Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.17023974T>ACA338270925SDHBc.470A>T (p.Gln157Leu)
c.599A>T (p.Gln200Leu)
c.641A>T (p.Gln214Leu)
n.575A>T
1g.17023974T>CCA16609928SDHBc.470A>G (p.Gln157Arg)
c.599A>G (p.Gln200Arg)
c.641A>G (p.Gln214Arg)
n.575A>G
 ClinVar dbSNP
1g.17023974T>GCA089682SDHBc.470A>C (p.Gln157Pro)
c.599A>C (p.Gln200Pro)
c.641A>C (p.Gln214Pro)
n.575A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.17023974T=CA1156078611SDHBc.470A= (p.Gln157=)
c.599A= (p.Gln200=)
c.641A= (p.Gln214=)
n.575A=
1g.17023975G>ACA10577671SDHBc.469C>T (p.Gln157Ter)
c.598C>T (p.Gln200Ter)
c.640C>T (p.Gln214Ter)
n.574C>T
 ClinVar dbSNP
1g.17023975G>CCA338270926SDHBc.469C>G (p.Gln157Glu)
c.598C>G (p.Gln200Glu)
c.640C>G (p.Gln214Glu)
n.574C>G
 dbSNP
1g.17023975G=CA1156078612SDHBc.469C= (p.Gln157=)
c.598C= (p.Gln200=)
c.640C= (p.Gln214=)
n.574C=
1g.17023975G>TCA338270927SDHBc.469C>A (p.Gln157Lys)
c.598C>A (p.Gln200Lys)
c.640C>A (p.Gln214Lys)
n.574C>A
1g.17023975_17023976delinsGCCA1156078613SDHBc.468_469delinsGC (p.Met156=)
c.597_598delinsGC (p.Met199=)
c.639_640delinsGC (p.Met213=)
n.573_574delinsGC
1g.17023976delCA645369141SDHBc.468del (p.Met156IlefsTer7)
c.597del (p.Met199IlefsTer7)
c.639del (p.Met213IlefsTer7)
n.573del
c.597del (p.Met199IlefsTer?)
 ClinVar dbSNP
1g.17023976C>ACA338270928SDHBc.468G>T (p.Met156Ile)
c.597G>T (p.Met199Ile)
c.639G>T (p.Met213Ile)
n.573G>T
1g.17023976C>GCA338270929SDHBc.468G>C (p.Met156Ile)
c.597G>C (p.Met199Ile)
c.639G>C (p.Met213Ile)
n.573G>C
1g.17023976C>TCA338270930SDHBc.468G>A (p.Met156Ile)
c.597G>A (p.Met199Ile)
c.639G>A (p.Met213Ile)
n.573G>A
1g.17023977A=CA1143519691SDHBc.467T= (p.Met156=)
c.596T= (p.Met199=)
c.638T= (p.Met213=)
n.572T=
1g.17023977A>CCA338270932SDHBc.467T>G (p.Met156Arg)
c.596T>G (p.Met199Arg)
c.638T>G (p.Met213Arg)
n.572T>G
 ClinVar
1g.17023977A>GCA016054SDHBc.467T>C (p.Met156Thr)
c.596T>C (p.Met199Thr)
c.638T>C (p.Met213Thr)
n.572T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17023977A>TCA338270931SDHBc.467T>A (p.Met156Lys)
c.596T>A (p.Met199Lys)
c.638T>A (p.Met213Lys)
n.572T>A
1g.17023978T>ACA089681SDHBc.466A>T (p.Met156Leu)
c.595A>T (p.Met199Leu)
c.637A>T (p.Met213Leu)
n.571A>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17023978T>CCA16609912SDHBc.466A>G (p.Met156Val)
c.595A>G (p.Met199Val)
c.637A>G (p.Met213Val)
n.571A>G
 ClinVar dbSNP gnomAD v4
1g.17023978T>GCA338270933SDHBc.466A>C (p.Met156Leu)
c.595A>C (p.Met199Leu)
c.637A>C (p.Met213Leu)
n.571A>C
1g.17023978T=CA1156078614SDHBc.466A= (p.Met156=)
c.595A= (p.Met199=)
c.637A= (p.Met213=)
n.571A=
1g.17023978dupCA2580060634SDHBc.466dup (p.Met156AsnfsTer9)
c.595dup (p.Met199AsnfsTer9)
c.637dup (p.Met213AsnfsTer9)
n.571dup
c.595dup (p.Met199AsnfsTer?)
 ClinVar
1g.17023979A=CA1156078615SDHBc.465T= (p.Leu155=)
c.594T= (p.Leu198=)
c.636T= (p.Leu212=)
n.570T=
1g.17023979A>CCA416082777SDHBc.465T>G (p.Leu155=)
c.594T>G (p.Leu198=)
c.636T>G (p.Leu212=)
n.570T>G
1g.17023979A>GCA18663154SDHBc.465T>C (p.Leu155=)
c.594T>C (p.Leu198=)
c.636T>C (p.Leu212=)
n.570T>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17023979A>TCA416082779SDHBc.465T>A (p.Leu155=)
c.594T>A (p.Leu198=)
c.636T>A (p.Leu212=)
n.570T>A
1g.17023980A=CA1156078616SDHBc.464T= (p.Leu155=)
c.593T= (p.Leu198=)
c.635T= (p.Leu212=)
n.569T=
1g.17023980A>CCA338270934SDHBc.464T>G (p.Leu155Arg)
c.593T>G (p.Leu198Arg)
c.635T>G (p.Leu212Arg)
n.569T>G
1g.17023980A>GCA338270935SDHBc.464T>C (p.Leu155Pro)
c.593T>C (p.Leu198Pro)
c.635T>C (p.Leu212Pro)
n.569T>C
 ClinVar gnomAD v4
1g.17023980A>TCA338270936SDHBc.464T>A (p.Leu155His)
c.593T>A (p.Leu198His)
c.635T>A (p.Leu212His)
n.569T>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17023981G>ACA338270937SDHBc.463C>T (p.Leu155Phe)
c.592C>T (p.Leu198Phe)
c.634C>T (p.Leu212Phe)
n.568C>T
 ClinVar dbSNP COSMIC
1g.17023981G>CCA338270938SDHBc.463C>G (p.Leu155Val)
c.592C>G (p.Leu198Val)
c.634C>G (p.Leu212Val)
n.568C>G
 ClinVar dbSNP
1g.17023981G=CA1156078617SDHBc.463C= (p.Leu155=)
c.592C= (p.Leu198=)
c.634C= (p.Leu212=)
n.568C=
1g.17023981G>TCA338270939SDHBc.463C>A (p.Leu155Ile)
c.592C>A (p.Leu198Ile)
c.634C>A (p.Leu212Ile)
n.568C>A
1g.17023982A>CCA416082798SDHBc.462T>G (p.Val154=)
c.591T>G (p.Val197=)
c.633T>G (p.Val211=)
n.567T>G
1g.17023982A>GCA416082801SDHBc.462T>C (p.Val154=)
c.591T>C (p.Val197=)
c.633T>C (p.Val211=)
n.567T>C
1g.17023982A>TCA416082804SDHBc.462T>A (p.Val154=)
c.591T>A (p.Val197=)
c.633T>A (p.Val211=)
n.567T>A
1g.17023983A>CCA338270940SDHBc.461T>G (p.Val154Gly)
c.590T>G (p.Val197Gly)
c.632T>G (p.Val211Gly)
n.566T>G
1g.17023983A>GCA338270941SDHBc.461T>C (p.Val154Ala)
c.590T>C (p.Val197Ala)
c.632T>C (p.Val211Ala)
n.566T>C
 ClinVar dbSNP COSMIC
1g.17023983A>TCA338270942SDHBc.461T>A (p.Val154Asp)
c.590T>A (p.Val197Asp)
c.632T>A (p.Val211Asp)
n.566T>A
1g.17023984C>ACA338270945SDHBc.460G>T (p.Val154Phe)
c.589G>T (p.Val197Phe)
c.631G>T (p.Val211Phe)
n.565G>T
1g.17023984C=CA1156078618SDHBc.460G= (p.Val154=)
c.589G= (p.Val197=)
c.631G= (p.Val211=)
n.565G=
1g.17023984C>GCA338270944SDHBc.460G>C (p.Val154Leu)
c.589G>C (p.Val197Leu)
c.631G>C (p.Val211Leu)
n.565G>C
 ClinVar dbSNP
1g.17023984C>TCA338270943SDHBc.460G>A (p.Val154Ile)
c.589G>A (p.Val197Ile)
c.631G>A (p.Val211Ile)
n.565G>A
 ClinVar dbSNP gnomAD v4
1g.17023985T>ACA416082822SDHBc.459A>T (p.Ala153=)
c.588A>T (p.Ala196=)
c.630A>T (p.Ala210=)
n.564A>T
1g.17023985T>CCA416082823SDHBc.459A>G (p.Ala153=)
c.588A>G (p.Ala196=)
c.630A>G (p.Ala210=)
n.564A>G
 gnomAD v4
1g.17023985T>GCA416082825SDHBc.459A>C (p.Ala153=)
c.588A>C (p.Ala196=)
c.630A>C (p.Ala210=)
n.564A>C
 ClinVar
1g.17023986G>ACA338270946SDHBc.458C>T (p.Ala153Val)
c.587C>T (p.Ala196Val)
c.629C>T (p.Ala210Val)
n.563C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17023986G>CCA338270947SDHBc.458C>G (p.Ala153Gly)
c.587C>G (p.Ala196Gly)
c.629C>G (p.Ala210Gly)
n.563C>G
1g.17023986G=CA1156078619SDHBc.458C= (p.Ala153=)
c.587C= (p.Ala196=)
c.629C= (p.Ala210=)
n.563C=
1g.17023986G>TCA338270948SDHBc.458C>A (p.Ala153Glu)
c.587C>A (p.Ala196Glu)
c.629C>A (p.Ala210Glu)
n.563C>A
1g.17023987C>ACA338270949SDHBc.457G>T (p.Ala153Ser)
c.586G>T (p.Ala196Ser)
c.628G>T (p.Ala210Ser)
n.562G>T
1g.17023987C>GCA338270950SDHBc.457G>C (p.Ala153Pro)
c.586G>C (p.Ala196Pro)
c.628G>C (p.Ala210Pro)
n.562G>C
1g.17023987C>TCA338270951SDHBc.457G>A (p.Ala153Thr)
c.586G>A (p.Ala196Thr)
c.628G>A (p.Ala210Thr)
n.562G>A
 dbSNP
1g.17023988A=CA1156078620SDHBc.456T= (p.Pro152=)
c.585T= (p.Pro195=)
c.627T= (p.Pro209=)
n.561T=
1g.17023988A>CCA416082841SDHBc.456T>G (p.Pro152=)
c.585T>G (p.Pro195=)
c.627T>G (p.Pro209=)
n.561T>G
1g.17023988A>GCA16609932SDHBc.456T>C (p.Pro152=)
c.585T>C (p.Pro195=)
c.627T>C (p.Pro209=)
n.561T>C
 ClinVar dbSNP
1g.17023988A>TCA416082844SDHBc.456T>A (p.Pro152=)
c.585T>A (p.Pro195=)
c.627T>A (p.Pro209=)
n.561T>A
1g.17023989G>ACA338270952SDHBc.455C>T (p.Pro152Leu)
c.584C>T (p.Pro195Leu)
c.626C>T (p.Pro209Leu)
n.560C>T
1g.17023989G>CCA338270953SDHBc.455C>G (p.Pro152Arg)
c.584C>G (p.Pro195Arg)
c.626C>G (p.Pro209Arg)
n.560C>G
 ClinVar dbSNP
1g.17023989G=CA1156078621SDHBc.455C= (p.Pro152=)
c.584C= (p.Pro195=)
c.626C= (p.Pro209=)
n.560C=
1g.17023989G>TCA338270954SDHBc.455C>A (p.Pro152His)
c.584C>A (p.Pro195His)
c.626C>A (p.Pro209His)
n.560C>A
1g.17023990G>ACA338270955SDHBc.454C>T (p.Pro152Ser)
c.583C>T (p.Pro195Ser)
c.625C>T (p.Pro209Ser)
n.559C>T
 ClinVar dbSNP
1g.17023990G>CCA338270956SDHBc.454C>G (p.Pro152Ala)
c.583C>G (p.Pro195Ala)
c.625C>G (p.Pro209Ala)
n.559C>G
1g.17023990G>TCA338270957SDHBc.454C>A (p.Pro152Thr)
c.583C>A (p.Pro195Thr)
c.625C>A (p.Pro209Thr)
n.559C>A
 ClinVar gnomAD v4
1g.17023990_17023991delinsTTCA2580060636SDHBc.453_454delinsAA (p.Pro152Thr)
c.582_583delinsAA (p.Pro195Thr)
c.624_625delinsAA (p.Pro209Thr)
n.558_559delinsAA
 ClinVar
1g.17023991C>ACA416082857SDHBc.453G>T (p.Gly151=)
c.582G>T (p.Gly194=)
c.624G>T (p.Gly208=)
n.558G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17023991C=CA1156078622SDHBc.453G= (p.Gly151=)
c.582G= (p.Gly194=)
c.624G= (p.Gly208=)
n.558G=
1g.17023991C>GCA416082860SDHBc.453G>C (p.Gly151=)
c.582G>C (p.Gly194=)
c.624G>C (p.Gly208=)
n.558G>C
1g.17023991C>TCA416082863SDHBc.453G>A (p.Gly151=)
c.582G>A (p.Gly194=)
c.624G>A (p.Gly208=)
n.558G>A
 ClinVar
1g.17023992C>ACA338270960SDHBc.452G>T (p.Gly151Val)
c.581G>T (p.Gly194Val)
c.623G>T (p.Gly208Val)
n.557G>T
1g.17023992C=CA1156078623SDHBc.452G= (p.Gly151=)
c.581G= (p.Gly194=)
c.623G= (p.Gly208=)
n.557G=
1g.17023992C>GCA338270959SDHBc.452G>C (p.Gly151Ala)
c.581G>C (p.Gly194Ala)
c.623G>C (p.Gly208Ala)
n.557G>C
1g.17023992C>TCA338270958SDHBc.452G>A (p.Gly151Glu)
c.581G>A (p.Gly194Glu)
c.623G>A (p.Gly208Glu)
n.557G>A
 ClinVar dbSNP
1g.17023993C>ACA338270961SDHBc.451G>T (p.Gly151Trp)
c.580G>T (p.Gly194Trp)
c.622G>T (p.Gly208Trp)
n.556G>T
1g.17023993C>GCA338270962SDHBc.451G>C (p.Gly151Arg)
c.580G>C (p.Gly194Arg)
c.622G>C (p.Gly208Arg)
n.556G>C
1g.17023993C>TCA338270963SDHBc.451G>A (p.Gly151Arg)
c.580G>A (p.Gly194Arg)
c.622G>A (p.Gly208Arg)
n.556G>A
 ClinVar
1g.17023993_17023995delinsCCACA1156078624SDHBc.449_451delinsTGG (p.Leu150=)
c.578_580delinsTGG (p.Leu193=)
c.620_622delinsTGG (p.Leu207=)
n.554_556delinsTGG
1g.17023995_17024008dupCA915941153SDHBc.438_451dup (p.Gly151GlufsTer17)
c.567_580dup (p.Gly194GlufsTer17)
c.609_622dup (p.Gly208GlufsTer17)
n.543_556dup
c.567_580dup (p.Gly194GlufsTer?)
 ClinVar dbSNP
1g.17023994C>ACA416082915SDHBc.450G>T (p.Leu150=)
c.579G>T (p.Leu193=)
c.621G>T (p.Leu207=)
n.555G>T
 dbSNP
1g.17023994C=CA1156078625SDHBc.450G= (p.Leu150=)
c.579G= (p.Leu193=)
c.621G= (p.Leu207=)
n.555G=
1g.17023994C>GCA416082909SDHBc.450G>C (p.Leu150=)
c.579G>C (p.Leu193=)
c.621G>C (p.Leu207=)
n.555G>C
 dbSNP
1g.17023994C>TCA416082912SDHBc.450G>A (p.Leu150=)
c.579G>A (p.Leu193=)
c.621G>A (p.Leu207=)
n.555G>A
1g.17023994_17023995delCA16609920SDHBc.449_450del (p.Leu150ArgfsTer14)
c.578_579del (p.Leu193ArgfsTer14)
c.620_621del (p.Leu207ArgfsTer14)
n.554_555del
c.578_579del (p.Leu193ArgfsTer?)
 ClinVar dbSNP
1g.17023995A>CCA338270964SDHBc.449T>G (p.Leu150Arg)
c.578T>G (p.Leu193Arg)
c.620T>G (p.Leu207Arg)
n.554T>G
1g.17023995A>GCA338270965SDHBc.449T>C (p.Leu150Pro)
c.578T>C (p.Leu193Pro)
c.620T>C (p.Leu207Pro)
n.554T>C
1g.17023995A>TCA338270966SDHBc.449T>A (p.Leu150Gln)
c.578T>A (p.Leu193Gln)
c.620T>A (p.Leu207Gln)
n.554T>A
 COSMIC
1g.17023996G>ACA416082925SDHBc.448C>T (p.Leu150=)
c.577C>T (p.Leu193=)
c.619C>T (p.Leu207=)
n.553C>T
 ClinVar dbSNP
1g.17023996G>CCA338270967SDHBc.448C>G (p.Leu150Val)
c.577C>G (p.Leu193Val)
c.619C>G (p.Leu207Val)
n.553C>G
 ClinVar
1g.17023996G=CA1156078626SDHBc.448C= (p.Leu150=)
c.577C= (p.Leu193=)
c.619C= (p.Leu207=)
n.553C=
1g.17023996G>TCA338270968SDHBc.448C>A (p.Leu150Met)
c.577C>A (p.Leu193Met)
c.619C>A (p.Leu207Met)
n.553C>A
1g.17023997A=CA1156078627SDHBc.447T= (p.Tyr149=)
c.576T= (p.Tyr192=)
c.618T= (p.Tyr206=)
n.552T=
1g.17023997A>CCA338270969SDHBc.447T>G (p.Tyr149Ter)
c.576T>G (p.Tyr192Ter)
c.618T>G (p.Tyr206Ter)
n.552T>G
1g.17023997A>GCA416082940SDHBc.447T>C (p.Tyr149=)
c.576T>C (p.Tyr192=)
c.618T>C (p.Tyr206=)
n.552T>C
 ClinVar dbSNP
1g.17023997A>TCA338270970SDHBc.447T>A (p.Tyr149Ter)
c.576T>A (p.Tyr192Ter)
c.618T>A (p.Tyr206Ter)
n.552T>A
1g.17023998T>ACA338270971SDHBc.446A>T (p.Tyr149Phe)
c.575A>T (p.Tyr192Phe)
c.617A>T (p.Tyr206Phe)
n.551A>T
1g.17023998T>CCA338270972SDHBc.446A>G (p.Tyr149Cys)
c.575A>G (p.Tyr192Cys)
c.617A>G (p.Tyr206Cys)
n.551A>G
 ClinVar
1g.17023998T>GCA338270973SDHBc.446A>C (p.Tyr149Ser)
c.575A>C (p.Tyr192Ser)
c.617A>C (p.Tyr206Ser)
n.551A>C
1g.17023998_17024008delinsTATTTGTCTCCCA1156078628SDHBc.436_446delinsGGAGACAAATA (p.Gly146=)
c.565_575delinsGGAGACAAATA (p.Gly189=)
c.607_617delinsGGAGACAAATA (p.Gly203=)
n.541_551delinsGGAGACAAATA
1g.17023999A>CCA338270976SDHBc.445T>G (p.Tyr149Asp)
c.574T>G (p.Tyr192Asp)
c.616T>G (p.Tyr206Asp)
n.550T>G
1g.17023999A>GCA338270975SDHBc.445T>C (p.Tyr149His)
c.574T>C (p.Tyr192His)
c.616T>C (p.Tyr206His)
n.550T>C
1g.17023999A>TCA338270974SDHBc.445T>A (p.Tyr149Asn)
c.574T>A (p.Tyr192Asn)
c.616T>A (p.Tyr206Asn)
n.550T>A
1g.17023999_17024008delCA016035SDHBc.436_445del (p.Gly146IlefsTer14)
c.565_574del (p.Gly189IlefsTer14)
c.607_616del (p.Gly203IlefsTer14)
n.541_550del
c.565_574del (p.Gly189IlefsTer?)
