Primary Site >> Stomach Cancer
Gene >> ARID1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26767943:26767943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3142C>T |
| AA Mutation | p.Pro1048Ser(p.P1048S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779126:26779126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528936858 |
| CDS Mutation | c.5228C>T |
| AA Mutation | p.Thr1743Met(p.T1743M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779933:26779933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6035G>A |
| AA Mutation | p.Gly2012Asp(p.G2012D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780671:26780671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6773T>G |
| AA Mutation | p.Leu2258Arg(p.L2258R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780157:26780157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6259G>A |
| AA Mutation | p.Gly2087Arg(p.G2087R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780482:26780482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6584T>C |
| AA Mutation | p.Leu2195Pro(p.L2195P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26731513:26731513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1712C>T |
| AA Mutation | p.Ser571Leu(p.S571L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774564:26774564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4337G>A |
| AA Mutation | p.Arg1446Gln(p.R1446Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780371:26780371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142069738 |
| CDS Mutation | c.6473G>A |
| AA Mutation | p.Arg2158Gln(p.R2158Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26767811:26767811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3010A>G |
| AA Mutation | p.Thr1004Ala(p.T1004A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26771297:26771297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3377C>T |
| AA Mutation | p.Ser1126Phe(p.S1126F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774786:26774786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4559G>A |
| AA Mutation | p.Gly1520Asp(p.G1520D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26762208:26762208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2308G>A |
| AA Mutation | p.Ala770Thr(p.A770T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780692:26780692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6794C>A |
| AA Mutation | p.Pro2265Gln(p.P2265Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779972:26779972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6074A>C |
| AA Mutation | p.Lys2025Thr(p.K2025T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779921:26779921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6023T>G |
| AA Mutation | p.Leu2008Arg(p.L2008R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26761423:26761423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2201A>G |
| AA Mutation | p.Asp734Gly(p.D734G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26773423:26773423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3793G>A |
| AA Mutation | p.Gly1265Ser(p.G1265S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26760995:26760995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2060C>A |
| AA Mutation | p.Pro687His(p.P687H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26762218:26762218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373690941 |
| CDS Mutation | c.2318C>T |
| AA Mutation | p.Pro773Leu(p.P773L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780208:26780208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6310T>C |
| AA Mutation | p.Ser2104Pro(p.S2104P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26773418:26773418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3788C>T |
| AA Mutation | p.Ala1263Val(p.A1263V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774873:26774873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4646G>T |
| AA Mutation | p.Gly1549Val(p.G1549V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779395:26779395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372213935 |
| CDS Mutation | c.5497C>T |
| AA Mutation | p.Arg1833Cys(p.R1833C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774435:26774435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4208A>T |
| AA Mutation | p.Gln1403Leu(p.Q1403L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779100:26779100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5202T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774859:26774859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146171057 |
| CDS Mutation | c.4632G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779769:26779769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761246391 |
| CDS Mutation | c.5871C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779199:26779199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5301A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779440:26779440(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.5548delG |
| AA Mutation | p.Asp1850ThrfsTer33(p.D1850Tfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26773839:26773851(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4042_4054delACCCCTTCTGGCA |
| AA Mutation | p.Thr1348AlafsTer129(p.T1348Afs*129) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26731570:26731573(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1771_1774delGCCT |
| AA Mutation | p.Ala591IlefsTer27(p.A591Ifs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26773840:26773840(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4046delC |
| AA Mutation | p.Pro1349LeufsTer132(p.P1349Lfs*132) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26771131:26771131(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3216delA |
| AA Mutation | p.Lys1072AsnfsTer21(p.K1072Nfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779317:26779318(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5419_5420delAG |
| AA Mutation | p.Ser1807Ter(p.S1807*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26731446:26731446(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1650delC |
| AA Mutation | p.Tyr551ThrfsTer68(p.Y551Tfs*68) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26762168:26762168(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2272delC |
| AA Mutation | p.Gln758ArgfsTer75(p.Q758Rfs*75) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779587:26779587(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.5693delC |
| AA Mutation | p.Pro1898HisfsTer25(p.P1898Hfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26729753:26729780(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1242_1269delACATGGGTACCCAGGGCAGCCATACGGG |
| AA Mutation | p.His415ProfsTer9(p.H415Pfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774626:26774626(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4403delC |
| AA Mutation | p.Pro1468LeufsTer13(p.P1468Lfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780044:26780044(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6147delG |
| AA Mutation | p.Trp2049CysfsTer86(p.W2049Cfs*86) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26762191:26762191(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2296delC |
| AA Mutation | p.Gln766SerfsTer67(p.Q766Sfs*67) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26775121:26775121(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4899delC |
| AA Mutation | p.Met1634Ter(p.M1634*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774777:26774777(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4555delC |
| AA Mutation | p.Gln1519ArgfsTer8(p.Q1519Rfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774698:26774705(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4472_4479delTTGCTCAG |
| AA Mutation | p.Val1491AlafsTer9(p.V1491Afs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780313:26780313(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.6420delC |
| AA Mutation | p.Phe2141SerfsTer59(p.F2141Sfs*59) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26761399:26761411(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2177_2189delCTCGGCCACCCAG |
| AA Mutation | p.Pro726LeufsTer12(p.P726Lfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26763003:26763003(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2451delC |
| AA Mutation | p.Leu818CysfsTer15(p.L818Cfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26732716:26732716(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1848delC |
| AA Mutation | p.Ser617GlnfsTer2(p.S617Qfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26762297:26762297(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2402delG |
| AA Mutation | p.Gly801ValfsTer32(p.G801Vfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780212:26780240(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6315_6343delCCTGGGCCCCAATGCCGTCCTTTCCCCGC |
| AA Mutation | p.Leu2106GlufsTer34(p.L2106Efs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26773685:26773685(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3977delC |
| AA Mutation | p.Pro1326ArgfsTer155(p.P1326Rfs*155) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774787:26774787(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4563delC |
| AA Mutation | p.Ala1522ProfsTer5(p.A1522Pfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26766258:26766291(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2772_2805delGGGAACTGGACCTCCTTATGGACAAGGGATTAAT |
| AA Mutation | p.Met924IlefsTer6(p.M924Ifs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774947:26774947(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4724delC |
| AA Mutation | p.Pro1575HisfsTer37(p.P1575Hfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774995:26774995(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4771delC |
| AA Mutation | p.Leu1591CysfsTer21(p.L1591Cfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26697225:26697225(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.827delG |
| AA Mutation | p.Gly276GlufsTer87(p.G276Efs*87) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26697278:26697278(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.879delC |
| AA Mutation | p.Thr294ProfsTer69(p.T294Pfs*69) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26761396:26761414(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2175_2193delACCTCGGCCACCCAGTGGC |
| AA Mutation | p.Pro726SerfsTer10(p.P726Sfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26761403:26761407(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2181_2185delGCCAC |
| AA Mutation | p.Pro728GlnfsTer87(p.P728Qfs*87) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774775:26774775(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4548delT |
| AA Mutation | p.Ala1517ProfsTer10(p.A1517Pfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774361:26774361(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4136delC |
| AA Mutation | p.Pro1379LeufsTer102(p.P1379Lfs*102) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26771310:26771313(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3392_3395delAGCC |
| AA Mutation | p.Gln1131LeufsTer29(p.Q1131Lfs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26774903:26774903(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4679delC |
| AA Mutation | p.Pro1560LeufsTer5(p.P1560Lfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26772612:26772612(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3524delC |
| AA Mutation | p.Pro1175HisfsTer5(p.P1175Hfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26771260:26771260(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3344delC |
| AA Mutation | p.Pro1115GlnfsTer46(p.P1115Qfs*46) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26731433:26731433(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1636delC |
| AA Mutation | p.Gln546ArgfsTer73(p.Q546Rfs*73) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26775102:26775102(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4875delA |
| AA Mutation | p.Ile1625MetfsTer10(p.I1625Mfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26771203:26771203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3283C>T |
| AA Mutation | p.Gln1095Ter(p.Q1095*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26780370:26780370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6472C>T |
| AA Mutation | p.Arg2158Ter(p.R2158*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26772562:26772562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3469G>T |
| AA Mutation | p.Gly1157Ter(p.G1157*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26774761:26774761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4534C>T |
| AA Mutation | p.Gln1512Ter(p.Q1512*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26731581:26731581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1780C>T |
| AA Mutation | p.Gln594Ter(p.Q594*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26779224:26779224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5326G>T |
| AA Mutation | p.Glu1776Ter(p.E1776*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26779816:26779816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5918G>A |
| AA Mutation | p.Trp1973Ter(p.W1973*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26760952:26760952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2017C>T |
| AA Mutation | p.Gln673Ter(p.Q673*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26732685:26732685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1813C>T |
| AA Mutation | p.Gln605Ter(p.Q605*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26731557:26731557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1756C>T |
| AA Mutation | p.Gln586Ter(p.Q586*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26763103:26763103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2550T>G |
| AA Mutation | p.Tyr850Ter(p.Y850*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26773821:26773821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4024C>T |
| AA Mutation | p.Gln1342Ter(p.Q1342*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26731456:26731456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1655C>A |
| AA Mutation | p.Ser552Ter(p.S552*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26696929:26696929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.526C>T |
| AA Mutation | p.Gln176Ter(p.Q176*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26779119:26779119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5221C>T |
| AA Mutation | p.Gln1741Ter(p.Q1741*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 84 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26780689:26780689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6791C>A |
| AA Mutation | p.Ser2264Ter(p.S2264*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 85 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26731305:26731305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1504C>T |
| AA Mutation | p.Gln502Ter(p.Q502*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 86 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26774608:26774608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4381C>T |
| AA Mutation | p.Arg1461Ter(p.R1461*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 87 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26772517:26772517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3424C>T |
| AA Mutation | p.Gln1142Ter(p.Q1142*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 88 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000324856 |
| Start | 26732676:26732676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1804G>T |
| AA Mutation | p.Glu602Ter(p.E602*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 89 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26780660:26780660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6762C>A |
| AA Mutation | p.Tyr2254Ter(p.Y2254*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 90 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26729723:26729723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1210C>T |
| AA Mutation | p.Gln404Ter(p.Q404*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 91 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26731239:26731239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1438C>T |
| AA Mutation | p.Gln480Ter(p.Q480*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 92 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26773660:26773660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3947C>A |
| AA Mutation | p.Ser1316Ter(p.S1316*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 93 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26761012:26761012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2077C>T |
| AA Mutation | p.Arg693Ter(p.R693*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 94 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26773866:26773866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4069C>T |
| AA Mutation | p.Gln1357Ter(p.Q1357*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 95 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26774563:26774563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4336C>T |
| AA Mutation | p.Arg1446Ter(p.R1446*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 96 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324856 |
| Start | 26779059:26779059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5161C>T |
| AA Mutation | p.Arg1721Ter(p.R1721*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 97 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26780735:26780736(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.6842dupT |
| AA Mutation | p.Leu2281PhefsTer104(p.L2281Ffs*104) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 98 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26731217:26731218(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1416_1417insA |
| AA Mutation | p.Gln473ThrfsTer150(p.Q473Tfs*150) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 99 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26773708:26773709(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3996dupG |
| AA Mutation | p.Gln1333AlafsTer5(p.Q1333Afs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 100 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26731445:26731446(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | null |
| CDS Mutation | c.1650dupC |
| AA Mutation | p.Tyr551LeufsTer72(p.Y551Lfs*72) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 101 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324856 |
| Start | 26779439:26779440(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs758608743 |
| CDS Mutation | c.5548dupG |
| AA Mutation | p.Asp1850GlyfsTer4(p.D1850Gfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |