Primary Site >> Stomach Cancer
Gene >> GYS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323798 |
| Start | 48991405:48991405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.197G>T |
| AA Mutation | p.Gly66Val(p.G66V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323798 |
| Start | 48978121:48978121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1206G>T |
| AA Mutation | p.Arg402Ser(p.R402S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323798 |
| Start | 48974324:48974324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1438G>C |
| AA Mutation | p.Glu480Gln(p.E480Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323798 |
| Start | 48985544:48985544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.740C>T |
| AA Mutation | p.Ala247Val(p.A247V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323798 |
| Start | 48977953:48977953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746669628 |
| CDS Mutation | c.1279A>G |
| AA Mutation | p.Met427Val(p.M427V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323798 |
| Start | 48969606:48969606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1896G>T |
| AA Mutation | p.Gln632His(p.Q632H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323798 |
| Start | 48982748:48982748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.913C>G |
| AA Mutation | p.Gln305Glu(p.Q305E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323798 |
| Start | 48977928:48977928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772459742 |
| CDS Mutation | c.1304C>T |
| AA Mutation | p.Thr435Met(p.T435M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323798 |
| Start | 48985919:48985919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.609C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323798 |
| Start | 48991449:48991449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754432159 |
| CDS Mutation | c.153G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323798 |
| Start | 48969411:48969411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752755917 |
| CDS Mutation | c.2091G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |