ClinVar Miner

List of variants in gene PPOX reported as uncertain significance

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Total variants: 149
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HGVS dbSNP gnomAD frequency
NM_001122764.3(PPOX):c.767C>G (p.Pro256Arg) rs12735723 0.00660
NM_001122764.3(PPOX):c.-246G>T rs114493458 0.00229
NM_001122764.3(PPOX):c.87+13C>T rs201155115 0.00078
NM_001122764.3(PPOX):c.617-6C>T rs200192089 0.00068
NM_001122764.3(PPOX):c.349C>T (p.Arg117Cys) rs190919484 0.00064
NM_001122764.3(PPOX):c.-251G>C rs368129128 0.00060
NM_001122764.3(PPOX):c.-1C>T rs148045152 0.00021
NM_001122764.3(PPOX):c.471+3G>A rs200920978 0.00021
NM_001122764.3(PPOX):c.360C>T (p.Pro120=) rs148730591 0.00017
NM_001122764.3(PPOX):c.668G>A (p.Arg223His) rs773741728 0.00010
NM_001122764.3(PPOX):c.322C>G (p.Leu108Val) rs144335388 0.00007
NM_001122764.3(PPOX):c.1248+4A>G rs775748399 0.00006
NM_001122764.3(PPOX):c.936G>A (p.Val312=) rs751511778 0.00006
NM_001122764.3(PPOX):c.-211C>A rs140693401 0.00005
NM_001122764.3(PPOX):c.1161G>C (p.Glu387Asp) rs140789684 0.00005
NM_001122764.3(PPOX):c.71C>T (p.Ala24Val) rs767225561 0.00005
NM_001122764.3(PPOX):c.1220C>T (p.Pro407Leu) rs772971420 0.00004
NM_001122764.3(PPOX):c.-149G>T rs186428034 0.00003
NM_001122764.3(PPOX):c.1390C>T (p.Arg464Cys) rs147480828 0.00003
NM_001122764.3(PPOX):c.799C>T (p.Arg267Cys) rs376945264 0.00003
NM_001122764.3(PPOX):c.800G>A (p.Arg267His) rs569993390 0.00003
NM_001122764.3(PPOX):c.1065G>C (p.Glu355Asp) rs759209914 0.00002
NM_001122764.3(PPOX):c.649C>T (p.Arg217Cys) rs751599052 0.00002
NM_001122764.3(PPOX):c.842A>G (p.His281Arg) rs1288034269 0.00002
NM_001122764.3(PPOX):c.844G>A (p.Val282Ile) rs145286580 0.00002
NM_001122764.3(PPOX):c.-180T>C rs886045450 0.00001
NM_001122764.3(PPOX):c.-2G>T rs779526273 0.00001
NM_001122764.3(PPOX):c.1003G>A (p.Val335Met) rs371812015 0.00001
NM_001122764.3(PPOX):c.1006C>G (p.Pro336Ala) rs1252661884 0.00001
NM_001122764.3(PPOX):c.1072G>A (p.Gly358Arg) rs374936130 0.00001
NM_001122764.3(PPOX):c.1139G>C (p.Ser380Thr) rs1269975991 0.00001
NM_001122764.3(PPOX):c.1175G>A (p.Arg392Gln) rs1001703993 0.00001
NM_001122764.3(PPOX):c.1259C>G (p.Pro420Arg) rs1661130879 0.00001
NM_001122764.3(PPOX):c.263G>T (p.Arg88Leu) rs943768360 0.00001
NM_001122764.3(PPOX):c.361C>A (p.Pro121Thr) rs532136485 0.00001
NM_001122764.3(PPOX):c.455G>A (p.Arg152His) rs758609195 0.00001
NM_001122764.3(PPOX):c.494G>A (p.Ser165Asn) rs762605289 0.00001
NM_001122764.3(PPOX):c.583C>T (p.Arg195Cys) rs768306133 0.00001
NM_001122764.3(PPOX):c.597G>T (p.Leu199=) rs769659160 0.00001
NM_001122764.3(PPOX):c.646A>G (p.Ile216Val) rs758572020 0.00001
NM_001122764.3(PPOX):c.650G>A (p.Arg217His) rs142407722 0.00001
NM_001122764.3(PPOX):c.661G>A (p.Ala221Thr) rs952064540 0.00001
NM_001122764.3(PPOX):c.667C>T (p.Arg223Cys) rs141116029 0.00001
NM_001122764.3(PPOX):c.689G>A (p.Arg230His) rs762308808 0.00001
NM_001122764.3(PPOX):c.70G>A (p.Ala24Thr) rs758933562 0.00001
NM_001122764.3(PPOX):c.742G>C (p.Gly248Arg) rs767772339 0.00001
NM_001122764.3(PPOX):c.79C>G (p.Pro27Ala) rs765694639 0.00001
NM_001122764.3(PPOX):c.910C>T (p.Arg304Cys) rs369952731 0.00001
NM_001122764.3(PPOX):c.988-3C>T rs751856317 0.00001
NM_001122764.3(PPOX):c.-174A>G rs886045451
NM_001122764.3(PPOX):c.100G>A (p.Glu34Lys) rs1659269072
NM_001122764.3(PPOX):c.1010C>G (p.Ser337Cys)
NM_001122764.3(PPOX):c.1014AGA[1] (p.Glu339del) rs2525339716
NM_001122764.3(PPOX):c.1018_1020del (p.Asp340del) rs1660909131
NM_001122764.3(PPOX):c.1024G>A (p.Gly342Arg)
NM_001122764.3(PPOX):c.1062T>C (p.Pro354=) rs771215757
NM_001122764.3(PPOX):c.1070A>C (p.Asp357Ala) rs2525341554
NM_001122764.3(PPOX):c.1087C>G (p.Leu363Val) rs886045455
NM_001122764.3(PPOX):c.1091_1092delinsAG (p.Arg364Lys) rs1660932843
NM_001122764.3(PPOX):c.1096A>C (p.Thr366Pro)
NM_001122764.3(PPOX):c.1097C>T (p.Thr366Ile) rs2525343102
NM_001122764.3(PPOX):c.1105C>A (p.Leu369Met)
NM_001122764.3(PPOX):c.1108_1119del (p.Gly370_Trp373del)
NM_001122764.3(PPOX):c.1114T>C (p.Ser372Pro) rs764652886
NM_001122764.3(PPOX):c.1115C>A (p.Ser372Tyr) rs1661012592
NM_001122764.3(PPOX):c.113G>C (p.Arg38Pro)
NM_001122764.3(PPOX):c.1154C>T (p.Ser385Phe) rs1484062472
NM_001122764.3(PPOX):c.1160A>G (p.Glu387Gly) rs2525350239
NM_001122764.3(PPOX):c.1198C>A (p.Gln400Lys) rs2101901963
NM_001122764.3(PPOX):c.1217T>C (p.Met406Thr) rs1479516823
NM_001122764.3(PPOX):c.1243C>T (p.His415Tyr) rs1301778268
NM_001122764.3(PPOX):c.1263G>C (p.Gln421His) rs370738994
NM_001122764.3(PPOX):c.1268C>T (p.Thr423Ile)
NM_001122764.3(PPOX):c.1281G>C (p.Trp427Cys) rs1057518798
NM_001122764.3(PPOX):c.1296A>G (p.Ser432=) rs1661206662
NM_001122764.3(PPOX):c.1315_1316delinsAT (p.Ala439Ile)
NM_001122764.3(PPOX):c.1316C>G (p.Ala439Gly) rs2525367722
NM_001122764.3(PPOX):c.1318C>T (p.His440Tyr) rs1661220672
NM_001122764.3(PPOX):c.1345G>A (p.Ala449Thr)
NM_001122764.3(PPOX):c.134C>A (p.Ser45Tyr) rs2525190265
NM_001122764.3(PPOX):c.1358G>A (p.Gly453Glu) rs1661249377
NM_001122764.3(PPOX):c.1361T>A (p.Val454Asp)
NM_001122764.3(PPOX):c.1391G>A (p.Arg464His)
NM_001122764.3(PPOX):c.1423C>G (p.Pro475Ala) rs1661292052
NM_001122764.3(PPOX):c.152G>A (p.Gly51Asp)
NM_001122764.3(PPOX):c.157A>G (p.Ile53Val) rs1171102735
NM_001122764.3(PPOX):c.164A>C (p.Glu55Ala)
NM_001122764.3(PPOX):c.182T>A (p.Ile61Asn) rs2525192004
NM_001122764.3(PPOX):c.208C>T (p.Arg70Trp) rs2525193268
NM_001122764.3(PPOX):c.218T>C (p.Leu73Pro) rs2525193705
NM_001122764.3(PPOX):c.230A>T (p.Glu77Val)
NM_001122764.3(PPOX):c.23T>C (p.Leu8Pro) rs1659110959
NM_001122764.3(PPOX):c.245C>T (p.Ser82Leu) rs1052597066
NM_001122764.3(PPOX):c.251T>G (p.Val84Gly) rs2525201326
NM_001122764.3(PPOX):c.26G>A (p.Gly9Asp)
NM_001122764.3(PPOX):c.270C>A (p.Asp90Glu)
NM_001122764.3(PPOX):c.271C>T (p.His91Tyr)
NM_001122764.3(PPOX):c.278C>T (p.Ala93Val) rs2525202835
NM_001122764.3(PPOX):c.292T>C (p.Phe98Leu)
NM_001122764.3(PPOX):c.31G>A (p.Gly11Ser) rs1571325591
NM_001122764.3(PPOX):c.31G>T (p.Gly11Cys) rs1571325591
NM_001122764.3(PPOX):c.332G>T (p.Gly111Val) rs2525204699
NM_001122764.3(PPOX):c.338+9A>G rs886045453
NM_001122764.3(PPOX):c.361C>G (p.Pro121Ala) rs532136485
NM_001122764.3(PPOX):c.362C>A (p.Pro121His)
NM_001122764.3(PPOX):c.367T>A (p.Ser123Thr) rs1064797018
NM_001122764.3(PPOX):c.38G>A (p.Ser13Asn) rs2101841884
NM_001122764.3(PPOX):c.419A>G (p.Lys140Arg)
NM_001122764.3(PPOX):c.427G>A (p.Asp143Asn) rs2525234704
NM_001122764.3(PPOX):c.441C>G (p.His147Gln) rs1659772587
NM_001122764.3(PPOX):c.488T>C (p.Met163Thr) rs1019141153
NM_001122764.3(PPOX):c.491A>G (p.Asp164Gly) rs2525248197
NM_001122764.3(PPOX):c.503G>T (p.Arg168Leu) rs41270025
NM_001122764.3(PPOX):c.522C>T (p.Asn174=) rs886045454
NM_001122764.3(PPOX):c.527G>A (p.Arg176His) rs1225937420
NM_001122764.3(PPOX):c.538A>G (p.Ile180Val) rs1200338773
NM_001122764.3(PPOX):c.545C>A (p.Ser182Tyr) rs745879127
NM_001122764.3(PPOX):c.559C>T (p.Leu187Phe) rs1659928956
NM_001122764.3(PPOX):c.567A>C (p.Gln189His)
NM_001122764.3(PPOX):c.590T>C (p.Ile197Thr) rs1553238545
NM_001122764.3(PPOX):c.599G>A (p.Gly200Asp)
NM_001122764.3(PPOX):c.611G>A (p.Gly204Glu) rs1293994558
NM_001122764.3(PPOX):c.616G>C (p.Gly206Arg) rs2525253886
NM_001122764.3(PPOX):c.617-3C>A rs2101876167
NM_001122764.3(PPOX):c.62T>A (p.Leu21Gln)
NM_001122764.3(PPOX):c.660G>T (p.Leu220Phe) rs1571367836
NM_001122764.3(PPOX):c.67C>T (p.Arg23Trp) rs373956753
NM_001122764.3(PPOX):c.688C>T (p.Arg230Cys) rs775261607
NM_001122764.3(PPOX):c.69G>T (p.Arg23=) rs886045452
NM_001122764.3(PPOX):c.708G>T (p.Leu236Phe) rs2101877634
NM_001122764.3(PPOX):c.710C>T (p.Pro237Leu)
NM_001122764.3(PPOX):c.719T>C (p.Leu240Pro) rs2525270371
NM_001122764.3(PPOX):c.761G>A (p.Gly254Asp) rs753605112
NM_001122764.3(PPOX):c.781A>C (p.Ser261Arg)
NM_001122764.3(PPOX):c.784C>T (p.Leu262Phe)
NM_001122764.3(PPOX):c.809T>C (p.Val270Ala) rs2525294551
NM_001122764.3(PPOX):c.82C>A (p.Pro28Thr) rs758987522
NM_001122764.3(PPOX):c.82C>G (p.Pro28Ala) rs758987522
NM_001122764.3(PPOX):c.83C>T (p.Pro28Leu) rs374585133
NM_001122764.3(PPOX):c.851G>T (p.Ser284Ile) rs2101886576
NM_001122764.3(PPOX):c.88-18_88-15del rs2525188022
NM_001122764.3(PPOX):c.8G>A (p.Arg3Gln) rs2101841312
NM_001122764.3(PPOX):c.950T>C (p.Val317Ala)
NM_001122764.3(PPOX):c.968_970del (p.Gly323del) rs1352842271
NM_001122764.3(PPOX):c.97G>T (p.Val33Leu) rs745790472
NM_001122764.3(PPOX):c.987+5G>T rs777244410
NM_001122764.3(PPOX):c.987+6A>T rs1255127950
NM_001122764.3(PPOX):c.987G>C (p.Gln329His) rs2101890627
NM_001122764.3(PPOX):c.997C>T (p.His333Tyr) rs2101898031

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