Primary Site >> Stomach Cancer
Gene >> PTPRF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43621153:43621153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5576T>A |
| AA Mutation | p.Met1859Lys(p.M1859K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000359947 |
| Start | 43617738:43617738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764399239 |
| CDS Mutation | c.4198G>A |
| AA Mutation | p.Val1400Ile(p.V1400I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43603772:43603772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758580532 |
| CDS Mutation | c.2620G>A |
| AA Mutation | p.Asp874Asn(p.D874N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43606391:43606391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376364770 |
| CDS Mutation | c.3635G>A |
| AA Mutation | p.Arg1212Gln(p.R1212Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43591346:43591346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1324G>A |
| AA Mutation | p.Gly442Ser(p.G442S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43619301:43619301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756962072 |
| CDS Mutation | c.4660C>T |
| AA Mutation | p.Arg1554Cys(p.R1554C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43619382:43619382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4741A>G |
| AA Mutation | p.Thr1581Ala(p.T1581A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43606280:43606280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200483026 |
| CDS Mutation | c.3524G>A |
| AA Mutation | p.Arg1175Gln(p.R1175Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43603991:43603991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372831256 |
| CDS Mutation | c.2839C>T |
| AA Mutation | p.Arg947Cys(p.R947C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43591242:43591242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373662568 |
| CDS Mutation | c.1220G>A |
| AA Mutation | p.Arg407His(p.R407H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43597817:43597817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1883T>C |
| AA Mutation | p.Val628Ala(p.V628A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43591187:43591187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1165G>A |
| AA Mutation | p.Val389Met(p.V389M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43621177:43621177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5600T>A |
| AA Mutation | p.Met1867Lys(p.M1867K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43617451:43617451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763477204 |
| CDS Mutation | c.4078G>A |
| AA Mutation | p.Asp1360Asn(p.D1360N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43603458:43603458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572629636 |
| CDS Mutation | c.2383G>A |
| AA Mutation | p.Val795Ile(p.V795I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43597853:43597853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1919C>G |
| AA Mutation | p.Thr640Ser(p.T640S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43617808:43617808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748798640 |
| CDS Mutation | c.4268C>T |
| AA Mutation | p.Thr1423Met(p.T1423M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43569758:43569758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771288963 |
| CDS Mutation | c.548G>A |
| AA Mutation | p.Arg183His(p.R183H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43553588:43553588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.188G>A |
| AA Mutation | p.Arg63His(p.R63H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43598873:43598873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2273G>A |
| AA Mutation | p.Gly758Glu(p.G758E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43591140:43591140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765844810 |
| CDS Mutation | c.1118G>A |
| AA Mutation | p.Arg373His(p.R373H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43597805:43597805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1871G>T |
| AA Mutation | p.Arg624Leu(p.R624L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43619807:43619807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5060G>A |
| AA Mutation | p.Arg1687His(p.R1687H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359947 |
| Start | 43620575:43620575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5360C>T |
| AA Mutation | p.Ala1787Val(p.A1787V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43603777:43603777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2625G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43591840:43591840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138493601 |
| CDS Mutation | c.1560C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43621166:43621166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138441028 |
| CDS Mutation | c.5589C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43597755:43597755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1821C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43605619:43605619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201860251 |
| CDS Mutation | c.3480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43609428:43609428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3903A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43606392:43606392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3636G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43621202:43621202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5625T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43588789:43588789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200014267 |
| CDS Mutation | c.738C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359947 |
| Start | 43620504:43620504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200578523 |
| CDS Mutation | c.5289C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359947 |
| Start | 43609493:43609493(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3971delC |
| AA Mutation | p.Pro1324GlnfsTer51(p.P1324Qfs*51) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000359947 |
| Start | 43621151:43621152(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.5574_5575insTAGCTACTCAGGAGGAGGCTGAGGT |
| AA Mutation | p.Met1859Ter(p.M1859*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359947 |
| Start | 43545111:43545112(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.40dupC |
| AA Mutation | p.Leu14ProfsTer17(p.L14Pfs*17) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |