List of variants in gene NPHP4 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_015102.5(NPHP4):c.2612-33G>A	rs3747989	0.83595
NM_015102.5(NPHP4):c.3231+41T>C	rs868163	0.64813
NM_015102.5(NPHP4):c.2802C>T (p.Arg934=)	rs3747992	0.36928
NM_015102.5(NPHP4):c.3570A>G (p.Glu1190=)	rs555164	0.35094
NM_015102.5(NPHP4):c.3645-38C>T	rs1287634	0.34998
NM_015102.5(NPHP4):c.3231+31A>G	rs905467	0.20383
NM_015102.5(NPHP4):c.1441+13A>G	rs7520105	0.17476
NM_015102.5(NPHP4):c.2643G>A (p.Ala881=)	rs3747990	0.11763
NM_015102.5(NPHP4):c.2485+38C>T	rs41280814	0.11752
NM_015102.5(NPHP4):c.1926G>A (p.Glu642=)	rs12120967	0.11732
NM_015102.5(NPHP4):c.1470C>T (p.Leu490=)	rs12116997	0.04804
NM_015102.5(NPHP4):c.86C>T (p.Thr29Met)	rs12142270	0.04382
NM_015102.5(NPHP4):c.2724G>A (p.Ser908=)	rs114545322	0.03032
NM_015102.5(NPHP4):c.1631C>G (p.Ala544Gly)	rs12093500	0.02840
NM_015102.5(NPHP4):c.2219G>A (p.Arg740His)	rs34248917	0.02256
NM_015102.5(NPHP4):c.3243G>C (p.Gly1081=)	rs41280800	0.01658
NM_015102.5(NPHP4):c.2808G>A (p.Thr936=)	rs17028857	0.01235
NM_015102.5(NPHP4):c.3479C>T (p.Pro1160Leu)	rs113445782	0.01143
NM_015102.5(NPHP4):c.2031C>T (p.Pro677=)	rs34373111	0.01102
NM_015102.5(NPHP4):c.1852G>A (p.Glu618Lys)	rs571655	0.01009
NM_015102.5(NPHP4):c.3876C>T (p.Gly1292=)	rs115526767	0.00982
NM_015102.5(NPHP4):c.2812G>A (p.Val938Met)	rs184961418	0.00460
NM_015102.5(NPHP4):c.1705C>G (p.Gln569Glu)	rs113413307	0.00443
NM_015102.5(NPHP4):c.511G>A (p.Ala171Thr)	rs113765431	0.00408
NM_015102.5(NPHP4):c.279+11G>A	rs113902159	0.00401
NM_015102.5(NPHP4):c.1503+10G>A	rs41307782	0.00367
NM_015102.5(NPHP4):c.3036C>T (p.Pro1012=)	rs34265978	0.00283
NM_015102.5(NPHP4):c.2868C>T (p.Ala956=)	rs138025088	0.00188
NM_015102.5(NPHP4):c.1196A>G (p.Glu399Gly)	rs117898549	0.00020
NM_015102.5(NPHP4):c.4141-32G>A

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