NM_002880.4(RAF1):c.909A>C (p.Thr303=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 9, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000037710.6
Allele description [Variation Report for NM_002880.4(RAF1):c.909A>C (p.Thr303=)]
NM_002880.4(RAF1):c.909A>C (p.Thr303=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024