NOTCH1 c.5007G>T ;(p.M1669I)

Variant ID: 9-139399136-C-A

NM_017617.3(NOTCH1):c.5007G>T;(p.M1669I)

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:

Mutational and transcriptomic profiling of acute leukemia of ambiguous lineage reveals obscure but clinically important lineage bias.

Haematologica
Lao, Zhen-Tang ZT; Ding, Ling-Wen LW; An, Omer O; Hattori, Norimichi N; Sun, Qiao-Yang QY; Tan, Kar-Tong KT; Mayakonda, Anand A; Chuan, Wong Gee WG; Madan, Vikas V; Lin, De-Chen DC; Yang, Henry H; Koeffler, H Phillip HP
Publication Date: 2019-05

Variant appearance in text: NOTCH1: M1669I
PubMed Link: 30514800
Variant Present in the following documents:
  • Main text
View BVdb publication page