Primary Site >> Stomach Cancer
Gene >> NEK6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320246 |
| Start | 124312633:124312633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.215C>T |
| AA Mutation | p.Ala72Val(p.A72V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320246 |
| Start | 124327373:124327373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.550G>A |
| AA Mutation | p.Gly184Ser(p.G184S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320246 |
| Start | 124339644:124339644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.696C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320246 |
| Start | 124327399:124327399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.576T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320246 |
| Start | 124339578:124339578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.630G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320246 |
| Start | 124327375:124327375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147517890 |
| CDS Mutation | c.552C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000320246 |
| Start | 124347789:124347789(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.803delC |
| AA Mutation | p.Pro268HisfsTer74(p.P268Hfs*74) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_lost |
| Transcription ID | ENST00000320246 |
| Start | 124350945:124350945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.940T>C |
| AA Mutation | p.Ter314ArgextTer17(p.*314Rext*17) |
| Mutation Classification | Nonstop_Mutation |
| Feature Type | Transcript |