PRRT2 c.37G>C ;(p.G13R)

Variant ID: 16-29824412-G-C

NM_145239.2(PRRT2):c.37G>C;(p.G13R)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.

American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01

Variant appearance in text: PRRT2: G13R; rs770164221
PubMed Link: 36413997
Variant Present in the following documents:
  • mmc4.xlsx, sheet 1
  • mmc3.xlsx, sheet 1
View BVdb publication page



Targeting Ras-RAF-ERK and its interactive pathways as a novel therapy for malignant gliomas.

Current Cancer Drug Targets
Lo, Hui-Wen HW
Publication Date: 2010-12

Variant appearance in text: PKC: G13R
PubMed Link: 20718706
Variant Present in the following documents:
  • Main text
View BVdb publication page