F2 c.1464G>C ;(p.T488=)

Variant ID: 11-46750379-G-C

NM_000506.3(F2):c.1464G>C;(p.T488=)

This variant was identified in 1 publication

View GRCh38 version.




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