NOTCH1 c.5035G>A ;(p.E1679K)

Variant ID: 9-139397766-C-T

NM_017617.3(NOTCH1):c.5035G>A;(p.E1679K)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Amplicon sequencing of colorectal cancer: variant calling in frozen and formalin-fixed samples.

Plos One
Betge, Johannes J; Kerr, Grainne G; Miersch, Thilo T; Leible, Svenja S; Erdmann, Gerrit G; Galata, Christian L CL; Zhan, Tianzuo T; Gaiser, Timo T; Post, Stefan S; Ebert, Matthias P MP; Horisberger, Karoline K; Boutros, Michael M
Publication Date: 2015

Variant appearance in text: NOTCH1: E1679K
PubMed Link: 26010451
Variant Present in the following documents:
  • pone.0127146.s011.pdf
  • pone.0127146.s013.xlsx, sheet 3
  • pone.0127146.s014.xlsx, sheet 3
View BVdb publication page