Primary Site >> Stomach Cancer
Gene >> SCG5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300175 |
| Start | 32684586:32684586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.406G>A |
| AA Mutation | p.Asp136Asn(p.D136N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300175 |
| Start | 32684638:32684638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202071901 |
| CDS Mutation | c.458C>T |
| AA Mutation | p.Pro153Leu(p.P153L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300175 |
| Start | 32696591:32696591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.621G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300175 |
| Start | 32643805:32643805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.213C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300175 |
| Start | 32643802:32643802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.210C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000300175 |
| Start | 32679870:32679870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764436055 |
| CDS Mutation | c.331C>T |
| AA Mutation | p.Gln111Ter(p.Q111*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |