Primary Site >> Stomach Cancer
Gene >> KIF7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394412 |
| Start | 89646966:89646966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1652T>C |
| AA Mutation | p.Leu551Pro(p.L551P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394412 |
| Start | 89642222:89642222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375985448 |
| CDS Mutation | c.2375C>T |
| AA Mutation | p.Ala792Val(p.A792V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394412 |
| Start | 89633858:89633858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757175418 |
| CDS Mutation | c.2420C>T |
| AA Mutation | p.Thr807Met(p.T807M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394412 |
| Start | 89628636:89628636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765907353 |
| CDS Mutation | c.3815C>T |
| AA Mutation | p.Pro1272Leu(p.P1272L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394412 |
| Start | 89628566:89628566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3885G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394412 |
| Start | 89633207:89633207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750064265 |
| CDS Mutation | c.2652C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394412 |
| Start | 89628581:89628581(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3870delC |
| AA Mutation | p.Glu1291ArgfsTer3(p.E1291Rfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394412 |
| Start | 89646978:89646978(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774048463 |
| CDS Mutation | c.1640delG |
| AA Mutation | p.Gly547AlafsTer5(p.G547Afs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394412 |
| Start | 89628691:89628691(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3760delC |
| AA Mutation | p.Leu1254SerfsTer22(p.L1254Sfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394412 |
| Start | 89628673:89628673(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3778delC |
| AA Mutation | p.Arg1260AlafsTer16(p.R1260Afs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394412 |
| Start | 89646909:89646909(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1709delG |
| AA Mutation | p.Gly570ValfsTer29(p.G570Vfs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394412 |
| Start | 89645120:89645120(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2084delC |
| AA Mutation | p.Pro695LeufsTer25(p.P695Lfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394412 |
| Start | 89646915:89646916(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs772716663 |
| CDS Mutation | c.1702dupC |
| AA Mutation | p.Leu568ProfsTer21(p.L568Pfs*21) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |