Primary Site >> Liver Cancer
Gene >> COPA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241704 |
| Start | 160339925:160339925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.212A>G |
| AA Mutation | p.Asp71Gly(p.D71G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241704 |
| Start | 160294554:160294554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2606C>T |
| AA Mutation | p.Ala869Val(p.A869V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241704 |
| Start | 160313160:160313160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.850G>A |
| AA Mutation | p.Val284Ile(p.V284I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241704 |
| Start | 160335300:160335300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.251G>T |
| AA Mutation | p.Arg84Leu(p.R84L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241704 |
| Start | 160325587:160325587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.562G>A |
| AA Mutation | p.Asp188Asn(p.D188N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241704 |
| Start | 160333652:160333652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.337G>T |
| AA Mutation | p.Asp113Tyr(p.D113Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241704 |
| Start | 160291829:160291829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141211632 |
| CDS Mutation | c.3248G>A |
| AA Mutation | p.Arg1083His(p.R1083H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241704 |
| Start | 160333647:160333647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.342T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |