ClinVar Miner

List of variants in gene USH2A reported as likely benign for not provided

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Total variants: 28
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HGVS dbSNP
GRCh37/hg19 1q41(chr1:215935660-216115708)x1
NC_000001.11:g.215846121del
NC_000001.11:g.216292378del
NM_206933.3(USH2A):c.10062G>C (p.Val3354=) rs200172376
NM_206933.3(USH2A):c.10246T>G (p.Cys3416Gly) rs527236140
NM_206933.3(USH2A):c.10470G>T (p.Val3490=) rs201401001
NM_206933.3(USH2A):c.11404G>A (p.Glu3802Lys) rs147900972
NM_206933.3(USH2A):c.12624C>T (p.Asp4208=)
NM_206933.3(USH2A):c.12743A>G (p.His4248Arg) rs145830318
NM_206933.3(USH2A):c.12817T>C (p.Tyr4273His) rs79654794
NM_206933.3(USH2A):c.1530C>T (p.Asp510=) rs200940197
NM_206933.3(USH2A):c.15433G>A (p.Val5145Ile) rs111033269
NM_206933.3(USH2A):c.2169G>A (p.Gly723=)
NM_206933.3(USH2A):c.2256T>C (p.His752=) rs111033281
NM_206933.3(USH2A):c.2522C>A (p.Ser841Tyr) rs111033282
NM_206933.3(USH2A):c.2643G>A (p.Gln881=)
NM_206933.3(USH2A):c.4445C>T (p.Thr1482Ile) rs200790812
NM_206933.3(USH2A):c.4680A>C (p.Ala1560=) rs1233583863
NM_206933.3(USH2A):c.5858C>G (p.Ala1953Gly) rs41302239
NM_206933.3(USH2A):c.5975A>G (p.Tyr1992Cys) rs41303287
NM_206933.3(USH2A):c.6462G>A (p.Leu2154=) rs1558203898
NM_206933.3(USH2A):c.6628C>G (p.Pro2210Ala) rs192115090
NM_206933.3(USH2A):c.688G>A (p.Val230Met) rs45500891
NM_206933.3(USH2A):c.7130A>G (p.Asn2377Ser) rs111033394
NM_206933.3(USH2A):c.7167C>T (p.Ser2389=)
NM_206933.3(USH2A):c.7300+29A>G
NM_206933.3(USH2A):c.8028G>A (p.Pro2676=) rs766443785
NM_206933.3(USH2A):c.9262G>A (p.Glu3088Lys) rs56056328

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