Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> VENTX

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000325980
Start 133240290:133240290(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755770897
CDS Mutation c.761C>T
AA Mutation p.Thr254Met(p.T254M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000325980
Start 133240089:133240089(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.560C>T
AA Mutation p.Ala187Val(p.A187V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000325980
Start 133240110:133240110(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.581C>T
AA Mutation p.Ala194Val(p.A194V)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> VENTX

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000325980
Start 133239717:133239717(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776964051
CDS Mutation c.283C>T
AA Mutation p.Arg95Cys(p.R95C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000325980
Start 133239953:133239953(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375001040
CDS Mutation c.424C>T
AA Mutation p.Arg142Cys(p.R142C)
Mutation Classification Missense_Mutation
Feature Type Transcript