Primary Site >> Stomach Cancer
Gene >> MKI67
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128111809:128111809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2096T>A |
| AA Mutation | p.Val699Glu(p.V699E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128115405:128115405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199572304 |
| CDS Mutation | c.1003G>A |
| AA Mutation | p.Ala335Thr(p.A335T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128107183:128107183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371337191 |
| CDS Mutation | c.4657G>A |
| AA Mutation | p.Ala1553Thr(p.A1553T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128102824:128102824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756109830 |
| CDS Mutation | c.9016G>A |
| AA Mutation | p.Val3006Ile(p.V3006I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128102607:128102607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9233A>G |
| AA Mutation | p.Lys3078Arg(p.K3078R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128105898:128105898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5942G>A |
| AA Mutation | p.Cys1981Tyr(p.C1981Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128109048:128109048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2792C>T |
| AA Mutation | p.Thr931Ile(p.T931I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128101419:128101419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9544C>T |
| AA Mutation | p.Leu3182Phe(p.L3182F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128102939:128102939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8901A>C |
| AA Mutation | p.Lys2967Asn(p.K2967N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128105913:128105913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5927T>G |
| AA Mutation | p.Ile1976Ser(p.I1976S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128107224:128107224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4616A>G |
| AA Mutation | p.His1539Arg(p.H1539R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128109151:128109151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2689A>G |
| AA Mutation | p.Asn897Asp(p.N897D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128102681:128102681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9159G>T |
| AA Mutation | p.Arg3053Ser(p.R3053S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128110445:128110445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2349G>C |
| AA Mutation | p.Leu783Phe(p.L783F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128107581:128107581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4259C>G |
| AA Mutation | p.Thr1420Arg(p.T1420R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128106202:128106202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5638A>G |
| AA Mutation | p.Ser1880Gly(p.S1880G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128104211:128104211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7629G>T |
| AA Mutation | p.Arg2543Ser(p.R2543S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128108313:128108313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs117795868 |
| CDS Mutation | c.3527C>T |
| AA Mutation | p.Thr1176Met(p.T1176M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128102590:128102590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528824310 |
| CDS Mutation | c.9250C>T |
| AA Mutation | p.Pro3084Ser(p.P3084S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128108800:128108800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3040C>T |
| AA Mutation | p.Pro1014Ser(p.P1014S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128101547:128101547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9416G>A |
| AA Mutation | p.Gly3139Glu(p.G3139E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128115905:128115905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.503C>T |
| AA Mutation | p.Ala168Val(p.A168V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128122929:128122929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.239T>C |
| AA Mutation | p.Val80Ala(p.V80A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128104845:128104845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182397079 |
| CDS Mutation | c.6995C>T |
| AA Mutation | p.Thr2332Met(p.T2332M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128101484:128101484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9479G>C |
| AA Mutation | p.Arg3160Thr(p.R3160T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128105997:128105997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5843C>T |
| AA Mutation | p.Ala1948Val(p.A1948V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128107207:128107207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4633G>A |
| AA Mutation | p.Val1545Ile(p.V1545I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128105768:128105768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750960623 |
| CDS Mutation | c.6072G>T |
| AA Mutation | p.Lys2024Asn(p.K2024N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128123154:128123154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.108C>G |
| AA Mutation | p.Asp36Glu(p.D36E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128101680:128101680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754001305 |
| CDS Mutation | c.9283C>T |
| AA Mutation | p.Arg3095Cys(p.R3095C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128104332:128104332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371949944 |
| CDS Mutation | c.7508G>A |
| AA Mutation | p.Arg2503Gln(p.R2503Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128104115:128104115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7725A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128110493:128110493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763613616 |
| CDS Mutation | c.2301G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128108894:128108894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2946C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128103356:128103356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8484A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128104313:128104313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368483125 |
| CDS Mutation | c.7527G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128103233:128103233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8607G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128115598:128115598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201621002 |
| CDS Mutation | c.810C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128109296:128109296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2544C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128108135:128108135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3705T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368654 |
| Start | 128114986:128114986(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1422delG |
| AA Mutation | p.Met474IlefsTer28(p.M474Ifs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368654 |
| Start | 128115210:128115210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142132992 |
| CDS Mutation | c.1198C>T |
| AA Mutation | p.Arg400Ter(p.R400*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |