Primary Site >> Stomach Cancer
Gene >> TM9SF3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371142 |
| Start | 96528127:96528127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1445G>A |
| AA Mutation | p.Gly482Asp(p.G482D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371142 |
| Start | 96565319:96565319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.406G>A |
| AA Mutation | p.Asp136Asn(p.D136N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371142 |
| Start | 96533115:96533115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1261T>C |
| AA Mutation | p.Ser421Pro(p.S421P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371142 |
| Start | 96562084:96562084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.476A>C |
| AA Mutation | p.Lys159Thr(p.K159T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371142 |
| Start | 96547970:96547970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.979A>G |
| AA Mutation | p.Thr327Ala(p.T327A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371142 |
| Start | 96559688:96559688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.631T>C |
| AA Mutation | p.Tyr211His(p.Y211H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371142 |
| Start | 96544167:96544167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1094T>G |
| AA Mutation | p.Leu365Arg(p.L365R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371142 |
| Start | 96544160:96544160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1101A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371142 |
| Start | 96528162:96528162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370713295 |
| CDS Mutation | c.1410G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371142 |
| Start | 96533164:96533164(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1212delT |
| AA Mutation | p.Phe404LeufsTer6(p.F404Lfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371142 |
| Start | 96527261:96527261(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1654delT |
| AA Mutation | p.Tyr552ThrfsTer14(p.Y552Tfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371142 |
| Start | 96576718:96576718(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773566859 |
| CDS Mutation | c.214delA |
| AA Mutation | p.Ser72ValfsTer31(p.S72Vfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |