TG c.172_175del ;(p.F58Rfs*47)

Variant ID: 8-133880462-GCTTC-G

NM_003235.4(TG):c.172_175del;(p.F58Rfs*47)

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: TG: 172_175del
PubMed Link: 35638715
Variant Present in the following documents:
  • 10.1177_10732748211062342.pdf
View BVdb publication page