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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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