ClinVar Miner

List of variants in gene PRX reported as benign for Charcot-Marie-Tooth disease, demyelinating, type 4F

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Total variants: 7
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HGVS dbSNP
NM_020956.2(PRX):c.*1688G>C rs146789340
NM_020956.2(PRX):c.306C>T (p.Thr102=) rs744389
NM_181882.2(PRX):c.1216G>A (p.Ala406Thr) rs117336941
NM_181882.2(PRX):c.2655T>C (p.Pro885=) rs268672
NM_181882.2(PRX):c.2763A>G (p.Ile921Met) rs268673
NM_181882.2(PRX):c.3248C>G (p.Pro1083Arg) rs3745202
NM_181882.2(PRX):c.4059_4061GGA[6] (p.Glu1361del) rs139624657

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