ClinVar Miner

List of variants in gene combination SNHG14, UBE3A reported as uncertain significance for not specified

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Total variants: 17
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NM_000462.5(UBE3A):c.498C>G (p.Ser166Arg) rs1566962361
NM_001354550.2(UBE3A):c.361+4191_361+4203delinsC rs797046089
NM_130838.3(UBE3A):c.1109A>G (p.Asn370Ser) rs147446244
NM_130838.3(UBE3A):c.1125A>T (p.Glu375Asp) rs114056442
NM_130838.3(UBE3A):c.1212C>T (p.Pro404=) rs1057520392
NM_130838.3(UBE3A):c.1560C>T (p.Ile520=) rs1057523671
NM_130838.3(UBE3A):c.1694-4A>G rs780429591
NM_130838.3(UBE3A):c.1697T>G (p.Met566Arg) rs587781244
NM_130838.3(UBE3A):c.1877G>C (p.Arg626Pro) rs374601913
NM_130838.3(UBE3A):c.2036A>C (p.Lys679Thr) rs202161423
NM_130838.3(UBE3A):c.2444C>G (p.Pro815Arg) rs863225069
NM_130838.3(UBE3A):c.397G>A (p.Val133Ile) rs199636913
NM_130838.3(UBE3A):c.599A>C (p.Asn200Thr) rs528422241
NM_130838.3(UBE3A):c.611T>C (p.Leu204Ser) rs587782922
NM_130838.3(UBE3A):c.755A>G (p.Asn252Ser) rs139928148
NM_130838.3(UBE3A):c.947T>C (p.Met316Thr) rs863225071
NM_130838.3(UBE3A):c.949A>T (p.Met317Leu) rs368318081

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