ClinVar Miner

List of variants reported as uncertain significance for Usher syndrome, type 1G

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Total variants: 52
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HGVS dbSNP
NM_173477.5(USH1G):c.*1018G>A rs780234900
NM_173477.5(USH1G):c.*1052C>T
NM_173477.5(USH1G):c.*1119G>A rs182142592
NM_173477.5(USH1G):c.*1130T>C
NM_173477.5(USH1G):c.*1154T>A
NM_173477.5(USH1G):c.*1174T>G
NM_173477.5(USH1G):c.*1191G>A
NM_173477.5(USH1G):c.*1376G>A
NM_173477.5(USH1G):c.*1447C>T
NM_173477.5(USH1G):c.*1719G>T rs886053384
NM_173477.5(USH1G):c.*1732C>T rs886053383
NM_173477.5(USH1G):c.*1922A>G
NM_173477.5(USH1G):c.*1987C>T rs886053381
NM_173477.5(USH1G):c.*198T>C
NM_173477.5(USH1G):c.*202G>A rs557845589
NM_173477.5(USH1G):c.*233C>G
NM_173477.5(USH1G):c.*256C>T
NM_173477.5(USH1G):c.*279G>T rs886053387
NM_173477.5(USH1G):c.*482C>T
NM_173477.5(USH1G):c.*498G>A rs569461974
NM_173477.5(USH1G):c.*49C>T rs199648830
NM_173477.5(USH1G):c.*567C>G
NM_173477.5(USH1G):c.*680C>G
NM_173477.5(USH1G):c.*704G>A
NM_173477.5(USH1G):c.*809C>A rs886053386
NM_173477.5(USH1G):c.*831C>T
NM_173477.5(USH1G):c.*95C>G rs886053388
NM_173477.5(USH1G):c.-173G>C rs570755897
NM_173477.5(USH1G):c.-2C>T rs758940726
NM_173477.5(USH1G):c.-76A>G
NM_173477.5(USH1G):c.-8C>T rs769903865
NM_173477.5(USH1G):c.1057G>A (p.Asp353Asn)
NM_173477.5(USH1G):c.1142T>C (p.Leu381Ser)
NM_173477.5(USH1G):c.1152C>T (p.Asp384=) rs569032124
NM_173477.5(USH1G):c.1170C>T (p.Ser390=) rs199724052
NM_173477.5(USH1G):c.1258C>G (p.Leu420Val) rs139897506
NM_173477.5(USH1G):c.126T>C (p.His42=)
NM_173477.5(USH1G):c.327C>T (p.Gly109=)
NM_173477.5(USH1G):c.344G>A (p.Arg115His) rs775117744
NM_173477.5(USH1G):c.348C>T (p.Tyr116=) rs886053390
NM_173477.5(USH1G):c.424G>C (p.Glu142Gln)
NM_173477.5(USH1G):c.436C>T (p.Arg146Cys) rs141791769
NM_173477.5(USH1G):c.474C>G (p.His158Gln) rs765860407
NM_173477.5(USH1G):c.478C>G (p.Arg160Gly) rs376527217
NM_173477.5(USH1G):c.501C>G (p.Arg167=) rs141688757
NM_173477.5(USH1G):c.563G>T (p.Arg188Leu) rs201123735
NM_173477.5(USH1G):c.566G>A (p.Arg189Gln) rs201644674
NM_173477.5(USH1G):c.635G>C (p.Gly212Ala)
NM_173477.5(USH1G):c.644del (p.Lys215fs) rs1567940040
NM_173477.5(USH1G):c.753C>T (p.Ser251=) rs886053389
NM_173477.5(USH1G):c.837C>G (p.Asp279Glu) rs142486910
NM_173477.5(USH1G):c.83C>T (p.Pro28Leu) rs145448362

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