ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
NM_014845.5(FIG4):c.1040-4T>C rs374343214
NM_014845.5(FIG4):c.1158T>C (p.His386=) rs370557879
NM_014845.5(FIG4):c.1272-16T>C rs1554303954
NM_014845.5(FIG4):c.1584-8T>A rs199522051
NM_014845.5(FIG4):c.173A>G (p.Tyr58Cys) rs145337669
NM_014845.5(FIG4):c.1751-3del rs1064794667
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.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.2199A>G (p.Glu733=) rs537464083
NM_014845.5(FIG4):c.2238G>A (p.Pro746=) rs753867543
NM_014845.5(FIG4):c.2459+7T>G rs575271308
NM_014845.5(FIG4):c.2460-17T>C rs201533992
NM_014845.5(FIG4):c.2547-5T>G rs200267243
NM_014845.5(FIG4):c.33G>C (p.Ser11=) rs527523781
NM_014845.5(FIG4):c.446+9G>A rs190287033
NM_014845.5(FIG4):c.447-16G>T rs200890189
NM_014845.5(FIG4):c.627A>G (p.Leu209=) rs140111406
NM_014845.5(FIG4):c.66+13dup rs755637236
NM_014845.5(FIG4):c.808A>G (p.Thr270Ala) rs61729092
NM_014845.6(FIG4):c.2377-11_2377-10del rs200535694

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