Primary Site >> Stomach Cancer
Gene >> SLC38A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398637 |
| Start | 46229190:46229190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200255614 |
| CDS Mutation | c.277G>A |
| AA Mutation | p.Ala93Thr(p.A93T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398637 |
| Start | 46204308:46204308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.815A>C |
| AA Mutation | p.Asn272Thr(p.N272T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398637 |
| Start | 46189022:46189022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1412C>T |
| AA Mutation | p.Pro471Leu(p.P471L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398637 |
| Start | 46198672:46198672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1075G>A |
| AA Mutation | p.Ala359Thr(p.A359T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398637 |
| Start | 46198738:46198738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1009G>A |
| AA Mutation | p.Val337Met(p.V337M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398637 |
| Start | 46209108:46209108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.334A>G |
| AA Mutation | p.Thr112Ala(p.T112A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398637 |
| Start | 46204331:46204331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.792T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398637 |
| Start | 46201153:46201153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148875371 |
| CDS Mutation | c.948C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |