ClinVar Miner

List of variants in gene PRX studied for not specified

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Total variants: 67
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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.2645T>C (p.Val882Ala) rs268671 0.59048
NM_181882.3(PRX):c.2655T>C (p.Pro885=) rs268672 0.56968
NM_181882.3(PRX):c.2763A>G (p.Ile921Met) rs268673 0.36279
NM_181882.3(PRX):c.3248C>G (p.Pro1083Arg) rs3745202 0.12427
NM_181882.3(PRX):c.306C>T (p.Thr102=) rs744389 0.12409
NM_181882.3(PRX):c.2017A>G (p.Met673Val) rs61735531 0.03414
NM_181882.3(PRX):c.2727C>T (p.Pro909=) rs61735546 0.03308
NM_181882.3(PRX):c.731C>T (p.Ala244Val) rs118071705 0.01410
NM_181882.3(PRX):c.3218A>G (p.Glu1073Gly) rs61733451 0.01078
NM_181882.3(PRX):c.2469G>A (p.Ala823=) rs61733450 0.00644
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.1216G>A (p.Ala406Thr) rs117336941 0.00456
NM_181882.3(PRX):c.-236G>A rs552436076 0.00317
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.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.3186G>T (p.Lys1062Asn) rs139188673 0.00105
NM_181882.3(PRX):c.3496C>T (p.Pro1166Ser) rs147826200 0.00093
NM_181882.3(PRX):c.2548C>G (p.Pro850Ala) rs141686828 0.00078
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.3708G>A (p.Ala1236=) rs202119177 0.00035
NM_181882.3(PRX):c.960G>A (p.Ser320=) rs775367319 0.00033
NM_181882.3(PRX):c.993G>A (p.Pro331=) rs146323928 0.00022
NM_181882.3(PRX):c.3209G>A (p.Arg1070Gln) rs146222815 0.00019
NM_181882.3(PRX):c.3549C>T (p.Tyr1183=) rs367876251 0.00017
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.1500A>G (p.Ser500=) rs777104457 0.00006
NM_181882.3(PRX):c.2296G>A (p.Val766Met) rs763619423 0.00006
NM_181882.3(PRX):c.4219T>G (p.Ser1407Ala) rs146468976 0.00006
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.3768G>T (p.Val1256=) rs367862999 0.00004
NM_181882.3(PRX):c.3852C>T (p.Ser1284=) rs567324732 0.00004
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.4152G>A (p.Ala1384=) rs756887163 0.00003
NM_181882.3(PRX):c.1080T>C (p.Leu360=) rs199882125 0.00002
NM_181882.3(PRX):c.2892C>G (p.Ile964Met) rs758668778 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.1529T>C (p.Met510Thr) rs780375180 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.3351C>T (p.Ala1117=) rs535934188 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.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.3248C>T (p.Pro1083Leu) rs3745202
NM_181882.3(PRX):c.3856G>A (p.Gly1286Ser) rs555523161
NM_181882.3(PRX):c.4059GGA[5] (p.Glu1360_Glu1361del) rs139624657
NM_181882.3(PRX):c.4172G>A (p.Arg1391Gln) rs917161355

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