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.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
 ClinVar
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
 ClinVar 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
 ClinVar
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
1g.17027827C>ACA338273039SDHBc.291G>T (p.Glu97Asp)
c.420G>T (p.Glu140Asp)
c.462G>T (p.Glu154Asp)
n.379G>T
n.396G>T
 dbSNP
1g.17027827C=CA1156080189SDHBc.291G= (p.Glu97=)
c.420G= (p.Glu140=)
c.462G= (p.Glu154=)
n.379G=
n.396G=
1g.17027827C>GCA338273042SDHBc.291G>C (p.Glu97Asp)
c.420G>C (p.Glu140Asp)
c.462G>C (p.Glu154Asp)
n.379G>C
n.396G>C
1g.17027827C>TCA416086167SDHBc.291G>A (p.Glu97=)
c.420G>A (p.Glu140=)
c.462G>A (p.Glu154=)
n.379G>A
n.396G>A
1g.17027828T>ACA338273045SDHBc.290A>T (p.Glu97Val)
c.419A>T (p.Glu140Val)
c.461A>T (p.Glu154Val)
n.378A>T
n.395A>T
1g.17027828T>CCA18665969SDHBc.290A>G (p.Glu97Gly)
c.419A>G (p.Glu140Gly)
c.461A>G (p.Glu154Gly)
n.378A>G
n.395A>G
 dbSNP
1g.17027828T>GCA338273064SDHBc.290A>C (p.Glu97Ala)
c.419A>C (p.Glu140Ala)
c.461A>C (p.Glu154Ala)
n.378A>C
n.395A>C
1g.17027828T=CA1145610940SDHBc.290A= (p.Glu97=)
c.419A= (p.Glu140=)
c.461A= (p.Glu154=)
n.378A=
n.395A=
1g.17027829C>ACA338273088SDHBc.289G>T (p.Glu97Ter)
c.418G>T (p.Glu140Ter)
c.460G>T (p.Glu154Ter)
n.377G>T
n.394G>T
1g.17027829C>GCA338273086SDHBc.289G>C (p.Glu97Gln)
c.418G>C (p.Glu140Gln)
c.460G>C (p.Glu154Gln)
n.377G>C
n.394G>C
1g.17027829C>TCA338273078SDHBc.289G>A (p.Glu97Lys)
c.418G>A (p.Glu140Lys)
c.460G>A (p.Glu154Lys)
n.377G>A
n.394G>A
1g.17027830A>CCA338273091SDHBc.288T>G (p.Ile96Met)
c.417T>G (p.Ile139Met)
c.459T>G (p.Ile153Met)
n.376T>G
n.393T>G
1g.17027830A>GCA416086179SDHBc.288T>C (p.Ile96=)
c.417T>C (p.Ile139=)
c.459T>C (p.Ile153=)
n.376T>C
n.393T>C
 ClinVar gnomAD v4
1g.17027830A>TCA416086181SDHBc.288T>A (p.Ile96=)
c.417T>A (p.Ile139=)
c.459T>A (p.Ile153=)
n.376T>A
n.393T>A
1g.17027831A=CA1156080190SDHBc.287T= (p.Ile96=)
c.416T= (p.Ile139=)
c.458T= (p.Ile153=)
n.375T=
n.392T=
1g.17027831A>CCA338273104SDHBc.287T>G (p.Ile96Ser)
c.416T>G (p.Ile139Ser)
c.458T>G (p.Ile153Ser)
n.375T>G
n.392T>G
1g.17027831A>GCA338273094SDHBc.287T>C (p.Ile96Thr)
c.416T>C (p.Ile139Thr)
c.458T>C (p.Ile153Thr)
n.375T>C
n.392T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17027831A>TCA338273097SDHBc.287T>A (p.Ile96Asn)
c.416T>A (p.Ile139Asn)
c.458T>A (p.Ile153Asn)
n.375T>A
n.392T>A
1g.17027832T>ACA338273110SDHBc.286A>T (p.Ile96Phe)
c.415A>T (p.Ile139Phe)
c.457A>T (p.Ile153Phe)
n.374A>T
n.391A>T
 ClinVar dbSNP
1g.17027832T>CCA338273114SDHBc.286A>G (p.Ile96Val)
c.415A>G (p.Ile139Val)
c.457A>G (p.Ile153Val)
n.374A>G
n.391A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17027832T>GCA338273130SDHBc.286A>C (p.Ile96Leu)
c.415A>C (p.Ile139Leu)
c.457A>C (p.Ile153Leu)
n.374A>C
n.391A>C
 gnomAD v4
1g.17027832T=CA1156080191SDHBc.286A= (p.Ile96=)
c.415A= (p.Ile139=)
c.457A= (p.Ile153=)
n.374A=
n.391A=
1g.17027833G>ACA416086199SDHBc.285C>T (p.Ser95=)
c.414C>T (p.Ser138=)
c.456C>T (p.Ser152=)
n.373C>T
n.390C>T
 ClinVar dbSNP
1g.17027833G>CCA416086202SDHBc.285C>G (p.Ser95=)
c.414C>G (p.Ser138=)
c.456C>G (p.Ser152=)
n.373C>G
n.390C>G
1g.17027833G=CA1156080192SDHBc.285C= (p.Ser95=)
c.414C= (p.Ser138=)
c.456C= (p.Ser152=)
n.373C=
n.390C=
1g.17027833G>TCA416086203SDHBc.285C>A (p.Ser95=)
c.414C>A (p.Ser138=)
c.456C>A (p.Ser152=)
n.373C>A
n.390C>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17027834G>ACA089629SDHBc.284C>T (p.Ser95Phe)
c.413C>T (p.Ser138Phe)
c.455C>T (p.Ser152Phe)
n.372C>T
n.389C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17027834G>CCA338273136SDHBc.284C>G (p.Ser95Cys)
c.413C>G (p.Ser138Cys)
c.455C>G (p.Ser152Cys)
n.372C>G
n.389C>G
1g.17027834G=CA1143415682SDHBc.284C= (p.Ser95=)
c.413C= (p.Ser138=)
c.455C= (p.Ser152=)
n.372C=
n.389C=
1g.17027834G>TCA338273140SDHBc.284C>A (p.Ser95Tyr)
c.413C>A (p.Ser138Tyr)
c.455C>A (p.Ser152Tyr)
n.372C>A
n.389C>A
 ClinVar dbSNP
1g.17027835A=CA1156080193SDHBc.283T= (p.Ser95=)
c.412T= (p.Ser138=)
c.454T= (p.Ser152=)
n.371T=
n.388T=
1g.17027835A>CCA338273142SDHBc.283T>G (p.Ser95Ala)
c.412T>G (p.Ser138Ala)
c.454T>G (p.Ser152Ala)
n.371T>G
n.388T>G
1g.17027835A>GCA10608342SDHBc.283T>C (p.Ser95Pro)
c.412T>C (p.Ser138Pro)
c.454T>C (p.Ser152Pro)
n.371T>C
n.388T>C
 ClinVar dbSNP gnomAD v4
1g.17027835A>TCA338273143SDHBc.283T>A (p.Ser95Thr)
c.412T>A (p.Ser138Thr)
c.454T>A (p.Ser152Thr)
n.371T>A
n.388T>A
1g.17027836T>ACA338273144SDHBc.282A>T (p.Lys94Asn)
c.411A>T (p.Lys137Asn)
c.453A>T (p.Lys151Asn)
n.370A>T
n.387A>T
1g.17027836T>CCA416086220SDHBc.282A>G (p.Lys94=)
c.411A>G (p.Lys137=)
c.453A>G (p.Lys151=)
n.370A>G
n.387A>G
 ClinVar dbSNP
1g.17027836T>GCA338273145SDHBc.282A>C (p.Lys94Asn)
c.411A>C (p.Lys137Asn)
c.453A>C (p.Lys151Asn)
n.370A>C
n.387A>C
1g.17027836T=CA1156080194SDHBc.282A= (p.Lys94=)
c.411A= (p.Lys137=)
c.453A= (p.Lys151=)
n.370A=
n.387A=
1g.17027838delCA2586964061SDHBc.282del (p.Lys94AsnfsTer7)
c.411del (p.Lys137AsnfsTer7)
c.453del (p.Lys151AsnfsTer7)
n.370del
n.387del
1g.17027836_17027840delCA2586964060SDHBc.278_282del (p.Tyr93PhefsTer3)
c.407_411del (p.Tyr136PhefsTer3)
c.449_453del (p.Tyr150PhefsTer3)
n.366_370del
n.383_387del
1g.17027837T>ACA338273146SDHBc.281A>T (p.Lys94Ile)
c.410A>T (p.Lys137Ile)
c.452A>T (p.Lys151Ile)
n.369A>T
n.386A>T
1g.17027837T>CCA338273152SDHBc.281A>G (p.Lys94Arg)
c.410A>G (p.Lys137Arg)
c.452A>G (p.Lys151Arg)
n.369A>G
n.386A>G
 ClinVar
1g.17027837T>GCA338273147SDHBc.281A>C (p.Lys94Thr)
c.410A>C (p.Lys137Thr)
c.452A>C (p.Lys151Thr)
n.369A>C
n.386A>C
 ClinVar
1g.17027838T>ACA338273153SDHBc.280A>T (p.Lys94Ter)
c.409A>T (p.Lys137Ter)
c.451A>T (p.Lys151Ter)
n.368A>T
n.385A>T
1g.17027838T>CCA338273154SDHBc.280A>G (p.Lys94Glu)
c.409A>G (p.Lys137Glu)
c.451A>G (p.Lys151Glu)
n.368A>G
n.385A>G
 ClinVar dbSNP
1g.17027838T>GCA338273155SDHBc.280A>C (p.Lys94Gln)
c.409A>C (p.Lys137Gln)
c.451A>C (p.Lys151Gln)
n.368A>C
n.385A>C
1g.17027839G>ACA416086240SDHBc.279C>T (p.Tyr93=)
c.408C>T (p.Tyr136=)
c.450C>T (p.Tyr150=)
n.367C>T
n.384C>T
 gnomAD v4
1g.17027839G>CCA338273181SDHBc.279C>G (p.Tyr93Ter)
c.408C>G (p.Tyr136Ter)
c.450C>G (p.Tyr150Ter)
n.367C>G
n.384C>G
 ClinVar dbSNP
1g.17027839G>TCA338273186SDHBc.279C>A (p.Tyr93Ter)
c.408C>A (p.Tyr136Ter)
c.450C>A (p.Tyr150Ter)
n.367C>A
n.384C>A
1g.17027840T>ACA338273198SDHBc.278A>T (p.Tyr93Phe)
c.407A>T (p.Tyr136Phe)
c.449A>T (p.Tyr150Phe)
n.366A>T
n.383A>T
1g.17027840T>CCA338273209SDHBc.278A>G (p.Tyr93Cys)
c.407A>G (p.Tyr136Cys)
c.449A>G (p.Tyr150Cys)
n.366A>G
n.383A>G
1g.17027840T>GCA338273242SDHBc.278A>C (p.Tyr93Ser)
c.407A>C (p.Tyr136Ser)
c.449A>C (p.Tyr150Ser)
n.366A>C
n.383A>C
1g.17027841A>CCA338273255SDHBc.277T>G (p.Tyr93Asp)
c.406T>G (p.Tyr136Asp)
c.448T>G (p.Tyr150Asp)
n.365T>G
n.382T>G
1g.17027841A>GCA338273265SDHBc.277T>C (p.Tyr93His)
c.406T>C (p.Tyr136His)
c.448T>C (p.Tyr150His)
n.365T>C
n.382T>C
 ClinVar dbSNP
1g.17027841A>TCA338273269SDHBc.277T>A (p.Tyr93Asn)
c.406T>A (p.Tyr136Asn)
c.448T>A (p.Tyr150Asn)
n.365T>A
n.382T>A
1g.17027841_17027844delinsACTGCA1156080195SDHBc.274_277delinsCAGT (p.Gln92=)
c.403_406delinsCAGT (p.Gln135=)
c.445_448delinsCAGT (p.Gln149=)
n.362_365delinsCAGT
n.379_382delinsCAGT
1g.17027842C>ACA18665993SDHBc.276G>T (p.Gln92His)
c.405G>T (p.Gln135His)
c.447G>T (p.Gln149His)
n.364G>T
n.381G>T
 ClinVar dbSNP gnomAD v4
1g.17027842C=CA1143411882SDHBc.276G= (p.Gln92=)
c.405G= (p.Gln135=)
c.447G= (p.Gln149=)
n.364G=
n.381G=
1g.17027842C>GCA338273273SDHBc.276G>C (p.Gln92His)
c.405G>C (p.Gln135His)
c.447G>C (p.Gln149His)
n.364G>C
n.381G>C
1g.17027842C>TCA416086252SDHBc.276G>A (p.Gln92=)
c.405G>A (p.Gln135=)
c.447G>A (p.Gln149=)
n.364G>A
n.381G>A
 ClinVar dbSNP
1g.17027842_17027844delinsAGATACCCA645509078SDHBc.274_276delinsGGTATCT (p.Gln92GlyfsTer7)
c.403_405delinsGGTATCT (p.Gln135GlyfsTer7)
c.445_447delinsGGTATCT (p.Gln149GlyfsTer7)
n.362_364delinsGGTATCT
n.379_381delinsGGTATCT
 ClinVar dbSNP
1g.17027843T>ACA338273280SDHBc.275A>T (p.Gln92Leu)
c.404A>T (p.Gln135Leu)
c.446A>T (p.Gln149Leu)
n.363A>T
n.380A>T
1g.17027843T>CCA338273300SDHBc.275A>G (p.Gln92Arg)
c.404A>G (p.Gln135Arg)
c.446A>G (p.Gln149Arg)
n.363A>G
n.380A>G
 ClinVar dbSNP
1g.17027843T>GCA338273303SDHBc.275A>C (p.Gln92Pro)
c.404A>C (p.Gln135Pro)
c.446A>C (p.Gln149Pro)
n.363A>C
n.380A>C
 ClinVar gnomAD v4
1g.17027843T=CA1156080196SDHBc.275A= (p.Gln92=)
c.404A= (p.Gln135=)
c.446A= (p.Gln149=)
n.363A=
n.380A=
1g.17027843_17027844delinsAGATACCCA2586964062SDHBc.274_275delinsGGTATCT (p.Gln92GlyfsTer11)
c.403_404delinsGGTATCT (p.Gln135GlyfsTer11)
c.445_446delinsGGTATCT (p.Gln149GlyfsTer11)
n.362_363delinsGGTATCT
n.379_380delinsGGTATCT
1g.17027845_17027846dupCA2580611151SDHBc.274_275dup (p.Gln92HisfsTer10)
c.403_404dup (p.Gln135HisfsTer10)
c.445_446dup (p.Gln149HisfsTer10)
n.362_363dup
n.379_380dup
 ClinVar dbSNP
1g.17027843_17027844insCCATACA658795406SDHBc.274_275insTATGG (p.Gln92LeufsTer11)
c.403_404insTATGG (p.Gln135LeufsTer11)
c.445_446insTATGG (p.Gln149LeufsTer11)
n.362_363insTATGG
n.379_380insTATGG
 ClinVar dbSNP
1g.17027844delCA2586964063SDHBc.274del (p.Gln92SerfsTer9)
c.403del (p.Gln135SerfsTer9)
c.445del (p.Gln149SerfsTer9)
n.362del
n.379del
1g.17027844G>ACA10577675SDHBc.274C>T (p.Gln92Ter)
c.403C>T (p.Gln135Ter)
c.445C>T (p.Gln149Ter)
n.362C>T
n.379C>T
 ClinVar dbSNP gnomAD v4
1g.17027844G>CCA338273308SDHBc.274C>G (p.Gln92Glu)
c.403C>G (p.Gln135Glu)
c.445C>G (p.Gln149Glu)
n.362C>G
n.379C>G
1g.17027844G=CA1156080197SDHBc.274C= (p.Gln92=)
c.403C= (p.Gln135=)
c.445C= (p.Gln149=)
n.362C=
n.379C=
1g.17027844G>TCA338273310SDHBc.274C>A (p.Gln92Lys)
c.403C>A (p.Gln135Lys)
c.445C>A (p.Gln149Lys)
n.362C>A
n.379C>A
 gnomAD v4
1g.17027845T>ACA416086267SDHBc.273A>T (p.Ala91=)
c.402A>T (p.Ala134=)
c.444A>T (p.Ala148=)
n.361A>T
n.378A>T
 ClinVar
1g.17027845T>CCA416086270SDHBc.273A>G (p.Ala91=)
c.402A>G (p.Ala134=)
c.444A>G (p.Ala148=)
n.361A>G
n.378A>G
1g.17027845T>GCA416086283SDHBc.273A>C (p.Ala91=)
c.402A>C (p.Ala134=)
c.444A>C (p.Ala148=)
n.361A>C
n.378A>C
1g.17027846G>ACA338273312SDHBc.272C>T (p.Ala91Val)
c.401C>T (p.Ala134Val)
c.443C>T (p.Ala148Val)
n.360C>T
n.377C>T
 ClinVar dbSNP
1g.17027846G>CCA338273314SDHBc.272C>G (p.Ala91Gly)
c.401C>G (p.Ala134Gly)
c.443C>G (p.Ala148Gly)
n.360C>G
n.377C>G
1g.17027846G=CA1156080199SDHBc.272C= (p.Ala91=)
c.401C= (p.Ala134=)
c.443C= (p.Ala148=)
n.360C=
n.377C=
1g.17027846G>TCA338273318SDHBc.272C>A (p.Ala91Glu)
c.401C>A (p.Ala134Glu)
c.443C>A (p.Ala148Glu)
n.360C>A
n.377C>A
1g.17027846_17027847delinsGCCA1156080198SDHBc.271_272delinsGC (p.Ala91=)
c.400_401delinsGC (p.Ala134=)
c.442_443delinsGC (p.Ala148=)
n.359_360delinsGC
n.376_377delinsGC
1g.17027847delCA10577676SDHBc.271del (p.Ala91HisfsTer10)
c.400del (p.Ala134HisfsTer10)
c.442del (p.Ala148HisfsTer10)
n.359del
n.376del
 ClinVar dbSNP
1g.17027847C>ACA338273327SDHBc.271G>T (p.Ala91Ser)
c.400G>T (p.Ala134Ser)
c.442G>T (p.Ala148Ser)
n.359G>T
n.376G>T
 ClinVar
1g.17027847C=CA1156080200SDHBc.271G= (p.Ala91=)
c.400G= (p.Ala134=)
c.442G= (p.Ala148=)
n.359G=
n.376G=
1g.17027847C>GCA338273330SDHBc.271G>C (p.Ala91Pro)
c.400G>C (p.Ala134Pro)
c.442G>C (p.Ala148Pro)
n.359G>C
n.376G>C
1g.17027847C>TCA338273338SDHBc.271G>A (p.Ala91Thr)
c.400G>A (p.Ala134Thr)
c.442G>A (p.Ala148Thr)
n.359G>A
n.376G>A
 ClinVar dbSNP
1g.17027848delCA658655539SDHBc.270del (p.Tyr90Ter)
c.399del (p.Tyr133Ter)
c.441del (p.Tyr147Ter)
n.358del
n.375del
1g.17027848A=CA1156080201SDHBc.270T= (p.Tyr90=)
c.399T= (p.Tyr133=)
c.441T= (p.Tyr147=)
n.358T=
n.375T=
1g.17027848A>CCA16609941SDHBc.270T>G (p.Tyr90Ter)
c.399T>G (p.Tyr133Ter)
c.441T>G (p.Tyr147Ter)
n.358T>G
n.375T>G
 ClinVar dbSNP
1g.17027848A>GCA416086308SDHBc.270T>C (p.Tyr90=)
c.399T>C (p.Tyr133=)
c.441T>C (p.Tyr147=)
n.358T>C
n.375T>C
 ClinVar dbSNP
1g.17027848A>TCA338273344SDHBc.270T>A (p.Tyr90Ter)
c.399T>A (p.Tyr133Ter)
c.441T>A (p.Tyr147Ter)
n.358T>A
n.375T>A
1g.17027849T>ACA338273349SDHBc.269A>T (p.Tyr90Phe)
c.398A>T (p.Tyr133Phe)
c.440A>T (p.Tyr147Phe)
n.357A>T
n.374A>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17027849T>CCA089628SDHBc.269A>G (p.Tyr90Cys)
c.398A>G (p.Tyr133Cys)
c.440A>G (p.Tyr147Cys)
n.357A>G
n.374A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17027849T>GCA338273355SDHBc.269A>C (p.Tyr90Ser)
c.398A>C (p.Tyr133Ser)
c.440A>C (p.Tyr147Ser)
n.357A>C
n.374A>C
1g.17027849T=CA1156080202SDHBc.269A= (p.Tyr90=)
c.398A= (p.Tyr133=)
c.440A= (p.Tyr147=)
n.357A=
n.374A=
1g.17027850A>CCA338273356SDHBc.268T>G (p.Tyr90Asp)
c.397T>G (p.Tyr133Asp)
c.439T>G (p.Tyr147Asp)
n.356T>G
n.373T>G
1g.17027850A>GCA338273359SDHBc.268T>C (p.Tyr90His)
c.397T>C (p.Tyr133His)
c.439T>C (p.Tyr147His)
n.356T>C
n.373T>C
 ClinVar
1g.17027850A>TCA338273377SDHBc.268T>A (p.Tyr90Asn)
c.397T>A (p.Tyr133Asn)
c.439T>A (p.Tyr147Asn)
n.356T>A
n.373T>A
1g.17027851G>ACA416086332SDHBc.267C>T (p.Phe89=)
c.396C>T (p.Phe132=)
c.438C>T (p.Phe146=)
n.355C>T
n.372C>T
 gnomAD v4
1g.17027851G>CCA338273382SDHBc.267C>G (p.Phe89Leu)
c.396C>G (p.Phe132Leu)
c.438C>G (p.Phe146Leu)
n.355C>G
n.372C>G
 ClinVar dbSNP
1g.17027851G=CA1156080203SDHBc.267C= (p.Phe89=)
c.396C= (p.Phe132=)
c.438C= (p.Phe146=)
n.355C=
n.372C=
1g.17027851G>TCA338273390SDHBc.267C>A (p.Phe89Leu)
c.396C>A (p.Phe132Leu)
c.438C>A (p.Phe146Leu)
n.355C>A
n.372C>A
 ClinVar dbSNP gnomAD v4
1g.17027852A>CCA338273393SDHBc.266T>G (p.Phe89Cys)
c.395T>G (p.Phe132Cys)
c.437T>G (p.Phe146Cys)
n.354T>G
n.371T>G
1g.17027852A>GCA338273397SDHBc.266T>C (p.Phe89Ser)
c.395T>C (p.Phe132Ser)
c.437T>C (p.Phe146Ser)
n.354T>C
n.371T>C
 ClinVar dbSNP
1g.17027852A>TCA338273400SDHBc.266T>A (p.Phe89Tyr)
c.395T>A (p.Phe132Tyr)
c.437T>A (p.Phe146Tyr)
n.354T>A
n.371T>A
1g.17027853delCA2586964064SDHBc.266del (p.Phe89SerfsTer12)
c.395del (p.Phe132SerfsTer12)
c.437del (p.Phe146SerfsTer12)
n.354del
n.371del
1g.17027853A=CA1156080204SDHBc.265T= (p.Phe89=)
c.394T= (p.Phe132=)
c.436T= (p.Phe146=)
n.353T=
n.370T=
1g.17027853A>CCA338273404SDHBc.265T>G (p.Phe89Val)
c.394T>G (p.Phe132Val)
c.436T>G (p.Phe146Val)
n.353T>G
n.370T>G
 ClinVar dbSNP gnomAD v4
1g.17027853A>GCA338273408SDHBc.265T>C (p.Phe89Leu)
c.394T>C (p.Phe132Leu)
c.436T>C (p.Phe146Leu)
n.353T>C
n.370T>C
1g.17027853A>TCA338273422SDHBc.265T>A (p.Phe89Ile)
c.394T>A (p.Phe132Ile)
c.436T>A (p.Phe146Ile)
n.353T>A
n.370T>A
1g.17027854delCA658655538SDHBc.264del (p.Phe89SerfsTer12)
c.393del (p.Phe132SerfsTer12)
c.435del (p.Phe146SerfsTer12)
n.352del
n.369del
1g.17027854G>ACA416086353SDHBc.264C>T (p.Asn88=)
c.393C>T (p.Asn131=)
c.435C>T (p.Asn145=)
n.352C>T
n.369C>T
 ClinVar dbSNP
1g.17027854G>CCA338273426SDHBc.264C>G (p.Asn88Lys)
c.393C>G (p.Asn131Lys)
c.435C>G (p.Asn145Lys)
n.352C>G
n.369C>G
1g.17027854G>TCA338273425SDHBc.264C>A (p.Asn88Lys)
c.393C>A (p.Asn131Lys)
c.435C>A (p.Asn145Lys)
n.352C>A
n.369C>A
1g.17027855T>ACA18666011SDHBc.263A>T (p.Asn88Ile)
c.392A>T (p.Asn131Ile)
c.434A>T (p.Asn145Ile)
n.351A>T
n.368A>T
 dbSNP gnomAD v4
1g.17027855T>CCA338273454SDHBc.263A>G (p.Asn88Ser)
c.392A>G (p.Asn131Ser)
c.434A>G (p.Asn145Ser)
n.351A>G
n.368A>G
 ClinVar gnomAD v4
1g.17027855T>GCA338273452SDHBc.263A>C (p.Asn88Thr)
c.392A>C (p.Asn131Thr)
c.434A>C (p.Asn145Thr)
n.351A>C
n.368A>C
1g.17027855T=CA1156080205SDHBc.263A= (p.Asn88=)
c.392A= (p.Asn131=)
c.434A= (p.Asn145=)
n.351A=
n.368A=
1g.17027856T>ACA338273455SDHBc.262A>T (p.Asn88Tyr)
c.391A>T (p.Asn131Tyr)
c.433A>T (p.Asn145Tyr)
n.350A>T
n.367A>T
1g.17027856T>CCA338273461SDHBc.262A>G (p.Asn88Asp)
c.391A>G (p.Asn131Asp)
c.433A>G (p.Asn145Asp)
n.350A>G
n.367A>G
1g.17027856T>GCA338273456SDHBc.262A>C (p.Asn88His)
c.391A>C (p.Asn131His)
c.433A>C (p.Asn145His)
n.350A>C
n.367A>C
1g.17027857G>ACA416086378SDHBc.261C>T (p.Ser87=)
c.390C>T (p.Ser130=)
c.432C>T (p.Ser144=)
n.349C>T
n.366C>T
 gnomAD v4
1g.17027857G>CCA338273466SDHBc.261C>G (p.Ser87Arg)
c.390C>G (p.Ser130Arg)
c.432C>G (p.Ser144Arg)
n.349C>G
n.366C>G
 gnomAD v4
1g.17027857G>TCA338273469SDHBc.261C>A (p.Ser87Arg)
c.390C>A (p.Ser130Arg)
c.432C>A (p.Ser144Arg)
n.349C>A
n.366C>A
 gnomAD v4 COSMIC
1g.17027858C>ACA338273480SDHBc.260G>T (p.Ser87Ile)
c.389G>T (p.Ser130Ile)
c.431G>T (p.Ser144Ile)
n.348G>T
n.365G>T
1g.17027858C>GCA338273484SDHBc.260G>C (p.Ser87Thr)
c.389G>C (p.Ser130Thr)
c.431G>C (p.Ser144Thr)
n.348G>C
n.365G>C
1g.17027858C>TCA338273488SDHBc.260G>A (p.Ser87Asn)
c.389G>A (p.Ser130Asn)
c.431G>A (p.Ser144Asn)
n.348G>A
n.365G>A
 gnomAD v4
1g.17027859T>ACA338273491SDHBc.259A>T (p.Ser87Cys)
c.388A>T (p.Ser130Cys)
c.430A>T (p.Ser144Cys)
n.347A>T
n.364A>T
1g.17027859T>CCA338273495SDHBc.259A>G (p.Ser87Gly)
c.388A>G (p.Ser130Gly)
c.430A>G (p.Ser144Gly)
n.347A>G
n.364A>G
1g.17027859T>GCA338273496SDHBc.259A>C (p.Ser87Arg)
c.388A>C (p.Ser130Arg)
c.430A>C (p.Ser144Arg)
n.347A>C
n.364A>C
1g.17027860C>ACA338273497SDHBc.258G>T (p.Leu86Phe)
c.387G>T (p.Leu129Phe)
c.429G>T (p.Leu143Phe)
n.346G>T
n.363G>T
 gnomAD v4
1g.17027860C>GCA338273498SDHBc.258G>C (p.Leu86Phe)
c.387G>C (p.Leu129Phe)
c.429G>C (p.Leu143Phe)
n.346G>C
n.363G>C
1g.17027860C>TCA416086399SDHBc.258G>A (p.Leu86=)
c.387G>A (p.Leu129=)
c.429G>A (p.Leu143=)
n.346G>A
n.363G>A
1g.17027861A>CCA338273499SDHBc.257T>G (p.Leu86Trp)
c.386T>G (p.Leu129Trp)
c.428T>G (p.Leu143Trp)
n.345T>G
n.362T>G
1g.17027861A>GCA338273500SDHBc.257T>C (p.Leu86Ser)
c.386T>C (p.Leu129Ser)
c.428T>C (p.Leu143Ser)
n.345T>C
n.362T>C
1g.17027861A>TCA338273501SDHBc.257T>A (p.Leu86Ter)
c.386T>A (p.Leu129Ter)
c.428T>A (p.Leu143Ter)
n.345T>A
n.362T>A
1g.17027863delCA2574235758SDHBc.257del (p.Leu86Ter)
c.386del (p.Leu129Ter)
c.428del (p.Leu143Ter)
n.345del
n.362del
1g.17027862A=CA1156080206SDHBc.256T= (p.Leu86=)
c.385T= (p.Leu129=)
c.427T= (p.Leu143=)
n.344T=
n.361T=
1g.17027862A>CCA338273502SDHBc.256T>G (p.Leu86Val)
c.385T>G (p.Leu129Val)
c.427T>G (p.Leu143Val)
n.344T>G
n.361T>G
1g.17027862A>GCA416086418SDHBc.256T>C (p.Leu86=)
c.385T>C (p.Leu129=)
c.427T>C (p.Leu143=)
n.344T>C
n.361T>C
1g.17027862A>TCA338273503SDHBc.256T>A (p.Leu86Met)
c.385T>A (p.Leu129Met)
c.427T>A (p.Leu143Met)
n.344T>A
n.361T>A
 ClinVar dbSNP gnomAD v4
1g.17027862_17027872delinsGCA2586964065SDHBc.253-7_256delinsC
c.382-7_385delinsC
c.424-7_427delinsC
n.341-7_344delinsC
n.358-7_361delinsC

Number of alleles fetched