AADAT[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3331138	NM_016228.4(AADAT):c.1246G>T (p.Val416Leu)	AADAT (V416L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482588	NM_016228.4(AADAT):c.1065T>A (p.Phe355Leu)	AADAT (F359L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131465	NM_016228.4(AADAT):c.964G>C (p.Val322Leu)	AADAT (V326L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245704	NM_016228.4(AADAT):c.634C>T (p.Arg212Cys)	AADAT (R212C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330221	NM_016228.4(AADAT):c.443G>C (p.Ser148Thr)	AADAT (S148T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131376	NM_016228.4(AADAT):c.381G>T (p.Met127Ile)	AADAT (M127I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611992	NM_016228.4(AADAT):c.199A>T (p.Met67Leu)	AADAT (M71L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338498	NM_016228.4(AADAT):c.65T>A (p.Met22Lys)	AADAT (M22K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar