Primary Site >> Stomach Cancer
Gene >> TFPI2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222543 |
| Start | 93889157:93889157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.338A>C |
| AA Mutation | p.Tyr113Ser(p.Y113S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222543 |
| Start | 93890311:93890311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.97G>A |
| AA Mutation | p.Ala33Thr(p.A33T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222543 |
| Start | 93890310:93890310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.98C>T |
| AA Mutation | p.Ala33Val(p.A33V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222543 |
| Start | 93890665:93890665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14G>A |
| AA Mutation | p.Arg5His(p.R5H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222543 |
| Start | 93889114:93889114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781284648 |
| CDS Mutation | c.381C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222543 |
| Start | 93890222:93890222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.186C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222543 |
| Start | 93887319:93887319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.573T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222543 |
| Start | 93887382:93887382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.510T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222543 |
| Start | 93890205:93890205(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs768025475 |
| CDS Mutation | c.203delG |
| AA Mutation | p.Gly68AlafsTer22(p.G68Afs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |