SPRED2
sprouty related EVH1 domain containing 2
Summary
SPRED2 is a member of the Sprouty (see SPRY1; MIM 602465)/SPRED family of proteins that regulate growth factor-induced activation of the MAP kinase cascade (see MAPK1; MIM 176948) (Nonami et al., 2004 [PubMed 15465815]).[supplied by OMIM, Mar 2008]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1422230015 | 2:65,540,672 | C/T | — | uncertain significance |
| rs138542483 | 2:65,540,699 | C/T | — | uncertain significance |
| rs2528679287 | 2:65,540,754 | C/T | — | uncertain significance |
| rs529301774 | 2:65,540,787 | T/C | — | uncertain significance |
| rs748586468 | 2:65,540,803 | G/T | — | uncertain significance |
| rs752921726 | 2:65,540,860 | C/G | — | uncertain significance |
| rs936514564 | 2:65,540,942 | T/A | — | uncertain significance |
| rs199737796 | 2:65,540,949 | T/G | — | uncertain significance |
| rs775641378 | 2:65,540,961 | A/G | — | uncertain significance |
| rs532860603 | 2:65,540,975 | C/T | — | uncertain significance |
| rs140044019 | 2:65,541,000 | G/A | — | uncertain significance |
| rs144709078 | 2:65,541,044 | C/T | — | uncertain significance |
| rs756607698 | 2:65,541,124 | C/G | — | uncertain significance |
| rs183246092 | 2:65,541,164 | G/A | — | uncertain significance |
| rs778032823 | 2:65,541,296 | G/C | — | uncertain significance |
| rs150461103 | 2:65,541,297 | G/A | — | uncertain significance |
| rs200299417 | 2:65,541,311 | G/A | — | likely benign |
| rs750670409 | 2:65,543,873 | C/G | — | uncertain significance |
| rs1338595320 | 2:65,543,883 | G/T | — | uncertain significance |
| rs777264148 | 2:65,543,888 | C/T | — | uncertain significance |
| rs201381865 | 2:65,543,932 | C/T | — | uncertain significance |
| rs745488120 | 2:65,543,966 | G/A | — | uncertain significance |
| rs369371372 | 2:65,543,992 | G/A | — | uncertain significance |
| rs2528766377 | 2:65,559,134 | T/C | — | uncertain significance |
| rs1361166793 | 2:65,559,161 | A/G | — | uncertain significance |
| rs2104216988 | 2:65,561,813 | A/G | — | pathogenic |
| rs200308305 | 2:65,571,284 | A/C | — | — |
| rs112455706 | 2:65,571,648 | G/A | — | likely benign |
| rs780902942 | 2:65,571,870 | G/A | — | pathogenic |
| rs61748094 | 2:65,571,889 | G/C | synonymous variant | — |
| rs761421595 | 2:65,571,948 | C/T | — | uncertain significance |
| rs61748095 | 2:65,571,976 | G/A | — | benign |
| rs201473537 | 2:65,572,013 | C/T | — | uncertain significance |
| rs7559283 | 2:65,578,368 | C/T | regulatory region variant | — |
| rs76704104 | 2:65,579,944 | G/A | intron variant | — |
| rs934734 | 2:65,595,586 | G/T | — | — |
| rs1858037 | 2:65,598,300 | T/C | — | — |
| rs906579 | 2:65,601,598 | T/G | — | — |
| rs906578 | 2:65,601,600 | C/A | intron variant | — |
| rs11689314 | 2:65,605,408 | G/T | intron variant | — |
| rs1876518 | 2:65,608,909 | C/T | regulatory region variant | — |
| rs268132 | 2:65,609,677 | T/G | — | — |
| rs3732102 | 2:65,614,509 | C/G | regulatory region variant | — |
| rs2661797 | 2:65,633,190 | G/A | intron variant | — |
| rs2661798 | 2:65,635,688 | A/T | intron variant | — |
| rs62141075 | 2:65,644,616 | C/T | intron variant | — |
| rs10166100 | 2:65,645,750 | C/T | intron variant | — |
| rs10166362 | 2:65,645,774 | G/C | — | — |
| rs7565437 | 2:65,646,966 | T/C | intron variant | — |
| rs12470883 | 2:65,651,851 | G/A | intron variant | — |
| rs7572922 | 2:65,652,156 | C/T | intron variant | — |
| rs2028150 | 2:65,655,012 | C/A | — | — |
| rs2028151 | 2:65,655,613 | A/C | — | — |
| rs7569257 | 2:65,656,976 | G/T | — | — |
| rs7576126 | 2:65,658,369 | G/C | — | — |
| rs750237615 | 2:65,659,112 | C/T | — | uncertain significance |
| rs12185577 | 2:65,659,488 | A/G | regulatory region variant | — |
| rs7584078 | 2:65,660,978 | C/A | upstream gene variant | — |
| rs12185610 | 2:65,661,468 | A/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.