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RUNDC3B c.239-3612T>G
Variant ID: 7-87326125-T-G
NM_001134405.1(
RUNDC3B
):c.239-3612T>G
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: rs12670317
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Pathway-based analysis using genome-wide association data from a Korean non-small cell lung cancer study.
Plos One
Lee, Donghoon D; Lee, Geon Kook GK; Yoon, Kyong-Ah KA; Lee, Jin Soo JS
Publication Date: 2013
Variant appearance in text: rs12670317
PubMed Link:
23762359
Variant Present in the following documents:
Main text
pone.0065396.pdf
View BVdb publication page