Primary Site >> Stomach Cancer
Gene >> C1GALT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223122 |
| Start | 7238675:7238675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.641T>C |
| AA Mutation | p.Val214Ala(p.V214A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223122 |
| Start | 7238455:7238455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.421G>T |
| AA Mutation | p.Asp141Tyr(p.D141Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223122 |
| Start | 7238830:7238830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.796T>A |
| AA Mutation | p.Phe266Ile(p.F266I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000223122 |
| Start | 7243555:7243555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.920C>T |
| AA Mutation | p.Ser307Phe(p.S307F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223122 |
| Start | 7243616:7243616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.981T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000223122 |
| Start | 7243601:7243601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746319437 |
| CDS Mutation | c.966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |