Primary Site >> Stomach Cancer
Gene >> AKAP4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50192801:50192801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1912C>T |
| AA Mutation | p.Leu638Phe(p.L638F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50197590:50197590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.128G>A |
| AA Mutation | p.Cys43Tyr(p.C43Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50194265:50194265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.448G>T |
| AA Mutation | p.Ala150Ser(p.A150S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50193497:50193497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1216G>A |
| AA Mutation | p.Ala406Thr(p.A406T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50193584:50193584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1129G>A |
| AA Mutation | p.Glu377Lys(p.E377K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50193281:50193281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1432G>A |
| AA Mutation | p.Asp478Asn(p.D478N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50193854:50193854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782646030 |
| CDS Mutation | c.859C>T |
| AA Mutation | p.Arg287Cys(p.R287C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50194301:50194301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.412C>T |
| AA Mutation | p.His138Tyr(p.H138Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50192605:50192605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2108C>T |
| AA Mutation | p.Ser703Phe(p.S703F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50193441:50193441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1272G>T |
| AA Mutation | p.Glu424Asp(p.E424D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50194151:50194151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.562A>G |
| AA Mutation | p.Asn188Asp(p.N188D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358526 |
| Start | 50193917:50193917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.796C>G |
| AA Mutation | p.Pro266Ala(p.P266A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358526 |
| Start | 50194050:50194050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.663C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358526 |
| Start | 50192934:50192934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1779C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358526 |
| Start | 50193573:50193573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140947270 |
| CDS Mutation | c.1140C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358526 |
| Start | 50194278:50194278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.435C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358526 |
| Start | 50192913:50192913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781891685 |
| CDS Mutation | c.1800A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358526 |
| Start | 50192863:50192885(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1828_1850delTCCACCTGTCAAAAGGAGAACCA |
| AA Mutation | p.Ser610ThrfsTer22(p.S610Tfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |