NM_001297.5(CNGB1):c.2700G>A (p.Thr900=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000955137.12
Allele description [Variation Report for NM_001297.5(CNGB1):c.2700G>A (p.Thr900=)]
NM_001297.5(CNGB1):c.2700G>A (p.Thr900=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024