NM_001040716.2(PC):c.2580C>T (p.Asp860=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 4, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000127317.2
Allele description [Variation Report for NM_001040716.2(PC):c.2580C>T (p.Asp860=)]
NM_001040716.2(PC):c.2580C>T (p.Asp860=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024