Primary Site >> Stomach Cancer
Gene >> GPLD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24436610:24436610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2324G>A |
| AA Mutation | p.Cys775Tyr(p.C775Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24456510:24456510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766726890 |
| CDS Mutation | c.1136C>T |
| AA Mutation | p.Ala379Val(p.A379V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24436632:24436632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2302C>G |
| AA Mutation | p.Leu768Val(p.L768V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24475137:24475137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.425T>G |
| AA Mutation | p.Leu142Arg(p.L142R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24489423:24489423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753872655 |
| CDS Mutation | c.89T>C |
| AA Mutation | p.Val30Ala(p.V30A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24436664:24436664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766133257 |
| CDS Mutation | c.2270G>A |
| AA Mutation | p.Arg757Gln(p.R757Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24437149:24437149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748536679 |
| CDS Mutation | c.2161G>A |
| AA Mutation | p.Val721Ile(p.V721I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24462787:24462787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.830A>G |
| AA Mutation | p.Asn277Ser(p.N277S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24447916:24447916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1639G>A |
| AA Mutation | p.Val547Met(p.V547M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24449845:24449845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144999503 |
| CDS Mutation | c.1390G>A |
| AA Mutation | p.Val464Met(p.V464M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24437182:24437182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2128A>C |
| AA Mutation | p.Ser710Arg(p.S710R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230036 |
| Start | 24460325:24460325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962A>G |
| AA Mutation | p.Asn321Ser(p.N321S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230036 |
| Start | 24446939:24446939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201729612 |
| CDS Mutation | c.1719C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230036 |
| Start | 24436684:24436684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770347454 |
| CDS Mutation | c.2250G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230036 |
| Start | 24436627:24436627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2307T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230036 |
| Start | 24445553:24445553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2013T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000230036 |
| Start | 24436712:24436713(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs749977099 |
| CDS Mutation | c.2221dupC |
| AA Mutation | p.Leu741ProfsTer22(p.L741Pfs*22) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |