ClinVar Miner

List of variants in gene ACTB reported as uncertain significance by Ambry Genetics

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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_001101.5(ACTB):c.1021A>G (p.Ile341Val) rs886041305
NM_001101.5(ACTB):c.170A>C (p.Glu57Ala) rs1784832645
NM_001101.5(ACTB):c.329T>G (p.Leu110Arg) rs1784829584
NM_001101.5(ACTB):c.406A>G (p.Ile136Val) rs1554329352
NM_001101.5(ACTB):c.537C>G (p.Asp179Glu) rs797044950
NM_001101.5(ACTB):c.645G>T (p.Lys215Asn) rs145017784
NM_001101.5(ACTB):c.685A>G (p.Thr229Ala)
NM_001101.5(ACTB):c.786C>A (p.Phe262Leu)

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