NM_006015.6(ARID1A):c.759C>G (p.Pro253=) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Dec 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001530802.7
Allele description [Variation Report for NM_006015.6(ARID1A):c.759C>G (p.Pro253=)]
NM_006015.6(ARID1A):c.759C>G (p.Pro253=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024