Primary Site >> Stomach Cancer
Gene >> SLC38A3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000614032 |
| Start | 50215574:50215574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780477983 |
| CDS Mutation | c.404G>A |
| AA Mutation | p.Arg135His(p.R135H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000614032 |
| Start | 50217423:50217423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.640G>A |
| AA Mutation | p.Gly214Ser(p.G214S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000614032 |
| Start | 50217252:50217252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.563A>G |
| AA Mutation | p.Asn188Ser(p.N188S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000614032 |
| Start | 50214708:50214708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.239T>C |
| AA Mutation | p.Met80Thr(p.M80T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000614032 |
| Start | 50215604:50215604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.434C>T |
| AA Mutation | p.Ala145Val(p.A145V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000614032 |
| Start | 50214259:50214259(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.63delG |
| AA Mutation | p.Leu22CysfsTer82(p.L22Cfs*82) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |