NM_004448.4(ERBB2):c.2308-14A>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002219666.7
Allele description [Variation Report for NM_004448.4(ERBB2):c.2308-14A>G]
NM_004448.4(ERBB2):c.2308-14A>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024