ClinVar Miner

List of variants in gene DAG1 reported as uncertain significance by Athena Diagnostics Inc

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_004393.6(DAG1):c.258G>C (p.Leu86Phe) rs145403829 0.00314
NM_004393.6(DAG1):c.1022C>T (p.Thr341Ile) rs148759919 0.00048
NM_004393.6(DAG1):c.1757C>T (p.Ser586Leu) rs371990100 0.00015
NM_004393.6(DAG1):c.965C>T (p.Thr322Ile) rs376602004 0.00014
NM_004393.6(DAG1):c.1307C>T (p.Thr436Met) rs143573515 0.00009
NM_004393.6(DAG1):c.1690C>A (p.Leu564Ile) rs199894361 0.00006
NM_004393.6(DAG1):c.1370G>A (p.Arg457Gln) rs756890406 0.00004
NM_004393.6(DAG1):c.2123C>T (p.Thr708Met) rs758254304 0.00004
NM_004393.6(DAG1):c.535T>A (p.Ser179Thr) rs201869343 0.00004
NM_004393.6(DAG1):c.1210A>G (p.Thr404Ala) rs769229834 0.00002
NM_004393.6(DAG1):c.1015G>A (p.Val339Met) rs763537489 0.00001
NM_004393.6(DAG1):c.2647A>G (p.Met883Val) rs754908618 0.00001
NM_004393.6(DAG1):c.1166G>A (p.Arg389Gln) rs764205302
NM_004393.6(DAG1):c.1442G>C (p.Arg481Pro) rs1256677839
NM_004393.6(DAG1):c.1487G>T (p.Arg496Leu) rs199519832
NM_004393.6(DAG1):c.1729A>G (p.Met577Val)
NM_004393.6(DAG1):c.1925G>A (p.Cys642Tyr) rs1559580460
NM_004393.6(DAG1):c.1955G>T (p.Arg652Leu) rs368810294
NM_004393.6(DAG1):c.212C>A (p.Thr71Lys) rs142572135
NM_004393.6(DAG1):c.532G>T (p.Val178Leu) rs1217933283
NM_004393.6(DAG1):c.838C>T (p.Pro280Ser) rs908394465

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