Primary Site >> Liver Cancer
Gene >> GRM5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305447 |
| Start | 89047252:89047252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.621G>T |
| AA Mutation | p.Lys207Asn(p.K207N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305447 |
| Start | 88508975:88508975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3256A>T |
| AA Mutation | p.Ser1086Cys(p.S1086C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305447 |
| Start | 88604881:88604881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1231C>A |
| AA Mutation | p.Leu411Ile(p.L411I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305447 |
| Start | 88597297:88597297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1450G>A |
| AA Mutation | p.Val484Ile(p.V484I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305447 |
| Start | 88653277:88653277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1038A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305447 |
| Start | 88849929:88849929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778245409 |
| CDS Mutation | c.888G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |