ClinVar Miner

List of variants in gene FIG4 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_014845.6(FIG4):c.1090A>T (p.Met364Leu) rs2295837 0.04647
NC_000006.12:g.109825565A>G rs76385456 0.02142
NM_014845.6(FIG4):c.2097-217C>T rs78154984 0.01518
NM_014845.6(FIG4):c.2546+158C>T rs7745191 0.01508
NM_014845.6(FIG4):c.1949-148A>G rs115395338 0.01355
NM_014845.5(FIG4):c.-182G>A rs55873083 0.01220
NM_014845.6(FIG4):c.776-270C>T rs112727135 0.01149
NM_014845.6(FIG4):c.1434+54G>A rs57159750 0.01033
NM_014845.6(FIG4):c.497+61G>A rs115467680 0.00992
NM_014845.6(FIG4):c.1138-284A>G rs111341099 0.00891
NM_014845.6(FIG4):c.497+175A>T rs111759494 0.00875
NM_014845.6(FIG4):c.1584-30A>C rs116602685 0.00742
NM_014845.6(FIG4):c.498-87T>C rs112790444 0.00683
NM_014845.6(FIG4):c.1138-291G>A rs113252524 0.00678
NM_014845.6(FIG4):c.1751-294A>G rs59852203 0.00670
NM_014845.6(FIG4):c.447-16G>T rs200890189 0.00618
NM_014845.6(FIG4):c.2377-71T>G rs186543204 0.00563
NM_014845.6(FIG4):c.66+10C>T rs200063827 0.00462
NM_014845.6(FIG4):c.498-145A>G rs192762300 0.00456
NM_014845.6(FIG4):c.*14C>T rs114136062 0.00408
NM_014845.6(FIG4):c.27C>T (p.Ile9=) rs141040807 0.00398
NM_014845.6(FIG4):c.1389-209T>G rs148001811 0.00366
NM_014845.6(FIG4):c.647-48C>T rs114219763 0.00352
NM_014845.6(FIG4):c.1889+309T>C rs182955642 0.00305
NM_014845.6(FIG4):c.173A>G (p.Tyr58Cys) rs145337669 0.00275
NM_014845.6(FIG4):c.446+9G>A rs190287033 0.00128
NM_014845.6(FIG4):c.627A>G (p.Leu209=) rs140111406 0.00119
NM_014845.6(FIG4):c.1584-8T>A rs199522051 0.00086
NM_014845.6(FIG4):c.834A>T (p.Lys278Asn) rs138048706 0.00029
NM_014845.6(FIG4):c.1305G>C (p.Val435=) rs145227623 0.00011
NM_014845.6(FIG4):c.1863C>A (p.Thr621=) rs201744761 0.00011
NM_014845.6(FIG4):c.102G>A (p.Thr34=) rs145711919 0.00010
NM_014845.6(FIG4):c.1138-45A>T rs201459736 0.00009
NM_014845.6(FIG4):c.2459+7T>G rs575271308 0.00009
NM_014845.6(FIG4):c.918C>T (p.Cys306=) rs369159531 0.00008
NM_014845.6(FIG4):c.535C>T (p.Leu179Phe) rs141116831 0.00006
NM_014845.6(FIG4):c.1341T>C (p.Phe447=) rs199651811 0.00005
NM_014845.6(FIG4):c.1040-4T>C rs374343214 0.00004
NM_014845.6(FIG4):c.2232C>T (p.Ser744=) rs760578430 0.00003
NM_014845.6(FIG4):c.2388A>G (p.Gln796=) rs1439788451 0.00003
NM_014845.6(FIG4):c.1620C>T (p.Thr540=) rs746367416 0.00002
NM_014845.6(FIG4):c.2599A>G (p.Arg867Gly) rs533419433 0.00002
NM_014845.6(FIG4):c.2238G>A (p.Pro746=) rs753867543 0.00001
NM_014845.6(FIG4):c.1137+10G>A rs1583671962
NM_014845.6(FIG4):c.1435-117TTTTTG[7] rs71018366
NM_014845.6(FIG4):c.1583+3A>G rs866431185
NM_014845.6(FIG4):c.1602T>C (p.Tyr534=) rs1583703907
NM_014845.6(FIG4):c.165+228C>T rs73535344
NM_014845.6(FIG4):c.2097-10C>G rs142482745
NM_014845.6(FIG4):c.2145G>A (p.Val715=) rs1583738268
NM_014845.6(FIG4):c.2459+59C>T rs77634668
NM_014845.6(FIG4):c.2546+17A>C rs1050332219
NM_014845.6(FIG4):c.2547-5T>G rs200267243
NM_014845.6(FIG4):c.2568G>A (p.Ser856=) rs140055056
NM_014845.6(FIG4):c.267G>A (p.Ala89=)
NM_014845.6(FIG4):c.289+280A>G rs73535347
NM_014845.6(FIG4):c.447-17dup rs764540259
NM_014845.6(FIG4):c.447-4_447-3dup rs11377100
NM_014845.6(FIG4):c.858A>G (p.Lys286=)

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