Primary Site >> Stomach Cancer
Gene >> DICER1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95096041:95096041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4879G>A |
| AA Mutation | p.Ala1627Thr(p.A1627T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95103372:95103372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776854466 |
| CDS Mutation | c.4024C>T |
| AA Mutation | p.Arg1342Cys(p.R1342C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95103408:95103408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3988T>C |
| AA Mutation | p.Tyr1330His(p.Y1330H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95115700:95115700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1874T>G |
| AA Mutation | p.Val625Gly(p.V625G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95096128:95096128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757177980 |
| CDS Mutation | c.4792G>A |
| AA Mutation | p.Asp1598Asn(p.D1598N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95091254:95091254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5476T>C |
| AA Mutation | p.Ser1826Pro(p.S1826P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95117662:95117662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1469G>A |
| AA Mutation | p.Arg490His(p.R490H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95091329:95091329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5401G>A |
| AA Mutation | p.Asp1801Asn(p.D1801N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95124647:95124647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.925G>A |
| AA Mutation | p.Val309Ile(p.V309I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343455 |
| Start | 95124595:95124595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.977T>C |
| AA Mutation | p.Val326Ala(p.V326A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343455 |
| Start | 95103493:95103493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3903G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343455 |
| Start | 95124648:95124648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142397473 |
| CDS Mutation | c.924C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343455 |
| Start | 95124315:95124315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1257T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343455 |
| Start | 95124243:95124243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776143079 |
| CDS Mutation | c.1329C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343455 |
| Start | 95133405:95133405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.54C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343455 |
| Start | 95103778:95103778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3618G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343455 |
| Start | 95103382:95103382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143454689 |
| CDS Mutation | c.4014G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |