NBEAL1

neurobeachin like 1

Summary

Predicted to enable protein kinase binding activity. Predicted to be involved in protein localization. Predicted to be active in cytosol and membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants158 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2351524	2:203,880,992	T/A	—	—
rs72932590	2:203,884,308	A/G	—	—
rs145538381	2:203,892,767	T/C	intron variant	—
rs375380888	2:203,899,079	A/G	—	—
rs181256816	2:203,904,305	T/C	regulatory region variant	—
rs185726277	2:203,904,306	G/A	regulatory region variant	—
rs1365576985	2:203,906,493	T/A	—	uncertain significance
rs1026720148	2:203,906,566	A/G	—	uncertain significance
rs2469477467	2:203,914,540	A/G	—	likely benign
rs754292716	2:203,914,550	C/T	—	uncertain significance
rs1159354664	2:203,914,613	T/A	—	uncertain significance
rs1339041271	2:203,914,628	G/T	—	uncertain significance
rs1368439283	2:203,914,656	C/T	—	uncertain significance
rs72934505	2:203,916,487	T/G	downstream gene variant	—
rs770286164	2:203,921,208	A/G	—	uncertain significance
rs146121994	2:203,922,075	A/G	—	likely benign
rs1469180645	2:203,922,163	C/T	—	uncertain significance
rs540055954	2:203,922,169	A/G	—	uncertain significance
rs530440261	2:203,933,118	G/A	—	uncertain significance
rs2061629800	2:203,933,191	C/G	—	uncertain significance
rs1407399646	2:203,942,507	A/G	—	uncertain significance
rs902384156	2:203,942,509	T/G	—	uncertain significance
rs2469617783	2:203,942,527	G/C	—	uncertain significance
rs1402685293	2:203,948,012	C/G	—	uncertain significance
rs563857369	2:203,948,020	G/A	—	uncertain significance
rs531118073	2:203,948,039	T/A	—	uncertain significance
rs1462174099	2:203,948,150	A/G	—	uncertain significance
rs1414098266	2:203,948,174	A/G	—	uncertain significance
rs59879855	2:203,955,273	T/C	intron variant	—
rs17473735	2:203,962,146	T/C	intron variant	—
rs7574314	2:203,964,137	T/C	intron variant	—
rs771630829	2:203,964,365	A/C	—	uncertain significance
rs2062462175	2:203,972,153	A/C	—	uncertain significance
rs2062466645	2:203,972,388	C/T	—	uncertain significance
rs745776175	2:203,972,424	T/G	—	uncertain significance
rs1421575812	2:203,972,493	A/G	—	uncertain significance
rs557628000	2:203,972,506	A/G	—	uncertain significance
rs148705424	2:203,972,519	G/A	—	benign
rs201228567	2:203,972,520	A/G	—	uncertain significance
rs2469783102	2:203,972,794	C/T	—	uncertain significance
rs2469783210	2:203,972,803	A/G	—	uncertain significance
rs1051082194	2:203,974,910	A/G	—	uncertain significance
rs748442036	2:203,974,934	G/A	—	uncertain significance
rs535516873	2:203,974,982	C/T	—	uncertain significance
rs760010055	2:203,974,985	A/G	—	uncertain significance
rs1265390907	2:203,976,705	A/G	—	uncertain significance
rs2469807462	2:203,976,725	G/T	—	uncertain significance
rs374880765	2:203,977,788	T/C	—	benign
rs2469814679	2:203,977,853	G/T	—	uncertain significance
rs377696347	2:203,977,910	C/T	—	uncertain significance
rs1436222888	2:203,977,979	G/A	—	uncertain significance
rs371316448	2:203,980,733	G/T	—	uncertain significance
rs374077480	2:203,980,738	A/G	—	uncertain significance
rs1056257155	2:203,980,740	G/C	—	uncertain significance
rs2086833	2:203,980,768	A/C	—	likely benign
rs757481460	2:203,980,775	T/G	—	likely benign
rs774601546	2:203,987,011	C/T	—	uncertain significance
rs1434156794	2:203,990,088	G/A	—	uncertain significance
rs2062917406	2:203,990,196	C/T	—	uncertain significance
rs778251406	2:203,990,718	A/G	—	uncertain significance
rs72934556	2:203,990,789	T/G	synonymous variant	—
rs1246280417	2:203,991,434	G/A	—	uncertain significance
rs2062949632	2:203,991,586	G/T	—	uncertain significance
rs1332159113	2:203,992,596	G/A	—	uncertain significance
rs2469897841	2:203,992,611	A/T	—	uncertain significance
rs983141405	2:203,992,634	A/C	—	uncertain significance
rs189753012	2:203,995,078	G/A	—	benign
rs781054666	2:203,995,126	G/T	—	uncertain significance
rs150511473	2:203,996,734	G/A	—	benign
rs1351630755	2:203,997,855	G/A	—	uncertain significance
rs573346429	2:203,997,858	A/G	—	likely benign
rs17408550	2:203,998,336	C/G	intron variant	—
rs1004558650	2:204,000,404	T/C	—	uncertain significance
rs771367200	2:204,000,407	A/G	—	uncertain significance
rs1016302692	2:204,000,425	C/G	—	uncertain significance
rs375751670	2:204,000,507	C/T	—	likely benign
rs1220127123	2:204,000,509	G/T	—	uncertain significance
rs138630576	2:204,000,571	A/G	—	likely benign
rs761396593	2:204,000,584	A/G	—	uncertain significance
rs565777332	2:204,000,713	A/G	—	uncertain significance
rs1314056599	2:204,000,732	G/T	—	uncertain significance
rs762790955	2:204,000,752	A/G	—	uncertain significance
rs372157805	2:204,000,763	T/G	—	uncertain significance
rs1438575606	2:204,000,935	T/C	—	likely benign
rs201308096	2:204,001,377	G/A	—	uncertain significance
rs1470450791	2:204,001,432	T/A	—	uncertain significance
rs556923204	2:204,003,033	G/A	—	uncertain significance
rs72934573	2:204,005,072	A/G	intron variant	—
rs72934583	2:204,009,057	T/G	intron variant	—
rs201260776	2:204,009,393	C/T	—	uncertain significance
rs751716136	2:204,009,423	T/A	—	uncertain significance
rs116563932	2:204,009,459	A/T	—	benign
rs201301987	2:204,009,470	A/G	—	uncertain significance
rs1273369237	2:204,009,527	C/T	—	uncertain significance
rs372750746	2:204,009,537	C/T	—	uncertain significance
rs2063468338	2:204,009,557	A/G	—	uncertain significance
rs754385841	2:204,009,594	A/G	—	likely benign
rs199533293	2:204,009,779	G/A	—	uncertain significance
rs758169950	2:204,009,786	A/G	—	uncertain significance
rs2063479460	2:204,009,879	T/A	—	uncertain significance

Showing 100 of 158 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.