"Ambry Genetics"[submitter] AND "CRCP"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3269440	NM_014478.5(CRCP):c.26C>T (p.Ala9Val)	CRCP (A9V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3077299	NM_014478.5(CRCP):c.73G>A (p.Glu25Lys)	CRCP (E25K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3269438	NM_014478.5(CRCP):c.79C>T (p.Arg27Cys)	CRCP (R27C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2254740	NM_014478.5(CRCP):c.123C>G (p.Asn41Lys)	CRCP (N41K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3269437	NM_014478.5(CRCP):c.169C>T (p.Pro57Ser)	CRCP (P24S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2509573	NM_014478.5(CRCP):c.269G>A (p.Arg90Gln)	CRCP (R13Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077298	NM_014478.5(CRCP):c.338T>C (p.Ile113Thr)	CRCP (I113T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518849	NM_014478.5(CRCP):c.358G>A (p.Val120Ile)	CRCP (V113I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225862	NM_014478.5(CRCP):c.424A>G (p.Met142Val)	CRCP (M135V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513585	NM_014478.5(CRCP):c.430G>A (p.Glu144Lys)	CRCP (E137K +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance