Primary Site >> Stomach Cancer
Gene >> DLL4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249749 |
| Start | 40934997:40934997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1120G>A |
| AA Mutation | p.Gly374Arg(p.G374R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249749 |
| Start | 40936267:40936267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771130564 |
| CDS Mutation | c.1280G>A |
| AA Mutation | p.Arg427His(p.R427H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249749 |
| Start | 40932322:40932322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.725G>A |
| AA Mutation | p.Arg242His(p.R242H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249749 |
| Start | 40937439:40937439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1965A>G |
| AA Mutation | p.Ile655Met(p.I655M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249749 |
| Start | 40930087:40930087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.307C>A |
| AA Mutation | p.Leu103Ile(p.L103I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249749 |
| Start | 40931537:40931537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375261574 |
| CDS Mutation | c.429C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |