NOTCH1 c.3286G>A ;(p.V1096M)

Variant ID: 9-139402723-C-T

NM_017617.3(NOTCH1):c.3286G>A;(p.V1096M)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Amplification of CDK4 and MDM2: a detailed study of a high-risk neuroblastoma subgroup.

Scientific Reports
Martinez-Monleon, Angela A; Kryh Öberg, Hanna H; Gaarder, Jennie J; Berbegall, Ana P AP; Javanmardi, Niloufar N; Djos, Anna A; Ussowicz, Marek M; Taschner-Mandl, Sabine S; Ambros, Inge M IM; Øra, Ingrid I; Sandstedt, Bengt B; Beiske, Klaus K; Ladenstein, Ruth R; Noguera, Rosa R; Ambros, Peter F PF; Gordon Murkes, Lena L; Ljungman, Gustaf G; Kogner, Per P; Fransson, Susanne S; Martinsson, Tommy T
Publication Date: 2022-07-20

Variant appearance in text: NOTCH1: 3286G>A; V1096M
PubMed Link: 35859155
Variant Present in the following documents:
  • 41598_2022_16455_MOESM2_ESM.xlsx, sheet 4
View BVdb publication page



Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations.

Oncotarget
Porkka, Noora N; Valo, Satu S; Nieminen, Taina T TT; Olkinuora, Alisa A; Mäki-Nevala, Satu S; Eldfors, Samuli S; Peltomäki, Päivi P
Publication Date: 2017-12-08

Variant appearance in text: NOTCH1: V1096M
PubMed Link: 29296220
Variant Present in the following documents:
  • oncotarget-08-108020-s006.xlsx, sheet 1
View BVdb publication page