CP c.2694T>G ;(p.I898M)

Variant ID: 3-148896386-A-C

NM_000096.3(CP):c.2694T>G;(p.I898M)

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:

The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials.

Frontiers In Genetics
Illés, Anett A; Csabán, Dóra D; Grosz, Zoltán Z; Balicza, Péter P; Gézsi, András A; Molnár, Viktor V; Bencsik, Renáta R; Gál, Anikó A; Klivényi, Péter P; Molnar, Maria Judit MJ
Publication Date: 2019

Variant appearance in text: CP: 2694T>G; I898M
PubMed Link: 31737044
Variant Present in the following documents:
  • Main text
  • fgene-10-01061.pdf
View BVdb publication page