NM_001931.5(DLAT):c.367G>T (p.Asp123Tyr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 25, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000518970.2
Allele description [Variation Report for NM_001931.5(DLAT):c.367G>T (p.Asp123Tyr)]
NM_001931.5(DLAT):c.367G>T (p.Asp123Tyr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024