Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> B3GNT8

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321702
Start 41425670:41425670(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768303766
CDS Mutation c.1109G>A
AA Mutation p.Arg370His(p.R370H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321702
Start 41425644:41425644(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1135G>T
AA Mutation p.Gly379Cys(p.G379C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321702
Start 41426079:41426079(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758478385
CDS Mutation c.700C>T
AA Mutation p.Arg234Cys(p.R234C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321702
Start 41426389:41426389(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.390G>T
AA Mutation p.Trp130Cys(p.W130C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000321702
Start 41426536:41426536(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.243delG
AA Mutation p.Ser82ProfsTer86(p.S82Pfs*86)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> B3GNT8

No Mutation Annotation!