Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADRA1D

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4248449:4248449(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.509A>G
AA Mutation p.Asp170Gly(p.D170G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4248102:4248102(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.856C>T
AA Mutation p.Arg286Cys(p.R286C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4248084:4248084(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs538270081
CDS Mutation c.874G>A
AA Mutation p.Val292Ile(p.V292I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4222115:4222115(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1127A>G
AA Mutation p.Gln376Arg(p.Q376R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4247955:4247955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1003G>A
AA Mutation p.Val335Met(p.V335M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4222091:4222091(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1151T>C
AA Mutation p.Phe384Ser(p.F384S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4248317:4248317(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.641C>T
AA Mutation p.Ala214Val(p.A214V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000379453
Start 4247989:4247989(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770973888
CDS Mutation c.969C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000379453
Start 4248520:4248520(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375396926
CDS Mutation c.438C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> ADRA1D

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379453
Start 4248253:4248253(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.705G>T
AA Mutation p.Trp235Cys(p.W235C)
Mutation Classification Missense_Mutation
Feature Type Transcript