RPS26

ribosomal protein S26

Summary

This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S26E family of ribosomal proteins. Mutations in this gene are found in Diamond-Blackfan anemia 10. There are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Aug 2017]

Known Variants109 total

rsidPosition (GRCh37)AllelesClassClinVar
rs7886546512:56,434,146G/Adownstream gene variant—
rs70570412:56,435,412G/A—benign
rs70570512:56,435,504G/Ccoding sequence variant—
rs7810800312:56,435,742T/G—benign
rs88604968612:56,435,802G/T—uncertain significance
rs189588993312:56,435,821T/G—uncertain significance
rs86869307812:56,435,850C/T—uncertain significance
rs88604968712:56,435,871C/T—uncertain significance
rs18880812112:56,435,916G/A—likely benign
rs37279415812:56,435,918C/T—likely benign
rs1711826212:56,435,920C/T—likely benign
rs20083184912:56,435,924C/T—likely benign
rs37348460612:56,435,926C/T—benign
rs113101712:56,435,929C/Gregulatory region variantbenign
rs37270842912:56,435,942G/T—likely benign
rs18117434912:56,435,948A/G—likely benign
rs37059891812:56,435,950G/C—uncertain significance
rs14395126712:56,435,951A/Cmissense variantpathogenic
rs189589426112:56,435,952T/G—pathogenic
rs14862286212:56,435,954G/A—pathogenic
rs213675349512:56,435,955T/G—likely pathogenic
rs20124821312:56,435,957A/C—uncertain significance
rs254072245512:56,435,958G/C—uncertain significance
rs74843702612:56,435,959T/G—uncertain significance
rs11575099312:56,435,960C/T—likely benign
rs54559571912:56,435,962T/A—likely benign
rs36886367712:56,435,963C/T—likely benign
rs136049159212:56,435,965T/C—likely benign
rs19991747412:56,435,966G/T—likely benign
rs76377072912:56,435,967C/T—likely benign
rs75986483712:56,435,973G/C—likely benign
rs795718712:56,436,111C/G—benign
rs74996648612:56,436,175C/T—likely benign
rs96215853812:56,436,196C/T—likely benign
rs77950792712:56,436,199C/T—likely benign
rs128889988212:56,436,202G/C—likely benign
rs213675377312:56,436,205G/T—conflicting classifications of pathogenicity
rs78620399812:56,436,207A/T—pathogenic
rs254072276212:56,436,214G/C—uncertain significance
rs75888402112:56,436,223G/A—likely benign
rs77119668112:56,436,247C/T—conflicting classifications of pathogenicity
rs79704591912:56,436,260C/Tstop gainedpathogenic
rs36883870012:56,436,265T/A—likely benign
rs139280192812:56,436,266A/C—uncertain significance
rs14816744912:56,436,268T/A—likely benign
rs76270125112:56,436,269C/G—uncertain significance
rs144012638512:56,436,270G/A—uncertain significance
rs254072281212:56,436,272T/C—uncertain significance
rs98656375812:56,436,274C/T—likely benign
rs254072281412:56,436,275A/G—uncertain significance
rs254072282412:56,436,282G/A—uncertain significance
rs254072282712:56,436,284G/T—uncertain significance
rs77398235812:56,436,286C/T—likely benign
rs76025576412:56,436,298C/T—conflicting classifications of pathogenicity
rs254072284412:56,436,300A/C—uncertain significance
rs147282712012:56,436,301G/A—likely benign
rs26760702312:56,436,302G/Amissense variantpathogenic
rs75329652012:56,436,304C/T—likely benign
rs254072286612:56,436,324T/A—uncertain significance
rs75882268712:56,436,325C/A—likely benign
rs254072287112:56,436,334C/T—likely benign
rs15071589612:56,436,349A/G—likely benign
rs129509264612:56,436,362A/G—uncertain significance
rs74591077712:56,436,373G/T—likely benign
rs254072289812:56,436,375G/A—uncertain significance
rs254072291112:56,436,387G/A—likely pathogenic
rs20184803512:56,436,392T/G—uncertain significance
rs74928537512:56,436,394G/C—likely benign
rs20119138712:56,436,396T/G—likely benign
rs20104075812:56,436,405C/G—likely benign
rs70570612:56,436,472T/G—benign
rs7145933512:56,436,917G/A—likely benign
rs19215419412:56,437,118C/G—likely benign
rs145579141012:56,437,127C/T—likely benign
rs37386117312:56,437,138A/G—likely benign
rs37017582812:56,437,148C/G—likely benign
rs189591814012:56,437,161A/T—pathogenic
rs137145161312:56,437,166G/A—likely benign
rs77624018312:56,437,172G/C—likely benign
rs130078139212:56,437,178A/G—likely benign
rs15022955112:56,437,184C/G—pathogenic
rs254072357112:56,437,186G/A—likely pathogenic
rs14894276512:56,437,224C/Tstop gainedpathogenic
rs76467336812:56,437,231G/C—uncertain significance
rs13905683612:56,437,235A/G—likely benign
rs76207552212:56,437,239C/T—uncertain significance
rs37381681612:56,437,253A/G—likely benign
rs76662166312:56,437,256C/T—likely benign
rs254072363812:56,437,260C/T—uncertain significance
rs77879170212:56,437,276C/T—uncertain significance
rs14597678412:56,437,277G/A—uncertain significance
rs254072366412:56,437,278G/C—likely pathogenic
rs159302380912:56,437,279T/A—likely pathogenic
rs189591975512:56,437,280G/A—uncertain significance
rs75828191312:56,437,284A/G—likely benign
rs7512544412:56,437,304G/T—benign
rs7749941312:56,437,305C/T—benign
rs55929382412:56,437,896C/T—likely benign
rs254072414512:56,437,901A/G—likely pathogenic
rs55429715612:56,437,905T/A—likely benign

Showing 100 of 109 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.