List of variants in gene ARAF reported as likely pathogenic for adenocarcinoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001654.5(ARAF):c.640T>G (p.Ser214Ala)	rs1057519876
NM_001654.5(ARAF):c.641C>G (p.Ser214Cys)	rs1057519786
NM_001654.5(ARAF):c.641C>T (p.Ser214Phe)	rs1057519786

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