CUX1 c.2284A>G ;(p.I762V)

Variant ID: 7-101844861-A-G

NM_181552.3(CUX1):c.2284A>G;(p.I762V)

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:

Implications of mutational spectrum in myelodysplastic syndromes based on targeted next-generation sequencing.

Oncotarget
Xu, Yuanyuan Y; Li, Yan Y; Xu, Qingyu Q; Chen, Yuelong Y; Lv, Na N; Jing, Yu Y; Dou, Liping L; Bo, Jian J; Hou, Guangyuan G; Guo, Jing J; Wang, Xiuli X; Wang, Lili L; Li, Yonghui Y; Chen, Chongjian C; Yu, Li L
Publication Date: 2017-10-10

Variant appearance in text: CUX1: 2284A>G; M762V
PubMed Link: 29137279
Variant Present in the following documents:
  • oncotarget-08-82475-s003.xls, sheet 1
View BVdb publication page