Primary Site >> Stomach Cancer
Gene >> DSP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7569267:7569267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368778031 |
| CDS Mutation | c.1501G>A |
| AA Mutation | p.Val501Ile(p.V501I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7580398:7580398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4208G>T |
| AA Mutation | p.Arg1403Met(p.R1403M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7581201:7581201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5011G>C |
| AA Mutation | p.Glu1671Gln(p.E1671Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7569286:7569286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1520C>T |
| AA Mutation | p.Ser507Phe(p.S507F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7569259:7569259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761051181 |
| CDS Mutation | c.1493C>T |
| AA Mutation | p.Pro498Leu(p.P498L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7582775:7582775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377715841 |
| CDS Mutation | c.5513G>A |
| AA Mutation | p.Arg1838His(p.R1838H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585583:7585583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8321T>C |
| AA Mutation | p.Leu2774Pro(p.L2774P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7583036:7583036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5774A>G |
| AA Mutation | p.Gln1925Arg(p.Q1925R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7575321:7575321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2463G>T |
| AA Mutation | p.Lys821Asn(p.K821N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7583771:7583771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6509A>C |
| AA Mutation | p.Lys2170Thr(p.K2170T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585066:7585066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745377828 |
| CDS Mutation | c.7804T>G |
| AA Mutation | p.Leu2602Val(p.L2602V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7558150:7558150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775015862 |
| CDS Mutation | c.308G>A |
| AA Mutation | p.Arg103Gln(p.R103Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7575455:7575455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764965132 |
| CDS Mutation | c.2597G>A |
| AA Mutation | p.Arg866His(p.R866H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7571497:7571497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372467697 |
| CDS Mutation | c.1816C>T |
| AA Mutation | p.Arg606Trp(p.R606W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7580656:7580656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4466T>C |
| AA Mutation | p.Leu1489Pro(p.L1489P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7583485:7583485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751050235 |
| CDS Mutation | c.6223C>T |
| AA Mutation | p.Arg2075Trp(p.R2075W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7584911:7584911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7649G>T |
| AA Mutation | p.Gly2550Val(p.G2550V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7559309:7559309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506G>A |
| AA Mutation | p.Gly169Asp(p.G169D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585540:7585540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8278G>A |
| AA Mutation | p.Ala2760Thr(p.A2760T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585315:7585315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8053G>A |
| AA Mutation | p.Ala2685Thr(p.A2685T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7576382:7576382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749051278 |
| CDS Mutation | c.2719C>T |
| AA Mutation | p.Arg907Cys(p.R907C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7580755:7580755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4565C>G |
| AA Mutation | p.Thr1522Arg(p.T1522R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7579691:7579691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3501G>T |
| AA Mutation | p.Lys1167Asn(p.K1167N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7570558:7570558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148147581 |
| CDS Mutation | c.1696G>A |
| AA Mutation | p.Ala566Thr(p.A566T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7583741:7583741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146642551 |
| CDS Mutation | c.6479G>A |
| AA Mutation | p.Arg2160Gln(p.R2160Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7584365:7584365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7103T>C |
| AA Mutation | p.Leu2368Ser(p.L2368S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7580613:7580613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4423A>C |
| AA Mutation | p.Thr1475Pro(p.T1475P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7580680:7580680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs727505037 |
| CDS Mutation | c.4490G>A |
| AA Mutation | p.Arg1497Gln(p.R1497Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7584560:7584560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7298G>A |
| AA Mutation | p.Cys2433Tyr(p.C2433Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7577834:7577834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2933T>C |
| AA Mutation | p.Ile978Thr(p.I978T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7559235:7559235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.432G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7577808:7577808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2907C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7565469:7565469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149701627 |
| CDS Mutation | c.888C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7574693:7574693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2334C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7584351:7584351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7089C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7584996:7584996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs28763970 |
| CDS Mutation | c.7734C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585767:7585767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8505C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7571499:7571499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1818G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7584960:7584960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7698T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7565478:7565478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121912992 |
| CDS Mutation | c.897C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585758:7585758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8496A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7583082:7583082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763026647 |
| CDS Mutation | c.5820T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000379802 |
| Start | 7583794:7583794(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6536delA |
| AA Mutation | p.Lys2179ArgfsTer8(p.K2179Rfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000379802 |
| Start | 7580276:7580276(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4091delA |
| AA Mutation | p.Asn1364IlefsTer32(p.N1364Ifs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000379802 |
| Start | 7579870:7579870(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3684delA |
| AA Mutation | p.Glu1229ArgfsTer21(p.E1229Rfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000379802 |
| Start | 7555815:7555815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.268C>T |
| AA Mutation | p.Gln90Ter(p.Q90*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000379802 |
| Start | 7584262:7584262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369482721 |
| CDS Mutation | c.7000C>T |
| AA Mutation | p.Arg2334Ter(p.R2334*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |