NM_017721.5(CC2D1A):c.1838C>T (p.Ala613Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 26, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000502288.6
Allele description [Variation Report for NM_017721.5(CC2D1A):c.1838C>T (p.Ala613Val)]
NM_017721.5(CC2D1A):c.1838C>T (p.Ala613Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 9, 2023