ClinVar Miner

List of variants in gene ACTB reported by Ambry Genetics

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001101.5(ACTB):c.124-3C>T rs1189379541 0.00002
NM_001101.5(ACTB):c.1021A>G (p.Ile341Val) rs886041305
NM_001101.5(ACTB):c.1097dup (p.Ser368fs) rs1554329078
NM_001101.5(ACTB):c.170A>C (p.Glu57Ala) rs1784832645
NM_001101.5(ACTB):c.259C>G (p.His87Asp) rs1554329552
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.547C>T (p.Arg183Trp) rs104894003
NM_001101.5(ACTB):c.589G>A (p.Gly197Ser) rs1554329317
NM_001101.5(ACTB):c.617G>A (p.Arg206Gln) rs886039472
NM_001101.5(ACTB):c.625G>A (p.Val209Met) rs587779777
NM_001101.5(ACTB):c.645G>T (p.Lys215Asn) rs145017784
NM_001101.5(ACTB):c.685A>G (p.Thr229Ala)
NM_001101.5(ACTB):c.773C>T (p.Pro258Leu) rs1554329281
NM_001101.5(ACTB):c.779C>A (p.Ala260Glu) rs1784808970
NM_001101.5(ACTB):c.786C>A (p.Phe262Leu)
NM_001101.5(ACTB):c.888C>G (p.Asn296Lys) rs769182426
NM_001101.5(ACTB):c.987_990dup (p.Ala331fs) rs1784799235

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