"Ambry Genetics"[submitter] AND "RCAN2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3152678	NM_001251974.2(RCAN2):c.596G>C (p.Gly199Ala)	RCAN2 (G153A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319835	NM_001251974.2(RCAN2):c.461A>G (p.Gln154Arg)	RCAN2 (Q108R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305520	NM_001251974.2(RCAN2):c.445C>G (p.Pro149Ala)	RCAN2 (P103A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480392	NM_001251974.2(RCAN2):c.414G>C (p.Glu138Asp)	RCAN2 (E138D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623103	NM_001251974.2(RCAN2):c.273C>A (p.Phe91Leu)	RCAN2 (F91L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551237	NM_001251974.2(RCAN2):c.226-76532G>A	LOC101926915, RCAN2 (V18M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar