NM_001004758.1(OR51S1):c.775T>C (p.Tyr259His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004646453.1
Allele description [Variation Report for NM_001004758.1(OR51S1):c.775T>C (p.Tyr259His)]
NM_001004758.1(OR51S1):c.775T>C (p.Tyr259His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024