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


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.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
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



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.150473362C>A
NM_015203 RPRD2 chr1:g.150473757A>C
NM_015203 RPRD2 chr1:g.150473930A>G
NM_015203 RPRD2 chr1:g.150475304T>C
NM_015203 RPRD2 chr1:g.150475512G>T
NM_015203 RPRD2 chr1:g.150475556G>C
NM_015203 RPRD2 chr1:g.150475569G>A
NM_015203 RPRD2 chr1:g.150475957G>A
NM_015203 RPRD2 chr1:g.150476212G>A
NM_015203 RPRD2 chr1:g.150476475AAAAC>-