Primary Site >> Stomach Cancer
Gene >> KIF1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10339801:10339801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775773486 |
| CDS Mutation | c.3455C>T |
| AA Mutation | p.Thr1152Met(p.T1152M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10296978:10296978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771169398 |
| CDS Mutation | c.1943C>A |
| AA Mutation | p.Pro648His(p.P648H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10326142:10326142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2707C>T |
| AA Mutation | p.Arg903Cys(p.R903C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10258499:10258499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.190G>A |
| AA Mutation | p.Asp64Asn(p.D64N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10296636:10296636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1832G>A |
| AA Mutation | p.Arg611Lys(p.R611K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10339792:10339792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3446C>A |
| AA Mutation | p.Ala1149Glu(p.A1149E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10363305:10363305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4327G>A |
| AA Mutation | p.Glu1443Lys(p.E1443K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10261921:10261921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.380T>G |
| AA Mutation | p.Phe127Cys(p.F127C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10295683:10295683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201531774 |
| CDS Mutation | c.1694G>A |
| AA Mutation | p.Arg565Gln(p.R565Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10295682:10295682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758740011 |
| CDS Mutation | c.1693C>T |
| AA Mutation | p.Arg565Trp(p.R565W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10276363:10276363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1001C>T |
| AA Mutation | p.Ala334Val(p.A334V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10334554:10334554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768340319 |
| CDS Mutation | c.2959G>A |
| AA Mutation | p.Val987Met(p.V987M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10321753:10321753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368066001 |
| CDS Mutation | c.2254C>T |
| AA Mutation | p.Arg752Trp(p.R752W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10324822:10324822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2602G>T |
| AA Mutation | p.Asp868Tyr(p.D868Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377086 |
| Start | 10371165:10371165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765259892 |
| CDS Mutation | c.4849C>T |
| AA Mutation | p.Arg1617Trp(p.R1617W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377086 |
| Start | 10324830:10324830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775697231 |
| CDS Mutation | c.2610C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377086 |
| Start | 10339802:10339802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574168097 |
| CDS Mutation | c.3456G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377086 |
| Start | 10276367:10276367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777030180 |
| CDS Mutation | c.1005T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377086 |
| Start | 10347776:10347776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3813G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377086 |
| Start | 10326273:10326273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138353787 |
| CDS Mutation | c.2838C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377086 |
| Start | 10321809:10321809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749823391 |
| CDS Mutation | c.2310C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377086 |
| Start | 10347812:10347813(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3854dupT |
| AA Mutation | p.Leu1285PhefsTer17(p.L1285Ffs*17) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000377086 |
| Start | 10258492:10258492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.184-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000377086 |
| Start | 10365111:10365113(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4380_4382delGAG |
| AA Mutation | p.Arg1462del(p.R1462del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |