Primary Site >> Stomach Cancer
Gene >> KIF27
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83870592:83870592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777539862 |
| CDS Mutation | c.2684C>T |
| AA Mutation | p.Pro895Leu(p.P895L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83842306:83842306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376993923 |
| CDS Mutation | c.3652C>T |
| AA Mutation | p.Arg1218Trp(p.R1218W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83837116:83837116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4091G>A |
| AA Mutation | p.Arg1364His(p.R1364H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83891440:83891440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1664T>G |
| AA Mutation | p.Leu555Arg(p.L555R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83887131:83887131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138059115 |
| CDS Mutation | c.2149C>T |
| AA Mutation | p.Arg717Cys(p.R717C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83908640:83908640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.311A>G |
| AA Mutation | p.Glu104Gly(p.E104G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83850225:83850225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370478477 |
| CDS Mutation | c.3430C>T |
| AA Mutation | p.Arg1144Trp(p.R1144W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83867802:83867802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566128018 |
| CDS Mutation | c.2816G>A |
| AA Mutation | p.Arg939His(p.R939H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83903757:83903757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141363838 |
| CDS Mutation | c.761C>T |
| AA Mutation | p.Thr254Met(p.T254M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83859263:83859263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3043A>C |
| AA Mutation | p.Lys1015Gln(p.K1015Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83899728:83899728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1535T>G |
| AA Mutation | p.Met512Arg(p.M512R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83880377:83880377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2563C>A |
| AA Mutation | p.Leu855Ile(p.L855I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83891387:83891387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1717G>A |
| AA Mutation | p.Ala573Thr(p.A573T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000297814 |
| Start | 83884018:83884018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2240G>T |
| AA Mutation | p.Gly747Val(p.G747V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83903652:83903652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.866C>T |
| AA Mutation | p.Ser289Leu(p.S289L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83903566:83903566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.952G>A |
| AA Mutation | p.Val318Ile(p.V318I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83889195:83889195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367944774 |
| CDS Mutation | c.1868G>A |
| AA Mutation | p.Arg623Gln(p.R623Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297814 |
| Start | 83880343:83880343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2597G>A |
| AA Mutation | p.Arg866Lys(p.R866K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297814 |
| Start | 83891460:83891460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1644G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297814 |
| Start | 83889173:83889173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1890C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297814 |
| Start | 83837271:83837271(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs775622981 |
| CDS Mutation | c.3936delC |
| AA Mutation | p.Ser1313ValfsTer5(p.S1313Vfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297814 |
| Start | 83891491:83891492(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1612dupA |
| AA Mutation | p.Ile538AsnfsTer13(p.I538Nfs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |