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F2 c.1464G>A ;(p.T488=)
Variant ID: 11-46750379-G-A
NM_000506.3(
F2
):c.1464G>A;(p.T488=)
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:
Genomic alterations in gastric cancers discovered via whole-exome sequencing.
Bmc Cancer
Zhang, Jie J; Qiu, Weiqing W; Liu, Hua H; Qian, Changlin C; Liu, Dujuan D; Wang, Hailong H; Hu, Ni N; Tang, Y Tom YT; Sun, Jianhua J; Shen, Zhiyong Z
Publication Date: 2018-12-19
Variant appearance in text: F2: T488T
PubMed Link:
30567531
Variant Present in the following documents:
12885_2018_5097_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page