NM_025251.3(ARHGAP39):c.389T>G (p.Val130Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004339369.1
Allele description [Variation Report for NM_025251.3(ARHGAP39):c.389T>G (p.Val130Gly)]
NM_025251.3(ARHGAP39):c.389T>G (p.Val130Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024