PDE11A c.1788+4329A>C

Variant ID: 2-178629722-T-G

NM_016953.3(PDE11A):c.1788+4329A>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-genome doubling drives oncogenic loss of chromatin segregation.

Nature
Lambuta, Ruxandra A RA; Nanni, Luca L; Liu, Yuanlong Y; Diaz-Miyar, Juan J; Iyer, Arvind A; Tavernari, Daniele D; Katanayeva, Natalya N; Ciriello, Giovanni G; Oricchio, Elisa E
Publication Date: 2023-03-15

Variant appearance in text: PDE11A: 1788+4329A>C
PubMed Link: 36922594
Variant Present in the following documents:
  • 41586_2023_5794_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page