ClinVar Miner

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

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Gene type:
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Total variants: 62
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HGVS dbSNP
NM_020956.2(PRX):c.*1028C>A rs200033507
NM_020956.2(PRX):c.*1198G>A rs146323928
NM_020956.2(PRX):c.*1334G>T rs754081921
NM_020956.2(PRX):c.*1486C>T rs76960467
NM_020956.2(PRX):c.*1705A>G rs777104457
NM_020956.2(PRX):c.*1779T>C rs149715830
NM_020956.2(PRX):c.*1783G>A rs567690884
NM_020956.2(PRX):c.*1830G>A rs139586219
NM_020956.2(PRX):c.*1856G>A rs61733448
NM_020956.2(PRX):c.*2032C>T rs751816156
NM_020956.2(PRX):c.*2169C>T rs118003416
NM_020956.2(PRX):c.*2248C>T rs56743160
NM_020956.2(PRX):c.*2306G>A rs116855701
NM_020956.2(PRX):c.*2459G>A rs147587689
NM_020956.2(PRX):c.*2512G>A rs148655811
NM_020956.2(PRX):c.*2846C>A rs375201649
NM_020956.2(PRX):c.*2980C>T rs201792838
NM_020956.2(PRX):c.*3578G>A rs148939995
NM_020956.2(PRX):c.*3701C>T rs147826200
NM_020956.2(PRX):c.*3907C>T rs139950446
NM_020956.2(PRX):c.*3913G>A rs202119177
NM_020956.2(PRX):c.*4007G>C rs146061247
NM_020956.2(PRX):c.*4036C>G rs577796628
NM_020956.2(PRX):c.*4051G>A rs143289108
NM_020956.2(PRX):c.*4144G>A rs140109585
NM_020956.2(PRX):c.*4152C>T rs142762689
NM_020956.2(PRX):c.*4249G>C rs76088917
NM_020956.2(PRX):c.*4264_*4266GGA[5] rs139624657
NM_020956.2(PRX):c.*650G>A rs142436391
NM_020956.2(PRX):c.*745G>A rs371243093
NM_020956.2(PRX):c.*759G>A rs76756143
NM_020956.2(PRX):c.*802C>T rs144157275
NM_020956.2(PRX):c.*847C>A rs551628239
NM_020956.2(PRX):c.*952C>T rs3814289
NM_020956.2(PRX):c.*999G>T rs374837022
NM_020956.2(PRX):c.-20A>C rs780315081
NM_020956.2(PRX):c.336G>A (p.Val112=) rs369268369
NM_181882.3(PRX):c.1077C>G (p.Arg359=) rs0
NM_181882.3(PRX):c.1113A>G (p.Glu371=) rs137930942
NM_181882.3(PRX):c.1491C>G (p.Pro497=) rs1224453835
NM_181882.3(PRX):c.1638A>G (p.Val546=) rs0
NM_181882.3(PRX):c.1695A>G (p.Pro565=) rs0
NM_181882.3(PRX):c.1695A>T (p.Pro565=) rs0
NM_181882.3(PRX):c.1818G>A (p.Pro606=) rs0
NM_181882.3(PRX):c.1857A>G (p.Pro619=) rs0
NM_181882.3(PRX):c.1950C>T (p.Pro650=) rs0
NM_181882.3(PRX):c.1986C>T (p.Val662=) rs0
NM_181882.3(PRX):c.2295C>T (p.Asp765=) rs0
NM_181882.3(PRX):c.2400G>A (p.Lys800=) rs0
NM_181882.3(PRX):c.2424G>A (p.Lys808=) rs0
NM_181882.3(PRX):c.2649G>A (p.Glu883=) rs0
NM_181882.3(PRX):c.2715C>A (p.Thr905=) rs188765166
NM_181882.3(PRX):c.2724G>T (p.Leu908=) rs0
NM_181882.3(PRX):c.300G>A (p.Val100=) rs0
NM_181882.3(PRX):c.3195C>T (p.Ser1065=) rs0
NM_181882.3(PRX):c.3423G>A (p.Ala1141=) rs0
NM_181882.3(PRX):c.3519A>C (p.Thr1173=) rs0
NM_181882.3(PRX):c.3768G>T (p.Val1256=) rs0
NM_181882.3(PRX):c.4059_4061GGA[8] (p.Glu1361dup) rs139624657
NM_181882.3(PRX):c.4146C>T (p.Gly1382=) rs0
NM_181882.3(PRX):c.717G>T (p.Pro239=) rs761293957
NM_181882.3(PRX):c.861C>T (p.Ala287=) rs0

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