ClinVar Miner

List of variants in gene PRX reported as likely benign for not specified

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Gene type:
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Total variants: 60
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HGVS dbSNP
NM_020956.2(PRX):c.-19G>A rs758480824
NM_020956.2(PRX):c.-20A>C rs780315081
NM_020956.2(PRX):c.-236G>A rs552436076
NM_020956.2(PRX):c.-9A>C rs200766544
NM_020956.2(PRX):c.102A>C (p.Val34=) rs761347226
NM_020956.2(PRX):c.108C>A (p.Gly36=) rs771407657
NM_020956.2(PRX):c.133C>G (p.Arg45Gly) rs115090201
NM_020956.2(PRX):c.237C>T (p.Asp79=) rs376174896
NM_020956.2(PRX):c.27+12C>T rs376353333
NM_020956.2(PRX):c.27+13G>A rs780222566
NM_020956.2(PRX):c.285C>T (p.Cys95=) rs531527827
NM_020956.2(PRX):c.306C>T (p.Thr102=) rs744389
NM_020956.2(PRX):c.354G>A (p.Lys118=) rs1044654884
NM_020956.2(PRX):c.399G>A (p.Pro133=) rs147585269
NM_181882.2(PRX):c.1002G>T (p.Gly334=) rs755650027
NM_181882.2(PRX):c.1080T>C (p.Leu360=) rs199882125
NM_181882.2(PRX):c.1500A>G (p.Ser500=) rs777104457
NM_181882.2(PRX):c.1574T>C (p.Val525Ala) rs149715830
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.1680A>C (p.Ser560=) rs1194012098
NM_181882.2(PRX):c.1725G>A (p.Pro575=) rs1043949955
NM_181882.2(PRX):c.1827C>T (p.Pro609=) rs751816156
NM_181882.2(PRX):c.1964C>T (p.Pro655Leu) rs118003416
NM_181882.2(PRX):c.2043C>T (p.Pro681=) rs56743160
NM_181882.2(PRX):c.2164A>G (p.Met722Val) rs376309142
NM_181882.2(PRX):c.2254G>A (p.Glu752Lys) rs147587689
NM_181882.2(PRX):c.2265G>A (p.Leu755=) rs370753668
NM_181882.2(PRX):c.2268G>A (p.Pro756=) rs570227186
NM_181882.2(PRX):c.2307G>A (p.Pro769=) rs148655811
NM_181882.2(PRX):c.2494G>C (p.Val832Leu) rs116139153
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.2645T>C (p.Val882Ala) rs268671
NM_181882.2(PRX):c.2655T>C (p.Pro885=) rs268672
NM_181882.2(PRX):c.2763A>G (p.Ile921Met) rs268673
NM_181882.2(PRX):c.2775C>T (p.Val925=) rs201792838
NM_181882.2(PRX):c.2832T>C (p.Ala944=) rs145226687
NM_181882.2(PRX):c.2967C>G (p.Leu989=) rs1057522657
NM_181882.2(PRX):c.3186G>T (p.Lys1062Asn) rs139188673
NM_181882.2(PRX):c.3248C>G (p.Pro1083Arg) rs3745202
NM_181882.2(PRX):c.3366G>A (p.Gln1122=) rs952933935
NM_181882.2(PRX):c.3373G>A (p.Gly1125Ser) rs148939995
NM_181882.2(PRX):c.3394G>A (p.Gly1132Arg) rs268674
NM_181882.2(PRX):c.3496C>T (p.Pro1166Ser) rs147826200
NM_181882.2(PRX):c.3708G>A (p.Ala1236=) rs202119177
NM_181882.2(PRX):c.3775G>A (p.Glu1259Lys) rs751742049
NM_181882.2(PRX):c.3802G>C (p.Ala1268Pro) rs146061247
NM_181882.2(PRX):c.3831C>G (p.Pro1277=) rs577796628
NM_181882.2(PRX):c.3846G>A (p.Ser1282=) rs143289108
NM_181882.2(PRX):c.3852C>T (p.Ser1284=) rs567324732
NM_181882.2(PRX):c.3856G>A (p.Gly1286Ser) rs555523161
NM_181882.2(PRX):c.3947C>T (p.Ala1316Val) rs142762689
NM_181882.2(PRX):c.4152G>A (p.Ala1384=) rs756887163
NM_181882.2(PRX):c.4206C>T (p.Pro1402=) rs771992595
NM_181882.2(PRX):c.540G>A (p.Pro180=) rs371243093
NM_181882.2(PRX):c.554G>A (p.Arg185His) rs76756143
NM_181882.2(PRX):c.642C>A (p.Pro214=) rs551628239
NM_181882.2(PRX):c.823C>A (p.Leu275Ile) rs200033507
NM_181882.2(PRX):c.960G>A (p.Ser320=) rs775367319

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