Primary Site >> Stomach Cancer

Gene >> DUSP9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000342782
Start 153649585:153649585(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.727T>G
AA Mutation p.Phe243Val(p.F243V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000342782
Start 153649366:153649366(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781935257
CDS Mutation c.508G>A
AA Mutation p.Asp170Asn(p.D170N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000342782
Start 153649517:153649517(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.659C>T
AA Mutation p.Ala220Val(p.A220V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000342782
Start 153650281:153650281(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375976650
CDS Mutation c.1131C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000342782
Start 153649656:153649656(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs137969779
CDS Mutation c.798G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000342782
Start 153650035:153650035(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.885C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000342782
Start 153650219:153650219(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1074delG
AA Mutation p.Gln359ArgfsTer77(p.Q359Rfs*77)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000342782
Start 153650218:153650219(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1074dupG
AA Mutation p.Gln359AlafsTer18(p.Q359Afs*18)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript