TERT c.179G>A ;(p.W60*)

Variant ID: 5-1294926-C-T

NM_198253.2(TERT):c.179G>A;(p.W60*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer.

British Journal Of Cancer
Trotman, Jamie J; Armstrong, Ruth R; Firth, Helen H; Trayers, Claire C; Watkins, James J; Allinson, Kieren K; Jacques, Thomas S TS; Nicholson, James C JC; Burke, G A Amos GAA; , ; Behjati, Sam S; Murray, Matthew J MJ; Hook, Catherine E CE; Tarpey, Patrick P
Publication Date: 2022-07

Variant appearance in text: TERT: 179G>A
PubMed Link: 35449451
Variant Present in the following documents:
  • 41416_2022_1788_MOESM4_ESM.pdf
View BVdb publication page



High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants.

Nature Medicine
Razavi, Pedram P; Li, Bob T BT; Brown, David N DN; Jung, Byoungsok B; Hubbell, Earl E; Shen, Ronglai R; Abida, Wassim W; Juluru, Krishna K; De Bruijn, Ino I; Hou, Chenlu C; Venn, Oliver O; Lim, Raymond R; Anand, Aseem A; Maddala, Tara T; Gnerre, Sante S; Vijaya Satya, Ravi R; Liu, Qinwen Q; Shen, Ling L; Eattock, Nicholas N; Yue, Jeanne J; Blocker, Alexander W AW; Lee, Mark M; Sehnert, Amy A; Xu, Hui H; Hall, Megan P MP; Santiago-Zayas, Angie A; Novotny, William F WF; Isbell, James M JM; Rusch, Valerie W VW; Plitas, George G; Heerdt, Alexandra S AS; Ladanyi, Marc M; Hyman, David M DM; Jones, David R DR; Morrow, Monica M; Riely, Gregory J GJ; Scher, Howard I HI; Rudin, Charles M CM; Robson, Mark E ME; Diaz, Luis A LA; Solit, David B DB; Aravanis, Alexander M AM; Reis-Filho, Jorge S JS
Publication Date: 2019-12

Variant appearance in text: TERT: Trp60Ter
PubMed Link: 31768066
Variant Present in the following documents:
  • NIHMS1541314-supplement-1541314_Sup_Tab.xlsx, sheet 5
View BVdb publication page