TET2 c.3368del ;(p.P1123Lfs*14)

Variant ID: 4-106158465-AC-A

NM_001127208.2(TET2):c.3368del;(p.P1123Lfs*14)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A comprehensive analysis of candidate genes in familial pancreatic cancer families reveals a high frequency of potentially pathogenic germline variants.

Ebiomedicine
Earl, Julie J; Galindo-Pumariño, Cristina C; Encinas, Jessica J; Barreto, Emma E; Castillo, Maria E ME; Pachón, Vanessa V; Ferreiro, Reyes R; Rodríguez-Garrote, Mercedes M; González-Martínez, Silvia S; Ramon Y Cajal, Teresa T; Diaz, Luis Robles LR; Chirivella-Gonzalez, Isabel I; Rodriguez, Montse M; de Castro, Eva Martínez EM; García-Seisdedos, David D; Muñoz, Gloria G; Rosa, Juan Manuel Rosa JMR; Marquez, Mirari M; Malats, Nuría N; Carrato, Alfredo A
Publication Date: 2020-03

Variant appearance in text: TET2: 3368delC
PubMed Link: 32113160
Variant Present in the following documents:
  • Main text
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