CLASRP

CLK4 associating serine/arginine rich protein

Summary

Predicted to be involved in RNA splicing and mRNA processing. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants63 total

rsidPosition (GRCh37)AllelesClassClinVar
rs55300823519:45,547,138T/C——
rs14718820619:45,552,587T/Cdownstream gene variant—
rs74706840619:45,556,119C/A—uncertain significance
rs76603283719:45,556,128A/T—uncertain significance
rs1166785119:45,556,130C/G—likely benign
rs75245189619:45,556,132C/G—uncertain significance
rs15059473119:45,556,134C/T—uncertain significance
rs120308145919:45,556,378G/A—uncertain significance
rs92521880919:45,556,381C/T—uncertain significance
rs251368285519:45,556,420A/C—uncertain significance
rs20132302019:45,556,432G/A—uncertain significance
rs75394993819:45,559,717A/G—uncertain significance
rs13955324219:45,561,012G/A—uncertain significance
rs14380088219:45,561,107G/A—likely benign
rs36851470319:45,562,528G/A—uncertain significance
rs193825285419:45,563,660G/A—uncertain significance
rs75432985119:45,563,686G/T—uncertain significance
rs147763226019:45,563,855G/A—uncertain significance
rs18624290319:45,565,409T/C—likely benign
rs133783082319:45,565,420G/A—uncertain significance
rs96985775019:45,565,423G/A—uncertain significance
rs77456458319:45,567,283T/G—uncertain significance
rs75825779519:45,567,304C/T—uncertain significance
rs57099109719:45,567,344C/T—uncertain significance
rs57301551319:45,567,431C/A—uncertain significance
rs74543391819:45,567,484C/T—uncertain significance
rs116206621519:45,567,678C/T—uncertain significance
rs129898578619:45,567,692G/T—uncertain significance
rs76619308219:45,567,737C/G—uncertain significance
rs101508721819:45,567,745G/C—uncertain significance
rs132868748719:45,567,759C/G—uncertain significance
rs156842069419:45,567,767C/G—uncertain significance
rs97361819219:45,567,798G/A—uncertain significance
rs77914987419:45,567,806T/G—uncertain significance
rs125036706119:45,567,810G/A—uncertain significance
rs74804204319:45,567,842C/T—uncertain significance
rs36929494419:45,567,854C/T—uncertain significance
rs148791862019:45,567,864G/A—uncertain significance
rs75767201019:45,567,878C/T—uncertain significance
rs75060802419:45,570,599C/T—uncertain significance
rs76456644919:45,570,616C/A—uncertain significance
rs138537817619:45,570,617C/T—uncertain significance
rs77714977519:45,570,618G/A—uncertain significance
rs146591642019:45,570,621A/G—uncertain significance
rs97883658219:45,570,632G/A—uncertain significance
rs76875914619:45,570,633G/A—uncertain significance
rs75060314919:45,570,635C/T—uncertain significance
rs127710167519:45,570,636G/A—uncertain significance
rs104769657119:45,570,683C/T—uncertain significance
rs75515738419:45,570,695C/T—uncertain significance
rs104725196619:45,570,701C/T—uncertain significance
rs57266550919:45,570,702G/A—uncertain significance
rs100997799119:45,570,756G/T—uncertain significance
rs75185362119:45,570,774A/G—uncertain significance
rs77897242219:45,570,792C/T—uncertain significance
rs88869217319:45,570,807T/C—uncertain significance
rs55125639719:45,570,818G/C—uncertain significance
rs251371233419:45,571,712G/A—uncertain significance
rs251371423719:45,572,461A/T—uncertain significance
rs196717643319:45,572,500G/A—uncertain significance
rs14293984219:45,573,333G/A—uncertain significance
rs75439620419:45,574,089C/T—uncertain significance
rs13999598419:45,574,482G/Cdownstream gene variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.