Primary Site >> Stomach Cancer
Gene >> DTX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257600 |
| Start | 113077431:113077431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.267G>A |
| AA Mutation | p.Met89Ile(p.M89I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257600 |
| Start | 113093542:113093542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1007T>C |
| AA Mutation | p.Met336Thr(p.M336T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257600 |
| Start | 113095377:113095377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771660342 |
| CDS Mutation | c.1601G>A |
| AA Mutation | p.Arg534His(p.R534H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257600 |
| Start | 113058314:113058314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.122C>T |
| AA Mutation | p.Thr41Met(p.T41M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257600 |
| Start | 113077577:113077577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.413C>T |
| AA Mutation | p.Pro138Leu(p.P138L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257600 |
| Start | 113077469:113077469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.305C>T |
| AA Mutation | p.Ala102Val(p.A102V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257600 |
| Start | 113095103:113095103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1448C>T |
| AA Mutation | p.Pro483Leu(p.P483L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257600 |
| Start | 113077429:113077429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.265A>G |
| AA Mutation | p.Met89Val(p.M89V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257600 |
| Start | 113077522:113077522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.358G>T |
| AA Mutation | p.Ala120Ser(p.A120S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257600 |
| Start | 113096718:113096718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1642C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257600 |
| Start | 113077455:113077455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.291C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257600 |
| Start | 113095095:113095095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766112060 |
| CDS Mutation | c.1440T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |