Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRIP13

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000166345
Start 904183:904183(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.571G>T
AA Mutation p.Ala191Ser(p.A191S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000166345
Start 896739:896739(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.333T>G
AA Mutation p.Asn111Lys(p.N111K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000166345
Start 904194:904194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.582G>T
AA Mutation p.Gln194His(p.Q194H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000166345
Start 908059:908059(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377734782
CDS Mutation c.744C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000166345
Start 894800:894800(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.106G>T
AA Mutation p.Glu36Ter(p.E36*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> TRIP13

No Mutation Annotation!