Primary Site >> Stomach Cancer
Gene >> HPSE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311412 |
| Start | 83313218:83313218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.569C>T |
| AA Mutation | p.Ala190Val(p.A190V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311412 |
| Start | 83301039:83301039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565705065 |
| CDS Mutation | c.1393C>T |
| AA Mutation | p.Arg465Trp(p.R465W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311412 |
| Start | 83300987:83300987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1445C>A |
| AA Mutation | p.Pro482His(p.P482H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311412 |
| Start | 83322314:83322314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.278G>A |
| AA Mutation | p.Arg93Lys(p.R93K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311412 |
| Start | 83301047:83301047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1385A>G |
| AA Mutation | p.Lys462Arg(p.K462R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000311412 |
| Start | 83310031:83310031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.890A>G |
| AA Mutation | p.His297Arg(p.H297R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311412 |
| Start | 83322279:83322279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747014307 |
| CDS Mutation | c.313G>A |
| AA Mutation | p.Asp105Asn(p.D105N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311412 |
| Start | 83306293:83306293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1116A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000311412 |
| Start | 83309456:83309456(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.930delT |
| AA Mutation | p.Leu311Ter(p.L311*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000311412 |
| Start | 83319366:83319367(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.476dupA |
| AA Mutation | p.Phe160ValfsTer44(p.F160Vfs*44) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |