NM_001379270.1(CNGA1):c.1092T>A (p.Pro364=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002603185.3
Allele description [Variation Report for NM_001379270.1(CNGA1):c.1092T>A (p.Pro364=)]
NM_001379270.1(CNGA1):c.1092T>A (p.Pro364=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024