Primary Site >> Stomach Cancer
Gene >> MAPKAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265960 |
| Start | 125444530:125444530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759492877 |
| CDS Mutation | c.1414G>A |
| AA Mutation | p.Ala472Thr(p.A472T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265960 |
| Start | 125585625:125585625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377752331 |
| CDS Mutation | c.601G>A |
| AA Mutation | p.Ala201Thr(p.A201T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265960 |
| Start | 125484445:125484445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1205T>C |
| AA Mutation | p.Leu402Pro(p.L402P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265960 |
| Start | 125657716:125657716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.433C>T |
| AA Mutation | p.Arg145Cys(p.R145C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265960 |
| Start | 125506364:125506364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1012G>T |
| AA Mutation | p.Asp338Tyr(p.D338Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265960 |
| Start | 125506405:125506405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779168610 |
| CDS Mutation | c.971G>A |
| AA Mutation | p.Arg324His(p.R324H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265960 |
| Start | 125672328:125672328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.247C>T |
| AA Mutation | p.Arg83Cys(p.R83C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265960 |
| Start | 125672487:125672487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.88G>A |
| AA Mutation | p.Val30Ile(p.V30I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265960 |
| Start | 125559752:125559752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.729C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265960 |
| Start | 125585602:125585602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746312500 |
| CDS Mutation | c.624G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265960 |
| Start | 125559741:125559741(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.740delC |
| AA Mutation | p.Pro247ArgfsTer27(p.P247Rfs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265960 |
| Start | 125669887:125669887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.280C>T |
| AA Mutation | p.Arg94Ter(p.R94*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |