ClinVar Miner

List of variants in gene FGD4 reported as uncertain significance for Charcot-Marie-Tooth disease, type 4H

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Total variants: 106
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HGVS dbSNP
NM_001304480.1(FGD4):c.193A>T (p.Ile65Leu) rs886049253
NM_001304480.1(FGD4):c.301C>A (p.Pro101Thr) rs199744649
NM_001304481.1(FGD4):c.8del (p.Gly3fs) rs1357153004
NM_139241.3(FGD4):c.*1006C>T rs886049260
NM_139241.3(FGD4):c.*1160G>A rs540745195
NM_139241.3(FGD4):c.*1259A>G
NM_139241.3(FGD4):c.*1274G>A rs570269532
NM_139241.3(FGD4):c.*131A>G
NM_139241.3(FGD4):c.*1351A>T
NM_139241.3(FGD4):c.*1354A>G rs886049261
NM_139241.3(FGD4):c.*1356T>G rs886049262
NM_139241.3(FGD4):c.*1365T>C
NM_139241.3(FGD4):c.*1375C>T
NM_139241.3(FGD4):c.*1485T>C rs55970127
NM_139241.3(FGD4):c.*1530T>C
NM_139241.3(FGD4):c.*1704C>G rs886049263
NM_139241.3(FGD4):c.*1781G>A rs886049264
NM_139241.3(FGD4):c.*1866T>G rs886049265
NM_139241.3(FGD4):c.*1908G>C rs886049266
NM_139241.3(FGD4):c.*2026A>G rs765502938
NM_139241.3(FGD4):c.*2096T>A
NM_139241.3(FGD4):c.*2192G>A
NM_139241.3(FGD4):c.*2264G>A
NM_139241.3(FGD4):c.*2309G>A
NM_139241.3(FGD4):c.*2374G>T rs753715337
NM_139241.3(FGD4):c.*2462C>A rs575272682
NM_139241.3(FGD4):c.*2487C>A
NM_139241.3(FGD4):c.*2648G>A
NM_139241.3(FGD4):c.*2813C>T rs148195158
NM_139241.3(FGD4):c.*2859G>A
NM_139241.3(FGD4):c.*3022A>G
NM_139241.3(FGD4):c.*3037C>A rs886049267
NM_139241.3(FGD4):c.*3044T>C rs747748956
NM_139241.3(FGD4):c.*3150A>G rs542871416
NM_139241.3(FGD4):c.*3195T>G
NM_139241.3(FGD4):c.*3438C>T rs886049269
NM_139241.3(FGD4):c.*3482G>T rs886049270
NM_139241.3(FGD4):c.*3543G>C
NM_139241.3(FGD4):c.*368T>C
NM_139241.3(FGD4):c.*3814A>G rs886049271
NM_139241.3(FGD4):c.*3905A>G rs886049273
NM_139241.3(FGD4):c.*3937A>G
NM_139241.3(FGD4):c.*3940G>A
NM_139241.3(FGD4):c.*3994A>G
NM_139241.3(FGD4):c.*4118G>A
NM_139241.3(FGD4):c.*411A>G rs886049256
NM_139241.3(FGD4):c.*4268A>G rs542163387
NM_139241.3(FGD4):c.*4317T>G
NM_139241.3(FGD4):c.*4347T>C
NM_139241.3(FGD4):c.*4446A>G
NM_139241.3(FGD4):c.*4756A>G rs763037960
NM_139241.3(FGD4):c.*4832G>A
NM_139241.3(FGD4):c.*4862C>A rs886049275
NM_139241.3(FGD4):c.*4925A>T rs886049276
NM_139241.3(FGD4):c.*4977G>C rs575914495
NM_139241.3(FGD4):c.*497T>C rs886049257
NM_139241.3(FGD4):c.*5020G>C rs886049277
NM_139241.3(FGD4):c.*5072A>G rs886049278
NM_139241.3(FGD4):c.*5152C>T rs886049279
NM_139241.3(FGD4):c.*5153G>A
NM_139241.3(FGD4):c.*5223G>A rs886049280
NM_139241.3(FGD4):c.*5243C>T
NM_139241.3(FGD4):c.*5265A>G
NM_139241.3(FGD4):c.*5309C>T rs556209722
NM_139241.3(FGD4):c.*5321G>A
NM_139241.3(FGD4):c.*5329G>C rs886049281
NM_139241.3(FGD4):c.*5389A>G
NM_139241.3(FGD4):c.*69T>C
NM_139241.3(FGD4):c.*712C>T
NM_139241.3(FGD4):c.*734G>A rs886049258
NM_139241.3(FGD4):c.*762G>T rs886049259
NM_139241.3(FGD4):c.*795G>A rs112398567
NM_139241.3(FGD4):c.-246+9C>T rs531501340
NM_139241.3(FGD4):c.-289A>G rs56168193
NM_139241.3(FGD4):c.-370G>A rs184708096
NM_139241.3(FGD4):c.-421A>C rs192626243
NM_139241.3(FGD4):c.-433C>G
NM_139241.3(FGD4):c.-447T>C rs886049252
NM_139241.3(FGD4):c.-448C>G
NM_139241.3(FGD4):c.-455C>A
NM_139241.3(FGD4):c.1132+13T>C rs762177862
NM_139241.3(FGD4):c.1191+6T>C
NM_139241.3(FGD4):c.1198C>G (p.Leu400Val) rs750265200
NM_139241.3(FGD4):c.1366C>A (p.Pro456Thr) rs138160928
NM_139241.3(FGD4):c.1525_1527del (p.Lys509del)
NM_139241.3(FGD4):c.1569T>C (p.Phe523=)
NM_139241.3(FGD4):c.1711C>G (p.Pro571Ala) rs144693221
NM_139241.3(FGD4):c.1761+12T>G
NM_139241.3(FGD4):c.1814G>A (p.Gly605Asp) rs886049255
NM_139241.3(FGD4):c.2095A>G (p.Met699Val)
NM_139241.3(FGD4):c.2149G>A (p.Val717Met) rs61753359
NM_139241.3(FGD4):c.255A>T (p.Ala85=) rs139357821
NM_139241.3(FGD4):c.310G>A (p.Glu104Lys) rs752621629
NM_139241.3(FGD4):c.329T>C (p.Leu110Pro) rs142609007
NM_139241.3(FGD4):c.374C>T (p.Thr125Met)
NM_139241.3(FGD4):c.398A>G (p.Asp133Gly) rs759415605
NM_139241.3(FGD4):c.479G>A (p.Gly160Asp) rs201826412
NM_139241.3(FGD4):c.50C>G (p.Pro17Arg) rs371407163
NM_139241.3(FGD4):c.569T>C (p.Leu190Pro) rs144980336
NM_139241.3(FGD4):c.635A>G (p.Asn212Ser) rs147969494
NM_139241.3(FGD4):c.731C>T (p.Ser244Leu)
NM_139241.3(FGD4):c.852A>G (p.Arg284=) rs773609461
NM_139241.3(FGD4):c.894G>T (p.Met298Ile)
NM_139241.3(FGD4):c.956G>A (p.Arg319His) rs533939591
NM_139241.3(FGD4):c.993+4A>T rs767855809
NM_139241.3(FGD4):c.994-4A>G rs886049254

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