PPP1R9A c.2344T>C ;(p.L782=)

Variant ID: 7-94879515-T-C

NM_001166160.1(PPP1R9A):c.2344T>C;(p.L782=)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

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: PPP1R9A: 2344T>C; Leu782=
PubMed Link: 36922594
Variant Present in the following documents:
  • 41586_2023_5794_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page