Primary Site >> Stomach Cancer

Gene >> USP15

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000280377
Start 62314866:62314866(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.425G>A
AA Mutation p.Gly142Glu(p.G142E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000280377
Start 62391310:62391310(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376173861
CDS Mutation c.2114C>T
AA Mutation p.Thr705Met(p.T705M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000280377
Start 62404259:62404259(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2830C>G
AA Mutation p.Leu944Val(p.L944V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000280377
Start 62383852:62383852(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779630870
CDS Mutation c.1102C>T
AA Mutation p.Arg368Cys(p.R368C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000280377
Start 62392311:62392311(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2349delA
AA Mutation p.Lys783AsnfsTer4(p.K783Nfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence stop_gained;inframe_insertion
Transcription ID ENST00000280377
Start 62383938:62383939(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1188_1189insCCTGCTTTCTAA
AA Mutation p.Leu396_Asn397insProAlaPheTer(p.L396_N397insPAF*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript