ClinVar Miner

List of variants in gene USH1C reported as uncertain significance for Usher syndrome, type 1C

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Total variants: 60
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HGVS dbSNP
NM_005709.4(USH1C):c.*127C>T rs552838747
NM_005709.4(USH1C):c.*172C>T rs886048058
NM_005709.4(USH1C):c.*408A>C rs886048057
NM_005709.4(USH1C):c.-71T>G rs571065113
NM_005709.4(USH1C):c.105-4A>G rs201374986
NM_005709.4(USH1C):c.1086-13G>T rs200490320
NM_005709.4(USH1C):c.114C>T (p.Asp38=) rs137962152
NM_005709.4(USH1C):c.1220G>A (p.Gly407Glu) rs143923730
NM_005709.4(USH1C):c.1285-2684C>T rs146451547
NM_005709.4(USH1C):c.1365C>G (p.Leu455=) rs151251262
NM_005709.4(USH1C):c.1380+15G>A rs886048059
NM_005709.4(USH1C):c.1478A>G (p.His493Arg) rs868121889
NM_005709.4(USH1C):c.1541C>A (p.Thr514Asn) rs397517877
NM_005709.4(USH1C):c.186T>C (p.Ile62=) rs200239508
NM_005709.4(USH1C):c.403G>A (p.Val135Ile) rs145013633
NM_005709.4(USH1C):c.406C>T (p.Arg136Trp) rs368903400
NM_005709.4(USH1C):c.464G>C (p.Arg155Pro) rs142730611
NM_005709.4(USH1C):c.496C>T (p.His166Tyr) rs367996370
NM_005709.4(USH1C):c.634G>A (p.Val212Ile) rs886048060
NM_005709.4(USH1C):c.684C>T (p.Ser228=) rs149172005
NM_005709.4(USH1C):c.759+10G>T rs368528034
NM_005709.4(USH1C):c.789C>G (p.Gly263=) rs376197674
NM_005709.4(USH1C):c.790G>A (p.Val264Ile) rs79875849
NM_005709.4(USH1C):c.845G>A (p.Arg282His) rs779111365
NM_005709.4(USH1C):c.851T>A (p.Leu284Gln) rs756485601
NM_005709.4(USH1C):c.881G>A (p.Arg294Gln) rs773481791
NM_005709.4(USH1C):c.883G>A (p.Glu295Lys) rs200127622
NM_005709.4(USH1C):c.921G>A (p.Ala307=) rs778447994
NM_153676.4(USH1C):c.*110C>G
NM_153676.4(USH1C):c.*117C>G
NM_153676.4(USH1C):c.*241C>G
NM_153676.4(USH1C):c.*427T>C
NM_153676.4(USH1C):c.-109A>T
NM_153676.4(USH1C):c.-60T>G
NM_153676.4(USH1C):c.1064G>T (p.Arg355Ile)
NM_153676.4(USH1C):c.1085+7A>G
NM_153676.4(USH1C):c.1211-1106G>A
NM_153676.4(USH1C):c.1211-1175G>C
NM_153676.4(USH1C):c.164G>A (p.Arg55His) rs1042393529
NM_153676.4(USH1C):c.192G>A (p.Pro64=) rs1040470628
NM_153676.4(USH1C):c.200C>T (p.Pro67Leu)
NM_153676.4(USH1C):c.2253G>A (p.Lys751=)
NM_153676.4(USH1C):c.2362G>A (p.Gly788Arg)
NM_153676.4(USH1C):c.2410G>A (p.Ala804Thr) rs150593932
NM_153676.4(USH1C):c.2419G>A (p.Gly807Ser) rs142652588
NM_153676.4(USH1C):c.2437T>G (p.Tyr813Asp)
NM_153676.4(USH1C):c.2487C>T (p.Gly829=) rs142801489
NM_153676.4(USH1C):c.2490+6A>C
NM_153676.4(USH1C):c.2541T>C (p.Asp847=)
NM_153676.4(USH1C):c.381G>T (p.Gly127=) rs41282942
NM_153676.4(USH1C):c.388G>A (p.Val130Ile) rs55843567
NM_153676.4(USH1C):c.540C>T (p.Leu180=) rs145510974
NM_153676.4(USH1C):c.570G>A (p.Ser190=) rs756709989
NM_153676.4(USH1C):c.669C>A (p.Gly223=) rs144761543
NM_153676.4(USH1C):c.66G>A (p.Glu22=) rs768165881
NM_153676.4(USH1C):c.674+4G>A rs202095395
NM_153676.4(USH1C):c.875C>G (p.Ala292Gly)
NM_153676.4(USH1C):c.880C>T (p.Arg294Trp) rs555152976
NM_153676.4(USH1C):c.923G>A (p.Arg308Gln)
NM_153676.4(USH1C):c.946G>C (p.Glu316Gln) rs35336155

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