UTP20

UTP20 small subunit processome component

Summary

UTP20 is a component of the U3 small nucleolar RNA (snoRNA) (SNORD3A; MIM 180710) protein complex (U3 snoRNP) and is involved in 18S rRNA processing (Wang et al., 2007 [PubMed 17498821]).[supplied by OMIM, Jun 2009]

Known Variants157 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1047957812	12:101,674,067	A/C	—	likely benign
rs2499546972	12:101,674,083	A/G	—	uncertain significance
rs78240090	12:101,674,902	A/G	—	benign
rs1181779838	12:101,674,945	C/T	—	uncertain significance
rs149447402	12:101,679,595	A/G	—	uncertain significance
rs143875613	12:101,679,652	C/G	—	uncertain significance
rs2499551930	12:101,680,121	G/T	—	uncertain significance
rs147399996	12:101,680,176	C/T	—	uncertain significance
rs139691544	12:101,680,177	G/A	—	likely benign
rs2499552033	12:101,680,187	A/G	—	uncertain significance
rs147632286	12:101,680,272	T/C	—	uncertain significance
rs142220773	12:101,680,273	G/A	—	benign
rs555371440	12:101,682,775	A/G	—	uncertain significance
rs749123222	12:101,683,970	C/G	—	uncertain significance
rs111551110	12:101,684,060	A/C	—	benign
rs372093743	12:101,684,530	G/A	—	likely benign
rs767936184	12:101,684,571	T/C	—	uncertain significance
rs760272496	12:101,684,584	G/A	—	uncertain significance
rs148951374	12:101,684,594	C/T	—	likely benign
rs2499556024	12:101,684,610	T/A	—	uncertain significance
rs75817013	12:101,685,540	C/T	—	benign
rs148365055	12:101,685,586	A/C	—	uncertain significance
rs951390222	12:101,685,600	A/T	—	uncertain significance
rs75620118	12:101,685,643	C/A	—	benign
rs759335513	12:101,685,652	G/A	—	uncertain significance
rs544207946	12:101,685,761	C/T	—	uncertain significance
rs79571582	12:101,685,838	A/T	—	conflicting classifications of pathogenicity
rs2290720	12:101,687,043	C/A	intron variant	—
rs373930284	12:101,693,782	G/A	—	uncertain significance
rs376003744	12:101,693,825	G/A	—	uncertain significance
rs748832576	12:101,696,313	G/T	—	uncertain significance
rs765693560	12:101,700,478	T/G	—	uncertain significance
rs753671569	12:101,702,060	A/G	—	uncertain significance
rs370762874	12:101,702,119	G/C	—	uncertain significance
rs749099686	12:101,705,507	C/T	—	uncertain significance
rs548791318	12:101,705,510	G/A	—	uncertain significance
rs142042282	12:101,705,544	A/G	—	uncertain significance
rs773438686	12:101,705,900	C/G	—	uncertain significance
rs1291147923	12:101,711,269	C/T	—	uncertain significance
rs759190580	12:101,711,306	G/A	—	uncertain significance
rs1371519214	12:101,711,321	G/A	—	uncertain significance
rs767156921	12:101,711,427	G/C	—	uncertain significance
rs376164687	12:101,713,345	G/A	—	uncertain significance
rs201830409	12:101,713,357	T/G	—	uncertain significance
rs2499582717	12:101,714,648	C/G	—	uncertain significance
rs200779998	12:101,714,697	C/T	—	uncertain significance
rs899621964	12:101,715,295	A/T	—	uncertain significance
rs374755767	12:101,715,313	A/C	—	uncertain significance
rs539396900	12:101,715,361	G/A	—	uncertain significance
rs577310747	12:101,720,867	A/G	—	uncertain significance
rs375521157	12:101,720,975	T/C	—	uncertain significance
rs375681505	12:101,723,054	G/A	—	uncertain significance
rs376634646	12:101,723,060	G/A	—	uncertain significance
rs142628447	12:101,723,088	G/A	—	uncertain significance
rs767466953	12:101,723,134	T/G	—	uncertain significance
rs759344498	12:101,723,198	G/A	—	uncertain significance
rs372292737	12:101,727,119	G/A	—	uncertain significance
rs1404807430	12:101,727,134	T/C	—	uncertain significance
rs1478629957	12:101,731,857	C/G	—	uncertain significance
rs762081637	12:101,731,871	A/C	—	uncertain significance
rs2499594874	12:101,731,876	A/G	—	uncertain significance
rs185536134	12:101,731,902	C/A	—	uncertain significance
rs138765948	12:101,731,954	T/C	—	likely benign
rs150082822	12:101,731,968	A/G	—	uncertain significance
rs767111217	12:101,731,983	G/A	—	uncertain significance
rs746321279	12:101,732,609	G/A	—	uncertain significance
rs142261987	12:101,732,628	T/C	—	benign
rs761558757	12:101,732,646	G/T	—	uncertain significance
rs765081808	12:101,732,647	T/A	—	uncertain significance
rs377526182	12:101,732,685	A/T	—	uncertain significance
rs1363688234	12:101,732,719	C/A	—	uncertain significance
rs1368396871	12:101,734,327	A/G	—	uncertain significance
rs750590866	12:101,734,365	C/T	—	uncertain significance
rs768010423	12:101,736,234	T/C	—	uncertain significance
rs577001413	12:101,736,302	A/G	—	uncertain significance
rs376859385	12:101,736,331	C/A	—	uncertain significance
rs200766524	12:101,736,357	C/T	—	uncertain significance
rs2270861	12:101,736,381	A/G	intron variant	—
rs775896086	12:101,736,587	G/T	—	uncertain significance
rs199880162	12:101,736,761	G/A	—	uncertain significance
rs768900064	12:101,736,764	G/A	—	uncertain significance
rs145374811	12:101,736,784	G/C	—	uncertain significance
rs1378239261	12:101,736,797	T/A	—	uncertain significance
rs753785975	12:101,736,859	C/A	—	uncertain significance
rs1869258327	12:101,738,403	A/G	—	uncertain significance
rs746376511	12:101,738,446	A/C	—	uncertain significance
rs140971531	12:101,738,481	C/T	—	uncertain significance
rs1362498186	12:101,738,509	G/T	—	uncertain significance
rs138618335	12:101,739,443	G/C	—	uncertain significance
rs2499601803	12:101,739,450	T/C	—	uncertain significance
rs149336135	12:101,740,290	T/C	—	uncertain significance
rs57083693	12:101,742,180	T/C	intron variant	—
rs1390137775	12:101,745,835	T/A	—	uncertain significance
rs1869550110	12:101,745,963	T/C	—	uncertain significance
rs373208716	12:101,746,893	T/C	—	uncertain significance
rs772682870	12:101,748,612	G/A	—	likely benign
rs776367536	12:101,748,697	G/A	—	uncertain significance
rs138643360	12:101,748,718	C/T	—	likely benign
rs1014340936	12:101,748,727	C/T	—	uncertain significance
rs370227791	12:101,748,826	C/T	—	uncertain significance

Showing 100 of 157 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.