Primary Site >> Stomach Cancer
Gene >> NEK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366999 |
| Start | 211670300:211670300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776935855 |
| CDS Mutation | c.746C>T |
| AA Mutation | p.Thr249Met(p.T249M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366999 |
| Start | 211673620:211673620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778979955 |
| CDS Mutation | c.418C>T |
| AA Mutation | p.Arg140Trp(p.R140W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366999 |
| Start | 211663441:211663441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769036822 |
| CDS Mutation | c.1323C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366999 |
| Start | 211669236:211669236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.862C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366999 |
| Start | 211674310:211674310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.300G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000366999 |
| Start | 211669113:211669113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140995957 |
| CDS Mutation | c.985C>T |
| AA Mutation | p.Gln329Ter(p.Q329*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |