Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FUS

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000254108
Start 31185116:31185116(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749434237
CDS Mutation c.701G>A
AA Mutation p.Arg234His(p.R234H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000254108
Start 31185099:31185099(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151073460
CDS Mutation c.684C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000254108
Start 31191069:31191069(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1500T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000254108
Start 31184324:31184324(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.455delC
AA Mutation p.Pro152LeufsTer33(p.P152Lfs*33)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000254108
Start 31182541:31182541(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.67C>T
AA Mutation p.Gln23Ter(p.Q23*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> FUS

Mutation ID 1
Mutation Consequence synonymous_variant
Transcription ID ENST00000254108
Start 31185099:31185099(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151073460
CDS Mutation c.684C>T
Mutation Classification Silent
Feature Type Transcript