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CFTR c.401G>A ;(p.R134K)
Variant ID: 7-117171080-G-A
NM_000492.3(
CFTR
):c.401G>A;(p.R134K)
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:
Integrative analysis reveals clinically relevant molecular fingerprints in pancreatic cancer.
Molecular Therapy. Nucleic Acids
Song, Libin L; Qi, Simin S; Hu, Wei W; Fang, Zhixiao Z; Yu, Dehua D; Liu, Teng T; Wu, Jingni J; Wu, Yangjun Y; Wu, Aiwei A; Feng, Lanyun L; Xie, Jing J; Zhang, Bo B; He, Wenguang W; Ning, Zhouyu Z; Liu, Luming L; Qin, Jiang-Jiang JJ; Li, Shengli S
Publication Date: 2021-12-03
Variant appearance in text: CFTR: 401G>A; R134K
PubMed Link:
34513290
Variant Present in the following documents:
mmc3.xlsx, sheet 1
View BVdb publication page
Computational Functional Genomics-Based AmpliSeq™ Panel for Next-Generation Sequencing of Key Genes of Pain.
International Journal Of Molecular Sciences
Kringel, Dario D; Malkusch, Sebastian S; Kalso, Eija E; Lötsch, Jörn J
Publication Date: 2021-01-16
Variant appearance in text: CFTR: R134K
PubMed Link:
33467215
Variant Present in the following documents:
ijms-22-00878.pdf
View BVdb publication page