CPPED1
calcineurin like phosphoesterase domain containing 1
Summary
Predicted to enable metal ion binding activity and phosphoprotein phosphatase activity. Predicted to be involved in chromatin remodeling and regulation of transcription by RNA polymerase II. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201868301 | 16:12,758,816 | C/T | — | uncertain significance |
| rs374948695 | 16:12,758,847 | C/T | — | uncertain significance |
| rs750146328 | 16:12,758,881 | G/C | — | uncertain significance |
| rs769093197 | 16:12,758,904 | C/A | — | uncertain significance |
| rs200926687 | 16:12,758,931 | C/T | — | uncertain significance |
| rs1596435258 | 16:12,758,958 | A/C | — | uncertain significance |
| rs113283093 | 16:12,787,563 | G/C | — | — |
| rs374136858 | 16:12,798,484 | C/T | — | uncertain significance |
| rs754364791 | 16:12,798,490 | T/A | — | uncertain significance |
| rs200745290 | 16:12,798,554 | G/T | — | uncertain significance |
| rs754208671 | 16:12,798,555 | T/A | — | uncertain significance |
| rs1398298637 | 16:12,798,559 | T/C | — | uncertain significance |
| rs1280674686 | 16:12,798,581 | G/T | — | uncertain significance |
| rs188370439 | 16:12,798,607 | A/G | missense variant | — |
| rs775083202 | 16:12,798,613 | G/A | — | uncertain significance |
| rs376749320 | 16:12,798,675 | C/T | — | uncertain significance |
| rs2506030865 | 16:12,798,685 | G/A | — | uncertain significance |
| rs775720619 | 16:12,798,786 | T/A | — | uncertain significance |
| rs754923212 | 16:12,798,798 | G/T | — | uncertain significance |
| rs202093661 | 16:12,798,844 | C/A | — | uncertain significance |
| rs2080041973 | 16:12,798,847 | T/C | — | uncertain significance |
| rs182902514 | 16:12,798,867 | C/T | — | uncertain significance |
| rs186670586 | 16:12,798,882 | G/A | missense variant | — |
| rs977743533 | 16:12,798,900 | G/A | — | uncertain significance |
| rs145263702 | 16:12,802,898 | T/C | intron variant | — |
| rs541069222 | 16:12,813,519 | C/T | — | — |
| rs147619057 | 16:12,817,762 | T/G | regulatory region variant | — |
| rs187985594 | 16:12,838,629 | C/T | upstream gene variant | — |
| rs115649478 | 16:12,847,867 | T/A | regulatory region variant | — |
| rs141818280 | 16:12,864,364 | T/C | intron variant | — |
| rs4781333 | 16:12,870,861 | C/G | — | — |
| rs190461752 | 16:12,873,023 | C/T | intron variant | — |
| rs117751320 | 16:12,873,572 | T/C | intron variant | — |
| rs771169265 | 16:12,875,104 | T/C | — | uncertain significance |
| rs1047462940 | 16:12,875,116 | A/G | — | uncertain significance |
| rs201377568 | 16:12,875,153 | C/T | — | uncertain significance |
| rs779595149 | 16:12,875,168 | C/T | — | uncertain significance |
| rs2506086437 | 16:12,875,174 | C/G | — | uncertain significance |
| rs199747827 | 16:12,875,200 | C/T | — | uncertain significance |
| rs200680134 | 16:12,875,240 | C/T | — | uncertain significance |
| rs376408924 | 16:12,875,249 | C/T | — | uncertain significance |
| rs748242 | 16:12,882,336 | C/A | — | — |
| rs7201202 | 16:12,883,543 | T/C | intron variant | — |
| rs8050485 | 16:12,889,417 | A/C | — | — |
| rs147840198 | 16:12,889,906 | C/T | intron variant | — |
| rs3748977 | 16:12,897,522 | G/A | regulatory region variant | — |
| rs766353865 | 16:12,897,567 | C/A | — | likely benign |
| rs778946142 | 16:12,897,575 | G/C | — | uncertain significance |
| rs3748976 | 16:12,897,578 | G/A | missense variant | — |
| rs376260811 | 16:12,897,586 | C/G | — | uncertain significance |
| rs1201455043 | 16:12,897,609 | C/G | — | uncertain significance |
| rs765975173 | 16:12,897,626 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.