WNK2

WNK lysine deficient protein kinase 2

Summary

The protein encoded by this gene is a cytoplasmic serine-threonine kinase that belongs to the protein kinase superfamily. The protein plays an important role in the regulation of electrolyte homeostasis, cell signaling survival, and proliferation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]

Known Variants147 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1298800136	9:95,947,251	C/G	—	uncertain significance
rs967634460	9:95,947,443	C/T	—	uncertain significance
rs756744238	9:95,947,471	A/G	—	uncertain significance
rs561768961	9:95,947,474	G/T	—	uncertain significance
rs960249386	9:95,947,560	G/A	—	uncertain significance
rs2538312423	9:95,947,591	A/C	—	uncertain significance
rs1349074328	9:95,947,618	C/T	—	uncertain significance
rs776345682	9:95,947,623	G/A	—	uncertain significance
rs759495885	9:95,947,662	G/C	—	uncertain significance
rs2538316244	9:95,947,698	C/T	—	uncertain significance
rs769132071	9:95,947,720	G/C	—	uncertain significance
rs1214485177	9:95,947,723	A/C	—	uncertain significance
rs368882633	9:95,947,742	G/C	—	uncertain significance
rs12349094	9:95,953,313	C/T	intron variant	—
rs968476403	9:95,992,003	G/A	—	uncertain significance
rs2539382855	9:95,993,187	A/G	—	uncertain significance
rs112615506	9:95,997,081	C/T	—	benign
rs757320091	9:96,002,146	G/A	—	uncertain significance
rs2539652347	9:96,002,248	C/T	—	uncertain significance
rs954257525	9:96,003,016	A/C	—	—
rs368033232	9:96,009,855	G/A	—	uncertain significance
rs267602319	9:96,009,863	C/T	—	likely benign
rs1009895513	9:96,009,892	C/G	—	uncertain significance
rs951353462	9:96,010,002	C/A	—	uncertain significance
rs2539846393	9:96,010,072	A/G	—	uncertain significance
rs2539971087	9:96,015,240	T/C	—	uncertain significance
rs376724876	9:96,015,243	G/A	—	uncertain significance
rs1051362149	9:96,015,252	C/A	—	uncertain significance
rs778381714	9:96,015,261	C/T	—	uncertain significance
rs561344476	9:96,015,293	C/G	—	uncertain significance
rs865994207	9:96,015,329	C/G	—	uncertain significance
rs1416742672	9:96,015,348	A/G	—	uncertain significance
rs2539975320	9:96,015,360	C/T	—	uncertain significance
rs2540045581	9:96,018,596	G/A	—	uncertain significance
rs201601244	9:96,018,606	C/T	—	uncertain significance
rs776341036	9:96,018,614	G/C	—	uncertain significance
rs375452200	9:96,018,624	C/T	—	uncertain significance
rs56062309	9:96,018,651	C/T	—	uncertain significance
rs756206792	9:96,018,658	G/C	—	uncertain significance
rs2540049258	9:96,018,708	C/T	—	uncertain significance
rs56137205	9:96,018,743	G/A	—	benign
rs1291909055	9:96,019,247	G/T	—	uncertain significance
rs777610809	9:96,019,290	C/G	—	uncertain significance
rs762929680	9:96,019,309	C/T	—	uncertain significance
rs41278262	9:96,019,311	C/A	—	likely benign
rs757872385	9:96,019,321	C/T	—	uncertain significance
rs1232053034	9:96,019,344	G/A	—	uncertain significance
rs760619944	9:96,019,376	G/T	—	uncertain significance
rs138191048	9:96,019,399	C/A	—	uncertain significance
rs746036582	9:96,021,264	G/A	—	likely benign
rs148781404	9:96,021,274	C/T	—	uncertain significance
rs542691515	9:96,021,303	G/C	—	uncertain significance
rs758491161	9:96,021,318	C/A	—	uncertain significance
rs755076404	9:96,021,388	C/T	—	uncertain significance
rs781211295	9:96,021,392	G/C	—	uncertain significance
rs45534637	9:96,021,423	C/T	—	likely benign
rs1414905895	9:96,021,432	C/T	—	uncertain significance
rs2540126043	9:96,021,454	C/T	—	uncertain significance
rs759690956	9:96,021,472	C/T	—	uncertain significance
rs746654332	9:96,021,510	G/A	—	uncertain significance
rs759885169	9:96,021,537	G/A	—	uncertain significance
rs112172724	9:96,021,553	G/C	—	benign
rs1588245686	9:96,021,666	C/T	—	uncertain significance
rs2540141705	9:96,021,754	C/T	—	uncertain significance
rs748423242	9:96,021,819	G/A	—	uncertain significance
rs368330463	9:96,021,820	C/T	—	uncertain significance
rs2540144929	9:96,021,826	C/T	—	uncertain significance
rs761567201	9:96,021,844	T/C	—	uncertain significance
rs754297681	9:96,024,153	G/A	—	uncertain significance
rs758413292	9:96,024,167	G/C	—	likely benign
rs2540202896	9:96,024,274	G/A	—	uncertain significance
rs151176657	9:96,024,318	C/T	—	uncertain significance
rs754565876	9:96,024,342	G/A	—	uncertain significance
rs367669560	9:96,024,954	G/T	—	uncertain significance
rs147603907	9:96,024,956	A/G	—	uncertain significance
rs149146046	9:96,025,903	G/A	—	likely benign
rs771940274	9:96,025,967	C/T	—	uncertain significance
rs142000432	9:96,026,254	A/G	—	uncertain significance
rs752561971	9:96,030,052	G/A	—	uncertain significance
rs61753900	9:96,030,088	G/A	—	uncertain significance
rs149250469	9:96,030,193	G/A	—	uncertain significance
rs756654439	9:96,030,324	A/G	—	uncertain significance
rs56072286	9:96,030,919	C/T	—	likely benign
rs55821719	9:96,030,961	C/T	—	likely benign
rs753326828	9:96,030,966	C/T	—	uncertain significance
rs549169030	9:96,030,978	A/C	—	uncertain significance
rs143326467	9:96,051,266	G/A	—	likely benign
rs1324530625	9:96,051,309	G/A	—	uncertain significance
rs750056272	9:96,051,313	T/C	—	likely benign
rs141554117	9:96,051,327	G/C	—	uncertain significance
rs373618412	9:96,051,331	C/T	—	uncertain significance
rs1848903785	9:96,051,355	A/T	—	uncertain significance
rs768532688	9:96,051,369	G/T	—	uncertain significance
rs762557499	9:96,051,384	G/A	—	uncertain significance
rs754198927	9:96,051,415	C/T	—	likely benign
rs1338197093	9:96,051,439	C/T	—	uncertain significance
rs547984904	9:96,051,469	C/G	—	uncertain significance
rs1381197850	9:96,051,474	C/T	—	uncertain significance
rs577622915	9:96,051,490	A/G	—	uncertain significance
rs777710522	9:96,051,526	C/T	—	uncertain significance

Showing 100 of 147 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.