"Ambry Genetics"[submitter] AND "KRTAP7-1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3117131	NM_181606.3(KRTAP7-1):c.128G>A (p.Gly43Asp)	KRTAP7-1 (G43D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289767	NM_181606.3(KRTAP7-1):c.85C>T (p.Pro29Ser)	KRTAP7-1 (P29S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117132	NM_181606.3(KRTAP7-1):c.59A>G (p.Asn20Ser)	KRTAP7-1 (N20S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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