ClinVar Miner

List of variants in gene FOXG1 reported as uncertain significance for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NC_000014.8:g.(?_29236466)_(29237975_?)dup
NM_005249.5(FOXG1):c.115_117CAC[1] (p.His40del)
NM_005249.5(FOXG1):c.1397G>A (p.Gly466Glu) rs1566446008
NM_005249.5(FOXG1):c.141_143CCA[4] (p.His55_His57del) rs587783630
NM_005249.5(FOXG1):c.141_143CCA[5] (p.His56_His57del) rs587783630
NM_005249.5(FOXG1):c.149A>G (p.His50Arg)
NM_005249.5(FOXG1):c.158_172del (p.His53_His57del) rs1462202735
NM_005249.5(FOXG1):c.193C>T (p.Pro65Ser)
NM_005249.5(FOXG1):c.209_235del (p.Gln70_Pro78del) rs587783634
NM_005249.5(FOXG1):c.218A>C (p.Gln73Pro) rs760663911
NM_005249.5(FOXG1):c.219G>T (p.Gln73His)
NM_005249.5(FOXG1):c.251C>G (p.Pro84Arg) rs866815665
NM_005249.5(FOXG1):c.271C>A (p.Pro91Thr) rs1555321245
NM_005249.5(FOXG1):c.314_318delinsAGCCGCCGCCA (p.Pro105_Pro106insGlnPro) rs1594383202
NM_005249.5(FOXG1):c.394G>A (p.Gly132Ser)
NM_005249.5(FOXG1):c.430G>A (p.Glu144Lys) rs797045583
NM_005249.5(FOXG1):c.443G>A (p.Gly148Asp) rs781726187
NM_005249.5(FOXG1):c.456G>T (p.Gly152=) rs587783637
NM_005249.5(FOXG1):c.458G>T (p.Gly153Val) rs1555321286
NM_005249.5(FOXG1):c.460_462GAG[1] (p.Glu155del) rs1175471807
NM_005249.5(FOXG1):c.466_468AAG[1] (p.Lys157del) rs1424025007
NM_005249.5(FOXG1):c.471G>T (p.Lys157Asn)
NM_005249.5(FOXG1):c.554G>C (p.Ser185Thr) rs1057516138
NM_005249.5(FOXG1):c.565C>G (p.Leu189Val) rs1555321308
NM_005249.5(FOXG1):c.645C>G (p.Phe215Leu) rs1057518165
NM_005249.5(FOXG1):c.655C>G (p.Arg219Gly) rs1555321323
NM_005249.5(FOXG1):c.670G>A (p.Gly224Ser) rs727503935
NM_005249.5(FOXG1):c.672C>G (p.Gly224=) rs587783639
NM_005249.5(FOXG1):c.681C>G (p.Asn227Lys) rs786205012
NM_005249.5(FOXG1):c.797T>G (p.Ile266Ser)

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