ClinVar Miner

List of variants in gene ACTG1 reported as uncertain significance by GeneDx

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_001614.5(ACTG1):c.193C>T (p.Leu65=) rs1275470163 0.00001
NM_001614.5(ACTG1):c.208C>T (p.Pro70Ser) rs1568062708 0.00001
NM_001614.5(ACTG1):c.417G>C (p.Val139=) rs1367861495 0.00001
NM_001614.5(ACTG1):c.913A>G (p.Met305Val) rs1555666484 0.00001
NM_001614.5(ACTG1):c.920C>T (p.Pro307Leu) rs782354322 0.00001
NM_001614.5(ACTG1):c.-6-1G>T rs2031861888
NM_001614.5(ACTG1):c.1013C>T (p.Ser338Leu) rs1192977984
NM_001614.5(ACTG1):c.1051A>G (p.Thr351Ala) rs727502880
NM_001614.5(ACTG1):c.1086CGA[1] (p.Asp363del)
NM_001614.5(ACTG1):c.136G>T (p.Gly46Cys) rs2143784290
NM_001614.5(ACTG1):c.192C>A (p.Ile64=)
NM_001614.5(ACTG1):c.213T>G (p.Ile71Met) rs782047199
NM_001614.5(ACTG1):c.229A>G (p.Thr77Ala)
NM_001614.5(ACTG1):c.237G>A (p.Trp79Ter) rs2143783424
NM_001614.5(ACTG1):c.280C>G (p.Leu94Val) rs782388764
NM_001614.5(ACTG1):c.327C>T (p.Pro109=)
NM_001614.5(ACTG1):c.349_352del (p.Glu117fs) rs2143782665
NM_001614.5(ACTG1):c.359C>G (p.Thr120Ser)
NM_001614.5(ACTG1):c.424C>G (p.Leu142Val)
NM_001614.5(ACTG1):c.494T>C (p.Ile165Thr) rs2143778877
NM_001614.5(ACTG1):c.525C>G (p.Ile175Met) rs146667866
NM_001614.5(ACTG1):c.569T>C (p.Met190Thr)
NM_001614.5(ACTG1):c.670G>T (p.Glu224Ter) rs2143777663
NM_001614.5(ACTG1):c.689C>T (p.Ala230Val) rs782124831
NM_001614.5(ACTG1):c.718T>C (p.Tyr240His) rs1555666640
NM_001614.5(ACTG1):c.737A>T (p.Gln246Leu) rs1568061110
NM_001614.5(ACTG1):c.742A>G (p.Ile248Val)
NM_001614.5(ACTG1):c.755A>T (p.Asn252Ile) rs886041873
NM_001614.5(ACTG1):c.805A>G (p.Met269Val) rs2143775987
NM_001614.5(ACTG1):c.859G>A (p.Val287Met) rs2143775561
NM_001614.5(ACTG1):c.868C>T (p.Arg290Cys) rs1555666501
NM_001614.5(ACTG1):c.872A>G (p.Lys291Arg) rs1568060667
NM_001614.5(ACTG1):c.932A>T (p.Asp311Val)
NM_001614.5(ACTG1):c.940C>G (p.Gln314Glu) rs1555666471
NM_001614.5(ACTG1):c.991G>A (p.Ala331Thr) rs11549200
NM_001614.5(ACTG1):c.998C>G (p.Pro333Arg)

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