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ARHGEF1 c.2007G>A ;(p.L669=)
Variant ID: 19-42408381-G-A
NM_004706.3(
ARHGEF1
):c.2007G>A;(p.L669=)
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:
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: ARHGEF1: L669L
PubMed Link:
29221171
Variant Present in the following documents:
oncotarget-08-95841-s002.xlsx, sheet 1
oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page