ClinVar Miner

List of variants in gene FOXG1 reported as uncertain significance by GeneDx

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_005249.5(FOXG1):c.506G>C (p.Gly169Ala) rs796052480 0.00003
NM_005249.5(FOXG1):c.131A>C (p.His44Pro) rs1555321183 0.00001
NM_005249.5(FOXG1):c.355G>T (p.Ala119Ser) rs796052459 0.00001
NM_005249.5(FOXG1):c.103G>A (p.Ala35Thr) rs767463607
NM_005249.5(FOXG1):c.1214G>T (p.Cys405Phe) rs2138662115
NM_005249.5(FOXG1):c.134_148del (p.Pro45_His49del) rs1881776474
NM_005249.5(FOXG1):c.1375T>G (p.Ser459Ala) rs796052473
NM_005249.5(FOXG1):c.141CCA[10] (p.His55_His57dup) rs587783630
NM_005249.5(FOXG1):c.1441G>A (p.Gly481Arg)
NM_005249.5(FOXG1):c.1442G>A (p.Gly481Glu) rs2138662380
NM_005249.5(FOXG1):c.202C>T (p.Pro68Ser) rs796052479
NM_005249.5(FOXG1):c.219GCC[8] (p.Pro79_Pro80dup) rs786200975
NM_005249.5(FOXG1):c.315GCC[5] (p.Pro111_Pro112dup) rs1319234983
NM_005249.5(FOXG1):c.317C>T (p.Pro106Leu)
NM_005249.5(FOXG1):c.321GCCACC[3] (p.Pro111_Pro112dup) rs796052475
NM_005249.5(FOXG1):c.340G>A (p.Ala114Thr)
NM_005249.5(FOXG1):c.347T>G (p.Leu116Arg)
NM_005249.5(FOXG1):c.424C>T (p.Pro142Ser) rs2138660823
NM_005249.5(FOXG1):c.430G>A (p.Glu144Lys) rs797045583
NM_005249.5(FOXG1):c.455G>A (p.Gly152Glu) rs796052460
NM_005249.5(FOXG1):c.459G>A (p.Gly153=) rs1057520968
NM_005249.5(FOXG1):c.503G>T (p.Gly168Val) rs148157138
NM_005249.5(FOXG1):c.617G>T (p.Gly206Val)
NM_005249.5(FOXG1):c.836C>A (p.Thr279Asn)
NM_005249.5(FOXG1):c.844G>A (p.Ala282Thr) rs796052470
NM_005249.5(FOXG1):c.880T>C (p.Ser294Pro) rs796052471
NM_005249.5(FOXG1):c.953A>T (p.His318Leu) rs2138661790

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