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ULK4 c.2193+15336A>G
Variant ID: 3-41815817-T-C
NM_017886.2(
ULK4
):c.2193+15336A>G
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: ULK4: 2193+15336A>G; rs1167843787
PubMed Link:
36922594
Variant Present in the following documents:
41586_2023_5794_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page