"Epithelial Biology; Institute of Medical Biology, Singapore"[submitte - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 66543	NM_002276.5(KRT19):c.685G>A (p.Val229Met)	KRT19 (V229M)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 66542	NM_002276.5(KRT19):c.552C>T (p.Asn184=)	KRT19	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 66540	NM_002276.5(KRT19):c.471T>C (p.Asn157=)	KRT19	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 66539	NM_002276.5(KRT19):c.179C>G (p.Ala60Gly)	KRT19 (A60G)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 66544	NM_002276.5(KRT19):c.90C>T (p.Ala30=)	KRT19	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 66541	NM_002276.5(KRT19):c.49G>A (p.Gly17Ser)	KRT19 (G17S)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 66538	NM_002276.4(KRT19):c.-99G>C	KRT19	Single nucleotide variant	not provided	Gnot provided

ClinVar