Primary Site >> Stomach Cancer
Gene >> GALNT9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397325 |
| Start | 132197953:132197953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763735503 |
| CDS Mutation | c.406C>T |
| AA Mutation | p.Arg136Trp(p.R136W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397325 |
| Start | 132197234:132197234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.587G>C |
| AA Mutation | p.Arg196Pro(p.R196P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397325 |
| Start | 132203573:132203573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758686830 |
| CDS Mutation | c.97C>T |
| AA Mutation | p.Arg33Cys(p.R33C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397325 |
| Start | 132197152:132197152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.669G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397325 |
| Start | 132203580:132203580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199528726 |
| CDS Mutation | c.90C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397325 |
| Start | 132203571:132203571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544376030 |
| CDS Mutation | c.99C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |