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: PAR-CLIP and HITS-CLIP [73 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_020342 SLC39A10 chr2:g.195657538G>A
NM_020342 SLC39A10 chr2:g.195657736C>G
hsa_circ_0057553 SLC39A10 chr2:g.195680046A>G
hsa_circ_0057553 SLC39A10 chr2:g.195680065A>C
hsa_circ_0057553 SLC39A10 chr2:g.195680078T>C
hsa_circ_0057553 SLC39A10 chr2:g.195680126A>G
hsa_circ_0057553 SLC39A10 chr2:g.195680139C>T
hsa_circ_0057553 SLC39A10 chr2:g.195680188G>A
hsa_circ_0057553 SLC39A10 chr2:g.195680238A>C
hsa_circ_0057553 SLC39A10 chr2:g.195680301A>G
hsa_circ_0057553 SLC39A10 chr2:g.195680471C>T
hsa_circ_0057553 SLC39A10 chr2:g.195680480C>T
hsa_circ_0057553 SLC39A10 chr2:g.195680492C>A
hsa_circ_0057553 SLC39A10 chr2:g.195680509A>G
hsa_circ_0057553 SLC39A10 chr2:g.195680517AC>A
hsa_circ_0057553 SLC39A10 chr2:g.195680528G>T
hsa_circ_0057553 SLC39A10 chr2:g.195680556C>T
hsa_circ_0057553 SLC39A10 chr2:g.195680650C>T
hsa_circ_0057553 SLC39A10 chr2:g.195680821A>T
hsa_circ_0057553 SLC39A10 chr2:g.195680836G>A
hsa_circ_0057555 SLC39A10 chr2:g.195681006A>G
hsa_circ_0057555 SLC39A10 chr2:g.195681021G>T
hsa_circ_0057555 SLC39A10 chr2:g.195683744A>G
hsa_circ_0057555 SLC39A10 chr2:g.195683752C>T
hsa_circ_0057555 SLC39A10 chr2:g.195683756T>C
hsa_circ_0057555 SLC39A10 chr2:g.195683781G>C
hsa_circ_0057555 SLC39A10 chr2:g.195683787C>G
hsa_circ_0057555 SLC39A10 chr2:g.195683787C>T
hsa_circ_0057555 SLC39A10 chr2:g.195683791G>T
hsa_circ_0057555 SLC39A10 chr2:g.195683798C>G
hsa_circ_0057555 SLC39A10 chr2:g.195683798C>T
hsa_circ_0057555 SLC39A10 chr2:g.195683824G>A
hsa_circ_0057555 SLC39A10 chr2:g.195683825C>T
hsa_circ_0057555 SLC39A10 chr2:g.195687750C>A
hsa_circ_0057555 SLC39A10 chr2:g.195708765T>G
hsa_circ_0057555 SLC39A10 chr2:g.195713543G>A
hsa_circ_0057555 SLC39A10 chr2:g.195713554G>T
hsa_circ_0057555 SLC39A10 chr2:g.195716708G>C
hsa_circ_0057555 SLC39A10 chr2:g.195716712C>G
hsa_circ_0057555 SLC39A10 chr2:g.195716712C>T
hsa_circ_0057555 SLC39A10 chr2:g.195716831G>A
hsa_circ_0057555 SLC39A10 chr2:g.195716840A>G
hsa_circ_0057555 SLC39A10 chr2:g.195716846C>A
hsa_circ_0057555 SLC39A10 chr2:g.195716859A>C
hsa_circ_0057555 SLC39A10 chr2:g.195716883C>T
hsa_circ_0057555 SLC39A10 chr2:g.195716888C>T
hsa_circ_0057555 SLC39A10 chr2:g.195716912G>A
hsa_circ_0057555 SLC39A10 chr2:g.195716918G>A
hsa_circ_0057555 SLC39A10 chr2:g.195716918G>T
hsa_circ_0057555 SLC39A10 chr2:g.195716926A>C
hsa_circ_0057555 SLC39A10 chr2:g.195728182G>A
hsa_circ_0057555 SLC39A10 chr2:g.195728200C>T
hsa_circ_0057555 SLC39A10 chr2:g.195728207T>C
hsa_circ_0057555 SLC39A10 chr2:g.195728216A>G
hsa_circ_0057555 SLC39A10 chr2:g.195728219T>C
hsa_circ_0057555 SLC39A10 chr2:g.195728244A>G
hsa_circ_0057555 SLC39A10 chr2:g.195728257G>T
hsa_circ_0057555 SLC39A10 chr2:g.195728271T>C
hsa_circ_0057555 SLC39A10 chr2:g.195728323T>C
hsa_circ_0057555 SLC39A10 chr2:g.195728344G>C
hsa_circ_0057555 SLC39A10 chr2:g.195734926G>A
hsa_circ_0057555 SLC39A10 chr2:g.195734934C>T
hsa_circ_0057555 SLC39A10 chr2:g.195734942G>T
hsa_circ_0057555 SLC39A10 chr2:g.195734994G>C
hsa_circ_0057555 SLC39A10 chr2:g.195735005C>T
hsa_circ_0057555 SLC39A10 chr2:g.195735010A>C
hsa_circ_0057555 SLC39A10 chr2:g.195735020T>G
hsa_circ_0057555 SLC39A10 chr2:g.195735107C>T
hsa_circ_0057555 SLC39A10 chr2:g.195735487A>G
hsa_circ_0057555 SLC39A10 chr2:g.195736230G>C
hsa_circ_0057555 SLC39A10 chr2:g.195736406T>C
hsa_circ_0057555 SLC39A10 chr2:g.195737117T>A
hsa_circ_0057555 SLC39A10 chr2:g.195737227C>G



Somatic mutations that alter predicted mRNA-miRNA target sites [6 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_001127257 SLC39A10 chr2:g.195735107C>T
NM_001127257 SLC39A10 chr2:g.195735487A>G
NM_020342 SLC39A10 chr2:g.195736230G>C
NM_020342 SLC39A10 chr2:g.195736406T>C
NM_020342 SLC39A10 chr2:g.195737117T>A
NM_020342 SLC39A10 chr2:g.195737227C>G