NM_006015.6(ARID1A):c.372C>T (p.Gly124=) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001587675.6
Allele description [Variation Report for NM_006015.6(ARID1A):c.372C>T (p.Gly124=)]
NM_006015.6(ARID1A):c.372C>T (p.Gly124=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024