NM_019098.5(CNGB3):c.159C>G (p.Leu53=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002146710.6
Allele description [Variation Report for NM_019098.5(CNGB3):c.159C>G (p.Leu53=)]
NM_019098.5(CNGB3):c.159C>G (p.Leu53=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024