Primary Site >> Stomach Cancer
Gene >> RP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626557:54626557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2675C>T |
| AA Mutation | p.Ala892Val(p.A892V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621426:54621426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376303499 |
| CDS Mutation | c.460C>T |
| AA Mutation | p.Arg154Trp(p.R154W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621385:54621385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147736171 |
| CDS Mutation | c.419A>G |
| AA Mutation | p.His140Arg(p.H140R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621111:54621111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374931762 |
| CDS Mutation | c.145G>A |
| AA Mutation | p.Gly49Ser(p.G49S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54624760:54624760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.878C>G |
| AA Mutation | p.Ser293Cys(p.S293C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629718:54629718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5836T>A |
| AA Mutation | p.Phe1946Ile(p.F1946I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621390:54621390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367600337 |
| CDS Mutation | c.424G>A |
| AA Mutation | p.Val142Ile(p.V142I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54624715:54624715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.833T>C |
| AA Mutation | p.Val278Ala(p.V278A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54622279:54622279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.778A>G |
| AA Mutation | p.Ser260Gly(p.S260G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621399:54621399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.433G>A |
| AA Mutation | p.Ala145Thr(p.A145T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621472:54621472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747000732 |
| CDS Mutation | c.506C>T |
| AA Mutation | p.Ala169Val(p.A169V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54624750:54624750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.868T>G |
| AA Mutation | p.Leu290Val(p.L290V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54628057:54628057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780518944 |
| CDS Mutation | c.4175A>G |
| AA Mutation | p.Asn1392Ser(p.N1392S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54628864:54628864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4982C>G |
| AA Mutation | p.Ser1661Cys(p.S1661C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621150:54621150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.184T>C |
| AA Mutation | p.Ser62Pro(p.S62P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54630042:54630042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6160C>G |
| AA Mutation | p.Leu2054Val(p.L2054V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621413:54621413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.447G>A |
| AA Mutation | p.Met149Ile(p.M149I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54628417:54628417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4535A>C |
| AA Mutation | p.Lys1512Thr(p.K1512T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626993:54626993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3111A>C |
| AA Mutation | p.Lys1037Asn(p.K1037N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629896:54629896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6014G>A |
| AA Mutation | p.Arg2005Lys(p.R2005K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627874:54627874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3992A>T |
| AA Mutation | p.Glu1331Val(p.E1331V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54622249:54622249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.748G>A |
| AA Mutation | p.Val250Met(p.V250M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629047:54629047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5165G>A |
| AA Mutation | p.Gly1722Asp(p.G1722D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629560:54629560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755363836 |
| CDS Mutation | c.5678G>A |
| AA Mutation | p.Gly1893Asp(p.G1893D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621069:54621069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.103G>A |
| AA Mutation | p.Ala35Thr(p.A35T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627679:54627679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3797A>G |
| AA Mutation | p.Lys1266Arg(p.K1266R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626569:54626569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2687C>T |
| AA Mutation | p.Ala896Val(p.A896V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627465:54627465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3583G>A |
| AA Mutation | p.Gly1195Arg(p.G1195R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54630078:54630078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149282954 |
| CDS Mutation | c.6196G>A |
| AA Mutation | p.Asp2066Asn(p.D2066N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629630:54629630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5748A>C |
| AA Mutation | p.Gln1916His(p.Q1916H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627726:54627726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3844C>T |
| AA Mutation | p.Pro1282Ser(p.P1282S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54630324:54630324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6442G>C |
| AA Mutation | p.Glu2148Gln(p.E2148Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54620985:54620985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.19A>C |
| AA Mutation | p.Thr7Pro(p.T7P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629007:54629007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747095891 |
| CDS Mutation | c.5125G>A |
| AA Mutation | p.Val1709Met(p.V1709M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627672:54627672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3790G>A |
| AA Mutation | p.Val1264Ile(p.V1264I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54630280:54630280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6398T>C |
| AA Mutation | p.Leu2133Pro(p.L2133P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627352:54627352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3470C>T |
| AA Mutation | p.Ser1157Phe(p.S1157F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54625840:54625840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1958G>A |
| AA Mutation | p.Gly653Asp(p.G653D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626557:54626557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2675C>A |
| AA Mutation | p.Ala892Glu(p.A892E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629942:54629942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6060T>G |
| AA Mutation | p.Asn2020Lys(p.N2020K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54625179:54625179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1297G>A |
| AA Mutation | p.Asp433Asn(p.D433N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621225:54621225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.259C>T |
| AA Mutation | p.Arg87Trp(p.R87W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629835:54629835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5953A>T |
| AA Mutation | p.Ile1985Phe(p.I1985F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629913:54629913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6031A>G |
| AA Mutation | p.Asn2011Asp(p.N2011D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627618:54627618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3736G>A |
| AA Mutation | p.Ala1246Thr(p.A1246T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629263:54629263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5381G>A |
| AA Mutation | p.Gly1794Asp(p.G1794D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54622140:54622140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267601948 |
| CDS Mutation | c.639C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621338:54621338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.372G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54625229:54625229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1347C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54620999:54620999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.33C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54628400:54628400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4518G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54628727:54628727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751632799 |
| CDS Mutation | c.4845C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621563:54621563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748104371 |
| CDS Mutation | c.597C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621494:54621494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.528C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621278:54621278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.312C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621113:54621113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571521776 |
| CDS Mutation | c.147C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621572:54621572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.606C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627503:54627503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3621T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54622125:54622125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.624C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627959:54627959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780936508 |
| CDS Mutation | c.4077T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626735:54626735(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2857delT |
| AA Mutation | p.Ser953GlnfsTer12(p.S953Qfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626253:54626253(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2377delA |
| AA Mutation | p.Arg793GlufsTer55(p.R793Efs*55) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220676 |
| Start | 54621419:54621419(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.458delC |
| AA Mutation | p.Pro153HisfsTer4(p.P153Hfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627719:54627719(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3843delT |
| AA Mutation | p.Pro1282LeufsTer12(p.P1282Lfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220676 |
| Start | 54628817:54628817(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4941delT |
| AA Mutation | p.Pro1648LeufsTer62(p.P1648Lfs*62) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627912:54627912(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4034delT |
| AA Mutation | p.Leu1345Ter(p.L1345*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000220676 |
| Start | 54629547:54629547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5665C>T |
| AA Mutation | p.Gln1889Ter(p.Q1889*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000220676 |
| Start | 54628746:54628746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4864G>T |
| AA Mutation | p.Glu1622Ter(p.E1622*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000220676 |
| Start | 54629693:54629693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5811T>A |
| AA Mutation | p.Tyr1937Ter(p.Y1937*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220676 |
| Start | 54626576:54626577(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | null |
| CDS Mutation | c.2700dupA |
| AA Mutation | p.Pro901ThrfsTer2(p.P901Tfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220676 |
| Start | 54627718:54627719(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs769601671 |
| CDS Mutation | c.3843dupT |
| AA Mutation | p.Pro1282SerfsTer2(p.P1282Sfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220676 |
| Start | 54629901:54629902(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.6025dupA |
| AA Mutation | p.Arg2009LysfsTer3(p.R2009Kfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |