DDB2 c.1024-535C>T

Variant ID: 11-47258853-C-T

NM_000107.2(DDB2):c.1024-535C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs3824866
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk.

Neuron
, ; ,
Publication Date: 2016-10-19

Variant appearance in text: rs3824866
PubMed Link: 27764667
Variant Present in the following documents:
  • Main text
View BVdb publication page



Comprehensive pathway-based interrogation of genetic variations in the nucleotide excision DNA repair pathway and risk of bladder cancer.

Cancer
Xing, Jinliang J; Dinney, Colin P CP; Shete, Sanjay S; Huang, Maosheng M; Hildebrandt, Michelle A MA; Chen, Zhinan Z; Gu, Jian J
Publication Date: 2012-01-01

Variant appearance in text: rs3824866
PubMed Link: 21692063
Variant Present in the following documents:
  • Main text
View BVdb publication page