Primary Site >> Stomach Cancer

Gene >> DDX58

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32493806:32493806(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.378T>G
AA Mutation p.Asp126Glu(p.D126E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32487539:32487539(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139635230
CDS Mutation c.1307C>T
AA Mutation p.Ala436Val(p.A436V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32492460:32492460(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757063794
CDS Mutation c.502C>T
AA Mutation p.Pro168Ser(p.P168S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32488857:32488857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.830T>G
AA Mutation p.Ile277Arg(p.I277R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32481368:32481368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1610C>T
AA Mutation p.Ala537Val(p.A537V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32488797:32488797(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765663574
CDS Mutation c.890C>T
AA Mutation p.Ala297Val(p.A297V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32492513:32492513(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.449C>T
AA Mutation p.Ala150Val(p.A150V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32457296:32457296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2604C>G
AA Mutation p.Asn868Lys(p.N868K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32487521:32487521(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1325T>C
AA Mutation p.Val442Ala(p.V442A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000379883
Start 32485237:32485237(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1418A>G
AA Mutation p.Tyr473Cys(p.Y473C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000379883
Start 32457365:32457365(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2535A>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000379883
Start 32467895:32467895(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2052A>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000379883
Start 32481359:32481359(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1619delT
AA Mutation p.Leu540TyrfsTer21(p.L540Yfs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000379883
Start 32459464:32459464(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2388delA
AA Mutation p.Lys796AsnfsTer28(p.K796Nfs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000379883
Start 32487590:32487590(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1256delA
AA Mutation p.Asn419ThrfsTer20(p.N419Tfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence start_lost
Transcription ID ENST00000379883
Start 32526166:32526166(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1A>G
AA Mutation p.Met1?(p.M1?)
Mutation Classification Translation_Start_Site
Feature Type Transcript