Primary Site >> Stomach Cancer
Gene >> GRPR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380289 |
| Start | 16124315:16124315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.362T>C |
| AA Mutation | p.Leu121Pro(p.L121P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380289 |
| Start | 16150423:16150423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.532T>G |
| AA Mutation | p.Phe178Val(p.F178V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380289 |
| Start | 16150420:16150420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.529G>A |
| AA Mutation | p.Val177Met(p.V177M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380289 |
| Start | 16152592:16152592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1102G>A |
| AA Mutation | p.Val368Met(p.V368M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380289 |
| Start | 16124267:16124267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.314G>T |
| AA Mutation | p.Arg105Ile(p.R105I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380289 |
| Start | 16152637:16152637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1147T>C |
| AA Mutation | p.Tyr383His(p.Y383H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380289 |
| Start | 16152627:16152627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1137T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380289 |
| Start | 16124046:16124046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768056683 |
| CDS Mutation | c.93C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |