NM_001378615.1(CC2D2A):c.4560T>C (p.Asn1520=) AND Meckel syndrome, type 6
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001147771.4
Allele description [Variation Report for NM_001378615.1(CC2D2A):c.4560T>C (p.Asn1520=)]
NM_001378615.1(CC2D2A):c.4560T>C (p.Asn1520=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023