ClinVar Miner

List of variants in gene NDRG1 reported as uncertain significance for Charcot-Marie-Tooth disease

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Total variants: 20
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HGVS dbSNP
NM_006096.3(NDRG1):c.1101C>T (p.Ser367=) rs201959970
NM_006096.3(NDRG1):c.1109C>G (p.Ala370Gly) rs367925853
NM_006096.3(NDRG1):c.1109C>T (p.Ala370Val) rs367925853
NM_006096.3(NDRG1):c.122A>G (p.His41Arg) rs2233318
NM_006096.3(NDRG1):c.538-1G>A rs11575976
NM_006096.3(NDRG1):c.63+6T>C rs199597649
NM_006096.3(NDRG1):c.664G>A (p.Gly222Ser) rs199995009
NM_006096.3(NDRG1):c.686A>G (p.Asn229Ser) rs137993172
NM_006096.4(NDRG1):c.1081C>G (p.Arg361Gly) rs0
NM_006096.4(NDRG1):c.12G>T (p.Glu4Asp) rs0
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.488T>C (p.Ile163Thr) rs0
NM_006096.4(NDRG1):c.4T>G (p.Ser2Ala) rs0
NM_006096.4(NDRG1):c.634C>T (p.Arg212Cys) rs0
NM_006096.4(NDRG1):c.635G>A (p.Arg212His) rs0
NM_006096.4(NDRG1):c.637C>A (p.Gln213Lys) rs0
NM_006096.4(NDRG1):c.703C>T rs772268356
NM_006096.4(NDRG1):c.706G>A (p.Asp236Asn) rs0
NM_006096.4(NDRG1):c.895G>A (p.Ala299Thr) rs0

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