ClinVar Miner

List of variants in gene PRX reported as likely benign for Charcot-Marie-Tooth disease type 4

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Gene type:
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Total variants: 28
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HGVS dbSNP
NM_020956.2(PRX):c.*1141A>G rs752086513
NM_020956.2(PRX):c.*1231A>C rs150772010
NM_020956.2(PRX):c.*1256C>T rs73933276
NM_020956.2(PRX):c.*1420C>T rs377184301
NM_020956.2(PRX):c.*1574G>A rs142064826
NM_020956.2(PRX):c.*1666G>A rs757009052
NM_020956.2(PRX):c.*1830G>A rs139586219
NM_020956.2(PRX):c.*2140C>T rs763132536
NM_020956.2(PRX):c.*2169C>T rs118003416
NM_020956.2(PRX):c.*2222A>G rs61735531
NM_020956.2(PRX):c.*2497C>T rs142637195
NM_020956.2(PRX):c.*2512G>A rs148655811
NM_020956.2(PRX):c.*2932C>T rs61735546
NM_020956.2(PRX):c.*3121G>T rs1555800751
NM_020956.2(PRX):c.*3423A>G rs61733451
NM_020956.2(PRX):c.*3453C>G rs3745202
NM_020956.2(PRX):c.*3907C>T rs139950446
NM_020956.2(PRX):c.*4009C>T rs553825184
NM_020956.2(PRX):c.*4429C>G rs1555800370
NM_020956.2(PRX):c.*802C>G rs144157275
NM_020956.2(PRX):c.*936C>T rs118071705
NM_020956.2(PRX):c.*976C>T rs1555801357
NM_020956.2(PRX):c.*999G>T rs374837022
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.306C>T (p.Thr102=) rs744389

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