ClinVar Miner

List of variants in gene FGA reported as uncertain significance for amyloidosis

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP gnomAD frequency
NM_021871.4(FGA):c.1417G>A (p.Asp473Asn) rs200378626 0.00048
NM_021871.4(FGA):c.1823G>C (p.Gly608Ala) rs370873387 0.00006
NM_021871.4(FGA):c.1838A>G (p.His613Arg) rs201686865 0.00004
NM_021871.4(FGA):c.765G>A (p.Pro255=) rs779582722 0.00004
NM_021871.4(FGA):c.923G>A (p.Arg308Gln) rs760992799 0.00004
NM_021871.4(FGA):c.1718G>A (p.Arg573His) rs78506343 0.00003
NM_021871.4(FGA):c.1918C>G (p.Pro640Ala) rs199571440 0.00002
NM_021871.4(FGA):c.8C>T (p.Ser3Phe) rs771156473 0.00002
NM_000508.5(FGA):c.2089G>A (p.Gly697Ser) rs771023837 0.00001
NM_021871.4(FGA):c.1025G>A (p.Gly342Glu) rs774664670 0.00001
NM_021871.4(FGA):c.1463G>A (p.Gly488Asp) rs1382669489 0.00001
NM_021871.4(FGA):c.1470C>G (p.Asp490Glu) rs1335171406 0.00001
NM_021871.4(FGA):c.1615G>A (p.Glu539Lys) rs1190260696 0.00001
NM_021871.4(FGA):c.1760C>G (p.Thr587Arg) rs1309799184 0.00001
NM_021871.4(FGA):c.1915A>G (p.Lys639Glu) rs1424019951 0.00001
NM_021871.4(FGA):c.346G>A (p.Asp116Asn) rs886059153 0.00001
NM_021871.4(FGA):c.822C>T (p.Ser274=) rs886059150 0.00001
NM_021871.4(FGA):c.919A>G (p.Asn307Asp) rs750564329 0.00001
NM_000508.5(FGA):c.2350C>T (p.Gln784Ter) rs148824832
NM_021871.4(FGA):c.100G>A (p.Val34Met)
NM_021871.4(FGA):c.1099C>T (p.Arg367Cys)
NM_021871.4(FGA):c.1102G>A (p.Gly368Arg)
NM_021871.4(FGA):c.1103G>A (p.Gly368Glu)
NM_021871.4(FGA):c.1106G>A (p.Ser369Asn)
NM_021871.4(FGA):c.1117T>C (p.Trp373Arg)
NM_021871.4(FGA):c.1120A>G (p.Thr374Ala)
NM_021871.4(FGA):c.1169C>A (p.Ser390Tyr)
NM_021871.4(FGA):c.1207G>A (p.Ala403Thr) rs1730710209
NM_021871.4(FGA):c.122A>T (p.Glu41Val)
NM_021871.4(FGA):c.1247T>C (p.Val416Ala)
NM_021871.4(FGA):c.124A>G (p.Arg42Gly)
NM_021871.4(FGA):c.1339G>C (p.Glu447Gln)
NM_021871.4(FGA):c.1367C>T (p.Thr456Ile)
NM_021871.4(FGA):c.1419T>A (p.Asp473Glu)
NM_021871.4(FGA):c.1426A>G (p.Lys476Glu)
NM_021871.4(FGA):c.14G>A (p.Arg5Lys)
NM_021871.4(FGA):c.1529G>A (p.Arg510His)
NM_021871.4(FGA):c.1553C>G (p.Ala518Gly)
NM_021871.4(FGA):c.1603C>T (p.Pro535Ser)
NM_021871.4(FGA):c.1621G>C (p.Val541Leu) rs1578795080
NM_021871.4(FGA):c.1631C>T (p.Thr544Ile)
NM_021871.4(FGA):c.1633G>A (p.Glu545Lys)
NM_021871.4(FGA):c.1643G>A (p.Gly548Asp)
NM_021871.4(FGA):c.164G>C (p.Cys55Ser)
NM_021871.4(FGA):c.1670C>G (p.Thr557Arg)
NM_021871.4(FGA):c.1673A>G (p.Lys558Arg)
NM_021871.4(FGA):c.1717C>G (p.Arg573Gly)
NM_021871.4(FGA):c.1784C>T (p.Thr595Ile)
NM_021871.4(FGA):c.1827T>A (p.Ser609Arg)
NM_021871.4(FGA):c.1832C>T (p.Ala611Val)
NM_021871.4(FGA):c.1858A>G (p.Lys620Glu)
NM_021871.4(FGA):c.1868A>G (p.His623Arg)
NM_021871.4(FGA):c.1875A>C (p.Lys625Asn)
NM_021871.4(FGA):c.1925T>C (p.Leu642Pro)
NM_021871.4(FGA):c.19G>A (p.Val7Ile)
NM_021871.4(FGA):c.214G>C (p.Gly72Arg)
NM_021871.4(FGA):c.215G>A (p.Gly72Glu) rs1730803914
NM_021871.4(FGA):c.23G>C (p.Cys8Ser)
NM_021871.4(FGA):c.248A>G (p.Asn83Ser)
NM_021871.4(FGA):c.295A>G (p.Asn99Asp)
NM_021871.4(FGA):c.40G>A (p.Val14Met)
NM_021871.4(FGA):c.40G>T (p.Val14Leu)
NM_021871.4(FGA):c.428G>A (p.Arg143His)
NM_021871.4(FGA):c.510+13C>T
NM_021871.4(FGA):c.531C>G (p.Ile177Met)
NM_021871.4(FGA):c.533G>A (p.Arg178Gln)
NM_021871.4(FGA):c.569G>A (p.Arg190His)
NM_021871.4(FGA):c.614A>G (p.Glu205Gly) rs886059152
NM_021871.4(FGA):c.645T>C (p.Ser215=)
NM_021871.4(FGA):c.648A>G (p.Arg216=)
NM_021871.4(FGA):c.666A>T (p.Pro222=) rs886059151
NM_021871.4(FGA):c.688C>T (p.Pro230Ser)
NM_021871.4(FGA):c.696G>T (p.Leu232Phe)
NM_021871.4(FGA):c.761T>C (p.Met254Thr)
NM_021871.4(FGA):c.784G>A (p.Glu262Lys)
NM_021871.4(FGA):c.804G>A (p.Glu268=)
NM_021871.4(FGA):c.838G>A (p.Gly280Arg)
NM_021871.4(FGA):c.84A>T (p.Leu28=)
NM_021871.4(FGA):c.856C>G (p.Pro286Ala)
NM_021871.4(FGA):c.873T>G (p.Ser291Arg)
NM_021871.4(FGA):c.896G>A (p.Ser299Asn)
NM_021871.4(FGA):c.908G>A (p.Gly303Glu)
NM_021871.4(FGA):c.974G>A (p.Ser325Asn)
NM_021871.4(FGA):c.97G>A (p.Gly33Ser)
NM_021871.4(FGA):c.99C>T (p.Gly33=)

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