NM_001005283.3(OR9Q2):c.647T>C (p.Val216Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 18, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004094238.1
Allele description [Variation Report for NM_001005283.3(OR9Q2):c.647T>C (p.Val216Ala)]
NM_001005283.3(OR9Q2):c.647T>C (p.Val216Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 19, 2024