ClinVar Miner

List of variants in gene DNM2 reported as uncertain significance by GeneDx

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Total variants: 26
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HGVS dbSNP
NM_001005360.2(DNM2):c.1004A>T (p.Gln335Leu) rs759996048
NM_001005360.2(DNM2):c.1051G>A (p.Val351Met) rs876661176
NM_001005360.2(DNM2):c.1273C>A (p.Leu425Met) rs879253980
NM_001005360.2(DNM2):c.1352G>A (p.Arg451Gln) rs749154067
NM_001005360.2(DNM2):c.1370A>G (p.Glu457Gly) rs1555711301
NM_001005360.2(DNM2):c.1384A>G (p.Thr462Ala) rs201575500
NM_001005360.2(DNM2):c.1418A>T (p.Asp473Val) rs766613900
NM_001005360.2(DNM2):c.1423-9C>G rs371006369
NM_001005360.2(DNM2):c.142C>T (p.Leu48=) rs753989925
NM_001005360.2(DNM2):c.1809C>G (p.Ile603Met) rs780409124
NM_001005360.2(DNM2):c.1903G>A (p.Glu635Lys) rs761198315
NM_001005360.2(DNM2):c.1912G>A (p.Ala638Thr) rs587778236
NM_001005360.2(DNM2):c.1934T>C (p.Met645Thr) rs879253969
NM_001005360.2(DNM2):c.1969C>T (p.Arg657Cys) rs772920450
NM_001005360.2(DNM2):c.1973A>G (p.Asn658Ser) rs753175954
NM_001005360.2(DNM2):c.2276G>A (p.Ser759Asn) rs879254300
NM_001005360.2(DNM2):c.2365C>G (p.Pro789Ala) rs876661218
NM_001005360.2(DNM2):c.2576_2581delCCATTA (p.Thr859_Ile860del) rs876661117
NM_001005360.2(DNM2):c.316G>A (p.Asp106Asn) rs375151459
NM_001005360.2(DNM2):c.677C>T (p.Pro226Leu) rs779734638
NM_001005360.2(DNM2):c.736A>T (p.Lys246Ter) rs1555707649
NM_001005360.2(DNM2):c.839C>T (p.Thr280Met) rs202155679
NM_001005360.2(DNM2):c.868C>T (p.Arg290Trp) rs587778235
NM_001005360.2(DNM2):c.8A>G (p.Asn3Ser) rs890297188
NM_001005360.2(DNM2):c.953G>A (p.Arg318Gln) rs879254323
NM_001005360.2(DNM2):c.992A>G (p.Gln331Arg) rs879254084

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