Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.17023929G>ACA2643676633SDHBc.471+44C>T (n.471+44C>T)
c.600+44C>T (n.600+44C>T)
c.642+44C>T (n.642+44C>T)
n.576+44C>T
 gnomAD v4
1g.17023929G>TCA2643676634SDHBc.471+44C>A (n.471+44C>A)
c.600+44C>A (n.600+44C>A)
c.642+44C>A (n.642+44C>A)
n.576+44C>A
 gnomAD v4
1g.17023930C=CA1156078589SDHBc.471+43G= (n.471+43G=)
c.600+43G= (n.600+43G=)
c.642+43G= (n.642+43G=)
n.576+43G=
1g.17023930C>GCA521037920SDHBc.471+43G>C (n.471+43G>C)
c.600+43G>C (n.600+43G>C)
c.642+43G>C (n.642+43G>C)
n.576+43G>C
 dbSNP gnomAD v2 gnomAD v4
1g.17023930C>TCA2643676639SDHBc.471+43G>A (n.471+43G>A)
c.600+43G>A (n.600+43G>A)
c.642+43G>A (n.642+43G>A)
n.576+43G>A
 gnomAD v4
1g.17023931T>CCA089688SDHBc.471+42A>G (n.471+42A>G)
c.600+42A>G (n.600+42A>G)
c.642+42A>G (n.642+42A>G)
n.576+42A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.17023931T=CA1156078590SDHBc.471+42A= (n.471+42A=)
c.600+42A= (n.600+42A=)
c.642+42A= (n.642+42A=)
n.576+42A=
1g.17023932T>CCA521037924SDHBc.471+41A>G (n.471+41A>G)
c.600+41A>G (n.600+41A>G)
c.642+41A>G (n.642+41A>G)
n.576+41A>G
 dbSNP gnomAD v2 gnomAD v4
1g.17023932T=CA1156078591SDHBc.471+41A= (n.471+41A=)
c.600+41A= (n.600+41A=)
c.642+41A= (n.642+41A=)
n.576+41A=
1g.17023933G>ACA2574235401SDHBc.471+40C>T (n.471+40C>T)
c.600+40C>T (n.600+40C>T)
c.642+40C>T (n.642+40C>T)
n.576+40C>T
 gnomAD v4
1g.17023933G>CCA2643676648SDHBc.471+40C>G (n.471+40C>G)
c.600+40C>G (n.600+40C>G)
c.642+40C>G (n.642+40C>G)
n.576+40C>G
 gnomAD v4
1g.17023933G>TCA2643676649SDHBc.471+40C>A (n.471+40C>A)
c.600+40C>A (n.600+40C>A)
c.642+40C>A (n.642+40C>A)
n.576+40C>A
 gnomAD v4
1g.17023934A>TCA2643676654SDHBc.471+39T>A (n.471+39T>A)
c.600+39T>A (n.600+39T>A)
c.642+39T>A (n.642+39T>A)
n.576+39T>A
 gnomAD v4
1g.17023935G>ACA890985801SDHBc.471+38C>T (n.471+38C>T)
c.600+38C>T (n.600+38C>T)
c.642+38C>T (n.642+38C>T)
n.576+38C>T
 dbSNP gnomAD v3 gnomAD v4
1g.17023935G=CA1156078592SDHBc.471+38C= (n.471+38C=)
c.600+38C= (n.600+38C=)
c.642+38C= (n.642+38C=)
n.576+38C=
1g.17023935G>TCA2574235404SDHBc.471+38C>A (n.471+38C>A)
c.600+38C>A (n.600+38C>A)
c.642+38C>A (n.642+38C>A)
n.576+38C>A
 gnomAD v4
1g.17023936T>ACA2643676659SDHBc.471+37A>T (n.471+37A>T)
c.600+37A>T (n.600+37A>T)
c.642+37A>T (n.642+37A>T)
n.576+37A>T
 gnomAD v4
1g.17023936T>CCA18663106SDHBc.471+37A>G (n.471+37A>G)
c.600+37A>G (n.600+37A>G)
c.642+37A>G (n.642+37A>G)
n.576+37A>G
 dbSNP
1g.17023936T=CA1156078593SDHBc.471+37A= (n.471+37A=)
c.600+37A= (n.600+37A=)
c.642+37A= (n.642+37A=)
n.576+37A=
1g.17023937T>ACA2742639256SDHBc.471+36A>T (n.471+36A>T)
c.600+36A>T (n.600+36A>T)
c.642+36A>T (n.642+36A>T)
n.576+36A>T
1g.17023939C>ACA2643676660SDHBc.471+34G>T (n.471+34G>T)
c.600+34G>T (n.600+34G>T)
c.642+34G>T (n.642+34G>T)
n.576+34G>T
 gnomAD v4
1g.17023942T>ACA2643676665SDHBc.471+31A>T (n.471+31A>T)
c.600+31A>T (n.600+31A>T)
c.642+31A>T (n.642+31A>T)
n.576+31A>T
 gnomAD v4
1g.17023944dupCA2643676662SDHBc.471+31dup (n.471+31dup)
c.600+31dup (n.600+31dup)
c.642+31dup (n.642+31dup)
n.576+31dup
 gnomAD v4
1g.17023943T>CCA2643676668SDHBc.471+30A>G (n.471+30A>G)
c.600+30A>G (n.600+30A>G)
c.642+30A>G (n.642+30A>G)
n.576+30A>G
 gnomAD v4
1g.17023945C>TCA2574235408SDHBc.471+28G>A (n.471+28G>A)
c.600+28G>A (n.600+28G>A)
c.642+28G>A (n.642+28G>A)
n.576+28G>A
 gnomAD v4
1g.17023946T>CCA2643676669SDHBc.471+27A>G (n.471+27A>G)
c.600+27A>G (n.600+27A>G)
c.642+27A>G (n.642+27A>G)
n.576+27A>G
 gnomAD v4
1g.17023947C>ACA637814SDHBc.471+26G>T (n.471+26G>T)
c.600+26G>T (n.600+26G>T)
c.642+26G>T (n.642+26G>T)
n.576+26G>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17023947C=CA1143466721SDHBc.471+26G= (n.471+26G=)
c.600+26G= (n.600+26G=)
c.642+26G= (n.642+26G=)
n.576+26G=
1g.17023947C>TCA2643676672SDHBc.471+26G>A (n.471+26G>A)
c.600+26G>A (n.600+26G>A)
c.642+26G>A (n.642+26G>A)
n.576+26G>A
 gnomAD v4
1g.17023947_17023959delinsCTTAAAGCAATTACA1156078594SDHBc.471+14_471+26delinsTAATTGCTTTAAG (n.471+14_471+26delinsTAATTGCTTTAAG)
c.600+14_600+26delinsTAATTGCTTTAAG (n.600+14_600+26delinsTAATTGCTTTAAG)
c.642+14_642+26delinsTAATTGCTTTAAG (n.642+14_642+26delinsTAATTGCTTTAAG)
n.576+14_576+26delinsTAATTGCTTTAAG
1g.17023948T>CCA1156078595SDHBc.471+25A>G (n.471+25A>G)
c.600+25A>G (n.600+25A>G)
c.642+25A>G (n.642+25A>G)
n.576+25A>G
 dbSNP
1g.17023948T=CA1156078596SDHBc.471+25A= (n.471+25A=)
c.600+25A= (n.600+25A=)
c.642+25A= (n.642+25A=)
n.576+25A=
1g.17023948_17023959delCA637815SDHBc.471+14_471+25del (n.471+14_471+25del)
c.600+14_600+25del (n.600+14_600+25del)
c.642+14_642+25del (n.642+14_642+25del)
n.576+14_576+25del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17023953G>ACA18663116SDHBc.471+20C>T (n.471+20C>T)
c.600+20C>T (n.600+20C>T)
c.642+20C>T (n.642+20C>T)
n.576+20C>T
 dbSNP
1g.17023953G>CCA2580060630SDHBc.471+20C>G (n.471+20C>G)
c.600+20C>G (n.600+20C>G)
c.642+20C>G (n.642+20C>G)
n.576+20C>G
 ClinVar
1g.17023953G=CA1143356053SDHBc.471+20C= (n.471+20C=)
c.600+20C= (n.600+20C=)
c.642+20C= (n.642+20C=)
n.576+20C=
1g.17023953G>TCA18663118SDHBc.471+20C>A (n.471+20C>A)
c.600+20C>A (n.600+20C>A)
c.642+20C>A (n.642+20C>A)
n.576+20C>A
 dbSNP gnomAD v4
1g.17023955A>GCA2643676690SDHBc.471+18T>C (n.471+18T>C)
c.600+18T>C (n.600+18T>C)
c.642+18T>C (n.642+18T>C)
n.576+18T>C
 gnomAD v4
1g.17023956A=CA1143427988SDHBc.471+17T= (n.471+17T=)
c.600+17T= (n.600+17T=)
c.642+17T= (n.642+17T=)
n.576+17T=
1g.17023956A>GCA089687SDHBc.471+17T>C (n.471+17T>C)
c.600+17T>C (n.600+17T>C)
c.642+17T>C (n.642+17T>C)
n.576+17T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17023956A>TCA2643676697SDHBc.471+17T>A (n.471+17T>A)
c.600+17T>A (n.600+17T>A)
c.642+17T>A (n.642+17T>A)
n.576+17T>A
 gnomAD v4
1g.17023957T>CCA521037927SDHBc.471+16A>G (n.471+16A>G)
c.600+16A>G (n.600+16A>G)
c.642+16A>G (n.642+16A>G)
n.576+16A>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17023957T=CA1156078597SDHBc.471+16A= (n.471+16A=)
c.600+16A= (n.600+16A=)
c.642+16A= (n.642+16A=)
n.576+16A=
1g.17023958T>CCA089686SDHBc.471+15A>G (n.471+15A>G)
c.600+15A>G (n.600+15A>G)
c.642+15A>G (n.642+15A>G)
n.576+15A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17023958T>GCA2643676706SDHBc.471+15A>C (n.471+15A>C)
c.600+15A>C (n.600+15A>C)
c.642+15A>C (n.642+15A>C)
n.576+15A>C
 gnomAD v4
1g.17023958T=CA1143596044SDHBc.471+15A= (n.471+15A=)
c.600+15A= (n.600+15A=)
c.642+15A= (n.642+15A=)
n.576+15A=
1g.17023959A=CA1156078598SDHBc.471+14T= (n.471+14T=)
c.600+14T= (n.600+14T=)
c.642+14T= (n.642+14T=)
n.576+14T=
1g.17023959A>GCA521037928SDHBc.471+14T>C (n.471+14T>C)
c.600+14T>C (n.600+14T>C)
c.642+14T>C (n.642+14T>C)
n.576+14T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17023959A>TCA2643676716SDHBc.471+14T>A (n.471+14T>A)
c.600+14T>A (n.600+14T>A)
c.642+14T>A (n.642+14T>A)
n.576+14T>A
 gnomAD v4
1g.17023960A>CCA2643676718SDHBc.471+13T>G (n.471+13T>G)
c.600+13T>G (n.600+13T>G)
c.642+13T>G (n.642+13T>G)
n.576+13T>G
 gnomAD v4
1g.17023961G>TCA2643676719SDHBc.471+12C>A (n.471+12C>A)
c.600+12C>A (n.600+12C>A)
c.642+12C>A (n.642+12C>A)
n.576+12C>A
 gnomAD v4
1g.17023962G>ACA521037929SDHBc.471+11C>T (n.471+11C>T)
c.600+11C>T (n.600+11C>T)
c.642+11C>T (n.642+11C>T)
n.576+11C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17023962G=CA1156078599SDHBc.471+11C= (n.471+11C=)
c.600+11C= (n.600+11C=)
c.642+11C= (n.642+11C=)
n.576+11C=
1g.17023962G>TCA2742639257SDHBc.471+11C>A (n.471+11C>A)
c.600+11C>A (n.600+11C>A)
c.642+11C>A (n.642+11C>A)
n.576+11C>A
1g.17023963A=CA1156078600SDHBc.471+10T= (n.471+10T=)
c.600+10T= (n.600+10T=)
c.642+10T= (n.642+10T=)
n.576+10T=
1g.17023963A>CCA2740090525SDHBc.471+10T>G (n.471+10T>G)
c.600+10T>G (n.600+10T>G)
c.642+10T>G (n.642+10T>G)
n.576+10T>G
 ClinVar
1g.17023963A>GCA089683SDHBc.471+10T>C (n.471+10T>C)
c.600+10T>C (n.600+10T>C)
c.642+10T>C (n.642+10T>C)
n.576+10T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17023963A>TCA2499214296SDHBc.471+10T>A (n.471+10T>A)
c.600+10T>A (n.600+10T>A)
c.642+10T>A (n.642+10T>A)
n.576+10T>A
 ClinVar dbSNP
1g.17023964G>ACA1156078602SDHBc.471+9C>T (n.471+9C>T)
c.600+9C>T (n.600+9C>T)
c.642+9C>T (n.642+9C>T)
n.576+9C>T
 ClinVar dbSNP gnomAD v4
1g.17023964G>CCA2573130771SDHBc.471+9C>G (n.471+9C>G)
c.600+9C>G (n.600+9C>G)
c.642+9C>G (n.642+9C>G)
n.576+9C>G
 ClinVar dbSNP
1g.17023964G=CA1156078601SDHBc.471+9C= (n.471+9C=)
c.600+9C= (n.600+9C=)
c.642+9C= (n.642+9C=)
n.576+9C=
1g.17023964G>TCA2643676721SDHBc.471+9C>A (n.471+9C>A)
c.600+9C>A (n.600+9C>A)
c.642+9C>A (n.642+9C>A)
n.576+9C>A
 gnomAD v4
1g.17023965C>GCA2643676725SDHBc.471+8G>C (n.471+8G>C)
c.600+8G>C (n.600+8G>C)
c.642+8G>C (n.642+8G>C)
n.576+8G>C
 gnomAD v4
1g.17023965C>TCA2580060631SDHBc.471+8G>A (n.471+8G>A)
c.600+8G>A (n.600+8G>A)
c.642+8G>A (n.642+8G>A)
n.576+8G>A
 ClinVar gnomAD v4
1g.17023966A=CA1148460506SDHBc.471+7T= (n.471+7T=)
c.600+7T= (n.600+7T=)
c.642+7T= (n.642+7T=)
n.576+7T=
1g.17023966A>GCA089692SDHBc.471+7T>C (n.471+7T>C)
c.600+7T>C (n.600+7T>C)
c.642+7T>C (n.642+7T>C)
n.576+7T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17023966_17023973delinsACCTCACCCA1156078603SDHBc.471_471+7delinsGGTGAGGT
c.600_600+7delinsGGTGAGGT
c.642_642+7delinsGGTGAGGT
n.576_576+7delinsGGTGAGGT
1g.17023967C=CA1156078604SDHBc.471+6G= (n.471+6G=)
c.600+6G= (n.600+6G=)
c.642+6G= (n.642+6G=)
n.576+6G=
1g.17023967C>TCA521037932SDHBc.471+6G>A (n.471+6G>A)
c.600+6G>A (n.600+6G>A)
c.642+6G>A (n.642+6G>A)
n.576+6G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.17023967_17023973delCA10577670SDHBc.471_471+6del
c.600_600+6del
c.642_642+6del
n.576_576+6del
 ClinVar dbSNP
1g.17023968C=CA1156078605SDHBc.471+5G= (n.471+5G=)
c.600+5G= (n.600+5G=)
c.642+5G= (n.642+5G=)
n.576+5G=
1g.17023968C>TCA089691SDHBc.471+5G>A (n.471+5G>A)
c.600+5G>A (n.600+5G>A)
c.642+5G>A (n.642+5G>A)
n.576+5G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.17023969T>ACA999082463SDHBc.471+4A>T (n.471+4A>T)
c.600+4A>T (n.600+4A>T)
c.642+4A>T (n.642+4A>T)
n.576+4A>T
 dbSNP gnomAD v3 gnomAD v4
1g.17023969T>CCA658656884SDHBc.471+4A>G (n.471+4A>G)
c.600+4A>G (n.600+4A>G)
c.642+4A>G (n.642+4A>G)
n.576+4A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.17023969T=CA1156078606SDHBc.471+4A= (n.471+4A=)
c.600+4A= (n.600+4A=)
c.642+4A= (n.642+4A=)
n.576+4A=
1g.17023970C=CA1156078607SDHBc.471+3G= (n.471+3G=)
c.600+3G= (n.600+3G=)
c.642+3G= (n.642+3G=)
n.576+3G=
1g.17023970C>TCA10581745SDHBc.471+3G>A (n.471+3G>A)
c.600+3G>A (n.600+3G>A)
c.642+3G>A (n.642+3G>A)
n.576+3G>A
 ClinVar dbSNP
1g.17023971A=CA1156078608SDHBc.471+2T= (n.471+2T=)
c.600+2T= (n.600+2T=)
c.642+2T= (n.642+2T=)
n.576+2T=
1g.17023971A>CCA338270919SDHBc.471+2T>G (n.471+2T>G)
c.600+2T>G (n.600+2T>G)
c.642+2T>G (n.642+2T>G)
n.576+2T>G
 ClinVar dbSNP
1g.17023971A>GCA338270918SDHBc.471+2T>C (n.471+2T>C)
c.600+2T>C (n.600+2T>C)
c.642+2T>C (n.642+2T>C)
n.576+2T>C
1g.17023971A>TCA338270917SDHBc.471+2T>A (n.471+2T>A)
c.600+2T>A (n.600+2T>A)
c.642+2T>A (n.642+2T>A)
n.576+2T>A
1g.17023972C>ACA338270922SDHBc.471+1G>T (n.471+1G>T)
c.600+1G>T (n.600+1G>T)
c.642+1G>T (n.642+1G>T)
n.576+1G>T
1g.17023972C=CA1156078609SDHBc.471+1G= (n.471+1G=)
c.600+1G= (n.600+1G=)
c.642+1G= (n.642+1G=)
n.576+1G=
1g.17023972C>GCA338270920SDHBc.471+1G>C (n.471+1G>C)
c.600+1G>C (n.600+1G>C)
c.642+1G>C (n.642+1G>C)
n.576+1G>C
 ClinVar dbSNP
1g.17023972C>TCA338270921SDHBc.471+1G>A (n.471+1G>A)
c.600+1G>A (n.600+1G>A)
c.642+1G>A (n.642+1G>A)
n.576+1G>A
 ClinVar dbSNP gnomAD v2
1g.17023973C>ACA338270923SDHBc.471G>T (p.Gln157His)
c.600G>T (p.Gln200His)
c.642G>T (p.Gln214His)
n.576G>T
 ClinVar dbSNP
1g.17023973C=CA1156078610SDHBc.471G= (p.Gln157=)
c.600G= (p.Gln200=)
c.642G= (p.Gln214=)
n.576G=
1g.17023973C>GCA338270924SDHBc.471G>C (p.Gln157His)
c.600G>C (p.Gln200His)
c.642G>C (p.Gln214His)
n.576G>C
 ClinVar dbSNP gnomAD v4
1g.17023973C>TCA416082740SDHBc.471G>A (p.Gln157=)
c.600G>A (p.Gln200=)
c.642G>A (p.Gln214=)
n.576G>A
 dbSNP gnomAD v2 gnomAD v4
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

Number of alleles fetched