NM_000059.4(BRCA2):c.7830G>T (p.Val2610=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 25, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002411551.9
Allele description [Variation Report for NM_000059.4(BRCA2):c.7830G>T (p.Val2610=)]
NM_000059.4(BRCA2):c.7830G>T (p.Val2610=)
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
-
Homo sapiens isolate Bul7062 mitochondrion, complete genome
Homo sapiens isolate Bul7062 mitochondrion, complete genomegi|373446404|gb|JQ245807.1|Nucleotide
-
SLC35B2 [Python bivittatus]
SLC35B2 [Python bivittatus]Gene ID:103060787Gene
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Last Updated: Sep 16, 2024