PGLYRP2 c.776C>T ;(p.T259M)

Variant ID: 19-15586705-G-A

NM_052890.3(PGLYRP2):c.776C>T;(p.T259M)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


SMAP is a pipeline for sample matching in proteogenomics.

Nature Communications
Li, Ling L; Niu, Mingming M; Erickson, Alyssa A; Luo, Jie J; Rowbotham, Kincaid K; Guo, Kai K; Huang, He H; Li, Yuxin Y; Jiang, Yi Y; Hur, Junguk J; Liu, Chunyu C; Peng, Junmin J; Wang, Xusheng X
Publication Date: 2022-02-08

Variant appearance in text: PGLYRP2: T259M
PubMed Link: 35136070
Variant Present in the following documents:
  • 41467_2022_28411_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Extrachromosomal driver mutations in glioblastoma and low-grade glioma.

Nature Communications
Nikolaev, Sergey S; Santoni, Federico F; Garieri, Marco M; Makrythanasis, Periklis P; Falconnet, Emilie E; Guipponi, Michel M; Vannier, Anne A; Radovanovic, Ivan I; Bena, Frederique F; Forestier, Françoise F; Schaller, Karl K; Dutoit, Valerie V; Clement-Schatlo, Virginie V; Dietrich, Pierre-Yves PY; Antonarakis, Stylianos E SE
Publication Date: 2014-12-04

Variant appearance in text: PGLYRP2: T259M
PubMed Link: 25471132
Variant Present in the following documents:
  • NIHMS60838-supplement-Supplementary_Data_2.xlsx, sheet 2
View BVdb publication page