NOTCH1 c.4613A>T ;(p.D1538V)

Variant ID: 9-139399530-T-A

NM_017617.3(NOTCH1):c.4613A>T;(p.D1538V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical genomic profiling to identify actionable alterations for investigational therapies in patients with diverse sarcomas.

Oncotarget
Groisberg, Roman R; Hong, David S DS; Holla, Vijaykumar V; Janku, Filip F; Piha-Paul, Sarina S; Ravi, Vinod V; Benjamin, Robert R; Kumar Patel, Shreyas S; Somaiah, Neeta N; Conley, Anthony A; Ali, Siraj M SM; Schrock, Alexa B AB; Ross, Jeffrey S JS; Stephens, Philip J PJ; Miller, Vincent A VA; Sen, Shiraj S; Herzog, Cynthia C; Meric-Bernstam, Funda F; Subbiah, Vivek V
Publication Date: 2017-06-13

Variant appearance in text: NOTCH1: D1538V
PubMed Link: 28424409
Variant Present in the following documents:
  • Main text
  • oncotarget-08-39254.pdf
View BVdb publication page