ClinVar Miner

List of variants reported as uncertain significance for Charcot-Marie-Tooth disease, type 4D

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ClinVar version:
Total variants: 78
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HGVS dbSNP
NC_000008.11:g.133297281T>G
NM_001135242.2(NDRG1):c.1081C>T (p.Arg361Cys) rs779065972
NM_006096.3(NDRG1):c.*1195G>T rs561506934
NM_006096.3(NDRG1):c.*1296C>T rs886062711
NM_006096.3(NDRG1):c.*1340G>A rs12668
NM_006096.3(NDRG1):c.*1706G>A rs781277187
NM_006096.3(NDRG1):c.*184G>A rs778104868
NM_006096.3(NDRG1):c.*201A>T rs886062715
NM_006096.3(NDRG1):c.*2C>T rs200367524
NM_006096.3(NDRG1):c.*306C>T rs886062714
NM_006096.3(NDRG1):c.*402C>T rs551081194
NM_006096.3(NDRG1):c.*618T>G rs886062713
NM_006096.3(NDRG1):c.*677C>T rs886062712
NM_006096.3(NDRG1):c.-123T>G rs886062718
NM_006096.3(NDRG1):c.-128C>T rs886062719
NM_006096.3(NDRG1):c.-157C>T rs545130040
NM_006096.3(NDRG1):c.-173G>A rs886062720
NM_006096.3(NDRG1):c.-19+14C>G rs886062716
NM_006096.3(NDRG1):c.-64G>A rs886062717
NM_006096.3(NDRG1):c.-8G>A rs200465804
NM_006096.3(NDRG1):c.1027C>T (p.Arg343Cys) rs146613168
NM_006096.3(NDRG1):c.1028G>A (p.Arg343His) rs144714216
NM_006096.3(NDRG1):c.1046G>A (p.Gly349Asp) rs1209851405
NM_006096.3(NDRG1):c.1101C>T (p.Ser367=) rs201959970
NM_006096.3(NDRG1):c.1155C>T (p.Ala385=) rs774605205
NM_006096.3(NDRG1):c.196G>A (p.Gly66Ser) rs780329667
NM_006096.3(NDRG1):c.304G>A (p.Gly102Ser) rs200433822
NM_006096.3(NDRG1):c.307G>C (p.Ala103Pro) rs374160497
NM_006096.3(NDRG1):c.31G>A (p.Ala11Thr) rs145871479
NM_006096.3(NDRG1):c.331A>C (p.Met111Leu) rs2233328
NM_006096.3(NDRG1):c.373G>A (p.Val125Ile) rs200593999
NM_006096.3(NDRG1):c.528C>G (p.Ala176=) rs191237702
NM_006096.3(NDRG1):c.613G>A (p.Val205Met) rs138839833
NM_006096.3(NDRG1):c.63+6T>C rs199597649
NM_006096.3(NDRG1):c.663C>T (p.Pro221=) rs377225752
NM_006096.3(NDRG1):c.664G>A (p.Gly222Ser) rs199995009
NM_006096.3(NDRG1):c.686A>G (p.Asn229Ser) rs137993172
NM_006096.3(NDRG1):c.789G>A (p.Ser263=) rs61755062
NM_006096.3(NDRG1):c.891+5G>A rs150968034
NM_006096.3(NDRG1):c.894G>A (p.Pro298=) rs368061370
NM_006096.3(NDRG1):c.944-13C>T rs753312340
NM_006096.3(NDRG1):c.956G>A (p.Ser319Asn) rs1564277421
NM_006096.3(NDRG1):c.973C>T (p.Arg325Trp) rs141078746
NM_006096.4(NDRG1):c.*1179G>C
NM_006096.4(NDRG1):c.*1299C>T
NM_006096.4(NDRG1):c.*1300G>C
NM_006096.4(NDRG1):c.*1339C>T
NM_006096.4(NDRG1):c.*1361C>A
NM_006096.4(NDRG1):c.*1621C>T
NM_006096.4(NDRG1):c.*228G>A
NM_006096.4(NDRG1):c.*308C>T
NM_006096.4(NDRG1):c.*31T>G
NM_006096.4(NDRG1):c.*392G>A
NM_006096.4(NDRG1):c.*403G>A
NM_006096.4(NDRG1):c.*48C>A
NM_006096.4(NDRG1):c.*525G>A
NM_006096.4(NDRG1):c.*791C>T
NM_006096.4(NDRG1):c.*854G>A
NM_006096.4(NDRG1):c.*91G>A
NM_006096.4(NDRG1):c.-99A>G
NM_006096.4(NDRG1):c.1000G>A (p.Val334Ile)
NM_006096.4(NDRG1):c.1041C>T (p.Ser347=)
NM_006096.4(NDRG1):c.1087C>T (p.Arg363Cys)
NM_006096.4(NDRG1):c.270C>T (p.Ala90=)
NM_006096.4(NDRG1):c.322G>A (p.Ala108Thr)
NM_006096.4(NDRG1):c.387T>G (p.Phe129Leu)
NM_006096.4(NDRG1):c.403A>G (p.Ile135Val) rs202118022
NM_006096.4(NDRG1):c.448G>T (p.Ala150Ser) rs150796527
NM_006096.4(NDRG1):c.4T>G (p.Ser2Ala)
NM_006096.4(NDRG1):c.528C>T (p.Ala176=) rs191237702
NM_006096.4(NDRG1):c.537+18C>T
NM_006096.4(NDRG1):c.583C>T (p.Leu195Phe)
NM_006096.4(NDRG1):c.594+10G>A rs751843731
NM_006096.4(NDRG1):c.594+9C>T rs373172944
NM_006096.4(NDRG1):c.634C>T (p.Arg212Cys)
NM_006096.4(NDRG1):c.874C>A (p.Leu292Ile) rs745520295
NM_006096.4(NDRG1):c.951G>A (p.Ser317=)
NM_006096.4(NDRG1):c.987C>T (p.Ala329=) rs778770054

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