Primary Site >> Stomach Cancer
Gene >> PLAT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220809 |
| Start | 42193127:42193127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.59T>G |
| AA Mutation | p.Val20Gly(p.V20G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220809 |
| Start | 42178905:42178905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774851580 |
| CDS Mutation | c.1522G>A |
| AA Mutation | p.Ala508Thr(p.A508T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220809 |
| Start | 42176144:42176144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747692088 |
| CDS Mutation | c.1538C>T |
| AA Mutation | p.Ser513Leu(p.S513L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220809 |
| Start | 42193131:42193131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.55T>C |
| AA Mutation | p.Phe19Leu(p.F19L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220809 |
| Start | 42180509:42180509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140012141 |
| CDS Mutation | c.1066G>A |
| AA Mutation | p.Ala356Thr(p.A356T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220809 |
| Start | 42181969:42181969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.857T>C |
| AA Mutation | p.Leu286Pro(p.L286P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220809 |
| Start | 42180009:42180009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776556278 |
| CDS Mutation | c.1280G>A |
| AA Mutation | p.Arg427His(p.R427H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220809 |
| Start | 42180372:42180372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374730133 |
| CDS Mutation | c.1092G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220809 |
| Start | 42187499:42187499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536186900 |
| CDS Mutation | c.438C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |