RRM2B c.*732A>G

Variant ID: 8-103219629-T-C

NM_015713.4(RRM2B):c.*732A>G

This variant was identified in 4 publications

View GRCh38 version.




Publications:


PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs16869269
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs16869269
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
  • oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page



Targeted resequencing of the microRNAome and 3'UTRome reveals functional germline DNA variants with altered prevalence in epithelial ovarian cancer.

Oncogene
Chen, X X; Paranjape, T T; Stahlhut, C C; McVeigh, T T; Keane, F F; Nallur, S S; Miller, N N; Kerin, M M; Deng, Y Y; Yao, X X; Zhao, H H; Weidhaas, J B JB; Slack, F J FJ
Publication Date: 2015-04-16

Variant appearance in text: rs16869269
PubMed Link: 24909162
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants in MicroRNA biosynthesis pathways and binding sites modify ovarian cancer risk, survival, and treatment response.

Cancer Research
Liang, Dong D; Meyer, Larissa L; Chang, David W DW; Lin, Jie J; Pu, Xia X; Ye, Yuanqing Y; Gu, Jian J; Wu, Xifeng X; Lu, Karen K
Publication Date: 2010-12-01

Variant appearance in text: rs16869269
PubMed Link: 21118967
Variant Present in the following documents:
  • Main text
View BVdb publication page