Primary Site >> Stomach Cancer
Gene >> BMPR1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372037 |
| Start | 86923438:86923438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1405G>C |
| AA Mutation | p.Asp469His(p.D469H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372037 |
| Start | 86917210:86917210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.752G>A |
| AA Mutation | p.Gly251Asp(p.G251D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372037 |
| Start | 86899870:86899870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.410C>T |
| AA Mutation | p.Thr137Ile(p.T137I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372037 |
| Start | 86917234:86917234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.776C>T |
| AA Mutation | p.Ala259Val(p.A259V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372037 |
| Start | 86919429:86919429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1126T>C |
| AA Mutation | p.Cys376Arg(p.C376R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000372037 |
| Start | 86919469:86919469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1166G>T |
| AA Mutation | p.Ser389Ile(p.S389I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372037 |
| Start | 86917318:86917318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.860A>G |
| AA Mutation | p.Asn287Ser(p.N287S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372037 |
| Start | 86923381:86923381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs55932635 |
| CDS Mutation | c.1348G>A |
| AA Mutation | p.Val450Met(p.V450M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000372037 |
| Start | 86890165:86890165(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.176delT |
| AA Mutation | p.Leu59Ter(p.L59*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000372037 |
| Start | 86923600:86923600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs786201040 |
| CDS Mutation | c.1480C>T |
| AA Mutation | p.Arg494Ter(p.R494*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000372037 |
| Start | 86917216:86917216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.758G>A |
| AA Mutation | p.Trp253Ter(p.W253*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000372037 |
| Start | 86921668:86921668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1315G>T |
| AA Mutation | p.Glu439Ter(p.E439*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000372037 |
| Start | 86899882:86899883(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.424_428dupGTCAT |
| AA Mutation | p.Ile143MetfsTer3(p.I143Mfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000372037 |
| Start | 86892216:86892217(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.324dupT |
| AA Mutation | p.Gln109SerfsTer23(p.Q109Sfs*23) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000372037 |
| Start | 86890226:86890226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.230+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |