"Database of Curated Mutations (DoCM)"[submitter] AND "ARAF"[gene] - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376367	NM_001654.5(ARAF):c.640T>G (p.Ser214Ala)	ARAF (S214A +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma, sporadic +2 more	GLikely pathogenic
Select item 376366	NM_001654.5(ARAF):c.641C>T (p.Ser214Phe)	ARAF (S214F +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma, sporadic +2 more	GLikely pathogenic
Select item 376137	NM_001654.5(ARAF):c.641C>G (p.Ser214Cys)	ARAF (S214C +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma, sporadic +2 more	GLikely pathogenic

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