Bibliome.ai browser hg19
Search
About
Stats
FAQ
DDX10 c.1742A>T ;(p.E581V)
Variant ID: 11-108593966-A-T
NM_004398.2(
DDX10
):c.1742A>T;(p.E581V)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Nucleic Acids Research
Tang, Xiaojia X; Baheti, Saurabh S; Shameer, Khader K; Thompson, Kevin J KJ; Wills, Quin Q; Niu, Nifang N; Holcomb, Ilona N IN; Boutet, Stephane C SC; Ramakrishnan, Ramesh R; Kachergus, Jennifer M JM; Kocher, Jean-Pierre A JP; Weinshilboum, Richard M RM; Wang, Liewei L; Thompson, E Aubrey EA; Kalari, Krishna R KR
Publication Date: 2014-12-16
Variant appearance in text: DDX10: E581V
PubMed Link:
25352556
Variant Present in the following documents:
supp_gku1005_nar-01266-met-n-2014-File014.xlsx, sheet 5
View BVdb publication page