TSC1 c.772G>T ;(p.E258*)

Variant ID: 9-135787810-C-A

NM_000368.4(TSC1):c.772G>T;(p.E258*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Analysis of renal cancer cell lines from two major resources enables genomics-guided cell line selection.

Nature Communications
Sinha, Rileen R; Winer, Andrew G AG; Chevinsky, Michael M; Jakubowski, Christopher C; Chen, Ying-Bei YB; Dong, Yiyu Y; Tickoo, Satish K SK; Reuter, Victor E VE; Russo, Paul P; Coleman, Jonathan A JA; Sander, Chris C; Hsieh, James J JJ; Hakimi, A Ari AA
Publication Date: 2017-05-10

Variant appearance in text: TSC1: E258*
PubMed Link: 28489074
Variant Present in the following documents:
  • ncomms15165.pdf
View BVdb publication page



High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing.

Cancer Discovery
Wagle, Nikhil N; Berger, Michael F MF; Davis, Matthew J MJ; Blumenstiel, Brendan B; Defelice, Matthew M; Pochanard, Panisa P; Ducar, Matthew M; Van Hummelen, Paul P; Macconaill, Laura E LE; Hahn, William C WC; Meyerson, Matthew M; Gabriel, Stacey B SB; Garraway, Levi A LA
Publication Date: 2012-01

Variant appearance in text: TSC1: E258*
PubMed Link: 22585170
Variant Present in the following documents:
  • Main text
View BVdb publication page