PALM

paralemmin

Summary

This gene encodes a member of the paralemmin protein family. The product of this gene is a prenylated and palmitoylated phosphoprotein that associates with the cytoplasmic face of plasma membranes and is implicated in plasma membrane dynamics in neurons and other cell types. Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Jul 2008]

Known Variants201 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1246588804	19:709,160	G/A	—	likely benign
rs1017987900	19:709,163	C/G	—	likely benign
rs2512122885	19:709,166	T/A	—	likely benign
rs7247549	19:722,165	G/C	—	—
rs116863980	19:725,066	G/A	intron variant	—
rs1485256889	19:726,128	C/T	—	likely benign
rs369962423	19:726,133	C/T	—	likely benign
rs369812602	19:726,134	G/A	—	likely benign
rs372771354	19:726,146	C/T	—	conflicting classifications of pathogenicity
rs760993265	19:726,158	C/T	—	uncertain significance
rs377213814	19:726,159	G/A	—	likely benign
rs981610291	19:726,164	A/C	—	uncertain significance
rs370247624	19:726,199	C/T	—	likely benign
rs10408458	19:726,200	G/A	—	benign
rs201470230	19:726,202	C/T	—	benign
rs748674089	19:726,206	C/T	—	likely benign
rs772530131	19:726,207	C/T	—	likely benign
rs771247993	19:726,209	C/T	—	likely benign
rs1169108954	19:726,990	A/C	—	likely benign
rs1342223766	19:726,994	G/C	—	likely benign
rs1233749177	19:726,995	G/T	—	likely benign
rs1292766679	19:726,997	C/T	—	likely benign
rs1210670058	19:726,999	T/C	—	likely benign
rs1164178517	19:727,002	C/T	—	likely benign
rs566820585	19:727,020	C/T	—	uncertain significance
rs201995410	19:727,021	G/A	—	uncertain significance
rs200597947	19:727,027	C/T	—	uncertain significance
rs746107055	19:727,028	G/A	—	likely benign
rs200449881	19:727,031	G/A	—	likely benign
rs1036438626	19:727,034	C/T	—	likely benign
rs2032689585	19:727,035	G/C	—	uncertain significance
rs2512153823	19:727,039	A/C	—	uncertain significance
rs1001270877	19:727,045	G/A	—	uncertain significance
rs1034205750	19:727,047	C/T	—	uncertain significance
rs768648371	19:727,061	C/T	—	likely benign
rs2032691961	19:727,091	A/G	—	uncertain significance
rs761610939	19:727,092	C/T	—	uncertain significance
rs372993106	19:727,093	G/A	—	uncertain significance
rs750056429	19:727,096	C/T	—	likely benign
rs142161853	19:727,097	G/A	—	benign
rs1178460930	19:727,099	G/A	—	likely benign
rs113692988	19:727,105	G/A	—	benign
rs2144880814	19:727,108	C/T	—	likely benign
rs3746168	19:727,544	C/G	—	benign
rs3746169	19:727,550	T/C	—	benign
rs3746170	19:727,552	C/T	—	benign
rs866669931	19:727,577	G/A	—	uncertain significance
rs756317240	19:727,601	C/T	—	uncertain significance
rs150664829	19:727,605	G/A	—	benign
rs556522898	19:727,653	C/T	—	likely benign
rs762376900	19:727,654	G/A	—	uncertain significance
rs139932478	19:727,656	C/T	—	likely benign
rs750941783	19:727,669	C/T	—	uncertain significance
rs149265619	19:727,670	G/A	—	uncertain significance
rs941199731	19:727,681	G/T	—	uncertain significance
rs370151535	19:731,084	C/T	—	likely benign
rs765662362	19:731,098	G/A	—	likely benign
rs752808504	19:731,113	G/A	—	likely benign
rs751753740	19:731,123	C/T	—	uncertain significance
rs757247313	19:731,124	G/A	—	conflicting classifications of pathogenicity
rs144513487	19:731,135	G/A	—	uncertain significance
rs1050457	19:731,144	A/G	—	benign
rs374481450	19:731,158	C/T	—	likely benign
rs550477288	19:731,161	G/A	—	likely benign
rs528324611	19:731,163	C/T	—	uncertain significance
rs368636400	19:731,169	C/T	—	uncertain significance
rs200527631	19:731,170	G/A	—	benign
rs76698799	19:731,176	A/G	—	benign
rs139966536	19:731,180	C/T	—	likely benign
rs756128231	19:731,181	G/A	—	uncertain significance
rs2511972316	19:731,184	C/A	—	uncertain significance
rs568795902	19:731,193	C/T	—	uncertain significance
rs746327383	19:731,213	C/T	—	uncertain significance
rs775703604	19:731,214	G/C	—	uncertain significance
rs774675588	19:731,243	C/G	—	uncertain significance
rs1254493259	19:734,159	C/T	—	likely benign
rs377577439	19:734,174	C/T	—	uncertain significance
rs758029885	19:734,177	C/G	—	uncertain significance
rs763743478	19:734,178	G/T	—	likely benign
rs143530661	19:734,182	G/A	—	uncertain significance
rs2511977659	19:734,183	G/T	—	uncertain significance
rs907706996	19:734,186	C/T	—	uncertain significance
rs1220597480	19:734,203	T/C	—	likely benign
rs772340580	19:734,204	C/T	—	likely benign
rs200182434	19:734,214	C/G	—	benign
rs147995718	19:735,999	C/T	—	benign
rs375468860	19:736,000	G/A	—	likely benign
rs746118405	19:736,013	G/A	—	likely benign
rs141526024	19:736,022	A/T	—	uncertain significance
rs749219002	19:736,025	G/A	—	uncertain significance
rs774184824	19:736,032	C/T	—	likely benign
rs747841598	19:736,034	A/G	—	uncertain significance
rs772962279	19:736,037	C/T	—	uncertain significance
rs757576004	19:736,067	T/C	—	uncertain significance
rs767889561	19:736,073	A/G	—	uncertain significance
rs778249420	19:740,332	C/T	—	likely benign
rs754102497	19:740,335	C/T	—	likely benign
rs754960807	19:740,336	G/A	—	likely benign
rs752646507	19:740,344	C/T	—	likely benign
rs758455631	19:740,345	G/A	—	likely benign

Showing 100 of 201 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.