ClinVar Miner

List of variants in gene PRX reported by PreventionGenetics, part of Exact Sciences

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_181882.3(PRX):c.3394G>A (p.Gly1132Arg) rs268674 0.95976
NM_181882.3(PRX):c.445G>A (p.Ala149Thr) rs142436391 0.00193
NM_181882.3(PRX):c.2254G>A (p.Glu752Lys) rs147587689 0.00185
NM_181882.3(PRX):c.3838G>C (p.Glu1280Gln) rs146205352 0.00135
NM_181882.3(PRX):c.823C>A (p.Leu275Ile) rs200033507 0.00108
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.960G>A (p.Ser320=) rs775367319 0.00033
NM_181882.3(PRX):c.2106C>T (p.Pro702=) rs183461864 0.00027
NM_181882.3(PRX):c.2190C>G (p.Pro730=) rs1336238948 0.00021
NM_181882.3(PRX):c.3549C>T (p.Tyr1183=) rs367876251 0.00017
NM_181882.3(PRX):c.1578G>A (p.Ser526=) rs567690884 0.00016
NM_181882.3(PRX):c.2449C>T (p.Arg817Cys) rs147441856 0.00014
NM_181882.3(PRX):c.1836C>T (p.Ala612=) rs574899855 0.00010
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.4017C>A (p.Ser1339Arg) rs758057597 0.00008
NM_181882.3(PRX):c.2164A>G (p.Met722Val) rs376309142 0.00005
NM_181882.3(PRX):c.2100C>T (p.Ala700=) rs757528702 0.00004
NM_181882.3(PRX):c.1461G>A (p.Pro487=) rs757009052 0.00003
NM_181882.3(PRX):c.1827C>T (p.Pro609=) rs751816156 0.00003
NM_181882.3(PRX):c.3707C>T (p.Ala1236Val) rs142501082 0.00003
NM_181882.3(PRX):c.840G>A (p.Pro280=) rs773272074 0.00003
NM_181882.3(PRX):c.502C>T (p.Arg168Trp) rs374193988 0.00002
NM_181882.3(PRX):c.-237C>T
NM_181882.3(PRX):c.1168del (p.Arg390fs)
NM_181882.3(PRX):c.1279A>C (p.Ile427Leu)
NM_181882.3(PRX):c.1900A>G (p.Met634Val) rs201204029
NM_181882.3(PRX):c.2247A>G (p.Lys749=)
NM_181882.3(PRX):c.3900C>T (p.Ala1300=)
NM_181882.3(PRX):c.861C>T (p.Ala287=) rs535958285

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