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SBF2 c.619+9864C>T
Variant ID: 11-10040135-G-A
NM_030962.3(
SBF2
):c.619+9864C>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:
A single-nucleotide-polymorphism in the 5'-flanking region of MSX1 gene as a predictive marker candidate for platinum-based therapy of esophageal carcinoma.
Therapeutic Advances In Medical Oncology
Mori, Takahiro T; Ueno, Kazuko K; Tokunaga, Katsushi K; Kawai, Yosuke Y; Matsuda, Koichi K; Nishida, Nao N; Komine, Keigo K; Saito, Sakae S; Nagasaki, Masao M; ,
Publication Date: 2022
Variant appearance in text: rs11042590
PubMed Link:
35251318
Variant Present in the following documents:
Main text
10.1177_17588359221080580.pdf
View BVdb publication page