TP53 c.368_369del ;(p.T123Mfs*25)

Variant ID: 17-7579318-AAG-A

NM_000546.5(TP53):c.368_369del;(p.T123Mfs*25)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing.

Bmc Medical Genomics
Cheng, Donavan T DT; Prasad, Meera M; Chekaluk, Yvonne Y; Benayed, Ryma R; Sadowska, Justyna J; Zehir, Ahmet A; Syed, Aijazuddin A; Wang, Yan Elsa YE; Somar, Joshua J; Li, Yirong Y; Yelskaya, Zarina Z; Wong, Donna D; Robson, Mark E ME; Offit, Kenneth K; Berger, Michael F MF; Nafa, Khedoudja K; Ladanyi, Marc M; Zhang, Liying L
Publication Date: 2017-05-19

Variant appearance in text: TP53: 368_369delCT; T123fs
PubMed Link: 28526081
Variant Present in the following documents:
  • Main text
  • 12920_2017_Article_271.pdf
View BVdb publication page