CCND2 c.785G>A ;(p.R262H)

Variant ID: 12-4409090-G-A

NM_001759.3(CCND2):c.785G>A;(p.R262H)

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Genomic Profiling on an Unselected Solid Tumor Population Reveals a Highly Mutated Wnt/β-Catenin Pathway Associated with Oncogenic EGFR Mutations.

Journal Of Personalized Medicine
Jiang, Jingrui J; Protopopov, Alexei A; Sun, Ruobai R; Lyle, Stephen S; Russell, Meaghan M
Publication Date: 2018-04-09

Variant appearance in text: CCND2: R262H
PubMed Link: 29642553
Variant Present in the following documents:
  • Main text
  • jpm-08-00013.pdf
View BVdb publication page



Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers.

Plos One
Pritchard, Antonia L AL; Johansson, Peter A PA; Nathan, Vaishnavi V; Howlie, Madeleine M; Symmons, Judith J; Palmer, Jane M JM; Hayward, Nicholas K NK
Publication Date: 2018

Variant appearance in text: CCND2: 785G>A; Arg262His; rs142170178
PubMed Link: 29641532
Variant Present in the following documents:
  • pone.0194098.s003.xlsx, sheet 10
View BVdb publication page



Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Scientific Reports
Chen, Xiaowei Sylvia XS; Reader, Rose H RH; Hoischen, Alexander A; Veltman, Joris A JA; Simpson, Nuala H NH; Francks, Clyde C; Newbury, Dianne F DF; Fisher, Simon E SE
Publication Date: 2017-04-25

Variant appearance in text: CCND2: R262H; rs142170178
PubMed Link: 28440294
Variant Present in the following documents:
  • srep46105-s2.xls, sheet 8
View BVdb publication page



Subclones in B-lymphoma cell lines: isogenic models for the study of gene regulation.

Oncotarget
Quentmeier, Hilmar H; Pommerenke, Claudia C; Ammerpohl, Ole O; Geffers, Robert R; Hauer, Vivien V; MacLeod, Roderick A F RA; Nagel, Stefan S; Romani, Julia J; Rosati, Emanuela E; Rosén, Anders A; Uphoff, Cord C CC; Zaborski, Margarete M; Drexler, Hans G HG
Publication Date: 2016-09-27

Variant appearance in text: CCND2: R262H
PubMed Link: 27566572
Variant Present in the following documents:
  • oncotarget-07-63456-s001.pdf
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: CCND2: R262H
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page