Primary Site >> Stomach Cancer
Gene >> AOC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253799 |
| Start | 42849185:42849185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1688A>T |
| AA Mutation | p.Gln563Leu(p.Q563L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253799 |
| Start | 42845706:42845706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1080G>T |
| AA Mutation | p.Gln360His(p.Q360H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253799 |
| Start | 42849239:42849239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760916686 |
| CDS Mutation | c.1742G>A |
| AA Mutation | p.Arg581His(p.R581H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253799 |
| Start | 42845806:42845806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765912640 |
| CDS Mutation | c.1180C>T |
| AA Mutation | p.Arg394Trp(p.R394W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253799 |
| Start | 42845471:42845471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845T>C |
| AA Mutation | p.Val282Ala(p.V282A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253799 |
| Start | 42845128:42845128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.502C>A |
| AA Mutation | p.Leu168Met(p.L168M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253799 |
| Start | 42846171:42846171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1545G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253799 |
| Start | 42849135:42849135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1638T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253799 |
| Start | 42845617:42845617(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.993delT |
| AA Mutation | p.Phe331LeufsTer11(p.F331Lfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253799 |
| Start | 42850322:42850322(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs779518566 |
| CDS Mutation | c.2249delC |
| AA Mutation | p.Pro750LeufsTer58(p.P750Lfs*58) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253799 |
| Start | 42845331:42845331(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.708delC |
| AA Mutation | p.Val237TrpfsTer60(p.V237Wfs*60) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253799 |
| Start | 42844924:42844924(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.303delC |
| AA Mutation | p.Lys102ArgfsTer33(p.K102Rfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253799 |
| Start | 42849137:42849137(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1644delC |
| AA Mutation | p.Trp549GlyfsTer12(p.W549Gfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |