ClinVar Miner

List of variants in gene PRX reported as likely benign by Molecular Genetics Laboratory, London Health Sciences Centre

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Gene type:
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Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_181882.3(PRX):c.4044G>C (p.Gly1348=) rs76088917 0.00620
NM_181882.3(PRX):c.1281C>T (p.Ile427=) rs76960467 0.00551
NM_181882.3(PRX):c.3802G>C (p.Ala1268Pro) rs146061247 0.00332
NM_181882.3(PRX):c.554G>A (p.Arg185His) rs76756143 0.00292
NM_181882.3(PRX):c.3702C>T (p.Gly1234=) rs139950446 0.00291
NM_181882.3(PRX):c.3846G>A (p.Ser1282=) rs143289108 0.00288
NM_181882.3(PRX):c.2043C>T (p.Pro681=) rs56743160 0.00259
NM_181882.3(PRX):c.445G>A (p.Ala149Thr) rs142436391 0.00193
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.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.3496C>T (p.Pro1166Ser) rs147826200 0.00093
NM_181882.3(PRX):c.1964C>T (p.Pro655Leu) rs118003416 0.00059
NM_181882.3(PRX):c.1625G>A (p.Arg542Gln) rs139586219 0.00058
NM_181882.3(PRX):c.1651G>A (p.Val551Met) rs61733448 0.00047
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.993G>A (p.Pro331=) rs146323928 0.00022
NM_181882.3(PRX):c.1578G>A (p.Ser526=) rs567690884 0.00016
NM_181882.3(PRX):c.-20A>C rs780315081 0.00015
NM_181882.3(PRX):c.794G>T (p.Gly265Val) rs374837022 0.00013
NM_181882.3(PRX):c.1129G>T (p.Val377Leu) rs754081921 0.00011
NM_181882.3(PRX):c.1500A>G (p.Ser500=) rs777104457 0.00006
NM_181882.3(PRX):c.597C>T (p.Ala199=) rs144157275 0.00006
NM_181882.3(PRX):c.642C>A (p.Pro214=) rs551628239 0.00005
NM_181882.3(PRX):c.2715C>A (p.Thr905=) rs188765166 0.00004
NM_181882.3(PRX):c.3768G>T (p.Val1256=) rs367862999 0.00004
NM_181882.3(PRX):c.747C>T (p.Pro249=) rs3814289 0.00004
NM_181882.3(PRX):c.1827C>T (p.Pro609=) rs751816156 0.00003
NM_181882.3(PRX):c.2295C>T (p.Asp765=) rs377360814 0.00003
NM_181882.3(PRX):c.2649G>A (p.Glu883=) rs747871484 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.1950C>T (p.Pro650=) rs761824931 0.00002
NM_181882.3(PRX):c.336G>A (p.Val112=) rs369268369 0.00002
NM_181882.3(PRX):c.3423G>A (p.Ala1141=) rs370800046 0.00002
NM_181882.3(PRX):c.1113A>G (p.Glu371=) rs137930942 0.00001
NM_181882.3(PRX):c.2307G>A (p.Pro769=) rs148655811 0.00001
NM_181882.3(PRX):c.1077C>G (p.Arg359=) rs1357784205
NM_181882.3(PRX):c.1491C>G (p.Pro497=) rs1224453835
NM_181882.3(PRX):c.1638A>G (p.Val546=) rs774541568
NM_181882.3(PRX):c.1695A>G (p.Pro565=) rs1000191235
NM_181882.3(PRX):c.1695A>T (p.Pro565=) rs1000191235
NM_181882.3(PRX):c.1818G>A (p.Pro606=) rs768022787
NM_181882.3(PRX):c.1857A>G (p.Pro619=) rs779898963
NM_181882.3(PRX):c.1986C>T (p.Val662=) rs1279008110
NM_181882.3(PRX):c.2400G>A (p.Lys800=) rs2079430394
NM_181882.3(PRX):c.2424G>A (p.Lys808=) rs2079430194
NM_181882.3(PRX):c.2641C>A (p.Arg881=) rs375201649
NM_181882.3(PRX):c.2724G>T (p.Leu908=) rs2079426389
NM_181882.3(PRX):c.300G>A (p.Val100=) rs747794739
NM_181882.3(PRX):c.3195C>T (p.Ser1065=) rs2079420208
NM_181882.3(PRX):c.3519A>C (p.Thr1173=) rs567285703
NM_181882.3(PRX):c.3831C>G (p.Pro1277=) rs577796628
NM_181882.3(PRX):c.4059GGA[5] (p.Glu1360_Glu1361del) rs139624657
NM_181882.3(PRX):c.4059GGA[8] (p.Glu1361dup) rs139624657
NM_181882.3(PRX):c.4146C>T (p.Gly1382=) rs2079405908
NM_181882.3(PRX):c.717G>T (p.Pro239=) rs761293957
NM_181882.3(PRX):c.861C>T (p.Ala287=) rs535958285

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