Primary Site >> Stomach Cancer

Gene >> EXOG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000287675
Start 38523925:38523925(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.670G>A
AA Mutation p.Val224Ile(p.V224I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000287675
Start 38524125:38524125(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.870C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000287675
Start 38497771:38497771(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.306G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000287675
Start 38524296:38524296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1041T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence inframe_deletion
Transcription ID ENST00000287675
Start 38524169:38524171(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.916_918delGAG
AA Mutation p.Glu306del(p.E306del)
Mutation Classification In_Frame_Del
Feature Type Transcript