ClinVar Miner

List of variants in gene FGD4 reported as likely benign for not provided

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Total variants: 21
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HGVS dbSNP
NM_001304481.1(FGD4):c.222C>A (p.Pro74=) rs1465471003
NM_139241.3(FGD4):c.-92-339A>G rs73305550
NM_139241.3(FGD4):c.1132+8_1132+9insG rs1555216986
NM_139241.3(FGD4):c.1398A>T (p.Thr466=) rs1220106574
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.1560C>T (p.Ile520=) rs61748364
NM_139241.3(FGD4):c.1635+221T>A rs12303795
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.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.2044-10T>C rs1592514932
NM_139241.3(FGD4):c.2214T>C (p.Ala738=) rs200144770
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.57G>A (p.Lys19=) rs1427707678
NM_139241.3(FGD4):c.601-154T>G rs12299653
NM_139241.3(FGD4):c.759C>A (p.Ile253=) rs1592364946
NM_139241.3(FGD4):c.873A>G (p.Lys291=) rs1224103433

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