NM_000059.4(BRCA2):c.3951T>C (p.Thr1317=) AND Breast-ovarian cancer, familial, susceptibility to, 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 29, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000495508.3
Allele description [Variation Report for NM_000059.4(BRCA2):c.3951T>C (p.Thr1317=)]
NM_000059.4(BRCA2):c.3951T>C (p.Thr1317=)
Condition(s)
-
Homo sapiens NOP56 ribonucleoprotein (NOP56), transcript variant 3, non-coding R...
Homo sapiens NOP56 ribonucleoprotein (NOP56), transcript variant 3, non-coding RNAgi|1701948223|ref|NR_145428.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024