UNC79

unc-79 subunit of NALCN channel complex

Summary

The NALCN channel is responsible for Na(+) leak currents. The protein encoded by this gene, along with UNC80, is an accessory subunit of the NALCN channel that contributes to the Ca(2+) sensitivity of the channel. [provided by RefSeq, Sep 2016]

Known Variants141 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs67021408	14:93,820,551	A/T	intron variant	—
rs8014875	14:93,828,290	G/A	intron variant	—
rs10144067	14:93,885,198	C/T	intron variant	—
rs4900184	14:93,900,609	T/C	downstream gene variant	—
rs10142298	14:93,909,792	C/T	intron variant	—
rs1242771	14:93,928,521	C/A	—	—
rs11160119	14:93,932,258	G/T	—	—
rs778061554	14:93,934,015	A/T	—	likely benign
rs745801030	14:93,934,016	G/T	—	likely benign
rs2547902476	14:93,934,097	A/T	—	uncertain significance
rs142898171	14:93,940,619	C/A	—	likely benign
rs150065550	14:93,944,029	G/A	—	uncertain significance
rs142058669	14:93,944,040	A/C	—	uncertain significance
rs777377323	14:93,954,049	C/G	—	uncertain significance
rs761723945	14:93,963,530	C/T	—	uncertain significance
rs12882384	14:93,985,447	A/C	—	—
rs2146506	14:93,992,735	T/C	intron variant	—
rs150368733	14:93,994,932	C/T	—	uncertain significance
rs2548437674	14:93,994,994	T/A	—	uncertain significance
rs765575094	14:93,998,910	A/G	—	uncertain significance
rs2548484648	14:93,998,919	A/T	—	uncertain significance
rs377687253	14:94,004,395	C/T	—	uncertain significance
rs2548532467	14:94,004,416	C/T	—	uncertain significance
rs755964933	14:94,004,471	C/T	—	uncertain significance
rs139796738	14:94,007,022	G/C	—	likely benign
rs759429125	14:94,007,061	C/T	—	uncertain significance
rs1264786788	14:94,008,846	C/T	—	uncertain significance
rs1567082034	14:94,008,870	C/T	—	uncertain significance
rs2548580145	14:94,008,875	G/A	—	uncertain significance
rs2548580616	14:94,008,924	G/C	—	uncertain significance
rs2548580817	14:94,008,948	C/G	—	uncertain significance
rs774399849	14:94,009,007	A/G	—	uncertain significance
rs1025196721	14:94,009,028	A/G	—	uncertain significance
rs942065	14:94,032,065	G/A	intron variant	—
rs143259547	14:94,041,411	C/T	—	uncertain significance
rs748885718	14:94,041,421	T/G	—	uncertain significance
rs147507350	14:94,041,488	G/T	—	uncertain significance
rs775625813	14:94,041,540	G/A	—	uncertain significance
rs576321999	14:94,044,213	G/A	—	uncertain significance
rs188822336	14:94,044,282	G/A	—	uncertain significance
rs181255610	14:94,044,294	G/A	—	uncertain significance
rs1267848033	14:94,044,364	G/T	—	uncertain significance
rs2548984389	14:94,046,504	C/T	—	uncertain significance
rs148393587	14:94,046,520	C/T	—	uncertain significance
rs80323573	14:94,046,523	T/C	—	uncertain significance
rs1566696810	14:94,046,613	A/C	—	uncertain significance
rs765545121	14:94,046,618	G/A	—	uncertain significance
rs1483265597	14:94,046,627	A/G	—	uncertain significance
rs200793911	14:94,046,630	G/A	—	uncertain significance
rs1166669395	14:94,046,654	A/G	—	uncertain significance
rs746598956	14:94,048,553	C/T	—	uncertain significance
rs767834661	14:94,048,653	G/T	—	uncertain significance
rs568643633	14:94,048,674	G/T	—	uncertain significance
rs140513716	14:94,053,005	T/C	—	uncertain significance
rs138158671	14:94,053,172	C/G	—	uncertain significance
rs149552452	14:94,053,227	A/G	—	uncertain significance
rs184571396	14:94,053,235	G/A	—	uncertain significance
rs2549174939	14:94,063,741	T/G	—	uncertain significance
rs2549237636	14:94,069,594	C/T	—	uncertain significance
rs770359445	14:94,069,668	C/T	—	uncertain significance
rs76171275	14:94,069,688	C/T	—	benign
rs2549239855	14:94,069,692	A/T	—	uncertain significance
rs1280817734	14:94,069,753	C/T	—	uncertain significance
rs12147136	14:94,072,304	A/T	—	—
rs1887195	14:94,075,104	C/T	intron variant	—
rs11851122	14:94,076,978	A/G	intron variant	—
rs967596948	14:94,079,150	A/G	—	likely benign
rs2066405972	14:94,079,154	C/T	—	uncertain significance
rs368292707	14:94,079,280	G/A	—	uncertain significance
rs2066418958	14:94,079,366	G/A	—	uncertain significance
rs146420696	14:94,079,368	T/C	—	uncertain significance
rs2549343494	14:94,079,421	A/G	—	uncertain significance
rs746984728	14:94,083,577	G/T	—	uncertain significance
rs34816083	14:94,084,641	C/T	—	conflicting classifications of pathogenicity
rs377416512	14:94,084,658	A/G	—	uncertain significance
rs1478080403	14:94,084,665	A/G	—	uncertain significance
rs532984210	14:94,087,310	C/G	—	likely benign
rs1330095646	14:94,088,007	A/T	—	uncertain significance
rs146432485	14:94,088,090	T/C	—	uncertain significance
rs1415839396	14:94,088,141	C/T	—	uncertain significance
rs2549426121	14:94,088,159	A/T	—	uncertain significance
rs2549426446	14:94,088,182	G/C	—	uncertain significance
rs2549426735	14:94,088,201	G/C	—	uncertain significance
rs141877928	14:94,088,203	C/T	—	uncertain significance
rs2139929706	14:94,088,206	A/C	—	likely benign
rs372911762	14:94,088,293	G/C	—	uncertain significance
rs1324912531	14:94,088,431	C/A	—	uncertain significance
rs2549430329	14:94,088,440	C/A	—	uncertain significance
rs78221379	14:94,088,455	A/G	—	uncertain significance
rs756129252	14:94,088,468	A/C	—	uncertain significance
rs780204528	14:94,088,488	C/T	—	uncertain significance
rs2549431684	14:94,088,524	G/C	—	uncertain significance
rs748828170	14:94,088,647	G/C	—	uncertain significance
rs539328393	14:94,088,687	A/C	—	uncertain significance
rs752803526	14:94,088,770	G/A	—	uncertain significance
rs2549436238	14:94,088,854	A/G	—	uncertain significance
rs781751585	14:94,088,933	C/A	—	uncertain significance
rs762001442	14:94,088,980	G/A	—	uncertain significance
rs766209009	14:94,088,993	C/T	—	uncertain significance
rs2549438130	14:94,089,044	A/G	—	uncertain significance

Showing 100 of 141 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.