KIT c.1053dup ;(p.N352Efs*6)

Variant ID: 4-55573390-T-TG

NM_000222.2(KIT):c.1053dup;(p.N352Efs*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:

Mutated WT1, FLT3-ITD, and NUP98-NSD1 Fusion in Various Combinations Define a Poor Prognostic Group in Pediatric Acute Myeloid Leukemia.

Journal Of Oncology
Niktoreh, Naghmeh N; Walter, Christiane C; Zimmermann, Martin M; von Neuhoff, Christine C; von Neuhoff, Nils N; Rasche, Mareike M; Waack, Katharina K; Creutzig, Ursula U; Hanenberg, Helmut H; Reinhardt, Dirk D
Publication Date: 2019

Variant appearance in text: KIT: 1053dupG
PubMed Link: 31467532
Variant Present in the following documents:
  • Main text
View BVdb publication page