NM_152432.4(ARHGAP42):c.2440C>G (p.Pro814Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004359097.1
Allele description [Variation Report for NM_152432.4(ARHGAP42):c.2440C>G (p.Pro814Ala)]
NM_152432.4(ARHGAP42):c.2440C>G (p.Pro814Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 10, 2024