SCAPER

S-phase cyclin A associated protein in the ER

Summary

Predicted to enable nucleic acid binding activity and zinc ion binding activity. Acts upstream of or within retina development in camera-type eye. Located in cytosol and nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants161 total

rsidPosition (GRCh37)AllelesClassClinVar
rs91824990415:76,640,977T/G—uncertain significance
rs204032788215:76,640,993A/G—uncertain significance
rs54181437115:76,641,003G/T—uncertain significance
rs254311017815:76,643,576A/G—uncertain significance
rs146091096815:76,643,593G/C—uncertain significance
rs20080509515:76,643,618C/G—uncertain significance
rs75367183715:76,646,318C/G—uncertain significance
rs77905948315:76,646,355T/G—uncertain significance
rs18743475315:76,646,371G/A—likely benign
rs254790541115:76,646,379A/G—uncertain significance
rs5838861115:76,646,455G/C—benign
rs78174759215:76,646,476G/A—likely benign
rs37498307315:76,668,519T/C—uncertain significance
rs254797225915:76,668,534C/G—uncertain significance
rs156702004315:76,668,540C/T—uncertain significance
rs19994012415:76,668,547T/C—conflicting classifications of pathogenicity
rs37401920515:76,668,578T/C—likely benign
rs376511515:76,673,716T/C—benign
rs130554229115:76,673,768C/T—pathogenic
rs37138757315:76,673,774A/G—uncertain significance
rs3602247615:76,673,785G/T—benign
rs54827554315:76,673,787T/C—likely benign
rs56985879915:76,673,792T/C—uncertain significance
rs20110356115:76,673,808C/T—benign
rs15062868215:76,673,827G/A—likely benign
rs204294289415:76,673,892T/C—uncertain significance
rs13881355315:76,673,928G/C—likely benign
rs19985938515:76,673,956C/T—likely benign
rs13797209215:76,696,901T/C—conflicting classifications of pathogenicity
rs374317615:76,696,914C/T—benign
rs78086643715:76,697,016C/T—uncertain significance
rs36976574415:76,697,024G/C—likely benign
rs1015251315:76,697,027A/G—benign
rs1163934515:76,717,989G/Aintron variant—
rs7623624515:76,721,294C/Gintron variant—
rs254814410815:76,726,419C/T—uncertain significance
rs77145483615:76,726,437C/T—uncertain significance
rs7345025315:76,726,440T/C—benign
rs160701715:76,726,465G/T—benign
rs119629874015:76,726,488G/A—uncertain significance
rs75404512815:76,726,527C/T—uncertain significance
rs3538257315:76,726,530T/C—conflicting classifications of pathogenicity
rs77632985715:76,726,617C/T—uncertain significance
rs19958663415:76,726,621A/G—likely benign
rs147716607115:76,726,659A/G—likely benign
rs1107259715:76,763,514C/A—benign
rs75788488915:76,763,554G/A—uncertain significance
rs78052343915:76,763,566A/G—uncertain significance
rs77045994715:76,763,609C/T—uncertain significance
rs76324115015:76,763,656T/C—uncertain significance
rs76905264915:76,763,658G/T—likely benign
rs37534852615:76,763,665T/C—uncertain significance
rs205014845715:76,763,677C/A—likely pathogenic
rs18853087115:76,781,806C/Tintron variant—
rs77465492015:76,797,210T/C—uncertain significance
rs148926523515:76,797,246C/T—uncertain significance
rs6792004515:76,800,084G/Aintron variant—
rs16690615:76,802,175C/Tintron variant—
rs49426815:76,815,713T/Cintron variant—
rs50600015:76,817,788T/Cintron variant—
rs28488415:76,828,289A/C——
rs7140521615:76,841,655T/A——
rs77094671715:76,866,550C/T—likely benign
rs77707229615:76,866,562T/C—likely benign
rs20004953215:76,866,632T/C—likely benign
rs6203042015:76,893,428T/Gintron variant—
rs18400329515:76,914,159T/A—likely benign
rs1243854015:76,943,213C/Gintron variant—
rs28002115:76,957,958A/G—benign
rs75549823315:76,958,017C/T—likely benign
rs77259767715:76,958,046G/A—uncertain significance
rs147509278215:76,958,081G/C—uncertain significance
rs136177732515:76,958,121A/G—uncertain significance
rs20205499515:76,958,128C/T—likely benign
rs11755275015:76,994,111T/C—benign
rs105350491915:76,994,121C/T—uncertain significance
rs77305154115:76,994,149C/T—uncertain significance
rs14689836515:76,994,150G/A—benign
rs37387965015:76,994,192T/A—likely benign
rs37082330415:76,995,198T/C—uncertain significance
rs123972546115:76,995,214G/A—pathogenic
rs119202827215:76,995,227A/T—likely pathogenic
rs254512847915:76,995,234G/A—uncertain significance
rs11685394115:76,995,269C/T—likely benign
rs205904215015:76,995,300C/T—uncertain significance
rs95146919115:76,995,302T/C—likely benign
rs76428700915:76,995,331T/A—uncertain significance
rs97833615115:76,998,312G/A—pathogenic
rs159827946915:76,998,328G/C—likely pathogenic
rs11749862715:77,021,058C/T—benign
rs155555816915:77,021,080T/C—pathogenic
rs7641223315:77,025,588T/A—benign
rs14469437915:77,025,687C/T—benign
rs37067971415:77,025,708A/G—benign
rs254550211715:77,025,709A/G—uncertain significance
rs240460215:77,030,792A/C——
rs13918784015:77,046,141C/T—conflicting classifications of pathogenicity
rs130215682815:77,046,280C/A—uncertain significance
rs37236593715:77,046,287C/T—likely benign
rs206302561215:77,057,343G/A—uncertain significance

Showing 100 of 161 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.