ClinVar Miner

List of variants in gene FGD4 reported as likely benign

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Gene type:
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Total variants: 95
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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.1113C>T (p.Cys371=)
NM_001370298.3(FGD4):c.1248-7G>A
NM_001370298.3(FGD4):c.1344A>G (p.Glu448=)
NM_001370298.3(FGD4):c.1440T>C (p.His480=)
NM_001370298.3(FGD4):c.1485C>T (p.Leu495=)
NM_001370298.3(FGD4):c.1488T>G (p.Leu496=)
NM_001370298.3(FGD4):c.1543+8C>T
NM_001370298.3(FGD4):c.1755C>T (p.Asn585=)
NM_001370298.3(FGD4):c.1923-6_1923-2del
NM_001370298.3(FGD4):c.2067A>G (p.Arg689=)
NM_001370298.3(FGD4):c.2262C>T (p.Ile754=)
NM_001370298.3(FGD4):c.2346G>T (p.Val782=)
NM_001370298.3(FGD4):c.2433G>A (p.Leu811=)
NM_001370298.3(FGD4):c.2436C>T (p.Tyr812=)
NM_001370298.3(FGD4):c.2490C>T (p.Gly830=)
NM_001370298.3(FGD4):c.2559C>T (p.Ser853=)
NM_001370298.3(FGD4):c.2652A>G (p.Pro884=)
NM_001370298.3(FGD4):c.2685T>C (p.Pro895=)
NM_001370298.3(FGD4):c.441T>C (p.Ser147=)
NM_001370298.3(FGD4):c.624G>A (p.Leu208=)
NM_001370298.3(FGD4):c.945A>G (p.Val315=)
NM_001370298.3(FGD4):c.999C>T (p.His333=)
NM_139241.3(FGD4):c.*167G>A
NM_139241.3(FGD4):c.*2103A>G rs55963204
NM_139241.3(FGD4):c.*2638A>G rs193167910
NM_139241.3(FGD4):c.*3367G>T rs188648275
NM_139241.3(FGD4):c.*3676A>G rs189489067
NM_139241.3(FGD4):c.*3920del rs144034303
NM_139241.3(FGD4):c.*4014C>A
NM_139241.3(FGD4):c.*4028A>G
NM_139241.3(FGD4):c.*4497G>A rs367545740
NM_139241.3(FGD4):c.*4585T>A
NM_139241.3(FGD4):c.*4831C>T rs145433607
NM_139241.3(FGD4):c.*5244G>A rs186014657
NM_139241.3(FGD4):c.-246+9C>T rs531501340
NM_139241.3(FGD4):c.-484C>A rs79370524
NM_139241.3(FGD4):c.-92-339A>G rs73305550
NM_139241.3(FGD4):c.1132+8_1132+9insG rs1555216986
NM_139241.3(FGD4):c.1191+13C>T rs557373932
NM_139241.3(FGD4):c.1191+7G>A
NM_139241.3(FGD4):c.1194G>A (p.Glu398=) rs746263549
NM_139241.3(FGD4):c.1198C>T (p.Leu400=)
NM_139241.3(FGD4):c.1366C>A (p.Pro456Thr) rs138160928
NM_139241.3(FGD4):c.1398A>T (p.Thr466=) rs1220106574
NM_139241.3(FGD4):c.1413T>G (p.Val471=)
NM_139241.3(FGD4):c.1431A>G (p.Lys477=) rs1023207495
NM_139241.3(FGD4):c.1494A>G (p.Thr498=) rs572887361
NM_139241.3(FGD4):c.1511+11C>T
NM_139241.3(FGD4):c.1512-7A>G rs200542541
NM_139241.3(FGD4):c.1542+7C>T rs1408854259
NM_139241.3(FGD4):c.1543-8T>C rs115061722
NM_139241.3(FGD4):c.1560C>T (p.Ile520=) rs61748364
NM_139241.3(FGD4):c.1635+10A>G rs374150424
NM_139241.3(FGD4):c.1635+221T>A rs12303795
NM_139241.3(FGD4):c.1659C>A (p.Ala553=) rs188104446
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.1722A>G (p.Ala574=) rs771910342
NM_139241.3(FGD4):c.1737G>A (p.Arg579=) rs372451301
NM_139241.3(FGD4):c.1758A>C (p.Gly586=) rs200761894
NM_139241.3(FGD4):c.1761+8A>T rs761674021
NM_139241.3(FGD4):c.1762-23T>G rs76834265
NM_139241.3(FGD4):c.1782C>T (p.Ser594=) rs147136365
NM_139241.3(FGD4):c.1920A>G (p.Val640=) rs909875227
NM_139241.3(FGD4):c.1950T>G (p.Leu650=) rs1358873743
NM_139241.3(FGD4):c.1962G>A (p.Glu654=) rs201822384
NM_139241.3(FGD4):c.201C>T (p.Leu67=) rs141920723
NM_139241.3(FGD4):c.2040C>T (p.Pro680=) rs1314359233
NM_139241.3(FGD4):c.2044-10T>C rs1592514932
NM_139241.3(FGD4):c.2106C>T (p.Ser702=) rs777555137
NM_139241.3(FGD4):c.2149G>A (p.Val717Met) rs61753359
NM_139241.3(FGD4):c.2205C>T (p.Ile735=) rs759982135
NM_139241.3(FGD4):c.2214T>C (p.Ala738=) rs200144770
NM_139241.3(FGD4):c.2220A>G (p.Thr740=)
NM_139241.3(FGD4):c.236C>T (p.Thr79Ile) rs145115430
NM_139241.3(FGD4):c.255A>T (p.Ala85=) rs139357821
NM_139241.3(FGD4):c.374C>T (p.Thr125Met) rs200732890
NM_139241.3(FGD4):c.417T>A (p.Pro139=) rs1295234161
NM_139241.3(FGD4):c.479G>A (p.Gly160Asp) rs201826412
NM_139241.3(FGD4):c.57G>A (p.Lys19=) rs1427707678
NM_139241.3(FGD4):c.601-154T>G rs12299653
NM_139241.3(FGD4):c.635A>G (p.Asn212Ser) rs147969494
NM_139241.3(FGD4):c.732G>A (p.Ser244=) rs34555341
NM_139241.3(FGD4):c.759C>A (p.Ile253=) rs1592364946
NM_139241.3(FGD4):c.783T>C (p.Asn261=) rs201678865
NM_139241.3(FGD4):c.837-13A>G
NM_139241.3(FGD4):c.837-16dup rs368420700
NM_139241.3(FGD4):c.852A>G (p.Arg284=) rs773609461
NM_139241.3(FGD4):c.873A>G (p.Lys291=) rs1224103433
NM_139241.3(FGD4):c.885C>T (p.Phe295=) rs151083690
NM_139241.3(FGD4):c.93-20C>G rs1592293275
NM_139241.3(FGD4):c.993+10C>T rs374656859

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