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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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