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NDUFAF2 c.127+3936A>G
Variant ID: 5-60245145-A-G
NM_174889.4(
NDUFAF2
):c.127+3936A>G
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Detection and clinical significance of DNA repair gene ERCC8 tag SNPs in gastric cancer.
The Turkish Journal Of Gastroenterology : The Official Journal Of Turkish Society Of Gastroenterology
Lu, Xingre X; Chen, Fengyu F; Liu, Xiaowen X; Yuan, Diao D; Zi, Yunju Y; He, Xiang X; Zhu, Deyong D
Publication Date: 2018-07
Variant appearance in text: rs158916
PubMed Link:
30249552
Variant Present in the following documents:
Main text
View BVdb publication page
Epistatic SNP interaction of ERCC6 with ERCC8 and their joint protein expression contribute to gastric cancer/atrophic gastritis risk.
Oncotarget
Jing, Jing-Jing JJ; Lu, You-Zhu YZ; Sun, Li-Ping LP; Liu, Jing-Wei JW; Gong, Yue-Hua YH; Xu, Qian Q; Dong, Nan-Nan NN; Yuan, Yuan Y
Publication Date: 2017-06-27
Variant appearance in text: rs158916
PubMed Link:
28562347
Variant Present in the following documents:
Main text
oncotarget-08-43140.pdf
View BVdb publication page
Polymorphisms of multiple genes involved in NER pathway predict prognosis of gastric cancer.
Oncotarget
Liu, Jingwei J; Deng, Na N; Xu, Qian Q; Sun, Liping L; Tu, Huakang H; Wang, Zhenning Z; Xing, Chengzhong C; Yuan, Yuan Y
Publication Date: 2016-07-26
Variant appearance in text: rs158916
PubMed Link:
27340861
Variant Present in the following documents:
Main text
oncotarget-07-48130.pdf
View BVdb publication page