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POLE c.286G>T ;(p.V96L)
Variant ID: 12-133256808-C-A
NM_006231.2(
POLE
):c.286G>T;(p.V96L)
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 sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.
Scientific Reports
Fransson, Susanne S; Martinez-Monleon, Angela A; Johansson, Mathias M; Sjöberg, Rose-Marie RM; Björklund, Caroline C; Ljungman, Gustaf G; Ek, Torben T; Kogner, Per P; Martinsson, Tommy T
Publication Date: 2020-12-31
Variant appearance in text: POLE: V96L
PubMed Link:
33384420
Variant Present in the following documents:
Main text
41598_2020_Article_78370.pdf
View BVdb publication page