List of variants reported as uncertain significance for Usher syndrome, type 1C by Illumina Clinical Services Laboratory,Illumina

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Total variants: 57

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HGVS	dbSNP
NM_153676.4(USH1C):c.*110C>G
NM_153676.4(USH1C):c.*117C>G
NM_153676.4(USH1C):c.*140C>T	rs886048058
NM_153676.4(USH1C):c.*241C>G
NM_153676.4(USH1C):c.*376A>C	rs886048057
NM_153676.4(USH1C):c.*427T>C
NM_153676.4(USH1C):c.*95C>T	rs552838747
NM_153676.4(USH1C):c.-109A>T
NM_153676.4(USH1C):c.-60T>G
NM_153676.4(USH1C):c.-71T>G	rs571065113
NM_153676.4(USH1C):c.105-4A>G	rs201374986
NM_153676.4(USH1C):c.1064G>T (p.Arg355Ile)
NM_153676.4(USH1C):c.1085+7A>G
NM_153676.4(USH1C):c.1086-13G>T	rs200490320
NM_153676.4(USH1C):c.114C>T (p.Asp38=)	rs137962152
NM_153676.4(USH1C):c.1211-1106G>A
NM_153676.4(USH1C):c.1211-1175G>A	rs143923730
NM_153676.4(USH1C):c.1211-1175G>C
NM_153676.4(USH1C):c.164G>A (p.Arg55His)	rs1042393529
NM_153676.4(USH1C):c.186T>C (p.Ile62=)	rs200239508
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.2265C>G (p.Leu755=)	rs151251262
NM_153676.4(USH1C):c.2280+15G>A	rs886048059
NM_153676.4(USH1C):c.2362G>A (p.Gly788Arg)
NM_153676.4(USH1C):c.2378A>G (p.His793Arg)	rs868121889
NM_153676.4(USH1C):c.2410G>A (p.Ala804Thr)	rs150593932
NM_153676.4(USH1C):c.2437T>G (p.Tyr813Asp)
NM_153676.4(USH1C):c.2441C>A (p.Thr814Asn)	rs397517877
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.403G>A (p.Val135Ile)	rs145013633
NM_153676.4(USH1C):c.406C>T (p.Arg136Trp)	rs368903400
NM_153676.4(USH1C):c.464G>C (p.Arg155Pro)	rs142730611
NM_153676.4(USH1C):c.496C>T (p.His166Tyr)	rs367996370
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.634G>A (p.Val212Ile)	rs886048060
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.684C>T (p.Ser228=)	rs149172005
NM_153676.4(USH1C):c.759+10G>T	rs368528034
NM_153676.4(USH1C):c.789C>G (p.Gly263=)	rs376197674
NM_153676.4(USH1C):c.790G>A (p.Val264Ile)	rs79875849
NM_153676.4(USH1C):c.845G>A (p.Arg282His)	rs779111365
NM_153676.4(USH1C):c.851T>A (p.Leu284Gln)	rs756485601
NM_153676.4(USH1C):c.875C>G (p.Ala292Gly)
NM_153676.4(USH1C):c.880C>T (p.Arg294Trp)	rs555152976
NM_153676.4(USH1C):c.881G>A (p.Arg294Gln)	rs773481791
NM_153676.4(USH1C):c.883G>A (p.Glu295Lys)	rs200127622
NM_153676.4(USH1C):c.921G>A (p.Ala307=)	rs778447994
NM_153676.4(USH1C):c.923G>A (p.Arg308Gln)
NM_153676.4(USH1C):c.946G>C (p.Glu316Gln)	rs35336155

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