ClinVar Miner

List of variants in gene FIG4 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 112
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HGVS dbSNP
NM_014845.5(FIG4):c.*14C>T rs114136062
NM_014845.5(FIG4):c.-182G>A rs55873083
NM_014845.5(FIG4):c.102G>A (p.Thr34=) rs145711919
NM_014845.5(FIG4):c.1040-4T>C rs374343214
NM_014845.5(FIG4):c.1090A>T (p.Met364Leu) rs2295837
NM_014845.5(FIG4):c.1138-45A>T rs201459736
NM_014845.5(FIG4):c.1158T>C (p.His386=) rs370557879
NM_014845.5(FIG4):c.122T>C (p.Ile41Thr) rs121908287
NM_014845.5(FIG4):c.1271+5A>G rs374583399
NM_014845.5(FIG4):c.1272-10C>G rs201293291
NM_014845.5(FIG4):c.1272-16T>C rs1554303954
NM_014845.5(FIG4):c.1305G>C (p.Val435=) rs145227623
NM_014845.5(FIG4):c.1350C>G (p.Arg450=) rs763035100
NM_014845.5(FIG4):c.1435-8C>T rs754607430
NM_014845.5(FIG4):c.1525C>T (p.Leu509=) rs146488614
NM_014845.5(FIG4):c.1584-8T>A rs199522051
NM_014845.5(FIG4):c.173A>G (p.Tyr58Cys) rs145337669
NM_014845.5(FIG4):c.1740T>C (p.Asn580=) rs1554304608
NM_014845.5(FIG4):c.1751-3del rs1064794667
NM_014845.5(FIG4):c.1755C>T (p.Ala585=) rs377111248
NM_014845.5(FIG4):c.1770C>T (p.Ser590=) rs1057524489
NM_014845.5(FIG4):c.1809G>A (p.Gly603=) rs148280593
NM_014845.5(FIG4):c.1812A>G (p.Lys604=) rs1399930708
NM_014845.5(FIG4):c.1863C>A (p.Thr621=) rs201744761
NM_014845.5(FIG4):c.1923G>A (p.Lys641=) rs140078026
NM_014845.5(FIG4):c.1940A>G (p.Tyr647Cys) rs150301327
NM_014845.5(FIG4):c.1949-15C>T rs778444771
NM_014845.5(FIG4):c.1983G>A (p.Val661=) rs1057524662
NM_014845.5(FIG4):c.2097-10C>G rs142482745
NM_014845.5(FIG4):c.2115C>T (p.Thr705=) rs201271644
NM_014845.5(FIG4):c.2154A>G (p.Pro718=) rs201138266
NM_014845.5(FIG4):c.2199A>G (p.Glu733=) rs537464083
NM_014845.5(FIG4):c.2223G>T (p.Thr741=) rs181012139
NM_014845.5(FIG4):c.2238G>A (p.Pro746=) rs753867543
NM_014845.5(FIG4):c.2241G>C (p.Pro747=) rs148589135
NM_014845.5(FIG4):c.2289G>A (p.Gly763=) rs756539176
NM_014845.5(FIG4):c.2382G>A (p.Val794=) rs1201567620
NM_014845.5(FIG4):c.243A>G (p.Lys81=) rs200257799
NM_014845.5(FIG4):c.2459+7T>G rs575271308
NM_014845.5(FIG4):c.2460-17T>C rs201533992
NM_014845.5(FIG4):c.2523G>A (p.Arg841=) rs1554309865
NM_014845.5(FIG4):c.2546+17A>C rs1050332219
NM_014845.5(FIG4):c.2547-5T>G rs200267243
NM_014845.5(FIG4):c.2568G>T (p.Ser856=) rs140055056
NM_014845.5(FIG4):c.27C>T (p.Ile9=) rs141040807
NM_014845.5(FIG4):c.300G>A (p.Arg100=) rs368831195
NM_014845.5(FIG4):c.33G>C (p.Ser11=) rs527523781
NM_014845.5(FIG4):c.350C>T (p.Ala117Val) rs551339249
NM_014845.5(FIG4):c.366T>C (p.His122=) rs772376305
NM_014845.5(FIG4):c.446+9G>A rs190287033
NM_014845.5(FIG4):c.447-16G>T rs200890189
NM_014845.5(FIG4):c.535C>T (p.Leu179Phe) rs141116831
NM_014845.5(FIG4):c.627A>G (p.Leu209=) rs140111406
