CAPSL
calcyphosine like
Summary
Predicted to enable calcium ion binding activity. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs72742463 | 5:35,904,173 | T/G | downstream gene variant | — |
| rs145807569 | 5:35,904,656 | C/G | — | uncertain significance |
| rs1345826 | 5:35,904,673 | T/C | — | benign |
| rs112464695 | 5:35,904,679 | T/C | — | uncertain significance |
| rs754662737 | 5:35,904,684 | T/C | — | uncertain significance |
| rs201508660 | 5:35,904,688 | C/T | — | uncertain significance |
| rs142885809 | 5:35,904,699 | A/G | — | uncertain significance |
| rs138016761 | 5:35,904,707 | G/T | — | uncertain significance |
| rs199954393 | 5:35,904,745 | T/A | — | uncertain significance |
| rs905926313 | 5:35,910,042 | C/T | — | uncertain significance |
| rs1261336427 | 5:35,910,063 | G/A | — | uncertain significance |
| rs1738173867 | 5:35,910,169 | C/A | — | uncertain significance |
| rs1043050074 | 5:35,910,515 | C/A | — | uncertain significance |
| rs1445898 | 5:35,910,529 | C/A | missense variant | — |
| rs890617341 | 5:35,910,545 | C/T | — | uncertain significance |
| rs1424175093 | 5:35,910,558 | C/T | — | uncertain significance |
| rs114583055 | 5:35,910,602 | A/C | — | uncertain significance |
| rs201588644 | 5:35,910,604 | T/G | — | uncertain significance |
| rs548080975 | 5:35,914,715 | G/A | — | — |
| rs768414245 | 5:35,921,096 | C/T | — | uncertain significance |
| rs767009111 | 5:35,921,127 | C/G | — | uncertain significance |
| rs200635899 | 5:35,921,161 | G/A | — | uncertain significance |
| rs1424955984 | 5:35,921,165 | T/A | — | uncertain significance |
| rs763465521 | 5:35,921,195 | C/G | — | uncertain significance |
| rs1479892478 | 5:35,921,219 | C/A | — | uncertain significance |
| rs696732 | 5:35,936,030 | C/T | upstream gene variant | — |
| rs2289878 | 5:35,939,777 | C/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.