BRAF c.138+10154T>A

Variant ID: 7-140614212-A-T

NM_004333.4(BRAF):c.138+10154T>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs11762469
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Association between single-nucleotide polymorphisms of BRAF and papillary thyroid carcinoma in a Chinese population.

Thyroid : Official Journal Of The American Thyroid Association
Zhang, Qiang Q; Song, Fangfang F; Zheng, Hong H; Zhu, Xiaoling X; Song, Fengju F; Yao, Xiaofeng X; Zhang, Lun L; Chen, Kexin K
Publication Date: 2013-01

Variant appearance in text: rs11762469
PubMed Link: 22973979
Variant Present in the following documents:
  • Main text
View BVdb publication page