Primary Site >> Stomach Cancer
Gene >> RAPGEF5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401957 |
| Start | 22167088:22167088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.356G>A |
| AA Mutation | p.Cys119Tyr(p.C119Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401957 |
| Start | 22157880:22157880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776916179 |
| CDS Mutation | c.623T>C |
| AA Mutation | p.Val208Ala(p.V208A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401957 |
| Start | 22136104:22136104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1441G>A |
| AA Mutation | p.Ala481Thr(p.A481T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401957 |
| Start | 22157878:22157878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.625G>A |
| AA Mutation | p.Asp209Asn(p.D209N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401957 |
| Start | 22145048:22145048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1273G>A |
| AA Mutation | p.Ala425Thr(p.A425T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000401957 |
| Start | 22167120:22167120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777857472 |
| CDS Mutation | c.324G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000401957 |
| Start | 22157856:22157856(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs770990761 |
| CDS Mutation | c.647delA |
| AA Mutation | p.Lys216ArgfsTer22(p.K216Rfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000401957 |
| Start | 22136082:22136082(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1463delA |
| AA Mutation | p.Lys488ArgfsTer2(p.K488Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344041 |
| Start | 22266978:22266979(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.322_323insC |
| AA Mutation | p.Lys108ThrfsTer8(p.K108Tfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |