ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
Download table as spreadsheet
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.*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=)
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=)
NM_181882.3(PRX):c.1695A>G (p.Pro565=)
NM_181882.3(PRX):c.1695A>T (p.Pro565=)
NM_181882.3(PRX):c.1818G>A (p.Pro606=)
NM_181882.3(PRX):c.1857A>G (p.Pro619=)
NM_181882.3(PRX):c.1950C>T (p.Pro650=)
NM_181882.3(PRX):c.1986C>T (p.Val662=)
NM_181882.3(PRX):c.2295C>T (p.Asp765=)
NM_181882.3(PRX):c.2400G>A (p.Lys800=)
NM_181882.3(PRX):c.2424G>A (p.Lys808=)
NM_181882.3(PRX):c.2649G>A (p.Glu883=)
NM_181882.3(PRX):c.2715C>A (p.Thr905=) rs188765166
NM_181882.3(PRX):c.2724G>T (p.Leu908=)
NM_181882.3(PRX):c.300G>A (p.Val100=)
NM_181882.3(PRX):c.3195C>T (p.Ser1065=)
NM_181882.3(PRX):c.3423G>A (p.Ala1141=)
NM_181882.3(PRX):c.3519A>C (p.Thr1173=)
NM_181882.3(PRX):c.3768G>T (p.Val1256=)
NM_181882.3(PRX):c.4059GGA[5] (p.Glu1360_Glu1361del) rs139624657
NM_181882.3(PRX):c.4059GGA[8] (p.Glu1361dup) rs139624657
NM_181882.3(PRX):c.4146C>T (p.Gly1382=)
NM_181882.3(PRX):c.717G>T (p.Pro239=) rs761293957
NM_181882.3(PRX):c.861C>T (p.Ala287=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.