Primary Site >> Stomach Cancer
Gene >> TPP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299427 |
| Start | 6615295:6615295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1301C>A |
| AA Mutation | p.Pro434His(p.P434H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299427 |
| Start | 6616487:6616487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.903G>T |
| AA Mutation | p.Gln301His(p.Q301H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299427 |
| Start | 6616804:6616804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.743G>T |
| AA Mutation | p.Gly248Val(p.G248V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299427 |
| Start | 6617690:6617690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.316G>A |
| AA Mutation | p.Ala106Thr(p.A106T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299427 |
| Start | 6617045:6617045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121908209 |
| CDS Mutation | c.617G>A |
| AA Mutation | p.Arg206His(p.R206H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299427 |
| Start | 6616842:6616842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.705C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299427 |
| Start | 6617353:6617353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.456G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299427 |
| Start | 6617017:6617017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766845531 |
| CDS Mutation | c.645C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299427 |
| Start | 6614968:6614968(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1449delG |
| AA Mutation | p.Ile484SerfsTer4(p.I484Sfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299427 |
| Start | 6614921:6614921(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1496delC |
| AA Mutation | p.Pro499LeufsTer20(p.P499Lfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000299427 |
| Start | 6617040:6617040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs119455955 |
| CDS Mutation | c.622C>T |
| AA Mutation | p.Arg208Ter(p.R208*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |