Primary Site >> Stomach Cancer
Gene >> SLC2A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426263 |
| Start | 42930631:42930631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.511G>A |
| AA Mutation | p.Ala171Thr(p.A171T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426263 |
| Start | 42931187:42931187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.134A>G |
| AA Mutation | p.Asn45Ser(p.N45S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426263 |
| Start | 42931190:42931190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.131A>G |
| AA Mutation | p.Tyr44Cys(p.Y44C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426263 |
| Start | 42929899:42929899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374080633 |
| CDS Mutation | c.653G>A |
| AA Mutation | p.Arg218His(p.R218H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426263 |
| Start | 42927687:42927687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1196C>A |
| AA Mutation | p.Pro399Gln(p.P399Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426263 |
| Start | 42931056:42931056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.265C>T |
| AA Mutation | p.Arg89Cys(p.R89C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000426263 |
| Start | 42927713:42927713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2236574 |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000426263 |
| Start | 42927668:42927668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769506294 |
| CDS Mutation | c.1215C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000426263 |
| Start | 42928944:42928944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748983257 |
| CDS Mutation | c.1062G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000426263 |
| Start | 42930803:42930803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755571737 |
| CDS Mutation | c.339G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |