Primary Site >> Stomach Cancer
Gene >> GPR152
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312457 |
| Start | 67452448:67452448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.277C>T |
| AA Mutation | p.His93Tyr(p.H93Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312457 |
| Start | 67451589:67451589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775290604 |
| CDS Mutation | c.1136C>T |
| AA Mutation | p.Thr379Met(p.T379M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312457 |
| Start | 67451979:67451979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.746T>C |
| AA Mutation | p.Leu249Pro(p.L249P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312457 |
| Start | 67451784:67451784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139892022 |
| CDS Mutation | c.941C>T |
| AA Mutation | p.Ala314Val(p.A314V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312457 |
| Start | 67451330:67451330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202233102 |
| CDS Mutation | c.1395G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312457 |
| Start | 67451786:67451786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144851549 |
| CDS Mutation | c.939C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |