ClinVar Miner

List of variants reported as likely benign for Rett syndrome, congenital variant

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Total variants: 18
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NM_005249.5(FOXG1):c.1122C>T (p.Tyr374=) rs777855975
NM_005249.5(FOXG1):c.1161G>A (p.Ser387=) rs147154860
NM_005249.5(FOXG1):c.1320C>G (p.Ser440=) rs1057524328
NM_005249.5(FOXG1):c.1323C>T (p.Ser441=) rs144434028
NM_005249.5(FOXG1):c.1399C>T (p.Leu467=) rs371279404
NM_005249.5(FOXG1):c.159C>T (p.His53=) rs769410384
NM_005249.5(FOXG1):c.164_166ACC[4] (p.His57dup) rs772407998
NM_005249.5(FOXG1):c.180G>C (p.Pro60=) rs1555321214
NM_005249.5(FOXG1):c.201G>T (p.Pro67=) rs587780944
NM_005249.5(FOXG1):c.209_211AGC[5] (p.Gln73dup) rs398124201
NM_005249.5(FOXG1):c.219_221GCC[7] (p.Pro80dup) rs786200975
NM_005249.5(FOXG1):c.245C>A (p.Pro82Gln) rs796052453
NM_005249.5(FOXG1):c.246G>C (p.Pro82=) rs1555321242
NM_005249.5(FOXG1):c.324A>G (p.Pro108=) rs750512461
NM_005249.5(FOXG1):c.417C>T (p.Pro139=) rs1018810212
NM_005249.5(FOXG1):c.447C>T (p.Ala149=) rs112803404
NM_005249.5(FOXG1):c.503G>C (p.Gly168Ala) rs148157138
NM_005249.5(FOXG1):c.594C>G (p.Pro198=) rs141088742

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