FLRT1

fibronectin leucine rich transmembrane protein 1

Summary

This gene encodes a member of the fibronectin leucine rich transmembrane protein (FLRT) family. The family members may function in cell adhesion and/or receptor signalling. Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix. The encoded protein shares sequence similarity with two other family members, FLRT2 and FLRT3. This gene is expressed in kidney and brain. [provided by RefSeq, Jul 2008]

Known Variants163 total

rsidPosition (GRCh37)AllelesClassClinVar
rs56266411:63,823,619C/Tintron variant—
rs498052011:63,833,088A/Cintron variant—
rs11756919111:63,851,888G/Aintron variant—
rs270154011:63,869,107T/C——
rs57274032611:63,869,793C/T——
rs498050411:63,873,083G/C——
rs65135911:63,876,201T/G——
rs5777924311:63,882,363G/Tdownstream gene variant—
rs249561086211:63,883,771C/A—uncertain significance
rs20065838511:63,883,775C/T—likely benign
rs13976822711:63,883,777C/G—uncertain significance
rs54732501211:63,883,796G/A—benign
rs14333766311:63,883,803G/A—conflicting classifications of pathogenicity
rs19985844511:63,883,825T/A—uncertain significance
rs104222414211:63,883,833C/A—likely benign
rs20058857011:63,883,847C/T—benign
rs77461094611:63,883,853C/G—uncertain significance
rs14606154511:63,883,856C/T—benign
rs95888163211:63,883,862C/T—likely benign
rs249561200511:63,883,894C/G—uncertain significance
rs194498310811:63,883,915G/A—uncertain significance
rs74995669911:63,883,919C/T—likely benign
rs77993478411:63,883,925C/T—likely benign
rs74923200811:63,883,926G/A—uncertain significance
rs77717787511:63,883,950G/C—uncertain significance
rs20004974011:63,883,967C/T—likely benign
rs77019328011:63,883,968G/A—uncertain significance
rs61439711:63,883,985C/T—benign
rs37041053711:63,883,990C/T—uncertain significance
rs20135492211:63,884,024C/T—likely benign
rs61403511:63,884,027C/T—benign
rs77107239011:63,884,029G/C—uncertain significance
rs77279484711:63,884,081C/T—likely benign
rs20061022011:63,884,119G/A—uncertain significance
rs20129602411:63,884,128G/A—uncertain significance
rs11699907311:63,884,146A/G—likely benign
rs75625092911:63,884,176C/T—uncertain significance
rs8006194111:63,884,182C/G—uncertain significance
rs77476393011:63,884,184C/T—uncertain significance
rs6173156811:63,884,196C/T—benign
rs134876300311:63,884,210C/A—uncertain significance
rs76759623611:63,884,234C/T—likely benign
rs75609048211:63,884,235G/A—uncertain significance
rs14168458011:63,884,252C/T—likely benign
rs94188046211:63,884,253G/A—uncertain significance
rs14801297911:63,884,262G/A—uncertain significance
rs138608434711:63,884,281T/G—uncertain significance
rs126630639211:63,884,320C/T—uncertain significance
rs56303698011:63,884,324G/C—likely benign
rs159093259711:63,884,406A/G—uncertain significance
rs56585825011:63,884,415C/T—uncertain significance
rs77176015711:63,884,416G/A—uncertain significance
rs75408805411:63,884,438G/A—likely benign
rs375112011:63,884,453C/T—benign
rs37711219711:63,884,459C/T—likely benign
rs156524156911:63,884,461A/T—uncertain significance
rs92860798411:63,884,462C/T—likely benign
rs375112111:63,884,474C/T—benign
rs75652757411:63,884,475C/T—uncertain significance
rs14615062511:63,884,501G/A—likely benign
rs77677315811:63,884,515C/T—uncertain significance
rs37702095211:63,884,516G/A—likely benign
rs13971111211:63,884,522C/T—likely benign
rs14582833111:63,884,525G/A—benign
rs3485699611:63,884,561A/G—benign
rs213462005811:63,884,564C/T—likely benign
rs75787552211:63,884,605C/T—uncertain significance
rs20220141311:63,884,609G/A—likely benign
rs77009889211:63,884,620G/T—uncertain significance
rs14539990211:63,884,632G/A—benign
rs18511533011:63,884,654C/A—uncertain significance
rs75786570211:63,884,672C/T—likely benign
rs77715013911:63,884,673G/A—uncertain significance
rs15121566211:63,884,684C/T—likely benign
rs14037001011:63,884,690G/A—likely benign
rs14988204911:63,884,716G/A—uncertain significance
rs77274499611:63,884,735T/C—likely benign
rs3524768011:63,884,747T/C—benign
rs76257738311:63,884,760G/C—uncertain significance
rs76364175611:63,884,766G/C—uncertain significance
rs75111577911:63,884,768G/A—likely benign
rs20210454311:63,884,779C/T—uncertain significance
rs194500593011:63,884,781G/A—uncertain significance
rs77910595411:63,884,784G/A—uncertain significance
rs159093352811:63,884,805A/C—uncertain significance
rs76702215411:63,884,830G/A—uncertain significance
rs57017631411:63,884,858C/A—uncertain significance
rs13844547911:63,884,859G/C—uncertain significance
rs74839246411:63,884,861G/C—likely benign
rs77393093511:63,884,881C/G—uncertain significance
rs14134285711:63,884,894C/T—likely benign
rs14340879111:63,884,897C/T—likely benign
rs116095283511:63,884,907G/A—uncertain significance
rs14838286811:63,884,909G/T—benign
rs13867674111:63,884,923C/T—likely benign
rs37453537911:63,884,941C/A—uncertain significance
rs36911201411:63,884,950C/T—uncertain significance
rs76417957711:63,884,951G/A—likely benign
rs91489638011:63,884,968T/A—uncertain significance
rs76903251611:63,884,992G/A—uncertain significance

Showing 100 of 163 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.