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DPYD c.151-69G>A
Variant ID: 1-98293821-C-T
NM_000110.3(
DPYD
):c.151-69G>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:
Case report: severe toxicity in an African-American patient receiving FOLFOX carrying uncommon allelic variants in DPYD.
Pharmacogenomics
Sissung, Tristan M TM; Cordes, Lisa L; Peer, Cody J CJ; Gandhy, Shruti S; Redman, Jason J; Strauss, Julius J; Figg, William D WD
Publication Date: 2021-01
Variant appearance in text: DPYD: 151-69G>A; rs115632870
PubMed Link:
33305610
Variant Present in the following documents:
Main text
View BVdb publication page
Pharmacogenomics Clinical Annotation Tool (PharmCAT).
Clinical Pharmacology And Therapeutics
Sangkuhl, Katrin K; Whirl-Carrillo, Michelle M; Whaley, Ryan M RM; Woon, Mark M; Lavertu, Adam A; Altman, Russ B RB; Carter, Lester L; Verma, Anurag A; Ritchie, Marylyn D MD; Klein, Teri E TE
Publication Date: 2020-01
Variant appearance in text: rs115632870
PubMed Link:
31306493
Variant Present in the following documents:
CPT-107-203-s004.pdf
View BVdb publication page