NM_000156.6(GAMT):c.471T>G (p.Phe157Leu) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 8, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000611035.1
Allele description [Variation Report for NM_000156.6(GAMT):c.471T>G (p.Phe157Leu)]
NM_000156.6(GAMT):c.471T>G (p.Phe157Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 4, 2023