ClinVar for MedGen (Select 349380) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2954035	NM_003000.3(SDHB):c.84_141dup (p.Asp48fs)	SDHB (D48fs)	Duplication (frameshift variant)	Pheochromocytoma +2 more	GPathogenic
Select item 2953788	NM_003000.3(SDHB):c.272G>C (p.Arg91Thr)	SDHB (R91T)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2953496	NM_003000.3(SDHB):c.690C>A (p.Arg230=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2952299	NM_003000.3(SDHB):c.154G>T (p.Ala52Ser)	SDHB (A52S)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2952214	NM_003000.3(SDHB):c.797T>A (p.Ile266Asn)	SDHB (I248N +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2951656	NM_003000.3(SDHB):c.233A>T (p.Lys78Met)	SDHB (K78M)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2951573	NM_003000.3(SDHB):c.128C>T (p.Ala43Val)	SDHB (A43V)	Single nucleotide variant (missense variant)	Hereditary pheochromocytoma-paraganglioma +3 more	GUncertain significance
Select item 2951425	NM_003000.3(SDHB):c.756C>T (p.Thr252=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2950880	NM_003000.3(SDHB):c.174G>A (p.Met58Ile)	SDHB (M58I)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2950703	NM_003000.3(SDHB):c.654G>C (p.Trp218Cys)	SDHB (W200C +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2950569	NM_003000.3(SDHB):c.424-5C>T	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2950230	NM_003000.3(SDHB):c.643-14C>A	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2950080	NM_003000.3(SDHB):c.500A>G (p.Lys167Arg)	SDHB (K167R +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2949817	NM_003000.3(SDHB):c.784del (p.Ala262fs)	SDHB (A244fs +1 more)	Deletion (frameshift variant)	Pheochromocytoma +2 more	GPathogenic
Select item 2949787	NM_003000.3(SDHB):c.286+17T>C	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2949595	NM_003000.3(SDHB):c.385C>A (p.Pro129Thr)	SDHB (P129T)	Single nucleotide variant (missense variant +1 more)	Pheochromocytoma +2 more	GUncertain significance
Select item 2949579	NM_003000.3(SDHB):c.146del (p.Pro49fs)	SDHB (P49fs)	Deletion (frameshift variant)	Pheochromocytoma +2 more	GPathogenic
Select item 2949466	NM_003000.3(SDHB):c.670G>A (p.Asp224Asn)	SDHB (D224N +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2949365	NM_003000.3(SDHB):c.766-4C>A	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2949287	NM_003000.3(SDHB):c.751_754del (p.Arg251fs)	SDHB (R233fs +1 more)	Deletion (frameshift variant)	Pheochromocytoma +2 more	GPathogenic
Select item 2949037	NM_003000.3(SDHB):c.541-12C>T	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2948917	NM_003000.3(SDHB):c.201-1G>C	SDHB	Single nucleotide variant (splice acceptor variant)	Pheochromocytoma +2 more	GPathogenic
Select item 2948913	NM_003000.3(SDHB):c.24C>G (p.Ser8=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2948912	NM_003000.3(SDHB):c.146C>A (p.Pro49Gln)	SDHB (P49Q)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2948839	NM_003000.3(SDHB):c.729C>T (p.Cys243=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2948490	NM_003000.3(SDHB):c.67C>T (p.Leu23=)	LOC129929542, SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2948406	NM_003000.3(SDHB):c.286G>C (p.Gly96Arg)	SDHB (G96R)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2948181	NM_003000.3(SDHB):c.411G>C (p.Lys137Asn)	SDHB (K137N)	Single nucleotide variant (missense variant +1 more)	Pheochromocytoma +2 more	GUncertain significance
Select item 2947609	NM_003000.3(SDHB):c.761C>G (p.Pro254Arg)	SDHB (P236R +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2947224	NM_003000.3(SDHB):c.236T>C (p.Ile79Thr)	SDHB (I79T)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2947194	NM_003000.3(SDHB):c.478A>G (p.Lys160Glu)	SDHB (K160E +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2947049	NM_003000.3(SDHB):c.281G>T (p.Arg94Ile)	SDHB (R94I)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2947022	NM_003000.3(SDHB):c.452A>G (p.Lys151Arg)	SDHB (K151R +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2946972	NM_003000.3(SDHB):c.424-14_424-13insCTC	SDHB	Insertion (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2946935	NM_003000.3(SDHB):c.287-10_295del	SDHB	Deletion (splice acceptor variant)	Pheochromocytoma +2 more	GLikely pathogenic
Select item 2946630	NM_003000.3(SDHB):c.456C>A (p.Ser152=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2946333	NM_003000.3(SDHB):c.283G>C (p.Glu95Gln)	SDHB (E95Q)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2946066	NM_003000.3(SDHB):c.273A>C (p.Arg91Ser)	SDHB (R91S)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2946014	NM_003000.3(SDHB):c.423+19C>T	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2945793	NM_003000.3(SDHB):c.766-18C>T	LOC129929541, SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2945656	NM_003000.3(SDHB):c.638T>G (p.Met213Arg)	SDHB (M213R +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2945424	NM_003000.3(SDHB):c.788T>C (p.Ile263Thr)	SDHB (I263T +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2945382	NM_003000.3(SDHB):c.60A>C (p.Gly20=)	LOC129929542, SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2945347	NM_003000.3(SDHB):c.712T>G (p.Phe238Val)	SDHB (F238V +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2945164	NM_003000.3(SDHB):c.287-20T>A	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2944626	NM_003000.3(SDHB):c.526G>A (p.Glu176Lys)	SDHB (E158K +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2943933	NM_003000.3(SDHB):c.80G>C (p.Arg27Pro)	SDHB (R27P)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2943668	NM_003000.3(SDHB):c.541-16T>G	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2943622	NM_003000.3(SDHB):c.556T>C (p.Cys186Arg)	SDHB (C168R +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2943611	NM_003000.3(SDHB):c.824A>T (p.Glu275Val)	SDHB (E257V +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2943394	NM_003000.3(SDHB):c.508dup (p.Tyr170fs)	SDHB (Y152fs +1 more)	Duplication (frameshift variant)	Pheochromocytoma +2 more	GPathogenic
Select item 2943055	NM_003000.3(SDHB):c.664T>C (p.Ser222Pro)	SDHB (S222P +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2942979	NM_003000.3(SDHB):c.777A>G (p.Pro259=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2942952	NM_003000.3(SDHB):c.73-19G>A	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2942785	NM_003000.3(SDHB):c.496G>C (p.Gly166Arg)	SDHB (G166R +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2942599	NM_003000.3(SDHB):c.598T>G (p.Trp200Gly)	SDHB (W182G +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2942161	NM_003000.3(SDHB):c.541-13_541-12insGCTCCTGCCTCTCTTTTTTTTTTTTTTTTTTTTTTTTNNNNNNNNNNGCGGCAAAGACTGAGACAGCTCCGCTGCCCGCTGAACTCCATCCTCCCGGCGGTCGGGCGGCGGCGGCTGCGC	SDHB	Microsatellite (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2941954	NM_003000.3(SDHB):c.423+11G>A	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2941917	NM_003000.3(SDHB):c.72+3G>C	LOC129929542, SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2941695	NM_003000.3(SDHB):c.824A>C (p.Glu275Ala)	SDHB (E257A +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2941552	NM_003000.3(SDHB):c.120_122del (p.Lys41del)	SDHB (K41del)	Deletion (inframe_deletion)	Pheochromocytoma +2 more	GUncertain significance
Select item 2941359	NM_003000.3(SDHB):c.383A>T (p.Tyr128Phe)	SDHB (Y128F)	Single nucleotide variant (missense variant +1 more)	Pheochromocytoma +2 more	GUncertain significance
Select item 2941318	NM_003000.3(SDHB):c.757T>C (p.Cys253Arg)	SDHB (C235R +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2940286	NM_003000.3(SDHB):c.649C>A (p.Arg217Ser)	SDHB (R199S +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2939494	NM_003000.3(SDHB):c.766-14T>C	LOC129929541, SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2939463	NM_003000.3(SDHB):c.145C>T (p.Pro49Ser)	SDHB (P49S)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2937937	NM_003000.3(SDHB):c.424-12T>C	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2937482	NM_003000.3(SDHB):c.212T>C (p.Met71Thr)	SDHB (M71T)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2937415	NM_003000.3(SDHB):c.749C>G (p.Thr250Arg)	SDHB (T232R +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2937373	NM_003000.3(SDHB):c.85G>T (p.Ala29Ser)	SDHB (A29S)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2936823	NM_003000.3(SDHB):c.643-20_643-18dup	SDHB	Duplication (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2936794	NM_003000.3(SDHB):c.287-20_287-18del	SDHB	Deletion (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2936398	NM_003000.3(SDHB):c.72+18A>C	LOC129929542, SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2936076	NM_003000.3(SDHB):c.335C>T (p.Ala112Val)	SDHB (A112V)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2935923	NM_003000.3(SDHB):c.765+9G>A	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2935216	NM_003000.3(SDHB):c.528G>A (p.Glu176=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2934317	NM_003000.3(SDHB):c.643-11T>G	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2934131	NM_003000.3(SDHB):c.434A>G (p.Asn145Ser)	SDHB (N145S +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2933282	NM_003000.3(SDHB):c.30G>A (p.Arg10=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2932979	NM_003000.3(SDHB):c.642+10T>G	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2932956	NM_003000.3(SDHB):c.72+15C>T	LOC129929542, SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2932870	NM_003000.3(SDHB):c.459T>C (p.Ile153=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2932625	NM_003000.3(SDHB):c.469T>C (p.Leu157=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2930833	NM_003000.3(SDHB):c.546G>A (p.Gly182=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2930455	NM_003000.3(SDHB):c.393A>G (p.Pro131=)	SDHB	Single nucleotide variant (synonymous variant +1 more)	Pheochromocytoma +2 more	GLikely benign
Select item 2930025	NM_003000.3(SDHB):c.765+20C>T	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2929845	NM_003000.3(SDHB):c.344G>T (p.Arg115Leu)	SDHB (R115L)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2928919	NM_003000.3(SDHB):c.90G>C (p.Gln30His)	SDHB (Q30H)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2927642	NM_003000.3(SDHB):c.766-18C>G	LOC129929541, SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2927412	NM_003000.3(SDHB):c.72+7C>G	LOC129929542, SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2927269	NM_003000.3(SDHB):c.424G>A (p.Asp142Asn)	SDHB (D124N +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2927111	NM_003000.3(SDHB):c.776C>T (p.Pro259Leu)	SDHB (P241L +1 more)	Single nucleotide variant (missense variant)	Hereditary pheochromocytoma-paraganglioma +3 more	GUncertain significance
Select item 2926399	NM_003000.3(SDHB):c.234G>C (p.Lys78Asn)	SDHB (K78N)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2925314	NM_003000.3(SDHB):c.630A>C (p.Ala210=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2925290	NM_003000.3(SDHB):c.607G>T (p.Gly203Ter)	SDHB (G203* +1 more)	Single nucleotide variant (nonsense)	Pheochromocytoma +2 more	GPathogenic
Select item 2925289	NM_003000.3(SDHB):c.670G>C (p.Asp224His)	SDHB (D206H +1 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance
Select item 2925288	NM_003000.3(SDHB):c.703C>T (p.Gln235Ter)	SDHB (Q235* +1 more)	Single nucleotide variant (nonsense)	Pheochromocytoma +2 more	GPathogenic
Select item 2925192	NM_003000.3(SDHB):c.287-9C>A	SDHB	Single nucleotide variant (intron variant)	Pheochromocytoma +2 more	GLikely benign
Select item 2924312	NM_003000.3(SDHB):c.396C>T (p.His132=)	SDHB	Single nucleotide variant (synonymous variant +1 more)	Pheochromocytoma +2 more	GLikely benign
Select item 2923067	NM_003000.3(SDHB):c.672T>C (p.Asp224=)	SDHB	Single nucleotide variant (synonymous variant)	Pheochromocytoma +2 more	GLikely benign

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