Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ST3GAL3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361392
Start 43920908:43920908(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1018C>T
AA Mutation p.Arg340Cys(p.R340C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361392
Start 43838269:43838269(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.260A>G
AA Mutation p.Lys87Arg(p.K87R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361392
Start 43930192:43930192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369157620
CDS Mutation c.1099G>A
AA Mutation p.Val367Ile(p.V367I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000361392
Start 43930152:43930152(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1059G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000361392
Start 43898279:43898279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.442C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000361392
Start 43920787:43920787(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766347682
CDS Mutation c.897C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000361392
Start 43920546:43920546(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.891+1delG
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000361392
Start 43920545:43920546(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.891+1dupG
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> ST3GAL3

Mutation ID 1
Mutation Consequence synonymous_variant
Transcription ID ENST00000361392
Start 43899547:43899547(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138286395
CDS Mutation c.564T>C
Mutation Classification Silent
Feature Type Transcript