ClinVar Miner

List of variants in gene FOXG1 reported as benign by GeneDx

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Gene type:
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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_005249.5(FOXG1):c.*13C>A rs151157846 0.01290
NM_005249.5(FOXG1):c.1233G>A (p.Ala411=) rs34654108 0.00801
NM_005249.5(FOXG1):c.447C>T (p.Ala149=) rs112803404 0.00126
NM_005249.5(FOXG1):c.489C>T (p.Gly163=) rs375378714 0.00062
NM_005249.5(FOXG1):c.503G>C (p.Gly168Ala) rs148157138 0.00048
NM_005249.5(FOXG1):c.201G>T (p.Pro67=) rs587780944 0.00029
NM_005249.5(FOXG1):c.1323C>T (p.Ser441=) rs144434028 0.00023
NM_005249.5(FOXG1):c.456G>T (p.Gly152=) rs587783637 0.00020
NM_005249.5(FOXG1):c.*4C>T rs774917687 0.00012
NM_005249.5(FOXG1):c.1161G>A (p.Ser387=) rs147154860 0.00012
NM_005249.5(FOXG1):c.594C>G (p.Pro198=) rs141088742 0.00010
NM_005249.5(FOXG1):c.1158C>G (p.Ala386=) rs143223844 0.00007
NM_005249.5(FOXG1):c.1399C>T (p.Leu467=) rs371279404 0.00006
NM_005249.5(FOXG1):c.162T>C (p.His54=) rs796052448 0.00004
NM_005249.5(FOXG1):c.165C>T (p.His55=) rs796052449 0.00004
NM_005249.5(FOXG1):c.1218C>G (p.Ser406=) rs587783628 0.00003
NM_005249.5(FOXG1):c.189G>T (p.Pro63=) rs796052451 0.00002
NM_005249.5(FOXG1):c.*100del rs68024132
NM_005249.5(FOXG1):c.-338_-337insA rs59954935
NM_005249.5(FOXG1):c.1032G>C (p.Val344=) rs765799544
NM_005249.5(FOXG1):c.105G>T (p.Ala35=) rs753859771
NM_005249.5(FOXG1):c.1086G>A (p.Leu362=) rs570981209
NM_005249.5(FOXG1):c.194CGC[6] (p.Pro69dup) rs761703699
NM_005249.5(FOXG1):c.209_232del (p.Gln70_Pro77del) rs794726920
NM_005249.5(FOXG1):c.219GCC[7] (p.Pro80dup) rs786200975
NM_005249.5(FOXG1):c.672C>G (p.Gly224=) rs587783639

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