Primary Site >> Stomach Cancer
Gene >> KIF11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260731 |
| Start | 92645537:92645537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2442G>C |
| AA Mutation | p.Glu814Asp(p.E814D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260731 |
| Start | 92613399:92613399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812A>G |
| AA Mutation | p.Asn271Ser(p.N271S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260731 |
| Start | 92613088:92613088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.747G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260731 |
| Start | 92653668:92653668(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3048delA |
| AA Mutation | p.Lys1016AsnfsTer52(p.K1016Nfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260731 |
| Start | 92649852:92649853(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2790_2791delAA |
| AA Mutation | p.Ser931LeufsTer11(p.S931Lfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260731 |
| Start | 92628861:92628861(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1276delA |
| AA Mutation | p.Ile426LeufsTer8(p.I426Lfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000260731 |
| Start | 92606717:92606717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527562872 |
| CDS Mutation | c.308+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |