NM_001393500.2(TOMT):c.404C>T (p.Thr135Met) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000900752.15
Allele description [Variation Report for NM_001393500.2(TOMT):c.404C>T (p.Thr135Met)]
NM_001393500.2(TOMT):c.404C>T (p.Thr135Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 23, 2024