NOTCH1 c.1457A>T ;(p.H486L)

Variant ID: 9-139411822-T-A

NM_017617.3(NOTCH1):c.1457A>T;(p.H486L)

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:

The Conundrum of Genetic "Drivers" in Benign Conditions.

Journal Of The National Cancer Institute
Kato, Shumei S; Lippman, Scott M SM; Flaherty, Keith T KT; Kurzrock, Razelle R
Publication Date: 2016-08

Variant appearance in text: NOTCH1: H486L
PubMed Link: 27059373
Variant Present in the following documents:
  • Main text
  • djw036.pdf
View BVdb publication page