POLE c.5448C>T ;(p.N1816=)

Variant ID: 12-133215815-G-A

NM_006231.2(POLE):c.5448C>T;(p.N1816=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Functional pre-therapeutic evaluation by genome editing of variants of uncertain significance of essential tumor suppressor genes.

Genome Medicine
Billaud, Amandine A; Chevalier, Louise-Marie LM; Augereau, Paule P; Frenel, Jean-Sebastien JS; Passot, Christophe C; Campone, Mario M; Morel, Alain A
Publication Date: 2021-11-09

Variant appearance in text: POLE: 5448C>T
PubMed Link: 34749799
Variant Present in the following documents:
  • 13073_2021_976_MOESM1_ESM.pdf
View BVdb publication page