Primary Site >> Liver Cancer
Gene >> TRIM58
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366481 |
| Start | 247876088:247876088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060G>A |
| AA Mutation | p.Glu354Lys(p.E354K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366481 |
| Start | 247875927:247875927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.899C>A |
| AA Mutation | p.Ala300Glu(p.A300E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366481 |
| Start | 247860698:247860698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.502A>G |
| AA Mutation | p.Thr168Ala(p.T168A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366481 |
| Start | 247857526:247857526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749287255 |
| CDS Mutation | c.280C>T |
| AA Mutation | p.Arg94Trp(p.R94W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366481 |
| Start | 247876152:247876152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1124C>A |
| AA Mutation | p.Pro375Gln(p.P375Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366481 |
| Start | 247876147:247876147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759619059 |
| CDS Mutation | c.1119C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |