SomamiR DB 2.0 Somatic mutations altering microRNA-ceRNA interactions |
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Browse genes associated with cancer risk that contain miRNA related somatic mutations |
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Somatic mutations that alter miRNA target sites: CLASH [9 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001297673 | RPRD2 | chr1:g.150364742A>G |
NM_001297673 | RPRD2 | chr1:g.150364743G>A |
NM_001297673 | RPRD2 | chr1:g.150470890A>T |
NM_001297673 | RPRD2 | chr1:g.150472078C>A |
NM_001297673 | RPRD2 | chr1:g.150472100C>A |
NM_001297673 | RPRD2 | chr1:g.150472941C>T |
NM_001297673 | RPRD2 | chr1:g.150472942C>T |
NM_001297673 | RPRD2 | chr1:g.150472953C>T |
NM_001297673 | RPRD2 | chr1:g.150472987A>G |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [102 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001297673 | RPRD2 | chr1:g.150473757A>C |
NM_001297673 | RPRD2 | chr1:g.150475512G>T |
NM_001297673 | RPRD2 | chr1:g.150475569G>A |
NM_001297673 | RPRD2 | chr1:g.150475957G>A |
NM_001297673 | RPRD2 | chr1:g.150476212G>A |
NM_001297673 | RPRD2 | chr1:g.150364812C>T |
NM_001297673 | RPRD2 | chr1:g.150364817A>C |
NM_001297673 | RPRD2 | chr1:g.150364834C>T |
hsa_circ_0006360 | RPRD2 | chr1:g.150417618T>C |
hsa_circ_0006360 | RPRD2 | chr1:g.150417621C>G |
hsa_circ_0006360 | RPRD2 | chr1:g.150417622T>G |
hsa_circ_0006360 | RPRD2 | chr1:g.150440952G>A |
hsa_circ_0006360 | RPRD2 | chr1:g.150440954A>C |
hsa_circ_0014013 | RPRD2 | chr1:g.150446273TC>T |
hsa_circ_0014013 | RPRD2 | chr1:g.150446381G>T |
hsa_circ_0014013 | RPRD2 | chr1:g.150446396G>T |
hsa_circ_0014013 | RPRD2 | chr1:g.150446403T>TA |
hsa_circ_0014013 | RPRD2 | chr1:g.150457357C>T |
hsa_circ_0014013 | RPRD2 | chr1:g.150457513C>T |
hsa_circ_0014013 | RPRD2 | chr1:g.150457540G>A |
hsa_circ_0014013 | RPRD2 | chr1:g.150457540G>T |
hsa_circ_0014017 | RPRD2 | chr1:g.150460208T>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150460225C>T |
hsa_circ_0014017 | RPRD2 | chr1:g.150464576C>G |
hsa_circ_0014017 | RPRD2 | chr1:g.150464586A>G |
hsa_circ_0014017 | RPRD2 | chr1:g.150464606A>C |
hsa_circ_0014017 | RPRD2 | chr1:g.150464631C>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150464648C>T |
hsa_circ_0014017 | RPRD2 | chr1:g.150464658G>T |
hsa_circ_0014017 | RPRD2 | chr1:g.150464684T>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150464688C>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150464689T>G |
hsa_circ_0014017 | RPRD2 | chr1:g.150470602C>T |
hsa_circ_0014017 | RPRD2 | chr1:g.150470615C>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150470628C>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150470629A>C |
hsa_circ_0014017 | RPRD2 | chr1:g.150470658C>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150470663C>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150470669A>G |
hsa_circ_0014017 | RPRD2 | chr1:g.150470790C>T |
hsa_circ_0014017 | RPRD2 | chr1:g.150470825C>T |
hsa_circ_0014017 | RPRD2 | chr1:g.150470835G>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150471009A>G |
hsa_circ_0014017 | RPRD2 | chr1:g.150471290A>C |
hsa_circ_0014017 | RPRD2 | chr1:g.150471304G>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150471316C>T |
hsa_circ_0014017 | RPRD2 | chr1:g.150471317G>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150471326G>A |
hsa_circ_0014017 | RPRD2 | chr1:g.150471350A>G |
hsa_circ_0014017 | RPRD2 | chr1:g.150471515C>T |
NM_001297673 | RPRD2 | chr1:g.150471762C>T |
NM_001297673 | RPRD2 | chr1:g.150471827A>T |
NM_001297673 | RPRD2 | chr1:g.150471899C>T |
NM_001297673 | RPRD2 | chr1:g.150471925G>A |
NM_001297673 | RPRD2 | chr1:g.150471933A>G |
NM_001297673 | RPRD2 | chr1:g.150471987TA>T |
NM_001297673 | RPRD2 | chr1:g.150471988A>T |
NM_001297673 | RPRD2 | chr1:g.150471993C>T |
NM_001297673 | RPRD2 | chr1:g.150472001G>A |
NM_001297673 | RPRD2 | chr1:g.150472016A>G |
NM_001297673 | RPRD2 | chr1:g.150472078C>A |
NM_001297673 | RPRD2 | chr1:g.150472100C>A |
NM_001297673 | RPRD2 | chr1:g.150472140A>G |
NM_001297673 | RPRD2 | chr1:g.150472145G>A |
NM_001297673 | RPRD2 | chr1:g.150472146C>T |
NM_001297673 | RPRD2 | chr1:g.150472147G>A |
NM_001297673 | RPRD2 | chr1:g.150472157C>G |
NM_001297673 | RPRD2 | chr1:g.150472171C>A |
NM_001297673 | RPRD2 | chr1:g.150472175A>G |
NM_001297673 | RPRD2 | chr1:g.150472230C>T |
NM_001297673 | RPRD2 | chr1:g.150472232A>G |
NM_001297673 | RPRD2 | chr1:g.150472242G>T |
NM_001297673 | RPRD2 | chr1:g.150472398C>T |
NM_001297673 | RPRD2 | chr1:g.150472402G>A |
NM_001297673 | RPRD2 | chr1:g.150472403G>T |
NM_001297673 | RPRD2 | chr1:g.150472447T>C |
NM_001297673 | RPRD2 | chr1:g.150472456C>T |
NM_001297673 | RPRD2 | chr1:g.150472457G>A |
NM_001297673 | RPRD2 | chr1:g.150472461A>G |
NM_001297673 | RPRD2 | chr1:g.150472492C>T |
NM_001297673 | RPRD2 | chr1:g.150472633C>T |
NM_001297673 | RPRD2 | chr1:g.150472643C>T |
NM_001297673 | RPRD2 | chr1:g.150472763C>T |
NM_001297673 | RPRD2 | chr1:g.150472767TC>T |
NM_001297673 | RPRD2 | chr1:g.150472770C>T |
NM_001297673 | RPRD2 | chr1:g.150472800G>C |
NM_001297673 | RPRD2 | chr1:g.150472810C>T |
NM_001297673 | RPRD2 | chr1:g.150472827C>T |
NM_001297673 | RPRD2 | chr1:g.150472831C>T |
NM_001297673 | RPRD2 | chr1:g.150472856G>T |
NM_001297673 | RPRD2 | chr1:g.150472911G>A |
NM_001297673 | RPRD2 | chr1:g.150472941C>T |
NM_001297673 | RPRD2 | chr1:g.150472942C>T |
NM_001297673 | RPRD2 | chr1:g.150472953C>T |
NM_001297673 | RPRD2 | chr1:g.150473090C>A |
NM_001297673 | RPRD2 | chr1:g.150473109TG>T |
NM_001297673 | RPRD2 | chr1:g.150473126G>T |
NM_001297673 | RPRD2 | chr1:g.150473290C>G |
NM_001297673 | RPRD2 | chr1:g.150473291C>T |
NM_001297673 | RPRD2 | chr1:g.150473295C>G |
NM_001297673 | RPRD2 | chr1:g.150473316C>T |
NM_001297673 | RPRD2 | chr1:g.150473320C>T |
Somatic mutations that alter predicted mRNA-miRNA target sites [10 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_015203 | RPRD2 | chr1:g.150475556G>C |
NM_015203 | RPRD2 | chr1:g.150475304T>C |
NM_015203 | RPRD2 | chr1:g.150476475AAAAC>- |
NM_015203 | RPRD2 | chr1:g.150475957G>A |
NM_015203 | RPRD2 | chr1:g.150473930A>G |
NM_015203 | RPRD2 | chr1:g.150473757A>C |
NM_015203 | RPRD2 | chr1:g.150475512G>T |
NM_015203 | RPRD2 | chr1:g.150476212G>A |
NM_015203 | RPRD2 | chr1:g.150473362C>A |
NM_015203 | RPRD2 | chr1:g.150475569G>A |