Primary Site >> Stomach Cancer

Gene >> ERG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000398919
Start 38403635:38403635(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs552037654
CDS Mutation c.484G>A
AA Mutation p.Val162Ile(p.V162I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000398919
Start 38423419:38423419(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.400G>A
AA Mutation p.Val134Met(p.V134M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000398919
Start 38383548:38383548(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1316C>T
AA Mutation p.Ala439Val(p.A439V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000398919
Start 38383727:38383727(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1137C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000398919
Start 38423528:38423528(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146525668
CDS Mutation c.291C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000398919
Start 38383412:38383412(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1452T>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000398919
Start 38383859:38383859(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1005C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000398919
Start 38383577:38383577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1287C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000398919
Start 38383505:38383505(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1359delT
AA Mutation p.Phe453LeufsTer59(p.F453Lfs*59)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000398919
Start 38400642:38400642(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.698delG
AA Mutation p.Gly233ValfsTer65(p.G233Vfs*65)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000398919
Start 38383632:38383632(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1232delC
AA Mutation p.Pro411ArgfsTer25(p.P411Rfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000398919
Start 38383504:38383505(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1359dupT
AA Mutation p.Ala454CysfsTer19(p.A454Cfs*19)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript