Primary Site >> Stomach Cancer
Gene >> APOB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21002251:21002251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13171C>G |
| AA Mutation | p.Pro4391Ala(p.P4391A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21033512:21033512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.911A>G |
| AA Mutation | p.Lys304Arg(p.K304R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21005214:21005214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11654C>T |
| AA Mutation | p.Ala3885Val(p.A3885V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21009963:21009963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6905G>T |
| AA Mutation | p.Gly2302Val(p.G2302V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21010967:21010967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5901A>C |
| AA Mutation | p.Lys1967Asn(p.K1967N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21006880:21006880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9988T>G |
| AA Mutation | p.Phe3330Val(p.F3330V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21007578:21007578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9290A>C |
| AA Mutation | p.Lys3097Thr(p.K3097T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21010041:21010041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6827T>C |
| AA Mutation | p.Ile2276Thr(p.I2276T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21004435:21004435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762783264 |
| CDS Mutation | c.11921C>T |
| AA Mutation | p.Ala3974Val(p.A3974V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21014482:21014482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3808G>T |
| AA Mutation | p.Asp1270Tyr(p.D1270Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21007891:21007891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8977G>A |
| AA Mutation | p.Asp2993Asn(p.D2993N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011288:21011288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199585500 |
| CDS Mutation | c.5580G>T |
| AA Mutation | p.Gln1860His(p.Q1860H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21019043:21019043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3070A>G |
| AA Mutation | p.Arg1024Gly(p.R1024G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011151:21011151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5717C>T |
| AA Mutation | p.Thr1906Ile(p.T1906I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21006223:21006223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10645A>C |
| AA Mutation | p.Asn3549His(p.N3549H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008923:21008923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7945G>A |
| AA Mutation | p.Glu2649Lys(p.E2649K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21010698:21010698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6170T>G |
| AA Mutation | p.Phe2057Cys(p.F2057C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21012570:21012570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200708197 |
| CDS Mutation | c.4298C>T |
| AA Mutation | p.Ser1433Leu(p.S1433L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21015453:21015453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199859104 |
| CDS Mutation | c.3425C>T |
| AA Mutation | p.Ser1142Leu(p.S1142L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21005461:21005461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11407C>T |
| AA Mutation | p.Pro3803Ser(p.P3803S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008115:21008115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8753A>G |
| AA Mutation | p.His2918Arg(p.H2918R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008757:21008757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201874707 |
| CDS Mutation | c.8111C>T |
| AA Mutation | p.Ala2704Val(p.A2704V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011413:21011413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5455C>A |
| AA Mutation | p.Leu1819Met(p.L1819M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21007461:21007461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199590149 |
| CDS Mutation | c.9407G>A |
| AA Mutation | p.Arg3136His(p.R3136H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21007857:21007857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9011C>A |
| AA Mutation | p.Ala3004Asp(p.A3004D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21002077:21002077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13345C>A |
| AA Mutation | p.Gln4449Lys(p.Q4449K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008433:21008433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8435C>A |
| AA Mutation | p.Ala2812Glu(p.A2812E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21029676:21029676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1580C>T |
| AA Mutation | p.Ala527Val(p.A527V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21005616:21005616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11252T>C |
| AA Mutation | p.Val3751Ala(p.V3751A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008421:21008421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8447A>C |
| AA Mutation | p.Asn2816Thr(p.N2816T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21042470:21042470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.128C>T |
| AA Mutation | p.Ala43Val(p.A43V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21025043:21025043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536328155 |
| CDS Mutation | c.2326T>C |
| AA Mutation | p.Tyr776His(p.Y776H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21005580:21005580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11288T>G |
| AA Mutation | p.Leu3763Arg(p.L3763R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21012457:21012457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4411T>G |
| AA Mutation | p.Leu1471Val(p.L1471V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21032448:21032448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192004342 |
| CDS Mutation | c.1258G>A |
| AA Mutation | p.Glu420Lys(p.E420K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21029752:21029752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767615659 |
| CDS Mutation | c.1504T>G |
| AA Mutation | p.Leu502Val(p.L502V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21015182:21015182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3587A>C |
| AA Mutation | p.Asp1196Ala(p.D1196A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011012:21011012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5856T>A |
| AA Mutation | p.His1952Gln(p.H1952Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21015140:21015140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3629G>C |
| AA Mutation | p.Arg1210Thr(p.R1210T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21006139:21006139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10729T>A |
| AA Mutation | p.Phe3577Ile(p.F3577I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21037195:21037195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.598G>T |
| AA Mutation | p.Ala200Ser(p.A200S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21012595:21012595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4273T>C |
| AA Mutation | p.Ser1425Pro(p.S1425P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011963:21011963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4905A>C |
| AA Mutation | p.Lys1635Asn(p.K1635N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21032387:21032387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1319C>T |
| AA Mutation | p.Ala440Val(p.A440V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21002970:21002970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12452T>C |
| AA Mutation | p.Leu4151Pro(p.L4151P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21003186:21003186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12236G>A |
| AA Mutation | p.Gly4079Glu(p.G4079E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21026822:21026822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2210A>T |
| AA Mutation | p.His737Leu(p.H737L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008614:21008614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8254G>T |
| AA Mutation | p.Val2752Leu(p.V2752L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21005971:21005971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10897T>C |
| AA Mutation | p.Trp3633Arg(p.W3633R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21019900:21019900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2822C>G |
| AA Mutation | p.Thr941Arg(p.T941R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011337:21011337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5531C>T |
| AA Mutation | p.Ser1844Phe(p.S1844F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21010104:21010104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6764A>C |
| AA Mutation | p.Lys2255Thr(p.K2255T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008698:21008698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8170C>A |
| AA Mutation | p.Pro2724Thr(p.P2724T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21022964:21022964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371884333 |
| CDS Mutation | c.2683G>A |
| AA Mutation | p.Ala895Thr(p.A895T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21019741:21019741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs41288783 |
| CDS Mutation | c.2981C>T |
| AA Mutation | p.Pro994Leu(p.P994L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21030001:21030001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1367A>G |
| AA Mutation | p.Asn456Ser(p.N456S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21042384:21042384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.214A>C |
| AA Mutation | p.Ser72Arg(p.S72R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233242 |
| Start | 21027943:21027943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1952C>A |
| AA Mutation | p.Ala651Asp(p.A651D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21009335:21009335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7533A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21005888:21005888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10980C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008003:21008003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8865T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21024969:21024969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2400G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21009905:21009905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6963T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21012512:21012512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4356A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21003044:21003044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12378C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21022926:21022926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs72653068 |
| CDS Mutation | c.2721C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21009143:21009143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7725A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21002804:21002804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12618G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21003137:21003137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749245462 |
| CDS Mutation | c.12285C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011939:21011939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200623857 |
| CDS Mutation | c.4929G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21006299:21006299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10569C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21001751:21001751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13671A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21002723:21002723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs56675344 |
| CDS Mutation | c.12699G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008144:21008144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755498745 |
| CDS Mutation | c.8724C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21011870:21011870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4998G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21010655:21010655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6213C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21019062:21019062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs558838327 |
| CDS Mutation | c.3051C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21004404:21004404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11952C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21007058:21007058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138010392 |
| CDS Mutation | c.9810C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21010340:21010340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6528A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233242 |
| Start | 21012076:21012076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760171163 |
| CDS Mutation | c.4792C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000233242 |
| Start | 21008274:21008274(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.8594delA |
| AA Mutation | p.Asn2865IlefsTer9(p.N2865Ifs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000233242 |
| Start | 21029954:21029954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767495928 |
| CDS Mutation | c.1414G>T |
| AA Mutation | p.Glu472Ter(p.E472*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |