Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> AKR1C4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263126
Start 5213139:5213139(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs529198618
CDS Mutation c.826C>T
AA Mutation p.Arg276Trp(p.R276W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263126
Start 5213101:5213101(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147757734
CDS Mutation c.788G>A
AA Mutation p.Arg263His(p.R263H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263126
Start 5213025:5213025(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.712G>T
AA Mutation p.Asp238Tyr(p.D238Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263126
Start 5206364:5206364(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.537G>T
AA Mutation p.Lys179Asn(p.K179N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000263126
Start 5205804:5205804(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781821647
CDS Mutation c.417C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> AKR1C4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263126
Start 5218746:5218746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.958T>G
AA Mutation p.Ser320Ala(p.S320A)
Mutation Classification Missense_Mutation
Feature Type Transcript