Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HOXD8

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313173
Start 176130774:176130774(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.408T>G
AA Mutation p.Phe136Leu(p.F136L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000313173
Start 176131521:176131521(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.782T>G
AA Mutation p.Phe261Cys(p.F261C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000313173
Start 176131415:176131415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.676A>G
AA Mutation p.Arg226Gly(p.R226G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000313173
Start 176131515:176131515(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143950622
CDS Mutation c.776A>G
AA Mutation p.Asp259Gly(p.D259G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000313173
Start 176130689:176130689(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.329delC
AA Mutation p.Pro110LeufsTer67(p.P110Lfs*67)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000313173
Start 176130730:176130730(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.369delC
AA Mutation p.Cys124AlafsTer53(p.C124Afs*53)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> HOXD8

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313173
Start 176131419:176131419(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.680G>T
AA Mutation p.Arg227Ile(p.R227I)
Mutation Classification Missense_Mutation
Feature Type Transcript