NM_173582.6(PGM2L1):c.1199AAG[1] (p.Glu401del) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003326839.5
Allele description [Variation Report for NM_173582.6(PGM2L1):c.1199AAG[1] (p.Glu401del)]
NM_173582.6(PGM2L1):c.1199AAG[1] (p.Glu401del)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024