Primary Site >> Stomach Cancer

Gene >> DDX4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000505374
Start 55792711:55792711(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1373C>T
AA Mutation p.Pro458Leu(p.P458L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000505374
Start 55763252:55763252(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.283G>T
AA Mutation p.Gly95Cys(p.G95C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000505374
Start 55764048:55764048(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.318C>A
AA Mutation p.Ser106Arg(p.S106R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000505374
Start 55798470:55798470(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1514T>C
AA Mutation p.Val505Ala(p.V505A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000505374
Start 55798550:55798550(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777699581
CDS Mutation c.1594G>A
AA Mutation p.Val532Ile(p.V532I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000505374
Start 55792660:55792660(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1322A>C
AA Mutation p.Lys441Thr(p.K441T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000505374
Start 55785756:55785756(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.749C>A
AA Mutation p.Pro250His(p.P250H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000505374
Start 55815129:55815129(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1944G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000505374
Start 55792787:55792787(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1449T>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000505374
Start 55792750:55792750(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1412C>G
AA Mutation p.Ser471Ter(p.S471*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000505374
Start 55786527:55786527(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.874G>T
AA Mutation p.Glu292Ter(p.E292*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript