Primary Site >> Stomach Cancer
Gene >> TSPAN5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305798 |
| Start | 98476269:98476269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.661T>G |
| AA Mutation | p.Cys221Gly(p.C221G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305798 |
| Start | 98476277:98476277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202045618 |
| CDS Mutation | c.653C>T |
| AA Mutation | p.Thr218Met(p.T218M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305798 |
| Start | 98476234:98476234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.696T>A |
| AA Mutation | p.Asn232Lys(p.N232K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305798 |
| Start | 98478731:98478731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373765263 |
| CDS Mutation | c.530G>A |
| AA Mutation | p.Arg177Gln(p.R177Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305798 |
| Start | 98486764:98486764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.253C>T |
| AA Mutation | p.Arg85Trp(p.R85W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305798 |
| Start | 98486805:98486805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212T>C |
| AA Mutation | p.Val71Ala(p.V71A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305798 |
| Start | 98478718:98478718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748663851 |
| CDS Mutation | c.543C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305798 |
| Start | 98482163:98482163(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.292delC |
| AA Mutation | p.Leu98TrpfsTer14(p.L98Wfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305798 |
| Start | 98478790:98478790(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.471delT |
| AA Mutation | p.Phe157LeufsTer8(p.F157Lfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |