List of variants in gene USP9X reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001039591.3(USP9X):c.420G>T (p.Trp140Cys)	rs1555919860
NM_001039591.3(USP9X):c.4406C>T (p.Pro1469Leu)	rs1010165716
NM_001039591.3(USP9X):c.538C>A (p.Pro180Thr)	rs2147035203
NM_001039591.3(USP9X):c.5632G>A (p.Gly1878Arg)

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