ClinVar Miner

List of variants in gene CDH3 reported as uncertain significance by Eurofins NTD LLC (GA)

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_001793.6(CDH3):c.1681G>A (p.Val561Met) rs151198926 0.00118
NM_001793.6(CDH3):c.1785C>T (p.Val595=) rs376302917 0.00063
NM_001793.6(CDH3):c.1443C>T (p.Asp481=) rs144403828 0.00053
NM_001793.6(CDH3):c.1222G>A (p.Val408Ile) rs145486898 0.00030
NM_001793.6(CDH3):c.821G>A (p.Arg274Gln) rs148598245 0.00028
NM_001793.6(CDH3):c.918C>T (p.Asp306=) rs201521473 0.00019
NM_001793.6(CDH3):c.2042G>A (p.Arg681Gln) rs758614807 0.00014
NM_001793.6(CDH3):c.2364C>T (p.Asp788=) rs144637479 0.00009
NM_001793.6(CDH3):c.2475C>T (p.Gly825=) rs543214840 0.00008
NM_001793.6(CDH3):c.1000G>A (p.Glu334Lys) rs772735028 0.00007
NM_001793.6(CDH3):c.1704G>A (p.Thr568=) rs561193756 0.00006
NM_001793.6(CDH3):c.1011G>C (p.Val337=) rs201726457 0.00004
NM_001793.6(CDH3):c.1081G>T (p.Ala361Ser) rs757205517 0.00003
NM_001793.6(CDH3):c.1652G>A (p.Arg551His) rs779413254 0.00003
NM_001793.6(CDH3):c.2178G>A (p.Pro726=) rs398123626 0.00003
NM_001793.6(CDH3):c.1932C>T (p.Val644=) rs750805163 0.00001
NM_001793.6(CDH3):c.2003-10A>G rs771535286 0.00001
NM_001793.6(CDH3):c.101C>T (p.Ala34Val) rs1555503894
NM_001793.6(CDH3):c.1178G>A (p.Arg393Lys) rs766325919
NM_001793.6(CDH3):c.119C>A (p.Ala40Glu) rs749703265
NM_001793.6(CDH3):c.2421T>G (p.Asp807Glu) rs886042659
NM_001793.6(CDH3):c.2430C>T (p.Asn810=) rs774229703

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