List of variants in gene FOXP3 reported as benign for hypersensitivity reaction disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 43

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HGVS	dbSNP	gnomAD frequency
NM_014009.4(FOXP3):c.543C>T (p.Ser181=)	rs2232367	0.03006
NM_014009.4(FOXP3):c.648-20G>A	rs2232368	0.01436
NM_014009.4(FOXP3):c.324G>A (p.Thr108=)	rs111856931	0.00245
NM_014009.4(FOXP3):c.648-13T>A	rs190739204	0.00201
NM_014009.4(FOXP3):c.210+16C>T	rs372471440	0.00165
NM_014009.4(FOXP3):c.176C>G (p.Ser59Cys)	rs199917616	0.00151
NM_014009.4(FOXP3):c.155G>T (p.Gly52Val)	rs17847095	0.00055
NM_014009.4(FOXP3):c.1044+17G>A	rs11465478	0.00026
NM_014009.4(FOXP3):c.340C>T (p.Arg114Trp)	rs200554980	0.00023
NM_014009.4(FOXP3):c.874G>A (p.Val292Ile)	rs74162067	0.00019
NM_014009.4(FOXP3):c.455-6C>T	rs373767482	0.00018
NM_014009.4(FOXP3):c.112G>T (p.Ala38Ser)	rs782239006	0.00014
NM_014009.4(FOXP3):c.249G>C (p.Gly83=)	rs782210800	0.00013
NM_014009.4(FOXP3):c.1278C>A (p.Asn426Lys)	rs369332983	0.00011
NM_014009.4(FOXP3):c.551C>T (p.Ser184Leu)	rs140222626	0.00011
NM_014009.4(FOXP3):c.624C>T (p.Phe208=)	rs148215677	0.00010
NM_014009.4(FOXP3):c.984G>A (p.Met328Ile)	rs367860281	0.00008
NM_014009.4(FOXP3):c.1221C>T (p.Thr407=)	rs373302430	0.00007
NM_014009.4(FOXP3):c.361C>T (p.His121Tyr)	rs782640594	0.00007
NM_014009.4(FOXP3):c.659C>T (p.Ala220Val)	rs2232369	0.00007
NM_014009.4(FOXP3):c.1147-13C>T	rs782632308	0.00006
NM_014009.4(FOXP3):c.1241G>A (p.Arg414His)	rs782786757	0.00006
NM_014009.4(FOXP3):c.1149C>T (p.Asn383=)	rs782267196	0.00005
NM_014009.4(FOXP3):c.873C>T (p.Val291=)	rs782371089	0.00005
NM_014009.4(FOXP3):c.1051C>T (p.Leu351=)	rs782127412	0.00003
NM_014009.4(FOXP3):c.495G>A (p.Pro165=)	rs781920028	0.00003
NM_014009.4(FOXP3):c.735+14G>A	rs782539969	0.00003
NM_014009.4(FOXP3):c.116G>A (p.Arg39Gln)	rs782639786	0.00002
NM_014009.4(FOXP3):c.352C>G (p.Leu118Val)	rs1373580534	0.00002
NM_014009.4(FOXP3):c.736-14G>A	rs76798919	0.00002
NM_014009.4(FOXP3):c.200C>T (p.Ser67Leu)	rs1382549860	0.00001
NM_014009.4(FOXP3):c.625G>A (p.Glu209Lys)	rs143048239	0.00001
NM_014009.4(FOXP3):c.959C>A (p.Thr320Lys)	rs781881326	0.00001
NM_014009.4(FOXP3):c.1045-11C>G	rs74162068
NM_014009.4(FOXP3):c.1147-12G>C
NM_014009.4(FOXP3):c.131C>G (p.Thr44Ser)
NM_014009.4(FOXP3):c.168CTC[1] (p.Ser60del)	rs781861708
NM_014009.4(FOXP3):c.316-3del	rs782086170
NM_014009.4(FOXP3):c.336C>T (p.His112=)	rs143632471
NM_014009.4(FOXP3):c.543-3dup
NM_014009.4(FOXP3):c.59C>T (p.Pro20Leu)	rs2066089076
NM_014009.4(FOXP3):c.826G>A (p.Asp276Asn)
NM_014009.4(FOXP3):c.968-13del

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