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COMT c.-91-780C>A
Variant ID: 22-19947942-C-A
NM_000754.4(
COMT
):c.-91-780C>A
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Grading Evolution and Contemporary Prognostic Biomarkers of Clinically Significant Prostate Cancer.
Cancers
Sopyllo, Konrad K; Erickson, Andrew M AM; Mirtti, Tuomas T
Publication Date: 2021-02-05
Variant appearance in text: rs16982844
PubMed Link:
33562508
Variant Present in the following documents:
Main text
cancers-13-00628.pdf
View BVdb publication page
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: rs16982844
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Localizing putative markers in genetic association studies by incorporating linkage disequilibrium into bayesian hierarchical models.
Human Heredity
Fridley, Brooke L BL; Jenkins, Gregory D GD
Publication Date: 2010
Variant appearance in text: rs16982844
PubMed Link:
20551675
Variant Present in the following documents:
Main text
View BVdb publication page