NM_000059.4(BRCA2):c.2661G>A (p.Glu887=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jan 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000220553.5
Allele description [Variation Report for NM_000059.4(BRCA2):c.2661G>A (p.Glu887=)]
NM_000059.4(BRCA2):c.2661G>A (p.Glu887=)
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
-
Mus musculus lectin, galactose binding, soluble 6 (Lgals6), mRNA
Mus musculus lectin, galactose binding, soluble 6 (Lgals6), mRNAgi|6754533|ref|NM_010707.1|Nucleotide
-
protein LURP-one-related 8 [Cucurbita maxima]
protein LURP-one-related 8 [Cucurbita maxima]gi|1280997791|ref|XP_022982605.1|Protein
-
protein LURP-one-related 8 [Cucumis sativus]
protein LURP-one-related 8 [Cucumis sativus]gi|449439787|ref|XP_004137667.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024