NM_004706.4(ARHGEF1):c.558C>T (p.Tyr186=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003816988.1
Allele description [Variation Report for NM_004706.4(ARHGEF1):c.558C>T (p.Tyr186=)]
NM_004706.4(ARHGEF1):c.558C>T (p.Tyr186=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024