NM_001001921.2(OR5AS1):c.953G>A (p.Arg318His) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004499530.1
Allele description [Variation Report for NM_001001921.2(OR5AS1):c.953G>A (p.Arg318His)]
NM_001001921.2(OR5AS1):c.953G>A (p.Arg318His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024