Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ODC1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000234111
Start 10444514:10444514(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.236C>T
AA Mutation p.Thr79Ile(p.T79I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000234111
Start 10444551:10444551(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745661230
CDS Mutation c.199G>A
AA Mutation p.Ala67Thr(p.A67T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000234111
Start 10440764:10440764(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763621553
CDS Mutation c.1346G>A
AA Mutation p.Arg449His(p.R449H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000234111
Start 10441820:10441820(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1023A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000234111
Start 10442036:10442036(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.889T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000234111
Start 10441880:10441880(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs548861296
CDS Mutation c.963C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000234111
Start 10444642:10444642(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.108T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000234111
Start 10443275:10443275(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs11538363
CDS Mutation c.705C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000234111
Start 10444228:10444228(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.316G>T
AA Mutation p.Glu106Ter(p.E106*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> ODC1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000234111
Start 10442134:10442134(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.791C>T
AA Mutation p.Pro264Leu(p.P264L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000234111
Start 10444154:10444154(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.390G>T
AA Mutation p.Met130Ile(p.M130I)
Mutation Classification Missense_Mutation
Feature Type Transcript