NM_017950.4(CCDC40):c.2784C>T (p.Ile928=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Feb 21, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000250560.10
Allele description [Variation Report for NM_017950.4(CCDC40):c.2784C>T (p.Ile928=)]
NM_017950.4(CCDC40):c.2784C>T (p.Ile928=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024