NM_001004487.1(OR13J1):c.266G>A (p.Arg89Gln) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004111194.1
Allele description [Variation Report for NM_001004487.1(OR13J1):c.266G>A (p.Arg89Gln)]
NM_001004487.1(OR13J1):c.266G>A (p.Arg89Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024