Primary Site >> Stomach Cancer
Gene >> COASY
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393818 |
| Start | 42565241:42565241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1317A>G |
| AA Mutation | p.Ile439Met(p.I439M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393818 |
| Start | 42563040:42563040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.418T>G |
| AA Mutation | p.Cys140Gly(p.C140G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393818 |
| Start | 42562951:42562951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.329C>T |
| AA Mutation | p.Pro110Leu(p.P110L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393818 |
| Start | 42564124:42564124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370902320 |
| CDS Mutation | c.864C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393818 |
| Start | 42564160:42564160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.900C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393818 |
| Start | 42562952:42562952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.330G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000393818 |
| Start | 42564097:42564097(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.840delC |
| AA Mutation | p.Ser281ProfsTer38(p.S281Pfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |