Primary Site >> Stomach Cancer

Gene >> DDX43

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370336
Start 73395010:73395010(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.105G>C
AA Mutation p.Leu35Phe(p.L35F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370336
Start 73413764:73413764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1475T>C
AA Mutation p.Val492Ala(p.V492A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370336
Start 73414035:73414035(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1562G>C
AA Mutation p.Arg521Thr(p.R521T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370336
Start 73400342:73400342(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.415T>G
AA Mutation p.Tyr139Asp(p.Y139D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370336
Start 73405758:73405758(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.730G>T
AA Mutation p.Asp244Tyr(p.D244Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000370336
Start 73413972:73413972(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144361613
CDS Mutation c.1499C>T
AA Mutation p.Ala500Val(p.A500V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000370336
Start 73400324:73400324(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.401delA
AA Mutation p.Lys134SerfsTer2(p.K134Sfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000370336
Start 73408009:73408009(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1092delA
AA Mutation p.Gly365ValfsTer2(p.G365Vfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000370336
Start 73408009:73408009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1087A>T
AA Mutation p.Lys363Ter(p.K363*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000370336
Start 73406421:73406421(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.865G>T
AA Mutation p.Gly289Ter(p.G289*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000370336
Start 73416161:73416161(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1882C>T
AA Mutation p.Gln628Ter(p.Q628*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript