MED23 c.1181C>A ;(p.P394H)

Variant ID: 6-131929108-G-T

NM_004830.3(MED23):c.1181C>A;(p.P394H)

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:

Integration of radiogenomic features for early prediction of pathological complete response in patients with triple-negative breast cancer and identification of potential therapeutic targets.

Journal Of Translational Medicine
Zhang, Ying Y; You, Chao C; Pei, Yuchen Y; Yang, Fan F; Li, Daqiang D; Jiang, Yi-Zhou YZ; Shao, Zhimin Z
Publication Date: 2022-06-07

Variant appearance in text: MED23: P394H
PubMed Link: 35672824
Variant Present in the following documents:
  • Main text
  • 12967_2022_Article_3452.pdf
View BVdb publication page