ClinVar Miner

List of variants in gene SLX4 reported as uncertain significance for Fanconi anemia, complementation group A

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Total variants: 11
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HGVS dbSNP
NM_032444.4(SLX4):c.1186C>G (p.Leu396Val)
NM_032444.4(SLX4):c.1372A>G (p.Lys458Glu) rs149126845
NM_032444.4(SLX4):c.1547C>T (p.Ala516Val) rs199683722
NM_032444.4(SLX4):c.2654C>T (p.Pro885Leu) rs147492092
NM_032444.4(SLX4):c.2878A>T (p.Ser960Cys)
NM_032444.4(SLX4):c.2941G>A (p.Gly981Arg) rs546628836
NM_032444.4(SLX4):c.3607C>G (p.Pro1203Ala)
NM_032444.4(SLX4):c.3830G>A (p.Ser1277Asn)
NM_032444.4(SLX4):c.4021A>G (p.Arg1341Gly)
NM_032444.4(SLX4):c.421G>T (p.Gly141Trp) rs137976282
NM_032444.4(SLX4):c.467C>A (p.Thr156Lys) rs144614070

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