Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DSC3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31029604:31029604(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.379G>A
AA Mutation p.Glu127Lys(p.E127K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31025845:31025845(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776850837
CDS Mutation c.545C>T
AA Mutation p.Pro182Leu(p.P182L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31025783:31025783(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757290041
CDS Mutation c.607C>T
AA Mutation p.Arg203Cys(p.R203C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31018081:31018081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1253C>A
AA Mutation p.Ser418Tyr(p.S418Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31031125:31031125(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.202G>T
AA Mutation p.Asp68Tyr(p.D68Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31008404:31008404(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1385T>A
AA Mutation p.Val462Glu(p.V462E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31029610:31029610(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.373A>T
AA Mutation p.Thr125Ser(p.T125S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31022427:31022427(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.851T>G
AA Mutation p.Ile284Ser(p.I284S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000360428
Start 31008074:31008074(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1605G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000360428
Start 31029623:31029623(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751115910
CDS Mutation c.360G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000360428
Start 31029569:31029569(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.414A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000360428
Start 31008463:31008463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1326A>G
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> DSC3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31024354:31024354(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.770G>T
AA Mutation p.Arg257Ile(p.R257I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360428
Start 31018121:31018121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1213A>G
AA Mutation p.Lys405Glu(p.K405E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence stop_gained
Transcription ID ENST00000360428
Start 31018167:31018167(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1167G>A
AA Mutation p.Trp389Ter(p.W389*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript