Primary Site >> Stomach Cancer
Gene >> SLC52A3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217254 |
| Start | 761159:761159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1277G>A |
| AA Mutation | p.Arg426His(p.R426H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217254 |
| Start | 765213:765213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752459961 |
| CDS Mutation | c.562G>A |
| AA Mutation | p.Ala188Thr(p.A188T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217254 |
| Start | 763524:763524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147369439 |
| CDS Mutation | c.1047G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217254 |
| Start | 763911:763911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.660C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217254 |
| Start | 763515:763515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1056C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217254 |
| Start | 761080:761080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1356C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217254 |
| Start | 765565:765565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.210C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217254 |
| Start | 765229:765229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139965967 |
| CDS Mutation | c.546G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |