List of variants in gene USH1C reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 18A

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_153676.4(USH1C):c.2611G>A (p.Ala871Thr)	rs56165709	0.00336
NM_153676.4(USH1C):c.403G>A (p.Val135Ile)	rs145013633	0.00234
NM_153676.4(USH1C):c.2167C>T (p.Gln723Ter)	rs146451547	0.00068
NM_153676.4(USH1C):c.2269C>T (p.Arg757Cys)	rs757163581	0.00006
NM_153676.4(USH1C):c.204G>T (p.Leu68=)	rs140945339	0.00002
NM_153676.4(USH1C):c.1910C>G (p.Thr637Ser)	rs754365594
NM_153676.4(USH1C):c.2013+1G>A
NM_153676.4(USH1C):c.2520C>A (p.Cys840Ter)
NM_153676.4(USH1C):c.2535T>A (p.Tyr845Ter)
NM_153676.4(USH1C):c.2546+1G>A
NM_153676.4(USH1C):c.434G>A (p.Cys145Tyr)
NM_153676.4(USH1C):c.671G>A (p.Cys224Tyr)
NM_153676.4(USH1C):c.876T>C (p.Ala292=)

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