Primary Site >> Liver Cancer
Gene >> IWS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295321 |
| Start | 127505279:127505279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.624G>T |
| AA Mutation | p.Met208Ile(p.M208I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295321 |
| Start | 127489932:127489932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2059A>T |
| AA Mutation | p.Arg687Trp(p.R687W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295321 |
| Start | 127486641:127486641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2240G>T |
| AA Mutation | p.Gly747Val(p.G747V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295321 |
| Start | 127492085:127492085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1933C>T |
| AA Mutation | p.Pro645Ser(p.P645S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295321 |
| Start | 127498183:127498183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1522G>C |
| AA Mutation | p.Ala508Pro(p.A508P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000295321 |
| Start | 127489848:127489848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757568675 |
| CDS Mutation | c.2143C>T |
| AA Mutation | p.Arg715Ter(p.R715*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |