Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TPM3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368530
Start 154170448:154170448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.727G>A
AA Mutation p.Ala243Thr(p.A243T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368530
Start 154170459:154170459(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs1051212
CDS Mutation c.716G>A
AA Mutation p.Arg239His(p.R239H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368530
Start 154191194:154191194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.235G>T
AA Mutation p.Ala79Ser(p.A79S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368530
Start 154191190:154191190(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.239C>T
AA Mutation p.Ala80Val(p.A80V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000368530
Start 154172922:154172922(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.552T>C
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> TPM3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368530
Start 154192001:154192001(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754704140
CDS Mutation c.18G>T
AA Mutation p.Lys6Asn(p.K6N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence stop_gained
Transcription ID ENST00000368530
Start 154170699:154170699(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.655G>T
AA Mutation p.Glu219Ter(p.E219*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript