NM_006431.3(CCT2):c.398C>T (p.Ala133Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001316924.6
Allele description [Variation Report for NM_006431.3(CCT2):c.398C>T (p.Ala133Val)]
NM_006431.3(CCT2):c.398C>T (p.Ala133Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024