Primary Site >> Liver Cancer
Gene >> SLC2A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314251 |
| Start | 171005350:171005350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769325995 |
| CDS Mutation | c.898T>C |
| AA Mutation | p.Tyr300His(p.Y300H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314251 |
| Start | 171014566:171014566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.274C>G |
| AA Mutation | p.Leu92Val(p.L92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314251 |
| Start | 171014632:171014632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.208A>C |
| AA Mutation | p.Ile70Leu(p.I70L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000314251 |
| Start | 170998194:170998194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749710583 |
| CDS Mutation | c.1373C>A |
| AA Mutation | p.Ala458Glu(p.A458E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314251 |
| Start | 171007214:171007214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773878999 |
| CDS Mutation | c.546C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314251 |
| Start | 171014567:171014567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.273A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |