ClinVar Miner

List of variants in gene FOXG1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
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.206C>A (p.Pro69Gln) rs727503933 0.00057
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.181C>T (p.Pro61Ser) rs762634382 0.00021
NM_005249.5(FOXG1):c.852G>A (p.Leu284=) rs537686463 0.00016
NM_005249.5(FOXG1):c.165C>T (p.His55=) rs796052449 0.00004
NM_005249.5(FOXG1):c.1311G>A (p.Arg437=) rs776918484 0.00003
NM_005249.5(FOXG1):c.1384A>G (p.Ser462Gly) rs752379833 0.00001
NM_005249.5(FOXG1):c.159C>T (p.His53=) rs769410384 0.00001
NM_005249.5(FOXG1):c.240G>A (p.Pro80=) rs1057521165 0.00001
NM_005249.5(FOXG1):c.1320C>G (p.Ser440=) rs1057524328
NM_005249.5(FOXG1):c.135C>T (p.Pro45=)
NM_005249.5(FOXG1):c.141CCA[5] (p.His56_His57del) rs587783630
NM_005249.5(FOXG1):c.209AGC[5] (p.Gln73dup) rs398124201
NM_005249.5(FOXG1):c.233_247del (p.Pro78_Pro82del) rs1466765630
NM_005249.5(FOXG1):c.268G>T (p.Ala90Ser) rs906816341
NM_005249.5(FOXG1):c.312C>G (p.Leu104=) rs1335648253
NM_005249.5(FOXG1):c.321G>A (p.Pro107=) rs1384634545
NM_005249.5(FOXG1):c.837C>G (p.Thr279=) rs570340475

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