Related gene-specific medical variations for Gene (Select 3868) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2433268	NM_005557.4(KRT16):c.905G>A (p.Arg302Lys)	KRT16 (R302K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 66610	NM_005557.4(KRT16):c.43A>T (p.Lys15Ter)	KRT16 (K15*)	Single nucleotide variant (nonsense)	not provided	Gnot provided
Select item 66607	NM_005557.4(KRT16):c.371_373del (p.Leu124_Asn125delinsHis)	KRT16	Deletion (inframe_indel)	not provided	Gnot provided
Select item 66606	NM_005557.4(KRT16):c.371T>C (p.Leu124Pro)	KRT16 (L124P)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 66604	NM_005557.4(KRT16):c.362T>A (p.Met121Lys)	KRT16 (M121K)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 66603	NM_005557.4(KRT16):c.316_327del (p.Phe106_Gly109del)	KRT16	Deletion (inframe_deletion)	not provided	Gnot provided
Select item 66602	NM_005557.4(KRT16):c.25del (p.Thr9fs)	KRT16 (T9fs)	Deletion (frameshift variant)	not provided	Gnot provided
Select item 66601	NM_005557.4(KRT16):c.1270del (p.Glu424fs)	KRT16 (E424fs)	Deletion (frameshift variant)	not provided	Gnot provided

ClinVar