MDN1 c.6842C>T ;(p.T2281I)

Variant ID: 6-90425390-G-A

NM_014611.1(MDN1):c.6842C>T;(p.T2281I)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Loss of heterozygosity of essential genes represents a widespread class of potential cancer vulnerabilities.

Nature Communications
Nichols, Caitlin A CA; Gibson, William J WJ; Brown, Meredith S MS; Kosmicki, Jack A JA; Busanovich, John P JP; Wei, Hope H; Urbanski, Laura M LM; Curimjee, Naomi N; Berger, Ashton C AC; Gao, Galen F GF; Cherniack, Andrew D AD; Dhe-Paganon, Sirano S; Paolella, Brenton R BR; Beroukhim, Rameen R
Publication Date: 2020-05-20

Variant appearance in text: MDN1: 6842C>T; Thr2281Ile; rs115497826
PubMed Link: 32433464
Variant Present in the following documents:
  • 41467_2020_16399_MOESM7_ESM.xlsx, sheet 1
  • 41467_2020_16399_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page