NM_178229.5(IQGAP3):c.3663T>C (p.Ala1221=) AND IQGAP3-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003926928.1
Allele description [Variation Report for NM_178229.5(IQGAP3):c.3663T>C (p.Ala1221=)]
NM_178229.5(IQGAP3):c.3663T>C (p.Ala1221=)
Condition(s)
- Name:
- IQGAP3-related disorder
- Synonyms:
- IQGAP3-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024