"Ambry Genetics"[submitter] AND "NTAQ1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2478014	NM_018024.3(NTAQ1):c.134A>G (p.Tyr45Cys)	NTAQ1 (Y45C)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3202544	NM_018024.3(NTAQ1):c.374A>G (p.Gln125Arg)	NTAQ1 (Q125R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202545	NM_018024.3(NTAQ1):c.445A>G (p.Met149Val)	NTAQ1 (M149V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202546	NM_018024.3(NTAQ1):c.474G>C (p.Glu158Asp)	NTAQ1 (E98D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202547	NM_018024.3(NTAQ1):c.515A>G (p.Lys172Arg)	NTAQ1 (K172R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202548	NM_018024.3(NTAQ1):c.548C>T (p.Pro183Leu)	NTAQ1 (P123L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202549	NM_018024.3(NTAQ1):c.568G>A (p.Val190Ile)	NTAQ1 (V190I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2539021	NM_018024.3(NTAQ1):c.583G>A (p.Glu195Lys)	NTAQ1 (E127K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar