ClinVar Miner

List of variants reported as likely benign for cataract 18

Included ClinVar conditions (1):
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Total variants: 31
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HGVS dbSNP
NM_024513.4(FYCO1):c.*1173C>T rs187327525
NM_024513.4(FYCO1):c.*1686A>G
NM_024513.4(FYCO1):c.*1748C>T rs149016664
NM_024513.4(FYCO1):c.*2238C>A
NM_024513.4(FYCO1):c.*2851C>T rs182350140
NM_024513.4(FYCO1):c.*3560C>A
NM_024513.4(FYCO1):c.*3725A>G rs547425913
NM_024513.4(FYCO1):c.*724C>A rs148133261
NM_024513.4(FYCO1):c.108G>A (p.Thr36=) rs558777911
NM_024513.4(FYCO1):c.1248G>A (p.Lys416=) rs149643762
NM_024513.4(FYCO1):c.1439C>T (p.Thr480Met) rs146711260
NM_024513.4(FYCO1):c.1474C>T (p.Arg492Trp) rs143704916
NM_024513.4(FYCO1):c.1659C>T (p.Leu553=) rs746026639
NM_024513.4(FYCO1):c.1985C>T (p.Ser662Phe) rs150785981
NM_024513.4(FYCO1):c.2006G>A (p.Ser669Asn) rs141155944
NM_024513.4(FYCO1):c.2109G>A (p.Gln703=) rs766375149
NM_024513.4(FYCO1):c.2199C>T (p.Leu733=)
NM_024513.4(FYCO1):c.2612G>A (p.Arg871Gln)
NM_024513.4(FYCO1):c.2814G>A (p.Glu938=) rs116798205
NM_024513.4(FYCO1):c.2844G>A (p.Glu948=) rs182162227
NM_024513.4(FYCO1):c.2865G>A (p.Gln955=) rs1575368474
NM_024513.4(FYCO1):c.3215C>T (p.Ala1072Val)
NM_024513.4(FYCO1):c.3322A>G (p.Lys1108Glu) rs73830668
NM_024513.4(FYCO1):c.3438-9_3438-8del
NM_024513.4(FYCO1):c.3779C>G (p.Pro1260Arg) rs144182297
NM_024513.4(FYCO1):c.3825G>A (p.Pro1275=) rs748985200
NM_024513.4(FYCO1):c.3903A>G (p.Thr1301=) rs144525738
NM_024513.4(FYCO1):c.4254C>A (p.Val1418=) rs1553620269
NM_024513.4(FYCO1):c.4319C>T (p.Thr1440Ile) rs41289612
NM_024513.4(FYCO1):c.753G>T (p.Glu251Asp) rs3821885
NM_024513.4(FYCO1):c.869G>A (p.Arg290His) rs146311777

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