Primary Site >> Stomach Cancer
Gene >> CAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372792 |
| Start | 40070459:40070459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1147G>A |
| AA Mutation | p.Asp383Asn(p.D383N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372792 |
| Start | 40064242:40064242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.310T>A |
| AA Mutation | p.Leu104Met(p.L104M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372792 |
| Start | 40070482:40070482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1170G>C |
| AA Mutation | p.Glu390Asp(p.E390D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372792 |
| Start | 40069755:40069755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781671919 |
| CDS Mutation | c.874C>A |
| AA Mutation | p.Pro292Thr(p.P292T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372792 |
| Start | 40059404:40059404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.58G>A |
| AA Mutation | p.Ala20Thr(p.A20T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372792 |
| Start | 40070222:40070222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1057A>T |
| AA Mutation | p.Ile353Leu(p.I353L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372792 |
| Start | 40064283:40064283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.351C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372792 |
| Start | 40067587:40067587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201296194 |
| CDS Mutation | c.678C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |