Primary Site >> Stomach Cancer
Gene >> BMP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378827 |
| Start | 6770258:6770258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.132G>T |
| AA Mutation | p.Gln44His(p.Q44H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378827 |
| Start | 6778676:6778676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.778A>G |
| AA Mutation | p.Ile260Val(p.I260V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378827 |
| Start | 6778589:6778589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.691G>T |
| AA Mutation | p.Ala231Ser(p.A231S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378827 |
| Start | 6778973:6778973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1075G>C |
| AA Mutation | p.Ala359Pro(p.A359P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378827 |
| Start | 6778804:6778804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374065751 |
| CDS Mutation | c.906C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378827 |
| Start | 6778576:6778576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770008690 |
| CDS Mutation | c.678C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378827 |
| Start | 6778527:6778527(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.633delC |
| AA Mutation | p.Ala212LeufsTer2(p.A212Lfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378827 |
| Start | 6778847:6778847(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.953delC |
| AA Mutation | p.Pro318ArgfsTer20(p.P318Rfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378827 |
| Start | 6778315:6778315(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.420delC |
| AA Mutation | p.Thr141ArgfsTer21(p.T141Rfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000378827 |
| Start | 6779032:6779033(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1135_1158dupAAGGTTGTATTAAAGAACTATCAG |
| AA Mutation | p.Lys379_Gln386dup(p.K379_Q386dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |