ClinVar Miner

List of variants in gene PRX reported as likely 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: 116
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HGVS dbSNP
NM_020956.2(PRX):c.*1028C>A rs200033507
NM_020956.2(PRX):c.*1141A>G rs752086513
NM_020956.2(PRX):c.*1198G>A rs146323928
NM_020956.2(PRX):c.*1231A>C rs150772010
NM_020956.2(PRX):c.*1334G>T rs754081921
NM_020956.2(PRX):c.*1420C>T rs377184301
NM_020956.2(PRX):c.*1486C>T rs76960467
NM_020956.2(PRX):c.*1574G>A rs142064826
NM_020956.2(PRX):c.*1666G>A rs757009052
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.*1829C>T rs201337455
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.*2041C>T rs574899855
NM_020956.2(PRX):c.*2140C>T rs763132536
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.*2434C>T rs144975214
NM_020956.2(PRX):c.*2459G>A rs147587689
NM_020956.2(PRX):c.*2497C>T rs142637195
NM_020956.2(PRX):c.*2512G>A rs148655811
NM_020956.2(PRX):c.*2699G>C rs116139153
NM_020956.2(PRX):c.*2846C>A rs375201649
NM_020956.2(PRX):c.*2935C>T rs878855283
NM_020956.2(PRX):c.*2980C>T rs201792838
NM_020956.2(PRX):c.*3037T>C rs145226687
NM_020956.2(PRX):c.*3121G>T rs1555800751
NM_020956.2(PRX):c.*3315A>G rs148600818
NM_020956.2(PRX):c.*3350G>A rs186086914
NM_020956.2(PRX):c.*3493C>A rs375122789
NM_020956.2(PRX):c.*3571G>A rs952933935
NM_020956.2(PRX):c.*3578G>A rs148939995
NM_020956.2(PRX):c.*3580C>T rs755560307
NM_020956.2(PRX):c.*3701C>T rs147826200
NM_020956.2(PRX):c.*3754C>T rs367876251
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.*4009C>T rs553825184
NM_020956.2(PRX):c.*4036C>G rs577796628
NM_020956.2(PRX):c.*4043G>C rs146205352
NM_020956.2(PRX):c.*4051G>A rs143289108
NM_020956.2(PRX):c.*4072C>T rs759245840
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.*4357G>A rs756887163
NM_020956.2(PRX):c.*4429C>G rs1555800370
NM_020956.2(PRX):c.*4522C>T rs372280596
NM_020956.2(PRX):c.*4735C>T rs189487790
NM_020956.2(PRX):c.*650G>A rs142436391
NM_020956.2(PRX):c.*698C>T rs555499679
NM_020956.2(PRX):c.*704C>T rs10425452
NM_020956.2(PRX):c.*745G>A rs371243093
NM_020956.2(PRX):c.*759G>A rs76756143
NM_020956.2(PRX):c.*785C>T rs45521038
NM_020956.2(PRX):c.*802C>G rs144157275
NM_020956.2(PRX):c.*802C>T rs144157275
NM_020956.2(PRX):c.*847C>A rs551628239
NM_020956.2(PRX):c.*924G>A rs77917609
NM_020956.2(PRX):c.*936C>T rs118071705
NM_020956.2(PRX):c.*952C>T rs3814289
NM_020956.2(PRX):c.*976C>T rs1555801357
NM_020956.2(PRX):c.*999G>T rs374837022
NM_020956.2(PRX):c.-20A>C rs780315081
NM_020956.2(PRX):c.-236G>A rs552436076
NM_020956.2(PRX):c.102A>C (p.Val34=) rs761347226
NM_020956.2(PRX):c.185-6C>T rs747043680
NM_020956.2(PRX):c.185-8G>A rs768814221
NM_020956.2(PRX):c.185-9C>T rs1555801635
NM_020956.2(PRX):c.27+8C>A rs769214562
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.1308G>A (p.Val436=) rs771496284
NM_181882.3(PRX):c.1491C>G (p.Pro497=) rs1224453835
NM_181882.3(PRX):c.1638A>G (p.Val546=)
NM_181882.3(PRX):c.1647G>C (p.Pro549=) rs202113722
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.1980G>T (p.Pro660=) rs777413169
NM_181882.3(PRX):c.1986C>T (p.Val662=)
NM_181882.3(PRX):c.2044G>A (p.Glu682Lys) rs761277865
NM_181882.3(PRX):c.2047G>A (p.Val683Met) rs575075163
NM_181882.3(PRX):c.2100C>T (p.Ala700=) rs757528702
NM_181882.3(PRX):c.2106C>T (p.Pro702=) rs183461864
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.2425C>T (p.Leu809=) rs145272609
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.3237T>C (p.Asp1079=) rs774823527
NM_181882.3(PRX):c.3294G>A (p.Glu1098=) rs1599651349
NM_181882.3(PRX):c.3423G>A (p.Ala1141=)
NM_181882.3(PRX):c.3519A>C (p.Thr1173=)
NM_181882.3(PRX):c.3531A>G (p.Ala1177=) rs1465687338
NM_181882.3(PRX):c.3588A>G (p.Gly1196=) rs372745419
NM_181882.3(PRX):c.3768G>T (p.Val1256=)
NM_181882.3(PRX):c.4059_4061GGA[8] (p.Glu1361dup) rs139624657
NM_181882.3(PRX):c.4146C>T (p.Gly1382=)
NM_181882.3(PRX):c.624C>T (p.Ala208=) rs777019611
NM_181882.3(PRX):c.717G>T (p.Pro239=) rs761293957
NM_181882.3(PRX):c.861C>T (p.Ala287=)
NM_181882.3(PRX):c.934C>T (p.Leu312=) rs369792380

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