ClinVar Miner

List of variants reported as uncertain significance for Acute lymphoid leukemia; Acute myeloid leukemia; Encephalopathy, acute, infection-induced, susceptibility to, 9 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005085.4(NUP214):c.3952G>A (p.Gly1318Arg)
NM_005085.4(NUP214):c.505C>A (p.Leu169Met)
NM_005085.4(NUP214):c.5251A>G (p.Ser1751Gly)
NM_005085.4(NUP214):c.6075-4G>A

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