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Integrated molecular analysis of clear-cell renal cell carcinoma.

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Nat Genet2013PMID 23797736stubpubmedProvenance
Source
PubMed
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-CIVIC-20260908-000001
Published

Abstract

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Linked entities

Linked entities (7)

How each link was made (MeSH, dictionary, registry reference, curation…) and whether it has been validated. Candidate links are not counted in entity statistics.

Validated 7

Curated evidence

Evidence citing this paper (4)

civicProvenance
Source
CIViC — Clinical Interpretation of Variants in Cancer
Dataset
CIViC evidence items
Version
civic-2026-09-08
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Evidence
expert curation
License
CC0 1.0
PMID
23797736
Run
ING-CIVIC-20260908-000001
Open at source
CuratedShowing 1–4 of 4 evidence items · levels, directions and significance as curated at the source; each row links to its CIViC record.
TherapyCancerTypeLevelDirection · significanceRating (1–5)StatusEvidenceSource
BAP1 Mutation2
(prognostic)Clear Cell Renal Cell CarcinomaPrognosticBSupports Poor Outcome5accepted
EID459

In patients with clear cell renal cell carcinoma, in a multivariate analysis those with mutations in BAP1 had worse overall survival than wild-type.

PMID 23797736 · Sato et al., 2013 · Open in CIViC

civic
〃Renal Cell CarcinomaCURATED_BROADERPrognosticBSupports Poor Outcome5accepted
EID460

In patients with clear cell renal cell carcinoma, in a multivariate analysis those with mutations in BAP1 had worse overall survival than wild-type.

PMID 23797736 · Sato et al., 2013 · Open in CIViC

civic
VHL S65L (c.194C>T)1
(predisposing)Von Hippel-Lindau DiseaseUNRESOLVEDPredisposingCSupports Uncertain Significance2accepted
EID6728

240 ccRCC specimens were genetically analyzed. 3 specimens (ccRCC-58, ccRCC-154, ccRCC-238) from 3 different patients were confirmed to carry the p.Ser65Leu; c.194C>T mutation. The mutation was found … (full text at CIViC)

PMID 23797736 · Sato et al., 2013 · Open in CIViC

civic
VHL Splice Site (c.464-1G>T)1
(predisposing)Von Hippel-Lindau DiseaseUNRESOLVEDPredisposingCSupports Uncertain Significance2submitted
EID6727

240 ccRCC specimens were analyzed. 3 specimens came from 3 different patients with confirmed germline mutations in the VHL gene. Two male unrelated patients, age 54 and 56 had a splice variant in the … (full text at CIViC)

PMID 23797736 · Sato et al., 2013 · Open in CIViC

civic