ClinVar Miner

List of variants in gene CDH3 reported as benign

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Gene type:
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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_001793.6(CDH3):c.2281-288T>C rs3114408 0.97807
NM_001793.6(CDH3):c.161-123T>C rs3118229 0.89885
NM_001793.6(CDH3):c.1570+297T>G rs3114401 0.89871
NM_001793.6(CDH3):c.390+37T>C rs2296410 0.87073
NM_001793.6(CDH3):c.*154G>T rs1886699 0.85426
NM_001793.6(CDH3):c.720G>A (p.Thr240=) rs2296409 0.63066
NM_001793.6(CDH3):c.813C>A (p.Thr271=) rs2296408 0.62977
NM_001793.6(CDH3):c.1424+23A>G rs2281850 0.62286
NM_001793.6(CDH3):c.1626T>C (p.Asn542=) rs2296405 0.62283
NM_001793.6(CDH3):c.1571-75G>A rs2296406 0.62263
NM_001793.6(CDH3):c.997-26T>C rs1886697 0.61791
NM_001793.6(CDH3):c.1796-137A>G rs2274240 0.61534
NM_001793.6(CDH3):c.1956G>A (p.Lys652=) rs2274239 0.61024
NM_001793.6(CDH3):c.2003-182C>A rs3785135 0.56438
NM_001793.6(CDH3):c.2003-220C>T rs3785134 0.56425
NM_001793.6(CDH3):c.2134-155C>T rs2296404 0.55631
NM_001793.6(CDH3):c.2239C>A (p.Arg747=) rs17715450 0.53279
NM_001793.6(CDH3):c.160+117G>A rs2236393 0.44521
NM_001793.6(CDH3):c.247-38A>G rs1952048 0.43462
NM_001793.6(CDH3):c.1183-119T>C rs4783661 0.38349
NM_001793.6(CDH3):c.1689G>C (p.Gln563His) rs1126933 0.32131
NM_001793.6(CDH3):c.997-139G>A rs1886698 0.30861
NM_001793.5(CDH3):c.-537A>G rs11644435 0.22872
NM_001793.6(CDH3):c.1570+177C>T rs3114400 0.20716
NM_001793.6(CDH3):c.692-247G>A rs57721399 0.18062
NM_001793.6(CDH3):c.692-129G>C rs112844902 0.05927
NM_001793.6(CDH3):c.1430G>A (p.Arg477His) rs34494880 0.04895
NM_001793.6(CDH3):c.692-248C>T rs112314027 0.03589
NM_001793.6(CDH3):c.1257G>A (p.Lys419=) rs11860187 0.02870
NM_001793.6(CDH3):c.2134-154G>A rs7185952 0.02785
NM_001793.6(CDH3):c.1285G>A (p.Val429Ile) rs34394404 0.00905
NM_001793.6(CDH3):c.2280+7C>T rs114709429 0.00779
NM_001793.6(CDH3):c.996+13C>T rs114408705 0.00573
NM_001793.6(CDH3):c.*195G>T rs114591853 0.00526
NM_001793.6(CDH3):c.2058C>T (p.Pro686=) rs116035854 0.00373
NM_001793.6(CDH3):c.2281-44G>T rs151140320 0.00355
NM_001793.6(CDH3):c.805A>C (p.Met269Leu) rs36038900 0.00341
NM_001793.6(CDH3):c.1500C>T (p.Thr500=) rs35232945 0.00241
NM_001793.6(CDH3):c.1087C>T (p.Arg363Cys) rs74026937 0.00225
NM_001793.6(CDH3):c.1236C>T (p.Asn412=) rs186599732 0.00111
NM_001793.6(CDH3):c.345T>C (p.Ser115=) rs138829996 0.00090
NM_001793.6(CDH3):c.141C>G (p.Pro47=) rs74619658 0.00086
NM_001793.6(CDH3):c.909G>T (p.Met303Ile) rs148535251 0.00061
NM_001793.6(CDH3):c.868-17C>T rs141338577 0.00059
NM_001793.6(CDH3):c.1568A>G (p.Asn523Ser) rs191805535 0.00024
NM_001793.6(CDH3):c.582A>C (p.Ser194=) rs148063369 0.00009
NM_001793.6(CDH3):c.2115G>A (p.Gly705=) rs200124759 0.00007
NM_001793.6(CDH3):c.1704G>A (p.Thr568=) rs561193756 0.00006
NM_001793.6(CDH3):c.1776G>A (p.Thr592=) rs766163524 0.00006
NM_001793.6(CDH3):c.109A>T (p.Thr37Ser) rs374627741 0.00004
NM_001793.4(CDH3):c.-629dup rs11440411
NM_001793.6(CDH3):c.2003-46A>G rs8060790
NM_001793.6(CDH3):c.2133+14_2133+22del rs569391693
NM_001793.6(CDH3):c.2281-45A>C rs3114409
NM_001793.6(CDH3):c.247-194del rs376882052
NM_001793.6(CDH3):c.612C>A (p.Ile204=) rs8049247

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