NM_001953.5(TYMP):c.1389C>T (p.Asp463=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001395089.15
Allele description [Variation Report for NM_001953.5(TYMP):c.1389C>T (p.Asp463=)]
NM_001953.5(TYMP):c.1389C>T (p.Asp463=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 26, 2024