ClinVar Miner

List of variants in gene FLNC reported as likely benign by PreventionGenetics

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Gene type:
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Total variants: 18
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HGVS dbSNP
NM_001458.4(FLNC):c.1813+36G>A rs142756348
NM_001458.4(FLNC):c.2122-27T>C rs117577125
NM_001458.4(FLNC):c.2125G>A (p.Ala709Thr) rs192725607
NM_001458.4(FLNC):c.2292C>T (p.Pro764=) rs369916201
NM_001458.4(FLNC):c.2389+12C>T rs370526829
NM_001458.4(FLNC):c.2415C>T (p.Cys805=) rs376800693
NM_001458.4(FLNC):c.3000T>C (p.Asp1000=) rs184454068
NM_001458.4(FLNC):c.366C>T (p.Ile122=) rs369120591
NM_001458.4(FLNC):c.3867G>A (p.Thr1289=) rs886038485
NM_001458.4(FLNC):c.4161C>T (p.Ile1387=) rs200288149
NM_001458.4(FLNC):c.5200-18C>T rs372184893
NM_001458.4(FLNC):c.5298+6G>A rs373553314
NM_001458.4(FLNC):c.5374G>A (p.Ala1792Thr) rs201348102
NM_001458.4(FLNC):c.5578C>T (p.Arg1860Cys) rs181067717
NM_001458.4(FLNC):c.5766G>A (p.Ala1922=) rs58914363
NM_001458.4(FLNC):c.597C>T (p.Ala199=) rs143942649
NM_001458.4(FLNC):c.7947C>T (p.Phe2649=) rs368849358
NM_001458.4(FLNC):c.969+14G>T rs765545958

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