List of variants in gene CNGA3 reported as benign

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.72T>C (p.Asp24=)	rs6727412	0.13838
NM_001298.3(CNGA3):c.*838T>C	rs13395005	0.06587
NM_001298.2(CNGA3):c.-286C>T	rs13408372	0.06490
NM_001298.3(CNGA3):c.396-84G>T	rs7562788	0.05319
NM_001298.3(CNGA3):c.674-48A>C	rs10184555	0.03666
NM_001298.3(CNGA3):c.*574C>T	rs13429817	0.03505
NM_001298.3(CNGA3):c.592G>A (p.Glu198Lys)	rs2271041	0.01129
NM_001298.3(CNGA3):c.458C>T (p.Thr153Met)	rs34314205	0.00836
NM_001298.3(CNGA3):c.215+11A>G	rs199755395	0.00490
NM_001298.3(CNGA3):c.1569C>T (p.Asn523=)	rs61752503	0.00467
NM_001298.3(CNGA3):c.143C>T (p.Pro48Leu)	rs62156348	0.00451
NM_001298.3(CNGA3):c.102-20C>T	rs111328717	0.00390
NM_001298.3(CNGA3):c.396-4G>A	rs114951127	0.00360
NM_001298.3(CNGA3):c.353A>G (p.Gln118Arg)	rs142837782	0.00305
NM_001298.3(CNGA3):c.1626C>T (p.Ser542=)	rs78583671	0.00275
NM_001298.3(CNGA3):c.790T>A (p.Leu264Ile)	rs73964088	0.00202
NM_001298.3(CNGA3):c.198C>T (p.Thr66=)	rs139544302	0.00147
NM_001298.3(CNGA3):c.1767C>T (p.Thr589=)	rs137950660	0.00102
NM_001298.3(CNGA3):c.81C>T (p.Arg27=)	rs148593890	0.00097
NM_001298.3(CNGA3):c.438C>T (p.Asn146=)	rs138720071	0.00083
NM_001298.3(CNGA3):c.682G>A (p.Glu228Lys)	rs147415641	0.00049
NM_001298.3(CNGA3):c.1863G>A (p.Ala621=)	rs181911949	0.00044
NM_001298.3(CNGA3):c.1101T>C (p.Gly367=)	rs200069389	0.00034
NM_001298.3(CNGA3):c.1746C>T (p.Asp582=)	rs77311157	0.00023
NM_001298.3(CNGA3):c.111G>A (p.Ser37=)	rs138888861	0.00018
NM_001298.3(CNGA3):c.59C>T (p.Thr20Ile)	rs143489966	0.00002
NM_001298.3(CNGA3):c.238C>T (p.Leu80=)	rs575326068	0.00001
NM_001298.3(CNGA3):c.450-12G>A	rs538751113	0.00001
NM_001298.3(CNGA3):c.102-16A>G	rs2279859
NM_001298.3(CNGA3):c.215+151T>C	rs937725
NM_001298.3(CNGA3):c.215+46T>G	rs58990587

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