Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RAB25

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361084
Start 156065959:156065959(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs566252037
CDS Mutation c.92G>A
AA Mutation p.Arg31Gln(p.R31Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361084
Start 156068423:156068423(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.393G>T
AA Mutation p.Gln131His(p.Q131H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361084
Start 156065937:156065937(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.70G>A
AA Mutation p.Gly24Arg(p.G24R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000361084
Start 156068405:156068405(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.375C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000361084
Start 156069681:156069681(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.444A>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> RAB25

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361084
Start 156066009:156066009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.142G>C
AA Mutation p.Glu48Gln(p.E48Q)
Mutation Classification Missense_Mutation
Feature Type Transcript