Primary Site >> Liver Cancer
Gene >> USP22
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261497 |
| Start | 21017982:21017982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.650G>A |
| AA Mutation | p.Ser217Asn(p.S217N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261497 |
| Start | 21006945:21006945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1273T>G |
| AA Mutation | p.Tyr425Asp(p.Y425D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261497 |
| Start | 21004284:21004284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370939634 |
| CDS Mutation | c.1453C>T |
| AA Mutation | p.Arg485Trp(p.R485W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261497 |
| Start | 21017988:21017988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.644G>A |
| AA Mutation | p.Ser215Asn(p.S215N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261497 |
| Start | 21021206:21021206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Gly109Ser(p.G109S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261497 |
| Start | 21015822:21015822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.768A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261497 |
| Start | 21015804:21015804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747593114 |
| CDS Mutation | c.786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261497 |
| Start | 21004951:21004951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1362G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |