Primary Site >> Liver Cancer
Gene >> XPO5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265351 |
| Start | 43549924:43549924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1739C>T |
| AA Mutation | p.Ser580Phe(p.S580F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265351 |
| Start | 43531540:43531540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2479C>T |
| AA Mutation | p.Pro827Ser(p.P827S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265351 |
| Start | 43524589:43524589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3359A>T |
| AA Mutation | p.Glu1120Val(p.E1120V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265351 |
| Start | 43546658:43546658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2255G>C |
| AA Mutation | p.Gly752Ala(p.G752A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265351 |
| Start | 43558561:43558561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1252A>T |
| AA Mutation | p.Ser418Cys(p.S418C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265351 |
| Start | 43558529:43558529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764721782 |
| CDS Mutation | c.1284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265351 |
| Start | 43525194:43525194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3087A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |