List of variants in gene FOXN1 reported as pathogenic for immune 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: 47

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HGVS	dbSNP	gnomAD frequency
NM_001369369.1(FOXN1):c.763C>T (p.Arg255Ter)	rs104894562	0.00001
NM_001369369.1(FOXN1):c.958C>T (p.Arg320Trp)	rs1288977950	0.00001
NC_000017.10:g.(?_26861752)_(26869835_?)del
NM_001369369.1(FOXN1):c.1010del (p.Gly337fs)	rs2151497970
NM_001369369.1(FOXN1):c.1021del (p.Arg341fs)
NM_001369369.1(FOXN1):c.1064del (p.Lys355fs)
NM_001369369.1(FOXN1):c.1086dup (p.Trp363fs)	rs1597566699
NM_001369369.1(FOXN1):c.1089_1103del (p.Trp363_Pro368delinsCys)	rs1597566726
NM_001369369.1(FOXN1):c.1151del (p.Leu384fs)
NM_001369369.1(FOXN1):c.118C>T (p.Gln40Ter)
NM_001369369.1(FOXN1):c.1201_1216del (p.Pro401fs)	rs1064793129
NM_001369369.1(FOXN1):c.1205del (p.Pro402fs)	rs2070011218
NM_001369369.1(FOXN1):c.1216_1247dup (p.Gly418fs)
NM_001369369.1(FOXN1):c.1220C>G (p.Ser407Ter)
NM_001369369.1(FOXN1):c.1283del (p.Pro428fs)	rs1597567692
NM_001369369.1(FOXN1):c.1314_1315dup (p.Leu439fs)
NM_001369369.1(FOXN1):c.1315del (p.Leu439fs)	rs1064796227
NM_001369369.1(FOXN1):c.1316del (p.Leu439fs)	rs2151498933
NM_001369369.1(FOXN1):c.1324_1336del (p.Leu442fs)
NM_001369369.1(FOXN1):c.1327del (p.Met444fs)	rs2151498964
NM_001369369.1(FOXN1):c.1364_1367del (p.Tyr455fs)	rs2151499024
NM_001369369.1(FOXN1):c.1366_1369dup (p.His457fs)	rs2070018439
NM_001369369.1(FOXN1):c.1367T>A (p.Leu456Ter)
NM_001369369.1(FOXN1):c.1370del (p.His457fs)	rs2151499042
NM_001369369.1(FOXN1):c.1376C>A (p.Ser459Ter)	rs745708044
NM_001369369.1(FOXN1):c.1392_1401del (p.Pro465fs)	rs1597567985
NM_001369369.1(FOXN1):c.1420C>T (p.Gln474Ter)	rs1438890364
NM_001369369.1(FOXN1):c.1431del (p.His478fs)
NM_001369369.1(FOXN1):c.1445_1449delinsCCA (p.Arg482fs)	rs1567887558
NM_001369369.1(FOXN1):c.1459_1460del (p.Thr487fs)	rs2151499311
NM_001369369.1(FOXN1):c.1465del (p.Gln489fs)	rs1169577591
NM_001369369.1(FOXN1):c.189del (p.Pro65fs)	rs2069719445
NM_001369369.1(FOXN1):c.246C>A (p.Cys82Ter)
NM_001369369.1(FOXN1):c.340C>T (p.Arg114Ter)
NM_001369369.1(FOXN1):c.455del (p.Pro152fs)	rs2151487481
NM_001369369.1(FOXN1):c.490del (p.Asp164fs)	rs2069729948
NM_001369369.1(FOXN1):c.562del (p.Ser188fs)	rs1597552140
NM_001369369.1(FOXN1):c.62del (p.Gly21fs)
NM_001369369.1(FOXN1):c.64G>T (p.Glu22Ter)	rs545707585
NM_001369369.1(FOXN1):c.690dup (p.Phe231fs)	rs2151490072
NM_001369369.1(FOXN1):c.6del (p.Ser3fs)
NM_001369369.1(FOXN1):c.723C>G (p.Tyr241Ter)	rs2151491863
NM_001369369.1(FOXN1):c.728_729dup (p.Pro244fs)	rs1597558200
NM_001369369.1(FOXN1):c.823del (p.Ser275fs)	rs2151492087
NM_001369369.1(FOXN1):c.880G>A (p.Val294Ile)
NM_001369369.1(FOXN1):c.933_936dup (p.Asp313fs)	rs1597566356
NM_001369369.1(FOXN1):c.98_114del (p.Leu33fs)

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