ClinVar Miner

List of variants in gene NPHP4 reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NM_015102.4(NPHP4):c.1024C>T (p.Arg342Cys) rs190940697
NM_015102.4(NPHP4):c.136-4delC rs143323188
NM_015102.4(NPHP4):c.1482G>A (p.Gln494=) rs199557439
NM_015102.4(NPHP4):c.1490C>G (p.Pro497Arg) rs375051705
NM_015102.4(NPHP4):c.1542G>A (p.Pro514=) rs35264155
NM_015102.4(NPHP4):c.1611+9C>T rs114900019
NM_015102.4(NPHP4):c.1622C>T (p.Pro541Leu) rs145255635
NM_015102.4(NPHP4):c.1631C>G (p.Ala544Gly) rs12093500
NM_015102.4(NPHP4):c.1852G>A (p.Glu618Lys) rs571655
NM_015102.4(NPHP4):c.2031C>T (p.Pro677=) rs34373111
NM_015102.4(NPHP4):c.2219G>A (p.Arg740His) rs34248917
NM_015102.4(NPHP4):c.2257G>A (p.Asp753Asn) rs148424288
NM_015102.4(NPHP4):c.2293G>A (p.Val765Ile) rs149244006
NM_015102.4(NPHP4):c.2542C>T (p.Arg848Trp) rs17472401
NM_015102.4(NPHP4):c.2557G>T (p.Asp853Tyr) rs199875059
NM_015102.4(NPHP4):c.2681A>G (p.His894Arg) rs113097479
NM_015102.4(NPHP4):c.2724G>A (p.Ser908=) rs114545322
NM_015102.4(NPHP4):c.2808G>A (p.Thr936=) rs17028857
NM_015102.4(NPHP4):c.2812G>A (p.Val938Met) rs184961418
NM_015102.4(NPHP4):c.2876G>A (p.Arg959Gln) rs12084067
NM_015102.4(NPHP4):c.2882G>A (p.Arg961His) rs183885357
NM_015102.4(NPHP4):c.3243G>C (p.Gly1081=) rs41280800
NM_015102.4(NPHP4):c.3329C>T (p.Ala1110Val) rs139767853
NM_015102.4(NPHP4):c.3479C>T (p.Pro1160Leu) rs113445782
NM_015102.4(NPHP4):c.3674C>T (p.Thr1225Met) rs144624477
NM_015102.4(NPHP4):c.3876C>T (p.Gly1292=) rs115526767
NM_015102.4(NPHP4):c.3894C>T (p.Ala1298=) rs60094861
NM_015102.4(NPHP4):c.4237G>A (p.Asp1413Asn) rs115910810
NM_015102.4(NPHP4):c.86C>T (p.Thr29Met) rs12142270

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