Primary Site >> Stomach Cancer
Gene >> SLC12A3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000563236 |
| Start | 56884162:56884162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201432183 |
| CDS Mutation | c.1783G>A |
| AA Mutation | p.Val595Met(p.V595M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000563236 |
| Start | 56872740:56872740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778585043 |
| CDS Mutation | c.1049C>T |
| AA Mutation | p.Ser350Leu(p.S350L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000563236 |
| Start | 56890318:56890318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768517795 |
| CDS Mutation | c.2330G>A |
| AA Mutation | p.Arg777Gln(p.R777Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000563236 |
| Start | 56879566:56879566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145929729 |
| CDS Mutation | c.1360G>A |
| AA Mutation | p.Ala454Thr(p.A454T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000563236 |
| Start | 56879087:56879087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775931992 |
| CDS Mutation | c.1195C>T |
| AA Mutation | p.Arg399Cys(p.R399C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000563236 |
| Start | 56884085:56884085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79351185 |
| CDS Mutation | c.1706C>T |
| AA Mutation | p.Ala569Val(p.A569V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000563236 |
| Start | 56870677:56870677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776260447 |
| CDS Mutation | c.793G>A |
| AA Mutation | p.Val265Met(p.V265M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000563236 |
| Start | 56869756:56869756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772589653 |
| CDS Mutation | c.533C>T |
| AA Mutation | p.Ser178Leu(p.S178L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000563236 |
| Start | 56869757:56869757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140931462 |
| CDS Mutation | c.534G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000563236 |
| Start | 56879568:56879568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372425406 |
| CDS Mutation | c.1362G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000563236 |
| Start | 56886389:56886389(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1956delC |
| AA Mutation | p.Asn653ThrfsTer19(p.N653Tfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000563236 |
| Start | 56870218:56870218(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.724delG |
| AA Mutation | p.Val242CysfsTer60(p.V242Cfs*60) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000563236 |
| Start | 56872415:56872416(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.923dupC |
| AA Mutation | p.Ser309IlefsTer2(p.S309Ifs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000563236 |
| Start | 56892985:56892986(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2454dupC |
| AA Mutation | p.Thr819HisfsTer20(p.T819Hfs*20) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |