ClinVar Miner

List of variants in gene USH2A reported as benign by ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories

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Total variants: 29
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HGVS dbSNP
NM_206933.2(USH2A):c.10232A>C (p.Glu3411Ala) rs10864198
NM_206933.2(USH2A):c.10552G>A (p.Val3518Ile) rs75397806
NM_206933.2(USH2A):c.11946G>A (p.Leu3982=) rs2820718
NM_206933.2(USH2A):c.12666A>G (p.Thr4222=) rs2797234
NM_206933.2(USH2A):c.12743A>G (p.His4248Arg) rs145830318
NM_206933.2(USH2A):c.13440G>A (p.Arg4480=) rs111033378
NM_206933.2(USH2A):c.13763C>A (p.Ser4588Tyr) rs78253373
NM_206933.2(USH2A):c.14074G>A (p.Gly4692Arg) rs45549044
NM_206933.2(USH2A):c.14333C>A (p.Ala4778Asp) rs113447586
NM_206933.2(USH2A):c.14454G>A (p.Pro4818=) rs137902779
NM_206933.2(USH2A):c.14513G>A (p.Gly4838Glu) rs41315587
NM_206933.2(USH2A):c.14960C>T (p.Ala4987Val) rs111033498
NM_206933.2(USH2A):c.15428G>A (p.Arg5143His) rs111033435
NM_206933.2(USH2A):c.2137G>C (p.Gly713Arg) rs696723
NM_206933.2(USH2A):c.3364T>G (p.Ser1122Ala) rs148135241
NM_206933.2(USH2A):c.373G>A (p.Ala125Thr) rs10779261
NM_206933.2(USH2A):c.4714C>T (p.Leu1572Phe) rs111033333
NM_206933.2(USH2A):c.504A>G (p.Thr168=) rs4253963
NM_206933.2(USH2A):c.5993G>A (p.Arg1998His) rs143624066
NM_206933.2(USH2A):c.6041A>C (p.Asn2014Thr) rs147883884
NM_206933.2(USH2A):c.6240G>T (p.Lys2080Asn) rs114402911
NM_206933.2(USH2A):c.6369C>T (p.Cys2123=) rs111033472
NM_206933.2(USH2A):c.6506T>C (p.Ile2169Thr) rs10864219
NM_206933.2(USH2A):c.6587G>C (p.Ser2196Thr) rs79444516
NM_206933.2(USH2A):c.6713A>C (p.Glu2238Ala) rs41277212
NM_206933.2(USH2A):c.688G>A (p.Val230Met) rs45500891
NM_206933.2(USH2A):c.8937A>G (p.Val2979=) rs139100097
NM_206933.2(USH2A):c.9296A>G (p.Asn3099Ser) rs41277194
NM_206933.3(USH2A):c.2522C>A (p.Ser841Tyr) rs111033282

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