Primary Site >> Stomach Cancer
Gene >> SLC4A8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453097 |
| Start | 51488796:51488796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2384T>G |
| AA Mutation | p.Ile795Ser(p.I795S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453097 |
| Start | 51450971:51450971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.226C>T |
| AA Mutation | p.Arg76Trp(p.R76W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000453097 |
| Start | 51453539:51453539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.414G>C |
| AA Mutation | p.Arg138Ser(p.R138S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453097 |
| Start | 51488714:51488714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2302C>T |
| AA Mutation | p.Arg768Cys(p.R768C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453097 |
| Start | 51488777:51488777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2365C>A |
| AA Mutation | p.Pro789Thr(p.P789T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453097 |
| Start | 51462420:51462420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1212C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453097 |
| Start | 51462360:51462360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775473317 |
| CDS Mutation | c.1152G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |