"Ambry Genetics"[submitter] AND "KRTAP12-1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3116921	NM_181686.2(KRTAP12-1):c.278C>T (p.Pro93Leu)	KRTAP12-1, TSPEAR (P93L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400366	NM_181686.2(KRTAP12-1):c.275C>T (p.Thr92Ile)	KRTAP12-1, TSPEAR (T92I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2316442	NM_181686.2(KRTAP12-1):c.209G>A (p.Cys70Tyr)	KRTAP12-1, TSPEAR (C70Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116920	NM_181686.2(KRTAP12-1):c.197C>T (p.Ala66Val)	KRTAP12-1, TSPEAR (A66V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2516150	NM_181686.2(KRTAP12-1):c.184C>A (p.Pro62Thr)	KRTAP12-1, TSPEAR (P62T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116919	NM_181686.2(KRTAP12-1):c.172G>A (p.Val58Met)	KRTAP12-1, TSPEAR (V58M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar