Primary Site >> Liver Cancer
Gene >> NES
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156669619:156669619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4569G>A |
| AA Mutation | p.Met1523Ile(p.M1523I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156671508:156671508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2680T>A |
| AA Mutation | p.Ser894Thr(p.S894T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156669699:156669699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4489G>T |
| AA Mutation | p.Gly1497Cys(p.G1497C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156670571:156670571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754373045 |
| CDS Mutation | c.3617G>T |
| AA Mutation | p.Gly1206Val(p.G1206V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156670418:156670418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3770G>T |
| AA Mutation | p.Gly1257Val(p.G1257V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156671967:156671967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2221C>A |
| AA Mutation | p.His741Asn(p.H741N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156669608:156669608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4580G>A |
| AA Mutation | p.Gly1527Asp(p.G1527D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368223 |
| Start | 156670930:156670930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3258A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368223 |
| Start | 156669523:156669523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148568870 |
| CDS Mutation | c.4665C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368223 |
| Start | 156671710:156671710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2478A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368223 |
| Start | 156670228:156670228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3960G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368223 |
| Start | 156673012:156673012(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs759081520 |
| CDS Mutation | c.1176delC |
| AA Mutation | p.Thr393HisfsTer9(p.T393Hfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |