NSMCE3

NSE3 component of SMC5/6 complex

Summary

The protein encoded by this gene is part of the SMC5-6 chromatin reorganizing complex and is a member of the MAGE superfamily. This is an intronless gene. [provided by RefSeq, May 2011]

Known Variants162 total

rsidPosition (GRCh37)AllelesClassClinVar
rs116303001515:29,561,008G/A—uncertain significance
rs74656722515:29,561,012G/A—uncertain significance
rs77647634215:29,561,021G/A—uncertain significance
rs102498227015:29,561,022C/T—likely benign
rs254379043815:29,561,029C/T—uncertain significance
rs14091358015:29,561,033C/T—uncertain significance
rs125028527015:29,561,034C/T—likely benign
rs146739648115:29,561,049T/C—likely benign
rs77426539115:29,561,058C/T—likely benign
rs254379110315:29,561,060C/G—uncertain significance
rs14518270915:29,561,064G/A—likely benign
rs76771337515:29,561,065T/C—uncertain significance
rs36924854815:29,561,070C/G—likely benign
rs92288642615:29,561,071G/A—uncertain significance
rs254379132015:29,561,072C/A—uncertain significance
rs75640745815:29,561,073T/C—likely benign
rs98717510915:29,561,084T/C—uncertain significance
rs134056080715:29,561,096T/C—uncertain significance
rs75767096815:29,561,100G/C—likely benign
rs254379253315:29,561,130C/T—likely benign
rs15127693815:29,561,146T/A—benign
rs204354197715:29,561,150T/A—uncertain significance
rs136376531015:29,561,151T/C—likely benign
rs77440523815:29,561,169T/C—likely benign
rs76759262815:29,561,172G/A—likely benign
rs204354248615:29,561,173T/C—uncertain significance
rs104278369215:29,561,180C/T—uncertain significance
rs77565374515:29,561,181G/A—likely benign
rs76091147015:29,561,187G/C—likely benign
rs129090865615:29,561,194G/A—uncertain significance
rs204354424515:29,561,211C/T—likely benign
rs37326017615:29,561,214G/A—likely benign
rs37532869315:29,561,229A/G—likely benign
rs75230293215:29,561,252T/C—uncertain significance
rs215304221715:29,561,257T/C—uncertain significance
rs75579900515:29,561,262G/A—likely benign
rs77763731315:29,561,271A/G—likely benign
rs131049046915:29,561,275T/C—uncertain significance
rs37772155515:29,561,287T/C—uncertain significance
rs122236003115:29,561,289G/C—likely benign
rs6174950615:29,561,291C/T—benign
rs76080880615:29,561,298G/T—likely benign
rs123942511415:29,561,304C/T—likely benign
rs76201384215:29,561,306G/T—uncertain significance
rs37010899015:29,561,311T/C—uncertain significance
rs75225182215:29,561,324T/C—uncertain significance
rs75574394215:29,561,325T/A—uncertain significance
rs133105567315:29,561,333T/C—uncertain significance
rs254379682115:29,561,335G/T—uncertain significance
rs14161930315:29,561,338T/C—likely benign
rs204354778715:29,561,340G/C—likely benign
rs139323252315:29,561,364G/A—likely benign
rs119828727915:29,561,367G/A—likely benign
rs74702931115:29,561,386G/A—likely benign
rs136287556415:29,561,389G/T—uncertain significance
rs77667369715:29,561,395C/T—uncertain significance
rs159614450015:29,561,406C/T—likely benign
rs77359508515:29,561,410A/T—uncertain significance
rs14705658915:29,561,415G/C—likely benign
rs134679530215:29,561,416G/A—uncertain significance
rs75212736415:29,561,420C/T—uncertain significance
rs56791635315:29,561,436C/A—likely benign
rs105297070615:29,561,438G/A—likely benign
rs37180665715:29,561,439G/A—likely benign
rs77989790615:29,561,442G/A—likely benign
rs78130791715:29,561,451G/A—likely benign
rs37529612415:29,561,454G/A—likely benign
rs254380060615:29,561,474C/G—uncertain significance
rs215304229815:29,561,478T/C—likely benign
rs215304230215:29,561,493C/G—likely benign
rs98772754615:29,561,496G/T—uncertain significance
rs254380122015:29,561,502G/A—likely benign
rs90589757115:29,561,511G/A—likely benign
rs75814637215:29,561,513G/T—uncertain significance
rs141964695615:29,561,520G/T—likely benign
rs37738673515:29,561,527T/C—uncertain significance
rs75140396015:29,561,529G/T—uncertain significance
rs159614471415:29,561,537C/T—uncertain significance
rs74824748815:29,561,539G/C—uncertain significance
rs204355475015:29,561,540G/A—uncertain significance
rs215304231715:29,561,541G/A—likely benign
rs77807594515:29,561,547G/A—likely benign
rs134509126715:29,561,550C/T—likely benign
rs37558149615:29,561,551T/C—likely benign
rs89725826715:29,561,562G/A—likely benign
rs204355601415:29,561,571C/T—likely benign
rs77587117315:29,561,574C/G—likely benign
rs117207608615:29,561,577T/A—likely benign
rs76131632815:29,561,579T/C—uncertain significance
rs77279922815:29,561,595C/T—likely benign
rs102986122615:29,561,601C/T—likely benign
rs76605842315:29,561,602T/C—uncertain significance
rs14505854615:29,561,606T/C—likely benign
rs76743212315:29,561,610G/A—likely benign
rs75618136615:29,561,616A/C—uncertain significance
rs77232448215:29,561,625G/A—likely benign
rs76919801615:29,561,640G/C—likely benign
rs254380468215:29,561,644A/G—uncertain significance
rs204355911815:29,561,651G/T—uncertain significance
rs204355923415:29,561,661C/T—likely benign

Showing 100 of 162 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.