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 [15 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001127208 | TET2 | chr4:g.105235572C>T |
NM_001127208 | TET2 | chr4:g.105235574A>G |
NM_001127208 | TET2 | chr4:g.105235575G>A |
NM_001127208 | TET2 | chr4:g.105235577C>T |
NM_001127208 | TET2 | chr4:g.105235586AA>A |
NM_001127208 | TET2 | chr4:g.105235587AC>A |
NM_001127208 | TET2 | chr4:g.105235589A>AA |
NM_001127208 | TET2 | chr4:g.105235590C>T |
NM_001127208 | TET2 | chr4:g.105235591G>A |
NM_001127208 | TET2 | chr4:g.105235600T>TG |
NM_001127208 | TET2 | chr4:g.105235602C>T |
NM_001127208 | TET2 | chr4:g.105235605C>T |
NM_001127208 | TET2 | chr4:g.105235605CC>C |
NM_001127208 | TET2 | chr4:g.105235606C>CC |
NM_001127208 | TET2 | chr4:g.105235611C>T |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [144 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
hsa_circ_0070561 | TET2 | chr4:g.105215023T>G |
hsa_circ_0070563 | TET2 | chr4:g.105238093A>G |
hsa_circ_0070564 | TET2 | chr4:g.105278502T>C |
hsa_circ_0070564 | TET2 | chr4:g.105279293G>C |
hsa_circ_0070563 | TET2 | chr4:g.105234161TG>T |
hsa_circ_0070563 | TET2 | chr4:g.105234165A>T |
hsa_circ_0070563 | TET2 | chr4:g.105234180C>T |
hsa_circ_0070563 | TET2 | chr4:g.105234183G>T |
hsa_circ_0070563 | TET2 | chr4:g.105234532T>TC |
hsa_circ_0070563 | TET2 | chr4:g.105234532TT>T |
hsa_circ_0070563 | TET2 | chr4:g.105234542T>TT |
hsa_circ_0070563 | TET2 | chr4:g.105234542TA>T |
hsa_circ_0070563 | TET2 | chr4:g.105234571GTG>G |
hsa_circ_0070563 | TET2 | chr4:g.105234571G>A |
hsa_circ_0070563 | TET2 | chr4:g.105234686C>A |
hsa_circ_0070563 | TET2 | chr4:g.105234691A>G |
hsa_circ_0070563 | TET2 | chr4:g.105234691A>AA |
hsa_circ_0070563 | TET2 | chr4:g.105234703GT>G |
hsa_circ_0070563 | TET2 | chr4:g.105234703GTCAG>G |
hsa_circ_0070563 | TET2 | chr4:g.105234705C>T |
hsa_circ_0070563 | TET2 | chr4:g.105234724CC>C |
hsa_circ_0070563 | TET2 | chr4:g.105234728TG>T |
hsa_circ_0070563 | TET2 | chr4:g.105234744T>G |
hsa_circ_0070563 | TET2 | chr4:g.105234745C>G |
hsa_circ_0070563 | TET2 | chr4:g.105234745C>T |
hsa_circ_0070563 | TET2 | chr4:g.105234746G>A |
hsa_circ_0070563 | TET2 | chr4:g.105234924GT>G |
hsa_circ_0070563 | TET2 | chr4:g.105234929T>TT |
hsa_circ_0070563 | TET2 | chr4:g.105234930G>C |
hsa_circ_0070563 | TET2 | chr4:g.105234939CC>C |
hsa_circ_0070563 | TET2 | chr4:g.105234943C>T |
hsa_circ_0070563 | TET2 | chr4:g.105234954AA>A |
hsa_circ_0070563 | TET2 | chr4:g.105234961T>TC |
hsa_circ_0070563 | TET2 | chr4:g.105234961TC>T |
hsa_circ_0070563 | TET2 | chr4:g.105234963C>T |
hsa_circ_0070563 | TET2 | chr4:g.105234974AAAGC>A |
hsa_circ_0070563 | TET2 | chr4:g.105234979T>TAGCT |
hsa_circ_0070563 | TET2 | chr4:g.105234979T>C |
hsa_circ_0070563 | TET2 | chr4:g.105234982C>T |
hsa_circ_0070563 | TET2 | chr4:g.105235031TGG>TT |
hsa_circ_0070563 | TET2 | chr4:g.105235033G>A |
hsa_circ_0070563 | TET2 | chr4:g.105235044GA>G |
hsa_circ_0070563 | TET2 | chr4:g.105235052T>A |
