ClinVar Miner

List of variants reported as benign for Rett syndrome, congenital variant by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 46
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HGVS dbSNP gnomAD frequency
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.206C>A (p.Pro69Gln) rs727503933 0.00057
NM_005249.5(FOXG1):c.209A>C (p.Gln70Pro) rs587783633 0.00026
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.218A>C (p.Gln73Pro) rs760663911 0.00015
NM_005249.5(FOXG1):c.376G>A (p.Gly126Ser) rs796052455 0.00006
NM_005249.5(FOXG1):c.251C>A (p.Pro84His) rs866815665 0.00004
NM_005249.5(FOXG1):c.455G>C (p.Gly152Ala) rs796052460 0.00004
NM_005249.5(FOXG1):c.418G>A (p.Val140Ile) rs1400545711 0.00002
NM_005249.5(FOXG1):c.107G>A (p.Ser36Asn) rs1881775466 0.00001
NM_005249.5(FOXG1):c.1384A>G (p.Ser462Gly) rs752379833 0.00001
NM_005249.5(FOXG1):c.256C>A (p.Gln86Lys) rs398124202 0.00001
NM_005249.5(FOXG1):c.275C>T (p.Ala92Val) rs1057520147 0.00001
NM_005249.5(FOXG1):c.308T>A (p.Leu103Gln) rs1276635464 0.00001
NM_005249.5(FOXG1):c.378C>T (p.Gly126=) rs572031458 0.00001
NM_005249.5(FOXG1):c.382G>T (p.Gly128Cys) rs1029176730 0.00001
NM_005249.5(FOXG1):c.457G>T (p.Gly153Trp) rs1881797133 0.00001
NM_005249.5(FOXG1):c.1003C>T (p.Pro335Ser)
NM_005249.5(FOXG1):c.1029C>T (p.Ser343=)
NM_005249.5(FOXG1):c.1086G>A (p.Leu362=) rs570981209
NM_005249.5(FOXG1):c.115C>T (p.His39Tyr)
NM_005249.5(FOXG1):c.1221C>T (p.Val407=)
NM_005249.5(FOXG1):c.1255C>T (p.Pro419Ser) rs2138662170
NM_005249.5(FOXG1):c.1381C>G (p.Pro461Ala) rs1881826897
NM_005249.5(FOXG1):c.1390A>G (p.Thr464Ala) rs1268719113
NM_005249.5(FOXG1):c.141CCA[6] (p.His57del) rs587783630
NM_005249.5(FOXG1):c.187C>T (p.Pro63Ser) rs1288532385
NM_005249.5(FOXG1):c.219GCC[7] (p.Pro80dup) rs786200975
NM_005249.5(FOXG1):c.241G>A (p.Ala81Thr) rs1240859292
NM_005249.5(FOXG1):c.256C>G (p.Gln86Glu) rs398124202
NM_005249.5(FOXG1):c.263G>C (p.Arg88Pro)
NM_005249.5(FOXG1):c.310C>G (p.Leu104Val)
NM_005249.5(FOXG1):c.322C>T (p.Pro108Ser) rs1881790056
NM_005249.5(FOXG1):c.329C>A (p.Pro110Gln)
NM_005249.5(FOXG1):c.362C>G (p.Ala121Gly) rs2138660693
NM_005249.5(FOXG1):c.443G>C (p.Gly148Ala)
NM_005249.5(FOXG1):c.453C>G (p.Ala151=)
NM_005249.5(FOXG1):c.454G>T (p.Gly152Trp)
NM_005249.5(FOXG1):c.475G>A (p.Ala159Thr)
NM_005249.5(FOXG1):c.672C>G (p.Gly224=) rs587783639
NM_005249.5(FOXG1):c.933G>A (p.Ser311=)
NM_005249.5(FOXG1):c.977G>A (p.Ser326Asn) rs748001255
NM_005249.5(FOXG1):c.991A>G (p.Thr331Ala)

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