ClinVar Miner

List of variants in gene NUP93 reported as likely pathogenic for Nephrotic syndrome

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Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_014669.5(NUP93):c.1162C>T (p.Arg388Trp) rs145146218 0.00070
NM_014669.5(NUP93):c.1772G>T (p.Gly591Val) rs145473779 0.00014
NM_014669.5(NUP93):c.575A>G (p.Tyr192Cys) rs201924382 0.00013
NM_014669.5(NUP93):c.2017C>T (p.Arg673Trp) rs1166462755 0.00001
NM_014669.5(NUP93):c.1886A>G (p.Tyr629Cys) rs757674160

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