NM_004448.4(ERBB2):c.3459A>C (p.Arg1153=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003059047.2
Allele description [Variation Report for NM_004448.4(ERBB2):c.3459A>C (p.Arg1153=)]
NM_004448.4(ERBB2):c.3459A>C (p.Arg1153=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024