Primary Site >> Stomach Cancer
Gene >> PTPRG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 61989712:61989712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.278C>T |
| AA Mutation | p.Ala93Val(p.A93V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62203414:62203414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779012226 |
| CDS Mutation | c.1619C>T |
| AA Mutation | p.Thr540Met(p.T540M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62203774:62203774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1979G>T |
| AA Mutation | p.Arg660Met(p.R660M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62195087:62195087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1244C>T |
| AA Mutation | p.Pro415Leu(p.P415L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62277031:62277031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3619A>G |
| AA Mutation | p.Asn1207Asp(p.N1207D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62269068:62269068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2908A>T |
| AA Mutation | p.Ser970Cys(p.S970C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62168062:62168062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932G>A |
| AA Mutation | p.Arg311His(p.R311H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 61748965:61748965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376043244 |
| CDS Mutation | c.173C>T |
| AA Mutation | p.Pro58Leu(p.P58L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62203456:62203456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1661C>T |
| AA Mutation | p.Ala554Val(p.A554V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62203336:62203336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756672469 |
| CDS Mutation | c.1541C>T |
| AA Mutation | p.Thr514Met(p.T514M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62273059:62273059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749173201 |
| CDS Mutation | c.3296G>A |
| AA Mutation | p.Arg1099His(p.R1099H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62231300:62231300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2364G>C |
| AA Mutation | p.Glu788Asp(p.E788D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 61989688:61989688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.254C>A |
| AA Mutation | p.Pro85His(p.P85H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62269135:62269135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773599761 |
| CDS Mutation | c.2975G>A |
| AA Mutation | p.Arg992His(p.R992H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62218977:62218977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2282A>G |
| AA Mutation | p.Tyr761Cys(p.Y761C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 61989723:61989723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.289G>A |
| AA Mutation | p.Glu97Lys(p.E97K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000474889 |
| Start | 62272961:62272961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3198A>C |
| AA Mutation | p.Arg1066Ser(p.R1066S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000474889 |
| Start | 62267798:62267798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557054933 |
| CDS Mutation | c.2853G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000474889 |
| Start | 62203358:62203358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1563C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000474889 |
| Start | 62195157:62195157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781007376 |
| CDS Mutation | c.1314G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000474889 |
| Start | 62267465:62267465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781276396 |
| CDS Mutation | c.2712C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000474889 |
| Start | 62157092:62157092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776285819 |
| CDS Mutation | c.708C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000474889 |
| Start | 62132658:62132658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753995594 |
| CDS Mutation | c.672C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000474889 |
| Start | 62203824:62203824(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2034delC |
| AA Mutation | p.Thr679ProfsTer48(p.T679Pfs*48) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000474889 |
| Start | 62218854:62218854(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2165delA |
| AA Mutation | p.Asn722ThrfsTer5(p.N722Tfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000474889 |
| Start | 62262867:62262867(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2633delA |
| AA Mutation | p.Asn878ThrfsTer7(p.N878Tfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000474889 |
| Start | 62267809:62267809(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2868delA |
| AA Mutation | p.Gly957GlufsTer24(p.G957Efs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |