NM_001393500.2(TOMT):c.123A>G (p.Ser41=) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Apr 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001553429.4
Allele description [Variation Report for NM_001393500.2(TOMT):c.123A>G (p.Ser41=)]
NM_001393500.2(TOMT):c.123A>G (p.Ser41=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024