ATP2B2 c.1541C>A ;(p.A514D)

Variant ID: 3-10413611-G-T

NM_001001331.2(ATP2B2):c.1541C>A;(p.A514D)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The genomic landscape of cutaneous SCC reveals drivers and a novel azathioprine associated mutational signature.

Nature Communications
Inman, Gareth J GJ; Wang, Jun J; Nagano, Ai A; Alexandrov, Ludmil B LB; Purdie, Karin J KJ; Taylor, Richard G RG; Sherwood, Victoria V; Thomson, Jason J; Hogan, Sarah S; Spender, Lindsay C LC; South, Andrew P AP; Stratton, Michael M; Chelala, Claude C; Harwood, Catherine A CA; Proby, Charlotte M CM; Leigh, Irene M IM
Publication Date: 2018-09-10

Variant appearance in text: ATP2B2: A514D
PubMed Link: 30202019
Variant Present in the following documents:
  • 41467_2018_6027_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Integration of genomics and histology revises diagnosis and enables effective therapy of refractory cancer of unknown primary with PDL1 amplification.

Cold Spring Harbor Molecular Case Studies
Gröschel, Stefan S; Bommer, Martin M; Hutter, Barbara B; Budczies, Jan J; Bonekamp, David D; Heining, Christoph C; Horak, Peter P; Fröhlich, Martina M; Uhrig, Sebastian S; Hübschmann, Daniel D; Geörg, Christina C; Richter, Daniela D; Pfarr, Nicole N; Pfütze, Katrin K; Wolf, Stephan S; Schirmacher, Peter P; Jäger, Dirk D; von Kalle, Christof C; Brors, Benedikt B; Glimm, Hanno H; Weichert, Wilko W; Stenzinger, Albrecht A; Fröhling, Stefan S
Publication Date: 2016-11

Variant appearance in text: ATP2B2: A514D
PubMed Link: 27900363
Variant Present in the following documents:
  • supp_mcs.a001180_SuppTabS1.xls, sheet 1
View BVdb publication page