ClinVar Miner

List of variants in gene PPOX reported as likely benign

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Gene type:
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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_001122764.3(PPOX):c.-128C>G rs72714915 0.05005
NM_001122764.3(PPOX):c.-151G>T rs115158839 0.01505
NM_001122764.3(PPOX):c.767C>G (p.Pro256Arg) rs12735723 0.00660
NM_001122764.3(PPOX):c.1248+5G>C rs140861330 0.00249
NM_001122764.3(PPOX):c.1206A>C (p.Gly402=) rs112762537 0.00140
NM_001122764.3(PPOX):c.684A>G (p.Ser228=) rs771649689 0.00013
NM_001122764.3(PPOX):c.1248+19C>T rs41270031 0.00011
NM_001122764.3(PPOX):c.1248+4A>G rs775748399 0.00006
NM_001122764.3(PPOX):c.1263G>A (p.Gln421=) rs370738994 0.00006
NM_001122764.3(PPOX):c.1071C>T (p.Asp357=) rs775262677 0.00005
NM_001122764.3(PPOX):c.1353T>C (p.Tyr451=) rs148292941 0.00005
NM_001122764.3(PPOX):c.71C>T (p.Ala24Val) rs767225561 0.00005
NM_001122764.3(PPOX):c.1098+9G>A rs201450061 0.00004
NM_001122764.3(PPOX):c.658T>C (p.Leu220=) rs547874675 0.00004
NM_001122764.3(PPOX):c.843C>T (p.His281=) rs150603927 0.00004
NM_001122764.3(PPOX):c.168T>C (p.Leu56=) rs756141647 0.00003
NM_001122764.3(PPOX):c.477G>A (p.Ala159=) rs764721329 0.00003
NM_001122764.3(PPOX):c.1421A>G (p.Glu474Gly) rs202103290 0.00002
NM_001122764.3(PPOX):c.219C>T (p.Leu73=) rs1293047678 0.00002
NM_001122764.3(PPOX):c.300C>T (p.Tyr100=) rs375823037 0.00002
NM_001122764.3(PPOX):c.844G>A (p.Val282Ile) rs145286580 0.00002
NM_001122764.3(PPOX):c.87+10C>T rs769695111 0.00002
NM_001122764.3(PPOX):c.1175G>A (p.Arg392Gln) rs1001703993 0.00001
NM_001122764.3(PPOX):c.213C>A (p.Thr71=) rs199710255 0.00001
NM_001122764.3(PPOX):c.306C>T (p.Gly102=) rs1422656757 0.00001
NM_001122764.3(PPOX):c.616+15A>G rs1214567328 0.00001
NM_001122764.3(PPOX):c.702G>A (p.Glu234=) rs2101877570 0.00001
NM_001122764.3(PPOX):c.72C>A (p.Ala24=) rs752272783 0.00001
NM_001122764.3(PPOX):c.744G>A (p.Gly248=) rs752880901 0.00001
NM_001122764.3(PPOX):c.1041G>T (p.Val347=) rs2101898518
NM_001122764.3(PPOX):c.1047C>T (p.Asp349=) rs749503356
NM_001122764.3(PPOX):c.1062T>C (p.Pro354=) rs771215757
NM_001122764.3(PPOX):c.1164G>C (p.Leu388=) rs1661027494
NM_001122764.3(PPOX):c.1249-10C>G
NM_001122764.3(PPOX):c.1249-12_1249-8del
NM_001122764.3(PPOX):c.1296A>G (p.Ser432=) rs1661206662
NM_001122764.3(PPOX):c.1317T>C (p.Ala439=) rs371241187
NM_001122764.3(PPOX):c.1317T>G (p.Ala439=) rs371241187
NM_001122764.3(PPOX):c.1413G>A (p.Leu471=)
NM_001122764.3(PPOX):c.276A>T (p.Pro92=) rs765401778
NM_001122764.3(PPOX):c.366C>T (p.Phe122=) rs2525232417
NM_001122764.3(PPOX):c.471+10G>C rs1208696772
NM_001122764.3(PPOX):c.471+14A>G rs1243106058
NM_001122764.3(PPOX):c.528T>G (p.Arg176=) rs2525250144
NM_001122764.3(PPOX):c.68G>A (p.Arg23Gln)
NM_001122764.3(PPOX):c.741G>T (p.Arg247Ser) rs149049124
NM_001122764.3(PPOX):c.747C>G (p.Val249=) rs755967832
NM_001122764.3(PPOX):c.78C>T (p.Cys26=)
NM_001122764.3(PPOX):c.807+13C>G rs1331723826
NM_001122764.3(PPOX):c.808-17T>C
NM_001122764.3(PPOX):c.87+8C>A rs2525181826
NM_001122764.3(PPOX):c.88-6C>T
NM_001122764.3(PPOX):c.972C>T (p.Ala324=) rs2525308812

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