Primary Site >> Stomach Cancer

Gene >> TRIM27

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000377199
Start 28904308:28904308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1304G>A
AA Mutation p.Arg435Gln(p.R435Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000377199
Start 28908996:28908996(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.863C>T
AA Mutation p.Thr288Met(p.T288M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000377199
Start 28904322:28904322(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1290G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000377199
Start 28920066:28920066(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.693C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000377199
Start 28909019:28909019(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.840delT
AA Mutation p.Phe280LeufsTer8(p.F280Lfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000377199
Start 28908835:28908835(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.892delA
AA Mutation p.Met298CysfsTer11(p.M298Cfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000377199
Start 28908812:28908813(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.910_914dupAAAAT
AA Mutation p.Gln306LysfsTer5(p.Q306Kfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 8
Mutation Consequence inframe_deletion
Transcription ID ENST00000377199
Start 28904264:28904266(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1346_1348delTCT
AA Mutation p.Phe449del(p.F449del)
Mutation Classification In_Frame_Del
Feature Type Transcript