NM_001378615.1(CC2D2A):c.2830-38G>T AND not specified
- Germline classification:
- Benign (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000114171.13
Allele description [Variation Report for NM_001378615.1(CC2D2A):c.2830-38G>T]
NM_001378615.1(CC2D2A):c.2830-38G>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024