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 [2 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_015570 AUTS2 chr7:g.70763208C>T
NM_015570 AUTS2 chr7:g.70763223T>C



Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [105 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
hsa_circ_0080413 AUTS2 chr7:g.69599765G>A
hsa_circ_0080413 AUTS2 chr7:g.69599766G>A
hsa_circ_0080413 AUTS2 chr7:g.69599787C>T
hsa_circ_0080413 AUTS2 chr7:g.69599843T>C
hsa_circ_0080413 AUTS2 chr7:g.69599852C>T
hsa_circ_0080413 AUTS2 chr7:g.69599858C>T
hsa_circ_0080413 AUTS2 chr7:g.69599859G>A
hsa_circ_0080413 AUTS2 chr7:g.69602592C>G
hsa_circ_0080413 AUTS2 chr7:g.69665185T>C
hsa_circ_0080413 AUTS2 chr7:g.69667790C>T
hsa_circ_0080413 AUTS2 chr7:g.69675877C>G
hsa_circ_0080413 AUTS2 chr7:g.69676250G>C
hsa_circ_0080413 AUTS2 chr7:g.69699972T>C
hsa_circ_0080413 AUTS2 chr7:g.69703528G>A
hsa_circ_0080413 AUTS2 chr7:g.69806227A>G
hsa_circ_0080417 AUTS2 chr7:g.69899325C>T
hsa_circ_0080417 AUTS2 chr7:g.69899332C>T
hsa_circ_0080417 AUTS2 chr7:g.69899337C>A
hsa_circ_0080417 AUTS2 chr7:g.69899341C>T
hsa_circ_0080417 AUTS2 chr7:g.69899342C>T
hsa_circ_0080417 AUTS2 chr7:g.69899342CAAG>C
hsa_circ_0080417 AUTS2 chr7:g.69899345G>C
hsa_circ_0080417 AUTS2 chr7:g.69899353G>A
hsa_circ_0080417 AUTS2 chr7:g.69899355G>T
hsa_circ_0080417 AUTS2 chr7:g.69899360A>G
hsa_circ_0080417 AUTS2 chr7:g.69899362T>C
hsa_circ_0080417 AUTS2 chr7:g.69899362T>G
hsa_circ_0080417 AUTS2 chr7:g.69918906C>T
hsa_circ_0080417 AUTS2 chr7:g.69948042A>G
hsa_circ_0080417 AUTS2 chr7:g.69986949G>A
hsa_circ_0080417 AUTS2 chr7:g.69993703T>C
hsa_circ_0080417 AUTS2 chr7:g.69998250T>G
hsa_circ_0080417 AUTS2 chr7:g.70078564A>T
hsa_circ_0080419 AUTS2 chr7:g.70234088A>C
hsa_circ_0080419 AUTS2 chr7:g.70314521G>C
hsa_circ_0080419 AUTS2 chr7:g.70483552C>G
hsa_circ_0080419 AUTS2 chr7:g.70505115C>T
hsa_circ_0080419 AUTS2 chr7:g.70505116C>G
hsa_circ_0080419 AUTS2 chr7:g.70525672T>C
hsa_circ_0080419 AUTS2 chr7:g.70528231GA>G
hsa_circ_0080419 AUTS2 chr7:g.70584491C>T
hsa_circ_0080417 AUTS2 chr7:g.70702673A>C
hsa_circ_0080417 AUTS2 chr7:g.70752492A>G
hsa_circ_0080417 AUTS2 chr7:g.70762925G>A
hsa_circ_0080417 AUTS2 chr7:g.70762930T>C
hsa_circ_0080417 AUTS2 chr7:g.70763060G>A
hsa_circ_0080417 AUTS2 chr7:g.70763063G>A
hsa_circ_0080417 AUTS2 chr7:g.70763074G>A
hsa_circ_0080417 AUTS2 chr7:g.70763098T>G
hsa_circ_0080417 AUTS2 chr7:g.70763103C>A
hsa_circ_0080417 AUTS2 chr7:g.70763292C>A
hsa_circ_0080417 AUTS2 chr7:g.70763302C>T
hsa_circ_0080417 AUTS2 chr7:g.70764786C>T
hsa_circ_0080417 AUTS2 chr7:g.70764789G>A
hsa_circ_0080417 AUTS2 chr7:g.70764795C>CA
hsa_circ_0080417 AUTS2 chr7:g.70764924C>T
hsa_circ_0080417 AUTS2 chr7:g.70764941T>A
hsa_circ_0080417 AUTS2 chr7:g.70764942C>T
hsa_circ_0080417 AUTS2 chr7:g.70766258C>T
hsa_circ_0080417 AUTS2 chr7:g.70766259G>A
hsa_circ_0080417 AUTS2 chr7:g.70766268C>T
hsa_circ_0080417 AUTS2 chr7:g.70771621C>A
hsa_circ_0080417 AUTS2 chr7:g.70772491C>T
hsa_circ_0080417 AUTS2 chr7:g.70774029C>T
hsa_circ_0080417 AUTS2 chr7:g.70774042C>T
hsa_circ_0080417 AUTS2 chr7:g.70774048C>T
hsa_circ_0080417 AUTS2 chr7:g.70774073C>T
hsa_circ_0080417 AUTS2 chr7:g.70781620G>A
hsa_circ_0080417 AUTS2 chr7:g.70781652G>T
hsa_circ_0080417 AUTS2 chr7:g.70781653A>G
hsa_circ_0080417 AUTS2 chr7:g.70781746C>T
hsa_circ_0080417 AUTS2 chr7:g.70784980C>G
hsa_circ_0080417 AUTS2 chr7:g.70784997C>T
hsa_circ_0080417 AUTS2 chr7:g.70784998C>T
NM_015570 AUTS2 chr7:g.70785971G>A
NM_015570 AUTS2 chr7:g.70786013C>T
NM_015570 AUTS2 chr7:g.70787388G>T
NM_015570 AUTS2 chr7:g.70790270C>T
NM_015570 AUTS2 chr7:g.70790278C>T
NM_015570 AUTS2 chr7:g.70790285C>T
NM_015570 AUTS2 chr7:g.70790354G>T
NM_015570 AUTS2 chr7:g.70790355AC>A
NM_015570 AUTS2 chr7:g.70790358C>T
NM_015570 AUTS2 chr7:g.70790372C>T
NM_015570 AUTS2 chr7:g.70790378C>T
NM_015570 AUTS2 chr7:g.70790383C>T
NM_015570 AUTS2 chr7:g.70790384G>A
NM_015570 AUTS2 chr7:g.70790384G>T
NM_015570 AUTS2 chr7:g.70790387C>T
NM_015570 AUTS2 chr7:g.70790393G>T
NM_015570 AUTS2 chr7:g.70790414C>T
NM_015570 AUTS2 chr7:g.70790430C>T
NM_015570 AUTS2 chr7:g.70790455G>A
NM_015570 AUTS2 chr7:g.70790705G>A
NM_015570 AUTS2 chr7:g.70790713G>A
NM_015570 AUTS2 chr7:g.70790714G>A
NM_015570 AUTS2 chr7:g.70790848C>T
NM_015570 AUTS2 chr7:g.70790854C>T
NM_015570 AUTS2 chr7:g.70790858A>G
NM_015570 AUTS2 chr7:g.70790950G>A
NM_015570 AUTS2 chr7:g.70791162A>G
NM_015570 AUTS2 chr7:g.70791218C>G
NM_015570 AUTS2 chr7:g.70791378T>A
NM_015570 AUTS2 chr7:g.70791819C>G
NM_015570 AUTS2 chr7:g.70792612G>A



Somatic mutations that alter predicted mRNA-miRNA target sites [9 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_015570 AUTS2 chr7:g.70791162A>G
NM_015570 AUTS2 chr7:g.70791202A>G
NM_015570 AUTS2 chr7:g.70791218C>G
NM_001127231 AUTS2 chr7:g.70791378T>A
NM_015570 AUTS2 chr7:g.70791569T>C
NM_015570 AUTS2 chr7:g.70791819C>G
NM_015570 AUTS2 chr7:g.70792149T>G
NM_015570 AUTS2 chr7:g.70792518G>A
NM_015570 AUTS2 chr7:g.70792612G>A