KRTAP15-1[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2331849	NM_181623.3(KRTAP15-1):c.104T>A (p.Ile35Asn)	KRTAP15-1 (I35N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116951	NM_181623.3(KRTAP15-1):c.105C>G (p.Ile35Met)	KRTAP15-1 (I35M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116952	NM_181623.3(KRTAP15-1):c.160A>G (p.Thr54Ala)	KRTAP15-1 (T54A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485854	NM_181623.3(KRTAP15-1):c.207A>T (p.Arg69Ser)	KRTAP15-1 (R69S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353644	NM_181623.3(KRTAP15-1):c.260G>A (p.Arg87His)	KRTAP15-1 (R87H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2345328	NM_181623.3(KRTAP15-1):c.409T>C (p.Tyr137His)	KRTAP15-1 (Y137H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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