Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IL10RA

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000227752
Start 117998776:117998776(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.872A>T
AA Mutation p.Asp291Val(p.D291V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000227752
Start 117989554:117989554(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368287711
CDS Mutation c.301C>T
AA Mutation p.Arg101Trp(p.R101W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000227752
Start 117993256:117993256(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748186383
CDS Mutation c.383G>A
AA Mutation p.Gly128Asp(p.G128D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000227752
Start 117999611:117999611(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1707C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> IL10RA

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000227752
Start 117998863:117998863(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.959G>A
AA Mutation p.Gly320Asp(p.G320D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence stop_gained
Transcription ID ENST00000227752
Start 117988486:117988486(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.172G>T
AA Mutation p.Glu58Ter(p.E58*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript