PRRT2 c.574G>T ;(p.G192W)

Variant ID: 16-29824949-G-T

NM_145239.2(PRRT2):c.574G>T;(p.G192W)

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:

Aberrant transcriptional networks in step-wise neurogenesis of paroxysmal kinesigenic dyskinesia-induced pluripotent stem cells.

Oncotarget
Li, Chun C; Ma, Yu Y; Zhang, Kunshan K; Gu, Junjie J; Tang, Fan F; Chen, Shengdi S; Cao, Li L; Li, Siguang S; Jin, Ying Y
Publication Date: 2016-08-16

Variant appearance in text: PRRT2: G192W
PubMed Link: 27449084
Variant Present in the following documents:
  • Main text
  • oncotarget-07-53611.pdf
View BVdb publication page