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

Gene information from NCBI Gene. Variant classifications from ClinVar.