Bibliome.ai browser hg19
Search
About
Stats
FAQ
IGF2BP3 c.237-17476C>T
Variant ID: 7-23475919-G-A
NM_006547.2(
IGF2BP3
):c.237-17476C>T
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:
Polymorphic variants of IGF2BP3 and SENCR have an impact on predisposition and/or progression of Ewing sarcoma.
Frontiers In Oncology
Martinelli, Marcella M; Mancarella, Caterina C; Scapoli, Luca L; Palmieri, Annalisa A; De Sanctis, Paola P; Ferrari, Cristina C; Pasello, Michela M; Zucchini, Cinzia C; Scotlandi, Katia K
Publication Date: 2022
Variant appearance in text: rs7782764
PubMed Link:
36338681
Variant Present in the following documents:
Main text
fonc-12-968884.pdf
View BVdb publication page