Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADRB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369295
Start 114044644:114044644(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.512C>T
AA Mutation p.Thr171Met(p.T171M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369295
Start 114045061:114045061(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.929G>A
AA Mutation p.Arg310Gln(p.R310Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369295
Start 114045190:114045190(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1058T>G
AA Mutation p.Leu353Arg(p.L353R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000369295
Start 114044840:114044840(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.708C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000369295
Start 114044651:114044651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.519G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000369295
Start 114045539:114045539(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1407C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000369295
Start 114044942:114044942(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.810G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000369295
Start 114044834:114044834(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.702C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> ADRB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369295
Start 114044598:114044598(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.466C>T
AA Mutation p.Arg156Cys(p.R156C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369295
Start 114044770:114044770(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.638C>A
AA Mutation p.Pro213His(p.P213H)
Mutation Classification Missense_Mutation
Feature Type Transcript