ClinVar Miner

List of variants in gene PRX reported as benign for Charcot-Marie-Tooth disease

Included ClinVar conditions (137):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_020956.2(PRX):c.*1097C>T rs185112635
NM_020956.2(PRX):c.*1256C>T rs73933276
NM_020956.2(PRX):c.*1421G>A rs117336941
NM_020956.2(PRX):c.*1486C>T rs76960467
NM_020956.2(PRX):c.*1688G>C rs146789340
NM_020956.2(PRX):c.*1830G>A rs139586219
NM_020956.2(PRX):c.*2041C>T rs574899855
NM_020956.2(PRX):c.*2169C>T rs118003416
NM_020956.2(PRX):c.*2222A>G rs61735531
NM_020956.2(PRX):c.*2248C>T rs56743160
NM_020956.2(PRX):c.*2306G>A rs116855701
NM_020956.2(PRX):c.*2674G>A rs61733450
NM_020956.2(PRX):c.*2850T>C rs268671
NM_020956.2(PRX):c.*2860T>C rs268672
NM_020956.2(PRX):c.*2932C>T rs61735546
NM_020956.2(PRX):c.*2968A>G rs268673
NM_020956.2(PRX):c.*2980C>T rs201792838
NM_020956.2(PRX):c.*3423A>G rs61733451
NM_020956.2(PRX):c.*3453C>G rs3745202
NM_020956.2(PRX):c.*3599G>A rs268674
NM_020956.2(PRX):c.*3907C>T rs139950446
NM_020956.2(PRX):c.*4007G>C rs146061247
NM_020956.2(PRX):c.*4051G>A rs143289108
NM_020956.2(PRX):c.*4057C>T rs567324732
NM_020956.2(PRX):c.*4249G>C rs76088917
NM_020956.2(PRX):c.*4264_*4266GGA[5] rs139624657
NM_020956.2(PRX):c.*4449_*4451dup rs771234852
NM_020956.2(PRX):c.*676G>A rs4803335
NM_020956.2(PRX):c.*698C>T rs555499679
NM_020956.2(PRX):c.*759G>A rs76756143
NM_020956.2(PRX):c.*936C>T rs118071705
NM_020956.2(PRX):c.133C>G (p.Arg45Gly) rs115090201
NM_020956.2(PRX):c.306C>T (p.Thr102=) rs744389
NM_181882.3(PRX):c.1539G>A (p.Pro513=) rs187786861
NM_181882.3(PRX):c.1836C>A (p.Ala612=)
NM_181882.3(PRX):c.3673G>A (p.Val1225Met)
NM_181882.3(PRX):c.944G>A (p.Arg315Gln) rs577197549

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