NM_019098.5(CNGB3):c.466T>G (p.Ser156Ala) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003687891.2
Allele description [Variation Report for NM_019098.5(CNGB3):c.466T>G (p.Ser156Ala)]
NM_019098.5(CNGB3):c.466T>G (p.Ser156Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024