ClinVar for PubMed (Select 26173966) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 428934	NM_003001.5(SDHC):c.405+1G>C	SDHC	Single nucleotide variant (splice donor variant +1 more)	Gastrointestinal stromal tumor +2 more	GPathogenic
Select item 189841	NM_003001.5(SDHC):c.224G>A (p.Gly75Asp)	SDHC (G75D +5 more)	Single nucleotide variant (missense variant)	Paragangliomas 3 +2 more	GPathogenic/Likely pathogenic
Select item 183814	NM_003000.3(SDHB):c.380T>G (p.Ile127Ser)	SDHB (I127S)	Single nucleotide variant (missense variant)	Paragangliomas 4 +5 more	GPathogenic/Likely pathogenic
Select item 183747	NM_003000.3(SDHB):c.600G>T (p.Trp200Cys)	SDHB (W200C)	Single nucleotide variant (missense variant)	not provided +5 more	GPathogenic/Likely pathogenic
Select item 142601	NM_004168.4(SDHA):c.91C>T (p.Arg31Ter)	SDHA (R31*)	Single nucleotide variant (nonsense)	Pilocytic astrocytoma +9 more	GPathogenic/Likely pathogenic
Select item 7244	NM_003001.5(SDHC):c.405+1G>A	SDHC	Single nucleotide variant (splice donor variant +1 more)	Gastrointestinal stromal tumor +1 more	GPathogenic

ClinVar