FGF14

fibroblast growth factor 14

Summary

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. A mutation in this gene is associated with autosomal dominant cerebral ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]

Known Variants145 total

rsidPosition (GRCh37)AllelesClassClinVar
rs18626544813:102,369,961T/Gregulatory region variant—
rs203492840913:102,373,233G/A—uncertain significance
rs203493032513:102,373,263A/G—uncertain significance
rs76132256813:102,373,409G/T—uncertain significance
rs88604993113:102,373,420C/G—uncertain significance
rs52964455913:102,373,440A/G—likely benign
rs1560813:102,373,563T/A—benign
rs104619713:102,373,569C/A—benign
rs54029261413:102,373,885T/G—uncertain significance
rs53593076413:102,373,922G/A—likely benign
rs203498892513:102,373,930C/T—uncertain significance
rs37276826913:102,373,982T/C—uncertain significance
rs14740482513:102,374,063C/T—likely benign
rs88604993213:102,374,109C/T—uncertain significance
rs88604993313:102,374,110G/A—uncertain significance
rs5855589813:102,374,118C/T—benign
rs75289642313:102,374,188G/A—uncertain significance
rs88604993413:102,374,207C/T—uncertain significance
rs121142641913:102,374,318C/G—uncertain significance
rs88604993513:102,374,398G/C—uncertain significance
rs88604993613:102,374,404G/T—uncertain significance
rs7937970013:102,374,437G/T—benign
rs203503684313:102,374,482A/G—uncertain significance
rs203503961613:102,374,523A/C—uncertain significance
rs54653648813:102,374,614C/G—benign
rs14179329813:102,374,627C/T—benign
rs15058034313:102,374,628G/A—uncertain significance
rs89752533113:102,374,646C/A—uncertain significance
rs7549891213:102,374,710T/G—benign
rs55739024213:102,374,767A/G—conflicting classifications of pathogenicity
rs203505865713:102,374,812T/C—uncertain significance
rs115933097313:102,374,820G/A—uncertain significance
rs19170544013:102,375,005G/C—benign
rs14966193313:102,375,150T/C—likely benign
rs3439770413:102,375,232T/C—likely benign
rs19953623913:102,375,233G/C—uncertain significance
rs77868465313:102,375,235A/G—likely benign
rs254888883913:102,375,242C/A—uncertain significance
rs75787932413:102,375,254G/A—uncertain significance
rs88604993813:102,375,261C/T—uncertain significance
rs74637452213:102,375,269G/A—uncertain significance
rs143238138713:102,375,273C/A—uncertain significance
rs15132564513:102,375,274C/T—uncertain significance
rs53595284213:102,375,275G/A—likely benign
rs96059644813:102,375,280C/T—likely benign
rs36837309213:102,375,282C/G—uncertain significance
rs133671164613:102,375,285C/T—uncertain significance
rs4128164413:102,375,289A/G—likely benign
rs76059587913:102,375,305C/T—uncertain significance
rs37590619913:102,375,320A/G—uncertain significance
rs57447628313:102,375,327G/A—benign
rs86711085413:102,375,334A/T—likely benign
rs55486414713:102,376,876G/A——
rs254890100813:102,378,988G/A—uncertain significance
rs13860734413:102,378,990T/A—likely benign
rs55650969313:102,379,005C/T—likely benign
rs155537076813:102,379,013T/A—uncertain significance
rs120474114513:102,379,017C/G—uncertain significance
rs19997091913:102,379,026A/G—likely benign
rs126898128413:102,379,029T/C—likely benign
rs155537078713:102,379,040T/A—pathogenic
rs159404330413:102,379,049C/T—uncertain significance
rs254890139013:102,379,057C/T—pathogenic
rs58777668513:102,379,082——pathogenic
rs254890153613:102,379,087A/C—uncertain significance
rs7708283113:102,379,088A/G—likely benign
rs77679475613:102,379,092G/A—uncertain significance
rs55869405313:102,379,101G/A—benign
rs121547194313:102,379,103T/C—uncertain significance
rs86587862713:102,379,130C/A—pathogenic
rs10489439313:102,379,135A/Gmissense variantpathogenic
rs203546614713:102,379,140G/T—uncertain significance
rs159404377013:102,379,141C/A—uncertain significance
rs75122671813:102,379,164T/G—likely benign
rs19110406513:102,379,174A/G—benign
rs14997579213:102,480,216C/G—likely benign
rs7412104413:102,480,228A/G—likely benign
rs56642996513:102,519,795A/G——
rs250185672713:102,521,074C/T—likely pathogenic
rs4128164613:102,521,099A/G—likely benign
rs214044787513:102,521,103A/T—uncertain significance
rs3407398213:102,521,110T/C—likely benign
rs74604083113:102,521,114C/G—uncertain significance
rs77993649813:102,521,131C/T—uncertain significance
rs155530190113:102,521,132C/T—conflicting classifications of pathogenicity
rs204487763613:102,521,168G/A—likely benign
rs155530192113:102,521,172A/G—uncertain significance
rs250185829813:102,521,180T/C—pathogenic
rs250192991613:102,527,531C/T—uncertain significance
rs142229098013:102,527,571G/C—uncertain significance
rs75721066013:102,527,579G/A—likely benign
rs13805146913:102,527,580G/A—uncertain significance
rs75895020713:102,527,584G/T—uncertain significance
rs122802200513:102,527,585C/A—uncertain significance
rs77503299213:102,527,607C/T—uncertain significance
rs37401082413:102,527,643G/T—conflicting classifications of pathogenicity
rs250193189913:102,527,647C/G—likely pathogenic
rs76804942713:102,527,655C/T—likely benign
rs93472639213:102,527,664T/C—likely benign
rs955775413:102,553,248G/Tintron variant—

Showing 100 of 145 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.