SIPA1L2
signal induced proliferation associated 1 like 2
Summary
This gene encodes a member of the signal-induced proliferation-associated 1 like family. Members of this family contain a GTPase activating domain, a PDZ domain and a C-terminal coiled-coil domain with a leucine zipper. A similar protein in rat acts as a GTPases for the small GTPase Rap. [provided by RefSeq, Sep 2015]
Known Variants121 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs980614544 | 1:232,534,935 | C/T | — | uncertain significance |
| rs1302135006 | 1:232,538,143 | G/A | — | uncertain significance |
| rs368811235 | 1:232,538,163 | C/T | — | uncertain significance |
| rs747122798 | 1:232,538,167 | G/T | — | uncertain significance |
| rs769994881 | 1:232,538,189 | T/G | — | uncertain significance |
| rs375851821 | 1:232,539,224 | C/T | — | uncertain significance |
| rs201002732 | 1:232,539,246 | G/T | — | uncertain significance |
| rs377108333 | 1:232,539,255 | C/A | — | uncertain significance |
| rs1332701851 | 1:232,539,309 | C/T | — | uncertain significance |
| rs2527190516 | 1:232,539,877 | A/G | — | uncertain significance |
| rs768457830 | 1:232,551,324 | C/T | — | uncertain significance |
| rs143986958 | 1:232,551,325 | G/A | — | benign |
| rs372530672 | 1:232,561,350 | T/G | — | uncertain significance |
| rs376047587 | 1:232,561,368 | C/A | — | uncertain significance |
| rs184013125 | 1:232,561,520 | G/A | — | benign |
| rs1437275578 | 1:232,564,238 | C/G | — | uncertain significance |
| rs369272322 | 1:232,564,264 | T/C | — | likely benign |
| rs61729754 | 1:232,564,288 | T/G | — | likely benign |
| rs140336758 | 1:232,567,984 | C/T | — | benign |
| rs748738977 | 1:232,567,994 | C/T | — | uncertain significance |
| rs200136990 | 1:232,568,054 | C/T | — | uncertain significance |
| rs775806931 | 1:232,568,108 | C/T | — | uncertain significance |
| rs201254048 | 1:232,568,146 | A/C | — | uncertain significance |
| rs749975241 | 1:232,568,198 | T/C | — | uncertain significance |
| rs35510641 | 1:232,574,894 | C/T | — | uncertain significance |
| rs2526841758 | 1:232,574,941 | G/C | — | uncertain significance |
| rs771646256 | 1:232,574,978 | C/T | — | likely benign |
| rs1294303927 | 1:232,574,989 | T/C | — | uncertain significance |
| rs762730850 | 1:232,575,001 | T/C | — | uncertain significance |
| rs189356281 | 1:232,575,051 | G/A | — | benign |
| rs1387815198 | 1:232,575,098 | T/C | — | uncertain significance |
| rs757818683 | 1:232,575,134 | C/T | — | uncertain significance |
| rs768311174 | 1:232,575,140 | C/A | — | uncertain significance |
| rs1271097797 | 1:232,575,158 | C/G | — | uncertain significance |
| rs368970454 | 1:232,575,166 | T/C | — | uncertain significance |
| rs200681906 | 1:232,575,219 | A/T | — | uncertain significance |
| rs6687568 | 1:232,576,612 | T/C | — | — |
| rs1307597254 | 1:232,577,056 | G/A | — | uncertain significance |
| rs901604617 | 1:232,577,522 | C/G | — | uncertain significance |
| rs757986732 | 1:232,577,592 | C/T | — | uncertain significance |
| rs1253734222 | 1:232,577,612 | C/A | — | uncertain significance |
| rs12740484 | 1:232,577,772 | G/A | intron variant | — |
| rs756059455 | 1:232,579,349 | C/A | — | uncertain significance |
| rs201649743 | 1:232,579,388 | C/T | — | uncertain significance |
| rs3737838 | 1:232,581,376 | G/A | — | benign |
| rs199716225 | 1:232,581,473 | G/C | — | uncertain significance |
| rs369338127 | 1:232,581,494 | T/C | — | uncertain significance |
| rs535183446 | 1:232,581,504 | T/C | — | uncertain significance |
| rs199691624 | 1:232,581,512 | C/T | — | uncertain significance |
| rs190456518 | 1:232,596,674 | C/T | — | benign |
| rs77184036 | 1:232,596,716 | G/A | — | benign |
| rs375820432 | 1:232,596,754 | C/T | — | uncertain significance |
| rs2527000621 | 1:232,596,847 | G/C | — | uncertain significance |
| rs758221105 | 1:232,596,861 | T/C | — | uncertain significance |
| rs757561167 | 1:232,600,615 | C/T | — | uncertain significance |
| rs368285385 | 1:232,600,626 | T/C | — | uncertain significance |
| rs755408418 | 1:232,600,635 | G/A | — | uncertain significance |
| rs777409320 | 1:232,600,638 | G/C | — | uncertain significance |
| rs200050453 | 1:232,600,667 | A/C | missense variant | uncertain significance |
| rs1247486415 | 1:232,600,719 | G/T | — | uncertain significance |
| rs372676461 | 1:232,600,725 | T/C | — | uncertain significance |
| rs200044884 | 1:232,600,762 | T/C | — | uncertain significance |
| rs200975807 | 1:232,600,796 | A/C | — | uncertain significance |
| rs748766418 | 1:232,600,798 | T/G | — | uncertain significance |
| rs779861491 | 1:232,600,822 | G/A | — | uncertain significance |
| rs774466058 | 1:232,600,859 | C/G | — | uncertain significance |
| rs1350561434 | 1:232,600,870 | C/A | — | uncertain significance |
| rs570763556 | 1:232,600,948 | C/T | — | uncertain significance |
| rs76102979 | 1:232,600,951 | T/C | — | uncertain significance |
| rs2527026071 | 1:232,600,966 | C/T | — | uncertain significance |
| rs116585138 | 1:232,600,994 | C/T | — | benign |
| rs746362891 | 1:232,601,013 | C/T | — | uncertain significance |
| rs372124843 | 1:232,601,076 | C/T | — | uncertain significance |
| rs1025305837 | 1:232,607,142 | G/A | — | uncertain significance |
| rs370159097 | 1:232,607,147 | T/C | — | uncertain significance |
| rs368842985 | 1:232,607,241 | C/T | — | uncertain significance |
| rs759522020 | 1:232,615,426 | G/C | — | uncertain significance |
| rs748986967 | 1:232,619,582 | C/T | — | uncertain significance |
| rs2527133973 | 1:232,619,694 | T/A | — | uncertain significance |
| rs141087091 | 1:232,626,671 | A/C | — | benign |
| rs773332496 | 1:232,649,688 | A/G | — | likely benign |
| rs183214964 | 1:232,649,696 | T/C | — | uncertain significance |
| rs755030916 | 1:232,649,699 | C/T | — | uncertain significance |
| rs376527949 | 1:232,649,809 | A/C | — | uncertain significance |
| rs202223211 | 1:232,649,818 | C/T | — | uncertain significance |
| rs376185035 | 1:232,649,881 | C/T | — | uncertain significance |
| rs780625282 | 1:232,649,900 | C/T | — | uncertain significance |
| rs1459222459 | 1:232,649,978 | G/A | — | uncertain significance |
| rs113255944 | 1:232,649,979 | C/A | — | uncertain significance |
| rs373207397 | 1:232,650,125 | G/A | — | uncertain significance |
| rs765732101 | 1:232,650,163 | G/A | — | uncertain significance |
| rs377255995 | 1:232,650,214 | A/C | — | uncertain significance |
| rs774847363 | 1:232,650,215 | G/A | — | uncertain significance |
| rs201519099 | 1:232,650,247 | C/T | — | uncertain significance |
| rs756271190 | 1:232,650,253 | A/C | — | uncertain significance |
| rs776163837 | 1:232,650,286 | G/A | — | uncertain significance |
| rs777962734 | 1:232,650,320 | C/T | — | uncertain significance |
| rs375893261 | 1:232,650,380 | A/G | — | uncertain significance |
| rs202105245 | 1:232,650,454 | A/G | — | uncertain significance |
| rs2527316987 | 1:232,650,641 | G/C | — | uncertain significance |
Showing 100 of 121 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.