Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GDA

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358399
Start 72149633:72149633(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.74C>A
AA Mutation p.Pro25His(p.P25H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000358399
Start 72225700:72225700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.738T>G
AA Mutation p.Asp246Glu(p.D246E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000358399
Start 72225772:72225772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.810T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000358399
Start 72228000:72228000(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.880C>T
AA Mutation p.Arg294Ter(p.R294*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence splice_donor_variant;intron_variant
Transcription ID ENST00000358399
Start 72225785:72225788(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.822+3_822+6delAAGT
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> GDA

Mutation ID 1
Mutation Consequence synonymous_variant
Transcription ID ENST00000358399
Start 72227993:72227993(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.873C>T
Mutation Classification Silent
Feature Type Transcript