Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IMP3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000314852
Start 75639784:75639784(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs543082666
CDS Mutation c.385G>A
AA Mutation p.Ala129Thr(p.A129T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000314852
Start 75639631:75639631(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.538T>G
AA Mutation p.Phe180Val(p.F180V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000314852
Start 75640049:75640049(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.120G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000314852
Start 75639860:75639860(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.309C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000314852
Start 75639671:75639671(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.498C>A
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> IMP3

No Mutation Annotation!