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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 14629	NM_153490.3(KRT13):c.356T>C (p.Leu119Pro)	KRT13 (L119P)	Single nucleotide variant (missense variant)	White sponge nevus 2	GPathogenic
Select item 66754	NM_153490.3(KRT13):c.344T>C (p.Leu115Pro)	KRT13 (L115P)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 66753	NM_153490.3(KRT13):c.341G>A (p.Arg114His)	KRT13 (R114H)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 66752	NM_153490.3(KRT13):c.335A>G (p.Asn112Ser)	KRT13 (N112S)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 66751	NM_153490.3(KRT13):c.332T>C (p.Leu111Pro)	KRT13 (L111P)	Single nucleotide variant (missense variant)	White sponge nevus 2	GPathogenic
Select item 66750	NM_153490.3(KRT13):c.323T>C (p.Met108Thr)	KRT13 (M108T)	Single nucleotide variant (missense variant)	not provided	Gnot provided

ClinVar