 ClinVar dbSNP
1g.17023999_17024008delinsATTTGTCTCCCA1148224197SDHBc.436_445delinsGGAGACAAAT (p.Gly146=)
c.565_574delinsGGAGACAAAT (p.Gly189=)
c.607_616delinsGGAGACAAAT (p.Gly203=)
n.541_550delinsGGAGACAAAT
1g.17024000T>ACA338270977SDHBc.444A>T (p.Lys148Asn)
c.573A>T (p.Lys191Asn)
c.615A>T (p.Lys205Asn)
n.549A>T
1g.17024000T>CCA416082979SDHBc.444A>G (p.Lys148=)
c.573A>G (p.Lys191=)
c.615A>G (p.Lys205=)
n.549A>G
 ClinVar dbSNP gnomAD v4
1g.17024000T>GCA338270979SDHBc.444A>C (p.Lys148Asn)
c.573A>C (p.Lys191Asn)
c.615A>C (p.Lys205Asn)
n.549A>C
1g.17024000T=CA1156078629SDHBc.444A= (p.Lys148=)
c.573A= (p.Lys191=)
c.615A= (p.Lys205=)
n.549A=
1g.17024001T>ACA338270981SDHBc.443A>T (p.Lys148Ile)
c.572A>T (p.Lys191Ile)
c.614A>T (p.Lys205Ile)
n.548A>T
1g.17024001T>CCA089679SDHBc.443A>G (p.Lys148Arg)
c.572A>G (p.Lys191Arg)
c.614A>G (p.Lys205Arg)
n.548A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17024001T>GCA338270985SDHBc.443A>C (p.Lys148Thr)
c.572A>C (p.Lys191Thr)
c.614A>C (p.Lys205Thr)
n.548A>C
 ClinVar dbSNP gnomAD v4
1g.17024001T=CA1156078630SDHBc.443A= (p.Lys148=)
c.572A= (p.Lys191=)
c.614A= (p.Lys205=)
n.548A=
1g.17024002T>ACA338270992SDHBc.442A>T (p.Lys148Ter)
c.571A>T (p.Lys191Ter)
c.613A>T (p.Lys205Ter)
n.547A>T
1g.17024002T>CCA338270988SDHBc.442A>G (p.Lys148Glu)
c.571A>G (p.Lys191Glu)
c.613A>G (p.Lys205Glu)
n.547A>G
1g.17024002T>GCA338270990SDHBc.442A>C (p.Lys148Gln)
c.571A>C (p.Lys191Gln)
c.613A>C (p.Lys205Gln)
n.547A>C
1g.17024003G>ACA416083456SDHBc.441C>T (p.Asp147=)
c.570C>T (p.Asp190=)
c.612C>T (p.Asp204=)
n.546C>T
 dbSNP gnomAD v4
1g.17024003G>CCA338270995SDHBc.441C>G (p.Asp147Glu)
c.570C>G (p.Asp190Glu)
c.612C>G (p.Asp204Glu)
n.546C>G
 ClinVar dbSNP
1g.17024003G=CA1156078631SDHBc.441C= (p.Asp147=)
c.570C= (p.Asp190=)
c.612C= (p.Asp204=)
n.546C=
1g.17024003G>TCA338270997SDHBc.441C>A (p.Asp147Glu)
c.570C>A (p.Asp190Glu)
c.612C>A (p.Asp204Glu)
n.546C>A
1g.17024004T>ACA338270999SDHBc.440A>T (p.Asp147Val)
c.569A>T (p.Asp190Val)
c.611A>T (p.Asp204Val)
n.545A>T
1g.17024004T>CCA338271001SDHBc.440A>G (p.Asp147Gly)
c.569A>G (p.Asp190Gly)
c.611A>G (p.Asp204Gly)
n.545A>G
1g.17024004T>GCA338271003SDHBc.440A>C (p.Asp147Ala)
c.569A>C (p.Asp190Ala)
c.611A>C (p.Asp204Ala)
n.545A>C
1g.17024005C>ACA338271008SDHBc.439G>T (p.Asp147Tyr)
c.568G>T (p.Asp190Tyr)
c.610G>T (p.Asp204Tyr)
n.544G>T
1g.17024005C=CA1156078632SDHBc.439G= (p.Asp147=)
c.568G= (p.Asp190=)
c.610G= (p.Asp204=)
n.544G=
1g.17024005C>GCA338271005SDHBc.439G>C (p.Asp147His)
c.568G>C (p.Asp190His)
c.610G>C (p.Asp204His)
n.544G>C
1g.17024005C>TCA338271007SDHBc.439G>A (p.Asp147Asn)
c.568G>A (p.Asp190Asn)
c.610G>A (p.Asp204Asn)
n.544G>A
 gnomAD v4
1g.17024006T>ACA416083482SDHBc.438A>T (p.Gly146=)
c.567A>T (p.Gly189=)
c.609A>T (p.Gly203=)
n.543A>T
1g.17024006T>CCA416083488SDHBc.438A>G (p.Gly146=)
c.567A>G (p.Gly189=)
c.609A>G (p.Gly203=)
n.543A>G
1g.17024006T>GCA416083490SDHBc.438A>C (p.Gly146=)
c.567A>C (p.Gly189=)
c.609A>C (p.Gly203=)
n.543A>C
 ClinVar dbSNP
1g.17024006T=CA1156078633SDHBc.438A= (p.Gly146=)
c.567A= (p.Gly189=)
c.609A= (p.Gly203=)
n.543A=
1g.17024006_17024007delinsTCCA1156078634SDHBc.437_438delinsGA (p.Gly146=)
c.566_567delinsGA (p.Gly189=)
c.608_609delinsGA (p.Gly203=)
n.542_543delinsGA
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.17024007C>ACA338271011SDHBc.437G>T (p.Gly146Val)
c.566G>T (p.Gly189Val)
c.608G>T (p.Gly203Val)
n.542G>T
 ClinVar
1g.17024007C=CA1156078635SDHBc.437G= (p.Gly146=)
c.566G= (p.Gly189=)
c.608G= (p.Gly203=)
n.542G=
1g.17024007C>GCA338271013SDHBc.437G>C (p.Gly146Ala)
c.566G>C (p.Gly189Ala)
c.608G>C (p.Gly203Ala)
n.542G>C
 ClinVar dbSNP
1g.17024007C>TCA338271014SDHBc.437G>A (p.Gly146Glu)
c.566G>A (p.Gly189Glu)
c.608G>A (p.Gly203Glu)
n.542G>A
 COSMIC
1g.17024008delCA658795407SDHBc.437del (p.Gly146GlufsTer17)
c.566del (p.Gly189GlufsTer17)
c.608del (p.Gly203GlufsTer17)
n.542del
c.566del (p.Gly189GlufsTer?)
 ClinVar dbSNP
1g.17024008C>ACA338271018SDHBc.436G>T (p.Gly146Ter)
c.565G>T (p.Gly189Ter)
c.607G>T (p.Gly203Ter)
n.541G>T
 ClinVar
1g.17024008C=CA1143487501SDHBc.436G= (p.Gly146=)
c.565G= (p.Gly189=)
c.607G= (p.Gly203=)
n.541G=
1g.17024008C>GCA338271019SDHBc.436G>C (p.Gly146Arg)
c.565G>C (p.Gly189Arg)
c.607G>C (p.Gly203Arg)
n.541G>C
1g.17024008C>TCA089678SDHBc.436G>A (p.Gly146Arg)
c.565G>A (p.Gly189Arg)
c.607G>A (p.Gly203Arg)
n.541G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.17024009G>ACA089677SDHBc.435C>T (p.Asn145=)
c.564C>T (p.Asn188=)
c.606C>T (p.Asn202=)
n.540C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17024009G>CCA338271024SDHBc.435C>G (p.Asn145Lys)
c.564C>G (p.Asn188Lys)
c.606C>G (p.Asn202Lys)
n.540C>G
 ClinVar dbSNP
1g.17024009G=CA1143365492SDHBc.435C= (p.Asn145=)
c.564C= (p.Asn188=)
c.606C= (p.Asn202=)
n.540C=
1g.17024009G>TCA338271026SDHBc.435C>A (p.Asn145Lys)
c.564C>A (p.Asn188Lys)
c.606C>A (p.Asn202Lys)
n.540C>A
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

Number of alleles fetched