ClinVar Miner

List of variants in gene FGA studied for hematologic disorder

Included ClinVar conditions (819):
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Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_021871.3(FGA):c.-58A>G rs2070011 0.65406
NM_021871.4(FGA):c.991A>G (p.Thr331Ala) rs6050 0.29256
NM_021871.4(FGA):c.1542T>C (p.Pro514=) rs4766 0.00426
NM_021871.4(FGA):c.1366A>G (p.Thr456Ala) rs2070031 0.00262
NM_021871.4(FGA):c.16A>G (p.Ile6Val) rs2070025 0.00250
NM_021871.4(FGA):c.181-14C>T rs190703077 0.00240
NM_021871.4(FGA):c.300G>A (p.Lys100=) rs112877216 0.00240
NM_021871.4(FGA):c.780G>A (p.Glu260=) rs145563362 0.00167
NM_021871.4(FGA):c.1417G>A (p.Asp473Asn) rs200378626 0.00048
NM_021871.4(FGA):c.1199C>T (p.Ser400Phe) rs184635235 0.00031
NM_021871.4(FGA):c.244A>C (p.Thr82Pro) rs199554805 0.00031
NM_021871.4(FGA):c.*50T>G rs369606098 0.00013
NM_021871.4(FGA):c.510+1G>T rs146387238 0.00009
NM_021871.4(FGA):c.616C>G (p.Gln206Glu) rs560732073 0.00009
NM_021871.4(FGA):c.1072G>A (p.Gly358Arg) rs201105899 0.00007
NM_021871.4(FGA):c.1444G>A (p.Val482Met) rs139146037 0.00006
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.450G>A (p.Gln150=) rs368446857 0.00002
NM_021871.4(FGA):c.502C>T (p.Arg168Ter) rs755117226 0.00002
NM_021871.4(FGA):c.8C>T (p.Ser3Phe) rs771156473 0.00002
NM_021871.4(FGA):c.904C>G (p.Pro302Ala) rs200203992 0.00002
NM_000508.3(FGA):c.103C>T (p.Arg35Cys) rs121909606 0.00001
NM_000508.5(FGA):c.2527T>C (p.Trp843Arg) rs1280924091 0.00001
NM_021871.4(FGA):c.1025G>A (p.Gly342Glu) rs774664670 0.00001
NM_021871.4(FGA):c.104G>A (p.Arg35His) rs121909607 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.1560C>T (p.Phe520=) rs778304190 0.00001
NM_021871.4(FGA):c.1634A>T (p.Glu545Val) rs121909612 0.00001
NM_021871.4(FGA):c.1912G>A (p.Gly638Arg) rs771429165 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.364+1G>A rs778779380 0.00001
NM_021871.4(FGA):c.532C>T (p.Arg178Ter) rs140911890 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
NC_000004.11:g.(?_155506411)_(155510715_155511785)del
NC_000004.11:g.(?_155506426)_(155511895_?)del
NC_000004.12:g.(154580323_154580329)_(154590210_154590216)del
NM_000508.3(FGA):c.1717C>T (p.Arg573Cys) rs121909613
NM_000508.5(FGA):c.2021T>C (p.Leu674Ser) rs2110806407
NM_000508.5(FGA):c.2024T>C (p.Ile675Thr) rs2110806390
NM_000508.5(FGA):c.2024T>G (p.Ile675Ser) rs2110806390
NM_000508.5(FGA):c.2128G>A (p.Gly710Ser) rs2110806103
NM_000508.5(FGA):c.2155del (p.Gln719fs) rs2110806028
NM_000508.5(FGA):c.2350C>T (p.Gln784Ter) rs148824832
NM_000508.5(FGA):c.2372A>T (p.Asp791Val) rs1479874554
NM_021871.4(FGA):c.*133G>A rs182736373
NM_021871.4(FGA):c.103C>G (p.Arg35Gly) rs121909606
NM_021871.4(FGA):c.1055del (p.Pro352fs) rs1299596156
NM_021871.4(FGA):c.1119G>A (p.Trp373Ter)
NM_021871.4(FGA):c.117del (p.Val40fs) rs762964798
NM_021871.4(FGA):c.1207G>A (p.Ala403Thr) rs1730710209
NM_021871.4(FGA):c.1486G>T (p.Asp496Tyr) rs2110809573
NM_021871.4(FGA):c.1517del (p.Leu506fs)
NM_021871.4(FGA):c.1754del (p.Ser585fs)
NM_021871.4(FGA):c.1930C>G (p.Pro644Ala) rs1730682953
NM_021871.4(FGA):c.364+5G>A rs891744509
NM_021871.4(FGA):c.431_432del (p.Lys144fs) rs934668242
NM_021871.4(FGA):c.448C>T (p.Gln150Ter) rs763715993
NM_021871.4(FGA):c.473dup (p.Asn158fs)
NM_021871.4(FGA):c.541C>T (p.Arg181Ter)
NM_021871.4(FGA):c.614A>G (p.Glu205Gly) rs886059152
NM_021871.4(FGA):c.666A>T (p.Pro222=) rs886059151
NM_021871.4(FGA):c.711dup (p.Lys238Ter) rs606231225
NM_021871.4(FGA):c.713del (p.Lys238fs)
NM_021871.4(FGA):c.811C>T (p.Arg271Ter) rs1578796476
NM_021871.4(FGA):c.829T>C (p.Tyr277His) rs1473392017
NM_021871.4(FGA):c.922C>T (p.Arg308Ter) rs776817952

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