NM_000059.4(BRCA2):c.6642T>C (p.Thr2214=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004517788.1
Allele description [Variation Report for NM_000059.4(BRCA2):c.6642T>C (p.Thr2214=)]
NM_000059.4(BRCA2):c.6642T>C (p.Thr2214=)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
PREDICTED: Homo sapiens uncharacterized lncRNA (LOC105376553), ncRNA
PREDICTED: Homo sapiens uncharacterized lncRNA (LOC105376553), ncRNAgi|2217285909|ref|XR_931034.3|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 1, 2024