Primary Site >> Stomach Cancer
Gene >> GPR132
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329797 |
| Start | 105051949:105051949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766876423 |
| CDS Mutation | c.188C>T |
| AA Mutation | p.Thr63Ile(p.T63I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329797 |
| Start | 105051347:105051347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777838540 |
| CDS Mutation | c.790G>A |
| AA Mutation | p.Val264Ile(p.V264I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329797 |
| Start | 105051992:105051992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.145T>C |
| AA Mutation | p.Tyr49His(p.Y49H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329797 |
| Start | 105051911:105051911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.226G>C |
| AA Mutation | p.Val76Leu(p.V76L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329797 |
| Start | 105051401:105051401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.736G>A |
| AA Mutation | p.Ala246Thr(p.A246T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329797 |
| Start | 105051531:105051531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.606C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329797 |
| Start | 105051204:105051204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.933C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329797 |
| Start | 105051699:105051699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780142285 |
| CDS Mutation | c.438C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329797 |
| Start | 105051912:105051912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371334440 |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |