NOTCH1 c.46_47delinsAT ;(p.A16M)

Variant ID: 9-139440192-GC-AT

NM_017617.3(NOTCH1):c.46_47delinsAT;(p.A16M)

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:

Large-scale analysis of acquired chromosomal alterations in non-tumor samples from patients with cancer.

Nature Biotechnology
Jakubek, Y A YA; Chang, K K; Sivakumar, S S; Yu, Y Y; Giordano, M R MR; Fowler, J J; Huff, C D CD; Kadara, H H; Vilar, E E; Scheet, P P
Publication Date: 2020-01

Variant appearance in text: NOTCH1: A16M
PubMed Link: 31685958
Variant Present in the following documents:
  • Main text
View BVdb publication page