Primary Site >> Stomach Cancer

Gene >> TRIM59

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000309784
Start 160438841:160438841(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.343T>A
AA Mutation p.Leu115Ile(p.L115I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000309784
Start 160438029:160438029(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1155A>G
AA Mutation p.Ile385Met(p.I385M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000309784
Start 160438410:160438410(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.774C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000309784
Start 160437985:160437986(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1198_1199insC
AA Mutation p.Ile400ThrfsTer10(p.I400Tfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript