Primary Site >> Stomach Cancer
Gene >> DLL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205143 |
| Start | 39504263:39504263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368487646 |
| CDS Mutation | c.845C>T |
| AA Mutation | p.Pro282Leu(p.P282L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205143 |
| Start | 39507078:39507078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1133G>A |
| AA Mutation | p.Arg378His(p.R378H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205143 |
| Start | 39507922:39507922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1766C>T |
| AA Mutation | p.Thr589Met(p.T589M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205143 |
| Start | 39505248:39505248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.890A>T |
| AA Mutation | p.Glu297Val(p.E297V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205143 |
| Start | 39507952:39507952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1796G>A |
| AA Mutation | p.Arg599His(p.R599H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205143 |
| Start | 39507317:39507317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1372G>A |
| AA Mutation | p.Gly458Ser(p.G458S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000205143 |
| Start | 39505273:39505273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372702131 |
| CDS Mutation | c.915C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000205143 |
| Start | 39507331:39507331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1386G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000205143 |
| Start | 39505261:39505261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148016836 |
| CDS Mutation | c.903G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000205143 |
| Start | 39507559:39507559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1614C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000205143 |
| Start | 39504164:39504164(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.746delC |
| AA Mutation | p.Thr249ArgfsTer63(p.T249Rfs*63) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000205143 |
| Start | 39507976:39507976(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1824delT |
| AA Mutation | p.Tyr610ThrfsTer8(p.Y610Tfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000205143 |
| Start | 39507932:39507932(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776323833 |
| CDS Mutation | c.1781delC |
| AA Mutation | p.Pro594ArgfsTer24(p.P594Rfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |