ClinVar Miner

List of variants in gene USH2A studied for Hearing impairment

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Total variants: 18
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NM_206933.3(USH2A):c.2168-1G>C rs748961218
NM_206933.3(USH2A):c.2522C>A (p.Ser841Tyr) rs111033282
NM_206933.3(USH2A):c.5118G>A (p.Trp1706Ter) rs1461319754
NM_206933.3(USH2A):c.8730T>A (p.Phe2910Leu) rs373811292
NM_206933.3(USH2A):c.908G>A (p.Arg303His) rs371777049
NM_206933.4(USH2A):c.10058C>T (p.Pro3353Leu)
NM_206933.4(USH2A):c.11864G>A (p.Trp3955Ter) rs111033364
NM_206933.4(USH2A):c.12458C>T (p.Ala4153Val)
NM_206933.4(USH2A):c.1270A>T (p.Met424Leu)
NM_206933.4(USH2A):c.14396C>T (p.Thr4799Ile)
NM_206933.4(USH2A):c.14519T>C (p.Leu4840Pro) rs143275144
NM_206933.4(USH2A):c.1585A>C (p.Thr529Pro)
NM_206933.4(USH2A):c.1898C>T (p.Ser633Leu)
NM_206933.4(USH2A):c.2035G>A (p.Gly679Arg)
NM_206933.4(USH2A):c.5320T>A (p.Leu1774Met)
NM_206933.4(USH2A):c.5919G>A (p.Val1973=)
NM_206933.4(USH2A):c.8452C>T (p.Pro2818Ser)
NM_206933.4(USH2A):c.9413G>C (p.Gly3138Ala)

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