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LRRK2 c.5338G>T ;(p.V1780F)
Variant ID: 12-40716141-G-T
NM_198578.3(
LRRK2
):c.5338G>T;(p.V1780F)
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:
Identification of sixteen novel candidate genes for late onset Parkinson's disease.
Molecular Neurodegeneration
Gialluisi, Alessandro A; Reccia, Mafalda Giovanna MG; Modugno, Nicola N; Nutile, Teresa T; Lombardi, Alessia A; Di Giovannantonio, Luca Giovanni LG; Pietracupa, Sara S; Ruggiero, Daniela D; Scala, Simona S; Gambardella, Stefano S; , ; Iacoviello, Licia L; Gianfrancesco, Fernando F; Acampora, Dario D; D'Esposito, Maurizio M; Simeone, Antonio A; Ciullo, Marina M; Esposito, Teresa T
Publication Date: 2021-06-21
Variant appearance in text: LRRK2: V1780F
PubMed Link:
34148545
Variant Present in the following documents:
13024_2021_455_MOESM1_ESM.pdf
View BVdb publication page