ClinVar for PubMed (Select 20503330) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2562717	NM_003000.3(SDHB):c.419T>A (p.Val140Asp)	SDHB (V140D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 1072824	NC_000001.10:g.(?_17345376)_(17371403_?)del	SDHB	Deletion	Gastrointestinal stromal tumor +2 more	GPathogenic
Select item 833509	NC_000001.11:g.(?_17018871)_(17044898_?)del	SDHB	Deletion	Pheochromocytoma +2 more	GPathogenic
Select item 830735	NC_000001.11:g.(?_17018871)_(17033155_?)del	SDHB	Deletion	Pheochromocytoma +2 more	GPathogenic
Select item 583909	NC_000001.11:g.(?_17018875)_(17033151_?)del	LOC129929541, SDHB	Deletion	Gastrointestinal stromal tumor +2 more	GPathogenic
Select item 18454	NM_003000.3(SDHB):c.418G>T (p.Val140Phe)	SDHB (V140F)	Single nucleotide variant (missense variant)	not provided +5 more	GPathogenic/Likely pathogenic

ClinVar