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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