Primary Site >> Stomach Cancer

Gene >> FLI1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000527786
Start 128758170:128758170(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200865469
CDS Mutation c.74C>T
AA Mutation p.Ala25Val(p.A25V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000527786
Start 128768221:128768221(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776142665
CDS Mutation c.334C>T
AA Mutation p.Pro112Ser(p.P112S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000527786
Start 128772797:128772797(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.401C>T
AA Mutation p.Thr134Ile(p.T134I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000527786
Start 128768247:128768247(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370809611
CDS Mutation c.360C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000527786
Start 128810547:128810547(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748983663
CDS Mutation c.918C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000527786
Start 128758192:128758192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs539499213
CDS Mutation c.96C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000527786
Start 128810541:128810541(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.912G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000527786
Start 128809179:128809179(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.804G>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000527786
Start 128810727:128810727(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1098C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000527786
Start 128768220:128768220(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.338delC
AA Mutation p.Pro113LeufsTer5(p.P113Lfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000527786
Start 128810909:128810910(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1286dupG
AA Mutation p.Ile430AsnfsTer12(p.I430Nfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript