"Ambry Genetics"[submitter] AND "RCOR1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2274411	NM_015156.4(RCOR1):c.107C>T (p.Ala36Val)	RCOR1 (A36V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312227	NM_015156.4(RCOR1):c.133G>A (p.Ala45Thr)	LOC130056530, RCOR1 (A45T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152743	NM_015156.4(RCOR1):c.181G>T (p.Ala61Ser)	LOC130056530, RCOR1 (A61S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152744	NM_015156.4(RCOR1):c.400G>T (p.Gly134Cys)	RCOR1 (G134C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152745	NM_015156.4(RCOR1):c.994A>G (p.Thr332Ala)	RCOR1 (T332A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152742	NM_015156.4(RCOR1):c.1346C>G (p.Thr449Ser)	LOC126862064, RCOR1 (T449S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar