Primary Site >> Liver Cancer
Gene >> ERC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288221 |
| Start | 56434520:56434520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.488T>A |
| AA Mutation | p.Leu163His(p.L163H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288221 |
| Start | 55992088:55992088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2224G>C |
| AA Mutation | p.Asp742His(p.D742H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288221 |
| Start | 55683850:55683850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2857G>C |
| AA Mutation | p.Glu953Gln(p.E953Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288221 |
| Start | 56434916:56434916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.92G>T |
| AA Mutation | p.Arg31Ile(p.R31I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288221 |
| Start | 55734798:55734798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749739992 |
| CDS Mutation | c.2685C>G |
| AA Mutation | p.Asp895Glu(p.D895E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288221 |
| Start | 56434603:56434603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141688594 |
| CDS Mutation | c.405C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |