Primary Site >> Stomach Cancer
Gene >> SLC6A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55672157:55672157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761057170 |
| CDS Mutation | c.626C>T |
| AA Mutation | p.Pro209Leu(p.P209L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55671964:55671964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.433G>A |
| AA Mutation | p.Ala145Thr(p.A145T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55656905:55656905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.211G>A |
| AA Mutation | p.Gly71Ser(p.G71S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55685247:55685247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.749T>G |
| AA Mutation | p.Phe250Cys(p.F250C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55694025:55694025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776659407 |
| CDS Mutation | c.934G>A |
| AA Mutation | p.Ala312Thr(p.A312T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55656929:55656929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.235G>A |
| AA Mutation | p.Val79Met(p.V79M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55656890:55656890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.196C>A |
| AA Mutation | p.Leu66Met(p.L66M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55672013:55672013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.482A>T |
| AA Mutation | p.Tyr161Phe(p.Y161F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55685151:55685151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.653T>C |
| AA Mutation | p.Val218Ala(p.V218A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55656767:55656767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.73C>A |
| AA Mutation | p.Leu25Ile(p.L25I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55692036:55692036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147833183 |
| CDS Mutation | c.902G>A |
| AA Mutation | p.Arg301His(p.R301H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379906 |
| Start | 55695333:55695333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1078G>A |
| AA Mutation | p.Ala360Thr(p.A360T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379906 |
| Start | 55656910:55656910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.216C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379906 |
| Start | 55656898:55656898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.204C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379906 |
| Start | 55696304:55696304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149035289 |
| CDS Mutation | c.1227C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |