"PreventionGenetics, part of Exact Sciences"[submitter] AND "KRT9"[gen - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3034210	NM_000226.4(KRT9):c.1668C>A (p.Gly556=)	KRT9	Single nucleotide variant (synonymous variant)	KRT9-related disorder	GLikely benign
Select item 3046581	NM_000226.4(KRT9):c.1394+8C>G	KRT9	Single nucleotide variant (intron variant)	KRT9-related disorder	GLikely benign
Select item 891512	NM_000226.4(KRT9):c.1290C>T (p.Ile430=)	KRT9	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 891760	NM_000226.4(KRT9):c.1120C>T (p.Arg374Trp)	KRT9 (R374W)	Single nucleotide variant (missense variant)	KRT9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 2636321	NM_000226.4(KRT9):c.566A>G (p.Tyr189Cys)	KRT9 (Y189C)	Single nucleotide variant (missense variant)	KRT9-related disorder	GUncertain significance
Select item 3055652	NM_000226.4(KRT9):c.354_377dup (p.Gly126_Tyr127insSerGlyGlyGlyPheGlyGlyGly)	KRT9	Duplication (inframe insertion)	KRT9-related disorder	GUncertain significance
Select item 3036315	NM_000226.4(KRT9):c.327G>A (p.Gly109=)	KRT9	Single nucleotide variant (synonymous variant)	KRT9-related disorder	GLikely benign
Select item 323139	NM_000226.4(KRT9):c.245G>A (p.Ser82Asn)	KRT9 (S82N)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 3044333	NM_000226.4(KRT9):c.87G>A (p.Arg29=)	KRT9	Single nucleotide variant (synonymous variant)	KRT9-related disorder	GLikely benign
Select item 3034059	NM_000226.4(KRT9):c.45C>T (p.Gly15=)	KRT9	Single nucleotide variant (synonymous variant)	KRT9-related disorder	GLikely benign