List of variants in gene USP9Y studied for syndrome caused by partial chromosomal deletion

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004654.4(USP9Y):c.3835C>G (p.Leu1279Val)
NM_004654.4(USP9Y):c.5924C>T (p.Thr1975Ile)
NM_004654.4(USP9Y):c.6343G>T (p.Gly2115Cys)
NM_004654.4(USP9Y):c.773+3_773+6del	rs778145751

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