PLXNB2

plexin B2

Summary

Members of the B class of plexins, such as PLXNB2 are transmembrane receptors that participate in axon guidance and cell migration in response to semaphorins (Perrot et al. (2002) [PubMed 12183458]).[supplied by OMIM, Mar 2008]

Known Variants166 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2519355233	22:50,714,152	T/G	—	uncertain significance
rs149124212	22:50,714,320	C/T	—	likely benign
rs180698014	22:50,714,389	G/A	—	uncertain significance
rs1309378692	22:50,714,391	G/A	—	uncertain significance
rs775068552	22:50,715,125	T/C	—	uncertain significance
rs201182504	22:50,716,039	G/A	—	uncertain significance
rs376134467	22:50,716,162	G/A	—	uncertain significance
rs2519416408	22:50,716,373	C/A	—	uncertain significance
rs187332808	22:50,716,375	G/A	—	uncertain significance
rs781634312	22:50,716,385	C/T	—	uncertain significance
rs2519422260	22:50,716,586	G/A	—	uncertain significance
rs2519435651	22:50,717,063	C/T	—	pathogenic
rs751388537	22:50,717,069	G/A	—	uncertain significance
rs199650688	22:50,717,092	G/A	—	uncertain significance
rs28718510	22:50,717,129	T/G	—	benign
rs371319008	22:50,717,293	C/T	—	uncertain significance
rs200623878	22:50,717,397	G/A	—	uncertain significance
rs774626695	22:50,717,428	T/C	—	uncertain significance
rs758488420	22:50,718,067	C/A	—	uncertain significance
rs2519464021	22:50,718,069	T/C	—	uncertain significance
rs764463882	22:50,718,120	T/G	—	uncertain significance
rs370462169	22:50,718,121	T/C	—	uncertain significance
rs755621229	22:50,718,952	C/T	—	uncertain significance
rs776823804	22:50,718,981	G/A	—	uncertain significance
rs776753345	22:50,719,041	G/A	—	uncertain significance
rs28540713	22:50,719,165	T/C	—	benign
rs200739841	22:50,719,174	T/C	—	uncertain significance
rs767904616	22:50,719,179	G/A	—	likely benign
rs200080652	22:50,719,238	G/T	—	uncertain significance
rs746941566	22:50,719,243	C/T	—	uncertain significance
rs201378041	22:50,719,246	G/A	—	uncertain significance
rs11547734	22:50,719,251	G/A	—	benign
rs2519503653	22:50,719,285	T/C	—	uncertain significance
rs757601022	22:50,719,292	C/T	—	uncertain significance
rs1212849563	22:50,719,316	C/T	—	uncertain significance
rs201960199	22:50,719,319	G/A	—	uncertain significance
rs748920566	22:50,719,339	T/C	—	uncertain significance
rs751262783	22:50,719,563	C/T	—	uncertain significance
rs778176942	22:50,719,613	T/C	—	uncertain significance
rs760225048	22:50,719,808	C/T	—	uncertain significance
rs754343905	22:50,719,810	G/A	—	uncertain significance
rs370284603	22:50,719,811	C/T	—	uncertain significance
rs768769541	22:50,719,833	G/A	—	likely benign
rs80199648	22:50,719,860	C/T	—	benign
rs201645775	22:50,719,920	G/A	—	likely benign
rs376149647	22:50,720,047	G/A	—	uncertain significance
rs1250714562	22:50,720,095	G/A	—	uncertain significance
rs751429886	22:50,720,114	C/T	—	uncertain significance
rs1266389693	22:50,720,285	G/A	—	uncertain significance
rs116468936	22:50,720,295	G/A	—	benign
rs2519539084	22:50,720,297	G/T	—	uncertain significance
rs1292876817	22:50,720,492	C/T	—	uncertain significance
rs201928186	22:50,720,591	C/G	intron variant	—
rs1234372437	22:50,720,613	C/T	—	pathogenic
rs372167877	22:50,720,614	G/A	—	uncertain significance
rs374289741	22:50,720,671	G/A	—	uncertain significance
rs746803740	22:50,720,719	G/A	—	uncertain significance
rs754762851	22:50,721,162	C/T	—	uncertain significance
rs957289874	22:50,721,167	G/A	—	uncertain significance
rs201068347	22:50,721,170	C/T	—	uncertain significance
rs200118373	22:50,721,177	C/T	—	uncertain significance
rs201704027	22:50,721,207	C/T	—	likely benign
rs200474256	22:50,721,250	C/T	—	uncertain significance
rs62621407	22:50,721,252	T/A	—	likely benign
rs749888275	22:50,721,287	T/C	—	uncertain significance
rs149805063	22:50,721,296	G/A	—	benign
rs777954936	22:50,721,488	G/A	—	uncertain significance
rs2066136321	22:50,721,504	T/C	—	uncertain significance
rs753303246	22:50,721,567	C/T	—	uncertain significance
rs754227017	22:50,721,572	G/A	—	uncertain significance
rs745882011	22:50,721,578	G/A	—	uncertain significance
rs200791148	22:50,721,785	T/C	—	uncertain significance
rs200111358	22:50,721,798	G/A	—	uncertain significance
rs763230043	22:50,721,830	C/A	—	uncertain significance
rs190910795	22:50,721,835	C/G	—	likely benign
rs1407238581	22:50,722,050	G/A	—	uncertain significance
rs200079670	22:50,722,077	C/T	—	uncertain significance
rs376030784	22:50,722,091	C/T	—	uncertain significance
rs770795215	22:50,722,103	C/T	—	likely benign
rs780232837	22:50,722,140	T/G	—	uncertain significance
rs376548374	22:50,722,143	G/A	—	uncertain significance
rs1212157084	22:50,722,270	T/A	—	pathogenic
rs370412897	22:50,722,273	C/T	—	uncertain significance
rs77569471	22:50,722,277	C/T	—	benign
rs375572338	22:50,722,278	G/A	—	uncertain significance
rs769514548	22:50,722,318	C/T	—	uncertain significance
rs551456267	22:50,722,336	C/T	—	uncertain significance
rs374234427	22:50,722,357	C/T	—	uncertain significance
rs1332617247	22:50,722,576	C/T	—	pathogenic
rs532944576	22:50,722,588	C/T	—	uncertain significance
rs370061884	22:50,722,600	C/T	—	uncertain significance
rs200165560	22:50,722,620	G/A	—	uncertain significance
rs200806827	22:50,722,646	G/A	—	likely benign
rs762799219	22:50,723,012	C/T	—	uncertain significance
rs201521733	22:50,723,013	G/A	—	uncertain significance
rs553785965	22:50,723,058	A/G	—	uncertain significance
rs200637738	22:50,723,068	G/C	—	uncertain significance
rs200360490	22:50,723,094	C/A	—	uncertain significance
rs769364893	22:50,724,273	C/T	—	uncertain significance
rs1010102713	22:50,724,308	A/C	—	uncertain significance

Showing 100 of 166 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.