NM_019066.5(MAGEL2):c.406G>A (p.Gly136Arg) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (4 submissions)
- Last evaluated:
- Nov 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000173481.22
Allele description [Variation Report for NM_019066.5(MAGEL2):c.406G>A (p.Gly136Arg)]
NM_019066.5(MAGEL2):c.406G>A (p.Gly136Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024