ClinVar Miner

List of variants in gene FUS reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_004960.4(FUS):c.833-29C>T rs72550862 0.01058
NM_004960.4(FUS):c.*41G>A rs80301724 0.00551
NM_004960.4(FUS):c.523+22C>T rs118174709 0.00529
NM_004960.4(FUS):c.273C>T (p.Tyr91=) rs73530286 0.00196
NM_004960.4(FUS):c.1566G>A (p.Arg522=) rs138901914 0.00095
NM_004960.4(FUS):c.198T>C (p.Tyr66=) rs144853447 0.00056
NM_004960.4(FUS):c.684C>T (p.Gly228=) rs151073460 0.00034
NM_004960.4(FUS):c.188A>G (p.Asn63Ser) rs140883211 0.00033
NM_004960.4(FUS):c.1080C>T (p.Ser360=) rs190724342 0.00022
NM_004960.4(FUS):c.*48G>A rs376510148 0.00014
NM_004960.4(FUS):c.1067-6C>T rs77813265 0.00014
NM_004960.4(FUS):c.339C>T (p.Tyr113=) rs770345118 0.00008
NM_004960.4(FUS):c.-44G>A rs370320909 0.00006
NM_004960.4(FUS):c.66G>A (p.Gly22=) rs147877613 0.00006
NM_004960.4(FUS):c.716A>G (p.Tyr239Cys) rs145013063 0.00002
NM_004960.4(FUS):c.821G>A (p.Arg274His) rs1415220872 0.00002
NM_004960.4(FUS):c.1561C>T (p.Arg521Cys) rs121909668 0.00001
NM_004960.4(FUS):c.181A>G (p.Ser61Gly) rs1481060391 0.00001
NM_004960.4(FUS):c.192A>G (p.Thr64=) rs776333956 0.00001
NM_004960.4(FUS):c.*132C>A rs565540429
NM_004960.4(FUS):c.*65_*66del rs2144143082
NM_004960.4(FUS):c.-6G>C
NM_004960.4(FUS):c.1226G>A (p.Gly409Glu)
NM_004960.4(FUS):c.1240G>A (p.Gly414Ser) rs370295006
NM_004960.4(FUS):c.1388A>G (p.His463Arg) rs2144138846
NM_004960.4(FUS):c.1400A>G (p.Asn467Ser)
NM_004960.4(FUS):c.1554_1557del (p.Gln519fs) rs2144142389
NM_004960.4(FUS):c.1556A>G (p.Gln519Arg)
NM_004960.4(FUS):c.1561C>G (p.Arg521Gly) rs121909668
NM_004960.4(FUS):c.1562G>A (p.Arg521His) rs121909671
NM_004960.4(FUS):c.1574C>T (p.Pro525Leu) rs886041390
NM_004960.4(FUS):c.412GGACAGCAGCAAAGCTAT[1] (p.138GQQQSY[1]) rs747579808
NM_004960.4(FUS):c.518_523del
NM_004960.4(FUS):c.608G>A (p.Gly203Asp) rs2079243802
NM_004960.4(FUS):c.669CGG[3] (p.Gly229_Gly231del) rs72550890
NM_004960.4(FUS):c.669CGG[4] (p.Gly230_Gly231del) rs72550890
NM_004960.4(FUS):c.669CGG[7] (p.Gly231dup) rs72550890
NM_004960.4(FUS):c.678C>T (p.Gly226=)
NM_004960.4(FUS):c.681C>T (p.Gly227=)
NM_004960.4(FUS):c.681_689del (p.Gly229_Gly231del) rs767564995
NM_004960.4(FUS):c.685GGT[6] (p.Gly229_Gly231dup) rs757651881
NM_004960.4(FUS):c.800-275C>G rs138631439

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