Primary Site >> Stomach Cancer
Gene >> ADAM17
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310823 |
| Start | 9536767:9536767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292G>C |
| AA Mutation | p.Val98Leu(p.V98L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310823 |
| Start | 9526193:9526193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548923032 |
| CDS Mutation | c.671C>T |
| AA Mutation | p.Thr224Met(p.T224M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310823 |
| Start | 9543177:9543177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.206T>C |
| AA Mutation | p.Leu69Pro(p.L69P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310823 |
| Start | 9491109:9491109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778028713 |
| CDS Mutation | c.2125C>T |
| AA Mutation | p.His709Tyr(p.H709Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310823 |
| Start | 9490235:9490235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2417C>T |
| AA Mutation | p.Ala806Val(p.A806V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310823 |
| Start | 9536705:9536705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373534760 |
| CDS Mutation | c.354C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |