PLXNB3

plexin B3

Summary

The protein encoded by this gene is a member of the plexin family. It functions as a receptor for semaphorin 5A, and plays a role in axon guidance, invasive growth and cell migration. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

Known Variants171 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs7059259	X:153,029,784	G/A	regulatory region variant	—
rs148960424	X:153,030,991	A/G	—	likely benign
rs781805567	X:153,030,995	G/A	—	likely benign
rs141960270	X:153,031,029	C/G	—	likely benign
rs904791368	X:153,031,715	G/A	—	uncertain significance
rs781990072	X:153,031,763	G/A	—	uncertain significance
rs782221652	X:153,032,344	G/A	—	uncertain significance
rs35537879	X:153,032,365	G/A	—	benign
rs372269937	X:153,032,373	C/G	—	uncertain significance
rs1409696454	X:153,032,389	C/T	—	uncertain significance
rs2522360651	X:153,032,475	A/G	—	uncertain significance
rs781795736	X:153,032,490	G/A	—	uncertain significance
rs2148413029	X:153,032,502	C/T	—	uncertain significance
rs2522361184	X:153,032,545	T/G	—	uncertain significance
rs528422651	X:153,032,576	C/T	—	likely benign
rs148423464	X:153,032,587	G/A	—	likely benign
rs368428119	X:153,032,656	G/A	—	conflicting classifications of pathogenicity
rs1215118708	X:153,032,679	G/A	—	uncertain significance
rs111247447	X:153,032,699	G/A	—	benign
rs112274376	X:153,032,762	C/T	—	benign
rs1440146266	X:153,032,818	C/G	—	uncertain significance
rs369077780	X:153,032,860	C/T	—	uncertain significance
rs149161688	X:153,032,943	C/T	—	uncertain significance
rs1557059703	X:153,032,954	G/A	—	likely benign
rs782468149	X:153,032,989	G/C	—	likely benign
rs782463555	X:153,033,000	G/A	—	uncertain significance
rs35669018	X:153,033,002	C/T	—	benign
rs782250509	X:153,033,060	C/T	—	uncertain significance
rs781948973	X:153,033,068	C/T	—	likely benign
rs370095364	X:153,033,117	G/A	—	uncertain significance
rs1557059892	X:153,033,230	C/G	—	likely benign
rs1557059915	X:153,033,291	G/C	—	uncertain significance
rs782600752	X:153,033,298	G/A	—	uncertain significance
rs782055449	X:153,033,339	G/A	—	uncertain significance
rs1006325245	X:153,033,348	C/T	—	uncertain significance
rs1314259821	X:153,033,354	G/A	—	uncertain significance
rs2522367776	X:153,033,367	T/C	—	likely benign
rs367873902	X:153,033,712	C/T	—	likely benign
rs782595075	X:153,033,733	C/G	—	uncertain significance
rs147527982	X:153,033,796	C/T	—	likely benign
rs1466003030	X:153,033,843	T/C	—	likely benign
rs2522373097	X:153,033,878	T/C	—	likely benign
rs1036115653	X:153,034,649	G/T	—	uncertain significance
rs782809682	X:153,034,654	C/G	—	uncertain significance
rs201696853	X:153,034,687	C/T	—	uncertain significance
rs34012054	X:153,034,688	G/A	—	benign
rs782275965	X:153,035,270	G/A	—	uncertain significance
rs145651760	X:153,035,284	G/A	—	benign
rs34461520	X:153,035,364	G/A	—	benign
rs781836984	X:153,035,383	G/A	—	likely benign
rs782438501	X:153,035,550	A/T	—	uncertain significance
rs2522391858	X:153,035,601	T/G	—	uncertain significance
rs146501701	X:153,035,673	G/C	—	uncertain significance
rs782283893	X:153,035,694	C/G	—	uncertain significance
rs2266879	X:153,035,798	G/A	missense variant	—
rs200197753	X:153,035,807	C/T	—	uncertain significance
rs374123296	X:153,035,825	G/A	—	uncertain significance
rs539782168	X:153,035,876	G/A	—	likely benign
rs73640825	X:153,035,893	G/A	—	benign
rs781950083	X:153,035,897	G/A	—	uncertain significance
rs147082716	X:153,035,990	G/A	—	uncertain significance
rs782469938	X:153,036,012	G/A	—	uncertain significance
rs781926148	X:153,036,027	C/A	—	uncertain significance
rs782809651	X:153,036,029	C/G	—	uncertain significance
rs781832307	X:153,036,044	G/A	—	uncertain significance
rs1476606812	X:153,036,068	G/A	—	uncertain significance
rs782481792	X:153,036,075	G/C	—	uncertain significance
rs147973343	X:153,036,078	C/T	—	benign
rs145979763	X:153,036,089	G/A	—	likely benign
rs139853034	X:153,036,095	G/A	—	likely benign
rs199908902	X:153,036,222	C/G	—	uncertain significance
rs150768754	X:153,036,225	G/A	—	likely benign
rs149945750	X:153,036,287	G/A	—	uncertain significance
rs373965130	X:153,036,313	G/A	—	uncertain significance
rs368450576	X:153,036,337	G/A	—	likely benign
rs782243052	X:153,036,411	C/T	—	likely benign
rs140681169	X:153,036,439	A/G	—	likely benign
rs782198887	X:153,036,504	G/A	—	uncertain significance
rs1603245520	X:153,036,519	C/T	—	uncertain significance
rs781946256	X:153,036,768	T/C	—	likely benign
rs1333735113	X:153,036,806	C/G	—	uncertain significance
rs1557061795	X:153,036,818	G/C	—	likely benign
rs2522401524	X:153,036,840	A/G	—	uncertain significance
rs151079204	X:153,036,848	T/C	—	benign
rs1557061813	X:153,036,849	G/A	—	likely benign
rs782155380	X:153,036,958	G/A	—	conflicting classifications of pathogenicity
rs138935872	X:153,036,971	C/T	—	benign
rs142380642	X:153,036,972	G/A	—	likely benign
rs144601801	X:153,037,030	G/A	—	uncertain significance
rs2522402937	X:153,037,039	G/A	—	uncertain significance
rs370781491	X:153,037,064	C/T	—	uncertain significance
rs375202688	X:153,037,078	G/C	—	uncertain significance
rs782525744	X:153,037,100	G/A	—	uncertain significance
rs138618805	X:153,037,386	G/T	—	uncertain significance
rs781969853	X:153,038,367	T/C	—	likely benign
rs372413645	X:153,038,408	G/A	—	uncertain significance
rs372170244	X:153,038,703	G/A	—	benign
rs2091953489	X:153,038,705	A/C	—	uncertain significance
rs2522416748	X:153,038,706	G/C	—	uncertain significance
rs782400714	X:153,038,720	G/A	—	likely benign

Showing 100 of 171 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.