Primary Site >> Stomach Cancer
Gene >> DRD5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782799:9782799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534674002 |
| CDS Mutation | c.770G>A |
| AA Mutation | p.Arg257His(p.R257H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782172:9782172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.143C>T |
| AA Mutation | p.Thr48Ile(p.T48I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9783035:9783035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749131704 |
| CDS Mutation | c.1006G>A |
| AA Mutation | p.Val336Ile(p.V336I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782759:9782759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.730A>G |
| AA Mutation | p.Thr244Ala(p.T244A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782834:9782834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773943990 |
| CDS Mutation | c.805G>A |
| AA Mutation | p.Ala269Thr(p.A269T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782802:9782802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.773G>T |
| AA Mutation | p.Arg258Met(p.R258M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9783053:9783053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1024G>A |
| AA Mutation | p.Asp342Asn(p.D342N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782094:9782094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.65C>T |
| AA Mutation | p.Ala22Val(p.A22V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9783281:9783281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760258996 |
| CDS Mutation | c.1252G>A |
| AA Mutation | p.Val418Ile(p.V418I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9783069:9783069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1040T>C |
| AA Mutation | p.Phe347Ser(p.F347S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782301:9782301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.272C>T |
| AA Mutation | p.Ala91Val(p.A91V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782670:9782670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.641C>T |
| AA Mutation | p.Ala214Val(p.A214V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782883:9782883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.854G>A |
| AA Mutation | p.Arg285His(p.R285H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782131:9782131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.102G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304374 |
| Start | 9782884:9782884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201697048 |
| CDS Mutation | c.855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |