NM_001374828.1(ARID1B):c.4864A>T (p.Met1622Leu) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 13, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002312006.9
Allele description [Variation Report for NM_001374828.1(ARID1B):c.4864A>T (p.Met1622Leu)]
NM_001374828.1(ARID1B):c.4864A>T (p.Met1622Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 26, 2024