NM_001953.5(TYMP):c.1389C>T (p.Asp463=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 30, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000438948.9
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:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024