Primary Site >> Stomach Cancer
Gene >> MAPK4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400384 |
| Start | 50729201:50729201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754538065 |
| CDS Mutation | c.1111C>T |
| AA Mutation | p.Arg371Trp(p.R371W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400384 |
| Start | 50729213:50729213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554214382 |
| CDS Mutation | c.1123G>A |
| AA Mutation | p.Ala375Thr(p.A375T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400384 |
| Start | 50664128:50664128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373566179 |
| CDS Mutation | c.170G>A |
| AA Mutation | p.Arg57His(p.R57H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400384 |
| Start | 50715178:50715178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767125390 |
| CDS Mutation | c.646G>A |
| AA Mutation | p.Gly216Ser(p.G216S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400384 |
| Start | 50729421:50729421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1331G>A |
| AA Mutation | p.Arg444His(p.R444H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400384 |
| Start | 50715142:50715142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.610A>G |
| AA Mutation | p.Asn204Asp(p.N204D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400384 |
| Start | 50664481:50664481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761132815 |
| CDS Mutation | c.523G>A |
| AA Mutation | p.Val175Ile(p.V175I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400384 |
| Start | 50664391:50664391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752206576 |
| CDS Mutation | c.433G>A |
| AA Mutation | p.Val145Met(p.V145M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400384 |
| Start | 50729764:50729764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1674C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400384 |
| Start | 50715162:50715162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.630C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400384 |
| Start | 50729332:50729332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776241189 |
| CDS Mutation | c.1242G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |