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

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2521632	NM_172370.5(DAOA):c.110C>A (p.Ser37Tyr)	DAOA, DAOA-AS1 (S37Y)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3270854	NM_172370.5(DAOA):c.130A>G (p.Ile44Val)	DAOA, DAOA-AS1 (I44V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3080047	NM_172370.5(DAOA):c.195T>C (p.His65=)	DAOA, DAOA-AS1 (M1T)	Single nucleotide variant (missense variant +3 more)	not specified	GLikely benign
Select item 3080048	NM_172370.5(DAOA):c.227A>G (p.His76Arg)	DAOA, DAOA-AS1 (H76R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335107	NM_172370.5(DAOA):c.238T>A (p.Ser80Thr)	DAOA, DAOA-AS1 (D15E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080049	NM_172370.5(DAOA):c.240A>C (p.Ser80=)	DAOA, DAOA-AS1 (H16P)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3270853	NM_172370.5(DAOA):c.282G>C (p.Glu94Asp)	DAOA, DAOA-AS1 (A126P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289174	NM_172370.5(DAOA):c.382C>G (p.Arg128Gly)	DAOA, DAOA-AS1 (R57G +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance