Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> COX4I1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000253452
Start 85804964:85804964(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201058411
CDS Mutation c.101C>T
AA Mutation p.Ser34Leu(p.S34L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000253452
Start 85805834:85805834(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772180664
CDS Mutation c.343G>A
AA Mutation p.Ala115Thr(p.A115T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000253452
Start 85805830:85805830(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.339C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000253452
Start 85801268:85801268(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.63A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence inframe_deletion
Transcription ID ENST00000253452
Start 85805066:85805068(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.206_208delCCT
AA Mutation p.Ser69del(p.S69del)
Mutation Classification In_Frame_Del
Feature Type Transcript

Rectum Cancer: Gene >> COX4I1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000253452
Start 85806753:85806753(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.389C>T
AA Mutation p.Pro130Leu(p.P130L)
Mutation Classification Missense_Mutation
Feature Type Transcript