Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> OXT

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000217386
Start 3071660:3071660(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5C>T
AA Mutation p.Ala2Val(p.A2V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000217386
Start 3072375:3072375(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.335C>T
AA Mutation p.Ala112Val(p.A112V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000217386
Start 3071722:3071722(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.67C>G
AA Mutation p.Gln23Glu(p.Q23E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000217386
Start 3071700:3071700(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.45G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000217386
Start 3071664:3071664(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> OXT

No Mutation Annotation!