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: 38
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HGVS dbSNP
NM_014845.5(FIG4):c.-182G>A rs55873083
NM_014845.5(FIG4):c.102G>A (p.Thr34=) rs145711919
NM_014845.5(FIG4):c.1138-45A>T rs201459736
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.1525C>T (p.Leu509=) rs146488614
NM_014845.5(FIG4):c.1923G>A (p.Lys641=) rs140078026
NM_014845.5(FIG4):c.2097-10C>G rs142482745
NM_014845.5(FIG4):c.243A>G (p.Lys81=) rs200257799
NM_014845.5(FIG4):c.2459+7T>G rs575271308
NM_014845.5(FIG4):c.2546+17A>C rs1050332219
NM_014845.5(FIG4):c.27C>T (p.Ile9=) rs141040807
NM_014845.5(FIG4):c.33G>C (p.Ser11=) rs527523781
NM_014845.5(FIG4):c.446+9G>A rs190287033
NM_014845.5(FIG4):c.535C>T (p.Leu179Phe) rs141116831
NM_014845.5(FIG4):c.762C>T (p.Phe254=) rs201013726
NM_014845.5(FIG4):c.776-270C>T rs112727135
NM_014845.6(FIG4):c.1137+10G>A rs1583671962
NM_014845.6(FIG4):c.1272-8C>T rs1583697467
NM_014845.6(FIG4):c.1443C>T (p.Ile481=) rs1583701662
NM_014845.6(FIG4):c.1602T>C (p.Tyr534=) rs1583703907
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.2235C>T (p.Ala745=) rs144830399
NM_014845.6(FIG4):c.2459+7T>C rs575271308
NM_014845.6(FIG4):c.2568G>A (p.Ser856=) rs140055056
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.516C>T (p.Ser172=) rs759246119
NM_014845.6(FIG4):c.54T>C (p.Tyr18=) rs746307320
NM_014845.6(FIG4):c.66+8C>T rs768404941
NM_014845.6(FIG4):c.717A>G (p.Lys239=) rs750904354
NM_014845.6(FIG4):c.811C>T (p.Leu271=) rs1360869637
NM_014845.6(FIG4):c.882T>C (p.Asp294=) rs776821372
NM_014845.6(FIG4):c.885T>A (p.Val295=) rs551491783

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