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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2273412	NM_000567.3(CRP):c.646G>A (p.Val216Met)	CRP (V216M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232682	NM_000567.3(CRP):c.635T>C (p.Val212Ala)	CRP (V79A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2403499	NM_000567.3(CRP):c.619G>C (p.Ala207Pro)	CRP (A74P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2529865	NM_000567.3(CRP):c.576C>G (p.Ile192Met)	CRP (I70M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2259287	NM_000567.3(CRP):c.496G>A (p.Gly166Arg)	CRP (G166R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2300884	NM_000567.3(CRP):c.212C>G (p.Ser71Trp)	CRP (S71W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar