Primary Site >> Stomach Cancer
Gene >> PTPRA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 3026759:3026759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377260441 |
| CDS Mutation | c.1687C>T |
| AA Mutation | p.Arg563Cys(p.R563C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 2988403:2988403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373627310 |
| CDS Mutation | c.667G>A |
| AA Mutation | p.Val223Met(p.V223M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 2988046:2988046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.542A>G |
| AA Mutation | p.Lys181Arg(p.K181R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 2964872:2964872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.85G>A |
| AA Mutation | p.Val29Ile(p.V29I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 2988445:2988445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773334274 |
| CDS Mutation | c.709G>A |
| AA Mutation | p.Asp237Asn(p.D237N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 2986800:2986800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.478T>A |
| AA Mutation | p.Ser160Thr(p.S160T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 2965049:2965049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.262A>G |
| AA Mutation | p.Thr88Ala(p.T88A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 3038078:3038078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2354A>G |
| AA Mutation | p.Tyr785Cys(p.Y785C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 3035685:3035685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2021G>A |
| AA Mutation | p.Arg674Gln(p.R674Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 3037242:3037242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2287A>G |
| AA Mutation | p.Thr763Ala(p.T763A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 3022793:3022793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1433G>A |
| AA Mutation | p.Arg478Gln(p.R478Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 2965005:2965005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.218C>T |
| AA Mutation | p.Pro73Leu(p.P73L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380393 |
| Start | 3035681:3035681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61742029 |
| CDS Mutation | c.2017G>A |
| AA Mutation | p.Val673Ile(p.V673I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380393 |
| Start | 3035858:3035858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761130690 |
| CDS Mutation | c.2115C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380393 |
| Start | 3026740:3026740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1668A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380393 |
| Start | 3021317:3021317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778195981 |
| CDS Mutation | c.1050C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |