Primary Site >> Liver Cancer
Gene >> SCRIB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320476 |
| Start | 143810511:143810511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759838353 |
| CDS Mutation | c.1498C>G |
| AA Mutation | p.Pro500Ala(p.P500A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320476 |
| Start | 143808960:143808960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1764G>T |
| AA Mutation | p.Gln588His(p.Q588H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320476 |
| Start | 143791182:143791182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4874T>C |
| AA Mutation | p.Leu1625Pro(p.L1625P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320476 |
| Start | 143793052:143793052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3941C>T |
| AA Mutation | p.Pro1314Leu(p.P1314L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320476 |
| Start | 143812946:143812946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754579272 |
| CDS Mutation | c.658C>T |
| AA Mutation | p.Arg220Trp(p.R220W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320476 |
| Start | 143805386:143805386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2396C>T |
| AA Mutation | p.Ala799Val(p.A799V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320476 |
| Start | 143803665:143803665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3396G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320476 |
| Start | 143809641:143809641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546935238 |
| CDS Mutation | c.1608C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |