Primary Site >> Liver Cancer
Gene >> CASR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000490131 |
| Start | 122275905:122275905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753238660 |
| CDS Mutation | c.1471A>G |
| AA Mutation | p.Ile491Val(p.I491V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000490131 |
| Start | 122262162:122262162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1127G>A |
| AA Mutation | p.Gly376Asp(p.G376D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000490131 |
| Start | 122261757:122261757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.722A>T |
| AA Mutation | p.Glu241Val(p.E241V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000490131 |
| Start | 122262279:122262279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs193922421 |
| CDS Mutation | c.1244G>A |
| AA Mutation | p.Arg415Gln(p.R415Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000490131 |
| Start | 122283767:122283767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1813T>C |
| AA Mutation | p.Phe605Leu(p.F605L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000490131 |
| Start | 122257171:122257171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.276G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |