.Tyr142Ter)
c.555C>A (p.Tyr185Ter)
c.597C>A (p.Tyr199Ter)
n.531C>A
1g.17024019T>ACA338271085SDHBc.425A>T (p.Tyr142Phe)
c.554A>T (p.Tyr185Phe)
c.596A>T (p.Tyr199Phe)
n.530A>T
1g.17024019T>CCA338271086SDHBc.425A>G (p.Tyr142Cys)
c.554A>G (p.Tyr185Cys)
c.596A>G (p.Tyr199Cys)
n.530A>G
 ClinVar dbSNP
1g.17024019T>GCA338271088SDHBc.425A>C (p.Tyr142Ser)
c.554A>C (p.Tyr185Ser)
c.596A>C (p.Tyr199Ser)
n.530A>C
1g.17024019T=CA1156078641SDHBc.425A= (p.Tyr142=)
c.554A= (p.Tyr185=)
c.596A= (p.Tyr199=)
n.530A=
1g.17024020A>CCA338271090SDHBc.424T>G (p.Tyr142Asp)
c.553T>G (p.Tyr185Asp)
c.595T>G (p.Tyr199Asp)
n.529T>G
1g.17024020A>GCA338271091SDHBc.424T>C (p.Tyr142His)
c.553T>C (p.Tyr185His)
c.595T>C (p.Tyr199His)
n.529T>C
1g.17024020A>TCA338271092SDHBc.424T>A (p.Tyr142Asn)
c.553T>A (p.Tyr185Asn)
c.595T>A (p.Tyr199Asn)
n.529T>A
1g.17024021G>ACA416083590SDHBc.423C>T (p.Ser141=)
c.552C>T (p.Ser184=)
c.594C>T (p.Ser198=)
n.528C>T
 dbSNP
1g.17024021G>CCA338271093SDHBc.423C>G (p.Ser141Arg)
c.552C>G (p.Ser184Arg)
c.594C>G (p.Ser198Arg)
n.528C>G
 ClinVar
1g.17024021G=CA1156078642SDHBc.423C= (p.Ser141=)
c.552C= (p.Ser184=)
c.594C= (p.Ser198=)
n.528C=
1g.17024021G>TCA338271095SDHBc.423C>A (p.Ser141Arg)
c.552C>A (p.Ser184Arg)
c.594C>A (p.Ser198Arg)
n.528C>A
1g.17024022C>ACA338271108SDHBc.422G>T (p.Ser141Ile)
c.551G>T (p.Ser184Ile)
c.593G>T (p.Ser198Ile)
n.527G>T
 ClinVar dbSNP gnomAD v4
1g.17024022C=CA1156078643SDHBc.422G= (p.Ser141=)
c.551G= (p.Ser184=)
c.593G= (p.Ser198=)
n.527G=
1g.17024022C>GCA338271110SDHBc.422G>C (p.Ser141Thr)
c.551G>C (p.Ser184Thr)
c.593G>C (p.Ser198Thr)
n.527G>C
 ClinVar dbSNP
1g.17024022C>TCA338271114SDHBc.422G>A (p.Ser141Asn)
c.551G>A (p.Ser184Asn)
c.593G>A (p.Ser198Asn)
n.527G>A
 dbSNP COSMIC
1g.17024023T>ACA338271118SDHBc.421A>T (p.Ser141Cys)
c.550A>T (p.Ser184Cys)
c.592A>T (p.Ser198Cys)
n.526A>T
1g.17024023T>CCA338271116SDHBc.421A>G (p.Ser141Gly)
c.550A>G (p.Ser184Gly)
c.592A>G (p.Ser198Gly)
n.526A>G
1g.17024023T>GCA338271115SDHBc.421A>C (p.Ser141Arg)
c.550A>C (p.Ser184Arg)
c.592A>C (p.Ser198Arg)
n.526A>C
 ClinVar dbSNP
1g.17024023T=CA1156078645SDHBc.421A= (p.Ser141=)
c.550A= (p.Ser184=)
c.592A= (p.Ser198=)
n.526A=
1g.17024023_17024024delinsTGCA1156078644SDHBc.420_421delinsCA (p.Pro140=)
c.549_550delinsCA (p.Pro183=)
c.591_592delinsCA (p.Pro197=)
n.525_526delinsCA
1g.17024024G>ACA416083614SDHBc.420C>T (p.Pro140=)
c.549C>T (p.Pro183=)
c.591C>T (p.Pro197=)
n.525C>T
 ClinVar
1g.17024024G>CCA416083631SDHBc.420C>G (p.Pro140=)
c.549C>G (p.Pro183=)
c.591C>G (p.Pro197=)
n.525C>G
 dbSNP
1g.17024024G>TCA416083627SDHBc.420C>A (p.Pro140=)
c.549C>A (p.Pro183=)
c.591C>A (p.Pro197=)
n.525C>A
1g.17024027delCA16609921SDHBc.420del (p.Ser141AlafsTer22)
c.549del (p.Ser184AlafsTer22)
c.591del (p.Ser198AlafsTer22)
n.525del
c.549del (p.Ser184AlafsTer?)
 ClinVar dbSNP
1g.17024025G>ACA338271122SDHBc.419C>T (p.Pro140Leu)
c.548C>T (p.Pro183Leu)
c.590C>T (p.Pro197Leu)
n.524C>T
 ClinVar dbSNP
1g.17024025G>CCA016001SDHBc.419C>G (p.Pro140Arg)
c.548C>G (p.Pro183Arg)
c.590C>G (p.Pro197Arg)
n.524C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17024025G=CA1140886353SDHBc.419C= (p.Pro140=)
c.548C= (p.Pro183=)
c.590C= (p.Pro197=)
n.524C=
1g.17024025G>TCA338271125SDHBc.419C>A (p.Pro140His)
c.548C>A (p.Pro183His)
c.590C>A (p.Pro197His)
n.524C>A
1g.17024026G>ACA338271129SDHBc.418C>T (p.Pro140Ser)
c.547C>T (p.Pro183Ser)
c.589C>T (p.Pro197Ser)
n.523C>T
 ClinVar dbSNP gnomAD v4
1g.17024026G>CCA338271133SDHBc.418C>G (p.Pro140Ala)
c.547C>G (p.Pro183Ala)
c.589C>G (p.Pro197Ala)
n.523C>G
1g.17024026G=CA1156078646SDHBc.418C= (p.Pro140=)
c.547C= (p.Pro183=)
c.589C= (p.Pro197=)
n.523C=
1g.17024026G>TCA338271136SDHBc.418C>A (p.Pro140Thr)
c.547C>A (p.Pro183Thr)
c.589C>A (p.Pro197Thr)
n.523C>A
1g.17024027G>ACA16609933SDHBc.417C>T (p.Cys139=)
c.546C>T (p.Cys182=)
c.588C>T (p.Cys196=)
n.522C>T
 ClinVar dbSNP gnomAD v4
1g.17024027G>CCA338271138SDHBc.417C>G (p.Cys139Trp)
c.546C>G (p.Cys182Trp)
c.588C>G (p.Cys196Trp)
n.522C>G
1g.17024027G=CA1156078647SDHBc.417C= (p.Cys139=)
c.546C= (p.Cys182=)
c.588C= (p.Cys196=)
n.522C=
1g.17024027G>TCA338271140SDHBc.417C>A (p.Cys139Ter)
c.546C>A (p.Cys182Ter)
c.588C>A (p.Cys196Ter)
n.522C>A
1g.17024027_17024038dupCA658820851SDHBc.406_417dup (p.Cys139_Pro140insSerThrSerCys)
c.535_546dup (p.Cys182_Pro183insSerThrSerCys)
c.577_588dup (p.Cys196_Pro197insSerThrSerCys)
n.511_522dup
1g.17024028C>ACA338271143SDHBc.416G>T (p.Cys139Phe)
c.545G>T (p.Cys182Phe)
c.587G>T (p.Cys196Phe)
n.521G>T
1g.17024028C=CA1156078648SDHBc.416G= (p.Cys139=)
c.545G= (p.Cys182=)
c.587G= (p.Cys196=)
n.521G=
1g.17024028C>GCA338271146SDHBc.416G>C (p.Cys139Ser)
c.545G>C (p.Cys182Ser)
c.587G>C (p.Cys196Ser)
n.521G>C
1g.17024028C>TCA10577672SDHBc.416G>A (p.Cys139Tyr)
c.545G>A (p.Cys182Tyr)
c.587G>A (p.Cys196Tyr)
n.521G>A
 ClinVar dbSNP gnomAD v4
1g.17024029A>CCA338271153SDHBc.415T>G (p.Cys139Gly)
c.544T>G (p.Cys182Gly)
c.586T>G (p.Cys196Gly)
n.520T>G
1g.17024029A>GCA338271152SDHBc.415T>C (p.Cys139Arg)
c.544T>C (p.Cys182Arg)
c.586T>C (p.Cys196Arg)
n.520T>C
 ClinVar dbSNP
1g.17024029A>TCA338271151SDHBc.415T>A (p.Cys139Ser)
c.544T>A (p.Cys182Ser)
c.586T>A (p.Cys196Ser)
n.520T>A
1g.17024030G>ACA416083664SDHBc.414C>T (p.Ser138=)
c.543C>T (p.Ser181=)
c.585C>T (p.Ser195=)
n.519C>T
 ClinVar
1g.17024030G>CCA338271156SDHBc.414C>G (p.Ser138Arg)
c.543C>G (p.Ser181Arg)
c.585C>G (p.Ser195Arg)
n.519C>G
1g.17024030G>TCA338271158SDHBc.414C>A (p.Ser138Arg)
c.543C>A (p.Ser181Arg)
c.585C>A (p.Ser195Arg)
n.519C>A
1g.17024031_17024033delCA658655547SDHBc.412_414del (p.Ser138del)
c.541_543del (p.Ser181del)
c.583_585del (p.Ser195del)
n.517_519del
1g.17024030_17024038dupCA2643676922SDHBc.406_414dup (p.Ser138_Cys139insSerThrSer)
c.535_543dup (p.Ser181_Cys182insSerThrSer)
c.577_585dup (p.Ser195_Cys196insSerThrSer)
n.511_519dup
 gnomAD v4
1g.17024031C>ACA338271167SDHBc.413G>T (p.Ser138Ile)
c.542G>T (p.Ser181Ile)
c.584G>T (p.Ser195Ile)
n.518G>T
 dbSNP
1g.17024031C=CA1156078649SDHBc.413G= (p.Ser138=)
c.542G= (p.Ser181=)
c.584G= (p.Ser195=)
n.518G=
1g.17024031C>GCA338271168SDHBc.413G>C (p.Ser138Thr)
c.542G>C (p.Ser181Thr)
c.584G>C (p.Ser195Thr)
n.518G>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17024031C>TCA338271170SDHBc.413G>A (p.Ser138Asn)
c.542G>A (p.Ser181Asn)
c.584G>A (p.Ser195Asn)
n.518G>A
 dbSNP
1g.17024032T>ACA338271174SDHBc.412A>T (p.Ser138Cys)
c.541A>T (p.Ser181Cys)
c.583A>T (p.Ser195Cys)
n.517A>T
1g.17024032T>CCA338271176SDHBc.412A>G (p.Ser138Gly)
c.541A>G (p.Ser181Gly)
c.583A>G (p.Ser195Gly)
n.517A>G
1g.17024032T>GCA338271179SDHBc.412A>C (p.Ser138Arg)
c.541A>C (p.Ser181Arg)
c.583A>C (p.Ser195Arg)
n.517A>C
1g.17024033G>ACA089674SDHBc.411C>T (p.Thr137=)
c.540C>T (p.Thr180=)
c.582C>T (p.Thr194=)
n.516C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024033G>CCA416083683SDHBc.411C>G (p.Thr137=)
c.540C>G (p.Thr180=)
c.582C>G (p.Thr194=)
n.516C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17024033G=CA1156078650SDHBc.411C= (p.Thr137=)
c.540C= (p.Thr180=)
c.582C= (p.Thr194=)
n.516C=
1g.17024033G>TCA416083686SDHBc.411C>A (p.Thr137=)
c.540C>A (p.Thr180=)
c.582C>A (p.Thr194=)
n.516C>A
1g.17024034G>ACA338271185SDHBc.410C>T (p.Thr137Ile)
c.539C>T (p.Thr180Ile)
c.581C>T (p.Thr194Ile)
n.515C>T
1g.17024034G>CCA18663196SDHBc.410C>G (p.Thr137Ser)
c.539C>G (p.Thr180Ser)
c.581C>G (p.Thr194Ser)
n.515C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17024034G=CA1143423247SDHBc.410C= (p.Thr137=)
c.539C= (p.Thr180=)
c.581C= (p.Thr194=)
n.515C=
1g.17024034G>TCA338271190SDHBc.410C>A (p.Thr137Asn)
c.539C>A (p.Thr180Asn)
c.581C>A (p.Thr194Asn)
n.515C>A
1g.17024035T>ACA338271196SDHBc.409A>T (p.Thr137Ser)
c.538A>T (p.Thr180Ser)
c.580A>T (p.Thr194Ser)
n.514A>T
1g.17024035T>CCA338271194SDHBc.409A>G (p.Thr137Ala)
c.538A>G (p.Thr180Ala)
c.580A>G (p.Thr194Ala)
n.514A>G
1g.17024035T>GCA338271192SDHBc.409A>C (p.Thr137Pro)
c.538A>C (p.Thr180Pro)
c.580A>C (p.Thr194Pro)
n.514A>C
1g.17024036G>ACA416083706SDHBc.408C>T (p.Ser136=)
c.537C>T (p.Ser179=)
c.579C>T (p.Ser193=)
n.513C>T
1g.17024036G>CCA338271199SDHBc.408C>G (p.Ser136Arg)
c.537C>G (p.Ser179Arg)
c.579C>G (p.Ser193Arg)
n.513C>G
1g.17024036G>TCA338271202SDHBc.408C>A (p.Ser136Arg)
c.537C>A (p.Ser179Arg)
c.579C>A (p.Ser193Arg)
n.513C>A
1g.17024037C>ACA338271204SDHBc.407G>T (p.Ser136Ile)
c.536G>T (p.Ser179Ile)
c.578G>T (p.Ser193Ile)
n.512G>T
 dbSNP
1g.17024037C=CA1156078651SDHBc.407G= (p.Ser136=)
c.536G= (p.Ser179=)
c.578G= (p.Ser193=)
n.512G=
1g.17024037C>GCA338271206SDHBc.407G>C (p.Ser136Thr)
c.536G>C (p.Ser179Thr)
c.578G>C (p.Ser193Thr)
n.512G>C
 dbSNP
1g.17024037C>TCA338271208SDHBc.407G>A (p.Ser136Asn)
c.536G>A (p.Ser179Asn)
c.578G>A (p.Ser193Asn)
n.512G>A
 ClinVar dbSNP
1g.17024038T>ACA338271211SDHBc.406A>T (p.Ser136Cys)
c.535A>T (p.Ser179Cys)
c.577A>T (p.Ser193Cys)
n.511A>T
1g.17024038T>CCA089673SDHBc.406A>G (p.Ser136Gly)
c.535A>G (p.Ser179Gly)
c.577A>G (p.Ser193Gly)
n.511A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024038T>GCA338271219SDHBc.406A>C (p.Ser136Arg)
c.535A>C (p.Ser179Arg)
c.577A>C (p.Ser193Arg)
n.511A>C
1g.17024038T=CA1156078652SDHBc.406A= (p.Ser136=)
c.535A= (p.Ser179=)
c.577A= (p.Ser193=)
n.511A=
1g.17024039A=CA1156078653SDHBc.405T= (p.Cys135=)
c.534T= (p.Cys178=)
c.576T= (p.Cys192=)
n.510T=
1g.17024039A>CCA338271222SDHBc.405T>G (p.Cys135Trp)
c.534T>G (p.Cys178Trp)
c.576T>G (p.Cys192Trp)
n.510T>G
1g.17024039A>GCA416083747SDHBc.405T>C (p.Cys135=)
c.534T>C (p.Cys178=)
c.576T>C (p.Cys192=)
n.510T>C
 dbSNP
1g.17024039A>TCA338271225SDHBc.405T>A (p.Cys135Ter)
c.534T>A (p.Cys178Ter)
c.576T>A (p.Cys192Ter)
n.510T>A
1g.17024040C>ACA338271227SDHBc.404G>T (p.Cys135Phe)
c.533G>T (p.Cys178Phe)
c.575G>T (p.Cys192Phe)
n.509G>T
1g.17024040C=CA1144228682SDHBc.404G= (p.Cys135=)
c.533G= (p.Cys178=)
c.575G= (p.Cys192=)
n.509G=
1g.17024040C>GCA015991SDHBc.404G>C (p.Cys135Ser)
c.533G>C (p.Cys178Ser)
c.575G>C (p.Cys192Ser)
n.509G>C
 ClinVar dbSNP
1g.17024040C>TCA015982SDHBc.404G>A (p.Cys135Tyr)
c.533G>A (p.Cys178Tyr)
c.575G>A (p.Cys192Tyr)
n.509G>A
 ClinVar dbSNP
1g.17024041A=CA1156078654SDHBc.403T= (p.Cys135=)
c.532T= (p.Cys178=)
c.574T= (p.Cys192=)
n.508T=
1g.17024041A>CCA338271235SDHBc.403T>G (p.Cys135Gly)
c.532T>G (p.Cys178Gly)
c.574T>G (p.Cys192Gly)
n.508T>G
1g.17024041A>GCA015973SDHBc.403T>C (p.Cys135Arg)
c.532T>C (p.Cys178Arg)
c.574T>C (p.Cys192Arg)
n.508T>C
 ClinVar dbSNP gnomAD v4
1g.17024041A>TCA338271243SDHBc.403T>A (p.Cys135Ser)
c.532T>A (p.Cys178Ser)
c.574T>A (p.Cys192Ser)
n.508T>A
1g.17024042G>ACA416083774SDHBc.402C>T (p.Cys134=)
c.531C>T (p.Cys177=)
c.573C>T (p.Cys191=)
n.507C>T
 ClinVar dbSNP gnomAD v4
1g.17024042G>CCA338271246SDHBc.402C>G (p.Cys134Trp)
c.531C>G (p.Cys177Trp)
c.573C>G (p.Cys191Trp)
n.507C>G
1g.17024042G>TCA338271248SDHBc.402C>A (p.Cys134Ter)
c.531C>A (p.Cys177Ter)
c.573C>A (p.Cys191Ter)
n.507C>A
1g.17024043delCA2586964047SDHBc.401del (p.Cys134SerfsTer29)
c.530del (p.Cys177SerfsTer29)
c.572del (p.Cys191SerfsTer29)
n.506del
c.530del (p.Cys177SerfsTer?)
1g.17024043C>ACA338271252SDHBc.401G>T (p.Cys134Phe)
c.530G>T (p.Cys177Phe)
c.572G>T (p.Cys191Phe)
n.506G>T
1g.17024043C=CA1156078655SDHBc.401G= (p.Cys134=)
c.530G= (p.Cys177=)
c.572G= (p.Cys191=)
n.506G=
1g.17024043C>GCA338271259SDHBc.401G>C (p.Cys134Ser)
c.530G>C (p.Cys177Ser)
c.572G>C (p.Cys191Ser)
n.506G>C
1g.17024043C>TCA338271262SDHBc.401G>A (p.Cys134Tyr)
c.530G>A (p.Cys177Tyr)
c.572G>A (p.Cys191Tyr)
n.506G>A
 ClinVar dbSNP
1g.17024044A>CCA338271265SDHBc.400T>G (p.Cys134Gly)
c.529T>G (p.Cys177Gly)
c.571T>G (p.Cys191Gly)
n.505T>G
1g.17024044A>GCA338271268SDHBc.400T>C (p.Cys134Arg)
c.529T>C (p.Cys177Arg)
c.571T>C (p.Cys191Arg)
n.505T>C
1g.17024044A>TCA338271269SDHBc.400T>A (p.Cys134Ser)
c.529T>A (p.Cys177Ser)
c.571T>A (p.Cys191Ser)
n.505T>A
1g.17024045G>ACA416083793SDHBc.399C>T (p.Ala133=)
c.528C>T (p.Ala176=)
c.570C>T (p.Ala190=)
n.504C>T
 gnomAD v4
1g.17024045G>CCA416083796SDHBc.399C>G (p.Ala133=)
c.528C>G (p.Ala176=)
c.570C>G (p.Ala190=)
n.504C>G
 ClinVar dbSNP
1g.17024045G>TCA416083801SDHBc.399C>A (p.Ala133=)
c.528C>A (p.Ala176=)
c.570C>A (p.Ala190=)
n.504C>A
1g.17024046G>ACA18663206SDHBc.398C>T (p.Ala133Val)
c.527C>T (p.Ala176Val)
c.569C>T (p.Ala190Val)
n.503C>T
 ClinVar dbSNP
1g.17024046G>CCA338271280SDHBc.398C>G (p.Ala133Gly)
c.527C>G (p.Ala176Gly)
c.569C>G (p.Ala190Gly)
n.503C>G
 dbSNP
1g.17024046G=CA1143513070SDHBc.398C= (p.Ala133=)
c.527C= (p.Ala176=)
c.569C= (p.Ala190=)
n.503C=
1g.17024046G>TCA338271289SDHBc.398C>A (p.Ala133Asp)
c.527C>A (p.Ala176Asp)
c.569C>A (p.Ala190Asp)
n.503C>A
 ClinVar
1g.17024047C>ACA338271297SDHBc.397G>T (p.Ala133Ser)
c.526G>T (p.Ala176Ser)
c.568G>T (p.Ala190Ser)
n.502G>T
 ClinVar
1g.17024047C=CA1143375003SDHBc.397G= (p.Ala133=)
c.526G= (p.Ala176=)
c.568G= (p.Ala190=)
n.502G=
1g.17024047C>GCA338271299SDHBc.397G>C (p.Ala133Pro)
c.526G>C (p.Ala176Pro)
c.568G>C (p.Ala190Pro)
n.502G>C
1g.17024047C>TCA089672SDHBc.397G>A (p.Ala133Thr)
c.526G>A (p.Ala176Thr)
c.568G>A (p.Ala190Thr)
n.502G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.17024049_17024050delCA2586964048SDHBc.396_397del (p.Ala133LeufsTer3)
c.525_526del (p.Ala176LeufsTer3)
c.567_568del (p.Ala190LeufsTer3)
n.501_502del
 gnomAD v4
1g.17024048A>CCA338271308SDHBc.396T>G (p.Cys132Trp)
c.525T>G (p.Cys175Trp)
c.567T>G (p.Cys189Trp)
n.501T>G
 ClinVar dbSNP
1g.17024048A>GCA416083814SDHBc.396T>C (p.Cys132=)
c.525T>C (p.Cys175=)
c.567T>C (p.Cys189=)
n.501T>C
 dbSNP
1g.17024048A>TCA338271309SDHBc.396T>A (p.Cys132Ter)
c.525T>A (p.Cys175Ter)
c.567T>A (p.Cys189Ter)
n.501T>A
1g.17024049C>ACA10577673SDHBc.395G>T (p.Cys132Phe)
c.524G>T (p.Cys175Phe)
c.566G>T (p.Cys189Phe)
n.500G>T
 ClinVar dbSNP
1g.17024049C=CA1156078656SDHBc.395G= (p.Cys132=)
c.524G= (p.Cys175=)
c.566G= (p.Cys189=)
n.500G=
1g.17024049C>GCA338271310SDHBc.395G>C (p.Cys132Ser)
c.524G>C (p.Cys175Ser)
c.566G>C (p.Cys189Ser)
n.500G>C
1g.17024049C>TCA338271313SDHBc.395G>A (p.Cys132Tyr)
c.524G>A (p.Cys175Tyr)
c.566G>A (p.Cys189Tyr)
n.500G>A
 ClinVar
1g.17024050A=CA1156078657SDHBc.394T= (p.Cys132=)
c.523T= (p.Cys175=)
c.565T= (p.Cys189=)
n.499T=
1g.17024050A>CCA338271317SDHBc.394T>G (p.Cys132Gly)
c.523T>G (p.Cys175Gly)
c.565T>G (p.Cys189Gly)
n.499T>G
1g.17024050A>GCA338271320SDHBc.394T>C (p.Cys132Arg)
c.523T>C (p.Cys175Arg)
c.565T>C (p.Cys189Arg)
n.499T>C
 ClinVar dbSNP
1g.17024050A>TCA338271324SDHBc.394T>A (p.Cys132Ser)
c.523T>A (p.Cys175Ser)
c.565T>A (p.Cys189Ser)
n.499T>A
1g.17024050dupCA658655546SDHBc.394dup (p.Cys132LeufsTer5)
c.523dup (p.Cys175LeufsTer5)
c.565dup (p.Cys189LeufsTer5)
n.499dup
1g.17024051G>ACA089671SDHBc.393C>T (p.Leu131=)
c.522C>T (p.Leu174=)
c.564C>T (p.Leu188=)
n.498C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024051G>CCA416083844SDHBc.393C>G (p.Leu131=)
c.522C>G (p.Leu174=)
c.564C>G (p.Leu188=)
n.498C>G
 dbSNP
1g.17024051G=CA1156078658SDHBc.393C= (p.Leu131=)
c.522C= (p.Leu174=)
c.564C= (p.Leu188=)
n.498C=
1g.17024051G>TCA416083842SDHBc.393C>A (p.Leu131=)
c.522C>A (p.Leu174=)
c.564C>A (p.Leu188=)
n.498C>A
1g.17024052A>CCA338271340SDHBc.392T>G (p.Leu131Arg)
c.521T>G (p.Leu174Arg)
c.563T>G (p.Leu188Arg)
n.497T>G
1g.17024052A>GCA338271345SDHBc.392T>C (p.Leu131Pro)
c.521T>C (p.Leu174Pro)
c.563T>C (p.Leu188Pro)
n.497T>C
1g.17024052A>TCA338271343SDHBc.392T>A (p.Leu131His)
c.521T>A (p.Leu174His)
c.563T>A (p.Leu188His)
n.497T>A
1g.17024053G>ACA338271355SDHBc.391C>T (p.Leu131Phe)
c.520C>T (p.Leu174Phe)
c.562C>T (p.Leu188Phe)
n.496C>T
 dbSNP gnomAD v2 gnomAD v4
1g.17024053G>CCA338271356SDHBc.391C>G (p.Leu131Val)
c.520C>G (p.Leu174Val)
c.562C>G (p.Leu188Val)
n.496C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17024053G=CA1156078659SDHBc.391C= (p.Leu131=)
c.520C= (p.Leu174=)
c.562C= (p.Leu188=)
n.496C=
1g.17024053G>TCA338271358SDHBc.391C>A (p.Leu131Ile)
c.520C>A (p.Leu174Ile)
c.562C>A (p.Leu188Ile)
n.496C>A
 ClinVar dbSNP
1g.17024054A=CA1156078660SDHBc.390T= (p.Ile130=)
c.519T= (p.Ile173=)
c.561T= (p.Ile187=)
n.495T=
1g.17024054A>CCA338271360SDHBc.390T>G (p.Ile130Met)
c.519T>G (p.Ile173Met)
c.561T>G (p.Ile187Met)
n.495T>G
1g.17024054A>GCA416083872SDHBc.390T>C (p.Ile130=)
c.519T>C (p.Ile173=)
c.561T>C (p.Ile187=)
n.495T>C
 dbSNP
1g.17024054A>TCA416083870SDHBc.390T>A (p.Ile130=)
c.519T>A (p.Ile173=)
c.561T>A (p.Ile187=)
n.495T>A
1g.17024054_17024055delCA658655545SDHBc.389_390del (p.Ile130ThrfsTer6)
c.518_519del (p.Ile173ThrfsTer6)
c.560_561del (p.Ile187ThrfsTer6)
n.494_495del
1g.17024055A>CCA338271361SDHBc.389T>G (p.Ile130Ser)
c.518T>G (p.Ile173Ser)
c.560T>G (p.Ile187Ser)
n.494T>G
1g.17024055A>GCA338271363SDHBc.389T>C (p.Ile130Thr)
c.518T>C (p.Ile173Thr)
c.560T>C (p.Ile187Thr)
n.494T>C
1g.17024055A>TCA338271362SDHBc.389T>A (p.Ile130Asn)
c.518T>A (p.Ile173Asn)
c.560T>A (p.Ile187Asn)
n.494T>A
 ClinVar
1g.17024056T>ACA338271364SDHBc.388A>T (p.Ile130Phe)
c.517A>T (p.Ile173Phe)
c.559A>T (p.Ile187Phe)
n.493A>T
1g.17024056T>CCA338271366SDHBc.388A>G (p.Ile130Val)
c.517A>G (p.Ile173Val)
c.559A>G (p.Ile187Val)
n.493A>G
 ClinVar dbSNP
1g.17024056T>GCA338271368SDHBc.388A>C (p.Ile130Leu)
c.517A>C (p.Ile173Leu)
c.559A>C (p.Ile187Leu)
n.493A>C
 ClinVar
1g.17024056T=CA1156078661SDHBc.388A= (p.Ile130=)
c.517A= (p.Ile173=)
c.559A= (p.Ile187=)
n.493A=
1g.17024057G>ACA416083897SDHBc.387C>T (p.Cys129=)
c.516C>T (p.Cys172=)
c.558C>T (p.Cys186=)
n.492C>T
 ClinVar dbSNP
1g.17024057G>CCA338271371SDHBc.387C>G (p.Cys129Trp)
c.516C>G (p.Cys172Trp)
c.558C>G (p.Cys186Trp)
n.492C>G
1g.17024057G=CA1156078662SDHBc.387C= (p.Cys129=)
c.516C= (p.Cys172=)
c.558C= (p.Cys186=)
n.492C=
1g.17024057G>TCA338271373SDHBc.387C>A (p.Cys129Ter)
c.516C>A (p.Cys172Ter)
c.558C>A (p.Cys186Ter)
n.492C>A
1g.17024058C>ACA338271374SDHBc.386G>T (p.Cys129Phe)
c.515G>T (p.Cys172Phe)
c.557G>T (p.Cys186Phe)
n.491G>T
1g.17024058C=CA1156078663SDHBc.386G= (p.Cys129=)
c.515G= (p.Cys172=)
c.557G= (p.Cys186=)
n.491G=
1g.17024058C>GCA338271376SDHBc.386G>C (p.Cys129Ser)
c.515G>C (p.Cys172Ser)
c.557G>C (p.Cys186Ser)
n.491G>C
 ClinVar dbSNP
1g.17024058C>TCA338271379SDHBc.386G>A (p.Cys129Tyr)
c.515G>A (p.Cys172Tyr)
c.557G>A (p.Cys186Tyr)
n.491G>A
 ClinVar dbSNP gnomAD v4
1g.17024059A>CCA338271382SDHBc.385T>G (p.Cys129Gly)
c.514T>G (p.Cys172Gly)
c.556T>G (p.Cys186Gly)
n.490T>G
1g.17024059A>GCA338271385SDHBc.385T>C (p.Cys129Arg)
c.514T>C (p.Cys172Arg)
c.556T>C (p.Cys186Arg)
n.490T>C
 ClinVar
1g.17024059A>TCA338271387SDHBc.385T>A (p.Cys129Ser)
c.514T>A (p.Cys172Ser)
c.556T>A (p.Cys186Ser)
n.490T>A
1g.17024060C>ACA338271400SDHBc.384G>T (p.Glu128Asp)
c.513G>T (p.Glu171Asp)
c.555G>T (p.Glu185Asp)
n.489G>T
1g.17024060C=CA1156078664SDHBc.384G= (p.Glu128=)
c.513G= (p.Glu171=)
c.555G= (p.Glu185=)
n.489G=
1g.17024060C>GCA338271396SDHBc.384G>C (p.Glu128Asp)
c.513G>C (p.Glu171Asp)
c.555G>C (p.Glu185Asp)
n.489G>C
 ClinVar
1g.17024060C>TCA089670SDHBc.384G>A (p.Glu128=)
c.513G>A (p.Glu171=)
c.555G>A (p.Glu185=)
n.489G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024061T>ACA338271405SDHBc.383A>T (p.Glu128Val)
c.512A>T (p.Glu171Val)
c.554A>T (p.Glu185Val)
n.488A>T
1g.17024061T>CCA015963SDHBc.383A>G (p.Glu128Gly)
c.512A>G (p.Glu171Gly)
c.554A>G (p.Glu185Gly)
n.488A>G
 ClinVar dbSNP
1g.17024061T>GCA338271409SDHBc.383A>C (p.Glu128Ala)
c.512A>C (p.Glu171Ala)
c.554A>C (p.Glu185Ala)
n.488A>C
1g.17024061T=CA1156078665SDHBc.383A= (p.Glu128=)
c.512A= (p.Glu171=)
c.554A= (p.Glu185=)
n.488A=
1g.17024062C>ACA338271414SDHBc.382G>T (p.Glu128Ter)
c.511G>T (p.Glu171Ter)
c.553G>T (p.Glu185Ter)
n.487G>T
 ClinVar dbSNP
1g.17024062C=CA1156078666SDHBc.382G= (p.Glu128=)
c.511G= (p.Glu171=)
c.553G= (p.Glu185=)
n.487G=
1g.17024062C>GCA338271423SDHBc.382G>C (p.Glu128Gln)
c.511G>C (p.Glu171Gln)
c.553G>C (p.Glu185Gln)
n.487G>C
 ClinVar dbSNP
1g.17024062C>TCA18663233SDHBc.382G>A (p.Glu128Lys)
c.511G>A (p.Glu171Lys)
c.553G>A (p.Glu185Lys)
n.487G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.17024063G>ACA089669SDHBc.381C>T (p.Tyr127=)
c.510C>T (p.Tyr170=)
c.552C>T (p.Tyr184=)
n.486C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17024063G>CCA338271432SDHBc.381C>G (p.Tyr127Ter)
c.510C>G (p.Tyr170Ter)
c.552C>G (p.Tyr184Ter)
n.486C>G
1g.17024063G=CA1143525358SDHBc.381C= (p.Tyr127=)
c.510C= (p.Tyr170=)
c.552C= (p.Tyr184=)
n.486C=
1g.17024063G>TCA338271429SDHBc.381C>A (p.Tyr127Ter)
c.510C>A (p.Tyr170Ter)
c.552C>A (p.Tyr184Ter)
n.486C>A
1g.17024063_17024065delinsCTGTATCA2586964051SDHBc.379_381delinsATACAG (p.Tyr127delinsIleGln)
c.508_510delinsATACAG (p.Tyr170delinsIleGln)
c.550_552delinsATACAG (p.Tyr184delinsIleGln)
n.484_486delinsATACAG
1g.17024064T>ACA338271433SDHBc.380A>T (p.Tyr127Phe)
c.509A>T (p.Tyr170Phe)
c.551A>T (p.Tyr184Phe)
n.485A>T
1g.17024064T>CCA338271435SDHBc.380A>G (p.Tyr127Cys)
c.509A>G (p.Tyr170Cys)
c.551A>G (p.Tyr184Cys)
n.485A>G
 ClinVar dbSNP
1g.17024064T>GCA338271437SDHBc.380A>C (p.Tyr127Ser)
c.509A>C (p.Tyr170Ser)
c.551A>C (p.Tyr184Ser)
n.485A>C
1g.17024065A=CA1156078667SDHBc.379T= (p.Tyr127=)
c.508T= (p.Tyr170=)
c.550T= (p.Tyr184=)
n.484T=
1g.17024065A>CCA338271438SDHBc.379T>G (p.Tyr127Asp)
c.508T>G (p.Tyr170Asp)
c.550T>G (p.Tyr184Asp)
n.484T>G
1g.17024065A>GCA338271439SDHBc.379T>C (p.Tyr127His)
c.508T>C (p.Tyr170His)
c.550T>C (p.Tyr184His)
n.484T>C
 ClinVar dbSNP
1g.17024065A>TCA338271440SDHBc.379T>A (p.Tyr127Asn)
c.508T>A (p.Tyr170Asn)
c.550T>A (p.Tyr184Asn)
n.484T>A
1g.17024065_17024071delCA658655543SDHBc.373_379del (p.Gly125ThrfsTer?)
c.502_508del (p.Gly168ThrfsTer?)
c.544_550del (p.Gly182ThrfsTer?)
n.478_484del
1g.17024066G>ACA416083972SDHBc.378C>T (p.Leu126=)
c.507C>T (p.Leu169=)
c.549C>T (p.Leu183=)
n.483C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17024066G>CCA416083977SDHBc.378C>G (p.Leu126=)
c.507C>G (p.Leu169=)
c.549C>G (p.Leu183=)
n.483C>G
 gnomAD v4 COSMIC
1g.17024066G=CA1156078668SDHBc.378C= (p.Leu126=)
c.507C= (p.Leu169=)
c.549C= (p.Leu183=)
n.483C=
1g.17024066G>TCA416083975SDHBc.378C>A (p.Leu126=)
c.507C>A (p.Leu169=)
c.549C>A (p.Leu183=)
n.483C>A
1g.17024067A>CCA338271442SDHBc.377T>G (p.Leu126Arg)
c.506T>G (p.Leu169Arg)
c.548T>G (p.Leu183Arg)
n.482T>G
1g.17024067A>GCA338271444SDHBc.377T>C (p.Leu126Pro)
c.506T>C (p.Leu169Pro)
c.548T>C (p.Leu183Pro)
n.482T>C
1g.17024067A>TCA338271445SDHBc.377T>A (p.Leu126His)
c.506T>A (p.Leu169His)
c.548T>A (p.Leu183His)
n.482T>A
1g.17024068G>ACA338271446SDHBc.376C>T (p.Leu126Phe)
c.505C>T (p.Leu169Phe)
c.547C>T (p.Leu183Phe)
n.481C>T
 ClinVar dbSNP gnomAD v4
1g.17024068G>CCA338271447SDHBc.376C>G (p.Leu126Val)
c.505C>G (p.Leu169Val)
c.547C>G (p.Leu183Val)
n.481C>G
1g.17024068G=CA1156078669SDHBc.376C= (p.Leu126=)
c.505C= (p.Leu169=)
c.547C= (p.Leu183=)
n.481C=
1g.17024068G>TCA338271449SDHBc.376C>A (p.Leu126Ile)
c.505C>A (p.Leu169Ile)
c.547C>A (p.Leu183Ile)
n.481C>A
1g.17024069C>ACA416083995SDHBc.375G>T (p.Gly125=)
c.504G>T (p.Gly168=)
c.546G>T (p.Gly182=)
n.480G>T
 dbSNP
1g.17024069C>GCA416083998SDHBc.375G>C (p.Gly125=)
c.504G>C (p.Gly168=)
c.546G>C (p.Gly182=)
n.480G>C
1g.17024069C>TCA416083993SDHBc.375G>A (p.Gly125=)
c.504G>A (p.Gly168=)
c.546G>A (p.Gly182=)
n.480G>A
 ClinVar gnomAD v4
1g.17024071delCA658655544SDHBc.375del (p.Leu126SerfsTer?)
c.504del (p.Leu169SerfsTer?)
c.546del (p.Leu183SerfsTer?)
n.480del
1g.17024070C>ACA338271452SDHBc.374G>T (p.Gly125Val)
c.503G>T (p.Gly168Val)
c.545G>T (p.Gly182Val)
n.479G>T
1g.17024070C=CA1156078670SDHBc.374G= (p.Gly125=)
c.503G= (p.Gly168=)
c.545G= (p.Gly182=)
n.479G=
1g.17024070C>GCA338271457SDHBc.374G>C (p.Gly125Ala)
c.503G>C (p.Gly168Ala)
c.545G>C (p.Gly182Ala)
n.479G>C
 ClinVar dbSNP gnomAD v4
1g.17024070C>TCA338271454SDHBc.374G>A (p.Gly125Glu)
c.503G>A (p.Gly168Glu)
c.545G>A (p.Gly182Glu)
n.479G>A
1g.17024071C>ACA338271459SDHBc.373G>T (p.Gly125Trp)
c.502G>T (p.Gly168Trp)
c.544G>T (p.Gly182Trp)
n.478G>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.17024071C=CA1143514970SDHBc.373G= (p.Gly125=)
c.502G= (p.Gly168=)
c.544G= (p.Gly182=)
n.478G=
1g.17024071C>GCA338271465SDHBc.373G>C (p.Gly125Arg)
c.502G>C (p.Gly168Arg)
c.544G>C (p.Gly182Arg)
n.478G>C
1g.17024071C>TCA089667SDHBc.373G>A (p.Gly125Arg)
c.502G>A (p.Gly168Arg)
c.544G>A (p.Gly182Arg)
n.478G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024071_17024076delCA2643676989SDHBc.370-2_373del
c.499-2_502del
c.541-2_544del
n.475-2_478del
 gnomAD v4
1g.17024072G>ACA089666SDHBc.372C>T (p.Asp124=)
c.501C>T (p.Asp167=)
c.543C>T (p.Asp181=)
n.477C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17024072G>CCA338271472SDHBc.372C>G (p.Asp124Glu)
c.501C>G (p.Asp167Glu)
c.543C>G (p.Asp181Glu)
n.477C>G
1g.17024072G=CA1143375935SDHBc.372C= (p.Asp124=)
c.501C= (p.Asp167=)
c.543C= (p.Asp181=)
n.477C=
1g.17024072G>TCA338271475SDHBc.372C>A (p.Asp124Glu)
c.501C>A (p.Asp167Glu)
c.543C>A (p.Asp181Glu)
n.477C>A
 ClinVar gnomAD v4
1g.17024074_17024078delCA2695202245SDHBc.370-2_372del
c.499-2_501del
c.541-2_543del
n.475-2_477del
1g.17024073T>ACA18663251SDHBc.371A>T (p.Asp124Val)
c.500A>T (p.Asp167Val)
c.542A>T (p.Asp181Val)
n.476A>T
 dbSNP
1g.17024073T>CCA338271481SDHBc.371A>G (p.Asp124Gly)
c.500A>G (p.Asp167Gly)
c.542A>G (p.Asp181Gly)
n.476A>G
 gnomAD v4
1g.17024073T>GCA338271484SDHBc.371A>C (p.Asp124Ala)
c.500A>C (p.Asp167Ala)
c.542A>C (p.Asp181Ala)
n.476A>C
1g.17024073T=CA1156078671SDHBc.371A= (p.Asp124=)
c.500A= (p.Asp167=)
c.542A= (p.Asp181=)
n.476A=
1g.17024074C>ACA338271490SDHBc.370G>T (p.Asp124Tyr)
c.499G>T (p.Asp167Tyr)
c.541G>T (p.Asp181Tyr)
n.475G>T
1g.17024074C=CA1143479027SDHBc.370G= (p.Asp124=)
c.499G= (p.Asp167=)
c.541G= (p.Asp181=)
n.475G=
1g.17024074C>GCA338271495SDHBc.370G>C (p.Asp124His)
c.499G>C (p.Asp167His)
c.541G>C (p.Asp181His)
n.475G>C
1g.17024074C>TCA089665SDHBc.370G>A (p.Asp124Asn)
c.499G>A (p.Asp167Asn)
c.541G>A (p.Asp181Asn)
n.475G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17024075dupCA2586964053SDHBc.370dup
c.499dup
c.541dup
n.475dup
1g.17024075C>ACA338271499SDHBc.370-1G>T (n.370-1G>T)
c.499-1G>T (n.499-1G>T)
c.541-1G>T (n.541-1G>T)
n.475-1G>T
 ClinVar dbSNP
1g.17024075C=CA1156078672SDHBc.370-1G= (n.370-1G=)
c.499-1G= (n.499-1G=)
c.541-1G= (n.541-1G=)
n.475-1G=
1g.17024075C>GCA338271505SDHBc.370-1G>C (n.370-1G>C)
c.499-1G>C (n.499-1G>C)
c.541-1G>C (n.541-1G>C)
n.475-1G>C
1g.17024075C>TCA338271507SDHBc.370-1G>A (n.370-1G>A)
c.499-1G>A (n.499-1G>A)
c.541-1G>A (n.541-1G>A)
n.475-1G>A
1g.17024076T>ACA338271509SDHBc.370-2A>T (n.370-2A>T)
c.499-2A>T (n.499-2A>T)
c.541-2A>T (n.541-2A>T)
n.475-2A>T
1g.17024076T>CCA015950SDHBc.370-2A>G (n.370-2A>G)
c.499-2A>G (n.499-2A>G)
c.541-2A>G (n.541-2A>G)
n.475-2A>G
 ClinVar dbSNP
1g.17024076T>GCA338271513SDHBc.370-2A>C (n.370-2A>C)
c.499-2A>C (n.499-2A>C)
c.541-2A>C (n.541-2A>C)
n.475-2A>C
1g.17024076T=CA1156078673SDHBc.370-2A= (n.370-2A=)
c.499-2A= (n.499-2A=)
c.541-2A= (n.541-2A=)
n.475-2A=
1g.17024077_17024078delCA2574235528SDHBc.370-3_370-2del (n.370-3_370-2del)
c.499-3_499-2del (n.499-3_499-2del)
c.541-3_541-2del (n.541-3_541-2del)
n.475-3_475-2del
1g.17024079_17024107dupCA637816SDHBc.370-30_370-2dup (n.370-30_370-2dup)
c.499-30_499-2dup (n.499-30_499-2dup)
c.541-30_541-2dup (n.541-30_541-2dup)
n.475-30_475-2dup
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17024077G>ACA089659SDHBc.370-3C>T (n.370-3C>T)
c.499-3C>T (n.499-3C>T)
c.541-3C>T (n.541-3C>T)
n.475-3C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17024077G>CCA2580060642SDHBc.370-3C>G (n.370-3C>G)
c.499-3C>G (n.499-3C>G)
c.541-3C>G (n.541-3C>G)
n.475-3C>G
 ClinVar dbSNP
1g.17024077G=CA1156078674SDHBc.370-3C= (n.370-3C=)
c.499-3C= (n.499-3C=)
c.541-3C= (n.541-3C=)
n.475-3C=
1g.17024077G>TCA2573130775SDHBc.370-3C>A (n.370-3C>A)
c.499-3C>A (n.499-3C>A)
c.541-3C>A (n.541-3C>A)
n.475-3C>A
 ClinVar dbSNP gnomAD v4
1g.17024078T>ACA2573130776SDHBc.370-4A>T (n.370-4A>T)
c.499-4A>T (n.499-4A>T)
c.541-4A>T (n.541-4A>T)
n.475-4A>T
 ClinVar dbSNP gnomAD v4
1g.17024078T>CCA1156078676SDHBc.370-4A>G (n.370-4A>G)
c.499-4A>G (n.499-4A>G)
c.541-4A>G (n.541-4A>G)
n.475-4A>G
 dbSNP
1g.17024078T=CA1156078675SDHBc.370-4A= (n.370-4A=)
c.499-4A= (n.499-4A=)
c.541-4A= (n.541-4A=)
n.475-4A=
1g.17024079A>GCA2499214297SDHBc.370-5T>C (n.370-5T>C)
c.499-5T>C (n.499-5T>C)
c.541-5T>C (n.541-5T>C)
n.475-5T>C
 ClinVar dbSNP gnomAD v4
1g.17024080T>ACA521038149SDHBc.370-6A>T (n.370-6A>T)
c.499-6A>T (n.499-6A>T)
c.541-6A>T (n.541-6A>T)
n.475-6A>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17024080T>CCA658795408SDHBc.370-6A>G (n.370-6A>G)
c.499-6A>G (n.499-6A>G)
c.541-6A>G (n.541-6A>G)
n.475-6A>G
 ClinVar dbSNP gnomAD v4
1g.17024080T=CA1156078677SDHBc.370-6A= (n.370-6A=)
c.499-6A= (n.499-6A=)
c.541-6A= (n.541-6A=)
n.475-6A=
1g.17024081G>ACA18663270SDHBc.370-7C>T (n.370-7C>T)
c.499-7C>T (n.499-7C>T)
c.541-7C>T (n.541-7C>T)
n.475-7C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17024081G>CCA2499214298SDHBc.370-7C>G (n.370-7C>G)
c.499-7C>G (n.499-7C>G)
c.541-7C>G (n.541-7C>G)
n.475-7C>G
 ClinVar dbSNP gnomAD v4
1g.17024081G=CA1143490350SDHBc.370-7C= (n.370-7C=)
c.499-7C= (n.499-7C=)
c.541-7C= (n.541-7C=)
n.475-7C=
1g.17024081G>TCA2643677017SDHBc.370-7C>A (n.370-7C>A)
c.499-7C>A (n.499-7C>A)
c.541-7C>A (n.541-7C>A)
n.475-7C>A
 gnomAD v4
1g.17024081_17024082delinsCTCA2582341893SDHBc.370-8_370-7delinsAG (n.370-8_370-7delinsAG)
c.499-8_499-7delinsAG (n.499-8_499-7delinsAG)
c.541-8_541-7delinsAG (n.541-8_541-7delinsAG)
n.475-8_475-7delinsAG
 ClinVar
1g.17024084delCA2643677016SDHBc.370-7del (n.370-7del)
c.499-7del (n.499-7del)
c.541-7del (n.541-7del)
n.475-7del
 gnomAD v4
1g.17024082G>ACA2574235543SDHBc.370-8C>T (n.370-8C>T)
c.499-8C>T (n.499-8C>T)
c.541-8C>T (n.541-8C>T)
n.475-8C>T
 ClinVar gnomAD v4
1g.17024082G>CCA915941154SDHBc.370-8C>G (n.370-8C>G)
c.499-8C>G (n.499-8C>G)
c.541-8C>G (n.541-8C>G)
n.475-8C>G
 ClinVar dbSNP
1g.17024082G=CA1156078678SDHBc.370-8C= (n.370-8C=)
c.499-8C= (n.499-8C=)
c.541-8C= (n.541-8C=)
n.475-8C=
1g.17024082G>TCA2643677019SDHBc.370-8C>A (n.370-8C>A)
c.499-8C>A (n.499-8C>A)
c.541-8C>A (n.541-8C>A)
n.475-8C>A
 gnomAD v4
1g.17024083_17024093dupCA658656887SDHBc.370-18_370-8dup (n.370-18_370-8dup)
c.499-18_499-8dup (n.499-18_499-8dup)
c.541-18_541-8dup (n.541-18_541-8dup)
n.475-18_475-8dup
 ClinVar dbSNP gnomAD v4
1g.17024083G>ACA089664SDHBc.370-9C>T (n.370-9C>T)
c.499-9C>T (n.499-9C>T)
c.541-9C>T (n.541-9C>T)
n.475-9C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024083G=CA1156078679SDHBc.370-9C= (n.370-9C=)
c.499-9C= (n.499-9C=)
c.541-9C= (n.541-9C=)
n.475-9C=
1g.17024083G>TCA2643677020SDHBc.370-9C>A (n.370-9C>A)
c.499-9C>A (n.499-9C>A)
c.541-9C>A (n.541-9C>A)
n.475-9C>A
 gnomAD v4
1g.17024084G>ACA18663280SDHBc.370-10C>T (n.370-10C>T)
c.499-10C>T (n.499-10C>T)
c.541-10C>T (n.541-10C>T)
n.475-10C>T
 ClinVar dbSNP gnomAD v4
1g.17024084G>CCA2643677021SDHBc.370-10C>G (n.370-10C>G)
c.499-10C>G (n.499-10C>G)
c.541-10C>G (n.541-10C>G)
n.475-10C>G
 gnomAD v4
1g.17024084G=CA1143388259SDHBc.370-10C= (n.370-10C=)
c.499-10C= (n.499-10C=)
c.541-10C= (n.541-10C=)
n.475-10C=
1g.17024084G>TCA2643677022SDHBc.370-10C>A (n.370-10C>A)
c.499-10C>A (n.499-10C>A)
c.541-10C>A (n.541-10C>A)
n.475-10C>A
 gnomAD v4
1g.17024085A=CA1156078680SDHBc.370-11T= (n.370-11T=)
c.499-11T= (n.499-11T=)
c.541-11T= (n.541-11T=)
n.475-11T=
1g.17024085A>CCA915941155SDHBc.370-11T>G (n.370-11T>G)
c.499-11T>G (n.499-11T>G)
c.541-11T>G (n.541-11T>G)
n.475-11T>G
 ClinVar dbSNP
1g.17024085A>GCA18663284SDHBc.370-11T>C (n.370-11T>C)
c.499-11T>C (n.499-11T>C)
c.541-11T>C (n.541-11T>C)
n.475-11T>C
 ClinVar dbSNP
1g.17024086G>ACA2643677027SDHBc.370-12C>T (n.370-12C>T)
c.499-12C>T (n.499-12C>T)
c.541-12C>T (n.541-12C>T)
n.475-12C>T
 ClinVar gnomAD v4
1g.17024086G>TCA2643677028SDHBc.370-12C>A (n.370-12C>A)
c.499-12C>A (n.499-12C>A)
c.541-12C>A (n.541-12C>A)
n.475-12C>A
 gnomAD v4
1g.17024090delCA2643677029SDHBc.370-13del (n.370-13del)
c.499-13del (n.499-13del)
c.541-13del (n.541-13del)
n.475-13del
 gnomAD v4
1g.17024089_17024090delCA2573130777SDHBc.370-14_370-13del (n.370-14_370-13del)
c.499-14_499-13del (n.499-14_499-13del)
c.541-14_541-13del (n.541-14_541-13del)
n.475-14_475-13del
 ClinVar dbSNP
1g.17024088A=CA1156078681SDHBc.370-14T= (n.370-14T=)
c.499-14T= (n.499-14T=)
c.541-14T= (n.541-14T=)
n.475-14T=
1g.17024088A>GCA999082566SDHBc.370-14T>C (n.370-14T>C)
c.499-14T>C (n.499-14T>C)
c.541-14T>C (n.541-14T>C)
n.475-14T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17024090A=CA1156078682SDHBc.370-16T= (n.370-16T=)
c.499-16T= (n.499-16T=)
c.541-16T= (n.541-16T=)
n.475-16T=
1g.17024090A>CCA2740090527SDHBc.370-16T>G (n.370-16T>G)
c.499-16T>G (n.499-16T>G)
c.541-16T>G (n.541-16T>G)
n.475-16T>G
 ClinVar
1g.17024090A>GCA2643677030SDHBc.370-16T>C (n.370-16T>C)
c.499-16T>C (n.499-16T>C)
c.541-16T>C (n.541-16T>C)
n.475-16T>C
 dbSNP gnomAD v4
1g.17024094_17024095delCA2580611149SDHBc.370-17_370-16del (n.370-17_370-16del)
c.499-17_499-16del (n.499-17_499-16del)
c.541-17_541-16del (n.541-17_541-16del)
n.475-17_475-16del
 ClinVar gnomAD v4
1g.17024091G>CCA1156078685SDHBc.370-17C>G (n.370-17C>G)
c.499-17C>G (n.499-17C>G)
c.541-17C>G (n.541-17C>G)
n.475-17C>G
 ClinVar dbSNP gnomAD v4
1g.17024091G=CA1156078684SDHBc.370-17C= (n.370-17C=)
c.499-17C= (n.499-17C=)
c.541-17C= (n.541-17C=)
n.475-17C=
1g.17024091G>TCA2643677032SDHBc.370-17C>A (n.370-17C>A)
c.499-17C>A (n.499-17C>A)
c.541-17C>A (n.541-17C>A)
n.475-17C>A
 gnomAD v4
1g.17024091dupCA1156078683SDHBc.370-17dup (n.370-17dup)
c.499-17dup (n.499-17dup)
c.541-17dup (n.541-17dup)
