"Ambry Genetics"[submitter] AND "PRKCH-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3218776	NM_006255.5(PRKCH):c.107A>G (p.Lys36Arg)	PRKCH, PRKCH-AS1 (K36R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218777	NM_006255.5(PRKCH):c.118C>G (p.Leu40Val)	PRKCH, PRKCH-AS1 (L40V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218781	NM_006255.5(PRKCH):c.153G>C (p.Gln51His)	PRKCH, PRKCH-AS1 (Q51H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310542	NM_006255.5(PRKCH):c.194A>G (p.Lys65Arg)	PRKCH, PRKCH-AS1 (K65R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218784	NM_006255.5(PRKCH):c.199A>G (p.Thr67Ala)	PRKCH, PRKCH-AS1 (T67A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303284	NM_006255.5(PRKCH):c.328C>T (p.Arg110Cys)	PRKCH, PRKCH-AS1 (R110C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218785	NM_006255.5(PRKCH):c.347A>G (p.Asp116Gly)	PRKCH, PRKCH-AS1 (D116G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar