Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CIAPIN1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394391
Start 57431165:57431165(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.732G>T
AA Mutation p.Lys244Asn(p.K244N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394391
Start 57434142:57434142(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.458A>G
AA Mutation p.Asn153Ser(p.N153S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000394391
Start 57432508:57432508(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747622608
CDS Mutation c.609C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000394391
Start 57440809:57440809(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.120C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000394391
Start 57440877:57440877(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.52A>T
AA Mutation p.Lys18Ter(p.K18*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000394391
Start 57432562:57432562(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.557-2A>G
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> CIAPIN1

No Mutation Annotation!