Bibliome.ai browser hg19
Search
About
Stats
FAQ
NOTCH1 c.1393_1394delinsTG ;(p.A465C)
Variant ID: 9-139412251-GC-CA
NM_017617.3(
NOTCH1
):c.1393_1394delinsTG;(p.A465C)
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:
TP53, PIK3CA, FBXW7 and KRAS Mutations in Esophageal Cancer Identified by Targeted Sequencing.
Cancer Genomics & Proteomics
Zheng, Huili H; Wang, Yan Y; Tang, Chuanning C; Jones, Lindsey L; Ye, Hua H; Zhang, Guangchun G; Cao, Weihai W; Li, Jingwen J; Liu, Lifeng L; Liu, Zhencong Z; Zhang, Chao C; Lou, Feng F; Liu, Zhiyuan Z; Li, Yangyang Y; Shi, Zhenfen Z; Zhang, Jingbo J; Zhang, Dandan D; Sun, Hong H; Dong, Haichao H; Dong, Zhishou Z; Guo, Baishuai B; Yan, H E HE; Lu, Qingyu Q; Huang, Xue X; Chen, Si-Yi SY
Publication Date: 2016
Variant appearance in text: NOTCH1: A465C
PubMed Link:
27107065
Variant Present in the following documents:
Main text
View BVdb publication page