NM_004333.6(BRAF):c.2127+3A>G AND Noonan syndrome 7
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001159454.4
Allele description [Variation Report for NM_004333.6(BRAF):c.2127+3A>G]
NM_004333.6(BRAF):c.2127+3A>G
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024