Primary Site >> Stomach Cancer

Gene >> DUSP8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000331588
Start 1556620:1556620(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1776C>A
AA Mutation p.Phe592Leu(p.F592L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000331588
Start 1558112:1558112(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.697G>A
AA Mutation p.Asp233Asn(p.D233N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000331588
Start 1558117:1558117(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.692T>C
AA Mutation p.Phe231Ser(p.F231S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000331588
Start 1557571:1557571(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.825C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000331588
Start 1558940:1558940(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.486C>A
Mutation Classification Silent
Feature Type Transcript