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RUNDC3B c.238+21887A>G
Variant ID: 7-87302140-A-G
NM_001134405.1(
RUNDC3B
):c.238+21887A>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: rs2157929
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Significant effect of polymorphisms in CYP2D6 and ABCC2 on clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients.
Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
Kiyotani, Kazuma K; Mushiroda, Taisei T; Imamura, Chiyo K CK; Hosono, Naoya N; Tsunoda, Tatsuhiko T; Kubo, Michiaki M; Tanigawara, Yusuke Y; Flockhart, David A DA; Desta, Zeruesenay Z; Skaar, Todd C TC; Aki, Fuminori F; Hirata, Koichi K; Takatsuka, Yuichi Y; Okazaki, Minoru M; Ohsumi, Shozo S; Yamakawa, Takashi T; Sasa, Mitsunori M; Nakamura, Yusuke Y; Zembutsu, Hitoshi H
Publication Date: 2010-03-10
Variant appearance in text: rs2157929
PubMed Link:
20124171
Variant Present in the following documents:
Main text
View BVdb publication page