NM_014845.5(FIG4):c.640G>A (p.Gly214Arg) rs529048339
NM_014845.5(FIG4):c.66+10C>T rs200063827
NM_014845.5(FIG4):c.66+13dup rs755637236
NM_014845.5(FIG4):c.705G>T (p.Leu235=) rs1026195072
NM_014845.5(FIG4):c.762C>T (p.Phe254=) rs201013726
NM_014845.5(FIG4):c.776-270C>T rs112727135
NM_014845.5(FIG4):c.808A>G (p.Thr270Ala) rs61729092
NM_014845.5(FIG4):c.834A>T (p.Lys278Asn) rs138048706
NM_014845.5(FIG4):c.870C>T (p.Asn290=) rs1236653957
NM_014845.5(FIG4):c.918C>T (p.Cys306=) rs369159531
NM_014845.6(FIG4):c.105A>G (p.Lys35=)
NM_014845.6(FIG4):c.1137+10G>A rs1583671962
NM_014845.6(FIG4):c.1272-10C>T rs201293291
NM_014845.6(FIG4):c.1272-8C>T rs1583697467
NM_014845.6(FIG4):c.1341T>C (p.Phe447=)
NM_014845.6(FIG4):c.1356T>C (p.Asp452=)
NM_014845.6(FIG4):c.1386A>G (p.Glu462=) rs764699770
NM_014845.6(FIG4):c.1443C>T (p.Ile481=) rs1583701662
NM_014845.6(FIG4):c.1536G>T (p.Leu512=)
NM_014845.6(FIG4):c.1602T>C (p.Tyr534=) rs1583703907
NM_014845.6(FIG4):c.1620C>T (p.Thr540=) rs746367416
NM_014845.6(FIG4):c.1750+11A>C
NM_014845.6(FIG4):c.1836A>G (p.Thr612=) rs1267198458
NM_014845.6(FIG4):c.1932A>G (p.Pro644=) rs767919652
NM_014845.6(FIG4):c.207C>T (p.Arg69=) rs1583643073
NM_014845.6(FIG4):c.2097-10C>T rs142482745
NM_014845.6(FIG4):c.2145G>A (p.Val715=) rs1583738268
NM_014845.6(FIG4):c.2180+20C>T
NM_014845.6(FIG4):c.2232C>T (p.Ser744=) rs760578430
NM_014845.6(FIG4):c.2235C>T (p.Ala745=) rs144830399
NM_014845.6(FIG4):c.2241G>A (p.Pro747=) rs148589135
NM_014845.6(FIG4):c.2319T>C (p.Ser773=)
NM_014845.6(FIG4):c.2377-11_2377-10del rs200535694
NM_014845.6(FIG4):c.2377-18T>C
NM_014845.6(FIG4):c.2377-20_2377-19insCT
NM_014845.6(FIG4):c.2406T>C (p.Tyr802=) rs765557108
NM_014845.6(FIG4):c.2459+7T>C rs575271308
NM_014845.6(FIG4):c.252G>A (p.Ser84=)
NM_014845.6(FIG4):c.2568G>A (p.Ser856=) rs140055056
NM_014845.6(FIG4):c.2574T>C (p.Asp858=) rs1583785957
NM_014845.6(FIG4):c.2640C>T (p.Ile880=) rs769813337
NM_014845.6(FIG4):c.2685C>T (p.Ser895=) rs764459799
NM_014845.6(FIG4):c.289+10C>A rs778732368
NM_014845.6(FIG4):c.289+17C>T
NM_014845.6(FIG4):c.351G>A (p.Ala117=) rs375963892
NM_014845.6(FIG4):c.401A>C (p.Tyr134Ser) rs571563767
NM_014845.6(FIG4):c.42G>A (p.Lys14=) rs552856153
NM_014845.6(FIG4):c.447-16delinsTT
NM_014845.6(FIG4):c.516C>T (p.Ser172=) rs759246119
NM_014845.6(FIG4):c.54T>C (p.Tyr18=) rs746307320
NM_014845.6(FIG4):c.658A>G (p.Ile220Val) rs565096937
NM_014845.6(FIG4):c.66+18G>A
NM_014845.6(FIG4):c.66+8C>T rs768404941
NM_014845.6(FIG4):c.717A>G (p.Lys239=) rs750904354
NM_014845.6(FIG4):c.744G>A (p.Leu248=)
NM_014845.6(FIG4):c.811C>T (p.Leu271=) rs1360869637
NM_014845.6(FIG4):c.876+8G>A rs923581334
NM_014845.6(FIG4):c.882T>C (p.Asp294=) rs776821372
NM_014845.6(FIG4):c.885T>A (p.Val295=) rs551491783

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