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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2265034	NM_002505.5(NFYA):c.34A>G (p.Thr12Ala)	NFYA, OARD1 (T12A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2332308	NM_002505.5(NFYA):c.120G>C (p.Gln40His)	NFYA, OARD1 (Q40H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2309849	NM_002505.5(NFYA):c.509A>G (p.Tyr170Cys)	NFYA, OARD1 (Y170C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2620871	NM_002505.5(NFYA):c.658G>A (p.Val220Ile)	NFYA, OARD1 (V220I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2309850	NM_002505.5(NFYA):c.704G>C (p.Gly235Ala)	NFYA, OARD1 (G206A +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2486987	NM_002505.5(NFYA):c.999C>G (p.Asn333Lys)	NFYA, OARD1 (N304K +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2292017	NM_002505.5(NFYA):c.1036G>C (p.Val346Leu)	NFYA, OARD1 (V346L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar