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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.
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: 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