Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RAB3D

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000222120
Start 11335777:11335777(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.235G>A
AA Mutation p.Ala79Thr(p.A79T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000222120
Start 11335492:11335492(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762283527
CDS Mutation c.427C>T
AA Mutation p.Arg143Cys(p.R143C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000222120
Start 11335511:11335511(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.408G>T
AA Mutation p.Lys136Asn(p.K136N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000222120
Start 11335467:11335467(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145958698
CDS Mutation c.452G>A
AA Mutation p.Arg151Gln(p.R151Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000222120
Start 11325575:11325575(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.483C>A
AA Mutation p.Phe161Leu(p.F161L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000222120
Start 11325526:11325526(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750538732
CDS Mutation c.532C>T
AA Mutation p.Arg178Cys(p.R178C)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> RAB3D

No Mutation Annotation!