NM_000156.6(GAMT):c.575C>T (p.Thr192Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 24, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002314717.9
Allele description [Variation Report for NM_000156.6(GAMT):c.575C>T (p.Thr192Met)]
NM_000156.6(GAMT):c.575C>T (p.Thr192Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 13, 2024