RNASET2

ribonuclease T2

Summary

This ribonuclease gene is a novel member of the Rh/T2/S-glycoprotein class of extracellular ribonucleases. It is a single copy gene that maps to 6q27, a region associated with human malignancies and chromosomal rearrangement. [provided by RefSeq, Jul 2008]

Known Variants147 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs9459805	6:167,336,151	A/G	intron variant	—
rs189853938	6:167,340,001	G/A	downstream gene variant	—
rs139552047	6:167,343,082	C/T	—	likely benign
rs934916857	6:167,343,096	G/A	—	uncertain significance
rs754430788	6:167,343,098	G/A	—	uncertain significance
rs759625896	6:167,343,099	G/A	—	uncertain significance
rs140357917	6:167,343,106	G/T	—	likely benign
rs1289032799	6:167,343,112	T/A	—	likely benign
rs2483186393	6:167,343,115	G/A	—	likely benign
rs146590748	6:167,343,140	C/T	—	likely benign
rs11159	6:167,343,141	G/A	—	benign
rs199823417	6:167,343,142	G/T	—	uncertain significance
rs201458874	6:167,343,148	G/A	—	likely benign
rs149922066	6:167,343,150	C/T	—	benign
rs537280779	6:167,343,151	G/A	—	likely benign
rs145013301	6:167,343,167	C/G	—	uncertain significance
rs149106779	6:167,343,179	T/G	—	uncertain significance
rs35716361	6:167,343,185	G/T	—	likely benign
rs74546166	6:167,343,187	C/T	—	conflicting classifications of pathogenicity
rs202105909	6:167,343,195	C/T	—	conflicting classifications of pathogenicity
rs35517174	6:167,343,199	C/G	—	conflicting classifications of pathogenicity
rs200901770	6:167,343,200	G/C	—	uncertain significance
rs41269593	6:167,343,204	C/T	—	likely benign
rs201960492	6:167,343,205	G/A	—	likely benign
rs777199814	6:167,343,207	T/C	—	uncertain significance
rs137968522	6:167,343,237	T/C	—	uncertain significance
rs776087270	6:167,343,246	G/C	—	uncertain significance
rs974396478	6:167,343,247	T/A	—	uncertain significance
rs762901010	6:167,343,257	C/T	—	uncertain significance
rs370545130	6:167,343,283	A/G	—	conflicting classifications of pathogenicity
rs192559541	6:167,343,296	A/G	—	benign
rs377095475	6:167,343,298	A/G	—	likely benign
rs201458320	6:167,343,299	G/T	—	benign
rs1191342507	6:167,344,532	C/T	—	uncertain significance
rs759190975	6:167,344,536	C/A	—	uncertain significance
rs121918137	6:167,344,549	A/G	missense variant	pathogenic
rs763011032	6:167,344,565	C/T	—	conflicting classifications of pathogenicity
rs1239284254	6:167,344,567	C/T	—	uncertain significance
rs1315470043	6:167,344,576	C/T	—	uncertain significance
rs1330770810	6:167,344,578	C/G	—	uncertain significance
rs13213697	6:167,344,583	G/A	—	benign
rs1217929196	6:167,344,587	G/A	—	uncertain significance
rs1583214018	6:167,344,589	A/G	—	likely benign
rs1447243603	6:167,344,597	A/G	—	uncertain significance
rs756845295	6:167,344,599	T/C	—	uncertain significance
rs2483191568	6:167,344,600	C/G	—	uncertain significance
rs1167563909	6:167,344,611	T/C	—	uncertain significance
rs368698284	6:167,344,620	C/T	—	likely benign
rs754184305	6:167,347,561	A/G	—	likely benign
rs771231451	6:167,347,623	C/A	—	uncertain significance
rs749067371	6:167,347,638	T/A	—	likely benign
rs143517894	6:167,352,252	C/T	—	likely benign
rs372938195	6:167,352,363	C/T	—	likely benign
rs374964582	6:167,352,364	G/A	—	likely benign
rs538845875	6:167,352,366	G/T	—	benign
rs773843764	6:167,352,367	G/C	—	likely benign
rs776901655	6:167,352,371	G/A	—	likely benign
rs752964226	6:167,352,375	G/A	—	likely benign
rs34346305	6:167,352,403	G/A	—	benign
rs140749759	6:167,352,448	C/T	—	likely benign
rs117003826	6:167,352,449	G/A	—	uncertain significance
rs769927092	6:167,352,462	C/T	—	uncertain significance
rs138906295	6:167,352,463	G/A	—	likely benign
rs775647997	6:167,352,466	G/A	—	likely benign
rs750265990	6:167,352,469	G/T	—	conflicting classifications of pathogenicity
rs373505402	6:167,352,478	C/T	—	likely benign
rs754432508	6:167,352,483	C/T	—	uncertain significance
rs2483208958	6:167,352,503	G/T	—	likely benign
rs2483216561	6:167,356,491	A/G	—	likely benign
rs370517169	6:167,356,495	G/C	—	likely benign
rs2483216603	6:167,356,506	C/A	—	pathogenic
rs374162593	6:167,356,513	C/T	—	likely benign
rs780445402	6:167,356,514	G/T	—	uncertain significance
rs149426644	6:167,356,519	C/T	—	conflicting classifications of pathogenicity
rs540010690	6:167,356,530	C/T	—	likely benign
rs772187999	6:167,356,542	G/A	—	likely benign
rs367656044	6:167,356,548	C/T	—	pathogenic
rs1280410103	6:167,356,552	T/C	—	uncertain significance
rs2483216820	6:167,356,574	G/T	—	uncertain significance
rs2128645761	6:167,356,579	T/C	—	pathogenic
rs112364937	6:167,360,153	T/C	—	likely benign
rs2128646363	6:167,360,156	T/A	—	likely benign
rs1261086042	6:167,360,167	T/C	—	uncertain significance
rs1239628395	6:167,360,184	A/T	—	uncertain significance
rs1441873284	6:167,360,186	T/C	—	uncertain significance
rs1434250650	6:167,360,198	G/T	—	pathogenic
rs886061240	6:167,360,207	C/T	—	uncertain significance
rs115956642	6:167,360,217	T/C	—	benign
rs184572250	6:167,360,224	G/A	—	conflicting classifications of pathogenicity
rs1778856869	6:167,360,241	T/C	—	uncertain significance
rs2236313	6:167,360,389	T/C	upstream gene variant	—
rs2483229419	6:167,362,051	C/T	—	likely benign
rs1583231802	6:167,362,060	T/C	—	likely benign
rs374897496	6:167,362,066	A/G	—	likely benign
rs2483229518	6:167,362,075	C/A	—	uncertain significance
rs761924699	6:167,362,101	C/T	—	uncertain significance
rs767762786	6:167,362,102	G/A	—	likely benign
rs750669368	6:167,362,107	G/A	—	pathogenic
rs2128646702	6:167,362,114	C/A	—	likely pathogenic
rs372239307	6:167,362,133	A/T	—	benign

Showing 100 of 147 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.