Primary Site >> Stomach Cancer

Gene >> DCAF8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000326837
Start 160240016:160240016(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.404C>T
AA Mutation p.Ala135Val(p.A135V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000326837
Start 160240073:160240073(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376611740
CDS Mutation c.347G>A
AA Mutation p.Arg116His(p.R116H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000326837
Start 160238617:160238617(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.854C>T
AA Mutation p.Ala285Val(p.A285V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000326837
Start 160218416:160218416(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1585C>T
AA Mutation p.Arg529Trp(p.R529W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000326837
Start 160222774:160222774(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766216059
CDS Mutation c.1317C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000326837
Start 160217652:160217652(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1734C>T
Mutation Classification Silent
Feature Type Transcript