Primary Site >> Stomach Cancer
Gene >> LRP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169185527:169185527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780200412 |
| CDS Mutation | c.9821G>A |
| AA Mutation | p.Ser3274Asn(p.S3274N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169275098:169275098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1913A>C |
| AA Mutation | p.Tyr638Ser(p.Y638S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169207175:169207175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199813044 |
| CDS Mutation | c.6545G>A |
| AA Mutation | p.Arg2182His(p.R2182H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169132659:169132659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13643A>T |
| AA Mutation | p.Asp4548Val(p.D4548V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169244867:169244867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3256T>C |
| AA Mutation | p.Cys1086Arg(p.C1086R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169185774:169185774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761574622 |
| CDS Mutation | c.9574C>T |
| AA Mutation | p.Arg3192Trp(p.R3192W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169175310:169175310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10651C>T |
| AA Mutation | p.Arg3551Cys(p.R3551C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169244858:169244858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763860226 |
| CDS Mutation | c.3265C>T |
| AA Mutation | p.Arg1089Cys(p.R1089C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169277809:169277809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1708C>T |
| AA Mutation | p.Arg570Cys(p.R570C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169201693:169201693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552943504 |
| CDS Mutation | c.8387G>A |
| AA Mutation | p.Arg2796His(p.R2796H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169176490:169176490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749628580 |
| CDS Mutation | c.10492C>T |
| AA Mutation | p.Arg3498Cys(p.R3498C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169205538:169205538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7656G>A |
| AA Mutation | p.Met2552Ile(p.M2552I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169174011:169174011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10922G>A |
| AA Mutation | p.Arg3641Gln(p.R3641Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169154533:169154533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12222C>A |
| AA Mutation | p.Phe4074Leu(p.F4074L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169175287:169175287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10674C>A |
| AA Mutation | p.Phe3558Leu(p.F3558L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169207038:169207038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6682C>T |
| AA Mutation | p.Leu2228Phe(p.L2228F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169241032:169241032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4001G>A |
| AA Mutation | p.Gly1334Asp(p.G1334D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000263816 |
| Start | 169177805:169177805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10391T>C |
| AA Mutation | p.Ile3464Thr(p.I3464T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169241345:169241345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3688T>C |
| AA Mutation | p.Cys1230Arg(p.C1230R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169259060:169259060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2478T>G |
| AA Mutation | p.Asn826Lys(p.N826K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169279436:169279436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760488801 |
| CDS Mutation | c.1501C>T |
| AA Mutation | p.Arg501Trp(p.R501W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169202782:169202782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8183G>T |
| AA Mutation | p.Gly2728Val(p.G2728V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000263816 |
| Start | 169139369:169139369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774009040 |
| CDS Mutation | c.13270G>A |
| AA Mutation | p.Ala4424Thr(p.A4424T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169241101:169241101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140748929 |
| CDS Mutation | c.3932G>A |
| AA Mutation | p.Arg1311His(p.R1311H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169216348:169216348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5731A>G |
| AA Mutation | p.Lys1911Glu(p.K1911E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169279525:169279525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1412A>C |
| AA Mutation | p.Asn471Thr(p.N471T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169207166:169207166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6554T>G |
| AA Mutation | p.Leu2185Arg(p.L2185R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169185935:169185935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs35086590 |
| CDS Mutation | c.9413G>T |
| AA Mutation | p.Arg3138Leu(p.R3138L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169177844:169177844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10352C>A |
| AA Mutation | p.Pro3451Gln(p.P3451Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169239625:169239625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4196C>G |
| AA Mutation | p.Ser1399Cys(p.S1399C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169172083:169172083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11195G>A |
| AA Mutation | p.Cys3732Tyr(p.C3732Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169220556:169220556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5546C>T |
| AA Mutation | p.Thr1849Ile(p.T1849I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169247490:169247490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2796A>T |
| AA Mutation | p.Arg932Ser(p.R932S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169156306:169156306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201753832 |
| CDS Mutation | c.12119G>A |
| AA Mutation | p.Ser4040Asn(p.S4040N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169177997:169177997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10199A>G |
| AA Mutation | p.His3400Arg(p.H3400R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169182316:169182316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9849G>T |
| AA Mutation | p.Lys3283Asn(p.K3283N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169244914:169244914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745389472 |
| CDS Mutation | c.3209C>T |
| AA Mutation | p.Ser1070Leu(p.S1070L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169188042:169188042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761770923 |
| CDS Mutation | c.9256C>T |
| AA Mutation | p.Arg3086Cys(p.R3086C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169279469:169279469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756451023 |
| CDS Mutation | c.1468C>T |
| AA Mutation | p.Arg490Cys(p.R490C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169246713:169246713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544224269 |
| CDS Mutation | c.3182G>A |
| AA Mutation | p.Gly1061Asp(p.G1061D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169226544:169226544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5272G>C |
| AA Mutation | p.Gly1758Arg(p.G1758R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169256228:169256228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2648G>A |
| AA Mutation | p.Arg883Gln(p.R883Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169241362:169241362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3671C>T |
| AA Mutation | p.Thr1224Ile(p.T1224I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169181548:169181548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10069T>A |
| AA Mutation | p.Ser3357Thr(p.S3357T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169318782:169318782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.290C>T |
| AA Mutation | p.Ser97Leu(p.S97L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169182188:169182188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9977T>A |
| AA Mutation | p.Leu3326His(p.L3326H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169188150:169188150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774960835 |
| CDS Mutation | c.9148G>A |
| AA Mutation | p.Val3050Ile(p.V3050I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169241015:169241015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4018A>G |
| AA Mutation | p.Asn1340Asp(p.N1340D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169169722:169169722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142613924 |
| CDS Mutation | c.11477C>T |
| AA Mutation | p.Ala3826Val(p.A3826V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169176489:169176489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534940314 |
| CDS Mutation | c.10493G>A |
| AA Mutation | p.Arg3498His(p.R3498H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169181472:169181472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10145C>T |
| AA Mutation | p.Ala3382Val(p.A3382V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169272938:169272938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538946388 |
| CDS Mutation | c.2105G>A |
| AA Mutation | p.Arg702His(p.R702H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169206529:169206529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7191C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169206346:169206346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7374A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169246925:169246925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2970G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169243416:169243416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3537T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169139571:169139571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532471990 |
| CDS Mutation | c.13239G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169206979:169206979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545476826 |
| CDS Mutation | c.6741C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169204250:169204250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7737T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169279380:169279380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1557A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169156314:169156314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745582154 |
| CDS Mutation | c.12111G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169270908:169270908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2316C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169225366:169225366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5482T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169191942:169191942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549070265 |
| CDS Mutation | c.8922C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263816 |
| Start | 169185739:169185739(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.9609delT |
| AA Mutation | p.Phe3203LeufsTer7(p.F3203Lfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263816 |
| Start | 169185809:169185809(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.9539delC |
| AA Mutation | p.Pro3180GlnfsTer30(p.P3180Qfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263816 |
| Start | 169231822:169231822(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5119delT |
| AA Mutation | p.Ser1707ProfsTer32(p.S1707Pfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263816 |
| Start | 169185693:169185693(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.9655delT |
| AA Mutation | p.Tyr3219ThrfsTer14(p.Y3219Tfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263816 |
| Start | 169188120:169188120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9178G>T |
| AA Mutation | p.Gly3060Ter(p.G3060*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263816 |
| Start | 169231789:169231789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5152C>T |
| AA Mutation | p.Gln1718Ter(p.Q1718*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263816 |
| Start | 169206924:169206924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6796G>T |
| AA Mutation | p.Glu2266Ter(p.E2266*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000263816 |
| Start | 169209639:169209639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753549113 |
| CDS Mutation | c.6283C>T |
| AA Mutation | p.Arg2095Ter(p.R2095*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263816 |
| Start | 169201826:169201826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8254C>T |
| AA Mutation | p.Arg2752Ter(p.R2752*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000263816 |
| Start | 169242955:169242955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752197557 |
| CDS Mutation | c.3667+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |