Primary Site >> Stomach Cancer
Gene >> SLC6A7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230671 |
| Start | 150203687:150203687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751132449 |
| CDS Mutation | c.1108G>A |
| AA Mutation | p.Val370Ile(p.V370I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230671 |
| Start | 150205588:150205588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1666G>T |
| AA Mutation | p.Val556Leu(p.V556L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230671 |
| Start | 150204000:150204000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139016893 |
| CDS Mutation | c.1294G>A |
| AA Mutation | p.Val432Met(p.V432M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230671 |
| Start | 150202429:150202429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941C>T |
| AA Mutation | p.Thr314Met(p.T314M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230671 |
| Start | 150202607:150202607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142379630 |
| CDS Mutation | c.991G>A |
| AA Mutation | p.Ala331Thr(p.A331T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230671 |
| Start | 150209517:150209517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1813A>T |
| AA Mutation | p.Met605Leu(p.M605L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230671 |
| Start | 150201143:150201143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145923003 |
| CDS Mutation | c.778C>T |
| AA Mutation | p.Arg260Cys(p.R260C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230671 |
| Start | 150204921:150204921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1527G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230671 |
| Start | 150197127:150197127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749927944 |
| CDS Mutation | c.435C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230671 |
| Start | 150197109:150197109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767456458 |
| CDS Mutation | c.417C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |