List of variants in gene GPR179 reported as benign for congenital stationary night blindness 1E

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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_001004334.4(GPR179):c.909= (p.Val303=)	rs9894059	0.24635
NM_001004334.4(GPR179):c.3448A>G (p.Lys1150Glu)	rs55727040	0.16088
NM_001004334.4(GPR179):c.7080T>G (p.Thr2360=)	rs58740367	0.05624
NM_001004334.4(GPR179):c.5605C>G (p.Gln1869Glu)	rs4399578	0.05465
NM_001004334.4(GPR179):c.*362G>A	rs4794777	0.05121
NM_001004334.4(GPR179):c.1478= (p.His493=)	rs4550493	0.04915
NM_001004334.4(GPR179):c.2650C>T (p.Arg884Trp)	rs72832277	0.04068
NM_001004334.4(GPR179):c.5930C>A (p.Pro1977His)	rs62073368	0.02067
NM_001004334.4(GPR179):c.5385C>T (p.Gly1795=)	rs72832276	0.01811
NM_001004334.4(GPR179):c.*613G>C	rs59996277	0.01442
NM_001004334.4(GPR179):c.*523G>A	rs143241101	0.01311
NM_001004334.4(GPR179):c.3881G>A (p.Arg1294Gln)	rs74742940	0.01287
NM_001004334.4(GPR179):c.3680A>G (p.Lys1227Arg)	rs138451517	0.01226
NM_001004334.4(GPR179):c.1595G>A (p.Arg532His)	rs59208852	0.01203
NM_001004334.4(GPR179):c.3569G>A (p.Arg1190Gln)	rs80172972	0.01140
NM_001004334.4(GPR179):c.921T>A (p.Ser307Arg)	rs137934209	0.01106
NM_001004334.4(GPR179):c.2924C>A (p.Ala975Asp)	rs111520301	0.01045
NM_001004334.4(GPR179):c.2392G>A (p.Ala798Thr)	rs78470373	0.01044
NM_001004334.4(GPR179):c.880C>T (p.Leu294=)	rs141320532	0.00905
NM_001004334.4(GPR179):c.2988G>A (p.Glu996=)	rs192591837	0.00838
NM_001004334.4(GPR179):c.3979G>A (p.Asp1327Asn)	rs112195635	0.00812
NM_001004334.4(GPR179):c.645G>A (p.Pro215=)	rs75688084	0.00639
NM_001004334.4(GPR179):c.508G>C (p.Gly170Arg)	rs77937007	0.00605
NM_001004334.4(GPR179):c.4141T>C (p.Cys1381Arg)	rs4398144	0.00592
NM_001004334.4(GPR179):c.628G>A (p.Gly210Ser)	rs148060036	0.00463
NM_001004334.4(GPR179):c.6824T>C (p.Leu2275Pro)	rs148601715	0.00108
NM_001004334.4(GPR179):c.1477C>T (p.His493Tyr)	rs114716738	0.00081
NM_001004334.4(GPR179):c.2022C>T (p.Asp674=)	rs79623844	0.00041
NM_001004334.4(GPR179):c.6798T>G (p.Phe2266Leu)	rs141146547	0.00025
NM_001004334.4(GPR179):c.3699= (p.Leu1233=)	rs35803744

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