ClinVar Miner

List of variants in gene FIG4 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_014845.5(FIG4):c.1051G>C (p.Asp351His) rs879253941
NM_014845.5(FIG4):c.1091T>A (p.Met364Lys) rs772677048
NM_014845.5(FIG4):c.1388+5G>T rs200730266
NM_014845.5(FIG4):c.1703A>G (p.Lys568Arg) rs1064797016
NM_014845.5(FIG4):c.2035C>T (p.Arg679Trp) rs188910818
NM_014845.5(FIG4):c.2080A>G (p.Met694Val) rs143531641
NM_014845.5(FIG4):c.2096G>A (p.Arg699His) rs750091928
NM_014845.5(FIG4):c.2200G>A (p.Glu734Lys) rs372846619
NM_014845.5(FIG4):c.2405A>G (p.Tyr802Cys) rs370293982
NM_014845.5(FIG4):c.2567C>T (p.Ser856Leu) rs200970494
NM_014845.5(FIG4):c.2639T>A (p.Ile880Asn) rs746915624
NM_014845.5(FIG4):c.263G>A (p.Arg88Gln) rs879254310
NM_014845.5(FIG4):c.506A>C (p.Tyr169Ser) rs770278572
NM_014845.5(FIG4):c.719G>C (p.Ser240Thr) rs772586786
NM_014845.5(FIG4):c.730C>T (p.Arg244Cys) rs138376077
NM_014845.6(FIG4):c.2433AGA[2] (p.Glu813del) rs876661144

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