NM_001379270.1(CNGA1):c.1298G>T (p.Trp433Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004023163.1
Allele description [Variation Report for NM_001379270.1(CNGA1):c.1298G>T (p.Trp433Leu)]
NM_001379270.1(CNGA1):c.1298G>T (p.Trp433Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024