hsa_circ_0070563 | TET2 | chr4:g.105235078CTT>CC |
hsa_circ_0070563 | TET2 | chr4:g.105235089C>T |
hsa_circ_0070563 | TET2 | chr4:g.105235092A>G |
hsa_circ_0070563 | TET2 | chr4:g.105235718T>G |
hsa_circ_0070563 | TET2 | chr4:g.105235719C>T |
hsa_circ_0070563 | TET2 | chr4:g.105235723CC>C |
hsa_circ_0070563 | TET2 | chr4:g.105235734AA>A |
hsa_circ_0070563 | TET2 | chr4:g.105235738A>G |
hsa_circ_0070563 | TET2 | chr4:g.105235740AT>A |
hsa_circ_0070563 | TET2 | chr4:g.105235742G>A |
hsa_circ_0070563 | TET2 | chr4:g.105235743AC>A |
hsa_circ_0070563 | TET2 | chr4:g.105235756A>AA |
hsa_circ_0070563 | TET2 | chr4:g.105235756AC>A |
hsa_circ_0070563 | TET2 | chr4:g.105235902C>T |
hsa_circ_0070563 | TET2 | chr4:g.105235908C>T |
hsa_circ_0070563 | TET2 | chr4:g.105235912C>G |
hsa_circ_0070563 | TET2 | chr4:g.105235913AC>A |
hsa_circ_0070563 | TET2 | chr4:g.105235914CAC>C |
hsa_circ_0070563 | TET2 | chr4:g.105235914CA>C |
hsa_circ_0070563 | TET2 | chr4:g.105235915A>C |
hsa_circ_0070563 | TET2 | chr4:g.105235924A>G |
hsa_circ_0070563 | TET2 | chr4:g.105236083C>A |
hsa_circ_0070563 | TET2 | chr4:g.105236086A>G |
hsa_circ_0070563 | TET2 | chr4:g.105236086ACT>A |
hsa_circ_0070563 | TET2 | chr4:g.105236088TCA>T |
hsa_circ_0070563 | TET2 | chr4:g.105236088TC>T |
hsa_circ_0070563 | TET2 | chr4:g.105236089C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236090ACA>A |
hsa_circ_0070563 | TET2 | chr4:g.105236091C>CA |
hsa_circ_0070563 | TET2 | chr4:g.105236094CT>C |
hsa_circ_0070563 | TET2 | chr4:g.105236100C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236102ACA>A |
hsa_circ_0070563 | TET2 | chr4:g.105236117ACAGG>A |
hsa_circ_0070563 | TET2 | chr4:g.105236118C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236121G>A |
hsa_circ_0070563 | TET2 | chr4:g.105236127C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236129AAC>A |
hsa_circ_0070563 | TET2 | chr4:g.105236133C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236137C>A |
hsa_circ_0070563 | TET2 | chr4:g.105236138A>AT |
hsa_circ_0070563 | TET2 | chr4:g.105236140C>CT |
hsa_circ_0070563 | TET2 | chr4:g.105236142C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236143A>G |
hsa_circ_0070563 | TET2 | chr4:g.105236149C>G |
hsa_circ_0070563 | TET2 | chr4:g.105236151C>CA |
hsa_circ_0070563 | TET2 | chr4:g.105236160C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236166C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236169C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236169C>CA |
hsa_circ_0070563 | TET2 | chr4:g.105236538C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236541T>C |
hsa_circ_0070563 | TET2 | chr4:g.105236543T>A |
hsa_circ_0070563 | TET2 | chr4:g.105236545TT>T |
hsa_circ_0070563 | TET2 | chr4:g.105236546T>TT |
hsa_circ_0070563 | TET2 | chr4:g.105236546T>G |
hsa_circ_0070563 | TET2 | chr4:g.105236562C>G |
hsa_circ_0070563 | TET2 | chr4:g.105236568C>T |
hsa_circ_0070563 | TET2 | chr4:g.105236573TC>T |
hsa_circ_0070563 | TET2 | chr4:g.105236574C>A |
hsa_circ_0070563 | TET2 | chr4:g.105236579TC>T |
hsa_circ_0070563 | TET2 | chr4:g.105236579TCACA>TAC |
hsa_circ_0070563 | TET2 | chr4:g.105236581A>G |
hsa_circ_0070563 | TET2 | chr4:g.105236583A>AA |
hsa_circ_0070563 | TET2 | chr4:g.105236585G>A |
hsa_circ_0070563 | TET2 | chr4:g.105236588C>A |
hsa_circ_0070563 | TET2 | chr4:g.105236592C>CC |
hsa_circ_0070564 | TET2 | chr4:g.105272630G>T |
hsa_circ_0070564 | TET2 | chr4:g.105272631T>G |
hsa_circ_0070564 | TET2 | chr4:g.105272631T>TTCTG |
hsa_circ_0070564 | TET2 | chr4:g.105272632T>TTT |
hsa_circ_0070564 | TET2 | chr4:g.105272637C>G |
hsa_circ_0070564 | TET2 | chr4:g.105275131C>T |
hsa_circ_0070564 | TET2 | chr4:g.105275134C>T |
hsa_circ_0070564 | TET2 | chr4:g.105275143CAG>CC |
hsa_circ_0070564 | TET2 | chr4:g.105275146C>T |
hsa_circ_0070564 | TET2 | chr4:g.105275149C>T |
hsa_circ_0070564 | TET2 | chr4:g.105275152C>T |
hsa_circ_0070564 | TET2 | chr4:g.105275155C>CAGC |
hsa_circ_0070564 | TET2 | chr4:g.105275245T>TA |
hsa_circ_0070564 | TET2 | chr4:g.105275246A>C |
hsa_circ_0070564 | TET2 | chr4:g.105275258C>A |
hsa_circ_0070564 | TET2 | chr4:g.105275267C>A |
hsa_circ_0070564 | TET2 | chr4:g.105275269G>A |
hsa_circ_0070564 | TET2 | chr4:g.105275270A>AT |
hsa_circ_0070564 | TET2 | chr4:g.105275304T>A |
hsa_circ_0070564 | TET2 | chr4:g.105275317C>T |
hsa_circ_0070564 | TET2 | chr4:g.105275389C>T |
hsa_circ_0070564 | TET2 | chr4:g.105275394T>A |
hsa_circ_0070564 | TET2 | chr4:g.105275394T>G |
hsa_circ_0070564 | TET2 | chr4:g.105275399C>A |
hsa_circ_0070564 | TET2 | chr4:g.105275403T>A |
hsa_circ_0070564 | TET2 | chr4:g.105275404C>T |
hsa_circ_0070564 | TET2 | chr4:g.105275408G>GG |
hsa_circ_0070564 | TET2 | chr4:g.105275527CCA>C |
hsa_circ_0070564 | TET2 | chr4:g.105275545T>TT |
hsa_circ_0070564 | TET2 | chr4:g.105275545TA>T |
hsa_circ_0070564 | TET2 | chr4:g.105275548C>T |
hsa_circ_0070564 | TET2 | chr4:g.105276448ACA>A |
hsa_circ_0070564 | TET2 | chr4:g.105276452A>G |
hsa_circ_0070564 | TET2 | chr4:g.105276461T>TT |
hsa_circ_0070564 | TET2 | chr4:g.105276509G>A |
Somatic mutations that alter predicted mRNA-miRNA target sites [20 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_017628 | TET2 | chr4:g.105241337A>C |
NM_017628 | TET2 | chr4:g.105237994A>G |
NM_001127208 | TET2 | chr4:g.105276602->G |
NM_001127208 | TET2 | chr4:g.105279146->T |
NM_017628 | TET2 | chr4:g.105241954C>T |
NM_017628 | TET2 | chr4:g.105242512T>C |
NM_001127208 | TET2 | chr4:g.105278502T>C |
NM_001127208 | TET2 | chr4:g.105278293A>T |
NM_017628 | TET2 | chr4:g.105238241T>C |
NM_017628 | TET2 | chr4:g.105239171T>C |
NM_001127208 | TET2 | chr4:g.105277680C>G |
NM_017628 | TET2 | chr4:g.105241964C>A |
NM_017628 | TET2 | chr4:g.105239846A>G |
NM_017628 | TET2 | chr4:g.105240759C>G |
NM_001127208 | TET2 | chr4:g.105278867A>G |
NM_017628 | TET2 | chr4:g.105238595T>G |
NM_017628 | TET2 | chr4:g.105238093A>G |
NM_017628 | TET2 | chr4:g.105237679C>T |
NM_017628 | TET2 | chr4:g.105239848A>T |
NM_001127208 | TET2 | chr4:g.105279293G>C |