ClinVar Miner

List of variants in gene CHRNA4 reported as uncertain significance for Seizures

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Total variants: 13
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HGVS dbSNP
NM_000744.6(CHRNA4):c.1108C>T (p.Arg370Trp) rs76378652
NM_000744.6(CHRNA4):c.1138A>G (p.Ser380Gly) rs187372416
NM_000744.6(CHRNA4):c.1144C>T (p.Pro382Ser) rs1568809115
NM_000744.6(CHRNA4):c.1228G>A (p.Val410Ile) rs121912272
NM_000744.6(CHRNA4):c.1273C>T (p.Pro425Ser) rs764808511
NM_000744.6(CHRNA4):c.1360G>A (p.Gly454Ser) rs78306886
NM_000744.6(CHRNA4):c.1454G>A (p.Arg485Gln) rs755416498
NM_000744.6(CHRNA4):c.1525G>A (p.Ala509Thr) rs142137599
NM_000744.6(CHRNA4):c.1721T>C (p.Ile574Thr)
NM_000744.6(CHRNA4):c.200G>A (p.Gly67Asp) rs1568819500
NM_000744.6(CHRNA4):c.274G>C (p.Glu92Gln) rs146651027
NM_000744.6(CHRNA4):c.622G>A (p.Glu208Lys) rs771249249
NM_000744.6(CHRNA4):c.971C>T (p.Thr324Met)

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