Primary Site >> Liver Cancer
Gene >> SERPINB3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283752 |
| Start | 63658539:63658539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.443A>G |
| AA Mutation | p.Asn148Ser(p.N148S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283752 |
| Start | 63655728:63655728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1102C>G |
| AA Mutation | p.Pro368Ala(p.P368A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283752 |
| Start | 63655937:63655937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377088096 |
| CDS Mutation | c.893C>T |
| AA Mutation | p.Thr298Met(p.T298M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283752 |
| Start | 63658538:63658538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.444C>A |
| AA Mutation | p.Asn148Lys(p.N148K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283752 |
| Start | 63655775:63655775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1055T>A |
| AA Mutation | p.Phe352Tyr(p.F352Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283752 |
| Start | 63655867:63655867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763567283 |
| CDS Mutation | c.963C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |