Primary Site >> Stomach Cancer
Gene >> DYRK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67657109:67657109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.202G>A |
| AA Mutation | p.Gly68Ser(p.G68S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67657806:67657806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575789813 |
| CDS Mutation | c.899C>T |
| AA Mutation | p.Thr300Met(p.T300M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67657689:67657689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752139842 |
| CDS Mutation | c.782G>A |
| AA Mutation | p.Arg261Gln(p.R261Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67657728:67657728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.821G>A |
| AA Mutation | p.Arg274Gln(p.R274Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67658354:67658354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748801595 |
| CDS Mutation | c.1447C>T |
| AA Mutation | p.Arg483Trp(p.R483W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67657142:67657142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.235C>T |
| AA Mutation | p.His79Tyr(p.H79Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67658157:67658157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140246773 |
| CDS Mutation | c.1250C>T |
| AA Mutation | p.Thr417Met(p.T417M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67657589:67657589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.682A>G |
| AA Mutation | p.Ile228Val(p.I228V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67657478:67657478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.571C>T |
| AA Mutation | p.Arg191Cys(p.R191C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67657628:67657628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.721G>A |
| AA Mutation | p.Asp241Asn(p.D241N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344096 |
| Start | 67658295:67658295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573469138 |
| CDS Mutation | c.1388G>A |
| AA Mutation | p.Arg463His(p.R463H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344096 |
| Start | 67657111:67657111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758935204 |
| CDS Mutation | c.204C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |