Primary Site >> Liver Cancer
Gene >> NUP210
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254508 |
| Start | 13327241:13327241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199638243 |
| CDS Mutation | c.4483G>A |
| AA Mutation | p.Ala1495Thr(p.A1495T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254508 |
| Start | 13341818:13341818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3158A>T |
| AA Mutation | p.Gln1053Leu(p.Q1053L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254508 |
| Start | 13360365:13360365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2059A>T |
| AA Mutation | p.Thr687Ser(p.T687S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254508 |
| Start | 13360319:13360319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2105A>G |
| AA Mutation | p.Asn702Ser(p.N702S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254508 |
| Start | 13335478:13335478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3819A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254508 |
| Start | 13371850:13371850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767996831 |
| CDS Mutation | c.1770G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |