KRTAP19-2[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2374084	NM_181608.2(KRTAP19-2):c.145A>T (p.Thr49Ser)	KRTAP19-2 (T49S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2355092	NM_181608.2(KRTAP19-2):c.85G>C (p.Gly29Arg)	KRTAP19-2 (G29R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116976	NM_181608.2(KRTAP19-2):c.58G>A (p.Gly20Ser)	KRTAP19-2 (G20S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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