ClinVar Miner

List of variants in gene FOXN1 reported as likely pathogenic for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001369369.1(FOXN1):c.1010del (p.Gly337fs) rs2151497970
NM_001369369.1(FOXN1):c.1049C>T (p.Pro350Leu)
NM_001369369.1(FOXN1):c.1135+1_1135+2delinsAG rs1064795660
NM_001369369.1(FOXN1):c.1168del (p.Glu390fs)
NM_001369369.1(FOXN1):c.1275_1278del (p.Leu426fs)
NM_001369369.1(FOXN1):c.1296del (p.Ile433fs)
NM_001369369.1(FOXN1):c.1315del (p.Leu439fs) rs1064796227
NM_001369369.1(FOXN1):c.1364_1367del (p.Tyr455fs) rs2151499024
NM_001369369.1(FOXN1):c.1367T>A (p.Leu456Ter)
NM_001369369.1(FOXN1):c.1392_1401del (p.Pro465fs) rs1597567985
NM_001369369.1(FOXN1):c.1418del (p.Pro473fs) rs1597568117
NM_001369369.1(FOXN1):c.1465del (p.Gln489fs) rs1169577591
NM_001369369.1(FOXN1):c.1579_1580del (p.Gly526_Thr527insTer)
NM_001369369.1(FOXN1):c.1585del (p.Leu529fs) rs1161194345
NM_001369369.1(FOXN1):c.699+1G>T rs1555609768
NM_001369369.1(FOXN1):c.723C>A (p.Tyr241Ter) rs2151491863
NM_001369369.1(FOXN1):c.880G>C (p.Val294Leu) rs1406320425
NM_001369369.1(FOXN1):c.907del (p.Glu303fs) rs1064796115
NM_001369369.1(FOXN1):c.928-2A>G rs2151497815
NM_001369369.1(FOXN1):c.962A>G (p.His321Arg) rs1057524466
NM_001369369.1(FOXN1):c.974T>C (p.Leu325Pro) rs1597566470

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