XRCC4 c.*406T>C

Variant ID: 5-82649467-T-C

NM_003401.3(XRCC4):c.*406T>C

This variant was identified in 7 publications

View GRCh38 version.




Publications:


BRCA2 3'-UTR Polymorphism rs15869 Alters Susceptibility to Papillary Thyroid Carcinoma via Binding hsa-mir-1178-3p.

Pharmacogenomics And Personalized Medicine
Guo, Nan N; Qu, Peng P; Li, Hao H; Liu, Liuli L; Jin, Hao H; Liu, Renqi R; Zhang, Zhen Z; Zhang, Xuan X; Li, Yingchun Y; Lu, Xiaobo X; Zhao, Yuejiao Y
Publication Date: 2021

Variant appearance in text: rs2035990
PubMed Link: 33986610
Variant Present in the following documents:
  • Main text
View BVdb publication page



MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis.

Cancer Medicine
Gholami, Morteza M; Larijani, Bagher B; Sharifi, Farshad F; Hasani-Ranjbar, Shirin S; Taslimi, Reza R; Bastami, Milad M; Atlasi, Rasha R; Amoli, Mahsa M MM
Publication Date: 2019-12

Variant appearance in text: rs2035990
PubMed Link: 31637880
Variant Present in the following documents:
  • Main text
  • CAM4-8-7477.pdf
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MicroRNA binding mediated Functional sequence variant in 3'-UTR of DNA repair Gene XPC in Age-related Cataract.

Scientific Reports
Zou, Xi X; Kang, Lihua L; Yang, Mei M; Wu, Jian J; Guan, Huaijin H
Publication Date: 2018-10-12

Variant appearance in text: rs2035990
PubMed Link: 30315181
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_33071.pdf
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A Decade of GWAS Results in Lung Cancer.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Bossé, Yohan Y; Amos, Christopher I CI
Publication Date: 2018-04

Variant appearance in text: rs2035990
PubMed Link: 28615365
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variant in DNA repair gene GTF2H4 is associated with lung cancer risk: a large-scale analysis of six published GWAS datasets in the TRICL consortium.

Carcinogenesis
Wang, Meilin M; Liu, Hongliang H; Liu, Zhensheng Z; Yi, Xiaohua X; Bickeboller, Heike H; Hung, Rayjean J RJ; Brennan, Paul P; Landi, Maria Teresa MT; Caporaso, Neil N; Christiani, David C DC; Doherty, Jennifer Anne JA; , ; Amos, Christopher I CI; Wei, Qingyi Q
Publication Date: 2016-09

Variant appearance in text: rs2035990
PubMed Link: 27288692
Variant Present in the following documents:
  • Main text
View BVdb publication page



A recessive variant of XRCC4 predisposes to non- BRCA1/2 breast cancer in chinese women and impairs the DNA damage response via dysregulated nuclear localization.

Oncotarget
He, Min M; Hu, Xin X; Chen, Li L; Cao, A-Yong AY; Yu, Ke-Da KD; Shi, Ting-Yan TY; Kuang, Xia-Ying XY; Shi, Wen-Biao WB; Ling, Hong H; Li, Shan S; Qiao, Feng F; Yao, Ling L; Wei, Qingyi Q; Di, Gen-Hong GH; Shao, Zhi-Ming ZM
Publication Date: 2014-12-15

Variant appearance in text: rs2035990
PubMed Link: 25360583
Variant Present in the following documents:
  • Main text
  • oncotarget-05-12218.pdf
  • oncotarget-05-12218-s001.pdf
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Genetic variants associated with protein C levels.

Journal Of Thrombosis And Haemostasis : Jth
Vossen, C Y CY; Koeleman, B P BP; Hasstedt, S J SJ; Nijman, I J IJ; Renkens, I J IJ; Callas, P W PW; Rosendaal, F R FR; Bovill, E G EG
Publication Date: 2013-04

Variant appearance in text: rs2035990
PubMed Link: 23387557
Variant Present in the following documents:
  • Main text
View BVdb publication page