CFTR c.4136+237C>T

Variant ID: 7-117305151-C-T

NM_000492.3(CFTR):c.4136+237C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Microsecond-timescale MD simulation of EGFR minor mutation predicts the structural flexibility of EGFR kinase core that reflects EGFR inhibitor sensitivity.

Npj Precision Oncology
Yoshizawa, Takahiro T; Uchibori, Ken K; Araki, Mitsugu M; Matsumoto, Shigeyuki S; Ma, Biao B; Kanada, Ryo R; Seto, Yosuke Y; Oh-Hara, Tomoko T; Koike, Sumie S; Ariyasu, Ryo R; Kitazono, Satoru S; Ninomiya, Hironori H; Takeuchi, Kengo K; Yanagitani, Noriko N; Takagi, Satoshi S; Kishi, Kazuma K; Fujita, Naoya N; Okuno, Yasushi Y; Nishio, Makoto M; Katayama, Ryohei R
Publication Date: 2021-04-16

Variant appearance in text: CFTR: 4136+237C>T; rs4148724
PubMed Link: 33863983
Variant Present in the following documents:
  • 41698_2021_170_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs4148724
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



MGST2 and WNT2 are candidate genes for comitant strabismus susceptibility in Japanese patients.

Peerj
Zhang, Jingjing J; Matsuo, Toshihiko T
Publication Date: 2017

Variant appearance in text: rs4148724
PubMed Link: 29062608
Variant Present in the following documents:
  • Main text
  • peerj-05-3935.pdf
View BVdb publication page