Primary Site >> Stomach Cancer
Gene >> CTDP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79713109:79713109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1001G>A |
| AA Mutation | p.Gly334Glu(p.G334E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79715181:79715181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1721A>C |
| AA Mutation | p.Gln574Pro(p.Q574P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79715153:79715153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1693G>A |
| AA Mutation | p.Gly565Arg(p.G565R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79710424:79710424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851C>T |
| AA Mutation | p.Thr284Met(p.T284M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79713085:79713085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760761980 |
| CDS Mutation | c.977C>T |
| AA Mutation | p.Thr326Met(p.T326M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79715256:79715256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149848787 |
| CDS Mutation | c.1796G>A |
| AA Mutation | p.Arg599His(p.R599H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79717994:79717994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148053048 |
| CDS Mutation | c.2395C>T |
| AA Mutation | p.Arg799Cys(p.R799C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79717859:79717859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142285723 |
| CDS Mutation | c.2260G>A |
| AA Mutation | p.Ala754Thr(p.A754T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79696018:79696018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143464787 |
| CDS Mutation | c.440C>T |
| AA Mutation | p.Thr147Met(p.T147M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000613122 |
| Start | 79715105:79715105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1645G>A |
| AA Mutation | p.Ala549Thr(p.A549T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000613122 |
| Start | 79729024:79729024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2535G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000613122 |
| Start | 79696022:79696022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147215606 |
| CDS Mutation | c.444G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000613122 |
| Start | 79717647:79717647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781342460 |
| CDS Mutation | c.2181G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000613122 |
| Start | 79715147:79715147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1687C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000613122 |
| Start | 79717825:79717825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780699468 |
| CDS Mutation | c.2226G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000613122 |
| Start | 79715506:79715506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756882272 |
| CDS Mutation | c.2046G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000613122 |
| Start | 79696043:79696043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767097152 |
| CDS Mutation | c.465C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000613122 |
| Start | 79713102:79713102(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.998delC |
| AA Mutation | p.Pro333LeufsTer12(p.P333Lfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000613122 |
| Start | 79710348:79710348(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.779delT |
| AA Mutation | p.Leu260Ter(p.L260*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000613122 |
| Start | 79710369:79710370(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.802dupT |
| AA Mutation | p.Ser268PhefsTer9(p.S268Ffs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |