NM_001903.5(CTNNA1):c.476A>T (p.Asp159Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001051746.6
Allele description [Variation Report for NM_001903.5(CTNNA1):c.476A>T (p.Asp159Val)]
NM_001903.5(CTNNA1):c.476A>T (p.Asp159Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024