LRRK2 c.5605_5606delinsCA ;(p.M1869Q)

Variant ID: 12-40717057-AT-CA

NM_198578.3(LRRK2):c.5605_5606delinsCA;(p.M1869Q)

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:

Mutations in the LRRK2 Roc-COR tandem domain link Parkinson's disease to Wnt signalling pathways.

Human Molecular Genetics
Sancho, Rosa M RM; Law, Bernard M H BM; Harvey, Kirsten K
Publication Date: 2009-10-15

Variant appearance in text: LRRK2: M1869Q
PubMed Link: 19625296
Variant Present in the following documents:
  • Main text
  • ddp337.pdf
View BVdb publication page