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.




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