Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.17027750_17028737del | CA645509076 | SDHB | c.117_369+1del c.246_498+1del c.288_540+1del n.205_458del n.276_474+1del | |
1 | g.17027783T>A | CA338272610 | SDHB | c.335A>T (p.Gln112Leu) c.464A>T (p.Gln155Leu) c.506A>T (p.Gln169Leu) n.423A>T n.440A>T | |
1 | g.17027783T>C | CA338272611 | SDHB | c.335A>G (p.Gln112Arg) c.464A>G (p.Gln155Arg) c.506A>G (p.Gln169Arg) n.423A>G n.440A>G | ClinVar |
1 | g.17027783T>G | CA338272620 | SDHB | c.335A>C (p.Gln112Pro) c.464A>C (p.Gln155Pro) c.506A>C (p.Gln169Pro) n.423A>C n.440A>C | |
1 | g.17027784G>A | CA16602226 | SDHB | c.334C>T (p.Gln112Ter) c.463C>T (p.Gln155Ter) c.505C>T (p.Gln169Ter) n.422C>T n.439C>T | ClinVar dbSNP gnomAD v4 |
1 | g.17027784G>C | CA338272629 | SDHB | c.334C>G (p.Gln112Glu) c.463C>G (p.Gln155Glu) c.505C>G (p.Gln169Glu) n.422C>G n.439C>G | ClinVar dbSNP gnomAD v4 |
1 | g.17027784G= | CA1156080168 | SDHB | c.334C= (p.Gln112=) c.463C= (p.Gln155=) c.505C= (p.Gln169=) n.422C= n.439C= | |
1 | g.17027784G>T | CA338272631 | SDHB | c.334C>A (p.Gln112Lys) c.463C>A (p.Gln155Lys) c.505C>A (p.Gln169Lys) n.422C>A n.439C>A | gnomAD v4 |
1 | g.17027785C>A | CA338272634 | SDHB | c.333G>T (p.Gln111His) c.462G>T (p.Gln154His) c.504G>T (p.Gln168His) n.421G>T n.438G>T | |
1 | g.17027785C>G | CA338272637 | SDHB | c.333G>C (p.Gln111His) c.462G>C (p.Gln154His) c.504G>C (p.Gln168His) n.421G>C n.438G>C | |
1 | g.17027785C>T | CA416085874 | SDHB | c.333G>A (p.Gln111=) c.462G>A (p.Gln154=) c.504G>A (p.Gln168=) n.421G>A n.438G>A | dbSNP |
1 | g.17027786T>A | CA338272659 | SDHB | c.332A>T (p.Gln111Leu) c.461A>T (p.Gln154Leu) c.503A>T (p.Gln168Leu) n.420A>T n.437A>T | |
1 | g.17027786T>C | CA338272655 | SDHB | c.332A>G (p.Gln111Arg) c.461A>G (p.Gln154Arg) c.503A>G (p.Gln168Arg) n.420A>G n.437A>G | ClinVar |
1 | g.17027786T>G | CA338272652 | SDHB | c.332A>C (p.Gln111Pro) c.461A>C (p.Gln154Pro) c.503A>C (p.Gln168Pro) n.420A>C n.437A>C | |
1 | g.17027786dup | CA2586964058 | SDHB | c.332dup (p.Gln112AlafsTer10) c.461dup (p.Gln155AlafsTer10) c.503dup (p.Gln169AlafsTer10) n.420dup n.437dup | |
1 | g.17027787G>A | CA338272662 | SDHB | c.331C>T (p.Gln111Ter) c.460C>T (p.Gln154Ter) c.502C>T (p.Gln168Ter) n.419C>T n.436C>T | ClinVar dbSNP |
1 | g.17027787G>C | CA338272676 | SDHB | c.331C>G (p.Gln111Glu) c.460C>G (p.Gln154Glu) c.502C>G (p.Gln168Glu) n.419C>G n.436C>G | |
1 | g.17027787G= | CA1156080169 | SDHB | c.331C= (p.Gln111=) c.460C= (p.Gln154=) c.502C= (p.Gln168=) n.419C= n.436C= | |
1 | g.17027787G>T | CA338272678 | SDHB | c.331C>A (p.Gln111Lys) c.460C>A (p.Gln154Lys) c.502C>A (p.Gln168Lys) n.419C>A n.436C>A | gnomAD v4 |
1 | g.17027787dup | CA658655542 | SDHB | c.331dup (p.Gln111ProfsTer11) c.460dup (p.Gln154ProfsTer11) c.502dup (p.Gln168ProfsTer11) n.419dup n.436dup | |
1 | g.17027788C>A | CA338272680 | SDHB | c.330G>T (p.Lys110Asn) c.459G>T (p.Lys153Asn) c.501G>T (p.Lys167Asn) n.418G>T n.435G>T | ClinVar dbSNP gnomAD v4 |
1 | g.17027788C= | CA1156080170 | SDHB | c.330G= (p.Lys110=) c.459G= (p.Lys153=) c.501G= (p.Lys167=) n.418G= n.435G= | |
1 | g.17027788C>G | CA338272684 | SDHB | c.330G>C (p.Lys110Asn) c.459G>C (p.Lys153Asn) c.501G>C (p.Lys167Asn) n.418G>C n.435G>C | |
1 | g.17027788C>T | CA416085892 | SDHB | c.330G>A (p.Lys110=) c.459G>A (p.Lys153=) c.501G>A (p.Lys167=) n.418G>A n.435G>A | ClinVar dbSNP gnomAD v4 |
1 | g.17027788_17027789delinsAG | CA1139655468 | SDHB | c.329_330delinsCT (p.Lys110Thr) c.458_459delinsCT (p.Lys153Thr) c.500_501delinsCT (p.Lys167Thr) n.417_418delinsCT n.434_435delinsCT | ClinVar |
1 | g.17027789T>A | CA338272687 | SDHB | c.329A>T (p.Lys110Met) c.458A>T (p.Lys153Met) c.500A>T (p.Lys167Met) n.417A>T n.434A>T | |
1 | g.17027789T>C | CA338272692 | SDHB | c.329A>G (p.Lys110Arg) c.458A>G (p.Lys153Arg) c.500A>G (p.Lys167Arg) n.417A>G n.434A>G | ClinVar |
1 | g.17027789T>G | CA338272693 | SDHB | c.329A>C (p.Lys110Thr) c.458A>C (p.Lys153Thr) c.500A>C (p.Lys167Thr) n.417A>C n.434A>C | gnomAD v4 |
1 | g.17027790T>A | CA16609934 | SDHB | c.328A>T (p.Lys110Ter) c.457A>T (p.Lys153Ter) c.499A>T (p.Lys167Ter) n.416A>T n.433A>T | ClinVar dbSNP |
1 | g.17027790T>C | CA338272695 | SDHB | c.328A>G (p.Lys110Glu) c.457A>G (p.Lys153Glu) c.499A>G (p.Lys167Glu) n.416A>G n.433A>G | |
1 | g.17027790T>G | CA338272696 | SDHB | c.328A>C (p.Lys110Gln) c.457A>C (p.Lys153Gln) c.499A>C (p.Lys167Gln) n.416A>C n.433A>C | |
1 | g.17027790T= | CA1156080171 | SDHB | c.328A= (p.Lys110=) c.457A= (p.Lys153=) c.499A= (p.Lys167=) n.416A= n.433A= | |
1 | g.17027791del | CA2830782440 | SDHB | c.327del (p.Lys110SerfsTer8) c.456del (p.Lys153SerfsTer8) c.498del (p.Lys167SerfsTer8) n.415del n.432del | |
1 | g.17027791G>A | CA416085918 | SDHB | c.327C>T (p.Gly109=) c.456C>T (p.Gly152=) c.498C>T (p.Gly166=) n.415C>T n.432C>T | |
1 | g.17027791G>C | CA416085915 | SDHB | c.327C>G (p.Gly109=) c.456C>G (p.Gly152=) c.498C>G (p.Gly166=) n.415C>G n.432C>G | |
1 | g.17027791G>T | CA416085919 | SDHB | c.327C>A (p.Gly109=) c.456C>A (p.Gly152=) c.498C>A (p.Gly166=) n.415C>A n.432C>A | |
1 | g.17027792C>A | CA338272697 | SDHB | c.326G>T (p.Gly109Val) c.455G>T (p.Gly152Val) c.497G>T (p.Gly166Val) n.414G>T n.431G>T | |
1 | g.17027792C= | CA1156080172 | SDHB | c.326G= (p.Gly109=) c.455G= (p.Gly152=) c.497G= (p.Gly166=) n.414G= n.431G= | |
1 | g.17027792C>G | CA338272698 | SDHB | c.326G>C (p.Gly109Ala) c.455G>C (p.Gly152Ala) c.497G>C (p.Gly166Ala) n.414G>C n.431G>C | |
1 | g.17027792C>T | CA16609936 | SDHB | c.326G>A (p.Gly109Asp) c.455G>A (p.Gly152Asp) c.497G>A (p.Gly166Asp) n.414G>A n.431G>A | ClinVar dbSNP gnomAD v4 |
1 | g.17027795_17027798del | CA2573334482 | SDHB | c.323_326del (p.Glu108AlafsTer9) c.452_455del (p.Glu151AlafsTer9) c.494_497del (p.Glu165AlafsTer9) n.411_414del n.428_431del | |
1 | g.17027793C>A | CA338272705 | SDHB | c.325G>T (p.Gly109Cys) c.454G>T (p.Gly152Cys) c.496G>T (p.Gly166Cys) n.413G>T n.430G>T | |
1 | g.17027793C>G | CA338272706 | SDHB | c.325G>C (p.Gly109Arg) c.454G>C (p.Gly152Arg) c.496G>C (p.Gly166Arg) n.413G>C n.430G>C | ClinVar |
1 | g.17027793C>T | CA338272701 | SDHB | c.325G>A (p.Gly109Ser) c.454G>A (p.Gly152Ser) c.496G>A (p.Gly166Ser) n.413G>A n.430G>A | gnomAD v4 |
1 | g.17027794T>A | CA338272708 | SDHB | c.324A>T (p.Glu108Asp) c.453A>T (p.Glu151Asp) c.495A>T (p.Glu165Asp) n.412A>T n.429A>T | |
1 | g.17027794T>C | CA416085942 | SDHB | c.324A>G (p.Glu108=) c.453A>G (p.Glu151=) c.495A>G (p.Glu165=) n.412A>G n.429A>G | gnomAD v4 |
1 | g.17027794T>G | CA338272710 | SDHB | c.324A>C (p.Glu108Asp) c.453A>C (p.Glu151Asp) c.495A>C (p.Glu165Asp) n.412A>C n.429A>C | |
1 | g.17027795T>A | CA338272712 | SDHB | c.323A>T (p.Glu108Val) c.452A>T (p.Glu151Val) c.494A>T (p.Glu165Val) n.411A>T n.428A>T | |
1 | g.17027795T>C | CA338272716 | SDHB | c.323A>G (p.Glu108Gly) c.452A>G (p.Glu151Gly) c.494A>G (p.Glu165Gly) n.411A>G n.428A>G | |
1 | g.17027795T>G | CA338272718 | SDHB | c.323A>C (p.Glu108Ala) c.452A>C (p.Glu151Ala) c.494A>C (p.Glu165Ala) n.411A>C n.428A>C | |
1 | g.17027796C>A | CA338272720 | SDHB | c.322G>T (p.Glu108Ter) c.451G>T (p.Glu151Ter) c.493G>T (p.Glu165Ter) n.410G>T n.427G>T | |
1 | g.17027796C>G | CA338272721 | SDHB | c.322G>C (p.Glu108Gln) c.451G>C (p.Glu151Gln) c.493G>C (p.Glu165Gln) n.410G>C n.427G>C | |
1 | g.17027796C>T | CA338272724 | SDHB | c.322G>A (p.Glu108Lys) c.451G>A (p.Glu151Lys) c.493G>A (p.Glu165Lys) n.410G>A n.427G>A | ClinVar dbSNP |
