Primary Site >> Liver Cancer
Gene >> NUAK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367157 |
| Start | 205321585:205321585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.44C>T |
| AA Mutation | p.Ser15Leu(p.S15L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367157 |
| Start | 205303545:205303545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1792G>C |
| AA Mutation | p.Asp598His(p.D598H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367157 |
| Start | 205308614:205308614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.471G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367157 |
| Start | 205304164:205304164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149020592 |
| CDS Mutation | c.1173G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000367157 |
| Start | 205321475:205321498(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.131_154delACCACAAGCACAACCTGCGGCACC |
| AA Mutation | p.His44_His51del(p.H44_H51del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |