SCYL3
SCY1 like pseudokinase 3
Summary
This gene encodes a protein with a kinase domain and four HEAT repeats. The encoded protein interacts with the C-terminal domain of ezrin, an ERM protein, and may play a role in cell adhesion and migration. Alternative splicing results in multiple transcript variants encoding multiple isoforms. [provided by RefSeq, Jun 2012]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1658901523 | 1:169,823,434 | A/G | — | uncertain significance |
| rs762265291 | 1:169,823,450 | C/G | — | uncertain significance |
| rs755867923 | 1:169,823,500 | C/T | — | uncertain significance |
| rs562214139 | 1:169,823,508 | A/G | — | uncertain significance |
| rs149349564 | 1:169,823,611 | C/T | — | uncertain significance |
| rs200694889 | 1:169,823,613 | C/T | — | uncertain significance |
| rs765072871 | 1:169,823,636 | C/G | — | uncertain significance |
| rs193246431 | 1:169,823,692 | C/A | — | uncertain significance |
| rs1386750013 | 1:169,823,695 | C/T | — | likely benign |
| rs376335762 | 1:169,823,707 | G/A | — | uncertain significance |
| rs2526400334 | 1:169,823,748 | T/G | — | uncertain significance |
| rs201275933 | 1:169,823,791 | C/T | — | uncertain significance |
| rs200214247 | 1:169,823,831 | G/C | — | uncertain significance |
| rs761949057 | 1:169,823,842 | T/C | — | uncertain significance |
| rs368350801 | 1:169,823,934 | G/A | — | uncertain significance |
| rs202107684 | 1:169,824,018 | G/A | — | uncertain significance |
| rs774315834 | 1:169,824,057 | T/C | — | uncertain significance |
| rs759769942 | 1:169,824,941 | C/G | — | uncertain significance |
| rs2526417221 | 1:169,824,999 | C/T | — | likely benign |
| rs1659094032 | 1:169,825,009 | A/G | — | uncertain significance |
| rs1175425742 | 1:169,825,024 | A/C | — | uncertain significance |
| rs190544301 | 1:169,825,044 | T/A | — | uncertain significance |
| rs764893802 | 1:169,825,088 | C/T | — | uncertain significance |
| rs551586973 | 1:169,825,089 | A/G | — | uncertain significance |
| rs146854464 | 1:169,831,847 | A/G | — | likely benign |
| rs187802198 | 1:169,831,929 | T/A | — | uncertain significance |
| rs1340905890 | 1:169,838,102 | G/A | — | uncertain significance |
| rs144588369 | 1:169,839,399 | G/C | — | uncertain significance |
| rs2526516981 | 1:169,839,494 | G/C | — | uncertain significance |
| rs1331964195 | 1:169,839,495 | G/A | — | uncertain significance |
| rs61733914 | 1:169,842,839 | T/A | — | uncertain significance |
| rs56066424 | 1:169,845,128 | G/T | — | likely benign |
| rs981079594 | 1:169,845,211 | C/T | — | uncertain significance |
| rs10800485 | 1:169,847,146 | C/T | regulatory region variant | — |
| rs767863788 | 1:169,847,926 | C/T | — | uncertain significance |
| rs10158922 | 1:169,853,439 | C/T | intron variant | — |
| rs910632621 | 1:169,857,825 | C/T | — | uncertain significance |
| rs756862893 | 1:169,857,851 | C/T | — | uncertain significance |
| rs749177865 | 1:169,857,906 | C/T | — | uncertain significance |
| rs2526632576 | 1:169,857,958 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.