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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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