Primary Site >> Stomach Cancer
Gene >> PDE10A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165435355:165435355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.389C>A |
| AA Mutation | p.Pro130His(p.P130H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165433036:165433036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.601A>T |
| AA Mutation | p.Ile201Phe(p.I201F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165395190:165395190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1466G>A |
| AA Mutation | p.Gly489Glu(p.G489E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165392741:165392741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770874774 |
| CDS Mutation | c.1531C>T |
| AA Mutation | p.Arg511Trp(p.R511W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165379300:165379300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1849C>T |
| AA Mutation | p.Arg617Cys(p.R617C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165343438:165343438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs117826255 |
| CDS Mutation | c.2020G>A |
| AA Mutation | p.Val674Ile(p.V674I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165433060:165433060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.577A>T |
| AA Mutation | p.Ile193Phe(p.I193F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165543458:165543458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.148A>G |
| AA Mutation | p.Lys50Glu(p.K50E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165418773:165418773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.830A>G |
| AA Mutation | p.Tyr277Cys(p.Y277C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165396438:165396438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1270T>C |
| AA Mutation | p.Ser424Pro(p.S424P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165333083:165333083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2282C>T |
| AA Mutation | p.Thr761Ile(p.T761I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165392780:165392780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1492T>G |
| AA Mutation | p.Leu498Val(p.L498V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366882 |
| Start | 165431429:165431429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.707A>G |
| AA Mutation | p.Gln236Arg(p.Q236R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366882 |
| Start | 165336194:165336194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs35370607 |
| CDS Mutation | c.2166C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366882 |
| Start | 165379262:165379262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1887T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366882 |
| Start | 165392712:165392712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1560G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | start_lost;splice_region_variant |
| Transcription ID | ENST00000366882 |
| Start | 165576448:165576448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762689447 |
| CDS Mutation | c.1A>G |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Translation_Start_Site |
| Feature Type | Transcript |