Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ABI1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000376142
Start 26751684:26751684(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1265A>C
AA Mutation p.Glu422Ala(p.E422A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000376142
Start 26823214:26823214(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775422208
CDS Mutation c.209A>G
AA Mutation p.Asn70Ser(p.N70S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000376142
Start 26751614:26751614(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1335G>T
AA Mutation p.Lys445Asn(p.K445N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000376142
Start 26768878:26768878(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.693T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000376142
Start 26748636:26748636(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1461C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000376142
Start 26759231:26759231(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763169008
CDS Mutation c.909G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000376142
Start 26759146:26759146(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.994G>T
AA Mutation p.Gly332Ter(p.G332*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> ABI1

Mutation ID 1
Mutation Consequence stop_gained
Transcription ID ENST00000376142
Start 26759182:26759182(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.958C>T
AA Mutation p.Arg320Ter(p.R320*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript