ClinVar Miner

List of variants in gene PRX reported as likely benign for demyelinating hereditary motor and sensory neuropathy

Included ClinVar conditions (46):
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Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP
NM_020956.2(PRX):c.*3578G>A rs148939995
NM_020956.2(PRX):c.133C>G (p.Arg45Gly) rs115090201
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.237C>T (p.Asp79=) rs376174896
NM_020956.2(PRX):c.27+8C>A rs769214562
NM_020956.2(PRX):c.306C>T (p.Thr102=) rs744389
NM_020956.2(PRX):c.336G>A (p.Val112=) rs369268369
NM_020956.2(PRX):c.75G>A (p.Ala25=) rs766160977
NM_181882.2(PRX):c.1026A>C (p.Ala342=) rs150772010
NM_181882.2(PRX):c.1051C>T (p.Pro351Ser) rs73933276
NM_181882.2(PRX):c.1129G>T (p.Val377Leu) rs754081921
NM_181882.2(PRX):c.1215C>T (p.Pro405=) rs377184301
NM_181882.2(PRX):c.1369G>A (p.Glu457Lys) rs142064826
NM_181882.2(PRX):c.1461G>A (p.Pro487=) rs757009052
NM_181882.2(PRX):c.1500A>G (p.Ser500=) rs777104457
NM_181882.2(PRX):c.1578G>A (p.Ser526=) rs567690884
NM_181882.2(PRX):c.1624C>T (p.Arg542Trp) rs201337455
NM_181882.2(PRX):c.1625G>A (p.Arg542Gln) rs139586219
NM_181882.2(PRX):c.1651G>A (p.Val551Met) rs61733448
NM_181882.2(PRX):c.1935C>T (p.Pro645=) rs763132536
NM_181882.2(PRX):c.1964C>T (p.Pro655Leu) rs118003416
NM_181882.2(PRX):c.1980G>A (p.Pro660=) rs777413169
NM_181882.2(PRX):c.2017A>G (p.Met673Val) rs61735531
NM_181882.2(PRX):c.2229C>T (p.Pro743=) rs144975214
NM_181882.2(PRX):c.2254G>A (p.Glu752Lys) rs147587689
NM_181882.2(PRX):c.2292C>T (p.Pro764=) rs142637195
NM_181882.2(PRX):c.2307G>A (p.Pro769=) rs148655811
NM_181882.2(PRX):c.2619C>T (p.Ala873=) rs761066015
NM_181882.2(PRX):c.2641C>A (p.Arg881=) rs375201649
NM_181882.2(PRX):c.2727C>T (p.Pro909=) rs61735546
NM_181882.2(PRX):c.2730C>T (p.Ala910=) rs878855283
NM_181882.2(PRX):c.2916G>T (p.Gly972=) rs1555800751
NM_181882.2(PRX):c.2943G>A (p.Gly981=) rs142228732
NM_181882.2(PRX):c.3145G>A (p.Gly1049Ser) rs186086914
NM_181882.2(PRX):c.3218A>G (p.Glu1073Gly) rs61733451
NM_181882.2(PRX):c.3248C>G (p.Pro1083Arg) rs3745202
NM_181882.2(PRX):c.3288C>A (p.Ile1096=) rs375122789
NM_181882.2(PRX):c.3375C>T (p.Gly1125=) rs755560307
NM_181882.2(PRX):c.3549C>T (p.Tyr1183=) rs367876251
NM_181882.2(PRX):c.3702C>T (p.Gly1234=) rs139950446
NM_181882.2(PRX):c.3708G>A (p.Ala1236=) rs202119177
NM_181882.2(PRX):c.3804C>T (p.Ala1268=) rs553825184
NM_181882.2(PRX):c.3831C>G (p.Pro1277=) rs577796628
NM_181882.2(PRX):c.3838G>C (p.Glu1280Gln) rs146205352
NM_181882.2(PRX):c.3867C>T (p.Ala1289=) rs759245840
NM_181882.2(PRX):c.3939G>A (p.Leu1313=) rs140109585
NM_181882.2(PRX):c.3947C>T (p.Ala1316Val) rs142762689
NM_181882.2(PRX):c.4224C>G (p.Pro1408=) rs1555800370
NM_181882.2(PRX):c.4317C>T (p.Ser1439=) rs372280596
NM_181882.2(PRX):c.445G>A (p.Ala149Thr) rs142436391
NM_181882.2(PRX):c.499C>T (p.Arg167Cys) rs10425452
NM_181882.2(PRX):c.540G>A (p.Pro180=) rs371243093
NM_181882.2(PRX):c.580C>T (p.Arg194Cys) rs45521038
NM_181882.2(PRX):c.597C>G (p.Ala199=) rs144157275
NM_181882.2(PRX):c.642C>A (p.Pro214=) rs551628239
NM_181882.2(PRX):c.719G>A (p.Arg240Gln) rs77917609
NM_181882.2(PRX):c.731C>T (p.Ala244Val) rs118071705
NM_181882.2(PRX):c.747C>T (p.Pro249=) rs3814289
NM_181882.2(PRX):c.771C>T (p.Ala257=) rs1555801357
NM_181882.2(PRX):c.794G>T (p.Gly265Val) rs374837022
NM_181882.2(PRX):c.936A>G (p.Leu312=) rs752086513
NM_181882.2(PRX):c.993G>A (p.Pro331=) rs146323928

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