ClinVar Miner

List of variants in gene USH2A reported as benign for none provided

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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP
NM_007123.5(USH2A):c.4457= (p.Lys1486=) rs1805049
NM_206933.3(USH2A):c.12612= (p.Thr4204=) rs2797235
NM_206933.3(USH2A):c.15297+3A>G rs57754754
NM_206933.3(USH2A):c.15562A>G (p.Ser5188Gly) rs58257972
NM_206933.3(USH2A):c.2522C>A (p.Ser841Tyr) rs111033282
NM_206933.3(USH2A):c.5857+17A>C rs74766738
NM_206933.3(USH2A):c.6317= (p.Thr2106=) rs6657250
NM_206933.3(USH2A):c.8681+18A>G rs41277198
NM_206933.4(USH2A):c.10232A>C (p.Glu3411Ala) rs10864198
NM_206933.4(USH2A):c.11389+9A>T rs12095085
NM_206933.4(USH2A):c.11677C>A (p.Pro3893Thr) rs41303285
NM_206933.4(USH2A):c.11907A>T (p.Pro3969=) rs61635304
NM_206933.4(USH2A):c.11946G>A (p.Leu3982=) rs2820718
NM_206933.4(USH2A):c.12666A>G (p.Thr4222=) rs2797234
NM_206933.4(USH2A):c.13440G>A (p.Arg4480=) rs111033378
NM_206933.4(USH2A):c.13763C>A (p.Ser4588Tyr) rs78253373
NM_206933.4(USH2A):c.14074G>A (p.Gly4692Arg) rs45549044
NM_206933.4(USH2A):c.14513G>A (p.Gly4838Glu) rs41315587
NM_206933.4(USH2A):c.14543G>A (p.Arg4848Gln) rs77211159
NM_206933.4(USH2A):c.14664G>A (p.Thr4888=) rs111033525
NM_206933.4(USH2A):c.14960C>T (p.Ala4987Val) rs111033498
NM_206933.4(USH2A):c.15076A>G (p.Lys5026Glu) rs41308435
NM_206933.4(USH2A):c.15091C>T (p.Arg5031Trp) rs56038610
NM_206933.4(USH2A):c.15428G>A (p.Arg5143His) rs111033435
NM_206933.4(USH2A):c.2137G>C (p.Gly713Arg) rs696723
NM_206933.4(USH2A):c.3364T>G (p.Ser1122Ala) rs148135241
NM_206933.4(USH2A):c.373G>A (p.Ala125Thr) rs10779261
NM_206933.4(USH2A):c.3945T>C (p.Asn1315=) rs41303257
NM_206933.4(USH2A):c.4371G>A (p.Ser1457=) rs56013136
NM_206933.4(USH2A):c.4560C>T (p.Ile1520=) rs148000219
NM_206933.4(USH2A):c.4586A>T (p.Lys1529Ile) rs41303255
NM_206933.4(USH2A):c.504A>G (p.Thr168=) rs4253963
NM_206933.4(USH2A):c.5572+15G>A rs17026052
NM_206933.4(USH2A):c.6240G>T (p.Lys2080Asn) rs114402911
NM_206933.4(USH2A):c.6257C>A (p.Thr2086Asn) rs149202379
NM_206933.4(USH2A):c.6506T>C (p.Ile2169Thr) rs10864219
NM_206933.4(USH2A):c.6587G>C (p.Ser2196Thr) rs79444516
NM_206933.4(USH2A):c.6713A>C (p.Glu2238Ala) rs41277212
NM_206933.4(USH2A):c.688G>A (p.Val230Met) rs45500891
NM_206933.4(USH2A):c.7130A>G (p.Asn2377Ser) rs111033394
NM_206933.4(USH2A):c.8656C>T (p.Leu2886Phe) rs41277200
NM_206933.4(USH2A):c.9296A>G (p.Asn3099Ser) rs41277194

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