IFNA10

interferon alpha 10

Summary

This gene encodes a protein that belongs to the type I interferon family of proteins, and is located in a cluster of alpha interferon genes on chromosome 9. Interferons are small regulatory molecules that function in cell signaling in response to viruses and other pathogens or tumor cells. This gene is intronless and the encoded protein is secreted. [provided by RefSeq, Aug 2013]

Known Variants25 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs149261728	9:21,206,532	C/T	—	uncertain significance
rs748009686	9:21,206,546	C/A	—	uncertain significance
rs1275950936	9:21,206,553	G/T	—	uncertain significance
rs762249251	9:21,206,570	G/A	—	uncertain significance
rs553280752	9:21,206,574	G/A	—	likely benign
rs141756650	9:21,206,578	T/A	—	uncertain significance
rs28368148	9:21,206,605	C/G	missense variant	—
rs139697457	9:21,206,660	T/G	—	uncertain significance
rs559723085	9:21,206,687	T/A	—	uncertain significance
rs2537264408	9:21,206,694	T/A	—	uncertain significance
rs369916950	9:21,206,699	G/T	—	uncertain significance
rs542010952	9:21,206,712	C/T	—	uncertain significance
rs146907935	9:21,206,817	C/T	—	likely benign
rs148182302	9:21,206,844	G/A	—	likely risk allele
rs781635594	9:21,206,882	T/C	—	uncertain significance
rs1062570	9:21,206,892	T/G	—	uncertain significance
rs748350258	9:21,206,898	C/T	—	uncertain significance
rs545860454	9:21,206,945	G/C	—	uncertain significance
rs746398984	9:21,206,954	G/C	—	uncertain significance
rs1238121993	9:21,206,956	G/C	—	uncertain significance
rs763865345	9:21,206,964	C/G	—	likely benign
rs138686794	9:21,206,983	C/A	—	uncertain significance
rs10113875	9:21,207,000	C/G	—	benign
rs10113876	9:21,207,005	C/G	—	benign
rs2537265088	9:21,207,054	T/G	—	uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.