Primary Site >> Stomach Cancer
Gene >> DPYD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97699484:97699484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.547T>C |
| AA Mutation | p.Ser183Pro(p.S183P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97593288:97593288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778601245 |
| CDS Mutation | c.1058G>A |
| AA Mutation | p.Arg353His(p.R353H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97593273:97593273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573299212 |
| CDS Mutation | c.1073G>A |
| AA Mutation | p.Arg358His(p.R358H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97193184:97193184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2507C>T |
| AA Mutation | p.Ala836Val(p.A836V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97450208:97450208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1756G>A |
| AA Mutation | p.Val586Ile(p.V586I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97515738:97515738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1728C>A |
| AA Mutation | p.Phe576Leu(p.F576L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97082466:97082466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2771T>C |
| AA Mutation | p.Val924Ala(p.V924A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97373614:97373614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2005T>G |
| AA Mutation | p.Leu669Val(p.L669V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97373568:97373568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2051G>A |
| AA Mutation | p.Cys684Tyr(p.C684Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97450120:97450120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1844A>C |
| AA Mutation | p.Glu615Ala(p.E615A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97593262:97593262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752020412 |
| CDS Mutation | c.1084G>A |
| AA Mutation | p.Val362Ile(p.V362I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97098541:97098541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2714C>T |
| AA Mutation | p.Ser905Leu(p.S905L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97450207:97450207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1757T>G |
| AA Mutation | p.Val586Gly(p.V586G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97593225:97593225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1121C>A |
| AA Mutation | p.Pro374His(p.P374H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97305265:97305265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2293G>A |
| AA Mutation | p.Val765Met(p.V765M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370192 |
| Start | 97573953:97573953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1146A>T |
| AA Mutation | p.Glu382Asp(p.E382D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370192 |
| Start | 97450119:97450119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1845G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370192 |
| Start | 97593263:97593263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372369973 |
| CDS Mutation | c.1083C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370192 |
| Start | 97305266:97305266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2292A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370192 |
| Start | 97306235:97306235(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2121delT |
| AA Mutation | p.Phe707LeufsTer4(p.F707Lfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000370192 |
| Start | 97082449:97082449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2788C>T |
| AA Mutation | p.Gln930Ter(p.Q930*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000370192 |
| Start | 97691743:97691743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.736G>T |
| AA Mutation | p.Glu246Ter(p.E246*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370192 |
| Start | 97699486:97699487(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs754785410 |
| CDS Mutation | c.544dupA |
| AA Mutation | p.Met182AsnfsTer3(p.M182Nfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |