FRMPD1

FERM and PDZ domain containing 1

Summary

Involved in establishment of protein localization to membrane and regulation of G protein-coupled receptor signaling pathway. Located in cell cortex and plasma membrane. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants118 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs4878712	9:37,654,257	G/A	intron variant	—
rs569779943	9:37,685,627	C/G	—	—
rs200161833	9:37,692,702	G/A	—	uncertain significance
rs142418624	9:37,692,711	C/G	—	uncertain significance
rs780133603	9:37,692,714	C/T	—	uncertain significance
rs146611803	9:37,692,715	G/A	—	uncertain significance
rs3747540	9:37,692,733	C/T	—	uncertain significance
rs2489252492	9:37,707,413	G/T	—	likely benign
rs1389274462	9:37,707,414	G/A	—	uncertain significance
rs150458691	9:37,707,448	A/T	—	likely benign
rs141611918	9:37,707,502	C/G	—	uncertain significance
rs202041675	9:37,707,504	C/T	—	uncertain significance
rs142593632	9:37,708,399	G/T	—	uncertain significance
rs1017054886	9:37,708,410	G/A	—	uncertain significance
rs200632259	9:37,708,450	A/G	—	uncertain significance
rs773296299	9:37,711,376	T/A	—	uncertain significance
rs373470102	9:37,711,388	C/T	—	uncertain significance
rs778026562	9:37,719,135	C/G	—	uncertain significance
rs763070434	9:37,729,762	G/A	—	uncertain significance
rs371862748	9:37,729,770	G/A	—	uncertain significance
rs148192224	9:37,731,012	G/A	—	uncertain significance
rs930651934	9:37,731,086	T/C	—	uncertain significance
rs771951665	9:37,732,326	G/A	—	uncertain significance
rs201737747	9:37,732,389	G/A	—	uncertain significance
rs746388440	9:37,733,566	G/C	—	uncertain significance
rs767160958	9:37,733,751	C/T	—	uncertain significance
rs1563958203	9:37,735,574	C/T	—	uncertain significance
rs370778859	9:37,735,615	A/G	—	uncertain significance
rs1432665838	9:37,735,646	C/T	—	uncertain significance
rs200633175	9:37,735,667	G/T	—	uncertain significance
rs61740795	9:37,735,680	G/A	synonymous variant	—
rs143999612	9:37,735,726	G/A	—	likely benign
rs2489322728	9:37,737,136	C/T	—	uncertain significance
rs755074216	9:37,737,138	T/A	—	uncertain significance
rs2489322798	9:37,737,160	G/T	—	uncertain significance
rs72724147	9:37,737,218	G/A	—	likely benign
rs1214579315	9:37,737,239	A/C	—	uncertain significance
rs372056992	9:37,740,128	G/A	—	uncertain significance
rs375221527	9:37,740,137	C/G	—	uncertain significance
rs748312449	9:37,740,152	C/T	—	uncertain significance
rs140481463	9:37,740,264	G/T	—	uncertain significance
rs368944021	9:37,740,287	G/A	—	uncertain significance
rs574623304	9:37,740,291	C/A	—	uncertain significance
rs2489331317	9:37,740,306	A/C	—	uncertain significance
rs748851489	9:37,740,339	C/T	—	uncertain significance
rs757376215	9:37,740,402	C/T	—	uncertain significance
rs764260619	9:37,740,470	G/A	—	likely benign
rs779949389	9:37,740,551	G/A	—	uncertain significance
rs766777202	9:37,740,595	C/A	—	uncertain significance
rs147985108	9:37,740,631	C/A	—	uncertain significance
rs768436248	9:37,740,635	G/A	—	likely benign
rs1824361058	9:37,740,698	A/C	—	uncertain significance
rs2489334498	9:37,740,723	C/T	—	uncertain significance
rs531669549	9:37,740,846	C/T	—	uncertain significance
rs144670594	9:37,740,876	C/T	—	likely benign
rs56124644	9:37,744,173	A/T	—	—
rs151326689	9:37,744,390	C/T	—	likely benign
rs2489346684	9:37,744,463	A/G	—	uncertain significance
rs34233395	9:37,744,565	G/T	—	likely benign
rs773313891	9:37,744,661	G/T	—	uncertain significance
rs201690567	9:37,744,665	C/T	—	uncertain significance
rs1192012449	9:37,744,734	T/C	—	uncertain significance
rs373579365	9:37,744,869	G/A	—	uncertain significance
rs746911046	9:37,744,871	A/G	—	uncertain significance
rs2489349540	9:37,744,878	C/A	—	uncertain significance
rs1824615189	9:37,744,898	G/A	—	uncertain significance
rs73447213	9:37,744,911	C/T	—	benign
rs1339955264	9:37,744,947	A/G	—	uncertain significance
rs1270261612	9:37,744,950	C/G	—	uncertain significance
rs1300301517	9:37,745,024	A/G	—	uncertain significance
rs377128806	9:37,745,025	T/C	—	likely benign
rs150600813	9:37,745,042	A/G	—	likely benign
rs2489351335	9:37,745,052	A/G	—	uncertain significance
rs1172892877	9:37,745,168	G/C	—	uncertain significance
rs2489352692	9:37,745,226	A/G	—	uncertain significance
rs35075933	9:37,745,304	G/A	—	benign
rs113193159	9:37,745,399	G/A	—	likely benign
rs2489353870	9:37,745,404	T/G	—	uncertain significance
rs2489354005	9:37,745,421	A/T	—	uncertain significance
rs62640013	9:37,745,437	C/T	—	benign
rs62640009	9:37,745,440	G/A	—	benign
rs781380445	9:37,745,501	G/A	—	likely benign
rs1824660278	9:37,745,525	C/T	—	uncertain significance
rs61170721	9:37,745,539	C/T	—	benign
rs200602863	9:37,745,550	C/T	—	uncertain significance
rs374057513	9:37,745,637	A/C	—	uncertain significance
rs57942614	9:37,745,678	G/A	—	benign
rs59640173	9:37,745,689	C/T	—	benign
rs143136317	9:37,745,735	G/A	—	uncertain significance
rs1271492709	9:37,745,751	C/T	—	uncertain significance
rs1424101219	9:37,745,801	G/A	—	likely benign
rs548307853	9:37,745,900	G/A	—	uncertain significance
rs748281395	9:37,745,962	G/C	—	uncertain significance
rs763498426	9:37,745,985	C/T	—	uncertain significance
rs2489359179	9:37,746,013	G/C	—	uncertain significance
rs1341563034	9:37,746,042	T/C	—	uncertain significance
rs113297576	9:37,746,062	C/T	—	uncertain significance
rs142476012	9:37,746,153	C/G	—	likely benign
rs1033297589	9:37,746,195	C/G	—	likely benign
rs761435424	9:37,746,210	C/T	—	uncertain significance

Showing 100 of 118 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.