Primary Site >> Stomach Cancer
Gene >> AKAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337714 |
| Start | 57106251:57106251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.787G>A |
| AA Mutation | p.Val263Ile(p.V263I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337714 |
| Start | 57114483:57114483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756066356 |
| CDS Mutation | c.2128G>A |
| AA Mutation | p.Val710Met(p.V710M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337714 |
| Start | 57107038:57107038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775916699 |
| CDS Mutation | c.1574C>T |
| AA Mutation | p.Ser525Leu(p.S525L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337714 |
| Start | 57111827:57111827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1878G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337714 |
| Start | 57116148:57116148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2319C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337714 |
| Start | 57111824:57111824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1875G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337714 |
| Start | 57118412:57118412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2532C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337714 |
| Start | 57106466:57106466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561844082 |
| CDS Mutation | c.1002T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000337714 |
| Start | 57105631:57105631(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.168delA |
| AA Mutation | p.Glu56AspfsTer12(p.E56Dfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |