NOTCH1 c.6343G>T ;(p.E2115*)

Variant ID: 9-139391848-C-A

NM_017617.3(NOTCH1):c.6343G>T;(p.E2115*)

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:

Mutation of SPINOPHILIN (PPP1R9B) found in human tumors promotes the tumorigenic and stemness properties of cells.

Theranostics
Verdugo-Sivianes, Eva M EM; Rojas, Ana M AM; Muñoz-Galván, Sandra S; Otero-Albiol, Daniel D; Carnero, Amancio A
Publication Date: 2021

Variant appearance in text: NOTCH1: E2115*
PubMed Link: 33537097
Variant Present in the following documents:
  • thnov11p3452s1.pdf
View BVdb publication page