Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TPM1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000403994
Start 63060920:63060920(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.544C>T
AA Mutation p.Arg182Trp(p.R182W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000403994
Start 63062249:63062249(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.674T>A
AA Mutation p.Ile225Asn(p.I225N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000358278
Start 63071166:63071166(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.849C>A
AA Mutation p.Asn283Lys(p.N283K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000403994
Start 63059666:63059666(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.478C>T
AA Mutation p.Arg160Cys(p.R160C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000403994
Start 63060867:63060867(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771589114
CDS Mutation c.493-2A>G
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 6
Mutation Consequence start_lost
Transcription ID ENST00000403994
Start 63042832:63042832(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3G>T
AA Mutation p.Met1?(p.M1?)
Mutation Classification Translation_Start_Site
Feature Type Transcript

Rectum Cancer: Gene >> TPM1

No Mutation Annotation!