RNF17

ring finger protein 17

Summary

This gene is similar to a mouse gene that encodes a testis-specific protein containing a RING finger domain. Alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, May 2010]

Known Variants74 total

rsidPosition (GRCh37)AllelesClassClinVar
rs37599391913:25,338,367G/C—uncertain significance
rs254153070013:25,338,424C/T—uncertain significance
rs37011289013:25,338,429A/G—uncertain significance
rs254155091813:25,341,490T/C—uncertain significance
rs74709560813:25,348,973G/C—uncertain significance
rs19984973113:25,348,979G/A—uncertain significance
rs77617464113:25,352,456T/C—uncertain significance
rs139108840213:25,352,495G/A—likely benign
rs129400272213:25,353,828T/G—uncertain significance
rs36866357813:25,356,007C/T—uncertain significance
rs14322967813:25,356,072T/C—likely benign
rs143797635213:25,362,235A/G—uncertain significance
rs76173719413:25,362,241A/G—uncertain significance
rs76590847313:25,362,250G/A—uncertain significance
rs76564454913:25,363,885A/G—uncertain significance
rs18377749813:25,367,202A/G—uncertain significance
rs15041653313:25,367,269C/T—uncertain significance
rs11478585213:25,367,292A/G—benign
rs6174831313:25,367,344A/G—benign
rs6174830213:25,367,388G/A—benign
rs76896449713:25,367,413T/C—uncertain significance
rs139414575013:25,367,414T/G—uncertain significance
rs56056356413:25,367,425C/T—uncertain significance
rs254172970213:25,367,432G/A—uncertain significance
rs254173018113:25,367,476A/G—uncertain significance
rs36767740413:25,370,379A/G—uncertain significance
rs950741313:25,373,634A/G—likely benign
rs14065041513:25,373,640A/G—uncertain significance
rs188510069513:25,374,514A/G—uncertain significance
rs254177885913:25,374,536C/T—uncertain significance
rs3413435413:25,374,538G/T—benign
rs15025693913:25,376,643C/T—likely benign
rs254180651913:25,378,456T/G—uncertain significance
rs76089577413:25,378,557A/G—uncertain significance
rs36825916413:25,399,793A/G—uncertain significance
rs77320180413:25,399,812G/A—likely benign
rs77816637613:25,406,002A/G—uncertain significance
rs19963101713:25,416,205G/A—uncertain significance
rs20068850313:25,417,893A/G—uncertain significance
rs76752180313:25,418,005T/G—uncertain significance
rs254126957613:25,418,006T/A—uncertain significance
rs36970523913:25,418,073A/G—uncertain significance
rs11519946813:25,418,782C/T—benign
rs77653215813:25,419,114G/A—uncertain significance
rs19150188613:25,421,623A/Gintron variant—
rs77733080013:25,424,552G/A—uncertain significance
rs74930504913:25,424,565T/C—uncertain significance
rs3420900313:25,425,647A/G—likely benign
rs105260850813:25,428,103A/G—uncertain significance
rs189221418413:25,428,154A/G—uncertain significance
rs75126595813:25,428,184G/A—uncertain significance
rs254137649013:25,428,211T/G—uncertain significance
rs77630781513:25,428,216G/A—uncertain significance
rs14109689513:25,428,230A/G—likely benign
rs76992191713:25,433,228G/C—uncertain significance
rs77311063313:25,433,286T/G—uncertain significance
rs7570477213:25,435,396C/T—benign
rs75423944913:25,435,521C/G—uncertain significance
rs75968475113:25,435,524C/T—uncertain significance
rs76441014713:25,439,068T/G—uncertain significance
rs36826697013:25,439,086G/A—uncertain significance
rs89093209313:25,439,090A/C—uncertain significance
rs254146841113:25,440,323A/G—likely benign
rs130568298013:25,442,754A/T—uncertain significance
rs57339421113:25,442,760A/G—uncertain significance
rs18849338213:25,444,744C/G—uncertain significance
rs135188006413:25,444,758A/T—uncertain significance
rs254150352713:25,444,766A/C—uncertain significance
rs37409308313:25,444,787G/A—uncertain significance
rs76771464013:25,448,257C/T—uncertain significance
rs76976520313:25,448,378C/T—uncertain significance
rs11472848513:25,451,201G/A—benign
rs254157268713:25,453,356A/G—uncertain significance
rs7346118213:25,453,409G/T—benign

Gene information from NCBI Gene. Variant classifications from ClinVar.