NOTCH1 c.797G>T ;(p.C266F)

Variant ID: 9-139413963-C-A

NM_017617.3(NOTCH1):c.797G>T;(p.C266F)

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:

The reliable assurance of detecting somatic mutations in cancer-related genes by next-generation sequencing: the results of external quality assessment in China.

Oncotarget
Zhang, Rui R; Ding, Jiansheng J; Han, Yanxi Y; Yi, Lang L; Xie, Jiehong J; Yang, Xin X; Fan, Gaowei G; Wang, Guojing G; Hao, Mingju M; Zhang, Dong D; Zhang, Kuo K; Lin, Guigao G; Li, Jinming J
Publication Date: 2016-09-06

Variant appearance in text: NOTCH1: 797G>T
PubMed Link: 27542269
Variant Present in the following documents:
  • oncotarget-07-58500.pdf
View BVdb publication page