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NRAS c.500_501delinsAT ;(p.R167H)
Variant ID: 1-115251225-TC-AT
NM_002524.4(
NRAS
):c.500_501delinsAT;(p.R167H)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Gain-of-Function Mutations in p53 in Cancer Invasiveness and Metastasis.
International Journal Of Molecular Sciences
Roszkowska, Katarzyna A KA; Gizinski, Slawomir S; Sady, Maria M; Gajewski, Zdzislaw Z; Olszewski, Maciej B MB
Publication Date: 2020-02-17
Variant appearance in text: NRAS: R167H
PubMed Link:
32079237
Variant Present in the following documents:
Main text
ijms-21-01334.pdf
View BVdb publication page
The Melding of Drug Screening Platforms for Melanoma.
Frontiers In Oncology
Couto, Gabriela Klein GK; Segatto, Natália Vieira NV; Oliveira, Thaís Larré TL; Seixas, Fabiana Kömmling FK; Schachtschneider, Kyle M KM; Collares, Tiago T
Publication Date: 2019
Variant appearance in text: NRAS: R167H
PubMed Link:
31293965
Variant Present in the following documents:
Main text
View BVdb publication page
Detecting protein variants by mass spectrometry: a comprehensive study in cancer cell-lines.
Genome Medicine
Alfaro, Javier A JA; Ignatchenko, Alexandr A; Ignatchenko, Vladimir V; Sinha, Ankit A; Boutros, Paul C PC; Kislinger, Thomas T
Publication Date: 2017-07-18
Variant appearance in text: NRAS: R167H
PubMed Link:
28716134
Variant Present in the following documents:
13073_2017_454_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page