ClinVar Miner

List of variants in gene PRX reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_181882.3(PRX):c.-243+159C>A rs268665 0.01116
NM_181882.3(PRX):c.185-167C>T rs117182727 0.00882
NM_181882.3(PRX):c.382-96C>T rs77238923 0.00553
NM_181882.3(PRX):c.-236G>A rs552436076 0.00317
NM_181882.3(PRX):c.554G>A (p.Arg185His) rs76756143 0.00292
NM_181882.3(PRX):c.3846G>A (p.Ser1282=) rs143289108 0.00288
NM_181882.3(PRX):c.892C>T (p.Pro298Ser) rs185112635 0.00262
NM_181882.3(PRX):c.2043C>T (p.Pro681=) rs56743160 0.00259
NM_181882.3(PRX):c.3373G>A (p.Gly1125Ser) rs148939995 0.00191
NM_181882.3(PRX):c.2254G>A (p.Glu752Lys) rs147587689 0.00185
NM_181882.3(PRX):c.719G>A (p.Arg240Gln) rs77917609 0.00140
NM_181882.3(PRX):c.3947C>T (p.Ala1316Val) rs142762689 0.00138
NM_181882.3(PRX):c.1574T>C (p.Val525Ala) rs149715830 0.00136
NM_181882.3(PRX):c.823C>A (p.Leu275Ile) rs200033507 0.00108
NM_181882.3(PRX):c.3110A>G (p.Glu1037Gly) rs148600818 0.00099
NM_181882.3(PRX):c.3496C>T (p.Pro1166Ser) rs147826200 0.00093
NM_181882.3(PRX):c.2494G>C (p.Val832Leu) rs116139153 0.00077
NM_181882.3(PRX):c.1651G>A (p.Val551Met) rs61733448 0.00047
NM_181882.3(PRX):c.2832T>C (p.Ala944=) rs145226687 0.00046
NM_181882.3(PRX):c.381+18G>A rs147585269 0.00046
NM_181882.3(PRX):c.2101G>A (p.Val701Met) rs116855701 0.00041
NM_181882.3(PRX):c.540G>A (p.Pro180=) rs371243093 0.00036
NM_181882.3(PRX):c.3708G>A (p.Ala1236=) rs202119177 0.00035
NM_181882.3(PRX):c.960G>A (p.Ser320=) rs775367319 0.00033
NM_181882.3(PRX):c.285C>T (p.Cys95=) rs531527827 0.00032
NM_181882.3(PRX):c.993G>A (p.Pro331=) rs146323928 0.00022
NM_181882.3(PRX):c.1624C>T (p.Arg542Trp) rs201337455 0.00018
NM_181882.3(PRX):c.-20A>C rs780315081 0.00015
NM_181882.3(PRX):c.-19G>A rs758480824 0.00009
NM_181882.3(PRX):c.2265G>A (p.Leu755=) rs370753668 0.00009
NM_181882.3(PRX):c.1369G>A (p.Glu457Lys) rs142064826 0.00008
NM_181882.3(PRX):c.1500A>G (p.Ser500=) rs777104457 0.00006
NM_181882.3(PRX):c.2164A>G (p.Met722Val) rs376309142 0.00005
NM_181882.3(PRX):c.237C>T (p.Asp79=) rs376174896 0.00005
NM_181882.3(PRX):c.642C>A (p.Pro214=) rs551628239 0.00005
NM_181882.3(PRX):c.3775G>A (p.Glu1259Lys) rs751742049 0.00004
NM_181882.3(PRX):c.3852C>T (p.Ser1284=) rs567324732 0.00004
NM_181882.3(PRX):c.1539G>A (p.Pro513=) rs187786861 0.00003
NM_181882.3(PRX):c.1827C>T (p.Pro609=) rs751816156 0.00003
NM_181882.3(PRX):c.2775C>T (p.Val925=) rs201792838 0.00003
NM_181882.3(PRX):c.3939G>A (p.Leu1313=) rs140109585 0.00003
NM_181882.3(PRX):c.4152G>A (p.Ala1384=) rs756887163 0.00003
NM_181882.3(PRX):c.1080T>C (p.Leu360=) rs199882125 0.00002
NM_181882.3(PRX):c.2496A>T (p.Val832=) rs777527307 0.00002
NM_181882.3(PRX):c.4206C>T (p.Pro1402=) rs771992595 0.00002
NM_181882.3(PRX):c.-9A>C rs200766544 0.00001
NM_181882.3(PRX):c.1113A>G (p.Glu371=) rs137930942 0.00001
NM_181882.3(PRX):c.2268G>A (p.Pro756=) rs570227186 0.00001
NM_181882.3(PRX):c.2307G>A (p.Pro769=) rs148655811 0.00001
NM_181882.3(PRX):c.2619C>T (p.Ala873=) rs761066015 0.00001
NM_181882.3(PRX):c.27+13G>A rs780222566 0.00001
NM_181882.3(PRX):c.3366G>A (p.Gln1122=) rs952933935 0.00001
NM_181882.3(PRX):c.354G>A (p.Lys118=) rs1044654884 0.00001
NM_181882.3(PRX):c.4350G>A (p.Pro1450=) rs768051108 0.00001
NC_000019.10:g.40413554dup rs112426896
NM_181882.3(PRX):c.-199+7G>A rs541213273
NM_181882.3(PRX):c.-99-20C>G rs148577357
NM_181882.3(PRX):c.1002G>T (p.Gly334=) rs755650027
NM_181882.3(PRX):c.1680A>C (p.Ser560=) rs1194012098
NM_181882.3(PRX):c.1725G>A (p.Pro575=) rs1043949955
NM_181882.3(PRX):c.2641C>A (p.Arg881=) rs375201649
NM_181882.3(PRX):c.27+12C>T rs376353333
NM_181882.3(PRX):c.2967C>G (p.Leu989=) rs1057522657
NM_181882.3(PRX):c.3831C>G (p.Pro1277=) rs577796628
NM_181882.3(PRX):c.3856G>A (p.Gly1286Ser) rs555523161

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