LRRK2 c.1663G>A ;(p.G555R)

Variant ID: 12-40668391-G-A

NM_198578.3(LRRK2):c.1663G>A;(p.G555R)

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:

A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing.

Movement Disorders : Official Journal Of The Movement Disorder Society
Lin, Chin-Hsien CH; Chen, Pei-Lung PL; Tai, Chun-Hwei CH; Lin, Hang-I HI; Chen, Chih-Shan CS; Chen, Meng-Ling ML; Wu, Ruey-Meei RM
Publication Date: 2019-04

Variant appearance in text: LRRK2: 1663G>A
PubMed Link: 30788857
Variant Present in the following documents:
  • Main text
  • MDS-34-506.pdf
View BVdb publication page