NRAS c.442_443insG ;(p.T148Sfs*6)

Variant ID: 1-115252197-G-GC

NM_002524.4(NRAS):c.442_443insG;(p.T148Sfs*6)

This variant was identified in 1 publication

View GRCh38 version.



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

Publications:

Enrichment of Double RUNX1 Mutations in Acute Leukemias of Ambiguous Lineage.

Frontiers In Oncology
Merati, Gabriele G; Rossi, Marianna M; Gallì, Anna A; Roncoroni, Elisa E; Zibellini, Silvia S; Rizzo, Ettore E; Pietra, Daniela D; Picone, Cristina C; Rocca, Barbara B; Cabrera, Claudia Patricia Tobar CPT; Gelli, Eleonora E; Santacroce, Eugenio E; Arcaini, Luca L; Zappasodi, Patrizia P
Publication Date: 2021

Variant appearance in text: NRAS: 442_443insG
PubMed Link: 34540694
Variant Present in the following documents:
  • DataSheet_1.pdf
View BVdb publication page