Primary Site >> Stomach Cancer
Gene >> CORO1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341356 |
| Start | 67440140:67440140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761036671 |
| CDS Mutation | c.985G>A |
| AA Mutation | p.Val329Ile(p.V329I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341356 |
| Start | 67441346:67441346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.623G>A |
| AA Mutation | p.Gly208Asp(p.G208D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341356 |
| Start | 67438419:67438419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2286624 |
| CDS Mutation | c.1427G>T |
| AA Mutation | p.Arg476Leu(p.R476L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341356 |
| Start | 67441216:67441216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747383937 |
| CDS Mutation | c.665G>A |
| AA Mutation | p.Arg222Gln(p.R222Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341356 |
| Start | 67441175:67441175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.706A>G |
| AA Mutation | p.Thr236Ala(p.T236A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341356 |
| Start | 67441149:67441149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.732G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341356 |
| Start | 67442008:67442008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774302969 |
| CDS Mutation | c.282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341356 |
| Start | 67438433:67438433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530415676 |
| CDS Mutation | c.1413C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000341356 |
| Start | 67440388:67440388(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.808delG |
| AA Mutation | p.Ala270ProfsTer38(p.A270Pfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |