Primary Site >> Stomach Cancer
Gene >> ALPL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374832 |
| Start | 21577421:21577421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138690664 |
| CDS Mutation | c.1348C>T |
| AA Mutation | p.Arg450Cys(p.R450C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374832 |
| Start | 21573712:21573712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745704006 |
| CDS Mutation | c.910G>A |
| AA Mutation | p.Val304Met(p.V304M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374832 |
| Start | 21575865:21575865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756418235 |
| CDS Mutation | c.1130C>T |
| AA Mutation | p.Ala377Val(p.A377V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374832 |
| Start | 21577596:21577596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1523C>A |
| AA Mutation | p.Ala508Glu(p.A508E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374832 |
| Start | 21560643:21560643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.79A>G |
| AA Mutation | p.Lys27Glu(p.K27E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374832 |
| Start | 21563139:21563139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.327C>A |
| AA Mutation | p.Asp109Glu(p.D109E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374832 |
| Start | 21564162:21564162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.594C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374832 |
| Start | 21561209:21561209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.294C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374832 |
| Start | 21564108:21564108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770068340 |
| CDS Mutation | c.540C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374832 |
| Start | 21575901:21575901(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs779683021 |
| CDS Mutation | c.1171delC |
| AA Mutation | p.Arg391ValfsTer12(p.R391Vfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374832 |
| Start | 21563196:21563196(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.388delG |
| AA Mutation | p.Val130Ter(p.V130*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374832 |
| Start | 21568112:21568112(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs769948289 |
| CDS Mutation | c.662delG |
| AA Mutation | p.Gly221ValfsTer56(p.G221Vfs*56) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000374832 |
| Start | 21576614:21576614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759017288 |
| CDS Mutation | c.1282C>T |
| AA Mutation | p.Arg428Ter(p.R428*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |