NM_001123385.2(BCOR):c.1260T>C (p.Asp420=) AND not specified
- Germline classification:
- Benign (4 submissions)
- Last evaluated:
- Mar 19, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000081809.22
Allele description [Variation Report for NM_001123385.2(BCOR):c.1260T>C (p.Asp420=)]
NM_001123385.2(BCOR):c.1260T>C (p.Asp420=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024