ClinVar Miner

List of variants in gene FAT4 reported as uncertain significance by GeneDx

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Total variants: 42
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HGVS dbSNP
NM_001291303.3(FAT4):c.2705TGG[1] (p.Val903del) rs541157165
NM_024582.4(FAT4):c.10055C>A (p.Thr3352Asn) rs145285004
NM_024582.4(FAT4):c.10193C>T (p.Ala3398Val) rs1553927211
NM_024582.4(FAT4):c.10787C>G (p.Ser3596Cys) rs558897707
NM_024582.4(FAT4):c.11147G>A (p.Arg3716His) rs139635339
NM_024582.4(FAT4):c.1163C>T (p.Pro388Leu) rs991371776
NM_024582.4(FAT4):c.12060C>T (p.Gly4020=) rs144476127
NM_024582.4(FAT4):c.1237A>G (p.Lys413Glu) rs1471306819
NM_024582.4(FAT4):c.12605C>T (p.Thr4202Ile) rs1173461199
NM_024582.4(FAT4):c.12641G>A (p.Arg4214His) rs148170326
NM_024582.4(FAT4):c.12763G>A (p.Glu4255Lys) rs143513466
NM_024582.4(FAT4):c.13174C>T (p.Pro4392Ser) rs772779154
NM_024582.4(FAT4):c.13411G>A (p.Val4471Ile) rs145835705
NM_024582.4(FAT4):c.13454C>T (p.Ala4485Val) rs141234678
NM_024582.4(FAT4):c.14660G>A (p.Arg4887Lys) rs35845544
NM_024582.4(FAT4):c.14671C>G (p.Arg4891Gly) rs765997899
NM_024582.4(FAT4):c.2896A>G (p.Ile966Val) rs778631726
NM_024582.4(FAT4):c.3065A>G (p.Asp1022Gly) rs372060616
NM_024582.4(FAT4):c.3328G>A (p.Glu1110Lys) rs377275274
NM_024582.4(FAT4):c.3424G>A (p.Val1142Met) rs202188213
NM_024582.4(FAT4):c.3682C>G (p.Gln1228Glu) rs200227715
NM_024582.4(FAT4):c.4250C>A (p.Pro1417His) rs201515596
NM_024582.4(FAT4):c.4257C>G (p.Ser1419Arg) rs377613970
NM_024582.4(FAT4):c.5275A>G (p.Ile1759Val) rs145639192
NM_024582.4(FAT4):c.5317G>T (p.Ala1773Ser) rs750458935
NM_024582.4(FAT4):c.5347G>A (p.Ala1783Thr) rs571447839
NM_024582.4(FAT4):c.5401C>T (p.Arg1801Trp) rs201887525
NM_024582.4(FAT4):c.5597C>T (p.Thr1866Met) rs141773516
NM_024582.4(FAT4):c.6094A>G (p.Thr2032Ala) rs147314754
NM_024582.4(FAT4):c.6554C>A (p.Thr2185Lys) rs1553968839
NM_024582.4(FAT4):c.6719C>T (p.Thr2240Ile) rs774192877
NM_024582.4(FAT4):c.6991G>A (p.Val2331Ile) rs752320782
NM_024582.4(FAT4):c.7103C>A (p.Ala2368Glu) rs116568645
NM_024582.4(FAT4):c.7196T>C (p.Ile2399Thr) rs140285782
NM_024582.4(FAT4):c.8015A>T (p.Asp2672Val) rs138655269
NM_024582.4(FAT4):c.8072C>T (p.Ser2691Leu) rs148918820
NM_024582.4(FAT4):c.8326A>G (p.Ile2776Val) rs773858750
NM_024582.4(FAT4):c.8725T>C (p.Tyr2909His) rs148655455
NM_024582.4(FAT4):c.8855T>G (p.Ile2952Arg) rs762222146
NM_024582.4(FAT4):c.9157C>A (p.Gln3053Lys) rs199778782
NM_024582.4(FAT4):c.9359T>C (p.Met3120Thr) rs371686578
NM_024582.4(FAT4):c.9596A>G (p.Tyr3199Cys) rs115895451

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