NM_006015.6(ARID1A):c.358C>T (p.Pro120Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 26, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000503505.6
Allele description [Variation Report for NM_006015.6(ARID1A):c.358C>T (p.Pro120Ser)]
NM_006015.6(ARID1A):c.358C>T (p.Pro120Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024