NM_019066.5(MAGEL2):c.1221G>A (p.Pro407=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000913828.4
Allele description [Variation Report for NM_019066.5(MAGEL2):c.1221G>A (p.Pro407=)]
NM_019066.5(MAGEL2):c.1221G>A (p.Pro407=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024