Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EIF5A2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295822
Start 170894369:170894369(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761918940
CDS Mutation c.325C>T
AA Mutation p.Arg109Cys(p.R109C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295822
Start 170907002:170907002(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.257G>T
AA Mutation p.Arg86Ile(p.R86I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000295822
Start 170893414:170893414(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.408T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000295822
Start 170894330:170894330(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.364G>T
AA Mutation p.Glu122Ter(p.E122*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> EIF5A2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295822
Start 170907002:170907002(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.257G>T
AA Mutation p.Arg86Ile(p.R86I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295822
Start 170907797:170907797(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747942434
CDS Mutation c.10G>A
AA Mutation p.Glu4Lys(p.E4K)
Mutation Classification Missense_Mutation
Feature Type Transcript