Primary Site >> Stomach Cancer
Gene >> PTPN13
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86689154:86689154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.510A>C |
| AA Mutation | p.Lys170Asn(p.K170N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86814547:86814547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7454A>C |
| AA Mutation | p.Lys2485Thr(p.K2485T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86689153:86689153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.509A>G |
| AA Mutation | p.Lys170Arg(p.K170R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86701751:86701751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1145G>A |
| AA Mutation | p.Arg382Gln(p.R382Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86758956:86758956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3436T>C |
| AA Mutation | p.Ser1146Pro(p.S1146P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86750864:86750864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3045G>T |
| AA Mutation | p.Leu1015Phe(p.L1015F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86762891:86762891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3718C>T |
| AA Mutation | p.Arg1240Trp(p.R1240W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86701322:86701322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373603386 |
| CDS Mutation | c.716A>C |
| AA Mutation | p.Lys239Thr(p.K239T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86775180:86775180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5518A>G |
| AA Mutation | p.Thr1840Ala(p.T1840A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86722399:86722399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1573G>A |
| AA Mutation | p.Ala525Thr(p.A525T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86741734:86741734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2405T>C |
| AA Mutation | p.Val802Ala(p.V802A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86814540:86814540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7447C>A |
| AA Mutation | p.Leu2483Ile(p.L2483I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86763144:86763144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3971A>T |
| AA Mutation | p.Asp1324Val(p.D1324V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86809962:86809962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765352499 |
| CDS Mutation | c.7277G>A |
| AA Mutation | p.Gly2426Glu(p.G2426E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86722270:86722270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575836236 |
| CDS Mutation | c.1444C>T |
| AA Mutation | p.Arg482Trp(p.R482W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86701521:86701521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.915G>T |
| AA Mutation | p.Leu305Phe(p.L305F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86763185:86763185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4012A>G |
| AA Mutation | p.Lys1338Glu(p.K1338E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86764660:86764660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4085A>C |
| AA Mutation | p.Lys1362Thr(p.K1362T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86758777:86758777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3413T>C |
| AA Mutation | p.Leu1138Ser(p.L1138S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411767 |
| Start | 86701574:86701574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115836094 |
| CDS Mutation | c.968G>A |
| AA Mutation | p.Arg323His(p.R323H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000411767 |
| Start | 86764661:86764661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4086G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000411767 |
| Start | 86814515:86814515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7422A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000411767 |
| Start | 86769848:86769848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4569G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000411767 |
| Start | 86701395:86701395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.789T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000411767 |
| Start | 86751057:86751057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3099T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000411767 |
| Start | 86803728:86803728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765749481 |
| CDS Mutation | c.6525C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000411767 |
| Start | 86769879:86769879(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4604delA |
| AA Mutation | p.Lys1535SerfsTer16(p.K1535Sfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000411767 |
| Start | 86769821:86769821(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4546delT |
| AA Mutation | p.Ser1516LeufsTer15(p.S1516Lfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000411767 |
| Start | 86716538:86716538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1204C>T |
| AA Mutation | p.Arg402Ter(p.R402*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000411767 |
| Start | 86766467:86766467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4279G>T |
| AA Mutation | p.Glu1427Ter(p.E1427*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000411767 |
| Start | 86762951:86762951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3778C>T |
| AA Mutation | p.Gln1260Ter(p.Q1260*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000411767 |
| Start | 86775261:86775261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5599C>T |
| AA Mutation | p.Arg1867Ter(p.R1867*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000411767 |
| Start | 86807660:86807660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6846C>A |
| AA Mutation | p.Cys2282Ter(p.C2282*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000411767 |
| Start | 86750532:86750532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773296258 |
| CDS Mutation | c.2713C>T |
| AA Mutation | p.Arg905Ter(p.R905*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |