NOTCH1 c.6889A>C ;(p.T2297P)

Variant ID: 9-139391302-T-G

NM_017617.3(NOTCH1):c.6889A>C;(p.T2297P)

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:

An activating intragenic deletion in NOTCH1 in human T-ALL.

Blood
Haydu, J Erika JE; De Keersmaecker, Kim K; Duff, Mary Kaye MK; Paietta, Elisabeth E; Racevskis, Janis J; Wiernik, Peter H PH; Rowe, Jacob M JM; Ferrando, Adolfo A
Publication Date: 2012-05-31

Variant appearance in text: NOTCH1: T2297P
PubMed Link: 22510873
Variant Present in the following documents:
  • Main text
View BVdb publication page