ClinVar Miner

List of variants in gene CNGA3 reported as uncertain significance for Retinal dystrophy

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Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_001298.3(CNGA3):c.1117G>A (p.Val373Met) rs552553452 0.00005
NM_001298.3(CNGA3):c.1557G>A (p.Met519Ile) rs199655686 0.00004
NM_001298.3(CNGA3):c.1048A>G (p.Arg350Gly) rs1692908768
NM_001298.3(CNGA3):c.1931T>C (p.Phe644Ser) rs878853359
NM_001298.3(CNGA3):c.649G>C (p.Asp217His) rs1692800358
NM_001298.3(CNGA3):c.907A>T (p.Ile303Phe) rs1305790956

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