NM_001353921.2(ARHGEF9):c.1033C>T (p.Arg345Trp) AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Jan 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001786341.5
Allele description [Variation Report for NM_001353921.2(ARHGEF9):c.1033C>T (p.Arg345Trp)]
NM_001353921.2(ARHGEF9):c.1033C>T (p.Arg345Trp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024