Primary Site >> Stomach Cancer
Gene >> DPYS
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000351513 |
| Start | 104451247:104451247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.422A>G |
| AA Mutation | p.Gln141Arg(p.Q141R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351513 |
| Start | 104424311:104424311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1171A>G |
| AA Mutation | p.Arg391Gly(p.R391G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351513 |
| Start | 104392863:104392863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1364T>A |
| AA Mutation | p.Val455Asp(p.V455D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351513 |
| Start | 104392852:104392852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1375G>T |
| AA Mutation | p.Asp459Tyr(p.D459Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351513 |
| Start | 104392954:104392954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1273T>G |
| AA Mutation | p.Phe425Val(p.F425V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351513 |
| Start | 104444380:104444380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661C>T |
| AA Mutation | p.Arg221Cys(p.R221C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351513 |
| Start | 104424316:104424316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1166A>C |
| AA Mutation | p.Tyr389Ser(p.Y389S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351513 |
| Start | 104429640:104429640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.855G>T |
| AA Mutation | p.Trp285Cys(p.W285C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351513 |
| Start | 104424311:104424311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1171A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351513 |
| Start | 104444351:104444351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374805521 |
| CDS Mutation | c.690G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351513 |
| Start | 104451366:104451366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141057778 |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351513 |
| Start | 104447348:104447348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188038278 |
| CDS Mutation | c.579G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000351513 |
| Start | 104392804:104392804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61758444 |
| CDS Mutation | c.1423C>T |
| AA Mutation | p.Arg475Ter(p.R475*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |