ClinVar Miner

List of variants in gene USH1C reported as likely benign

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Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP
NM_005709.3(USH1C):c.*218C>T rs1055577
NM_005709.3(USH1C):c.*243A>G rs1055581
NM_005709.3(USH1C):c.101A>G (p.His34Arg) rs75157409
NM_005709.3(USH1C):c.1086-12G>A rs11024318
NM_005709.3(USH1C):c.1086-13G>T rs200490320
NM_005709.3(USH1C):c.114C>T (p.Asp38=) rs137962152
NM_005709.3(USH1C):c.1211-4G>A rs199972595
NM_005709.3(USH1C):c.1243G>A (p.Ala415Thr) rs116996553
NM_005709.3(USH1C):c.1266G>A (p.Thr422=) rs35188020
NM_005709.3(USH1C):c.1284+1133C>T rs377439949
NM_005709.3(USH1C):c.1284+1167C>T rs978889964
NM_005709.3(USH1C):c.1284+6915G>A rs142669563
NM_005709.3(USH1C):c.1284+7552A>G rs397517872
NM_005709.3(USH1C):c.1284+7580G>A rs780428813
NM_005709.3(USH1C):c.1285-7549C>T rs1554956913
NM_005709.3(USH1C):c.1285-7549delC rs1554956916
NM_005709.3(USH1C):c.1285-7565G>C rs201101932
NM_005709.3(USH1C):c.1285-7567C>T rs727505247
NM_005709.3(USH1C):c.1326+12C>T rs17703528
NM_005709.3(USH1C):c.1518C>T (p.Asn506=) rs397517876
NM_005709.3(USH1C):c.1543C>T (p.Leu515=) rs148477093
NM_005709.3(USH1C):c.1599C>T (p.Ile533=) rs34581703
NM_005709.3(USH1C):c.1646+1080G>T rs571304936
NM_005709.3(USH1C):c.1646+1124C>T rs767767573
NM_005709.3(USH1C):c.1646+1151G>A rs201533059
NM_005709.3(USH1C):c.1647-1181G>A rs727504552
NM_005709.3(USH1C):c.264G>A (p.Val88=) rs397517879
NM_005709.3(USH1C):c.381G>T (p.Gly127=) rs41282942
NM_005709.3(USH1C):c.403G>A (p.Val135Ile) rs145013633
NM_005709.3(USH1C):c.497-4G>A rs397517881
NM_005709.3(USH1C):c.521+14C>G rs1235631667
NM_005709.3(USH1C):c.582C>T (p.Gly194=) rs397517882
NM_005709.3(USH1C):c.587G>A (p.Arg196Gln) rs397517883
NM_005709.3(USH1C):c.648G>A (p.Leu216=) rs77137413
NM_005709.3(USH1C):c.674+4G>A rs202095395
NM_005709.3(USH1C):c.921G>A (p.Ala307=) rs778447994
NM_005709.3(USH1C):c.946G>C (p.Glu316Gln) rs35336155
NM_153676.3(USH1C):c.*46T>C rs1055574
NM_153676.3(USH1C):c.1020-7G>A rs1554960567
NM_153676.3(USH1C):c.1188A>G (p.Pro396=) rs2240487
NM_153676.3(USH1C):c.1413+13C>T rs876657623
NM_153676.3(USH1C):c.1548G>C (p.Pro516=) rs780428813
NM_153676.3(USH1C):c.1731G>A (p.Pro577=) rs199572804
NM_153676.3(USH1C):c.1792C>T (p.Arg598Cys) rs111033520
NM_153676.3(USH1C):c.1823C>G (p.Pro608Arg) rs41282932
NM_153676.3(USH1C):c.186T>C (p.Ile62=) rs200239508
NM_153676.3(USH1C):c.1907G>A (p.Arg636His) rs138017852
NM_153676.3(USH1C):c.2013+5T>C rs371038786
NM_153676.3(USH1C):c.2046C>T (p.Gly682=) rs1554955894
NM_153676.3(USH1C):c.2112A>G (p.Pro704=) rs199532754
NM_153676.3(USH1C):c.2124T>C (p.Ser708=) rs369021714
NM_153676.3(USH1C):c.2184+10T>C rs200889109
NM_153676.3(USH1C):c.2340C>T (p.Val780=) rs10832796
NM_153676.3(USH1C):c.2457G>C (p.Glu819Asp) rs1064074
NM_153676.3(USH1C):c.248+7_248+20del rs749047869
NM_153676.3(USH1C):c.2490+12G>C rs2072232
NM_153676.3(USH1C):c.2538C>T (p.Asp846=) rs143860238
NM_153676.3(USH1C):c.2568A>G (p.Val856=) rs1385487954
NM_153676.3(USH1C):c.2591G>A (p.Arg864Gln) rs374696855
NM_153676.3(USH1C):c.2616C>T (p.Ala872=) rs141591891
NM_153676.3(USH1C):c.66G>A (p.Glu22=) rs768165881
NM_153676.3(USH1C):c.675-4G>A rs550964012
NM_153676.3(USH1C):c.684C>T (p.Ser228=) rs149172005
NM_153676.3(USH1C):c.760-4C>T rs374167444
NM_153676.3(USH1C):c.7C>A (p.Arg3=) rs876657624

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