Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BAX

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000345358
Start 48960857:48960857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.417G>T
AA Mutation p.Trp139Cys(p.W139C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000345358
Start 48960839:48960839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.399C>G
AA Mutation p.Ile133Met(p.I133M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000345358
Start 48955714:48955714(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs771158018
CDS Mutation c.121delG
AA Mutation p.Glu41ArgfsTer19(p.E41Rfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000345358
Start 48956224:48956224(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.265delC
AA Mutation p.Arg89GlufsTer44(p.R89Efs*44)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000345358
Start 48955597:48955597(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.86+1delG
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000345358
Start 48956244:48956244(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.280C>T
AA Mutation p.Arg94Ter(p.R94*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> BAX

No Mutation Annotation!