Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DCUN1D1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000292782
Start 182947582:182947582(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.571A>C
AA Mutation p.Lys191Gln(p.K191Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000292782
Start 182947324:182947324(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.614A>C
AA Mutation p.Lys205Thr(p.K205T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000292782
Start 182963977:182963977(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.293C>T
AA Mutation p.Ala98Val(p.A98V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000292782
Start 182965690:182965690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.67G>A
AA Mutation p.Glu23Lys(p.E23K)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> DCUN1D1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000292782
Start 182965720:182965720(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.37C>T
AA Mutation p.Arg13Cys(p.R13C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000292782
Start 182965568:182965568(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.189G>T
AA Mutation p.Lys63Asn(p.K63N)
Mutation Classification Missense_Mutation
Feature Type Transcript