NM_016249.4(MAGEC2):c.19G>A (p.Val7Ile) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001572768.2
Allele description [Variation Report for NM_016249.4(MAGEC2):c.19G>A (p.Val7Ile)]
NM_016249.4(MAGEC2):c.19G>A (p.Val7Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 2, 2024