NM_007357.3(COG2):c.1825G>A (p.Asp609Asn) AND Congenital disorder of glycosylation, type IIq
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 27, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001071427.5
Allele description [Variation Report for NM_007357.3(COG2):c.1825G>A (p.Asp609Asn)]
NM_007357.3(COG2):c.1825G>A (p.Asp609Asn)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024