Primary Site >> Stomach Cancer
Gene >> CNP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393892 |
| Start | 41968203:41968203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.139C>A |
| AA Mutation | p.Leu47Ile(p.L47I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393892 |
| Start | 41973899:41973899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1241C>G |
| AA Mutation | p.Ala414Gly(p.A414G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393892 |
| Start | 41968324:41968324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.260A>G |
| AA Mutation | p.Lys87Arg(p.K87R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393892 |
| Start | 41968379:41968379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.315G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393892 |
| Start | 41968316:41968316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782683469 |
| CDS Mutation | c.252C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393892 |
| Start | 41968622:41968622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.558G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |