Primary Site >> Stomach Cancer
Gene >> DDX27
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371764 |
| Start | 49235055:49235055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1487A>C |
| AA Mutation | p.Asn496Thr(p.N496T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371764 |
| Start | 49234948:49234948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1380G>T |
| AA Mutation | p.Arg460Ser(p.R460S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371764 |
| Start | 49233623:49233623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1280G>A |
| AA Mutation | p.Ser427Asn(p.S427N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371764 |
| Start | 49243639:49243639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2308G>C |
| AA Mutation | p.Glu770Gln(p.E770Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000622530 |
| Start | 49239050:49239050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1882G>A |
| AA Mutation | p.Ala628Thr(p.A628T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371764 |
| Start | 49226476:49226476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.740C>T |
| AA Mutation | p.Ala247Val(p.A247V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000371764 |
| Start | 49226535:49226535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.799G>T |
| AA Mutation | p.Gly267Cys(p.G267C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371764 |
| Start | 49241973:49241973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2071A>C |
| AA Mutation | p.Lys691Gln(p.K691Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371764 |
| Start | 49228751:49228751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.836G>A |
| AA Mutation | p.Arg279His(p.R279H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371764 |
| Start | 49230271:49230271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1046G>A |
| AA Mutation | p.Arg349Gln(p.R349Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371764 |
| Start | 49235068:49235068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1500G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371764 |
| Start | 49236216:49236216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1587T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371764 |
| Start | 49221455:49221455(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.192delC |
| AA Mutation | p.Ile65LeufsTer41(p.I65Lfs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371764 |
| Start | 49241967:49241967(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs766714372 |
| CDS Mutation | c.2072delA |
| AA Mutation | p.Lys691ArgfsTer4(p.K691Rfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |