BRAF c.139-6155G>A

Variant ID: 7-140556167-C-T

NM_004333.4(BRAF):c.139-6155G>A

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: rs1267621
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Chromosome band 7q34 deletions resulting in KIAA1549-BRAF and FAM131B-BRAF fusions in pediatric low-grade Gliomas.

Brain Pathology (Zurich, Switzerland)
Roth, Jacquelyn J JJ; Santi, Mariarita M; Pollock, Avrum N AN; Harding, Brian N BN; Rorke-Adams, Lucy B LB; Tooke, Laura S LS; Biegel, Jaclyn A JA
Publication Date: 2015-03

Variant appearance in text: rs1267621
PubMed Link: 25040262
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms of the BRAF gene predispose males to malignant melanoma.

Journal Of Carcinogenesis
Meyer, Peter P; Sergi, Consolato C; Garbe, Claus C
Publication Date: 2003-11-14

Variant appearance in text: rs1267621
PubMed Link: 14617374
Variant Present in the following documents:
  • Main text
  • 1477-3163-2-7.pdf
View BVdb publication page