List of variants in gene CNGA3 reported as uncertain significance by Molecular Genetics Laboratory, Institute for Ophthalmic Research

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.1343A>G (p.Lys448Arg)	rs190014426	0.00034
NM_001298.3(CNGA3):c.1615G>A (p.Val539Met)	rs374275399	0.00002
NM_001298.3(CNGA3):c.1347G>A (p.Lys449=)	rs778251470	0.00001
NM_001298.3(CNGA3):c.1A>T (p.Met1Leu)	rs1324338876	0.00001
NM_001298.3(CNGA3):c.609G>T (p.Trp203Cys)	rs757650055	0.00001
NM_001298.3(CNGA3):c.1889T>C (p.Val630Ala)	rs2104250774
NM_001298.3(CNGA3):c.450-15T>G	rs2104229048
NM_001298.3(CNGA3):c.479T>G (p.Val160Gly)	rs201713771
NM_001298.3(CNGA3):c.566G>A (p.Arg189Lys)	rs2104229996
NM_001298.3(CNGA3):c.66C>T (p.Asp22=)	rs2104175460
NM_001298.3(CNGA3):c.670A>G (p.Thr224Ala)	rs2104236067
NM_001298.3(CNGA3):c.743A>G (p.Gln248Arg)	rs2104245407
NM_001298.3(CNGA3):c.772C>G (p.Pro258Ala)	rs1477725731
NM_001298.3(CNGA3):c.796G>A (p.Val266Met)	rs536335712

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