Primary Site >> Liver Cancer
Gene >> GRIA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541091 |
| Start | 123464916:123464916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2128G>A |
| AA Mutation | p.Glu710Lys(p.E710K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541091 |
| Start | 123482835:123482835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2476G>A |
| AA Mutation | p.Gly826Ser(p.G826S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541091 |
| Start | 123417435:123417435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1534A>C |
| AA Mutation | p.Thr512Pro(p.T512P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541091 |
| Start | 123404876:123404876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1462A>G |
| AA Mutation | p.Lys488Glu(p.K488E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000541091 |
| Start | 123402997:123402997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1084C>A |
| AA Mutation | p.Gln362Lys(p.Q362K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000541091 |
| Start | 123428004:123428004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1941C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000541091 |
| Start | 123253469:123253469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.435G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000541091 |
| Start | 123253430:123253430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192636764 |
| CDS Mutation | c.396C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |