ATM c.1597A>G ;(p.R533G)

Variant ID: 11-108121789-A-G

NM_000051.3(ATM):c.1597A>G;(p.R533G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Mismatch Repair Deficiency and Somatic Mutations in Human Sinonasal Tumors.

Cancers
Hieggelke, Lena L; Heydt, Carina C; Castiglione, Roberta R; Rehker, Jan J; Merkelbach-Bruse, Sabine S; Riobello, Cristina C; Llorente, José Luis JL; Hermsen, Mario A MA; Buettner, Reinhard R
Publication Date: 2021-12-02

Variant appearance in text: ATM: R533G
PubMed Link: 34885191
Variant Present in the following documents:
  • Main text
  • cancers-13-06081.pdf
View BVdb publication page



Mismatch Repair Deficiency and Somatic Mutations in Human Sinonasal Tumors.

Cancers
Hieggelke, Lena L; Heydt, Carina C; Castiglione, Roberta R; Rehker, Jan J; Merkelbach-Bruse, Sabine S; Riobello, Cristina C; Llorente, José Luis JL; Hermsen, Mario A MA; Buettner, Reinhard R
Publication Date: 2021-12-02

Variant appearance in text: ATM: R533G
PubMed Link: 34885191
Variant Present in the following documents:
  • Main text
  • cancers-13-06081.pdf
View BVdb publication page



Kinome-wide decoding of network-attacking mutations rewiring cancer signaling.

Cell
Creixell, Pau P; Schoof, Erwin M EM; Simpson, Craig D CD; Longden, James J; Miller, Chad J CJ; Lou, Hua Jane HJ; Perryman, Lara L; Cox, Thomas R TR; Zivanovic, Nevena N; Palmeri, Antonio A; Wesolowska-Andersen, Agata A; Helmer-Citterich, Manuela M; Ferkinghoff-Borg, Jesper J; Itamochi, Hiroaki H; Bodenmiller, Bernd B; Erler, Janine T JT; Turk, Benjamin E BE; Linding, Rune R
Publication Date: 2015-09-24

Variant appearance in text: ATM: R533G
PubMed Link: 26388441
Variant Present in the following documents:
  • mmc4.xlsx, sheet 1
View BVdb publication page