"GeneDx"[submitter] AND "KRT8"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 66530	NM_002273.4(KRT8):c.1392G>T (p.Lys464Asn)	KRT8 (K464N +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1192140	NM_002273.4(KRT8):c.1265G>T (p.Gly422Val)	KRT8 (G422V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 66522	NM_002273.4(KRT8):c.1022G>A (p.Arg341His)	KRT8 (R341H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 66533	NM_002273.4(KRT8):c.187A>G (p.Ile63Val)	KRT8 (I63V +1 more)	Single nucleotide variant (missense variant +1 more)	Hepatitis C virus, susceptibility to +3 more	GBenign/Likely benign
Select item 1309232	NM_002273.4(KRT8):c.161A>G (p.Tyr54Cys)	KRT8 (Y54C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1276175	NM_002273.4(KRT8):c.-4T>C	KRT8	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 1259897	NM_001256282.2(KRT8):c.39-2208G>A	KRT8	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar