"Color Diagnostics, LLC DBA Color Health"[submitter] AND "SDHC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41776	NM_003001.5(SDHC):c.43C>T (p.Arg15Ter)	SDHC (R15*)	Single nucleotide variant (nonsense +3 more)	Gastrointestinal stromal tumor +4 more	GPathogenic
Select item 407054	NM_003001.5(SDHC):c.98C>T (p.Thr33Met)	SDHC (T33M +1 more)	Single nucleotide variant (missense variant +3 more)	not specified +5 more	GUncertain significance
Select item 239447	NM_003001.5(SDHC):c.120G>A (p.Arg40=)	SDHC	Single nucleotide variant (synonymous variant +2 more)	Gastrointestinal stromal tumor +5 more	GBenign/Likely benign
Select item 135194	NM_003001.5(SDHC):c.148C>T (p.Arg50Cys)	SDHC (R50C +2 more)	Single nucleotide variant (missense variant +2 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 239453	NM_003001.5(SDHC):c.295T>C (p.Tyr99His)	SDHC (Y99H +7 more)	Single nucleotide variant (missense variant +2 more)	Paragangliomas 3 +4 more	GConflicting classifications of pathogenicity
Select item 165182	NM_003001.5(SDHC):c.354T>C (p.Phe118=)	SDHC	Single nucleotide variant (synonymous variant +2 more)	not specified +4 more	GBenign/Likely benign
Select item 428933	NM_003001.5(SDHC):c.377A>G (p.Tyr126Cys)	SDHC (Y126C +7 more)	Single nucleotide variant (missense variant +2 more)	Gastrointestinal stromal tumor +4 more	GPathogenic/Likely pathogenic

ClinVar