NM_001353921.2(ARHGEF9):c.1488G>A (p.Ser496=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000827555.12
Allele description [Variation Report for NM_001353921.2(ARHGEF9):c.1488G>A (p.Ser496=)]
NM_001353921.2(ARHGEF9):c.1488G>A (p.Ser496=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 26, 2024