ClinVar Miner

List of variants reported as uncertain significance for Charcot-Marie-Tooth disease type 2P by Illumina Clinical Services Laboratory,Illumina

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Total variants: 43
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HGVS dbSNP
NM_138361.5(LRSAM1):c.*121C>T
NM_138361.5(LRSAM1):c.*238G>A rs886063459
NM_138361.5(LRSAM1):c.*350C>A rs764119919
NM_138361.5(LRSAM1):c.*356G>A
NM_138361.5(LRSAM1):c.*370C>T
NM_138361.5(LRSAM1):c.*392G>T
NM_138361.5(LRSAM1):c.*501C>T rs886063460
NM_138361.5(LRSAM1):c.*552A>G
NM_138361.5(LRSAM1):c.*588T>A rs886063461
NM_138361.5(LRSAM1):c.*597T>G rs751523580
NM_138361.5(LRSAM1):c.-127C>A
NM_138361.5(LRSAM1):c.-309A>G rs886063453
NM_138361.5(LRSAM1):c.-321A>G
NM_138361.5(LRSAM1):c.-338G>A rs886063451
NM_138361.5(LRSAM1):c.-35C>T
NM_138361.5(LRSAM1):c.-401C>T rs886063450
NM_138361.5(LRSAM1):c.-458A>G rs760403428
NM_138361.5(LRSAM1):c.-561C>T
NM_138361.5(LRSAM1):c.-567G>A
NM_138361.5(LRSAM1):c.-78C>T rs886063454
NM_138361.5(LRSAM1):c.1035C>T (p.Asp345=) rs766701971
NM_138361.5(LRSAM1):c.1073C>T (p.Ser358Leu) rs886063457
NM_138361.5(LRSAM1):c.1159+13A>T
NM_138361.5(LRSAM1):c.1199G>A (p.Arg400Gln) rs150344223
NM_138361.5(LRSAM1):c.1347+6C>T rs1588128875
NM_138361.5(LRSAM1):c.1422+15T>A
NM_138361.5(LRSAM1):c.1515G>A (p.Ser505=) rs140066362
NM_138361.5(LRSAM1):c.1660C>T (p.Arg554Trp) rs757208185
NM_138361.5(LRSAM1):c.1699-3C>T
NM_138361.5(LRSAM1):c.1772C>T (p.Ala591Val) rs139344911
NM_138361.5(LRSAM1):c.1834G>A (p.Gly612Ser)
NM_138361.5(LRSAM1):c.2110C>T (p.Arg704Cys) rs150984897
NM_138361.5(LRSAM1):c.2115C>T (p.Thr705=)
NM_138361.5(LRSAM1):c.2134G>A (p.Asp712Asn)
NM_138361.5(LRSAM1):c.390G>C (p.Gln130His)
NM_138361.5(LRSAM1):c.528G>A (p.Glu176=) rs1564255509
NM_138361.5(LRSAM1):c.593C>A (p.Ala198Glu) rs758867006
NM_138361.5(LRSAM1):c.598A>G (p.Ile200Val)
NM_138361.5(LRSAM1):c.615C>G (p.Cys205Trp) rs886063455
NM_138361.5(LRSAM1):c.620-3C>T rs373015900
NM_138361.5(LRSAM1):c.643C>A (p.Pro215Thr) rs765389102
NM_138361.5(LRSAM1):c.894G>A (p.Thr298=) rs771491533
NM_138361.5(LRSAM1):c.972G>A (p.Leu324=) rs940085400

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