NM_018287.7(ARHGAP12):c.1178C>T (p.Ala393Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004268975.1
Allele description [Variation Report for NM_018287.7(ARHGAP12):c.1178C>T (p.Ala393Val)]
NM_018287.7(ARHGAP12):c.1178C>T (p.Ala393Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024