Primary Site >> Stomach Cancer
Gene >> DZIP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347108 |
| Start | 95584748:95584748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2512C>T |
| AA Mutation | p.Pro838Ser(p.P838S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347108 |
| Start | 95641444:95641444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.448C>T |
| AA Mutation | p.Arg150Cys(p.R150C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347108 |
| Start | 95641359:95641359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.533A>C |
| AA Mutation | p.Lys178Thr(p.K178T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347108 |
| Start | 95589170:95589170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2011A>C |
| AA Mutation | p.Lys671Gln(p.K671Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347108 |
| Start | 95606048:95606048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1432G>T |
| AA Mutation | p.Ala478Ser(p.A478S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347108 |
| Start | 95587671:95587671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2086G>A |
| AA Mutation | p.Ala696Thr(p.A696T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347108 |
| Start | 95599410:95599410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1492T>C |
| AA Mutation | p.Ser498Pro(p.S498P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347108 |
| Start | 95633264:95633264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763110145 |
| CDS Mutation | c.655C>T |
| AA Mutation | p.Arg219Cys(p.R219C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347108 |
| Start | 95599409:95599409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755679148 |
| CDS Mutation | c.1493C>T |
| AA Mutation | p.Ser498Leu(p.S498L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347108 |
| Start | 95584854:95584854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760051137 |
| CDS Mutation | c.2406T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347108 |
| Start | 95584767:95584767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554454725 |
| CDS Mutation | c.2493C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347108 |
| Start | 95641742:95641742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.150G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347108 |
| Start | 95587645:95587645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111764824 |
| CDS Mutation | c.2112G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000347108 |
| Start | 95641656:95641656(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.236delA |
| AA Mutation | p.Lys79ArgfsTer9(p.K79Rfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000347108 |
| Start | 95586027:95586027(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2328delA |
| AA Mutation | p.Glu777LysfsTer6(p.E777Kfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000347108 |
| Start | 95584842:95584842(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2418delA |
| AA Mutation | p.Lys806AsnfsTer22(p.K806Nfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000347108 |
| Start | 95590339:95590339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756109756 |
| CDS Mutation | c.1783C>T |
| AA Mutation | p.Arg595Ter(p.R595*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |