Primary Site >> Stomach Cancer
Gene >> SLC15A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000489711 |
| Start | 121915266:121915266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.568T>A |
| AA Mutation | p.Ser190Thr(p.S190T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000489711 |
| Start | 121929344:121929344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372532662 |
| CDS Mutation | c.1549G>A |
| AA Mutation | p.Val517Met(p.V517M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000489711 |
| Start | 121928989:121928989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1349C>T |
| AA Mutation | p.Pro450Leu(p.P450L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000489711 |
| Start | 121922259:121922259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.737C>T |
| AA Mutation | p.Pro246Leu(p.P246L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000489711 |
| Start | 121923070:121923070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.898A>C |
| AA Mutation | p.Thr300Pro(p.T300P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000489711 |
| Start | 121939414:121939414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192276964 |
| CDS Mutation | c.1827G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000489711 |
| Start | 121924353:121924354(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1011dupT |
| AA Mutation | p.Val338CysfsTer23(p.V338Cfs*23) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |