Primary Site >> Stomach Cancer
Gene >> PLAGL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246229 |
| Start | 32197116:32197116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.827T>C |
| AA Mutation | p.Leu276Pro(p.L276P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246229 |
| Start | 32197041:32197041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.902A>G |
| AA Mutation | p.His301Arg(p.H301R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246229 |
| Start | 32197296:32197296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760026877 |
| CDS Mutation | c.647G>A |
| AA Mutation | p.Arg216His(p.R216H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246229 |
| Start | 32197203:32197203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.740T>G |
| AA Mutation | p.Leu247Arg(p.L247R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246229 |
| Start | 32197326:32197326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.617T>C |
| AA Mutation | p.Val206Ala(p.V206A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246229 |
| Start | 32201966:32201966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.213T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246229 |
| Start | 32197016:32197016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.927C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246229 |
| Start | 32196779:32196779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373499646 |
| CDS Mutation | c.1164G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |