"Ambry Genetics"[submitter] AND "KRT7-AS"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2267212	NM_005556.4(KRT7):c.1003G>A (p.Ala335Thr)	KRT7-AS, KRT7 (A335T)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2486505	NM_005556.4(KRT7):c.1021G>A (p.Glu341Lys)	KRT7, KRT7-AS (E341K)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2368910	NM_005556.4(KRT7):c.1024C>T (p.Arg342Cys)	KRT7, KRT7-AS (R342C)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2294573	NM_005556.4(KRT7):c.1088G>A (p.Arg363Gln)	KRT7-AS, KRT7 (R363Q)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2312379	NM_005556.4(KRT7):c.1118G>C (p.Arg373Pro)	KRT7-AS, KRT7 (R373P)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2212028	NM_005556.4(KRT7):c.1123T>C (p.Tyr375His)	KRT7, KRT7-AS (Y375H)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar