ClinVar Miner

List of variants in gene NPHS1 reported as benign

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Gene type:
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Total variants: 54
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HGVS dbSNP
NC_000019.10:g.35826057T>C
NC_000019.10:g.35826368A>G
NM_004646.3(NPHS1):c.*1119A>C rs74509387
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.1170+9G>A rs531263446
NM_004646.3(NPHS1):c.1175T>C (p.Leu392Pro) rs34320609
NM_004646.3(NPHS1):c.1183G>A (p.Gly395Ser) rs372069596
NM_004646.3(NPHS1):c.1223G>A (p.Arg408Gln) rs33950747
NM_004646.3(NPHS1):c.1233C>T (p.Asn411=) rs374218631
NM_004646.3(NPHS1):c.128T>C (p.Val43Ala) rs140626538
NM_004646.3(NPHS1):c.1320C>T (p.Pro440=) rs392702
NM_004646.3(NPHS1):c.1339G>A (p.Glu447Lys) rs28939695
NM_004646.3(NPHS1):c.151C>T (p.Leu51=) rs114385015
NM_004646.3(NPHS1):c.1610C>T (p.Thr537Met) rs368913905
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.1802G>C (p.Gly601Ala) rs114615449
NM_004646.3(NPHS1):c.1822G>A (p.Val608Ile) rs367976914
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.1930+12G>A rs528950
NM_004646.3(NPHS1):c.2072-6C>T rs200253809
NM_004646.3(NPHS1):c.2223C>T (p.Thr741=) rs2073901
NM_004646.3(NPHS1):c.2289C>T (p.Val763=) rs437168
NM_004646.3(NPHS1):c.2398C>T (p.Arg800Cys) rs114896482
NM_004646.3(NPHS1):c.2869G>C (p.Val957Leu) rs114849139
NM_004646.3(NPHS1):c.294C>T (p.Ile98=) rs2285450
NM_004646.3(NPHS1):c.2971G>C (p.Val991Leu) rs34736717
NM_004646.3(NPHS1):c.3130G>A (p.Glu1044Lys) rs370387270
NM_004646.3(NPHS1):c.3230A>G (p.Asn1077Ser) rs4806213
NM_004646.3(NPHS1):c.3315G>A (p.Ser1105=) rs2071327
NM_004646.3(NPHS1):c.3321G>A (p.Glu1107=) rs115670171
NM_004646.3(NPHS1):c.3418C>A (p.Arg1140Ser) rs143092783
NM_004646.3(NPHS1):c.3482-7A>T rs73928326
NM_004646.3(NPHS1):c.349G>A (p.Glu117Lys) rs3814995
NM_004646.3(NPHS1):c.3562G>A (p.Ala1188Thr) rs116700257
NM_004646.3(NPHS1):c.3595-9G>T rs77309273
NM_004646.3(NPHS1):c.3598C>T (p.Pro1200Ser) rs35240811
NM_004646.3(NPHS1):c.3702C>T (p.Phe1234=) rs141375888
NM_004646.3(NPHS1):c.396G>C (p.Leu132=) rs567149548
NM_004646.3(NPHS1):c.528T>C (p.Ser176=) rs539716201
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.697A>G (p.Thr233Ala) rs35238405
NM_004646.3(NPHS1):c.699C>T (p.Thr233=) rs144398621
NM_004646.3(NPHS1):c.791C>G (p.Pro264Arg) rs34982899
NM_004646.3(NPHS1):c.803G>A (p.Arg268Gln) rs115308424
NM_004646.3(NPHS1):c.840+6G>A rs369975773
NM_004646.3(NPHS1):c.881C>T (p.Thr294Ile) rs113825926
NM_004646.3(NPHS1):c.888G>A (p.Ala296=) rs531224038

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