NM_012249.4(RHOQ):c.482T>C (p.Val161Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004100309.1
Allele description [Variation Report for NM_012249.4(RHOQ):c.482T>C (p.Val161Ala)]
NM_012249.4(RHOQ):c.482T>C (p.Val161Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024