"Ambry Genetics"[submitter] AND "CORO1C"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2617351	NM_014325.4(CORO1C):c.1128G>C (p.Glu376Asp)	CORO1C (E382D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2262550	NM_014325.4(CORO1C):c.899C>T (p.Pro300Leu)	CORO1C (P300L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2588888	NM_014325.4(CORO1C):c.550C>T (p.Arg184Trp)	CORO1C (R190W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533795	NM_014325.4(CORO1C):c.337A>G (p.Asn113Asp)	CORO1C (N113D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2318653	NM_014325.4(CORO1C):c.82C>T (p.Arg28Trp)	LOC121466714, CORO1C (R28W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2475384	NM_014325.4(CORO1C):c.59A>G (p.Asn20Ser)	CORO1C, LOC121466714 (N26S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar