NM_001379270.1(CNGA1):c.-15+10288_-15+10290del AND CNGA1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 18, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003904271.1
Allele description [Variation Report for NM_001379270.1(CNGA1):c.-15+10288_-15+10290del]
NM_001379270.1(CNGA1):c.-15+10288_-15+10290del
Condition(s)
- Name:
- CNGA1-related disorder
- Synonyms:
- CNGA1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 26, 2024