List of variants in gene USH2A reported by Institute of Human Genetics, University Hospital Muenster

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_206933.4(USH2A):c.11864G>A (p.Trp3955Ter)	rs111033364	0.00013
NM_206933.4(USH2A):c.10561T>C (p.Trp3521Arg)	rs111033264	0.00007
NM_206933.4(USH2A):c.3086G>T (p.Gly1029Val)	rs768158580	0.00002
NM_206933.4(USH2A):c.9258+1G>A	rs748810737	0.00001
NM_206933.4(USH2A):c.12299ACA[1] (p.Asn4101del)	rs1657997491
NM_206933.4(USH2A):c.3730C>T (p.Gln1244Ter)	rs2528045584
NM_206933.4(USH2A):c.3934del (p.Ala1312fs)	rs2102464166
NM_206933.4(USH2A):c.7950dup (p.Asn2651fs)	rs886041502
NM_206933.4(USH2A):c.9270C>A (p.Cys3090Ter)	rs779572631

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