NM_001367823.1(ARHGEF18):c.2055C>T (p.Leu685=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 26, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001407630.6
Allele description [Variation Report for NM_001367823.1(ARHGEF18):c.2055C>T (p.Leu685=)]
NM_001367823.1(ARHGEF18):c.2055C>T (p.Leu685=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024