DIPK1C

divergent protein kinase domain 1C

Summary

This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. [provided by RefSeq, Nov 2011]

Known Variants45 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs200137210	18:72,103,756	G/C	—	uncertain significance
rs771408240	18:72,103,777	G/T	—	uncertain significance
rs750315649	18:72,103,819	G/A	—	uncertain significance
rs17089289	18:72,103,863	G/A	—	uncertain significance
rs758060528	18:72,103,933	G/A	—	uncertain significance
rs1559806	18:72,108,787	G/C	—	—
rs546862605	18:72,109,199	G/C	—	uncertain significance
rs772398139	18:72,109,206	C/T	—	uncertain significance
rs1233656178	18:72,109,230	C/T	—	uncertain significance
rs769310738	18:72,109,300	T/G	—	uncertain significance
rs1986140174	18:72,109,305	C/T	—	uncertain significance
rs935757644	18:72,109,327	C/T	—	uncertain significance
rs769699780	18:72,109,335	A/T	—	uncertain significance
rs372349870	18:72,109,676	T/G	—	—
rs1325579096	18:72,113,872	G/C	—	uncertain significance
rs563652633	18:72,113,897	G/A	—	uncertain significance
rs201867846	18:72,113,929	A/G	—	uncertain significance
rs376456185	18:72,113,941	C/G	—	uncertain significance
rs988849992	18:72,113,945	G/C	—	uncertain significance
rs200975934	18:72,113,999	G/A	—	uncertain significance
rs552295990	18:72,114,019	C/T	—	uncertain significance
rs758668760	18:72,114,071	A/G	—	uncertain significance
rs536902218	18:72,114,092	C/A	—	uncertain significance
rs2511986526	18:72,114,107	C/G	—	uncertain significance
rs1350823925	18:72,114,172	C/A	—	uncertain significance
rs372816832	18:72,114,185	G/T	—	uncertain significance
rs941744661	18:72,114,191	G/A	—	uncertain significance
rs371788036	18:72,114,245	C/T	—	uncertain significance
rs1010219417	18:72,114,268	A/G	—	uncertain significance
rs1021560841	18:72,114,269	T/A	—	likely benign
rs968812752	18:72,114,280	T/C	—	uncertain significance
rs562166193	18:72,114,362	C/T	—	uncertain significance
rs745801581	18:72,114,409	A/T	—	uncertain significance
rs556922449	18:72,114,461	C/G	—	uncertain significance
rs753937715	18:72,114,496	G/A	—	uncertain significance
rs1046814461	18:72,114,514	T/C	—	likely benign
rs140690292	18:72,118,711	G/A	intron variant	—
rs189267431	18:72,121,429	A/G	intron variant	—
rs149694131	18:72,123,652	G/C	regulatory region variant	—
rs1339739577	18:72,124,341	C/G	—	uncertain significance
rs755765487	18:72,124,378	G/T	—	likely benign
rs1404333895	18:72,124,407	C/T	—	uncertain significance
rs772257154	18:72,124,412	A/C	—	uncertain significance
rs1463682958	18:72,124,466	G/C	—	likely benign
rs927415192	18:72,124,487	C/G	—	uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.