Primary Site >> Stomach Cancer
Gene >> MAPK15
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338033 |
| Start | 143721327:143721327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371482487 |
| CDS Mutation | c.1120G>A |
| AA Mutation | p.Asp374Asn(p.D374N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338033 |
| Start | 143722192:143722192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1576G>T |
| AA Mutation | p.Gly526Trp(p.G526W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338033 |
| Start | 143722144:143722144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1528G>A |
| AA Mutation | p.Ala510Thr(p.A510T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338033 |
| Start | 143721646:143721646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1302G>T |
| AA Mutation | p.Lys434Asn(p.K434N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338033 |
| Start | 143721831:143721831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs576245505 |
| CDS Mutation | c.1409G>A |
| AA Mutation | p.Arg470Gln(p.R470Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338033 |
| Start | 143720797:143720797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185466475 |
| CDS Mutation | c.874C>T |
| AA Mutation | p.Arg292Trp(p.R292W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338033 |
| Start | 143721653:143721653(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1314delC |
| AA Mutation | p.Leu439Ter(p.L439*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338033 |
| Start | 143722149:143722149(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs782558070 |
| CDS Mutation | c.1538delG |
| AA Mutation | p.Gly513ValfsTer?(p.G513Vfs*?) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |