Primary Site >> Stomach Cancer
Gene >> KIF14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200618489:200618489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.235C>T |
| AA Mutation | p.Pro79Ser(p.P79S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200553408:200553408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4927A>G |
| AA Mutation | p.Ser1643Gly(p.S1643G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200605335:200605335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1694A>T |
| AA Mutation | p.Asp565Val(p.D565V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200555447:200555447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4361A>G |
| AA Mutation | p.Lys1454Arg(p.K1454R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200560813:200560813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4139A>G |
| AA Mutation | p.Gln1380Arg(p.Q1380R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200603909:200603909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373895990 |
| CDS Mutation | c.1793G>A |
| AA Mutation | p.Arg598Gln(p.R598Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200618323:200618323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.401A>G |
| AA Mutation | p.Lys134Arg(p.K134R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200590181:200590181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2905C>A |
| AA Mutation | p.Leu969Ile(p.L969I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200603937:200603937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1765G>A |
| AA Mutation | p.Glu589Lys(p.E589K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200589239:200589239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377490365 |
| CDS Mutation | c.3092T>C |
| AA Mutation | p.Met1031Thr(p.M1031T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200598361:200598361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2425G>A |
| AA Mutation | p.Asp809Asn(p.D809N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200601956:200601956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371788866 |
| CDS Mutation | c.2092G>A |
| AA Mutation | p.Ala698Thr(p.A698T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200615548:200615548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1174C>G |
| AA Mutation | p.His392Asp(p.H392D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200603245:200603245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1960C>T |
| AA Mutation | p.Arg654Cys(p.R654C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200592095:200592095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568570558 |
| CDS Mutation | c.2798T>C |
| AA Mutation | p.Met933Thr(p.M933T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200600426:200600426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2230T>C |
| AA Mutation | p.Cys744Arg(p.C744R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367350 |
| Start | 200570004:200570004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3568A>T |
| AA Mutation | p.Ser1190Cys(p.S1190C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367350 |
| Start | 200553439:200553439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754764767 |
| CDS Mutation | c.4896C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |