GRIP1

glutamate receptor interacting protein 1

Summary

This gene encodes a member of the glutamate receptor interacting protein family. The encoded scaffold protein binds to and mediates the trafficking and membrane organization of a number of transmembrane proteins. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, May 2010]

Known Variants574 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs760559161	12:66,741,288	C/T	—	uncertain significance
rs886049790	12:66,741,471	C/T	—	uncertain significance
rs144894732	12:66,741,485	C/T	—	likely benign
rs544816589	12:66,741,512	T/A	—	uncertain significance
rs886049791	12:66,741,537	A/T	—	uncertain significance
rs2054042410	12:66,741,583	C/A	—	uncertain significance
rs144864808	12:66,741,650	T/C	—	uncertain significance
rs1345779940	12:66,741,780	G/A	—	uncertain significance
rs138773990	12:66,741,869	A/T	—	uncertain significance
rs886049792	12:66,741,884	A/G	—	uncertain significance
rs2054060318	12:66,741,967	C/G	—	uncertain significance
rs867272684	12:66,741,978	A/C	—	uncertain significance
rs531925092	12:66,742,083	A/G	—	uncertain significance
rs191784180	12:66,742,132	G/A	—	uncertain significance
rs554240061	12:66,742,182	C/T	—	uncertain significance
rs1168308	12:66,742,183	A/G	—	benign
rs984899547	12:66,742,188	A/G	—	uncertain significance
rs572566894	12:66,742,300	T/C	—	likely benign
rs78619935	12:66,742,371	G/A	—	benign
rs886049795	12:66,742,382	C/T	—	uncertain significance
rs886049796	12:66,742,564	C/A	—	uncertain significance
rs541596282	12:66,742,565	C/T	—	likely benign
rs1344322970	12:66,742,571	G/T	—	uncertain significance
rs191549204	12:66,742,661	G/A	—	uncertain significance
rs200232418	12:66,742,700	C/T	—	uncertain significance
rs1284400061	12:66,742,706	T/C	—	uncertain significance
rs367666328	12:66,742,795	G/A	—	uncertain significance
rs199812266	12:66,742,817	T/A	—	conflicting classifications of pathogenicity
rs2054101493	12:66,742,820	T/C	—	likely benign
rs564771115	12:66,742,841	G/A	—	likely benign
rs2499568532	12:66,742,848	G/T	—	uncertain significance
rs780019018	12:66,742,850	C/T	—	likely benign
rs542462169	12:66,742,854	T/C	—	uncertain significance
rs536657259	12:66,742,882	A/T	—	uncertain significance
rs2054105422	12:66,742,883	A/G	—	likely benign
rs2054105713	12:66,742,889	T/G	—	likely benign
rs2499569379	12:66,742,892	T/C	—	likely benign
rs2054106599	12:66,742,901	T/C	—	likely benign
rs2054108274	12:66,742,928	T/G	—	likely benign
rs2499570113	12:66,742,931	G/T	—	uncertain significance
rs2499570225	12:66,742,937	A/G	—	likely benign
rs2499570303	12:66,742,940	A/T	—	likely benign
rs2054109253	12:66,742,949	G/A	—	likely benign
rs778582549	12:66,742,955	C/T	—	likely benign
rs2499570534	12:66,742,961	C/T	—	likely benign
rs201410285	12:66,742,963	C/T	—	conflicting classifications of pathogenicity
rs558365010	12:66,742,964	G/A	—	conflicting classifications of pathogenicity
rs750696929	12:66,742,971	G/C	—	uncertain significance
rs2499570812	12:66,742,976	G/A	—	likely benign
rs187691546	12:66,742,979	G/A	—	conflicting classifications of pathogenicity
rs116894395	12:66,742,987	C/G	—	uncertain significance
rs771473441	12:66,743,010	G/C	—	uncertain significance
rs767782069	12:66,743,018	A/G	—	likely benign
rs761396901	12:66,743,030	A/C	—	likely benign
rs935125650	12:66,743,034	G/T	—	likely benign
rs2499571707	12:66,743,035	T/C	—	likely benign
rs749423962	12:66,747,184	C/T	—	likely benign
rs2499608084	12:66,747,186	T/C	—	likely benign
rs1451672566	12:66,747,209	G/A	—	likely benign
rs772435411	12:66,747,212	A/G	—	likely benign
rs2499608869	12:66,747,233	A/G	—	likely benign
rs762619221	12:66,747,254	A/G	—	likely benign
rs369087420	12:66,747,257	A/T	—	uncertain significance
rs2499609588	12:66,747,283	G/A	—	likely benign
rs907504226	12:66,747,287	G/A	—	likely benign
rs372970620	12:66,747,308	A/G	—	conflicting classifications of pathogenicity
rs2054335071	12:66,747,311	G/A	—	likely benign
rs2499610217	12:66,747,328	C/T	—	uncertain significance
rs1565657679	12:66,747,329	C/T	—	likely benign
rs1468776161	12:66,747,349	G/A	—	likely benign
rs201508790	12:66,747,358	T/A	—	likely benign
rs2137084830	12:66,747,360	G/C	—	likely benign
rs780445888	12:66,747,361	G/C	—	likely benign
rs2499610622	12:66,747,362	A/G	—	likely benign
rs374870806	12:66,765,455	G/A	—	likely benign
rs2499782777	12:66,765,459	A/T	—	likely benign
rs369591677	12:66,765,460	G/A	—	likely benign
rs779023536	12:66,765,465	C/T	—	likely benign
rs780494377	12:66,765,475	T/C	—	uncertain significance
rs1310999738	12:66,765,477	G/A	—	likely benign
rs1321446217	12:66,765,480	C/A	—	likely benign
rs2137293909	12:66,765,485	C/T	—	uncertain significance
rs2499783531	12:66,765,489	A/G	—	likely benign
rs2499783583	12:66,765,495	T/C	—	likely benign
rs773895525	12:66,765,498	A/G	—	likely benign
rs2499784325	12:66,765,536	G/A	—	likely benign
rs765435720	12:66,765,537	G/A	—	likely benign
rs1263863090	12:66,765,570	G/A	—	likely benign
rs375330927	12:66,765,600	C/T	—	likely benign
rs540468070	12:66,765,601	G/A	—	uncertain significance
rs570235851	12:66,765,604	C/T	—	uncertain significance
rs761580569	12:66,765,605	G/A	—	uncertain significance
rs181527317	12:66,765,606	C/T	—	likely benign
rs371002374	12:66,765,607	G/C	—	uncertain significance
rs202030145	12:66,765,616	C/T	—	uncertain significance
rs766533364	12:66,765,617	G/A	—	uncertain significance
rs755528209	12:66,765,637	C/T	—	uncertain significance
rs753250239	12:66,765,642	C/A	—	likely benign
rs778224613	12:66,765,651	G/A	—	likely benign
rs199951418	12:66,765,652	C/T	—	uncertain significance

Showing 100 of 574 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.