NM_002633.3(PGM1):c.1501G>A (p.Val501Ile) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 4, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000441537.1
Allele description [Variation Report for NM_002633.3(PGM1):c.1501G>A (p.Val501Ile)]
NM_002633.3(PGM1):c.1501G>A (p.Val501Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024