NM_001042492.3(NF1):c.42C>G (p.Val14=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003172412.1
Allele description [Variation Report for NM_001042492.3(NF1):c.42C>G (p.Val14=)]
NM_001042492.3(NF1):c.42C>G (p.Val14=)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Dec 24, 2023