Primary Site >> Stomach Cancer
Gene >> PGK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373316 |
| Start | 78124902:78124902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.965A>G |
| AA Mutation | p.Lys322Arg(p.K322R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373316 |
| Start | 78125802:78125802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1226C>A |
| AA Mutation | p.Pro409His(p.P409H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373316 |
| Start | 78104366:78104366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.26T>G |
| AA Mutation | p.Leu9Arg(p.L9R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373316 |
| Start | 78123232:78123232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.794T>C |
| AA Mutation | p.Ile265Thr(p.I265T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373316 |
| Start | 78114107:78114107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.364C>A |
| AA Mutation | p.Leu122Ile(p.L122I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373316 |
| Start | 78123359:78123359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.921A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373316 |
| Start | 78123233:78123233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.795T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373316 |
| Start | 78117320:78117320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201516932 |
| CDS Mutation | c.426C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |