Primary Site >> Stomach Cancer
Gene >> SLC9C1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305815 |
| Start | 112278839:112278839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776718397 |
| CDS Mutation | c.208G>A |
| AA Mutation | p.Ala70Thr(p.A70T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305815 |
| Start | 112217452:112217452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1780G>T |
| AA Mutation | p.Gly594Cys(p.G594C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305815 |
| Start | 112202376:112202376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2196A>C |
| AA Mutation | p.Gln732His(p.Q732H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305815 |
| Start | 112264254:112264254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968A>G |
| AA Mutation | p.Glu323Gly(p.E323G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305815 |
| Start | 112208218:112208218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1946A>G |
| AA Mutation | p.Tyr649Cys(p.Y649C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305815 |
| Start | 112278776:112278776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.271A>G |
| AA Mutation | p.Thr91Ala(p.T91A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305815 |
| Start | 112264334:112264334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.888T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305815 |
| Start | 112202310:112202310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2262A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305815 |
| Start | 112204239:112204239(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2151delT |
| AA Mutation | p.Arg718ValfsTer9(p.R718Vfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305815 |
| Start | 112266270:112266270(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.846delT |
| AA Mutation | p.Phe282LeufsTer32(p.F282Lfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305815 |
| Start | 112169259:112169259(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2989delA |
| AA Mutation | p.Met997CysfsTer3(p.M997Cfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305815 |
| Start | 112286763:112286763(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs770572006 |
| CDS Mutation | c.29delT |
| AA Mutation | p.Phe10SerfsTer11(p.F10Sfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305815 |
| Start | 112204376:112204376(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761139813 |
| CDS Mutation | c.2014delT |
| AA Mutation | p.Ser672HisfsTer9(p.S672Hfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305815 |
| Start | 112286762:112286763(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs749004401 |
| CDS Mutation | c.29dupT |
| AA Mutation | p.Ser11GlnfsTer3(p.S11Qfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |