ClinVar Miner

List of variants reported as uncertain significance for Congenital nephrotic syndrome

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Total variants: 109
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HGVS dbSNP
NM_004646.3(NPHS1):c.*1020C>T rs564256430
NM_004646.3(NPHS1):c.*1021G>A rs536792618
NM_004646.3(NPHS1):c.*1040C>T rs181405524
NM_004646.3(NPHS1):c.*250G>A rs117894015
NM_004646.3(NPHS1):c.*529C>T rs148755697
NM_004646.3(NPHS1):c.*609G>A rs144206206
NM_004646.3(NPHS1):c.*759A>T rs886054345
NM_004646.3(NPHS1):c.*82G>T rs569295487
NM_004646.3(NPHS1):c.*958G>T rs886054344
NM_004646.3(NPHS1):c.-31C>T rs376050812
NM_004646.3(NPHS1):c.-57G>T rs140404523
NM_004646.3(NPHS1):c.1110T>C (p.Val370=) rs116459838
NM_004646.3(NPHS1):c.115G>A (p.Glu39Lys) rs375670819
NM_004646.3(NPHS1):c.1170+8G>A rs140808195
NM_004646.3(NPHS1):c.1183G>A (p.Gly395Ser) rs372069596
NM_004646.3(NPHS1):c.126G>T (p.Thr42=) rs145683325
NM_004646.3(NPHS1):c.128T>C (p.Val43Ala) rs140626538
NM_004646.3(NPHS1):c.1297C>T (p.Leu433Phe) rs730880173
NM_004646.3(NPHS1):c.14C>T (p.Thr5Met) rs191850409
NM_004646.3(NPHS1):c.151C>T (p.Leu51=) rs114385015
NM_004646.3(NPHS1):c.1598T>C (p.Leu533Pro) rs886054351
NM_004646.3(NPHS1):c.1610C>T (p.Thr537Met) rs368913905
NM_004646.3(NPHS1):c.1619C>A (p.Ala540Glu) rs149598144
NM_004646.3(NPHS1):c.1638T>G (p.Thr546=) rs115444936
NM_004646.3(NPHS1):c.1758-11C>G rs145554982
NM_004646.3(NPHS1):c.1758-8T>G rs187501631
NM_004646.3(NPHS1):c.1799A>G (p.Lys600Arg) rs566516658
NM_004646.3(NPHS1):c.1802G>C (p.Gly601Ala) rs114615449
NM_004646.3(NPHS1):c.1822G>A (p.Val608Ile) rs367976914
NM_004646.3(NPHS1):c.1861G>A (p.Val621Met) rs886054350
NM_004646.3(NPHS1):c.1899C>T (p.Thr633=) rs748680209
NM_004646.3(NPHS1):c.1908C>T (p.Ser636=) rs34761059
NM_004646.3(NPHS1):c.1926A>G (p.Val642=) rs114728208
NM_004646.3(NPHS1):c.1930+10C>T rs76131336
NM_004646.3(NPHS1):c.2072C>A (p.Ala691Glu) rs886054349
NM_004646.3(NPHS1):c.2469G>A (p.Ala823=) rs371646734
NM_004646.3(NPHS1):c.25G>A (p.Ala9Thr) rs376793744
NM_004646.3(NPHS1):c.2654A>T (p.Gln885Leu) rs886054348
NM_004646.3(NPHS1):c.2686C>G (p.Gln896Glu) rs771594710
NM_004646.3(NPHS1):c.2746G>T (p.Ala916Ser) rs138173172
NM_004646.3(NPHS1):c.2869G>C (p.Val957Leu) rs114849139
NM_004646.3(NPHS1):c.2916G>T (p.Arg972Ser) rs374762054
NM_004646.3(NPHS1):c.2961T>C (p.Tyr987=) rs201263480
NM_004646.3(NPHS1):c.3027C>T (p.Tyr1009=) rs762184939
NM_004646.3(NPHS1):c.3130G>A (p.Glu1044Lys) rs370387270
NM_004646.3(NPHS1):c.3166+14C>A rs886054347
NM_004646.3(NPHS1):c.3173C>T (p.Ser1058Leu) rs201503587
NM_004646.3(NPHS1):c.3206T>C (p.Leu1069Pro) rs756273676
NM_004646.3(NPHS1):c.3311+14T>C rs375587420
NM_004646.3(NPHS1):c.3364G>C (p.Glu1122Gln) rs548792892
NM_004646.3(NPHS1):c.3388-14C>T rs371907999
NM_004646.3(NPHS1):c.3419G>A (p.Arg1140His) rs369787477
NM_004646.3(NPHS1):c.3455C>T (p.Thr1152Met) rs143145248
NM_004646.3(NPHS1):c.3520C>T (p.His1174Tyr) rs115489112
NM_004646.3(NPHS1):c.3598C>T (p.Pro1200Ser) rs35240811
NM_004646.3(NPHS1):c.427G>C (p.Glu143Gln) rs540253444
NM_004646.3(NPHS1):c.428A>T (p.Glu143Val) rs781117481
NM_004646.3(NPHS1):c.43G>C (p.Gly15Arg) rs73928330
NM_004646.3(NPHS1):c.485C>G (p.Ser162Cys) rs376172729
NM_004646.3(NPHS1):c.492C>T (p.Asp164=) rs147569168
NM_004646.3(NPHS1):c.505C>A (p.Pro169Thr) rs886054353
NM_004646.3(NPHS1):c.563A>T (p.Asn188Ile) rs145125791
NM_004646.3(NPHS1):c.597G>A (p.Glu199=) rs61731102
NM_004646.3(NPHS1):c.658T>G (p.Ser220Ala) rs115333628
NM_004646.3(NPHS1):c.733A>C (p.Ile245Leu) rs370046047
NM_004646.3(NPHS1):c.888G>A (p.Ala296=) rs531224038
NM_004646.3(NPHS1):c.916G>A (p.Val306Met) rs769719915
NM_004646.4(NPHS1):c.*1111G>T
NM_004646.4(NPHS1):c.*272G>A
NM_004646.4(NPHS1):c.*272G>T
NM_004646.4(NPHS1):c.*287C>T
NM_004646.4(NPHS1):c.*419C>T
NM_004646.4(NPHS1):c.*483G>A
NM_004646.4(NPHS1):c.*751C>T
NM_004646.4(NPHS1):c.*757T>C
NM_004646.4(NPHS1):c.*760T>C
NM_004646.4(NPHS1):c.*765C>T
NM_004646.4(NPHS1):c.*865T>C
NM_004646.4(NPHS1):c.*888A>G
NM_004646.4(NPHS1):c.*962G>A
NM_004646.4(NPHS1):c.-140G>A
NM_004646.4(NPHS1):c.1196T>C (p.Met399Thr)
NM_004646.4(NPHS1):c.1315+7C>T
NM_004646.4(NPHS1):c.1342G>C (p.Gly448Arg)
NM_004646.4(NPHS1):c.1378C>T (p.Arg460Trp)
NM_004646.4(NPHS1):c.1790C>A (p.Ala597Asp)
NM_004646.4(NPHS1):c.1871G>T (p.Arg624Leu)
NM_004646.4(NPHS1):c.1989G>A (p.Glu663=)
NM_004646.4(NPHS1):c.218C>T (p.Pro73Leu)
NM_004646.4(NPHS1):c.2201T>G (p.Leu734Arg)
NM_004646.4(NPHS1):c.2285C>T (p.Thr762Ile)
NM_004646.4(NPHS1):c.2334+9C>A
NM_004646.4(NPHS1):c.2436C>G (p.Gly812=)
NM_004646.4(NPHS1):c.2504G>C (p.Arg835Thr)
NM_004646.4(NPHS1):c.2507-13C>T
NM_004646.4(NPHS1):c.2507-14C>T
NM_004646.4(NPHS1):c.2516A>T (p.Gln839Leu)
NM_004646.4(NPHS1):c.2705G>A (p.Ser902Asn)
NM_004646.4(NPHS1):c.2905C>T (p.Leu969=)
NM_004646.4(NPHS1):c.298G>T (p.Ala100Ser)
NM_004646.4(NPHS1):c.3275G>A (p.Arg1092His)
NM_004646.4(NPHS1):c.3337G>A (p.Glu1113Lys)
NM_004646.4(NPHS1):c.3545C>T (p.Thr1182Met)
NM_004646.4(NPHS1):c.3667G>A (p.Asp1223Asn)
NM_004646.4(NPHS1):c.3687C>T (p.Pro1229=)
NM_004646.4(NPHS1):c.3716A>T (p.His1239Leu)
NM_004646.4(NPHS1):c.407A>G (p.Lys136Arg)
NM_004646.4(NPHS1):c.475A>T (p.Asn159Tyr)
NM_004646.4(NPHS1):c.613A>T (p.Thr205Ser)

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