PC c.355_356delinsAC ;(p.G119T)

Variant ID: 11-66638917-CC-GT

NM_001040716.1(PC):c.355_356delinsAC;(p.G119T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical Significance of Gene Mutations and Polymorphic Variants and their Association with Prostate Cancer Risk in Polish Men.

Cancer Control : Journal Of The Moffitt Cancer Center
Heise, Marta M; Jarzemski, Piotr P; Nowak, Dagmara D; Bąk, Aneta A; Junkiert-Czarnecka, Anna A; Pilarska-Deltow, Maria M; Borysiak, Maciej M; Pilarska, Beata B; Haus, Olga O
Publication Date: 2022

Variant appearance in text: PC: G119T
PubMed Link: 35638715
Variant Present in the following documents:
  • Main text
  • 10.1177_10732748211062342.pdf
View BVdb publication page