Primary Site >> Stomach Cancer
Gene >> ASPH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379454 |
| Start | 61503432:61503432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371485848 |
| CDS Mutation | c.2204G>A |
| AA Mutation | p.Arg735Gln(p.R735Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379454 |
| Start | 61567257:61567257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1211C>T |
| AA Mutation | p.Thr404Ile(p.T404I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379454 |
| Start | 61553080:61553080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1577G>T |
| AA Mutation | p.Arg526Ile(p.R526I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379454 |
| Start | 61651110:61651110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758840739 |
| CDS Mutation | c.430G>A |
| AA Mutation | p.Glu144Lys(p.E144K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379454 |
| Start | 61562797:61562797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200072789 |
| CDS Mutation | c.1384G>A |
| AA Mutation | p.Val462Met(p.V462M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379454 |
| Start | 61517541:61517541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749030670 |
| CDS Mutation | c.2113G>A |
| AA Mutation | p.Ala705Thr(p.A705T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379454 |
| Start | 61637979:61637979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.857A>G |
| AA Mutation | p.Asn286Ser(p.N286S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379454 |
| Start | 61567300:61567300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1168G>C |
| AA Mutation | p.Glu390Gln(p.E390Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379454 |
| Start | 61562777:61562777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1404A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379454 |
| Start | 61503461:61503461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112982646 |
| CDS Mutation | c.2175C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379454 |
| Start | 61517596:61517596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2058G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379454 |
| Start | 61553106:61553106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373467138 |
| CDS Mutation | c.1551C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |