ClinVar Miner

List of variants in gene ACTB reported as uncertain significance by GeneDx

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_001101.5(ACTB):c.634A>G (p.Ile212Val) rs1382720283 0.00001
NM_001101.5(ACTB):c.804C>T (p.Gly268=) rs770089307 0.00001
NM_001101.5(ACTB):c.94C>T (p.Pro32Ser) rs779839358 0.00001
NM_001101.5(ACTB):c.1021A>C (p.Ile341Leu) rs886041305
NM_001101.5(ACTB):c.1028G>A (p.Gly343Asp) rs1057524783
NM_001101.5(ACTB):c.1085A>G (p.Tyr362Cys)
NM_001101.5(ACTB):c.1121G>A (p.Cys374Tyr)
NM_001101.5(ACTB):c.1125C>T (p.Phe375=)
NM_001101.5(ACTB):c.143G>A (p.Gly48Asp) rs886041268
NM_001101.5(ACTB):c.155C>T (p.Ser52Phe) rs886041271
NM_001101.5(ACTB):c.246G>A (p.Met82Ile)
NM_001101.5(ACTB):c.259C>T (p.His87Tyr) rs1554329552
NM_001101.5(ACTB):c.307G>A (p.Val103Met) rs587779772
NM_001101.5(ACTB):c.359C>G (p.Thr120Ser)
NM_001101.5(ACTB):c.389C>G (p.Pro130Arg) rs2128241308
NM_001101.5(ACTB):c.389C>T (p.Pro130Leu) rs2128241308
NM_001101.5(ACTB):c.400G>A (p.Val134Ile)
NM_001101.5(ACTB):c.432C>T (p.Ala144=) rs1254718824
NM_001101.5(ACTB):c.535G>C (p.Asp179His) rs1064796439
NM_001101.5(ACTB):c.553C>G (p.Leu185Val)
NM_001101.5(ACTB):c.561C>G (p.Asp187Glu) rs202099951
NM_001101.5(ACTB):c.673C>G (p.Gln225Glu) rs1784811545
NM_001101.5(ACTB):c.721G>A (p.Glu241Lys) rs2128241271
NM_001101.5(ACTB):c.739G>T (p.Val247Phe)
NM_001101.5(ACTB):c.754A>G (p.Asn252Asp) rs2128241265
NM_001101.5(ACTB):c.770G>A (p.Cys257Tyr) rs11546930
NM_001101.5(ACTB):c.810G>C (p.Glu270Asp) rs745973745
NM_001101.5(ACTB):c.825C>G (p.His275Gln)
NM_001101.5(ACTB):c.82C>G (p.Arg28Gly) rs886041270
NM_001101.5(ACTB):c.914T>C (p.Met305Thr) rs1784803788
NM_001101.5(ACTB):c.946_948del (p.Glu316del) rs2128241229
NM_001101.5(ACTB):c.985-43_993dup

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