NM_003073.5(SMARCB1):c.1145C>T (p.Ala382Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 5, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001017455.3
Allele description [Variation Report for NM_003073.5(SMARCB1):c.1145C>T (p.Ala382Val)]
NM_003073.5(SMARCB1):c.1145C>T (p.Ala382Val)
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
-
Oryza sativa Japonica Group cultivar Nipponbare chromosome 4, IRGSP-1.0
Oryza sativa Japonica Group cultivar Nipponbare chromosome 4, IRGSP-1.0gi|996703429|gnl|ASM:GCF_001433945| |NC_029259.1||gpp|GPC_000002165.1||gnl|NCBI_GENOMES|49349Nucleotide
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See more...Assertion and evidence details
Last Updated: Jun 23, 2024