Primary Site >> Stomach Cancer
Gene >> SLC23A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348729 |
| Start | 139379723:139379723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151281788 |
| CDS Mutation | c.880G>A |
| AA Mutation | p.Gly294Ser(p.G294S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348729 |
| Start | 139382586:139382586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.56C>A |
| AA Mutation | p.Pro19His(p.P19H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348729 |
| Start | 139380038:139380038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.686G>A |
| AA Mutation | p.Arg229His(p.R229H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348729 |
| Start | 139378590:139378590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1168G>A |
| AA Mutation | p.Gly390Arg(p.G390R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348729 |
| Start | 139379777:139379777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775489994 |
| CDS Mutation | c.826G>A |
| AA Mutation | p.Val276Met(p.V276M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000348729 |
| Start | 139378682:139378682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1076G>A |
| AA Mutation | p.Gly359Asp(p.G359D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348729 |
| Start | 139379715:139379715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780812554 |
| CDS Mutation | c.888C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348729 |
| Start | 139382576:139382576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755085859 |
| CDS Mutation | c.66G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |