Primary Site >> Stomach Cancer
Gene >> MUC5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1249911:1249911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13031C>A |
| AA Mutation | p.Pro4344His(p.P4344H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1247657:1247657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372303707 |
| CDS Mutation | c.10777G>A |
| AA Mutation | p.Gly3593Arg(p.G3593R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1242608:1242608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5728C>A |
| AA Mutation | p.Pro1910Thr(p.P1910T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243017:1243017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6137C>T |
| AA Mutation | p.Ala2046Val(p.A2046V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243773:1243773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6893C>A |
| AA Mutation | p.Pro2298His(p.P2298H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254713:1254713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764462339 |
| CDS Mutation | c.15497C>T |
| AA Mutation | p.Pro5166Leu(p.P5166L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1247234:1247234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10354G>A |
| AA Mutation | p.Ala3452Thr(p.A3452T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246419:1246419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369158178 |
| CDS Mutation | c.9539C>T |
| AA Mutation | p.Thr3180Met(p.T3180M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1251689:1251689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14809T>C |
| AA Mutation | p.Ser4937Pro(p.S4937P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254196:1254196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777182861 |
| CDS Mutation | c.15322C>T |
| AA Mutation | p.Arg5108Cys(p.R5108C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248115:1248115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11235G>T |
| AA Mutation | p.Gln3745His(p.Q3745H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1240294:1240294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3889A>T |
| AA Mutation | p.Arg1297Trp(p.R1297W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244369:1244369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7489A>G |
| AA Mutation | p.Ser2497Gly(p.S2497G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1251473:1251473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14593G>A |
| AA Mutation | p.Ala4865Thr(p.A4865T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1247277:1247277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762917439 |
| CDS Mutation | c.10397C>T |
| AA Mutation | p.Thr3466Met(p.T3466M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1255094:1255094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15718G>A |
| AA Mutation | p.Ala5240Thr(p.A5240T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1239494:1239494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3511T>G |
| AA Mutation | p.Cys1171Gly(p.C1171G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1240934:1240934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4054G>T |
| AA Mutation | p.Gly1352Cys(p.G1352C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244324:1244324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7444G>A |
| AA Mutation | p.Ala2482Thr(p.A2482T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1250076:1250076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13196C>T |
| AA Mutation | p.Ala4399Val(p.A4399V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1245426:1245426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780570757 |
| CDS Mutation | c.8546G>A |
| AA Mutation | p.Arg2849His(p.R2849H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1245663:1245663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377303931 |
| CDS Mutation | c.8783G>A |
| AA Mutation | p.Arg2928Gln(p.R2928Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254698:1254698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15482T>C |
| AA Mutation | p.Leu5161Pro(p.L5161P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1225693:1225693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.83C>A |
| AA Mutation | p.Pro28His(p.P28H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244784:1244784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7904G>A |
| AA Mutation | p.Ser2635Asn(p.S2635N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246266:1246266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377732364 |
| CDS Mutation | c.9386C>T |
| AA Mutation | p.Pro3129Leu(p.P3129L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254310:1254310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373377243 |
| CDS Mutation | c.15436G>A |
| AA Mutation | p.Val5146Ile(p.V5146I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1250015:1250015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13135A>C |
| AA Mutation | p.Thr4379Pro(p.T4379P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1229735:1229735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1148G>T |
| AA Mutation | p.Gly383Val(p.G383V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1250162:1250162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13282G>A |
| AA Mutation | p.Ala4428Thr(p.A4428T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1245851:1245851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8971T>C |
| AA Mutation | p.Trp2991Arg(p.W2991R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1242648:1242648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142667139 |
| CDS Mutation | c.5768C>T |
| AA Mutation | p.Thr1923Met(p.T1923M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244454:1244454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7574T>A |
| AA Mutation | p.Leu2525Gln(p.L2525Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1226743:1226743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780107364 |
| CDS Mutation | c.328G>A |
| AA Mutation | p.Ala110Thr(p.A110T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1232764:1232764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757494837 |
| CDS Mutation | c.2059G>A |
| AA Mutation | p.Val687Ile(p.V687I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1236423:1236423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368017279 |
| CDS Mutation | c.2918C>T |
| AA Mutation | p.Ala973Val(p.A973V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244732:1244732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7852G>A |
| AA Mutation | p.Ala2618Thr(p.A2618T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1251432:1251432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201730803 |
| CDS Mutation | c.14552C>T |
| AA Mutation | p.Pro4851Leu(p.P4851L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244501:1244501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7621C>T |
| AA Mutation | p.Pro2541Ser(p.P2541S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254311:1254311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15437T>C |
| AA Mutation | p.Val5146Ala(p.V5146A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1251578:1251578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200106435 |
| CDS Mutation | c.14698G>A |
| AA Mutation | p.Val4900Met(p.V4900M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1240340:1240340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3935C>A |
| AA Mutation | p.Thr1312Asn(p.T1312N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1249079:1249079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12199T>C |
| AA Mutation | p.Ser4067Pro(p.S4067P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254805:1254805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749312348 |
| CDS Mutation | c.15589G>A |
| AA Mutation | p.Val5197Ile(p.V5197I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248095:1248095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11215G>A |
| AA Mutation | p.Ala3739Thr(p.A3739T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243860:1243860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6980G>A |
| AA Mutation | p.Ser2327Asn(p.S2327N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1258345:1258345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756336123 |
| CDS Mutation | c.16571C>T |
| AA Mutation | p.Ser5524Leu(p.S5524L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244736:1244736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7856C>A |
| AA Mutation | p.Thr2619Asn(p.T2619N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529681 |
| Start | 1259801:1259801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752501699 |
| CDS Mutation | c.16759G>A |
| AA Mutation | p.Val5587Ile(p.V5587I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254880:1254880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563622514 |
| CDS Mutation | c.15664G>A |
| AA Mutation | p.Gly5222Ser(p.G5222S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254867:1254867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15651C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1241506:1241506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4626G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244245:1244245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774746614 |
| CDS Mutation | c.7365G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1242649:1242649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530408361 |
| CDS Mutation | c.5769G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1257616:1257616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768908012 |
| CDS Mutation | c.16356C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246174:1246174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9294C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1241587:1241587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369671175 |
| CDS Mutation | c.4707C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1235148:1235148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546384509 |
| CDS Mutation | c.2694C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1232505:1232505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762981010 |
| CDS Mutation | c.1899G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1247560:1247560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774465079 |
| CDS Mutation | c.10680G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244368:1244368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7488G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1245844:1245844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552609450 |
| CDS Mutation | c.8964G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243921:1243921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766599670 |
| CDS Mutation | c.7041C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246435:1246435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9555C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248556:1248556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11676C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254141:1254141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15267C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1249996:1249996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746438655 |
| CDS Mutation | c.13116G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243699:1243699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6819G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1247575:1247575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544046466 |
| CDS Mutation | c.10695G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1240191:1240191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243039:1243039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6159T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243789:1243789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375457073 |
| CDS Mutation | c.6909G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248139:1248139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761584395 |
| CDS Mutation | c.11259G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1241812:1241812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749776295 |
| CDS Mutation | c.4932G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1242109:1242109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5229G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248100:1248100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761306783 |
| CDS Mutation | c.11220C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1242388:1242388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752386600 |
| CDS Mutation | c.5508C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1251448:1251448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746714148 |
| CDS Mutation | c.14568C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1241458:1241458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376958594 |
| CDS Mutation | c.4578C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1254240:1254240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748622933 |
| CDS Mutation | c.15366G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246930:1246930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10050C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1252901:1252901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754101374 |
| CDS Mutation | c.15138C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243990:1243990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7110G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 84 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1249177:1249177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753882633 |
| CDS Mutation | c.12297G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 85 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000529681 |
| Start | 1235119:1235119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2735722 |
| CDS Mutation | c.2665C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 86 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1243487:1243487(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6612delC |
| AA Mutation | p.Ser2205AlafsTer29(p.S2205Afs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 87 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246251:1246251(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.9375delC |
| AA Mutation | p.Ser3126ProfsTer13(p.S3126Pfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 88 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1250022:1250022(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.13146delC |
| AA Mutation | p.Ser4383ProfsTer13(p.S4383Pfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 89 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1247213:1247213(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.10337delC |
| AA Mutation | p.Pro3446GlnfsTer45(p.P3446Qfs*45) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 90 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1250241:1250242(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.13361_13362delGC |
| AA Mutation | p.Ser4454AsnfsTer216(p.S4454Nfs*216) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 91 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1246923:1246923(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.10047delC |
| AA Mutation | p.Ser3350ProfsTer13(p.S3350Pfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 92 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1229288:1229288(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1100delC |
| AA Mutation | p.Pro367GlnfsTer105(p.P367Qfs*105) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 93 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1248507:1248507(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.11631delC |
| AA Mutation | p.Ser3878ProfsTer27(p.S3878Pfs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 94 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1230014:1230015(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1236dupG |
| AA Mutation | p.Leu413AlafsTer25(p.L413Afs*25) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 95 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1244540:1244541(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.7661dupA |
| AA Mutation | p.Thr2555AspfsTer126(p.T2555Dfs*126) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 96 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000529681 |
| Start | 1240860:1240861(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3983dupC |
| AA Mutation | p.Val1329GlyfsTer31(p.V1329Gfs*31) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 97 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000529681 |
| Start | 1240377:1240377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3970+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 98 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000529681 |
| Start | 1246093:1246095(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.9214_9216delTTC |
| AA Mutation | p.Phe3072del(p.F3072del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 99 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000529681 |
| Start | 1230548:1230550(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs151023614 |
| CDS Mutation | c.1420_1422delAAC |
| AA Mutation | p.Asn474del(p.N474del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |