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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2323924	NM_002073.4(GNAZ):c.32A>C (p.Glu11Ala)	GNAZ, RSPH14 (E11A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410877	NM_002073.4(GNAZ):c.62G>A (p.Arg21His)	GNAZ, RSPH14 (R21H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100583	NM_002073.4(GNAZ):c.428G>A (p.Arg143His)	GNAZ, RSPH14 (R143H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100584	NM_002073.4(GNAZ):c.493G>A (p.Ala165Thr)	RSPH14, GNAZ (A165T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454715	NM_002073.4(GNAZ):c.901G>A (p.Ala301Thr)	GNAZ, RSPH14 (A301T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100585	NM_002073.4(GNAZ):c.904G>A (p.Val302Ile)	GNAZ, RSPH14 (V302I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100586	NM_002073.4(GNAZ):c.921G>C (p.Gln307His)	GNAZ, RSPH14 (Q307H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar