NM_003073.5(SMARCB1):c.628+13C>T AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 21, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002255370.1
Allele description [Variation Report for NM_003073.5(SMARCB1):c.628+13C>T]
NM_003073.5(SMARCB1):c.628+13C>T
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
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neurotrophin 3, partial [Amphiesma stolatum]
neurotrophin 3, partial [Amphiesma stolatum]gi|2159029583|gb|UFQ72895.1|Protein
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brain derived neurotrophic factor, partial [Amphiesma stolatum]
brain derived neurotrophic factor, partial [Amphiesma stolatum]gi|2159029701|gb|UFQ72954.1|Protein
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Rhabditida cytochrome c oxidase subunit 1 gene, partial cds; mitochondrial.
Rhabditida cytochrome c oxidase subunit 1 gene, partial cds; mitochondrial.PopSet: 1573131177PopSet
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JGI_CAAO5586.fwd NIH_XGC_tropTe5 Xenopus tropicalis cDNA clone CAAO5586 5', mRNA...
JGI_CAAO5586.fwd NIH_XGC_tropTe5 Xenopus tropicalis cDNA clone CAAO5586 5', mRNA sequencegi|58727401|gnl|dbEST|27644562|gb|C 43.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024