LRRK2 c.2681A>T ;(p.D894V)

Variant ID: 12-40681333-A-T

NM_198578.3(LRRK2):c.2681A>T;(p.D894V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Pervasive occurrence of splice-site-creating mutations and their possible involvement in genetic disorders.

Npj Genomic Medicine
Sakaguchi, Narumi N; Suyama, Mikita M
Publication Date: 2022-03-18

Variant appearance in text: LRRK2: 2681A>T; Asp894Val; rs1198371319
PubMed Link: 35304488
Variant Present in the following documents:
  • 41525_2022_294_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page