NM_000059.4(BRCA2):c.3849A>C (p.Val1283=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Feb 23, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000777591.4
Allele description [Variation Report for NM_000059.4(BRCA2):c.3849A>C (p.Val1283=)]
NM_000059.4(BRCA2):c.3849A>C (p.Val1283=)
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
-
Mycobacterium xenopi 4042, whole genome shotgun sequencing project
Mycobacterium xenopi 4042, whole genome shotgun sequencing projectgi|576491613|gb|JAOB00000000.1|JAOB 000Nucleotide
-
ITGA9 integrin subunit alpha 9 [Homo sapiens]
ITGA9 integrin subunit alpha 9 [Homo sapiens]Gene ID:3680Gene
-
Gene Links for GEO Profiles (Select 131929444) (1)
Gene
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See more...Assertion and evidence details
Last Updated: Sep 1, 2024