NM_001379270.1(CNGA1):c.1298G>T (p.Trp433Leu) AND Retinitis pigmentosa
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001147265.4
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)
Assertion and evidence details
Last Updated: Sep 29, 2024