1 | g.17027797del | CA658655541 | SDHB | c.322del (p.Glu108LysfsTer10) c.451del (p.Glu151LysfsTer10) c.493del (p.Glu165LysfsTer10) n.410del n.427del | |
1 | g.17027797C>A | CA338272726 | SDHB | c.321G>T (p.Gln107His) c.450G>T (p.Gln150His) c.492G>T (p.Gln164His) n.409G>T n.426G>T | |
1 | g.17027797C>G | CA338272734 | SDHB | c.321G>C (p.Gln107His) c.450G>C (p.Gln150His) c.492G>C (p.Gln164His) n.409G>C n.426G>C | |
1 | g.17027797C>T | CA416085962 | SDHB | c.321G>A (p.Gln107=) c.450G>A (p.Gln150=) c.492G>A (p.Gln164=) n.409G>A n.426G>A | ClinVar dbSNP gnomAD v4 |
1 | g.17027797_17027798delinsCT | CA1156080173 | SDHB | c.320_321delinsAG (p.Gln107=) c.449_450delinsAG (p.Gln150=) c.491_492delinsAG (p.Gln164=) n.408_409delinsAG n.425_426delinsAG | |
1 | g.17027798del | CA658795404 | SDHB | c.320del (p.Gln107ArgfsTer11) c.449del (p.Gln150ArgfsTer11) c.491del (p.Gln164ArgfsTer11) n.408del n.425del | ClinVar dbSNP |
1 | g.17027798T>A | CA338272736 | SDHB | c.320A>T (p.Gln107Leu) c.449A>T (p.Gln150Leu) c.491A>T (p.Gln164Leu) n.408A>T n.425A>T | |
1 | g.17027798T>C | CA089634 | SDHB | c.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 |
1 | g.17027798T>G | CA338272743 | SDHB | c.320A>C (p.Gln107Pro) c.449A>C (p.Gln150Pro) c.491A>C (p.Gln164Pro) n.408A>C n.425A>C | |
1 | g.17027798T= | CA1148714518 | SDHB | c.320A= (p.Gln107=) c.449A= (p.Gln150=) c.491A= (p.Gln164=) n.408A= n.425A= | |
1 | g.17027799G>A | CA338272750 | SDHB | c.319C>T (p.Gln107Ter) c.448C>T (p.Gln150Ter) c.490C>T (p.Gln164Ter) n.407C>T n.424C>T | ClinVar dbSNP |
1 | g.17027799G>C | CA338272746 | SDHB | c.319C>G (p.Gln107Glu) c.448C>G (p.Gln150Glu) c.490C>G (p.Gln164Glu) n.407C>G n.424C>G | |
1 | g.17027799G= | CA1156080174 | SDHB | c.319C= (p.Gln107=) c.448C= (p.Gln150=) c.490C= (p.Gln164=) n.407C= n.424C= | |
1 | g.17027799G>T | CA338272748 | SDHB | c.319C>A (p.Gln107Lys) c.448C>A (p.Gln150Lys) c.490C>A (p.Gln164Lys) n.407C>A n.424C>A | |
1 | g.17027800A>C | CA416085976 | SDHB | c.318T>G (p.Ser106=) c.447T>G (p.Ser149=) c.489T>G (p.Ser163=) n.406T>G n.423T>G | |
1 | g.17027800A>G | CA416085979 | SDHB | c.318T>C (p.Ser106=) c.447T>C (p.Ser149=) c.489T>C (p.Ser163=) n.406T>C n.423T>C | |
1 | g.17027800A>T | CA416085981 | SDHB | c.318T>A (p.Ser106=) c.447T>A (p.Ser149=) c.489T>A (p.Ser163=) n.406T>A n.423T>A | |
1 | g.17027801G>A | CA089633 | SDHB | c.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 |
1 | g.17027801G>C | CA338272752 | SDHB | c.317C>G (p.Ser106Cys) c.446C>G (p.Ser149Cys) c.488C>G (p.Ser163Cys) n.405C>G n.422C>G | dbSNP |
1 | g.17027801G= | CA1156080175 | SDHB | c.317C= (p.Ser106=) c.446C= (p.Ser149=) c.488C= (p.Ser163=) n.405C= n.422C= | |
1 | g.17027801G>T | CA338272755 | SDHB | c.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 |
1 | g.17027802A= | CA1140495524 | SDHB | c.316T= (p.Ser106=) c.445T= (p.Ser149=) c.487T= (p.Ser163=) n.404T= n.421T= | |
1 | g.17027802A>C | CA338272759 | SDHB | c.316T>G (p.Ser106Ala) c.445T>G (p.Ser149Ala) c.487T>G (p.Ser163Ala) n.404T>G n.421T>G | |
1 | g.17027802A>G | CA015910 | SDHB | c.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 |
1 | g.17027802A>T | CA338272762 | SDHB | c.316T>A (p.Ser106Thr) c.445T>A (p.Ser149Thr) c.487T>A (p.Ser163Thr) n.404T>A n.421T>A | |
1 | g.17027803T>A | CA338272766 | SDHB | c.315A>T (p.Glu105Asp) c.444A>T (p.Glu148Asp) c.486A>T (p.Glu162Asp) n.403A>T n.420A>T | |
1 | g.17027803T>C | CA416085998 | SDHB | c.315A>G (p.Glu105=) c.444A>G (p.Glu148=) c.486A>G (p.Glu162=) n.403A>G n.420A>G | ClinVar dbSNP |
1 | g.17027803T>G | CA338272767 | SDHB | c.315A>C (p.Glu105Asp) c.444A>C (p.Glu148Asp) c.486A>C (p.Glu162Asp) n.403A>C n.420A>C | |
1 | g.17027803T= | CA1156080176 | SDHB | c.315A= (p.Glu105=) c.444A= (p.Glu148=) c.486A= (p.Glu162=) n.403A= n.420A= | |
1 | g.17027804T>A | CA338272770 | SDHB | c.314A>T (p.Glu105Val) c.443A>T (p.Glu148Val) c.485A>T (p.Glu162Val) n.402A>T n.419A>T | ClinVar |
1 | g.17027804T>C | CA338272772 | SDHB | c.314A>G (p.Glu105Gly) c.443A>G (p.Glu148Gly) c.485A>G (p.Glu162Gly) n.402A>G n.419A>G | ClinVar |
1 | g.17027804T>G | CA338272773 | SDHB | c.314A>C (p.Glu105Ala) c.443A>C (p.Glu148Ala) c.485A>C (p.Glu162Ala) n.402A>C n.419A>C | |
1 | g.17027805C>A | CA338272779 | SDHB | c.313G>T (p.Glu105Ter) c.442G>T (p.Glu148Ter) c.484G>T (p.Glu162Ter) n.401G>T n.418G>T | ClinVar dbSNP |
1 | g.17027805C>G | CA338272777 | SDHB | c.313G>C (p.Glu105Gln) c.442G>C (p.Glu148Gln) c.484G>C (p.Glu162Gln) n.401G>C n.418G>C | |
1 | g.17027805C>T | CA338272775 | SDHB | c.313G>A (p.Glu105Lys) c.442G>A (p.Glu148Lys) c.484G>A (p.Glu162Lys) n.401G>A n.418G>A | |
1 | g.17027806A>C | CA338272781 | SDHB | c.312T>G (p.Asp104Glu) c.441T>G (p.Asp147Glu) c.483T>G (p.Asp161Glu) n.400T>G n.417T>G | |
1 | g.17027806A>G | CA416086012 | SDHB | c.312T>C (p.Asp104=) c.441T>C (p.Asp147=) c.483T>C (p.Asp161=) n.400T>C n.417T>C | |
1 | g.17027806A>T | CA338272787 | SDHB | c.312T>A (p.Asp104Glu) c.441T>A (p.Asp147Glu) c.483T>A (p.Asp161Glu) n.400T>A n.417T>A | gnomAD v4 |
1 | g.17027807T>A | CA338272790 | SDHB | c.311A>T (p.Asp104Val) c.440A>T (p.Asp147Val) c.482A>T (p.Asp161Val) n.399A>T n.416A>T | ClinVar dbSNP |
1 | g.17027807T>C | CA18665939 | SDHB | c.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 |
1 | g.17027807T>G | CA338272795 | SDHB | c.311A>C (p.Asp104Ala) c.440A>C (p.Asp147Ala) c.482A>C (p.Asp161Ala) n.399A>C n.416A>C | |
1 | g.17027807T= | CA1156080178 | SDHB | c.311A= (p.Asp104=) c.440A= (p.Asp147=) c.482A= (p.Asp161=) n.399A= n.416A= | |
1 | g.17027807_17027808delinsTC | CA1156080177 | SDHB | c.310_311delinsGA (p.Asp104=) c.439_440delinsGA (p.Asp147=) c.481_482delinsGA (p.Asp161=) n.398_399delinsGA n.415_416delinsGA | |
1 | g.17027809_17027812del | CA2499214300 | SDHB | c.308_311del (p.Lys103MetfsTer14) c.437_440del (p.Lys146MetfsTer14) c.479_482del (p.Lys160MetfsTer14) n.396_399del n.413_416del | ClinVar dbSNP |
1 | g.17027809_17027829del | CA658655540 | SDHB | c.291_311del (p.Glu97_Lys103del) c.420_440del (p.Glu140_Lys146del) c.462_482del (p.Glu154_Lys160del) n.379_399del n.396_416del | |
1 | g.17027808C>A | CA338272803 | SDHB | c.310G>T (p.Asp104Tyr) c.439G>T (p.Asp147Tyr) c.481G>T (p.Asp161Tyr) n.398G>T n.415G>T | dbSNP |
1 | g.17027808C= | CA1156080180 | SDHB | c.310G= (p.Asp104=) c.439G= (p.Asp147=) c.481G= (p.Asp161=) n.398G= n.415G= | |
1 | g.17027808C>G | CA338272806 | SDHB | c.310G>C (p.Asp104His) c.439G>C (p.Asp147His) c.481G>C (p.Asp161His) n.398G>C n.415G>C | |
1 | g.17027808C>T | CA338272813 | SDHB | c.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 |
1 | g.17027809del | CA015897 | SDHB | c.310del (p.Asp104MetfsTer14) c.439del (p.Asp147MetfsTer14) c.481del (p.Asp161MetfsTer14) n.398del n.415del | ClinVar dbSNP |
1 | g.17027808_17027811delinsCCTT | CA1156080179 | SDHB | c.307_310delinsAAGG (p.Lys103=) c.436_439delinsAAGG (p.Lys146=) c.478_481delinsAAGG (p.Lys160=) n.395_398delinsAAGG n.412_415delinsAAGG | |
1 | g.17027809C>A | CA338272822 | SDHB | c.309G>T (p.Lys103Asn) c.438G>T (p.Lys146Asn) c.480G>T (p.Lys160Asn) n.397G>T n.414G>T | |
1 | g.17027809C= | CA1156080181 | SDHB | c.309G= (p.Lys103=) c.438G= (p.Lys146=) c.480G= (p.Lys160=) n.397G= n.414G= | |
1 | g.17027809C>G | CA338272824 | SDHB | c.309G>C (p.Lys103Asn) c.438G>C (p.Lys146Asn) c.480G>C (p.Lys160Asn) n.397G>C n.414G>C | gnomAD v4 |
1 | g.17027809C>T | CA416086043 | SDHB | c.309G>A (p.Lys103=) c.438G>A (p.Lys146=) c.480G>A (p.Lys160=) n.397G>A n.414G>A | ClinVar dbSNP |
1 | g.17027816_17027818del | CA521039145 | SDHB | c.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 |
1 | g.17027810T>A | CA338272826 | SDHB | c.308A>T (p.Lys103Met) c.437A>T (p.Lys146Met) c.479A>T (p.Lys160Met) n.396A>T n.413A>T | |
1 | g.17027810T>C | CA338272829 | SDHB | c.308A>G (p.Lys103Arg) c.437A>G (p.Lys146Arg) c.479A>G (p.Lys160Arg) n.396A>G n.413A>G | |
1 | g.17027810T>G | CA338272838 | SDHB | c.308A>C (p.Lys103Thr) c.437A>C (p.Lys146Thr) c.479A>C (p.Lys160Thr) n.396A>C n.413A>C | ClinVar dbSNP |
1 | g.17027810T= | CA1156080182 | SDHB | c.308A= (p.Lys103=) c.437A= (p.Lys146=) c.479A= (p.Lys160=) n.396A= n.413A= | |
1 | g.17027811T>A | CA338272842 | SDHB | c.307A>T (p.Lys103Ter) c.436A>T (p.Lys146Ter) c.478A>T (p.Lys160Ter) n.395A>T n.412A>T | |
1 | g.17027811T>C | CA338272846 | SDHB | c.307A>G (p.Lys103Glu) c.436A>G (p.Lys146Glu) c.478A>G (p.Lys160Glu) n.395A>G n.412A>G | ClinVar |
1 | g.17027811T>G | CA338272853 | SDHB | c.307A>C (p.Lys103Gln) c.436A>C (p.Lys146Gln) c.478A>C (p.Lys160Gln) n.395A>C n.412A>C | |
1 | g.17027812C>A | CA338272865 | SDHB | c.306G>T (p.Lys102Asn) c.435G>T (p.Lys145Asn) c.477G>T (p.Lys159Asn) n.394G>T n.411G>T | |
1 | g.17027812C>G | CA338272858 | SDHB | c.306G>C (p.Lys102Asn) c.435G>C (p.Lys145Asn) c.477G>C (p.Lys159Asn) n.394G>C n.411G>C | ClinVar |
1 | g.17027812C>T | CA416086063 | SDHB | c.306G>A (p.Lys102=) c.435G>A (p.Lys145=) c.477G>A (p.Lys159=) n.394G>A n.411G>A | ClinVar dbSNP gnomAD v4 |
1 | g.17027813T>A | CA338272867 | SDHB | c.305A>T (p.Lys102Met) c.434A>T (p.Lys145Met) c.476A>T (p.Lys159Met) n.393A>T n.410A>T | |
1 | g.17027813T>C | CA338272869 | SDHB | c.305A>G (p.Lys102Arg) c.434A>G (p.Lys145Arg) c.476A>G (p.Lys159Arg) n.393A>G n.410A>G | ClinVar gnomAD v4 |
1 | g.17027813T>G | CA338272871 | SDHB | c.305A>C (p.Lys102Thr) c.434A>C (p.Lys145Thr) c.476A>C (p.Lys159Thr) n.393A>C n.410A>C | |
1 | g.17027814T>A | CA338272873 | SDHB | c.304A>T (p.Lys102Ter) c.433A>T (p.Lys145Ter) c.475A>T (p.Lys159Ter) n.392A>T n.409A>T | |
1 | g.17027814T>C | CA338272876 | SDHB | c.304A>G (p.Lys102Glu) c.433A>G (p.Lys145Glu) c.475A>G (p.Lys159Glu) n.392A>G n.409A>G | |
1 | g.17027814T>G | CA338272897 | SDHB | c.304A>C (p.Lys102Gln) c.433A>C (p.Lys145Gln) c.475A>C (p.Lys159Gln) n.392A>C n.409A>C | |
1 | g.17027815C>A | CA338272900 | SDHB | c.303G>T (p.Lys101Asn) c.432G>T (p.Lys144Asn) c.474G>T (p.Lys158Asn) n.391G>T n.408G>T | |
1 | g.17027815C>G | CA338272908 | SDHB | c.303G>C (p.Lys101Asn) c.432G>C (p.Lys144Asn) c.474G>C (p.Lys158Asn) n.391G>C n.408G>C | |
1 | g.17027815C>T | CA416086088 | SDHB | c.303G>A (p.Lys101=) c.432G>A (p.Lys144=) c.474G>A (p.Lys158=) n.391G>A n.408G>A | gnomAD v4 |
1 | g.17027816T>A | CA338272912 | SDHB | c.302A>T (p.Lys101Met) c.431A>T (p.Lys144Met) c.473A>T (p.Lys158Met) n.390A>T n.407A>T | |
1 | g.17027816T>C | CA338272913 | SDHB | c.302A>G (p.Lys101Arg) c.431A>G (p.Lys144Arg) c.473A>G (p.Lys158Arg) n.390A>G n.407A>G | |
1 | g.17027816T>G | CA338272914 | SDHB | c.302A>C (p.Lys101Thr) c.431A>C (p.Lys144Thr) c.473A>C (p.Lys158Thr) n.390A>C n.407A>C | |
1 | g.17027817del | CA2580060651 | SDHB | c.302del (p.Lys101ArgfsTer17) c.431del (p.Lys144ArgfsTer17) c.473del (p.Lys158ArgfsTer17) n.390del n.407del | ClinVar |
1 | g.17027817T>A | CA338272917 | SDHB | c.301A>T (p.Lys101Ter) c.430A>T (p.Lys144Ter) c.472A>T (p.Lys158Ter) n.389A>T n.406A>T | |
1 | g.17027817T>C | CA338272916 | SDHB | c.301A>G (p.Lys101Glu) c.430A>G (p.Lys144Glu) c.472A>G (p.Lys158Glu) n.389A>G n.406A>G | ClinVar |
1 | g.17027817T>G | CA338272915 | SDHB | c.301A>C (p.Lys101Gln) c.430A>C (p.Lys144Gln) c.472A>C (p.Lys158Gln) n.389A>C n.406A>C | |
1 | g.17027818C>A | CA338272918 | SDHB | c.300G>T (p.Leu100Phe) c.429G>T (p.Leu143Phe) c.471G>T (p.Leu157Phe) n.388G>T n.405G>T | |
1 | g.17027818C>G | CA338272920 | SDHB | c.300G>C (p.Leu100Phe) c.429G>C (p.Leu143Phe) c.471G>C (p.Leu157Phe) n.388G>C n.405G>C | |
1 | g.17027818C>T | CA416086106 | SDHB | c.300G>A (p.Leu100=) c.429G>A (p.Leu143=) c.471G>A (p.Leu157=) n.388G>A n.405G>A | |
1 | g.17027818_17027819delinsCA | CA1156080183 | SDHB | c.299_300delinsTG (p.Leu100=) c.428_429delinsTG (p.Leu143=) c.470_471delinsTG (p.Leu157=) n.387_388delinsTG n.404_405delinsTG | |
1 | g.17027819A= | CA1156080184 | SDHB | c.299T= (p.Leu100=) c.428T= (p.Leu143=) c.470T= (p.Leu157=) n.387T= n.404T= | |
1 | g.17027819A>C | CA338272923 | SDHB | c.299T>G (p.Leu100Trp) c.428T>G (p.Leu143Trp) c.470T>G (p.Leu157Trp) n.387T>G n.404T>G | |
1 | g.17027819A>G | CA338272931 | SDHB | c.299T>C (p.Leu100Ser) c.428T>C (p.Leu143Ser) c.470T>C (p.Leu157Ser) n.387T>C n.404T>C | ClinVar dbSNP |
1 | g.17027819A>T | CA338272932 | SDHB | c.299T>A (p.Leu100Ter) c.428T>A (p.Leu143Ter) c.470T>A (p.Leu157Ter) n.387T>A n.404T>A | |
1 | g.17027821del | CA1139655469 | SDHB | c.299del (p.Leu100Ter) c.428del (p.Leu143Ter) c.470del (p.Leu157Ter) n.387del n.404del | ClinVar dbSNP gnomAD v4 |
1 | g.17027820A>C | CA338272935 | SDHB | c.298T>G (p.Leu100Val) c.427T>G (p.Leu143Val) c.469T>G (p.Leu157Val) n.386T>G n.403T>G | |
1 | g.17027820A>G | CA416086126 | SDHB | c.298T>C (p.Leu100=) c.427T>C (p.Leu143=) c.469T>C (p.Leu157=) n.386T>C n.403T>C | ClinVar gnomAD v4 |
1 | g.17027820A>T | CA338272936 | SDHB | c.298T>A (p.Leu100Met) c.427T>A (p.Leu143Met) c.469T>A (p.Leu157Met) n.386T>A n.403T>A | |
1 | g.17027821A= | CA1143370233 | SDHB | c.297T= (p.Tyr99=) c.426T= (p.Tyr142=) c.468T= (p.Tyr156=) n.385T= n.402T= | |
1 | g.17027821A>C | CA338272937 | SDHB | c.297T>G (p.Tyr99Ter) c.426T>G (p.Tyr142Ter) c.468T>G (p.Tyr156Ter) n.385T>G n.402T>G | |
1 | g.17027821A>G | CA18665949 | SDHB | c.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 |
1 | g.17027821A>T | CA338272940 | SDHB | c.297T>A (p.Tyr99Ter) c.426T>A (p.Tyr142Ter) c.468T>A (p.Tyr156Ter) n.385T>A n.402T>A | |
1 | g.17027822T>A | CA338272942 | SDHB | c.296A>T (p.Tyr99Phe) c.425A>T (p.Tyr142Phe) c.467A>T (p.Tyr156Phe) n.384A>T n.401A>T | |
1 | g.17027822T>C | CA338272951 | SDHB | c.296A>G (p.Tyr99Cys) c.425A>G (p.Tyr142Cys) c.467A>G (p.Tyr156Cys) n.384A>G n.401A>G | |
1 | g.17027822T>G | CA338272959 | SDHB | c.296A>C (p.Tyr99Ser) c.425A>C (p.Tyr142Ser) c.467A>C (p.Tyr156Ser) n.384A>C n.401A>C | |
1 | g.17027823A= | CA1156080185 | SDHB | c.295T= (p.Tyr99=) c.424T= (p.Tyr142=) c.466T= (p.Tyr156=) n.383T= n.400T= | |
1 | g.17027823A>C | CA338272980 | SDHB | c.295T>G (p.Tyr99Asp) c.424T>G (p.Tyr142Asp) c.466T>G (p.Tyr156Asp) n.383T>G n.400T>G | |
1 | g.17027823A>G | CA338272960 | SDHB | c.295T>C (p.Tyr99His) c.424T>C (p.Tyr142His) c.466T>C (p.Tyr156His) n.383T>C n.400T>C | dbSNP gnomAD v4 |
1 | g.17027823A>T | CA338272965 | SDHB | c.295T>A (p.Tyr99Asn) c.424T>A (p.Tyr142Asn) c.466T>A (p.Tyr156Asn) n.383T>A n.400T>A | |
1 | g.17027824del | CA2499214301 | SDHB | c.295del (p.Tyr99IlefsTer2) c.424del (p.Tyr142IlefsTer2) c.466del (p.Tyr156IlefsTer2) n.383del n.400del | ClinVar dbSNP |
1 | g.17027824A= | CA1156080186 | SDHB | c.294T= (p.Pro98=) c.423T= (p.Pro141=) c.465T= (p.Pro155=) n.382T= n.399T= | |
1 | g.17027824A>C | CA416086149 | SDHB | c.294T>G (p.Pro98=) c.423T>G (p.Pro141=) c.465T>G (p.Pro155=) n.382T>G n.399T>G | gnomAD v4 |
1 | g.17027824A>G | CA416086152 | SDHB | c.294T>C (p.Pro98=) c.423T>C (p.Pro141=) c.465T>C (p.Pro155=) n.382T>C n.399T>C | ClinVar dbSNP gnomAD v4 |
1 | g.17027824A>T | CA416086154 | SDHB | c.294T>A (p.Pro98=) c.423T>A (p.Pro141=) c.465T>A (p.Pro155=) n.382T>A n.399T>A | |
1 | g.17027825G>A | CA338272998 | SDHB | c.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 |
1 | g.17027825G>C | CA338273002 | SDHB | c.293C>G (p.Pro98Arg) c.422C>G (p.Pro141Arg) c.464C>G (p.Pro155Arg) n.381C>G n.398C>G | ClinVar |
1 | g.17027825G= | CA1156080187 | SDHB | c.293C= (p.Pro98=) c.422C= (p.Pro141=) c.464C= (p.Pro155=) n.381C= n.398C= | |
1 | g.17027825G>T | CA338273013 | SDHB | c.293C>A (p.Pro98His) c.422C>A (p.Pro141His) c.464C>A (p.Pro155His) n.381C>A n.398C>A | |
1 | g.17027826G>A | CA089630 | SDHB | c.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 |
1 | g.17027826G>C | CA338273026 | SDHB | c.292C>G (p.Pro98Ala) c.421C>G (p.Pro141Ala) c.463C>G (p.Pro155Ala) n.380C>G n.397C>G | |
1 | g.17027826G= | CA1156080188 | SDHB | c.292C= (p.Pro98=) c.421C= (p.Pro141=) c.463C= (p.Pro155=) n.380C= n.397C= | |
1 | g.17027826G>T | CA338273035 | SDHB | c.292C>A (p.Pro98Thr) c.421C>A (p.Pro141Thr) c.463C>A (p.Pro155Thr) n.380C>A n.397C>A | |
1 | g.17027827C>A | CA338273039 | SDHB | c.291G>T (p.Glu97Asp) c.420G>T (p.Glu140Asp) c.462G>T (p.Glu154Asp) n.379G>T n.396G>T | dbSNP |
1 | g.17027827C= | CA1156080189 | SDHB | c.291G= (p.Glu97=) c.420G= (p.Glu140=) c.462G= (p.Glu154=) n.379G= n.396G= | |
1 | g.17027827C>G | CA338273042 | SDHB | c.291G>C (p.Glu97Asp) c.420G>C (p.Glu140Asp) c.462G>C (p.Glu154Asp) n.379G>C n.396G>C | |
1 | g.17027827C>T | CA416086167 | SDHB | c.291G>A (p.Glu97=) c.420G>A (p.Glu140=) c.462G>A (p.Glu154=) n.379G>A n.396G>A | |
1 | g.17027828T>A | CA338273045 | SDHB | c.290A>T (p.Glu97Val) c.419A>T (p.Glu140Val) c.461A>T (p.Glu154Val) n.378A>T n.395A>T | |
1 | g.17027828T>C | CA18665969 | SDHB | c.290A>G (p.Glu97Gly) c.419A>G (p.Glu140Gly) c.461A>G (p.Glu154Gly) n.378A>G n.395A>G | dbSNP |
1 | g.17027828T>G | CA338273064 | SDHB | c.290A>C (p.Glu97Ala) c.419A>C (p.Glu140Ala) c.461A>C (p.Glu154Ala) n.378A>C n.395A>C | |
1 | g.17027828T= | CA1145610940 | SDHB | c.290A= (p.Glu97=) c.419A= (p.Glu140=) c.461A= (p.Glu154=) n.378A= n.395A= | |
1 | g.17027829C>A | CA338273088 | SDHB | c.289G>T (p.Glu97Ter) c.418G>T (p.Glu140Ter) c.460G>T (p.Glu154Ter) n.377G>T n.394G>T | |
1 | g.17027829C>G | CA338273086 | SDHB | c.289G>C (p.Glu97Gln) c.418G>C (p.Glu140Gln) c.460G>C (p.Glu154Gln) n.377G>C n.394G>C | |
1 | g.17027829C>T | CA338273078 | SDHB | c.289G>A (p.Glu97Lys) c.418G>A (p.Glu140Lys) c.460G>A (p.Glu154Lys) n.377G>A n.394G>A | |
1 | g.17027830A>C | CA338273091 | SDHB | c.288T>G (p.Ile96Met) c.417T>G (p.Ile139Met) c.459T>G (p.Ile153Met) n.376T>G n.393T>G | |
1 | g.17027830A>G | CA416086179 | SDHB | c.288T>C (p.Ile96=) c.417T>C (p.Ile139=) c.459T>C (p.Ile153=) n.376T>C n.393T>C | ClinVar gnomAD v4 |
1 | g.17027830A>T | CA416086181 | SDHB | c.288T>A (p.Ile96=) c.417T>A (p.Ile139=) c.459T>A (p.Ile153=) n.376T>A n.393T>A | |
1 | g.17027831A= | CA1156080190 | SDHB | c.287T= (p.Ile96=) c.416T= (p.Ile139=) c.458T= (p.Ile153=) n.375T= n.392T= | |
1 | g.17027831A>C | CA338273104 | SDHB | c.287T>G (p.Ile96Ser) c.416T>G (p.Ile139Ser) c.458T>G (p.Ile153Ser) n.375T>G n.392T>G | |
1 | g.17027831A>G | CA338273094 | SDHB | c.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 |
1 | g.17027831A>T | CA338273097 | SDHB | c.287T>A (p.Ile96Asn) c.416T>A (p.Ile139Asn) c.458T>A (p.Ile153Asn) n.375T>A n.392T>A | |
1 | g.17027832T>A | CA338273110 | SDHB | c.286A>T (p.Ile96Phe) c.415A>T (p.Ile139Phe) c.457A>T (p.Ile153Phe) n.374A>T n.391A>T | ClinVar dbSNP |
1 | g.17027832T>C | CA338273114 | SDHB | c.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 |
1 | g.17027832T>G | CA338273130 | SDHB | c.286A>C (p.Ile96Leu) c.415A>C (p.Ile139Leu) c.457A>C (p.Ile153Leu) n.374A>C n.391A>C | gnomAD v4 |
1 | g.17027832T= | CA1156080191 | SDHB | c.286A= (p.Ile96=) c.415A= (p.Ile139=) c.457A= (p.Ile153=) n.374A= n.391A= | |
1 | g.17027833G>A | CA416086199 | SDHB | c.285C>T (p.Ser95=) c.414C>T (p.Ser138=) c.456C>T (p.Ser152=) n.373C>T n.390C>T | ClinVar dbSNP |
1 | g.17027833G>C | CA416086202 | SDHB | c.285C>G (p.Ser95=) c.414C>G (p.Ser138=) c.456C>G (p.Ser152=) n.373C>G n.390C>G | |
1 | g.17027833G= | CA1156080192 | SDHB | c.285C= (p.Ser95=) c.414C= (p.Ser138=) c.456C= (p.Ser152=) n.373C= n.390C= | |
1 | g.17027833G>T | CA416086203 | SDHB | c.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 |
1 | g.17027834G>A | CA089629 | SDHB | c.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 |
1 | g.17027834G>C | CA338273136 | SDHB | c.284C>G (p.Ser95Cys) c.413C>G (p.Ser138Cys) c.455C>G (p.Ser152Cys) n.372C>G n.389C>G | |
1 | g.17027834G= | CA1143415682 | SDHB | c.284C= (p.Ser95=) c.413C= (p.Ser138=) c.455C= (p.Ser152=) n.372C= n.389C= | |
1 | g.17027834G>T | CA338273140 | SDHB | c.284C>A (p.Ser95Tyr) c.413C>A (p.Ser138Tyr) c.455C>A (p.Ser152Tyr) n.372C>A n.389C>A | ClinVar dbSNP |
1 | g.17027835A= | CA1156080193 | SDHB | c.283T= (p.Ser95=) c.412T= (p.Ser138=) c.454T= (p.Ser152=) n.371T= n.388T= | |
1 | g.17027835A>C | CA338273142 | SDHB | c.283T>G (p.Ser95Ala) c.412T>G (p.Ser138Ala) c.454T>G (p.Ser152Ala) n.371T>G n.388T>G | |
1 | g.17027835A>G | CA10608342 | SDHB | c.283T>C (p.Ser95Pro) c.412T>C (p.Ser138Pro) c.454T>C (p.Ser152Pro) n.371T>C n.388T>C | ClinVar dbSNP gnomAD v4 |
1 | g.17027835A>T | CA338273143 | SDHB | c.283T>A (p.Ser95Thr) c.412T>A (p.Ser138Thr) c.454T>A (p.Ser152Thr) n.371T>A n.388T>A | |
1 | g.17027836T>A | CA338273144 | SDHB | c.282A>T (p.Lys94Asn) c.411A>T (p.Lys137Asn) c.453A>T (p.Lys151Asn) n.370A>T n.387A>T | |
1 | g.17027836T>C | CA416086220 | SDHB | c.282A>G (p.Lys94=) c.411A>G (p.Lys137=) c.453A>G (p.Lys151=) n.370A>G n.387A>G | ClinVar dbSNP |
1 | g.17027836T>G | CA338273145 | SDHB | c.282A>C (p.Lys94Asn) c.411A>C (p.Lys137Asn) c.453A>C (p.Lys151Asn) n.370A>C n.387A>C | |
1 | g.17027836T= | CA1156080194 | SDHB | c.282A= (p.Lys94=) c.411A= (p.Lys137=) c.453A= (p.Lys151=) n.370A= n.387A= | |
1 | g.17027838del | CA2586964061 | SDHB | c.282del (p.Lys94AsnfsTer7) c.411del (p.Lys137AsnfsTer7) c.453del (p.Lys151AsnfsTer7) n.370del n.387del | |
1 | g.17027836_17027840del | CA2586964060 | SDHB | c.278_282del (p.Tyr93PhefsTer3) c.407_411del (p.Tyr136PhefsTer3) c.449_453del (p.Tyr150PhefsTer3) n.366_370del n.383_387del | |
1 | g.17027837T>A | CA338273146 | SDHB | c.281A>T (p.Lys94Ile) c.410A>T (p.Lys137Ile) c.452A>T (p.Lys151Ile) n.369A>T n.386A>T | |
1 | g.17027837T>C | CA338273152 | SDHB | c.281A>G (p.Lys94Arg) c.410A>G (p.Lys137Arg) c.452A>G (p.Lys151Arg) n.369A>G n.386A>G | ClinVar |
1 | g.17027837T>G | CA338273147 | SDHB | c.281A>C (p.Lys94Thr) c.410A>C (p.Lys137Thr) c.452A>C (p.Lys151Thr) n.369A>C n.386A>C | ClinVar |
1 | g.17027838T>A | CA338273153 | SDHB | c.280A>T (p.Lys94Ter) c.409A>T (p.Lys137Ter) c.451A>T (p.Lys151Ter) n.368A>T n.385A>T | |
1 | g.17027838T>C | CA338273154 | SDHB | c.280A>G (p.Lys94Glu) c.409A>G (p.Lys137Glu) c.451A>G (p.Lys151Glu) n.368A>G n.385A>G | ClinVar dbSNP |
1 | g.17027838T>G | CA338273155 | SDHB | c.280A>C (p.Lys94Gln) c.409A>C (p.Lys137Gln) c.451A>C (p.Lys151Gln) n.368A>C n.385A>C | |
1 | g.17027839G>A | CA416086240 | SDHB | c.279C>T (p.Tyr93=) c.408C>T (p.Tyr136=) c.450C>T (p.Tyr150=) n.367C>T n.384C>T | gnomAD v4 |
1 | g.17027839G>C | CA338273181 | SDHB | c.279C>G (p.Tyr93Ter) c.408C>G (p.Tyr136Ter) c.450C>G (p.Tyr150Ter) n.367C>G n.384C>G | ClinVar dbSNP |
1 | g.17027839G>T | CA338273186 | SDHB | c.279C>A (p.Tyr93Ter) c.408C>A (p.Tyr136Ter) c.450C>A (p.Tyr150Ter) n.367C>A n.384C>A | |
1 | g.17027840T>A | CA338273198 | SDHB | c.278A>T (p.Tyr93Phe) c.407A>T (p.Tyr136Phe) c.449A>T (p.Tyr150Phe) n.366A>T n.383A>T | |
1 | g.17027840T>C | CA338273209 | SDHB | c.278A>G (p.Tyr93Cys) c.407A>G (p.Tyr136Cys) c.449A>G (p.Tyr150Cys) n.366A>G n.383A>G | |
1 | g.17027840T>G | CA338273242 | SDHB | c.278A>C (p.Tyr93Ser) c.407A>C (p.Tyr136Ser) c.449A>C (p.Tyr150Ser) n.366A>C n.383A>C | |
1 | g.17027841A>C | CA338273255 | SDHB | c.277T>G (p.Tyr93Asp) c.406T>G (p.Tyr136Asp) c.448T>G (p.Tyr150Asp) n.365T>G n.382T>G | |
1 | g.17027841A>G | CA338273265 | SDHB | c.277T>C (p.Tyr93His) c.406T>C (p.Tyr136His) c.448T>C (p.Tyr150His) n.365T>C n.382T>C | ClinVar dbSNP |
1 | g.17027841A>T | CA338273269 | SDHB | c.277T>A (p.Tyr93Asn) c.406T>A (p.Tyr136Asn) c.448T>A (p.Tyr150Asn) n.365T>A n.382T>A | |
1 | g.17027841_17027844delinsACTG | CA1156080195 | SDHB | c.274_277delinsCAGT (p.Gln92=) c.403_406delinsCAGT (p.Gln135=) c.445_448delinsCAGT (p.Gln149=) n.362_365delinsCAGT n.379_382delinsCAGT | |
1 | g.17027842C>A | CA18665993 | SDHB | c.276G>T (p.Gln92His) c.405G>T (p.Gln135His) c.447G>T (p.Gln149His) n.364G>T n.381G>T | ClinVar dbSNP gnomAD v4 |
1 | g.17027842C= | CA1143411882 | SDHB | c.276G= (p.Gln92=) c.405G= (p.Gln135=) c.447G= (p.Gln149=) n.364G= n.381G= | |
1 | g.17027842C>G | CA338273273 | SDHB | c.276G>C (p.Gln92His) c.405G>C (p.Gln135His) c.447G>C (p.Gln149His) n.364G>C n.381G>C | |
1 | g.17027842C>T | CA416086252 | SDHB | c.276G>A (p.Gln92=) c.405G>A (p.Gln135=) c.447G>A (p.Gln149=) n.364G>A n.381G>A | ClinVar dbSNP |
1 | g.17027842_17027844delinsAGATACC | CA645509078 | SDHB | c.274_276delinsGGTATCT (p.Gln92GlyfsTer7) c.403_405delinsGGTATCT (p.Gln135GlyfsTer7) c.445_447delinsGGTATCT (p.Gln149GlyfsTer7) n.362_364delinsGGTATCT n.379_381delinsGGTATCT | ClinVar dbSNP |
1 | g.17027843T>A | CA338273280 | SDHB | c.275A>T (p.Gln92Leu) c.404A>T (p.Gln135Leu) c.446A>T (p.Gln149Leu) n.363A>T n.380A>T | |
1 | g.17027843T>C | CA338273300 | SDHB | c.275A>G (p.Gln92Arg) c.404A>G (p.Gln135Arg) c.446A>G (p.Gln149Arg) n.363A>G n.380A>G | ClinVar dbSNP |
1 | g.17027843T>G | CA338273303 | SDHB | c.275A>C (p.Gln92Pro) c.404A>C (p.Gln135Pro) c.446A>C (p.Gln149Pro) n.363A>C n.380A>C | ClinVar gnomAD v4 |
1 | g.17027843T= | CA1156080196 | SDHB | c.275A= (p.Gln92=) c.404A= (p.Gln135=) c.446A= (p.Gln149=) n.363A= n.380A= | |
1 | g.17027843_17027844delinsAGATACC | CA2586964062 | SDHB | c.274_275delinsGGTATCT (p.Gln92GlyfsTer11) c.403_404delinsGGTATCT (p.Gln135GlyfsTer11) c.445_446delinsGGTATCT (p.Gln149GlyfsTer11) n.362_363delinsGGTATCT n.379_380delinsGGTATCT | |
1 | g.17027845_17027846dup | CA2580611151 | SDHB | c.274_275dup (p.Gln92HisfsTer10) c.403_404dup (p.Gln135HisfsTer10) c.445_446dup (p.Gln149HisfsTer10) n.362_363dup n.379_380dup | ClinVar dbSNP |
1 | g.17027843_17027844insCCATA | CA658795406 | SDHB | c.274_275insTATGG (p.Gln92LeufsTer11) c.403_404insTATGG (p.Gln135LeufsTer11) c.445_446insTATGG (p.Gln149LeufsTer11) n.362_363insTATGG n.379_380insTATGG | ClinVar dbSNP |
1 | g.17027844del | CA2586964063 | SDHB | c.274del (p.Gln92SerfsTer9) c.403del (p.Gln135SerfsTer9) c.445del (p.Gln149SerfsTer9) n.362del n.379del | |
1 | g.17027844G>A | CA10577675 | SDHB | c.274C>T (p.Gln92Ter) c.403C>T (p.Gln135Ter) c.445C>T (p.Gln149Ter) n.362C>T n.379C>T | ClinVar dbSNP gnomAD v4 |
1 | g.17027844G>C | CA338273308 | SDHB | c.274C>G (p.Gln92Glu) c.403C>G (p.Gln135Glu) c.445C>G (p.Gln149Glu) n.362C>G n.379C>G | |
1 | g.17027844G= | CA1156080197 | SDHB | c.274C= (p.Gln92=) c.403C= (p.Gln135=) c.445C= (p.Gln149=) n.362C= n.379C= | |
1 | g.17027844G>T | CA338273310 | SDHB | c.274C>A (p.Gln92Lys) c.403C>A (p.Gln135Lys) c.445C>A (p.Gln149Lys) n.362C>A n.379C>A | gnomAD v4 |
1 | g.17027844_17027845delinsCCATAGA | CA2838032012 | SDHB | c.273_274delinsTCTATGG (p.Gln92LeufsTer11) c.402_403delinsTCTATGG (p.Gln135LeufsTer11) c.444_445delinsTCTATGG (p.Gln149LeufsTer11) n.361_362delinsTCTATGG n.378_379delinsTCTATGG | |
1 | g.17027845T>A | CA416086267 | SDHB | c.273A>T (p.Ala91=) c.402A>T (p.Ala134=) c.444A>T (p.Ala148=) n.361A>T n.378A>T | ClinVar |
1 | g.17027845T>C | CA416086270 | SDHB | c.273A>G (p.Ala91=) c.402A>G (p.Ala134=) c.444A>G (p.Ala148=) n.361A>G n.378A>G | |
1 | g.17027845T>G | CA416086283 | SDHB | c.273A>C (p.Ala91=) c.402A>C (p.Ala134=) c.444A>C (p.Ala148=) n.361A>C n.378A>C | |
1 | g.17027846G>A | CA338273312 | SDHB | c.272C>T (p.Ala91Val) c.401C>T (p.Ala134Val) c.443C>T (p.Ala148Val) n.360C>T n.377C>T | ClinVar dbSNP |
1 | g.17027846G>C | CA338273314 | SDHB | c.272C>G (p.Ala91Gly) c.401C>G (p.Ala134Gly) c.443C>G (p.Ala148Gly) n.360C>G n.377C>G | |
1 | g.17027846G= | CA1156080199 | SDHB | c.272C= (p.Ala91=) c.401C= (p.Ala134=) c.443C= (p.Ala148=) n.360C= n.377C= | |
1 | g.17027846G>T | CA338273318 | SDHB | c.272C>A (p.Ala91Glu) c.401C>A (p.Ala134Glu) c.443C>A (p.Ala148Glu) n.360C>A n.377C>A | |
1 | g.17027846_17027847delinsGC | CA1156080198 | SDHB | c.271_272delinsGC (p.Ala91=) c.400_401delinsGC (p.Ala134=) c.442_443delinsGC (p.Ala148=) n.359_360delinsGC n.376_377delinsGC | |
1 | g.17027847del | CA10577676 | SDHB | c.271del (p.Ala91HisfsTer10) c.400del (p.Ala134HisfsTer10) c.442del (p.Ala148HisfsTer10) n.359del n.376del | ClinVar dbSNP |
1 | g.17027847C>A | CA338273327 | SDHB | c.271G>T (p.Ala91Ser) c.400G>T (p.Ala134Ser) c.442G>T (p.Ala148Ser) n.359G>T n.376G>T | ClinVar |
1 | g.17027847C= | CA1156080200 | SDHB | c.271G= (p.Ala91=) c.400G= (p.Ala134=) c.442G= (p.Ala148=) n.359G= n.376G= | |
1 | g.17027847C>G | CA338273330 | SDHB | c.271G>C (p.Ala91Pro) c.400G>C (p.Ala134Pro) c.442G>C (p.Ala148Pro) n.359G>C n.376G>C | |
1 | g.17027847C>T | CA338273338 | SDHB | c.271G>A (p.Ala91Thr) c.400G>A (p.Ala134Thr) c.442G>A (p.Ala148Thr) n.359G>A n.376G>A | ClinVar dbSNP |
1 | g.17027848del | CA658655539 | SDHB | c.270del (p.Tyr90Ter) c.399del (p.Tyr133Ter) c.441del (p.Tyr147Ter) n.358del n.375del | |
1 | g.17027848A= | CA1156080201 | SDHB | c.270T= (p.Tyr90=) c.399T= (p.Tyr133=) c.441T= (p.Tyr147=) n.358T= n.375T= | |
1 | g.17027848A>C | CA16609941 | SDHB | c.270T>G (p.Tyr90Ter) c.399T>G (p.Tyr133Ter) c.441T>G (p.Tyr147Ter) n.358T>G n.375T>G | ClinVar dbSNP |
1 | g.17027848A>G | CA416086308 | SDHB | c.270T>C (p.Tyr90=) c.399T>C (p.Tyr133=) c.441T>C (p.Tyr147=) n.358T>C n.375T>C | ClinVar dbSNP |
1 | g.17027848A>T | CA338273344 | SDHB | c.270T>A (p.Tyr90Ter) c.399T>A (p.Tyr133Ter) c.441T>A (p.Tyr147Ter) n.358T>A n.375T>A | |
1 | g.17027849T>A | CA338273349 | SDHB | c.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 |
1 | g.17027849T>C | CA089628 | SDHB | c.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 |
1 | g.17027849T>G | CA338273355 | SDHB | c.269A>C (p.Tyr90Ser) c.398A>C (p.Tyr133Ser) c.440A>C (p.Tyr147Ser) n.357A>C n.374A>C | |
1 | g.17027849T= | CA1156080202 | SDHB | c.269A= (p.Tyr90=) c.398A= (p.Tyr133=) c.440A= (p.Tyr147=) n.357A= n.374A= | |
1 | g.17027850A>C | CA338273356 | SDHB | c.268T>G (p.Tyr90Asp) c.397T>G (p.Tyr133Asp) c.439T>G (p.Tyr147Asp) n.356T>G n.373T>G | |
1 | g.17027850A>G | CA338273359 | SDHB | c.268T>C (p.Tyr90His) c.397T>C (p.Tyr133His) c.439T>C (p.Tyr147His) n.356T>C n.373T>C | ClinVar |
1 | g.17027850A>T | CA338273377 | SDHB | c.268T>A (p.Tyr90Asn) c.397T>A (p.Tyr133Asn) c.439T>A (p.Tyr147Asn) n.356T>A n.373T>A | |
1 | g.17027851G>A | CA416086332 | SDHB | c.267C>T (p.Phe89=) c.396C>T (p.Phe132=) c.438C>T (p.Phe146=) n.355C>T n.372C>T | gnomAD v4 |
1 | g.17027851G>C | CA338273382 | SDHB | c.267C>G (p.Phe89Leu) c.396C>G (p.Phe132Leu) c.438C>G (p.Phe146Leu) n.355C>G n.372C>G | ClinVar dbSNP |
1 | g.17027851G= | CA1156080203 | SDHB | c.267C= (p.Phe89=) c.396C= (p.Phe132=) c.438C= (p.Phe146=) n.355C= n.372C= | |
1 | g.17027851G>T | CA338273390 | SDHB | c.267C>A (p.Phe89Leu) c.396C>A (p.Phe132Leu) c.438C>A (p.Phe146Leu) n.355C>A n.372C>A | ClinVar dbSNP gnomAD v4 |
1 | g.17027852A>C | CA338273393 | SDHB | c.266T>G (p.Phe89Cys) c.395T>G (p.Phe132Cys) c.437T>G (p.Phe146Cys) n.354T>G n.371T>G | |
1 | g.17027852A>G | CA338273397 | SDHB | c.266T>C (p.Phe89Ser) c.395T>C (p.Phe132Ser) c.437T>C (p.Phe146Ser) n.354T>C n.371T>C | ClinVar dbSNP |
1 | g.17027852A>T | CA338273400 | SDHB | c.266T>A (p.Phe89Tyr) c.395T>A (p.Phe132Tyr) c.437T>A (p.Phe146Tyr) n.354T>A n.371T>A | |
1 | g.17027853del | CA2586964064 | SDHB | c.266del (p.Phe89SerfsTer12) c.395del (p.Phe132SerfsTer12) c.437del (p.Phe146SerfsTer12) n.354del n.371del | |
1 | g.17027853A= | CA1156080204 | SDHB | c.265T= (p.Phe89=) c.394T= (p.Phe132=) c.436T= (p.Phe146=) n.353T= n.370T= | |
1 | g.17027853A>C | CA338273404 | SDHB | c.265T>G (p.Phe89Val) c.394T>G (p.Phe132Val) c.436T>G (p.Phe146Val) n.353T>G n.370T>G | ClinVar dbSNP gnomAD v4 |
1 | g.17027853A>G | CA338273408 | SDHB | c.265T>C (p.Phe89Leu) c.394T>C (p.Phe132Leu) c.436T>C (p.Phe146Leu) n.353T>C n.370T>C | |
1 | g.17027853A>T | CA338273422 | SDHB | c.265T>A (p.Phe89Ile) c.394T>A (p.Phe132Ile) c.436T>A (p.Phe146Ile) n.353T>A n.370T>A | |
1 | g.17027854del | CA658655538 | SDHB | c.264del (p.Phe89SerfsTer12) c.393del (p.Phe132SerfsTer12) c.435del (p.Phe146SerfsTer12) n.352del n.369del | |
1 | g.17027854G>A | CA416086353 | SDHB | c.264C>T (p.Asn88=) c.393C>T (p.Asn131=) c.435C>T (p.Asn145=) n.352C>T n.369C>T | ClinVar dbSNP |
1 | g.17027854G>C | CA338273426 | SDHB | c.264C>G (p.Asn88Lys) c.393C>G (p.Asn131Lys) c.435C>G (p.Asn145Lys) n.352C>G n.369C>G | |
1 | g.17027854G>T | CA338273425 | SDHB | c.264C>A (p.Asn88Lys) c.393C>A (p.Asn131Lys) c.435C>A (p.Asn145Lys) n.352C>A n.369C>A | |
1 | g.17027855T>A | CA18666011 | SDHB | c.263A>T (p.Asn88Ile) c.392A>T (p.Asn131Ile) c.434A>T (p.Asn145Ile) n.351A>T n.368A>T | dbSNP gnomAD v4 |
1 | g.17027855T>C | CA338273454 | SDHB | c.263A>G (p.Asn88Ser) c.392A>G (p.Asn131Ser) c.434A>G (p.Asn145Ser) n.351A>G n.368A>G | ClinVar gnomAD v4 |
1 | g.17027855T>G | CA338273452 | SDHB | c.263A>C (p.Asn88Thr) c.392A>C (p.Asn131Thr) c.434A>C (p.Asn145Thr) n.351A>C n.368A>C | |
1 | g.17027855T= | CA1156080205 | SDHB | c.263A= (p.Asn88=) c.392A= (p.Asn131=) c.434A= (p.Asn145=) n.351A= n.368A= | |
1 | g.17027856T>A | CA338273455 | SDHB | c.262A>T (p.Asn88Tyr) c.391A>T (p.Asn131Tyr) c.433A>T (p.Asn145Tyr) n.350A>T n.367A>T | |
1 | g.17027856T>C | CA338273461 | SDHB | c.262A>G (p.Asn88Asp) c.391A>G (p.Asn131Asp) c.433A>G (p.Asn145Asp) n.350A>G n.367A>G | |
1 | g.17027856T>G | CA338273456 | SDHB | c.262A>C (p.Asn88His) c.391A>C (p.Asn131His) c.433A>C (p.Asn145His) n.350A>C n.367A>C | |
1 | g.17027857G>A | CA416086378 | SDHB | c.261C>T (p.Ser87=) c.390C>T (p.Ser130=) c.432C>T (p.Ser144=) n.349C>T n.366C>T | gnomAD v4 |
1 | g.17027857G>C | CA338273466 | SDHB | c.261C>G (p.Ser87Arg) c.390C>G (p.Ser130Arg) c.432C>G (p.Ser144Arg) n.349C>G n.366C>G | gnomAD v4 |
1 | g.17027857G>T | CA338273469 | SDHB | c.261C>A (p.Ser87Arg) c.390C>A (p.Ser130Arg) c.432C>A (p.Ser144Arg) n.349C>A n.366C>A | gnomAD v4 COSMIC |
1 | g.17027858C>A | CA338273480 | SDHB | c.260G>T (p.Ser87Ile) c.389G>T (p.Ser130Ile) c.431G>T (p.Ser144Ile) n.348G>T n.365G>T | |
1 | g.17027858C>G | CA338273484 | SDHB | c.260G>C (p.Ser87Thr) c.389G>C (p.Ser130Thr) c.431G>C (p.Ser144Thr) n.348G>C n.365G>C | |
1 | g.17027858C>T | CA338273488 | SDHB | c.260G>A (p.Ser87Asn) c.389G>A (p.Ser130Asn) c.431G>A (p.Ser144Asn) n.348G>A n.365G>A | gnomAD v4 |
1 | g.17027859T>A | CA338273491 | SDHB | c.259A>T (p.Ser87Cys) c.388A>T (p.Ser130Cys) c.430A>T (p.Ser144Cys) n.347A>T n.364A>T | |
1 | g.17027859T>C | CA338273495 | SDHB | c.259A>G (p.Ser87Gly) c.388A>G (p.Ser130Gly) c.430A>G (p.Ser144Gly) n.347A>G n.364A>G | |
1 | g.17027859T>G | CA338273496 | SDHB | c.259A>C (p.Ser87Arg) c.388A>C (p.Ser130Arg) c.430A>C (p.Ser144Arg) n.347A>C n.364A>C | |
1 | g.17027860C>A | CA338273497 | SDHB | c.258G>T (p.Leu86Phe) c.387G>T (p.Leu129Phe) c.429G>T (p.Leu143Phe) n.346G>T n.363G>T | gnomAD v4 |
1 | g.17027860C>G | CA338273498 | SDHB | c.258G>C (p.Leu86Phe) c.387G>C (p.Leu129Phe) c.429G>C (p.Leu143Phe) n.346G>C n.363G>C | |
1 | g.17027860C>T | CA416086399 | SDHB | c.258G>A (p.Leu86=) c.387G>A (p.Leu129=) c.429G>A (p.Leu143=) n.346G>A n.363G>A | |
1 | g.17027861A>C | CA338273499 | SDHB | c.257T>G (p.Leu86Trp) c.386T>G (p.Leu129Trp) c.428T>G (p.Leu143Trp) n.345T>G n.362T>G | |
1 | g.17027861A>G | CA338273500 | SDHB | c.257T>C (p.Leu86Ser) c.386T>C (p.Leu129Ser) c.428T>C (p.Leu143Ser) n.345T>C n.362T>C | |
1 | g.17027861A>T | CA338273501 | SDHB | c.257T>A (p.Leu86Ter) c.386T>A (p.Leu129Ter) c.428T>A (p.Leu143Ter) n.345T>A n.362T>A | |
1 | g.17027863del | CA2574235758 | SDHB | c.257del (p.Leu86Ter) c.386del (p.Leu129Ter) c.428del (p.Leu143Ter) n.345del n.362del | |
1 | g.17027862A= | CA1156080206 | SDHB | c.256T= (p.Leu86=) c.385T= (p.Leu129=) c.427T= (p.Leu143=) n.344T= n.361T= | |
1 | g.17027862A>C | CA338273502 | SDHB | c.256T>G (p.Leu86Val) c.385T>G (p.Leu129Val) c.427T>G (p.Leu143Val) n.344T>G n.361T>G | |
1 | g.17027862A>G | CA416086418 | SDHB | c.256T>C (p.Leu86=) c.385T>C (p.Leu129=) c.427T>C (p.Leu143=) n.344T>C n.361T>C | |
1 | g.17027862A>T | CA338273503 | SDHB | c.256T>A (p.Leu86Met) c.385T>A (p.Leu129Met) c.427T>A (p.Leu143Met) n.344T>A n.361T>A | ClinVar dbSNP gnomAD v4 |
1 | g.17027862_17027872delinsG | CA2586964065 | SDHB | c.253-7_256delinsC c.382-7_385delinsC c.424-7_427delinsC n.341-7_344delinsC n.358-7_361delinsC | |
1 | g.17027863A>C | CA338273504 | SDHB | c.255T>G (p.Asp85Glu) c.384T>G (p.Asp128Glu) c.426T>G (p.Asp142Glu) n.343T>G n.360T>G | COSMIC |
1 | g.17027863A>G | CA416086424 | SDHB | c.255T>C (p.Asp85=) c.384T>C (p.Asp128=) c.426T>C (p.Asp142=) n.343T>C n.360T>C | ClinVar |
1 | g.17027863A>T | CA338273505 | SDHB | c.255T>A (p.Asp85Glu) c.384T>A (p.Asp128Glu) c.426T>A (p.Asp142Glu) n.343T>A n.360T>A | |
1 | g.17027864T>A | CA089626 | SDHB | c.254A>T (p.Asp85Val) c.383A>T (p.Asp128Val) c.425A>T (p.Asp142Val) n.342A>T n.359A>T | ClinVar dbSNP ExAC gnomAD v2 |
1 | g.17027864T>C | CA338273506 | SDHB | c.254A>G (p.Asp85Gly) c.383A>G (p.Asp128Gly) c.425A>G (p.Asp142Gly) n.342A>G n.359A>G | ClinVar dbSNP gnomAD v4 |
1 | g.17027864T>G | CA338273509 | SDHB | c.254A>C (p.Asp85Ala) c.383A>C (p.Asp128Ala) c.425A>C (p.Asp142Ala) n.342A>C n.359A>C | |
1 | g.17027864T= | CA1156080207 | SDHB | c.254A= (p.Asp85=) c.383A= (p.Asp128=) c.425A= (p.Asp142=) n.342A= n.359A= | |
1 | g.17027865C>A | CA338273513 | SDHB | c.253G>T (p.Asp85Tyr) c.382G>T (p.Asp128Tyr) c.424G>T (p.Asp142Tyr) n.341G>T n.358G>T | gnomAD v4 |
1 | g.17027865C= | CA1156080208 | SDHB | c.253G= (p.Asp85=) c.382G= (p.Asp128=) c.424G= (p.Asp142=) n.341G= n.358G= | |
1 | g.17027865C>G | CA338273517 | SDHB | c.253G>C (p.Asp85His) c.382G>C (p.Asp128His) c.424G>C (p.Asp142His) n.341G>C n.358G>C | gnomAD v4 |
1 | g.17027865C>T | CA338273520 | SDHB | c.253G>A (p.Asp85Asn) c.382G>A (p.Asp128Asn) c.424G>A (p.Asp142Asn) n.341G>A n.358G>A | ClinVar dbSNP |
1 | g.17027866C>A | CA338273529 | SDHB | c.253-1G>T (n.253-1G>T) c.382-1G>T (n.382-1G>T) c.424-1G>T (n.424-1G>T) n.341-1G>T n.358-1G>T | gnomAD v4 |
1 | g.17027866C= | CA1156080209 | SDHB | c.253-1G= (n.253-1G=) c.382-1G= (n.382-1G=) c.424-1G= (n.424-1G=) n.341-1G= n.358-1G= | |
1 | g.17027866C>G | CA338273530 | SDHB | c.253-1G>C (n.253-1G>C) c.382-1G>C (n.382-1G>C) c.424-1G>C (n.424-1G>C) n.341-1G>C n.358-1G>C | |
1 | g.17027866C>T | CA338273531 | SDHB | c.253-1G>A (n.253-1G>A) c.382-1G>A (n.382-1G>A) c.424-1G>A (n.424-1G>A) n.341-1G>A n.358-1G>A | ClinVar dbSNP |
1 | g.17027867del | CA2586964066 | SDHB | c.253-2del (n.253-2del) c.382-2del (n.382-2del) c.424-2del (n.424-2del) n.341-2del n.358-2del | dbSNP gnomAD v4 |
1 | g.17027867T>A | CA338273535 | SDHB | c.253-2A>T (n.253-2A>T) c.382-2A>T (n.382-2A>T) c.424-2A>T (n.424-2A>T) n.341-2A>T n.358-2A>T | |
1 | g.17027867T>C | CA338273533 | SDHB | c.253-2A>G (n.253-2A>G) c.382-2A>G (n.382-2A>G) c.424-2A>G (n.424-2A>G) n.341-2A>G n.358-2A>G | ClinVar dbSNP gnomAD v4 |
1 | g.17027867T>G | CA338273532 | SDHB | c.253-2A>C (n.253-2A>C) c.382-2A>C (n.382-2A>C) c.424-2A>C (n.424-2A>C) n.341-2A>C n.358-2A>C | |
1 | g.17027868_17027945del | CA2695197978 | SDHB | c.253-79_253-2del (n.253-79_253-2del) c.382-79_382-2del (n.382-79_382-2del) c.424-79_424-2del (n.424-79_424-2del) n.341-79_341-2del n.358-79_358-2del | ClinVar |
1 | g.17027868G>A | CA2643678113 | SDHB | c.253-3C>T (n.253-3C>T) c.382-3C>T (n.382-3C>T) c.424-3C>T (n.424-3C>T) n.341-3C>T n.358-3C>T | gnomAD v4 |
1 | g.17027868G>C | CA658655537 | SDHB | c.253-3C>G (n.253-3C>G) c.382-3C>G (n.382-3C>G) c.424-3C>G (n.424-3C>G) n.341-3C>G n.358-3C>G | ClinVar dbSNP |
1 | g.17027868G= | CA1156080210 | SDHB | c.253-3C= (n.253-3C=) c.382-3C= (n.382-3C=) c.424-3C= (n.424-3C=) n.341-3C= n.358-3C= | |
1 | g.17027868G>T | CA2643678114 | SDHB | c.253-3C>A (n.253-3C>A) c.382-3C>A (n.382-3C>A) c.424-3C>A (n.424-3C>A) n.341-3C>A n.358-3C>A | gnomAD v4 |
1 | g.17027869T>C | CA089624 | SDHB | c.253-4A>G (n.253-4A>G) c.382-4A>G (n.382-4A>G) c.424-4A>G (n.424-4A>G) n.341-4A>G n.358-4A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.17027869T= | CA1156080211 | SDHB | c.253-4A= (n.253-4A=) c.382-4A= (n.382-4A=) c.424-4A= (n.424-4A=) n.341-4A= n.358-4A= | |
1 | g.17027870G>A | CA2643678124 | SDHB | c.253-5C>T (n.253-5C>T) c.382-5C>T (n.382-5C>T) c.424-5C>T (n.424-5C>T) n.341-5C>T n.358-5C>T | ClinVar dbSNP gnomAD v4 |
1 | g.17027870G>C | CA658656889 | SDHB | c.253-5C>G (n.253-5C>G) c.382-5C>G (n.382-5C>G) c.424-5C>G (n.424-5C>G) n.341-5C>G n.358-5C>G | ClinVar dbSNP |
1 | g.17027870G= | CA1156080212 | SDHB | c.253-5C= (n.253-5C=) c.382-5C= (n.382-5C=) c.424-5C= (n.424-5C=) n.341-5C= n.358-5C= | |
1 | g.17027870G>T | CA2574235768 | SDHB | c.253-5C>A (n.253-5C>A) c.382-5C>A (n.382-5C>A) c.424-5C>A (n.424-5C>A) n.341-5C>A n.358-5C>A | gnomAD v4 |
1 | g.17027871dup | CA2499214302 | SDHB | c.253-5dup (n.253-5dup) c.382-5dup (n.382-5dup) c.424-5dup (n.424-5dup) n.341-5dup n.358-5dup | ClinVar dbSNP |
1 | g.17027871G>A | CA089625 | SDHB | c.253-6C>T (n.253-6C>T) c.382-6C>T (n.382-6C>T) c.424-6C>T (n.424-6C>T) n.341-6C>T n.358-6C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17027871G= | CA1144115745 | SDHB | c.253-6C= (n.253-6C=) c.382-6C= (n.382-6C=) c.424-6C= (n.424-6C=) n.341-6C= n.358-6C= | |
1 | g.17027871G>T | CA2643678136 | SDHB | c.253-6C>A (n.253-6C>A) c.382-6C>A (n.382-6C>A) c.424-6C>A (n.424-6C>A) n.341-6C>A n.358-6C>A | gnomAD v4 |
1 | g.17027872T>A | CA2499214303 | SDHB | c.253-7A>T (n.253-7A>T) c.382-7A>T (n.382-7A>T) c.424-7A>T (n.424-7A>T) n.341-7A>T n.358-7A>T | ClinVar dbSNP |
1 | g.17027872T>C | CA2643678142 | SDHB | c.253-7A>G (n.253-7A>G) c.382-7A>G (n.382-7A>G) c.424-7A>G (n.424-7A>G) n.341-7A>G n.358-7A>G | gnomAD v4 |
1 | g.17027872T>G | CA915941156 | SDHB | c.253-7A>C (n.253-7A>C) c.382-7A>C (n.382-7A>C) c.424-7A>C (n.424-7A>C) n.341-7A>C n.358-7A>C | ClinVar dbSNP |
1 | g.17027872T= | CA1156080213 | SDHB | c.253-7A= (n.253-7A=) c.382-7A= (n.382-7A=) c.424-7A= (n.424-7A=) n.341-7A= n.358-7A= | |
1 | g.17027873del | CA2574235772 | SDHB | c.253-7del (n.253-7del) c.382-7del (n.382-7del) c.424-7del (n.424-7del) n.341-7del n.358-7del | gnomAD v4 |
1 | g.17027873T>A | CA2643678146 | SDHB | c.253-8A>T (n.253-8A>T) c.382-8A>T (n.382-8A>T) c.424-8A>T (n.424-8A>T) n.341-8A>T n.358-8A>T | gnomAD v4 |
1 | g.17027873T>C | CA2643678147 | SDHB | c.253-8A>G (n.253-8A>G) c.382-8A>G (n.382-8A>G) c.424-8A>G (n.424-8A>G) n.341-8A>G n.358-8A>G | gnomAD v4 |
1 | g.17027873T= | CA1156080214 | SDHB | c.253-8A= (n.253-8A=) c.382-8A= (n.382-8A=) c.424-8A= (n.424-8A=) n.341-8A= n.358-8A= | |
1 | g.17027874A= | CA1143475256 | SDHB | c.253-9T= (n.253-9T=) c.382-9T= (n.382-9T=) c.424-9T= (n.424-9T=) n.341-9T= n.358-9T= | |
1 | g.17027874A>C | CA18666023 | SDHB | c.253-9T>G (n.253-9T>G) c.382-9T>G (n.382-9T>G) c.424-9T>G (n.424-9T>G) n.341-9T>G n.358-9T>G | ClinVar dbSNP |
1 | g.17027874A>G | CA2643678160 | SDHB | c.253-9T>C (n.253-9T>C) c.382-9T>C (n.382-9T>C) c.424-9T>C (n.424-9T>C) n.341-9T>C n.358-9T>C | gnomAD v4 |
1 | g.17027878_17027883dup | CA16617022 | SDHB | c.253-14_253-9dup (n.253-14_253-9dup) c.382-14_382-9dup (n.382-14_382-9dup) c.424-14_424-9dup (n.424-14_424-9dup) n.341-14_341-9dup n.358-14_358-9dup | ClinVar dbSNP gnomAD v4 |
1 | g.17027878_17027883del | CA2574235777 | SDHB | c.253-14_253-9del (n.253-14_253-9del) c.382-14_382-9del (n.382-14_382-9del) c.424-14_424-9del (n.424-14_424-9del) n.341-14_341-9del n.358-14_358-9del | ClinVar gnomAD v4 |
1 | g.17027878_17027886del | CA2499214304 | SDHB | c.253-17_253-9del (n.253-17_253-9del) c.382-17_382-9del (n.382-17_382-9del) c.424-17_424-9del (n.424-17_424-9del) n.341-17_341-9del n.358-17_358-9del | ClinVar dbSNP gnomAD v4 |
1 | g.17027875A= | CA1156080215 | SDHB | c.253-10T= (n.253-10T=) c.382-10T= (n.382-10T=) c.424-10T= (n.424-10T=) n.341-10T= n.358-10T= | |
1 | g.17027875A>C | CA2580060654 | SDHB | c.253-10T>G (n.253-10T>G) c.382-10T>G (n.382-10T>G) c.424-10T>G (n.424-10T>G) n.341-10T>G n.358-10T>G | ClinVar |
1 | g.17027876G>C | CA089612 | SDHB | c.253-11C>G (n.253-11C>G) c.382-11C>G (n.382-11C>G) c.424-11C>G (n.424-11C>G) n.341-11C>G n.358-11C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.17027876G= | CA1143356996 | SDHB | c.253-11C= (n.253-11C=) c.382-11C= (n.382-11C=) c.424-11C= (n.424-11C=) n.341-11C= n.358-11C= | |
1 | g.17027876G>T | CA2643678171 | SDHB | c.253-11C>A (n.253-11C>A) c.382-11C>A (n.382-11C>A) c.424-11C>A (n.424-11C>A) n.341-11C>A n.358-11C>A | gnomAD v4 |
1 | g.17027878_17027880dup | CA890972251 | SDHB | c.253-13_253-11dup (n.253-13_253-11dup) c.382-13_382-11dup (n.382-13_382-11dup) c.424-13_424-11dup (n.424-13_424-11dup) n.341-13_341-11dup n.358-13_358-11dup | ClinVar dbSNP gnomAD v4 |
1 | g.17027878_17027880del | CA2574235786 | SDHB | c.253-13_253-11del (n.253-13_253-11del) c.382-13_382-11del (n.382-13_382-11del) c.424-13_424-11del (n.424-13_424-11del) n.341-13_341-11del n.358-13_358-11del | |
1 | g.17027877A= | CA1156080216 | SDHB | c.253-12T= (n.253-12T=) c.382-12T= (n.382-12T=) c.424-12T= (n.424-12T=) n.341-12T= n.358-12T= | |
1 | g.17027877A>C | CA089613 | SDHB | c.253-12T>G (n.253-12T>G) c.382-12T>G (n.382-12T>G) c.424-12T>G (n.424-12T>G) n.341-12T>G n.358-12T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17027877A>G | CA2740090528 | SDHB | c.253-12T>C (n.253-12T>C) c.382-12T>C (n.382-12T>C) c.424-12T>C (n.424-12T>C) n.341-12T>C n.358-12T>C | ClinVar |
1 | g.17027878G>A | CA18666038 | SDHB | c.253-13C>T (n.253-13C>T) c.382-13C>T (n.382-13C>T) c.424-13C>T (n.424-13C>T) n.341-13C>T n.358-13C>T | ClinVar dbSNP gnomAD v4 |
1 | g.17027878G>C | CA2580060655 | SDHB | c.253-13C>G (n.253-13C>G) c.382-13C>G (n.382-13C>G) c.424-13C>G (n.424-13C>G) n.341-13C>G n.358-13C>G | ClinVar |
1 | g.17027878G= | CA1143449727 | SDHB | c.253-13C= (n.253-13C=) c.382-13C= (n.382-13C=) c.424-13C= (n.424-13C=) n.341-13C= n.358-13C= | |
1 | g.17027878G>T | CA2643678182 | SDHB | c.253-13C>A (n.253-13C>A) c.382-13C>A (n.382-13C>A) c.424-13C>A (n.424-13C>A) n.341-13C>A n.358-13C>A | gnomAD v4 |
1 | g.17027879del | CA2580060656 | SDHB | c.253-13del (n.253-13del) c.382-13del (n.382-13del) c.424-13del (n.424-13del) n.341-13del n.358-13del | ClinVar |
1 | g.17027878_17027890delinsGGAAGAAGAAGAA | CA1156080217 | SDHB | c.253-25_253-13delinsTTCTTCTTCTTCC (n.253-25_253-13delinsTTCTTCTTCTTCC) c.382-25_382-13delinsTTCTTCTTCTTCC (n.382-25_382-13delinsTTCTTCTTCTTCC) c.424-25_424-13delinsTTCTTCTTCTTCC (n.424-25_424-13delinsTTCTTCTTCTTCC) n.341-25_341-13delinsTTCTTCTTCTTCC n.358-25_358-13delinsTTCTTCTTCTTCC | |
1 | g.17027879G= | CA1156080218 | SDHB | c.253-14C= (n.253-14C=) c.382-14C= (n.382-14C=) c.424-14C= (n.424-14C=) n.341-14C= n.358-14C= | |
1 | g.17027879G>T | CA18666049 | SDHB | c.253-14C>A (n.253-14C>A) c.382-14C>A (n.382-14C>A) c.424-14C>A (n.424-14C>A) n.341-14C>A n.358-14C>A | dbSNP gnomAD v4 |
1 | g.17027879_17027880insGAG | CA2740090529 | SDHB | c.253-14_253-13insTCC (n.253-14_253-13insTCC) c.382-14_382-13insTCC (n.382-14_382-13insTCC) c.424-14_424-13insTCC (n.424-14_424-13insTCC) n.341-14_341-13insTCC n.358-14_358-13insTCC | ClinVar |
1 | g.17027879_17027902delinsGAAGAAGAAGAAGAAGAAGAAGAA | CA1140509650 | SDHB | c.253-37_253-14delinsTTCTTCTTCTTCTTCTTCTTCTTC (n.253-37_253-14delinsTTCTTCTTCTTCTTCTTCTTCTTC) c.382-37_382-14delinsTTCTTCTTCTTCTTCTTCTTCTTC (n.382-37_382-14delinsTTCTTCTTCTTCTTCTTCTTCTTC) c.424-37_424-14delinsTTCTTCTTCTTCTTCTTCTTCTTC (n.424-37_424-14delinsTTCTTCTTCTTCTTCTTCTTCTTC) n.341-37_341-14delinsTTCTTCTTCTTCTTCTTCTTCTTC n.358-37_358-14delinsTTCTTCTTCTTCTTCTTCTTCTTC | |
1 | g.17027900_17027902dup | CA134779 | SDHB | c.253-16_253-14dup (n.253-16_253-14dup) c.382-16_382-14dup (n.382-16_382-14dup) c.424-16_424-14dup (n.424-16_424-14dup) n.341-16_341-14dup n.358-16_358-14dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17027897_17027902dup | CA260527 | SDHB | c.253-19_253-14dup (n.253-19_253-14dup) c.382-19_382-14dup (n.382-19_382-14dup) c.424-19_424-14dup (n.424-19_424-14dup) n.341-19_341-14dup n.358-19_358-14dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17027894_17027902dup | CA637819 | SDHB | c.253-22_253-14dup (n.253-22_253-14dup) c.382-22_382-14dup (n.382-22_382-14dup) c.424-22_424-14dup (n.424-22_424-14dup) n.341-22_341-14dup n.358-22_358-14dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17027900_17027902del | CA637818 | SDHB | c.253-16_253-14del (n.253-16_253-14del) c.382-16_382-14del (n.382-16_382-14del) c.424-16_424-14del (n.424-16_424-14del) n.341-16_341-14del n.358-16_358-14del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17027897_17027902del | CA637817 | SDHB | c.253-19_253-14del (n.253-19_253-14del) c.382-19_382-14del (n.382-19_382-14del) c.424-19_424-14del (n.424-19_424-14del) n.341-19_341-14del n.358-19_358-14del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17027894_17027902del | CA521039164 | SDHB | c.253-22_253-14del (n.253-22_253-14del) c.382-22_382-14del (n.382-22_382-14del) c.424-22_424-14del (n.424-22_424-14del) n.341-22_341-14del n.358-22_358-14del | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17027891_17027902del | CA089615 | SDHB | c.253-25_253-14del (n.253-25_253-14del) c.382-25_382-14del (n.382-25_382-14del) c.424-25_424-14del (n.424-25_424-14del) n.341-25_341-14del n.358-25_358-14del | dbSNP ExAC gnomAD v4 |
1 | g.17027879_17027880insGAA | CA1139655470 | SDHB | c.253-15_253-14insTTC (n.253-15_253-14insTTC) c.382-15_382-14insTTC (n.382-15_382-14insTTC) c.424-15_424-14insTTC (n.424-15_424-14insTTC) n.341-15_341-14insTTC n.358-15_358-14insTTC | |
1 | g.17027880A>G | CA2643678225 | SDHB | c.253-15T>C (n.253-15T>C) c.382-15T>C (n.382-15T>C) c.424-15T>C (n.424-15T>C) n.341-15T>C n.358-15T>C | gnomAD v4 |
1 | g.17027880_17027881insGAA | CA1139770655 | SDHB | c.253-15_253-14insTCT (n.253-15_253-14insTCT) c.382-15_382-14insTCT (n.382-15_382-14insTCT) c.424-15_424-14insTCT (n.424-15_424-14insTCT) n.341-15_341-14insTCT n.358-15_358-14insTCT | |
1 | g.17027880_17027881insGAAGAA | CA1139770654 | SDHB | c.253-15_253-14insTCTTCT (n.253-15_253-14insTCTTCT) c.382-15_382-14insTCTTCT (n.382-15_382-14insTCTTCT) c.424-15_424-14insTCTTCT (n.424-15_424-14insTCTTCT) n.341-15_341-14insTCTTCT n.358-15_358-14insTCTTCT | |
1 | g.17027881A= | CA1156080219 | SDHB | c.253-16T= (n.253-16T=) c.382-16T= (n.382-16T=) c.424-16T= (n.424-16T=) n.341-16T= n.358-16T= | |
1 | g.17027881A>C | CA521039173 | SDHB | c.253-16T>G (n.253-16T>G) c.382-16T>G (n.382-16T>G) c.424-16T>G (n.424-16T>G) n.341-16T>G n.358-16T>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.17027881A>G | CA089614 | SDHB | c.253-16T>C (n.253-16T>C) c.382-16T>C (n.382-16T>C) c.424-16T>C (n.424-16T>C) n.341-16T>C n.358-16T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.17027882G>A | CA2643678246 | SDHB | c.253-17C>T (n.253-17C>T) c.382-17C>T (n.382-17C>T) c.424-17C>T (n.424-17C>T) n.341-17C>T n.358-17C>T | gnomAD v4 |
1 | g.17027882G= | CA1156080220 | SDHB | c.253-17C= (n.253-17C=) c.382-17C= (n.382-17C=) c.424-17C= (n.424-17C=) n.341-17C= n.358-17C= | |
1 | g.17027882G>T | CA2643678247 | SDHB | c.253-17C>A (n.253-17C>A) c.382-17C>A (n.382-17C>A) c.424-17C>A (n.424-17C>A) n.341-17C>A n.358-17C>A | gnomAD v4 |
1 | g.17027883_17027884insGAAGAA | CA1139770653 | SDHB | c.253-18_253-17insTCTTCT (n.253-18_253-17insTCTTCT) c.382-18_382-17insTCTTCT (n.382-18_382-17insTCTTCT) c.424-18_424-17insTCTTCT (n.424-18_424-17insTCTTCT) n.341-18_341-17insTCTTCT n.358-18_358-17insTCTTCT | |
1 | g.17027883_17027884delinsAA | CA1144232707 | SDHB | c.253-19_253-18delinsTT (n.253-19_253-18delinsTT) c.382-19_382-18delinsTT (n.382-19_382-18delinsTT) c.424-19_424-18delinsTT (n.424-19_424-18delinsTT) n.341-19_341-18delinsTT n.358-19_358-18delinsTT | |
1 | g.17027884dup | CA18666089 | SDHB | c.253-18dup (n.253-18dup) c.382-18dup (n.382-18dup) c.424-18dup (n.424-18dup) n.341-18dup n.358-18dup | dbSNP |
1 | g.17027887_17027888insTAAGAA | CA2838289598 | SDHB | c.253-18_253-17insATTCTT (n.253-18_253-17insATTCTT) c.382-18_382-17insATTCTT (n.382-18_382-17insATTCTT) c.424-18_424-17insATTCTT (n.424-18_424-17insATTCTT) n.341-18_341-17insATTCTT n.358-18_358-17insATTCTT |