TP53 c.800_806del ;(p.R267Pfs*76)

Variant ID: 17-7577132-GCTGTTCC-G

NM_000546.5(TP53):c.800_806del;(p.R267Pfs*76)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


TP53 alterations in Wilms tumour represent progression events with strong intratumour heterogeneity that are closely linked but not limited to anaplasia.

The Journal Of Pathology. Clinical Research
Wegert, Jenny J; Vokuhl, Christian C; Ziegler, Barbara B; Ernestus, Karen K; Leuschner, Ivo I; Furtwängler, Rhoikos R; Graf, Norbert N; Gessler, Manfred M
Publication Date: 2017-10

Variant appearance in text: TP53: 800_806del
PubMed Link: 29085664
Variant Present in the following documents:
  • Main text
  • CJP2-3-234.pdf
View BVdb publication page



Targeted next generation sequencing of parotid gland cancer uncovers genetic heterogeneity.

Oncotarget
Grünewald, Inga I; Vollbrecht, Claudia C; Meinrath, Jeannine J; Meyer, Moritz F MF; Heukamp, Lukas C LC; Drebber, Uta U; Quaas, Alexander A; Beutner, Dirk D; Hüttenbrink, Karl-Bernd KB; Wardelmann, Eva E; Hartmann, Wolfgang W; Büttner, Reinhard R; Odenthal, Margarete M; Stenner, Markus M
Publication Date: 2015-07-20

Variant appearance in text: N/A
PubMed Link: 26053092
Variant Present in the following documents:
View BVdb publication page