Primary Site >> Stomach Cancer
Gene >> GPER1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1092098:1092098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.370T>C |
| AA Mutation | p.Tyr124His(p.Y124H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1092516:1092516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564861434 |
| CDS Mutation | c.788C>T |
| AA Mutation | p.Ala263Val(p.A263V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1092129:1092129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773015616 |
| CDS Mutation | c.401C>T |
| AA Mutation | p.Ser134Leu(p.S134L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1092291:1092291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.563C>T |
| AA Mutation | p.Ala188Val(p.A188V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1092515:1092515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.787G>A |
| AA Mutation | p.Ala263Thr(p.A263T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1092161:1092161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776489649 |
| CDS Mutation | c.433G>A |
| AA Mutation | p.Val145Ile(p.V145I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1091793:1091793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370224401 |
| CDS Mutation | c.65C>T |
| AA Mutation | p.Ala22Val(p.A22V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1092788:1092788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060G>A |
| AA Mutation | p.Ala354Thr(p.A354T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1091823:1091823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.95A>G |
| AA Mutation | p.Asn32Ser(p.N32S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297469 |
| Start | 1092642:1092642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.914C>A |
| AA Mutation | p.Thr305Lys(p.T305K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297469 |
| Start | 1092109:1092109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780063298 |
| CDS Mutation | c.381C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |