ClinVar Miner

List of variants in gene ANO3 reported as uncertain significance by GeneDx

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_031418.4(ANO3):c.1215G>A (p.Met405Ile) rs751046509 0.00003
NM_031418.4(ANO3):c.100C>G (p.Arg34Gly) rs373387931 0.00001
NM_031418.4(ANO3):c.1540C>T (p.Arg514Cys) rs1161758979 0.00001
NM_031418.4(ANO3):c.2449G>A (p.Glu817Lys) rs1393695079 0.00001
NM_031418.4(ANO3):c.2453G>C (p.Gly818Ala) rs750997370 0.00001
NM_031418.4(ANO3):c.2891A>C (p.His964Pro) rs779541748 0.00001
NM_031418.4(ANO3):c.2905C>T (p.Arg969Trp) rs373975805 0.00001
NM_031418.4(ANO3):c.428C>T (p.Ser143Phe) rs778338592 0.00001
NM_031418.4(ANO3):c.610G>A (p.Asp204Asn) rs1316389828 0.00001
NM_031418.4(ANO3):c.613A>G (p.Ile205Val) rs375180741 0.00001
NM_031418.4(ANO3):c.914G>A (p.Arg305Gln) rs772297446 0.00001
NM_031418.4(ANO3):c.1003T>A (p.Ser335Thr) rs1025522523
NM_031418.4(ANO3):c.1007dup (p.Tyr336Ter) rs2134196843
NM_031418.4(ANO3):c.101G>A (p.Arg34Gln)
NM_031418.4(ANO3):c.1067A>G (p.His356Arg) rs1254174023
NM_031418.4(ANO3):c.1088A>G (p.His363Arg) rs1057521380
NM_031418.4(ANO3):c.1102C>G (p.Arg368Gly) rs376935363
NM_031418.4(ANO3):c.1228G>C (p.Ala410Pro)
NM_031418.4(ANO3):c.1290C>G (p.Ser430Arg)
NM_031418.4(ANO3):c.1506C>A (p.Asp502Glu)
NM_031418.4(ANO3):c.166C>T (p.Leu56Phe)
NM_031418.4(ANO3):c.1699G>A (p.Gly567Arg) rs2132929609
NM_031418.4(ANO3):c.1760T>C (p.Ile587Thr) rs2538936048
NM_031418.4(ANO3):c.1765C>T (p.Gln589Ter)
NM_031418.4(ANO3):c.2118C>A (p.Asn706Lys) rs2538999479
NM_031418.4(ANO3):c.2301C>G (p.Ile767Met) rs1590669609
NM_031418.4(ANO3):c.2326C>T (p.Pro776Ser)
NM_031418.4(ANO3):c.2365C>G (p.Leu789Val) rs2539007732
NM_031418.4(ANO3):c.2458G>T (p.Gly820Cys)
NM_031418.4(ANO3):c.2459G>A (p.Gly820Asp) rs1853395441
NM_031418.4(ANO3):c.2657+1G>T
NM_031418.4(ANO3):c.2723A>G (p.His908Arg)
NM_031418.4(ANO3):c.2810A>G (p.Asp937Gly) rs2133106169
NM_031418.4(ANO3):c.2939G>A (p.Trp980Ter)
NM_031418.4(ANO3):c.2945_2946delinsGC (p.Ter982Cys)
NM_031418.4(ANO3):c.340G>C (p.Asp114His) rs868398613
NM_031418.4(ANO3):c.427_430del (p.Ser143fs)
NM_031418.4(ANO3):c.49A>G (p.Met17Val)
NM_031418.4(ANO3):c.657G>A (p.Lys219=)
NM_031418.4(ANO3):c.702C>G (p.Cys234Trp) rs886037882
NM_031418.4(ANO3):c.709A>G (p.Thr237Ala) rs2134167847
NM_031418.4(ANO3):c.771G>C (p.Trp257Cys)
NM_031418.4(ANO3):c.785C>T (p.Pro262Leu)
NM_031418.4(ANO3):c.992T>A (p.Ile331Lys) rs751447376

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