n.475-17dup
 dbSNP
1g.17024093G>CCA089648SDHBc.370-19C>G (n.370-19C>G)
c.499-19C>G (n.499-19C>G)
c.541-19C>G (n.541-19C>G)
n.475-19C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024093G=CA1156078686SDHBc.370-19C= (n.370-19C=)
c.499-19C= (n.499-19C=)
c.541-19C= (n.541-19C=)
n.475-19C=
1g.17024093G>TCA2574235555SDHBc.370-19C>A (n.370-19C>A)
c.499-19C>A (n.499-19C>A)
c.541-19C>A (n.541-19C>A)
n.475-19C>A
1g.17024095G>ACA1156078688SDHBc.370-21C>T (n.370-21C>T)
c.499-21C>T (n.499-21C>T)
c.541-21C>T (n.541-21C>T)
n.475-21C>T
 dbSNP
1g.17024095G=CA1156078687SDHBc.370-21C= (n.370-21C=)
c.499-21C= (n.499-21C=)
c.541-21C= (n.541-21C=)
n.475-21C=
1g.17024095G>TCA2643677037SDHBc.370-21C>A (n.370-21C>A)
c.499-21C>A (n.499-21C>A)
c.541-21C>A (n.541-21C>A)
n.475-21C>A
 gnomAD v4
1g.17024096G>TCA2643677038SDHBc.370-22C>A (n.370-22C>A)
c.499-22C>A (n.499-22C>A)
c.541-22C>A (n.541-22C>A)
n.475-22C>A
 gnomAD v4
1g.17024097C>ACA089650SDHBc.370-23G>T (n.370-23G>T)
c.499-23G>T (n.499-23G>T)
c.541-23G>T (n.541-23G>T)
n.475-23G>T
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024097C=CA1148896358SDHBc.370-23G= (n.370-23G=)
c.499-23G= (n.499-23G=)
c.541-23G= (n.541-23G=)
n.475-23G=
1g.17024097C>TCA089649SDHBc.370-23G>A (n.370-23G>A)
c.499-23G>A (n.499-23G>A)
c.541-23G>A (n.541-23G>A)
n.475-23G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024098A>TCA2643677040SDHBc.370-24T>A (n.370-24T>A)
c.499-24T>A (n.499-24T>A)
c.541-24T>A (n.541-24T>A)
n.475-24T>A
 gnomAD v4
1g.17024099G>ACA1156078690SDHBc.370-25C>T (n.370-25C>T)
c.499-25C>T (n.499-25C>T)
c.541-25C>T (n.541-25C>T)
n.475-25C>T
 dbSNP
1g.17024099G>CCA089651SDHBc.370-25C>G (n.370-25C>G)
c.499-25C>G (n.499-25C>G)
c.541-25C>G (n.541-25C>G)
n.475-25C>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17024099G=CA1156078689SDHBc.370-25C= (n.370-25C=)
c.499-25C= (n.499-25C=)
c.541-25C= (n.541-25C=)
n.475-25C=
1g.17024099G>TCA2643677041SDHBc.370-25C>A (n.370-25C>A)
c.499-25C>A (n.499-25C>A)
c.541-25C>A (n.541-25C>A)
n.475-25C>A
 gnomAD v4
1g.17024101A=CA1148237128SDHBc.370-27T= (n.370-27T=)
c.499-27T= (n.499-27T=)
c.541-27T= (n.541-27T=)
n.475-27T=
1g.17024101A>CCA089652SDHBc.370-27T>G (n.370-27T>G)
c.499-27T>G (n.499-27T>G)
c.541-27T>G (n.541-27T>G)
n.475-27T>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17024101A>TCA2574235561SDHBc.370-27T>A (n.370-27T>A)
c.499-27T>A (n.499-27T>A)
c.541-27T>A (n.541-27T>A)
n.475-27T>A
1g.17024102G>TCA2643677043SDHBc.370-28C>A (n.370-28C>A)
c.499-28C>A (n.499-28C>A)
c.541-28C>A (n.541-28C>A)
n.475-28C>A
 gnomAD v4
1g.17024103C>ACA2643677044SDHBc.370-29G>T (n.370-29G>T)
c.499-29G>T (n.499-29G>T)
c.541-29G>T (n.541-29G>T)
n.475-29G>T
 gnomAD v4
1g.17024104T>CCA2643677045SDHBc.370-30A>G (n.370-30A>G)
c.499-30A>G (n.499-30A>G)
c.541-30A>G (n.541-30A>G)
n.475-30A>G
 gnomAD v4
1g.17024104T>GCA2643677046SDHBc.370-30A>C (n.370-30A>C)
c.499-30A>C (n.499-30A>C)
c.541-30A>C (n.541-30A>C)
n.475-30A>C
 gnomAD v4
1g.17024105_17024110delinsTGTGACCA1156078691SDHBc.370-36_370-31delinsGTCACA (n.370-36_370-31delinsGTCACA)
c.499-36_499-31delinsGTCACA (n.499-36_499-31delinsGTCACA)
c.541-36_541-31delinsGTCACA (n.541-36_541-31delinsGTCACA)
n.475-36_475-31delinsGTCACA
1g.17024106G>ACA089653SDHBc.370-32C>T (n.370-32C>T)
c.499-32C>T (n.499-32C>T)
c.541-32C>T (n.541-32C>T)
n.475-32C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024106G>CCA521038163SDHBc.370-32C>G (n.370-32C>G)
c.499-32C>G (n.499-32C>G)
c.541-32C>G (n.541-32C>G)
n.475-32C>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17024106G=CA1156078692SDHBc.370-32C= (n.370-32C=)
c.499-32C= (n.499-32C=)
c.541-32C= (n.541-32C=)
n.475-32C=
1g.17024106G>TCA2643677050SDHBc.370-32C>A (n.370-32C>A)
c.499-32C>A (n.499-32C>A)
c.541-32C>A (n.541-32C>A)
n.475-32C>A
 gnomAD v4
1g.17024107_17024111delCA521038159SDHBc.370-36_370-32del (n.370-36_370-32del)
c.499-36_499-32del (n.499-36_499-32del)
c.541-36_541-32del (n.541-36_541-32del)
n.475-36_475-32del
 dbSNP gnomAD v2 gnomAD v4
1g.17024107T>CCA089654SDHBc.370-33A>G (n.370-33A>G)
c.499-33A>G (n.499-33A>G)
c.541-33A>G (n.541-33A>G)
n.475-33A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024107T=CA1156078693SDHBc.370-33A= (n.370-33A=)
c.499-33A= (n.499-33A=)
c.541-33A= (n.541-33A=)
n.475-33A=
1g.17024108G>TCA2574235567SDHBc.370-34C>A (n.370-34C>A)
c.499-34C>A (n.499-34C>A)
c.541-34C>A (n.541-34C>A)
n.475-34C>A
 gnomAD v4
1g.17024109A=CA1148413905SDHBc.370-35T= (n.370-35T=)
c.499-35T= (n.499-35T=)
c.541-35T= (n.541-35T=)
n.475-35T=
1g.17024109A>CCA2695245765SDHBc.370-35T>G (n.370-35T>G)
c.499-35T>G (n.499-35T>G)
c.541-35T>G (n.541-35T>G)
n.475-35T>G
 dbSNP
1g.17024109A>GCA089655SDHBc.370-35T>C (n.370-35T>C)
c.499-35T>C (n.499-35T>C)
c.541-35T>C (n.541-35T>C)
n.475-35T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024110C=CA1145031135SDHBc.370-36G= (n.370-36G=)
c.499-36G= (n.499-36G=)
c.541-36G= (n.541-36G=)
n.475-36G=
1g.17024110C>TCA089656SDHBc.370-36G>A (n.370-36G>A)
c.499-36G>A (n.499-36G>A)
c.541-36G>A (n.541-36G>A)
n.475-36G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched