"PreventionGenetics, part of Exact Sciences"[submitter] AND "KRT3"[gen - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2059950	NM_057088.3(KRT3):c.1802G>A (p.Gly601Asp)	KRT3 (G601D)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3044013	NM_057088.3(KRT3):c.1571-5C>G	KRT3	Single nucleotide variant (intron variant)	KRT3-related disorder	GBenign
Select item 734361	NM_057088.3(KRT3):c.1342G>A (p.Glu448Lys)	KRT3, LOC126861527 (E448K)	Single nucleotide variant (missense variant)	KRT3-related disorder +1 more	GLikely benign
Select item 3056671	NM_057088.3(KRT3):c.1248C>T (p.Ser416=)	KRT3, LOC126861527	Single nucleotide variant (synonymous variant)	KRT3-related disorder	GLikely benign
Select item 3039625	NM_057088.3(KRT3):c.1224G>A (p.Gly408=)	KRT3, LOC126861527	Single nucleotide variant (synonymous variant)	KRT3-related disorder	GLikely benign
Select item 3042885	NM_057088.3(KRT3):c.1161C>G (p.Ala387=)	KRT3	Single nucleotide variant (synonymous variant)	KRT3-related disorder	GLikely benign
Select item 3039603	NM_057088.3(KRT3):c.1017C>T (p.Tyr339=)	KRT3	Single nucleotide variant (synonymous variant)	KRT3-related disorder	GLikely benign
Select item 3032771	NM_057088.3(KRT3):c.866+7G>C	KRT3	Single nucleotide variant (intron variant)	KRT3-related disorder	GLikely benign
Select item 3049215	NM_057088.3(KRT3):c.595C>T (p.Arg199Trp)	KRT3 (R199W)	Single nucleotide variant (missense variant)	KRT3-related disorder	GLikely benign
Select item 787397	NM_057088.3(KRT3):c.250C>T (p.Arg84Trp)	KRT3 (R84W)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2042004	NM_057088.3(KRT3):c.93T>C (p.Cys31=)	KRT3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3050237	NM_057088.3(KRT3):c.72C>T (p.Ser24=)	KRT3	Single nucleotide variant (synonymous variant)	KRT3-related disorder	GLikely benign