NM_000551.4(VHL):c.209A>T (p.Glu70Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004520897.1
Allele description [Variation Report for NM_000551.4(VHL):c.209A>T (p.Glu70Val)]
NM_000551.4(VHL):c.209A>T (p.Glu70Val)
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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STAG2 Mutations Reshape the Cohesin-Structured Spatial Chromatin Architecture to...
STAG2 Mutations Reshape the Cohesin-Structured Spatial Chromatin Architecture to Drive Gene Regulation in Acute myeloid Leukemia [DNAInputSeq]STAG2 Mutations Reshape the Cohesin-Structured Spatial Chromatin Architecture to Drive Gene Regulation in Acute myeloid Leukemia [DNAInputSeq]BioProject
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CBTC949.rev NICHD_XGC_tropBone1 Xenopus tropicalis cDNA clone IMAGE:8933303 3', ...
CBTC949.rev NICHD_XGC_tropBone1 Xenopus tropicalis cDNA clone IMAGE:8933303 3', mRNA sequencegi|126271493|gnl|dbEST|45045322|gb| 770.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024