NYNRIN

NYN domain and retroviral integrase containing

Summary

Predicted to enable RNA endonuclease activity and mRNA binding activity. Predicted to be involved in DNA integration; DNA synthesis involved in DNA repair; and DNA-templated DNA replication. Predicted to be located in membrane. Predicted to be active in cytoplasmic ribonucleoprotein granule and nucleus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants167 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs751013349	14:24,868,537	C/T	—	likely benign
rs762516672	14:24,868,600	T/C	—	uncertain significance
rs1594735750	14:24,868,637	T/C	—	likely benign
rs11625026	14:24,869,746	C/T	intron variant	—
rs72694393	14:24,874,193	G/T	intron variant	—
rs12437083	14:24,874,235	A/T	—	—
rs116410758	14:24,877,062	C/T	—	benign
rs77367832	14:24,877,064	A/G	—	benign
rs200331786	14:24,877,070	C/T	—	benign
rs1646798420	14:24,877,079	A/G	—	uncertain significance
rs756142193	14:24,877,120	C/T	—	uncertain significance
rs146351794	14:24,877,161	A/G	—	benign
rs10148781	14:24,877,215	C/T	—	benign
rs557266750	14:24,877,219	C/G	—	uncertain significance
rs189369960	14:24,877,239	C/T	—	benign
rs370323848	14:24,877,351	G/T	—	uncertain significance
rs760640899	14:24,877,427	C/A	—	uncertain significance
rs202195057	14:24,877,468	G/A	—	uncertain significance
rs746196710	14:24,877,499	G/A	—	likely benign
rs2502380019	14:24,877,505	G/C	—	uncertain significance
rs1449993834	14:24,877,547	C/T	—	uncertain significance
rs1284985312	14:24,877,609	G/A	—	uncertain significance
rs756824618	14:24,877,666	C/T	—	likely benign
rs74036628	14:24,877,699	A/G	—	benign
rs748289213	14:24,877,724	A/G	—	uncertain significance
rs572019723	14:24,877,884	T/C	—	likely benign
rs1194880007	14:24,877,916	G/A	—	uncertain significance
rs1459542080	14:24,877,932	A/G	—	uncertain significance
rs772650230	14:24,877,953	C/A	—	uncertain significance
rs113119792	14:24,877,969	G/C	—	uncertain significance
rs1400158279	14:24,878,053	C/T	—	likely benign
rs748401666	14:24,878,274	C/T	—	uncertain significance
rs1477949724	14:24,878,288	C/A	—	uncertain significance
rs2042893896	14:24,878,297	A/C	—	likely benign
rs777654963	14:24,878,306	G/C	—	uncertain significance
rs12437434	14:24,878,370	C/T	—	benign
rs1421951732	14:24,878,388	C/T	—	uncertain significance
rs149771079	14:24,878,399	G/A	—	likely benign
rs763697962	14:24,878,471	G/C	—	uncertain significance
rs367907615	14:24,878,484	C/G	—	uncertain significance
rs12897153	14:24,878,485	A/G	—	benign
rs765047927	14:24,878,495	G/A	—	uncertain significance
rs375728700	14:24,878,519	G/A	—	uncertain significance
rs199653140	14:24,878,552	A/G	—	conflicting classifications of pathogenicity
rs183366368	14:24,878,569	C/T	—	benign
rs1451015837	14:24,878,673	C/G	—	uncertain significance
rs2042898135	14:24,878,827	T/G	—	uncertain significance
rs2502383653	14:24,878,899	A/G	—	likely benign
rs376129072	14:24,878,916	G/C	—	uncertain significance
rs145306004	14:24,878,921	A/C	—	likely benign
rs774339840	14:24,878,965	A/T	—	uncertain significance
rs1594740369	14:24,878,968	A/G	—	likely benign
rs1361415676	14:24,879,005	C/T	—	uncertain significance
rs751868586	14:24,879,041	C/T	—	uncertain significance
rs554700851	14:24,879,060	C/T	—	uncertain significance
rs2502384181	14:24,879,107	G/C	—	uncertain significance
rs2042900866	14:24,879,135	C/T	—	uncertain significance
rs186691420	14:24,879,148	C/T	—	likely benign
rs200984430	14:24,879,161	G/C	—	likely benign
rs2042902002	14:24,879,233	C/T	—	likely benign
rs200054578	14:24,879,247	G/A	—	likely benign
rs772825031	14:24,879,261	A/G	—	uncertain significance
rs559761812	14:24,879,263	C/A	—	uncertain significance
rs267603971	14:24,879,269	C/T	—	uncertain significance
rs2502384667	14:24,879,333	C/T	—	uncertain significance
rs377683866	14:24,879,356	G/A	—	uncertain significance
rs751504287	14:24,879,359	C/A	—	uncertain significance
rs762063546	14:24,879,377	C/T	—	uncertain significance
rs765443117	14:24,879,378	G/A	—	uncertain significance
rs62000678	14:24,879,391	T/C	—	benign
rs1185391559	14:24,879,426	C/T	—	likely benign
rs142174010	14:24,879,430	C/T	—	benign
rs142217007	14:24,880,557	C/T	—	benign
rs547499850	14:24,880,587	C/T	—	uncertain significance
rs376923106	14:24,880,588	G/A	—	likely benign
rs2502388660	14:24,882,203	G/A	—	likely benign
rs751644731	14:24,882,210	G/A	—	uncertain significance
rs770637725	14:24,882,289	T/C	—	uncertain significance
rs2273634	14:24,882,312	C/G	—	benign
rs2332328	14:24,883,058	C/T	intron variant	—
rs2042932100	14:24,883,864	G/A	—	uncertain significance
rs2502390787	14:24,883,866	G/A	—	likely benign
rs8017377	14:24,883,887	G/A	missense variant	benign
rs201369368	14:24,883,896	G/A	—	uncertain significance
rs181160538	14:24,883,899	C/A	—	likely benign
rs200803889	14:24,883,964	G/T	—	likely benign
rs140818379	14:24,883,994	G/A	—	likely benign
rs376159917	14:24,884,006	C/T	—	uncertain significance
rs763907941	14:24,884,074	G/A	—	uncertain significance
rs936733579	14:24,884,113	A/G	—	uncertain significance
rs1164608993	14:24,884,133	G/T	—	uncertain significance
rs762649803	14:24,884,197	A/G	—	uncertain significance
rs374795039	14:24,884,272	A/T	—	uncertain significance
rs912019927	14:24,884,277	A/C	—	uncertain significance
rs757541061	14:24,884,366	C/G	—	likely benign
rs200952720	14:24,884,426	G/C	—	uncertain significance
rs777661158	14:24,884,436	C/T	—	uncertain significance
rs369620295	14:24,884,450	C/T	—	uncertain significance
rs765518334	14:24,884,497	G/A	—	uncertain significance
rs376021092	14:24,884,506	A/G	—	uncertain significance

Showing 100 of 167 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.