ClinVar Miner

List of variants in gene CHD4 reported as benign for not provided

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Gene type:
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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_001273.5(CHD4):c.417G>T (p.Glu139Asp) rs1639122 0.54444
NM_001273.5(CHD4):c.4371-5C>T rs7316626 0.23149
NM_001273.5(CHD4):c.4909+20T>G rs55670476 0.16159
NM_001273.5(CHD4):c.1362C>T (p.Val454=) rs11539542 0.13722
NM_001273.5(CHD4):c.1548C>T (p.Pro516=) rs11539543 0.13698
NM_001273.5(CHD4):c.13C>T (p.Leu5=) rs2267974 0.02674
NM_001273.5(CHD4):c.100+18G>A rs71584862 0.02662
NM_001273.5(CHD4):c.799+18T>C rs115269629 0.02533
NM_001273.5(CHD4):c.1686+3A>G rs61759471 0.02250
NM_001273.5(CHD4):c.4943C>T (p.Ser1648Leu) rs35512811 0.02250
NM_001273.5(CHD4):c.4587G>A (p.Lys1529=) rs34863790 0.02049
NM_001273.5(CHD4):c.1848G>A (p.Gly616=) rs61753200 0.01192
NM_001273.5(CHD4):c.1483-5C>T rs139702202 0.01036
NM_001273.5(CHD4):c.5292T>C (p.Pro1764=) rs71584868 0.00534
NM_001273.5(CHD4):c.633G>A (p.Glu211=) rs111569582 0.00473
NM_001273.5(CHD4):c.3466-6C>T rs147135592 0.00391
NM_001273.5(CHD4):c.4161C>T (p.Pro1387=) rs115174844 0.00390
NM_001273.5(CHD4):c.420T>G (p.Asp140Glu) rs74790047 0.00239
NM_001273.5(CHD4):c.5178T>C (p.Tyr1726=) rs149961532 0.00133
NM_001273.5(CHD4):c.5217C>T (p.Ala1739=) rs34509399 0.00129
NM_001273.5(CHD4):c.2238C>T (p.Asp746=) rs141301378 0.00101
NM_001273.5(CHD4):c.1947C>T (p.Tyr649=) rs138856908 0.00090
NM_001273.5(CHD4):c.1992C>T (p.Tyr664=) rs116849726 0.00089
NM_001273.5(CHD4):c.3087A>G (p.Ala1029=) rs143645855 0.00082
NM_001273.5(CHD4):c.2397A>C (p.Pro799=) rs138250427 0.00066
NM_001273.5(CHD4):c.1686+9A>G rs201167959 0.00063
NM_001273.5(CHD4):c.1209G>A (p.Lys403=) rs149884399 0.00060
NM_001273.5(CHD4):c.2610C>T (p.Leu870=) rs61759470 0.00047
NM_001273.5(CHD4):c.101-5T>A rs201854884 0.00046
NM_001273.5(CHD4):c.5002G>C (p.Glu1668Gln) rs201047688 0.00042
NM_001273.5(CHD4):c.87C>G (p.Pro29=) rs142820101 0.00035
NM_001273.5(CHD4):c.5529C>T (p.Asn1843=) rs201751048 0.00026
NM_001273.5(CHD4):c.1800C>T (p.Asn600=) rs144662304 0.00016
NM_001273.5(CHD4):c.3091-8G>T rs201313750 0.00016
NM_001273.5(CHD4):c.2734T>C (p.Leu912=) rs142502385 0.00011
NM_001273.5(CHD4):c.800-3T>C rs746196724 0.00010
NM_001273.5(CHD4):c.223-12G>A rs200831097 0.00008
NM_001273.5(CHD4):c.687G>A (p.Ala229=) rs546882640 0.00006
NM_001273.5(CHD4):c.4323C>T (p.Thr1441=) rs201490082 0.00004
NM_001273.5(CHD4):c.3772C>T (p.Leu1258=) rs758929074 0.00003
NM_001273.5(CHD4):c.1040G>A (p.Arg347Gln)
NM_001273.5(CHD4):c.1046C>T (p.Thr349Ile) rs774036270
NM_001273.5(CHD4):c.1137C>T (p.Gly379=)
NM_001273.5(CHD4):c.1243-5T>C
NM_001273.5(CHD4):c.143C>G (p.Thr48Ser)
NM_001273.5(CHD4):c.1586C>T (p.Thr529Met)
NM_001273.5(CHD4):c.1638A>G (p.Lys546=)
NM_001273.5(CHD4):c.1698C>T (p.His566=)
NM_001273.5(CHD4):c.1875C>T (p.His625=)
NM_001273.5(CHD4):c.1911C>T (p.His637=)
NM_001273.5(CHD4):c.2274T>C (p.Thr758=)
NM_001273.5(CHD4):c.2335C>T (p.Leu779=)
NM_001273.5(CHD4):c.2520G>A (p.Glu840=) rs538710424
NM_001273.5(CHD4):c.38C>T (p.Ala13Val)
NM_001273.5(CHD4):c.438+3G>A rs61753201
NM_001273.5(CHD4):c.456T>C (p.Ala152=)
NM_001273.5(CHD4):c.4677T>A (p.Pro1559=)
NM_001273.5(CHD4):c.4780-20del
NM_001273.5(CHD4):c.495C>T (p.His165=)
NM_001273.5(CHD4):c.5119+59G>T
NM_001273.5(CHD4):c.5454C>G (p.Leu1818=) rs572734539
NM_001273.5(CHD4):c.5503C>T (p.Leu1835=)
NM_001273.5(CHD4):c.5722-17C>T rs116460731

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