ClinVar Miner

List of variants in gene FGD4 reported by GeneDx

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Total variants: 60
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HGVS dbSNP
NM_001304481.1(FGD4):c.20C>G (p.Thr7Ser) rs187853007
NM_001304481.1(FGD4):c.220C>A (p.Pro74Thr) rs199744649
NM_001304481.1(FGD4):c.222C>A (p.Pro74=) rs1465471003
NM_001370298.3(FGD4):c.1808_1809del (p.Thr603fs) rs886039361
NM_001370298.3(FGD4):c.2173-322del rs150852537
NM_001370298.3(FGD4):c.2298_2302del (p.Lys767fs) rs751035912
NM_001370298.3(FGD4):c.2298_2302dup (p.Gly768fs) rs751035912
NM_139241.3(FGD4):c.-246+9C>T rs531501340
NM_139241.3(FGD4):c.-92-339A>G rs73305550
NM_139241.3(FGD4):c.-93+1G>A rs1057518446
NM_139241.3(FGD4):c.1133-135G>A rs10844252
NM_139241.3(FGD4):c.1133-236T>G rs1004968
NM_139241.3(FGD4):c.1191+13C>T rs557373932
NM_139241.3(FGD4):c.1203G>C (p.Lys401Asn) rs1131691394
NM_139241.3(FGD4):c.1278A>C (p.Glu426Asp) rs879254000
NM_139241.3(FGD4):c.1305G>A (p.Arg435=) rs10844253
NM_139241.3(FGD4):c.1329C>A (p.Tyr443Ter) rs886041200
NM_139241.3(FGD4):c.1338+200A>C rs10844254
NM_139241.3(FGD4):c.1348A>G (p.Met450Val) rs201186597
NM_139241.3(FGD4):c.1366C>A (p.Pro456Thr) rs138160928
NM_139241.3(FGD4):c.1512-7A>G rs200542541
NM_139241.3(FGD4):c.1515T>C (p.Ser505=) rs60803891
NM_139241.3(FGD4):c.1518G>A (p.Ala506=) rs11052110
NM_139241.3(FGD4):c.1543-8T>C rs115061722
NM_139241.3(FGD4):c.1562A>G (p.Asp521Gly) rs141237776
NM_139241.3(FGD4):c.1635+221T>A rs12303795
NM_139241.3(FGD4):c.1636-292C>T rs11052111
NM_139241.3(FGD4):c.1659C>G (p.Ala553=) rs188104446
NM_139241.3(FGD4):c.1711C>A (p.Pro571Thr) rs144693221
NM_139241.3(FGD4):c.1711C>G (p.Pro571Ala) rs144693221
NM_139241.3(FGD4):c.1712C>A (p.Pro571His) rs145071617
NM_139241.3(FGD4):c.1737G>A (p.Arg579=) rs372451301
NM_139241.3(FGD4):c.1761+200G>A rs1909510
NM_139241.3(FGD4):c.1761+8A>T rs761674021
NM_139241.3(FGD4):c.1762-23T>G rs76834265
NM_139241.3(FGD4):c.1762-257C>T rs11831099
NM_139241.3(FGD4):c.1782C>T (p.Ser594=) rs147136365
NM_139241.3(FGD4):c.1962G>A (p.Glu654=) rs201822384
NM_139241.3(FGD4):c.2005dup (p.Gln669fs) rs1555224772
NM_139241.3(FGD4):c.2040C>T (p.Pro680=) rs1314359233
NM_139241.3(FGD4):c.2044-236G>A rs10771973
NM_139241.3(FGD4):c.2044-46A>G rs74073032
NM_139241.3(FGD4):c.2149G>A (p.Val717Met) rs61753359
NM_139241.3(FGD4):c.2176G>T (p.Glu726Ter) rs771529170
NM_139241.3(FGD4):c.255A>T (p.Ala85=) rs139357821
NM_139241.3(FGD4):c.329T>C (p.Leu110Pro) rs142609007
NM_139241.3(FGD4):c.381A>G (p.Ile127Met) rs774466701
NM_139241.3(FGD4):c.435C>G (p.Asp145Glu) rs904582
NM_139241.3(FGD4):c.479G>A (p.Gly160Asp) rs201826412
NM_139241.3(FGD4):c.484G>C (p.Gly162Arg) rs774679169
NM_139241.3(FGD4):c.50C>G (p.Pro17Arg) rs371407163
NM_139241.3(FGD4):c.569T>A (p.Leu190Gln) rs144980336
NM_139241.3(FGD4):c.601-154T>G rs12299653
NM_139241.3(FGD4):c.732G>A (p.Ser244=) rs34555341
NM_139241.3(FGD4):c.837-149T>G rs4931640
NM_139241.3(FGD4):c.837-16dup rs368420700
NM_139241.3(FGD4):c.837-37T>A rs4931641
NM_139241.3(FGD4):c.955C>T (p.Arg319Cys) rs1131691854
NM_139241.3(FGD4):c.993+10C>T rs374656859
NM_139241.3(FGD4):c.993+149T>C rs7964734

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