Primary Site >> Stomach Cancer
Gene >> DRD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362072 |
| Start | 113424600:113424600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.52T>C |
| AA Mutation | p.Trp18Arg(p.W18R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362072 |
| Start | 113410863:113410863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1196G>C |
| AA Mutation | p.Cys399Ser(p.C399S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362072 |
| Start | 113412726:113412726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968C>T |
| AA Mutation | p.Ala323Val(p.A323V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362072 |
| Start | 113416895:113416895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.500C>T |
| AA Mutation | p.Ser167Phe(p.S167F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362072 |
| Start | 113424431:113424431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.221T>A |
| AA Mutation | p.Val74Asp(p.V74D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362072 |
| Start | 113416866:113416866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571869697 |
| CDS Mutation | c.529G>A |
| AA Mutation | p.Ala177Thr(p.A177T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362072 |
| Start | 113415495:113415495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649C>T |
| AA Mutation | p.Arg217Cys(p.R217C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362072 |
| Start | 113415461:113415461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.683G>A |
| AA Mutation | p.Ser228Asn(p.S228N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000362072 |
| Start | 113415592:113415592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.552T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000362072 |
| Start | 113424415:113424415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759920076 |
| CDS Mutation | c.237C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000362072 |
| Start | 113424511:113424511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.141C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000362072 |
| Start | 113424583:113424583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200831689 |
| CDS Mutation | c.69C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |