List of variants in gene NUBPL reported as uncertain significance for Inborn genetic diseases

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_025152.3(NUBPL):c.593A>C (p.Asn198Thr)	rs11558436	0.00480
NM_025152.3(NUBPL):c.413G>A (p.Gly138Asp)	rs201412882	0.00071
NM_025152.3(NUBPL):c.382+3A>G	rs777457120	0.00001
NM_025152.3(NUBPL):c.109-4A>G
NM_025152.3(NUBPL):c.17G>A (p.Arg6His)
NM_025152.3(NUBPL):c.218C>A (p.Ala73Asp)
NM_025152.3(NUBPL):c.430A>G (p.Met144Val)
NM_025152.3(NUBPL):c.523G>A (p.Gly175Ser)
NM_025152.3(NUBPL):c.601A>G (p.Ile201Val)
NM_025152.3(NUBPL):c.652G>A (p.Ala218Thr)

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