Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CD3G

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000532917
Start 118351652:118351652(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.464C>T
AA Mutation p.Pro155Leu(p.P155L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000532917
Start 118349785:118349785(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201752677
CDS Mutation c.122C>T
AA Mutation p.Ser41Leu(p.S41L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000532917
Start 118349868:118349868(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs570768621
CDS Mutation c.213delA
AA Mutation p.Lys71AsnfsTer40(p.K71Nfs*40)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 4
Mutation Consequence splice_donor_variant
Transcription ID ENST00000532917
Start 118352489:118352489(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.*18+2T>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> CD3G

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000532917
Start 118349843:118349843(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750576395
CDS Mutation c.180G>T
AA Mutation p.Lys60Asn(p.K60N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence frameshift_variant
Transcription ID ENST00000532917
Start 118350645:118350645(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.401delA
AA Mutation p.Tyr134SerfsTer46(p.Y134Sfs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript