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SLC24A3 c.142+9934A>G
Variant ID: 20-19203562-A-G
NM_020689.3(
SLC24A3
):c.142+9934A>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: SLC24A3: 142+9934A>G
PubMed Link:
36922594
Variant Present in the following documents:
41586_2023_5794_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page