"Ambry Genetics"[submitter] AND "KRTAP3-2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3117023	NM_031959.3(KRTAP3-2):c.220A>G (p.Thr74Ala)	KRTAP3-2 (T74A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117022	NM_031959.3(KRTAP3-2):c.220A>C (p.Thr74Pro)	KRTAP3-2 (T74P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225161	NM_031959.3(KRTAP3-2):c.146A>G (p.Asp49Gly)	KRTAP3-2 (D49G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117025	NM_031959.3(KRTAP3-2):c.74C>A (p.Ser25Tyr)	KRTAP3-2 (S25Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611758	NM_031959.3(KRTAP3-2):c.64T>G (p.Ser22Ala)	KRTAP3-2 (S22A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216790	NM_031959.3(KRTAP3-2):c.40G>T (p.Gly14Trp)	KRTAP3-2 (G14W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117024	NM_031959.3(KRTAP3-2):c.37A>G (p.Thr13Ala)	KRTAP3-2 (T13A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar