ClinVar (all) for Orgtrack (Select 500124) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 56170	NM_002273.4(KRT8):c.1412G>A (p.Gly471Glu)	KRT8 (G471E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 56169	NM_002273.4(KRT8):c.1340C>T (p.Ala447Val)	KRT8 (A447V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 56168	NM_002273.4(KRT8):c.1033G>T (p.Ala345Ser)	KRT8 (A345S +1 more)	Single nucleotide variant (missense variant +1 more)	Hepatitis C virus, susceptibility to	Gnot provided
Select item 56167	NM_000224.3(KRT18):c.134G>C (p.Arg45Pro)	KRT18, KRT8 +1 more (R45P)	Single nucleotide variant (missense variant +1 more)	Hepatitis C virus, susceptibility to	Gnot provided
Select item 56166	NM_000224.3(KRT18):c.282C>T (p.Tyr94=)	LOC106096416, KRT18 +1 more	Single nucleotide variant (synonymous variant +1 more)	Hepatitis C virus, susceptibility to	Gnot provided
Select item 56165	NM_000224.3(KRT18):c.1230C>G (p.Thr410=)	KRT18, LOC106096416	Single nucleotide variant (synonymous variant)	Hepatitis C virus, susceptibility to	Gnot provided

ClinVar