Primary Site >> Stomach Cancer
Gene >> ADAM10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260408 |
| Start | 58621556:58621556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1426A>G |
| AA Mutation | p.Ser476Gly(p.S476G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260408 |
| Start | 58627853:58627853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1207G>A |
| AA Mutation | p.Glu403Lys(p.E403K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260408 |
| Start | 58633223:58633223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201536086 |
| CDS Mutation | c.1149C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260408 |
| Start | 58621493:58621493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260408 |
| Start | 58717604:58717604(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.179delT |
| AA Mutation | p.Leu60TyrfsTer3(p.L60Yfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260408 |
| Start | 58610345:58610345(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1977delA |
| AA Mutation | p.Ala660GlnfsTer29(p.A660Qfs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260408 |
| Start | 58717648:58717648(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.135delA |
| AA Mutation | p.Lys45AsnfsTer18(p.K45Nfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |