Primary Site >> Stomach Cancer
Gene >> NET1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355029 |
| Start | 5429206:5429206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.232A>G |
| AA Mutation | p.Ser78Gly(p.S78G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355029 |
| Start | 5455012:5455012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1091A>G |
| AA Mutation | p.Tyr364Cys(p.Y364C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355029 |
| Start | 5451837:5451837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.263G>T |
| AA Mutation | p.Ser88Ile(p.S88I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355029 |
| Start | 5452485:5452485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760269274 |
| CDS Mutation | c.491T>C |
| AA Mutation | p.Met164Thr(p.M164T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355029 |
| Start | 5456727:5456727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1524T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355029 |
| Start | 5456146:5456146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186691846 |
| CDS Mutation | c.1257C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |