Bibliome.ai browser hg19
Search
About
Stats
FAQ
LRRK2 c.6055_6057delinsAAG ;(p.G2019K)
Variant ID: 12-40734202-GGC-AAG
NM_198578.3(
LRRK2
):c.6055_6057delinsAAG;(p.G2019K)
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:
Age-dependent dopamine transporter dysfunction and Serine129 phospho-α-synuclein overload in G2019S LRRK2 mice.
Acta Neuropathologica Communications
Longo, Francesco F; Mercatelli, Daniela D; Novello, Salvatore S; Arcuri, Ludovico L; Brugnoli, Alberto A; Vincenzi, Fabrizio F; Russo, Isabella I; Berti, Giulia G; Mabrouk, Omar S OS; Kennedy, Robert T RT; Shimshek, Derya R DR; Varani, Katia K; Bubacco, Luigi L; Greggio, Elisa E; Morari, Michele M
Publication Date: 2017-03-14
Variant appearance in text: LRRK2: G2019K
PubMed Link:
28292328
Variant Present in the following documents:
Main text
40478_2017_Article_426.pdf
View BVdb publication page