MPHOSPH9 c.2266G>T ;(p.G756*)

Variant ID: 12-123665733-C-A

NM_022782.3(MPHOSPH9):c.2266G>T;(p.G756*)

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: MPHOSPH9: G756X
PubMed Link: 30567531
Variant Present in the following documents:
  • 12885_2018_5097_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page