NM_013964.5(NRG1):c.414T>C (p.Gly138=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000961861.4
Allele description [Variation Report for NM_013964.5(NRG1):c.414T>C (p.Gly138=)]
NM_013964.5(NRG1):c.414T>C (p.Gly138=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024