NM_001005198.2(OR8G5):c.580A>G (p.Ile194Val) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004365395.1
Allele description [Variation Report for NM_001005198.2(OR8G5):c.580A>G (p.Ile194Val)]
NM_001005198.2(OR8G5):c.580A>G (p.Ile194Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024