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.




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
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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