PRRT2 c.*406G>A

Variant ID: 16-29826365-G-A

NM_145239.2(PRRT2):c.*406G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Biological networks in Parkinson's disease: an insight into the epigenetic mechanisms associated with this disease.

Bmc Genomics
Chatterjee, Paulami P; Roy, Debjani D; Bhattacharyya, Malay M; Bandyopadhyay, Sanghamitra S
Publication Date: 2017-09-12

Variant appearance in text: rs1045968
PubMed Link: 28899360
Variant Present in the following documents:
  • Main text
  • 12864_2017_Article_4098.pdf
View BVdb publication page



MiRNA-Related SNPs and Risk of Esophageal Adenocarcinoma and Barrett's Esophagus: Post Genome-Wide Association Analysis in the BEACON Consortium.

Plos One
Buas, Matthew F MF; Onstad, Lynn L; Levine, David M DM; Risch, Harvey A HA; Chow, Wong-Ho WH; Liu, Geoffrey G; Fitzgerald, Rebecca C RC; Bernstein, Leslie L; Ye, Weimin W; Bird, Nigel C NC; Romero, Yvonne Y; Casson, Alan G AG; Corley, Douglas A DA; Shaheen, Nicholas J NJ; Wu, Anna H AH; Gammon, Marilie D MD; Reid, Brian J BJ; Hardie, Laura J LJ; Peters, Ulrike U; Whiteman, David C DC; Vaughan, Thomas L TL
Publication Date: 2015

Variant appearance in text: rs1045968
PubMed Link: 26039359
Variant Present in the following documents:
  • Main text
  • pone.0128617.pdf
View BVdb publication page



PRRT2 c.649dupC mutation derived from de novo in paroxysmal kinesigenic dyskinesia.

Cns Neuroscience & Therapeutics
Li, Hong-Fu HF; Ni, Wang W; Xiong, Zhi-Qi ZQ; Xu, Jianfeng J; Wu, Zhi-Ying ZY
Publication Date: 2013-01

Variant appearance in text: rs1045968
PubMed Link: 23176561
Variant Present in the following documents:
  • Main text
View BVdb publication page