"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "KRT86"[gen - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2643010	NM_001320198.2(KRT86):c.-5+10305del	KRT81, KRT86	Deletion (3 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 1701200	NM_002281.4(KRT81):c.1453G>A (p.Val485Met)	KRT86, KRT81 (V485M)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1275631	NM_002281.4(KRT81):c.946C>T (p.Arg316Cys)	KRT81, KRT86 (R316C)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign/Likely benign
Select item 2643011	NM_002281.4(KRT81):c.138C>T (p.Gly46=)	KRT81, KRT86	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1219942	NM_001320198.2(KRT86):c.60C>G (p.Pro20=)	KRT81, KRT86	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 444296	NM_001320198.2(KRT86):c.884C>G (p.Ser295Cys)	KRT81, KRT86 (S295C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2643012	NM_001320198.2(KRT86):c.947G>A (p.Arg316His)	KRT81, KRT86 (R316H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2643013	NM_001320198.2(KRT86):c.993G>A (p.Arg331=)	KRT81, KRT86	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 7609	NM_001320198.2(KRT86):c.1237G>A (p.Glu413Lys)	KRT81, KRT86 (E413K)	Single nucleotide variant (missense variant)	not provided	GPathogenic