ClinVar Miner

List of variants in gene DNM1 reported as uncertain significance by GeneDx

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_004408.4(DNM1):c.796C>T (p.Arg266Cys) rs138053929 0.00006
NM_004408.4(DNM1):c.1390A>G (p.Ile464Val) rs992608425 0.00003
NM_004408.4(DNM1):c.1186C>T (p.His396Tyr) rs1835103565 0.00001
NM_004408.4(DNM1):c.1408C>T (p.Arg470Cys) rs762553379 0.00001
NM_004408.4(DNM1):c.788C>T (p.Pro263Leu) rs930963855 0.00001
NM_004408.4(DNM1):c.890G>A (p.Arg297Gln) rs1321080189 0.00001
NM_004408.4(DNM1):c.1025del (p.Lys342fs)
NM_004408.4(DNM1):c.1027C>T (p.Arg343Cys)
NM_004408.4(DNM1):c.1082G>A (p.Arg361His) rs1172228858
NM_004408.4(DNM1):c.1102G>A (p.Glu368Lys) rs1835087040
NM_004408.4(DNM1):c.1282G>A (p.Val428Met) rs868805405
NM_004408.4(DNM1):c.1324T>C (p.Cys442Arg)
NM_004408.4(DNM1):c.1393C>T (p.Arg465Trp) rs772264918
NM_004408.4(DNM1):c.1409G>C (p.Arg470Pro)
NM_004408.4(DNM1):c.1468C>G (p.His490Asp)
NM_004408.4(DNM1):c.1493+4A>T
NM_004408.4(DNM1):c.1587T>A (p.Asn529Lys)
NM_004408.4(DNM1):c.1723G>A (p.Val575Met) rs748647924
NM_004408.4(DNM1):c.1872C>T (p.Gly624=) rs1367619284
NM_004408.4(DNM1):c.1973A>T (p.Gln658Leu)
NM_004408.4(DNM1):c.2009T>C (p.Met670Thr) rs1437208936
NM_004408.4(DNM1):c.2076+5G>A rs1829321597
NM_004408.4(DNM1):c.2154_2166delinsCAT (p.Ala719fs)
NM_004408.4(DNM1):c.2197_2199dup (p.His733_Ala734insHis)
NM_004408.4(DNM1):c.2534+2T>G
NM_004408.4(DNM1):c.604G>A (p.Gly202Arg) rs1057524561
NM_004408.4(DNM1):c.679dup (p.Leu227fs)
NM_004408.4(DNM1):c.683G>A (p.Arg228His) rs866946278
NM_004408.4(DNM1):c.701T>G (p.Val234Gly)
NM_004408.4(DNM1):c.739G>A (p.Asp247Asn)
NM_004408.4(DNM1):c.925_927del (p.Lys309del)
NM_004408.4(DNM1):c.929A>G (p.Glu310Gly) rs1835069996
NM_004408.4(DNM1):c.933G>A (p.Val311=)
NM_004408.4(DNM1):c.952C>T (p.Arg318Cys) rs892194903

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