ClinVar Miner

List of variants in gene combination SNHG14, UBE3A reported as likely benign for History of neurodevelopmental disorder

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Total variants: 8
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NM_000462.5(UBE3A):c.1278C>T (p.Asp426=) rs149506027
NM_000462.5(UBE3A):c.1776C>T (p.Tyr592=) rs139082033
NM_130838.3(UBE3A):c.162G>A (p.Lys54=)
NM_130838.3(UBE3A):c.2262C>T (p.Asp754=)
NM_130838.3(UBE3A):c.2310C>T (p.Ile770=) rs767254317
NM_130838.3(UBE3A):c.2370C>T (p.Asp790=) rs1566825584
NM_130838.3(UBE3A):c.2538C>T (p.Ala846=)
NM_130838.3(UBE3A):c.346T>C (p.Leu116=) rs1566962877

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