NM_032380.5(GFM2):c.2082T>C (p.Val694=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jan 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001697528.14
Allele description [Variation Report for NM_032380.5(GFM2):c.2082T>C (p.Val694=)]
NM_032380.5(GFM2):c.2082T>C (p.Val694=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024