Primary Site >> Stomach Cancer
Gene >> PTER
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378000 |
| Start | 16511209:16511209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1003G>A |
| AA Mutation | p.Asp335Asn(p.D335N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378000 |
| Start | 16511050:16511050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376388470 |
| CDS Mutation | c.844C>T |
| AA Mutation | p.Arg282Cys(p.R282C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378000 |
| Start | 16484546:16484546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.162G>T |
| AA Mutation | p.Met54Ile(p.M54I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378000 |
| Start | 16511245:16511245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1039A>C |
| AA Mutation | p.Thr347Pro(p.T347P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | stop_retained_variant |
| Transcription ID | ENST00000378000 |
| Start | 16511256:16511256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1050G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378000 |
| Start | 16486543:16486543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.624A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378000 |
| Start | 16484547:16484547(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.167delA |
| AA Mutation | p.Asn56IlefsTer18(p.N56Ifs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378000 |
| Start | 16484568:16484568(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.188delA |
| AA Mutation | p.Asn63ThrfsTer11(p.N63Tfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000378000 |
| Start | 16486559:16486559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370033967 |
| CDS Mutation | c.640C>T |
| AA Mutation | p.Arg214Ter(p.R214*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |