Primary Site >> Stomach Cancer
Gene >> KIF5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302418 |
| Start | 32018545:32018545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201506716 |
| CDS Mutation | c.2324G>A |
| AA Mutation | p.Arg775Gln(p.R775Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302418 |
| Start | 32017281:32017281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2623A>G |
| AA Mutation | p.Lys875Glu(p.K875E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302418 |
| Start | 32022928:32022928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1834G>A |
| AA Mutation | p.Glu612Lys(p.E612K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302418 |
| Start | 32038181:32038181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.480C>A |
| AA Mutation | p.Asn160Lys(p.N160K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302418 |
| Start | 32038789:32038789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.431A>G |
| AA Mutation | p.Asp144Gly(p.D144G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302418 |
| Start | 32022868:32022868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1894T>C |
| AA Mutation | p.Cys632Arg(p.C632R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302418 |
| Start | 32017352:32017352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200746362 |
| CDS Mutation | c.2552G>A |
| AA Mutation | p.Arg851His(p.R851H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302418 |
| Start | 32035973:32035973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.733G>T |
| AA Mutation | p.Gly245Cys(p.G245C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302418 |
| Start | 32033935:32033935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772429092 |
| CDS Mutation | c.1215C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302418 |
| Start | 32028509:32028509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1644A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302418 |
| Start | 32040453:32040453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.219A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302418 |
| Start | 32034835:32034835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.966C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302418 |
| Start | 32022898:32022898(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1864delA |
| AA Mutation | p.Met622TrpfsTer8(p.M622Wfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000302418 |
| Start | 32018317:32018317(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2438delA |
| AA Mutation | p.Lys813ArgfsTer62(p.K813Rfs*62) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302418 |
| Start | 32022897:32022898(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs777526028 |
| CDS Mutation | c.1864dupA |
| AA Mutation | p.Met622AsnfsTer5(p.M622Nfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000302418 |
| Start | 32023037:32023037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768804971 |
| CDS Mutation | c.1726-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |