NM_001378615.1(CC2D2A):c.4098A>C (p.Glu1366Asp) AND Meckel syndrome, type 6
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000407949.5
Allele description [Variation Report for NM_001378615.1(CC2D2A):c.4098A>C (p.Glu1366Asp)]
NM_001378615.1(CC2D2A):c.4098A>C (p.Glu1366Asp)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024