BRAF c.139-8728C>G

Variant ID: 7-140558740-G-C

NM_004333.4(BRAF):c.139-8728C>G

This variant was identified in 3 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: rs17161747
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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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: rs17161747
PubMed Link: 22973979
Variant Present in the following documents:
  • Main text
View BVdb publication page



Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer.

British Journal Of Cancer
Quaye, L L; Song, H H; Ramus, S J SJ; Gentry-Maharaj, A A; Høgdall, E E; DiCioccio, R A RA; McGuire, V V; Wu, A H AH; Van Den Berg, D J DJ; Pike, M C MC; Wozniak, E E; Doherty, J A JA; Rossing, M A MA; Ness, R B RB; Moysich, K B KB; Høgdall, C C; Blaakaer, J J; , ; Easton, D F DF; Ponder, B A J BA; Jacobs, I J IJ; Menon, U U; Whittemore, A S AS; Krüger-Kjaer, S S; Pearce, C L CL; Pharoah, P D P PD; Gayther, S A SA
Publication Date: 2009-03-24

Variant appearance in text: rs17161747
PubMed Link: 19240718
Variant Present in the following documents:
  • Main text
  • 6604947a.pdf
View BVdb publication page