NM_001379270.1(CNGA1):c.1229T>C (p.Ile410Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 24, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001870665.5
Allele description [Variation Report for NM_001379270.1(CNGA1):c.1229T>C (p.Ile410Thr)]
NM_001379270.1(CNGA1):c.1229T>C (p.Ile410Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 11, 2024