Primary Site >> Stomach Cancer
Gene >> NEK8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268766 |
| Start | 28737692:28737692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845C>T |
| AA Mutation | p.Ala282Val(p.A282V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268766 |
| Start | 28741171:28741171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1826G>A |
| AA Mutation | p.Gly609Asp(p.G609D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000268766 |
| Start | 28734774:28734774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.256G>A |
| AA Mutation | p.Gly86Ser(p.G86S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268766 |
| Start | 28734159:28734159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.224C>T |
| AA Mutation | p.Ala75Val(p.A75V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268766 |
| Start | 28741434:28741434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776486944 |
| CDS Mutation | c.1913G>A |
| AA Mutation | p.Gly638Asp(p.G638D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268766 |
| Start | 28737363:28737363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779175681 |
| CDS Mutation | c.676C>T |
| AA Mutation | p.Arg226Trp(p.R226W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268766 |
| Start | 28734985:28734985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.467G>A |
| AA Mutation | p.Ser156Asn(p.S156N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268766 |
| Start | 28737733:28737733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756135134 |
| CDS Mutation | c.886A>G |
| AA Mutation | p.Arg296Gly(p.R296G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268766 |
| Start | 28740938:28740938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1685C>A |
| AA Mutation | p.Pro562His(p.P562H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268766 |
| Start | 28734983:28734983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.465C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268766 |
| Start | 28737494:28737494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.807G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268766 |
| Start | 28737877:28737877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.948C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000268766 |
| Start | 28741978:28741978(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2076delC |
| AA Mutation | p.Ter693GlufsTer11(p.*693Efs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000268766 |
| Start | 28741445:28741445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763288569 |
| CDS Mutation | c.1924C>T |
| AA Mutation | p.Arg642Ter(p.R642*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000268766 |
| Start | 28741477:28741478(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1958dupG |
| AA Mutation | p.Leu654ThrfsTer9(p.L654Tfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |