GNAT2

G protein subunit alpha transducin 2

Summary

Transducin is a 3-subunit guanine nucleotide-binding protein (G protein) which stimulates the coupling of rhodopsin and cGMP-phoshodiesterase during visual impulses. The transducin alpha subunits in rods and cones are encoded by separate genes. This gene encodes the alpha subunit in cones. [provided by RefSeq, Jul 2008]

Known Variants191 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs572222112	1:110,145,874	G/T	—	uncertain significance
rs116688317	1:110,145,926	C/G	—	uncertain significance
rs2524329757	1:110,145,983	A/G	—	uncertain significance
rs61754627	1:110,145,984	G/A	—	uncertain significance
rs765538494	1:110,145,988	G/A	—	likely benign
rs2101121104	1:110,146,006	T/G	—	uncertain significance
rs753014058	1:110,146,010	A/G	—	uncertain significance
rs758178456	1:110,146,016	A/G	—	uncertain significance
rs1570560469	1:110,146,043	T/A	—	uncertain significance
rs1257988049	1:110,146,071	T/C	—	uncertain significance
rs1476110210	1:110,146,074	T/C	—	uncertain significance
rs139314029	1:110,146,075	G/C	—	uncertain significance
rs1419203047	1:110,146,092	T/C	—	uncertain significance
rs950519744	1:110,146,098	C/T	—	uncertain significance
rs368195234	1:110,146,103	C/T	—	uncertain significance
rs748981899	1:110,146,104	G/A	—	pathogenic
rs34723289	1:110,146,108	A/G	—	conflicting classifications of pathogenicity
rs2101121277	1:110,146,109	T/C	—	uncertain significance
rs200137591	1:110,146,110	T/C	—	uncertain significance
rs200883344	1:110,146,113	G/A	—	conflicting classifications of pathogenicity
rs2524330271	1:110,146,119	G/C	—	uncertain significance
rs1309275044	1:110,146,132	T/C	—	uncertain significance
rs1553226355	1:110,146,135	G/T	—	likely pathogenic
rs1315297448	1:110,146,141	C/G	—	likely benign
rs765445143	1:110,146,144	C/T	—	likely benign
rs200056419	1:110,146,145	G/A	—	uncertain significance
rs751249807	1:110,146,153	A/G	—	likely benign
rs1025845483	1:110,146,154	T/C	—	uncertain significance
rs757147586	1:110,146,155	A/G	—	conflicting classifications of pathogenicity
rs750410966	1:110,146,164	T/C	—	uncertain significance
rs200224608	1:110,146,166	C/T	—	uncertain significance
rs2524330471	1:110,146,170	G/T	—	likely benign
rs374107405	1:110,146,181	A/T	—	likely benign
rs1266946606	1:110,146,561	C/T	—	likely benign
rs925715201	1:110,146,573	C/T	—	uncertain significance
rs373436662	1:110,146,577	A/G	—	likely benign
rs779967692	1:110,146,602	T/G	—	uncertain significance
rs753280339	1:110,146,609	T/C	—	uncertain significance
rs1465582550	1:110,146,613	G/C	—	uncertain significance
rs754570281	1:110,146,622	C/T	—	likely benign
rs1649516067	1:110,146,626	A/G	—	conflicting classifications of pathogenicity
rs368906691	1:110,146,629	A/T	—	uncertain significance
rs771880106	1:110,146,632	T/A	—	uncertain significance
rs1193859398	1:110,146,641	T/A	—	uncertain significance
rs1452869796	1:110,146,650	A/G	—	uncertain significance
rs2101121948	1:110,146,666	C/T	—	uncertain significance
rs762929495	1:110,146,668	G/A	—	uncertain significance
rs768833008	1:110,146,669	C/A	—	uncertain significance
rs2101121964	1:110,146,670	A/G	—	likely benign
rs2524332079	1:110,146,685	A/G	—	uncertain significance
rs1341749258	1:110,146,703	A/G	—	likely benign
rs1412729148	1:110,146,705	G/T	—	uncertain significance
rs147849105	1:110,146,714	C/T	—	uncertain significance
rs760527034	1:110,146,718	C/T	—	uncertain significance
rs535592857	1:110,146,719	A/G	—	uncertain significance
rs142609327	1:110,146,722	C/T	—	uncertain significance
rs754414120	1:110,146,723	G/A	—	uncertain significance
rs764762846	1:110,146,724	A/G	—	likely benign
rs942543744	1:110,146,730	G/A	—	likely benign
rs372583779	1:110,146,745	A/G	—	likely benign
rs758064816	1:110,146,746	T/C	—	uncertain significance
rs114388354	1:110,146,849	C/T	intron variant	—
rs17024258	1:110,147,321	C/T	intron variant	—
rs748179055	1:110,148,575	A/G	—	likely benign
rs377096148	1:110,148,583	G/A	—	likely benign
rs566052246	1:110,148,584	C/A	—	likely benign
rs1553226581	1:110,148,587	C/G	—	likely pathogenic
rs1557918544	1:110,148,590	A/G	—	likely pathogenic
rs2524336820	1:110,148,592	C/G	—	uncertain significance
rs2101123698	1:110,148,593	A/G	—	uncertain significance
rs140788789	1:110,148,597	C/T	—	uncertain significance
rs367863835	1:110,148,598	G/A	—	likely benign
rs758050645	1:110,148,611	A/G	—	uncertain significance
rs1649580303	1:110,148,633	G/C	—	uncertain significance
rs201230566	1:110,148,640	A/G	—	conflicting classifications of pathogenicity
rs1649580974	1:110,148,662	C/T	—	uncertain significance
rs779352893	1:110,148,685	C/T	—	likely benign
rs995152260	1:110,148,689	C/G	—	uncertain significance
rs1557918619	1:110,148,692	T/A	—	pathogenic
rs140231308	1:110,148,694	G/A	—	likely benign
rs551776784	1:110,148,703	C/A	—	conflicting classifications of pathogenicity
rs1570562309	1:110,148,707	C/T	—	pathogenic
rs1557918635	1:110,148,719	A/T	—	likely pathogenic
rs1649583816	1:110,148,722	C/G	—	likely pathogenic
rs1557918638	1:110,148,723	T/G	—	pathogenic
rs199666763	1:110,148,730	A/G	—	uncertain significance
rs200962508	1:110,148,913	G/T	—	likely benign
rs2524338147	1:110,148,920	A/G	—	likely benign
rs767182806	1:110,148,924	A/G	—	uncertain significance
rs1488296684	1:110,148,925	C/T	—	uncertain significance
rs750089687	1:110,148,940	A/G	—	likely benign
rs2524338207	1:110,148,946	T/C	—	uncertain significance
rs759910267	1:110,148,949	C/T	—	uncertain significance
rs376412882	1:110,148,950	G/A	—	likely benign
rs753083112	1:110,148,954	A/T	—	uncertain significance
rs370869387	1:110,148,966	A/G	—	uncertain significance
rs751633351	1:110,148,969	A/T	—	uncertain significance
rs201798524	1:110,148,970	T/C	—	uncertain significance
rs1799875	1:110,148,974	C/A	—	likely benign
rs746117122	1:110,148,975	G/A	—	uncertain significance

Showing 100 of 191 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.