List of variants in gene FOXP3 reported as likely benign for digestive system disorder

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: 103

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HGVS	dbSNP	gnomAD frequency
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.874G>A (p.Val292Ile)	rs74162067	0.00019
NM_014009.4(FOXP3):c.1278C>A (p.Asn426Lys)	rs369332983	0.00011
NM_014009.4(FOXP3):c.30G>A (p.Ser10=)	rs142994383	0.00010
NM_014009.4(FOXP3):c.647+19T>G	rs371187277	0.00008
NM_014009.4(FOXP3):c.1241G>A (p.Arg414His)	rs782786757	0.00006
NM_014009.4(FOXP3):c.825C>T (p.Ser275=)	rs1405637345	0.00006
NM_014009.4(FOXP3):c.1240C>T (p.Arg414Cys)	rs781854593	0.00005
NM_014009.4(FOXP3):c.1295G>A (p.Ter432=)	rs782112916	0.00004
NM_014009.4(FOXP3):c.323C>T (p.Thr108Met)	rs782572328	0.00004
NM_014009.4(FOXP3):c.331G>A (p.Ala111Thr)	rs1424687079	0.00004
NM_014009.4(FOXP3):c.670C>G (p.Leu224Val)	rs373242883	0.00004
NM_014009.4(FOXP3):c.895C>T (p.Arg299Trp)	rs200928046	0.00004
NM_014009.4(FOXP3):c.1051C>T (p.Leu351=)	rs782127412	0.00003
NM_014009.4(FOXP3):c.246C>T (p.Ser82=)	rs368483472	0.00003
NM_014009.4(FOXP3):c.495G>A (p.Pro165=)	rs781920028	0.00003
NM_014009.4(FOXP3):c.634G>C (p.Glu212Gln)	rs140794570	0.00003
NM_014009.4(FOXP3):c.105G>A (p.Leu35=)	rs782359163	0.00002
NM_014009.4(FOXP3):c.1116C>A (p.Ala372=)	rs1303706775	0.00002
NM_014009.4(FOXP3):c.1146+17T>C	rs782486668	0.00002
NM_014009.4(FOXP3):c.1200C>T (p.Ser400=)	rs201723322	0.00002
NM_014009.4(FOXP3):c.201G>A (p.Ser67=)	rs1296610779	0.00002
NM_014009.4(FOXP3):c.525T>C (p.Ser175=)	rs1441216420	0.00002
NM_014009.4(FOXP3):c.611G>A (p.Cys204Tyr)	rs368066149	0.00002
NM_014009.4(FOXP3):c.69G>A (p.Ser23=)	rs376670807	0.00002
NM_014009.4(FOXP3):c.736-14G>A	rs76798919	0.00002
NM_014009.4(FOXP3):c.896G>A (p.Arg299Gln)	rs782188307	0.00002
NM_014009.4(FOXP3):c.1032G>A (p.Thr344=)	rs781905807	0.00001
NM_014009.4(FOXP3):c.1045-13C>T	rs781966644	0.00001
NM_014009.4(FOXP3):c.119G>A (p.Gly40Asp)	rs781805416	0.00001
NM_014009.4(FOXP3):c.124G>A (p.Gly42Arg)	rs782178764	0.00001
NM_014009.4(FOXP3):c.211-20C>A	rs781982592	0.00001
NM_014009.4(FOXP3):c.315+8C>T	rs782558220	0.00001
NM_014009.4(FOXP3):c.552G>A (p.Ser184=)	rs782085584	0.00001
NM_014009.4(FOXP3):c.631C>G (p.Pro211Ala)	rs374109896	0.00001
NM_014009.4(FOXP3):c.647+16C>T	rs2066075855	0.00001
NM_014009.4(FOXP3):c.648-15C>T	rs1183403474	0.00001
NM_014009.4(FOXP3):c.711G>A (p.Glu237=)	rs1557116204	0.00001
NM_014009.4(FOXP3):c.805G>A (p.Ala269Thr)	rs781999579	0.00001
NM_014009.4(FOXP3):c.817-9C>T	rs1166432395	0.00001
NM_014009.4(FOXP3):c.1026C>T (p.Tyr342=)
NM_014009.4(FOXP3):c.1044+16C>T
NM_014009.4(FOXP3):c.1045-11C>G	rs74162068
NM_014009.4(FOXP3):c.1045-11C>T	rs74162068
NM_014009.4(FOXP3):c.1045-14C>T
NM_014009.4(FOXP3):c.1045-15C>A
NM_014009.4(FOXP3):c.1045-15_1045-9del	rs1428795908
NM_014009.4(FOXP3):c.1045-17C>T	rs2147944472
NM_014009.4(FOXP3):c.1045-6T>C
NM_014009.4(FOXP3):c.1080C>G (p.Leu360=)	rs2147944398
NM_014009.4(FOXP3):c.1119C>T (p.Phe373=)
NM_014009.4(FOXP3):c.1146+16G>C
NM_014009.4(FOXP3):c.1146+8C>T
NM_014009.4(FOXP3):c.1191G>T (p.Arg397=)
NM_014009.4(FOXP3):c.1227T>C (p.Asp409=)
NM_014009.4(FOXP3):c.1248A>T (p.Lys416Asn)	rs2066029945
NM_014009.4(FOXP3):c.1277A>G (p.Asn426Ser)
NM_014009.4(FOXP3):c.1285C>T (p.Pro429Ser)
NM_014009.4(FOXP3):c.129A>G (p.Gly43=)	rs1602687640
NM_014009.4(FOXP3):c.162C>T (p.Ala54=)
NM_014009.4(FOXP3):c.174T>C (p.Ser58=)
NM_014009.4(FOXP3):c.195A>T (p.Pro65=)
NM_014009.4(FOXP3):c.205C>G (p.Leu69Val)
NM_014009.4(FOXP3):c.211-17C>A	rs2147949241
NM_014009.4(FOXP3):c.226C>G (p.Leu76Val)
NM_014009.4(FOXP3):c.288C>A (p.Leu96=)	rs942280481
NM_014009.4(FOXP3):c.315+9G>A
NM_014009.4(FOXP3):c.316-13A>G	rs2066082389
NM_014009.4(FOXP3):c.316-4C>T	rs977920377
NM_014009.4(FOXP3):c.318C>T (p.Leu106=)
NM_014009.4(FOXP3):c.336C>T (p.His112=)	rs143632471
NM_014009.4(FOXP3):c.372G>A (p.Glu124=)
NM_014009.4(FOXP3):c.408C>T (p.Thr136=)	rs782613398
NM_014009.4(FOXP3):c.420C>G (p.Val140=)
NM_014009.4(FOXP3):c.444C>T (p.Gly148=)
NM_014009.4(FOXP3):c.455-14G>A	rs914653327
NM_014009.4(FOXP3):c.455-19G>A
NM_014009.4(FOXP3):c.486C>T (p.Ser162=)	rs1557116474
NM_014009.4(FOXP3):c.492G>A (p.Glu164=)	rs2147948631
NM_014009.4(FOXP3):c.542+8G>A
NM_014009.4(FOXP3):c.543-16C>T
NM_014009.4(FOXP3):c.543-4C>T	rs782430715
NM_014009.4(FOXP3):c.543-5C>T
NM_014009.4(FOXP3):c.552G>T (p.Ser184=)	rs782085584
NM_014009.4(FOXP3):c.606C>T (p.Pro202=)
NM_014009.4(FOXP3):c.647+11del	rs2066075881
NM_014009.4(FOXP3):c.660G>A (p.Ala220=)
NM_014009.4(FOXP3):c.702C>T (p.Leu234=)	rs2066065548
NM_014009.4(FOXP3):c.735+13C>T
NM_014009.4(FOXP3):c.735+17G>A
NM_014009.4(FOXP3):c.748_750del (p.Lys250del)	rs1557116163
NM_014009.4(FOXP3):c.762T>C (p.Ser254=)
NM_014009.4(FOXP3):c.786G>A (p.Gly262=)
NM_014009.4(FOXP3):c.817-10C>G
NM_014009.4(FOXP3):c.817-11C>T
NM_014009.4(FOXP3):c.817-5C>T	rs1602682433
NM_014009.4(FOXP3):c.84T>C (p.Ala28=)
NM_014009.4(FOXP3):c.912C>T (p.Ser304=)	rs2147946006
NM_014009.4(FOXP3):c.954C>T (p.Asn318=)
NM_014009.4(FOXP3):c.968-12A>G
NM_014009.4(FOXP3):c.968-17T>A
NM_014009.4(FOXP3):c.981C>T (p.Asn327=)

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