AKAP6 c.3588+6982G>A

Variant ID: 14-33250081-G-A

NM_004274.4(AKAP6):c.3588+6982G>A

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations.

Cancer Biology & Medicine
Mo, Zongchao Z; Xin, Junyi J; Chai, Ruichao R; Woo, Peter Y M PYM; Chan, Danny T M DTM; Wang, Jiguang J
Publication Date: 2022-11-01

Variant appearance in text: rs10131032
PubMed Link: 36350002
Variant Present in the following documents:
  • Main text
  • cbm-19-1440.pdf
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Epidemiology of Brain and Other CNS Tumors.

Current Neurology And Neuroscience Reports
Ostrom, Quinn T QT; Francis, Stephen S SS; Barnholtz-Sloan, Jill S JS
Publication Date: 2021-11-24

Variant appearance in text: rs10131032
PubMed Link: 34817716
Variant Present in the following documents:
  • Main text
  • 11910_2021_Article_1152.pdf
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The Genetic Architecture of Gliomagenesis-Genetic Risk Variants Linked to Specific Molecular Subtypes.

Cancers
Wu, Wendy Yi-Ying WY; Johansson, Gunnar G; Wibom, Carl C; Brännström, Thomas T; Malmström, Annika A; Henriksson, Roger R; Golovleva, Irina I; Bondy, Melissa L ML; Andersson, Ulrika U; Dahlin, Anna M AM; Melin, Beatrice B
Publication Date: 2019-12-12

Variant appearance in text: rs10131032
PubMed Link: 31842352
Variant Present in the following documents:
  • Main text
  • cancers-11-02001.pdf
  • cancers-11-02001-s001.pdf
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Risk factors for childhood and adult primary brain tumors.

Neuro-Oncology
Ostrom, Quinn T QT; Adel Fahmideh, Maral M; Cote, David J DJ; Muskens, Ivo S IS; Schraw, Jeremy M JM; Scheurer, Michael E ME; Bondy, Melissa L ML
Publication Date: 2019-11-04

Variant appearance in text: rs10131032
PubMed Link: 31301133
Variant Present in the following documents:
  • Main text
View BVdb publication page



Use of Mendelian Randomization for Identifying Risk Factors for Brain Tumors.

Frontiers In Genetics
Howell, Amy Elizabeth AE; Zheng, Jie J; Haycock, Philip C PC; McAleenan, Alexandra A; Relton, Caroline C; Martin, Richard M RM; Kurian, Kathreena M KM
Publication Date: 2018

Variant appearance in text: rs10131032
PubMed Link: 30483309
Variant Present in the following documents:
  • Main text
  • fgene-09-00525.pdf
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Diffuse gliomas classified by 1p/19q co-deletion, TERT promoter and IDH mutation status are associated with specific genetic risk loci.

Acta Neuropathologica
Labreche, Karim K; Kinnersley, Ben B; Berzero, Giulia G; Di Stefano, Anna Luisa AL; Rahimian, Amithys A; Detrait, Ines I; Marie, Yannick Y; Grenier-Boley, Benjamin B; Hoang-Xuan, Khe K; Delattre, Jean-Yves JY; Idbaih, Ahmed A; Houlston, Richard S RS; Sanson, Marc M
Publication Date: 2018-05

Variant appearance in text: rs10131032
PubMed Link: 29460007
Variant Present in the following documents:
  • Main text
  • 401_2018_Article_1825.pdf
  • 401_2018_1825_MOESM1_ESM.pdf
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Genome-Wide Association Studies in Glioma.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Kinnersley, Ben B; Houlston, Richard S RS; Bondy, Melissa L ML
Publication Date: 2018-04

Variant appearance in text: rs10131032
PubMed Link: 29382702
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.

Nature Genetics
Melin, Beatrice S BS; Barnholtz-Sloan, Jill S JS; Wrensch, Margaret R MR; Johansen, Christoffer C; Il'yasova, Dora D; Kinnersley, Ben B; Ostrom, Quinn T QT; Labreche, Karim K; Chen, Yanwen Y; Armstrong, Georgina G; Liu, Yanhong Y; Eckel-Passow, Jeanette E JE; Decker, Paul A PA; Labussière, Marianne M; Idbaih, Ahmed A; Hoang-Xuan, Khe K; Di Stefano, Anna-Luisa AL; Mokhtari, Karima K; Delattre, Jean-Yves JY; Broderick, Peter P; Galan, Pilar P; Gousias, Konstantinos K; Schramm, Johannes J; Schoemaker, Minouk J MJ; Fleming, Sarah J SJ; Herms, Stefan S; Heilmann, Stefanie S; Nöthen, Markus M MM; Wichmann, Heinz-Erich HE; Schreiber, Stefan S; Swerdlow, Anthony A; Lathrop, Mark M; Simon, Matthias M; Sanson, Marc M; Andersson, Ulrika U; Rajaraman, Preetha P; Chanock, Stephen S; Linet, Martha M; Wang, Zhaoming Z; Yeager, Meredith M; , ; Wiencke, John K JK; Hansen, Helen H; McCoy, Lucie L; Rice, Terri T; Kosel, Matthew L ML; Sicotte, Hugues H; Amos, Christopher I CI; Bernstein, Jonine L JL; Davis, Faith F; Lachance, Dan D; Lau, Ching C; Merrell, Ryan T RT; Shildkraut, Joellen J; Ali-Osman, Francis F; Sadetzki, Siegal S; Scheurer, Michael M; Shete, Sanjay S; Lai, Rose K RK; Claus, Elizabeth B EB; Olson, Sara H SH; Jenkins, Robert B RB; Houlston, Richard S RS; Bondy, Melissa L ML
Publication Date: 2017-05

Variant appearance in text: rs10131032
PubMed Link: 28346443
Variant Present in the following documents:
  • Main text
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Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
Liu, Yanhong Y; Shete, Sanjay S; Etzel, Carol J CJ; Scheurer, Michael M; Alexiou, George G; Armstrong, Georgina G; Tsavachidis, Spyros S; Liang, Fu-Wen FW; Gilbert, Mark M; Aldape, Ken K; Armstrong, Terri T; Houlston, Richard R; Hosking, Fay F; Robertson, Lindsay L; Xiao, Yuanyuan Y; Wiencke, John J; Wrensch, Margaret M; Andersson, Ulrika U; Melin, Beatrice S BS; Bondy, Melissa M
Publication Date: 2010-05-10

Variant appearance in text: rs10131032
PubMed Link: 20368557
Variant Present in the following documents:
  • Main text
View BVdb publication page