PDCD11

programmed cell death 11

Summary

PDCD11 is a NF-kappa-B (NFKB1; 164011)-binding protein that colocalizes with U3 RNA (MIM 180710) in the nucleolus and is required for rRNA maturation and generation of 18S rRNA (Sweet et al., 2003 [PubMed 14624448]; Sweet et al., 2008 [PubMed 17654514]).[supplied by OMIM, Oct 2008]

Known Variants111 total

rsidPosition (GRCh37)AllelesClassClinVar
rs56043848310:105,158,188C/T—uncertain significance
rs77816399010:105,160,222G/A—likely benign
rs104862197010:105,160,227T/C—uncertain significance
rs37032601410:105,162,893C/T—uncertain significance
rs254063093810:105,162,933T/C—uncertain significance
rs254063531610:105,165,836C/T—uncertain significance
rs15124671310:105,165,861C/G—uncertain significance
rs13942389410:105,166,424C/T—likely benign
rs254063657110:105,166,437A/T—uncertain significance
rs254063677510:105,166,516C/T—uncertain significance
rs77263797510:105,169,475C/T—uncertain significance
rs14135268210:105,169,504G/A—uncertain significance
rs101853811810:105,169,505T/A—uncertain significance
rs1119168310:105,170,649G/Tintron variant—
rs77981423710:105,172,904G/C—uncertain significance
rs20034263310:105,172,918C/A—uncertain significance
rs54831401310:105,172,931G/A—uncertain significance
rs14346054410:105,172,966C/G—uncertain significance
rs203091119610:105,173,000A/G—uncertain significance
rs254064693210:105,173,002G/A—uncertain significance
rs76013896610:105,173,054A/C—uncertain significance
rs76286444110:105,173,077C/T—uncertain significance
rs75344465210:105,173,726A/C—uncertain significance
rs203095301810:105,173,736C/T—uncertain significance
rs20123047310:105,173,778G/A—uncertain significance
rs74897492810:105,174,777A/C—uncertain significance
rs254065014810:105,174,815G/C—uncertain significance
rs37204544610:105,174,821G/C—uncertain significance
rs56057568610:105,174,868C/T—uncertain significance
rs147379514710:105,174,883A/C—uncertain significance
rs54970240710:105,174,907G/A—uncertain significance
rs14851163710:105,176,341G/A—uncertain significance
rs254065263310:105,176,348A/G—uncertain significance
rs134978590310:105,176,363C/G—uncertain significance
rs75676648810:105,176,474C/T—uncertain significance
rs76554421210:105,177,597C/T—uncertain significance
rs103544906510:105,177,649G/A—uncertain significance
rs20139081310:105,177,658A/G—uncertain significance
rs36762842510:105,178,203G/A—uncertain significance
rs54012700610:105,178,281A/T—uncertain significance
rs20069505010:105,178,347A/G—uncertain significance
rs74533171610:105,178,350C/T—uncertain significance
rs76945286510:105,178,357G/A—uncertain significance
rs6175151010:105,178,380G/A—likely benign
rs95378137810:105,179,314C/G—uncertain significance
rs156476575610:105,179,344A/T—uncertain significance
rs14280836210:105,179,448G/A—uncertain significance
rs74816996110:105,179,455C/T—uncertain significance
rs3543580810:105,180,910C/Tintron variant—
rs254066029310:105,181,141C/T—uncertain significance
rs75985084610:105,181,181A/G—uncertain significance
rs76463453110:105,181,197G/C—uncertain significance
rs75219569910:105,181,227G/A—likely benign
rs78102258810:105,181,243G/T—uncertain significance
rs56053790110:105,181,262T/G—uncertain significance
rs54393658510:105,182,765C/G—uncertain significance
rs254066305210:105,182,769C/A—uncertain significance
rs14205255510:105,182,781C/T—uncertain significance
rs37737551010:105,182,788G/A—uncertain significance
rs77831423010:105,182,841G/A—uncertain significance
rs78045054610:105,183,374G/A—uncertain significance
rs229651210:105,184,688G/Aintron variant—
rs254066610710:105,184,741C/G—uncertain significance
rs13837116010:105,184,817C/T—uncertain significance
rs19962439210:105,184,834T/C—uncertain significance
rs127416782710:105,185,216C/T—uncertain significance
rs37005405110:105,185,249G/T—uncertain significance
rs254066964610:105,187,088A/G—uncertain significance
rs14042903510:105,187,096A/G—uncertain significance
rs76621919110:105,187,127C/T—uncertain significance
rs74866553810:105,187,142G/A—uncertain significance
rs74756813010:105,193,714G/A—uncertain significance
rs6176096910:105,193,754G/A—uncertain significance
rs254067896810:105,193,775T/G—uncertain significance
rs203204512110:105,193,778C/G—uncertain significance
rs76190030310:105,194,033G/A—likely benign
rs254068066110:105,194,576G/A—uncertain significance
rs20011545410:105,194,696C/T—likely benign
rs76605797010:105,197,794G/A—uncertain significance
rs11394059710:105,199,624C/T—uncertain significance
rs19132123310:105,200,111G/A—uncertain significance
rs36899348810:105,200,156A/T—uncertain significance
rs203233133510:105,200,178G/A—uncertain significance
rs121231087910:105,200,304G/A—uncertain significance
rs76102266510:105,200,306G/T—uncertain significance
rs36912507310:105,200,318C/T—uncertain significance
rs77254637710:105,200,492A/G—uncertain significance
rs74644028710:105,200,563C/T—uncertain significance
rs74968303310:105,200,573A/G—uncertain significance
rs76593161610:105,200,594A/G—likely benign
rs6175151310:105,201,595A/C—likely benign
rs131477414110:105,201,601G/A—uncertain significance
rs254069110010:105,201,602C/G—uncertain significance
rs53246876610:105,201,665C/T—uncertain significance
rs74536288510:105,201,686C/G—likely benign
rs57689425610:105,202,030C/T—uncertain significance
rs76339761610:105,202,075G/A—uncertain significance
rs14034338410:105,202,123C/G—uncertain significance
rs123545190610:105,202,984C/T—uncertain significance
rs254069437010:105,203,019G/A—uncertain significance

Showing 100 of 111 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.