ClinVar Miner

List of variants in gene FAT4 reported as benign by GeneDx

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Total variants: 65
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HGVS dbSNP
NM_024582.4(FAT4):c.-326A>G rs7677005
NM_024582.4(FAT4):c.10152A>G (p.Ala3384=) rs144585931
NM_024582.4(FAT4):c.10571G>A (p.Gly3524Asp) rs1567047
NM_024582.4(FAT4):c.10804A>C (p.Ile3602Leu) rs76491994
NM_024582.4(FAT4):c.1101A>G (p.Val367=) rs57692448
NM_024582.4(FAT4):c.11399C>T (p.Ser3800Phe) rs75380987
NM_024582.4(FAT4):c.11423A>G (p.His3808Arg) rs114637892
NM_024582.4(FAT4):c.11482A>G (p.Lys3828Glu) rs17009684
NM_024582.4(FAT4):c.11618G>A (p.Ser3873Asn) rs12650153
NM_024582.4(FAT4):c.11795-123C>T rs4146009
NM_024582.4(FAT4):c.11814A>G (p.Ser3938=) rs17009721
NM_024582.4(FAT4):c.11899+83A>C rs10010645
NM_024582.4(FAT4):c.12064C>T (p.Arg4022Trp) rs138019311
NM_024582.4(FAT4):c.12065G>A (p.Arg4022Gln) rs28515675
NM_024582.4(FAT4):c.12207+207C>T rs17009745
NM_024582.4(FAT4):c.12208-270C>T rs67399037
NM_024582.4(FAT4):c.12208-5C>T rs17009761
NM_024582.4(FAT4):c.12208-72G>A rs35472819
NM_024582.4(FAT4):c.12500C>T (p.Thr4167Ile) rs115822434
NM_024582.4(FAT4):c.12598+306T>C rs11737550
NM_024582.4(FAT4):c.12599-58C>T rs10026069
NM_024582.4(FAT4):c.12813G>A (p.Val4271=) rs6824160
NM_024582.4(FAT4):c.12816+28T>G rs11098815
NM_024582.4(FAT4):c.12846C>T (p.Ser4282=) rs17009819
NM_024582.4(FAT4):c.12849T>C (p.Asp4283=) rs78040862
NM_024582.4(FAT4):c.12903C>T (p.Asp4301=) rs17009825
NM_024582.4(FAT4):c.13078+219A>T rs1395237
NM_024582.4(FAT4):c.13078+227G>C rs1395236
NM_024582.4(FAT4):c.1358A>T (p.Gln453Leu) rs6847454
NM_024582.4(FAT4):c.13599G>A (p.Lys4533=) rs75469760
NM_024582.4(FAT4):c.13617G>A (p.Glu4539=) rs62312781
NM_024582.4(FAT4):c.14129C>G (p.Ser4710Cys) rs147662558
NM_024582.4(FAT4):c.14177G>A (p.Arg4726Lys) rs72675395
NM_024582.4(FAT4):c.14355C>T (p.Val4785=) rs1014865
NM_024582.4(FAT4):c.14598A>G (p.Arg4866=) rs1014866
NM_024582.4(FAT4):c.14657C>G (p.Ala4886Gly) rs35340865
NM_024582.4(FAT4):c.14914C>T (p.Pro4972Ser) rs1014867
NM_024582.4(FAT4):c.2420C>T (p.Ala807Val) rs1039808
NM_024582.4(FAT4):c.2919C>T (p.Val973=) rs144356360
NM_024582.4(FAT4):c.2944T>C (p.Leu982=) rs2940779
NM_024582.4(FAT4):c.3096A>G (p.Ala1032=) rs57537930
NM_024582.4(FAT4):c.3687G>C (p.Val1229=) rs7657251
NM_024582.4(FAT4):c.3769C>G (p.Gln1257Glu) rs36052762
NM_024582.4(FAT4):c.405C>T (p.Phe135=) rs72928772
NM_024582.4(FAT4):c.4305C>T (p.Ile1435=) rs2710555
NM_024582.4(FAT4):c.5176-82C>T rs11946554
NM_024582.4(FAT4):c.5569+266T>C rs6833240
NM_024582.4(FAT4):c.5760T>C (p.Asp1920=) rs958415
NM_024582.4(FAT4):c.6219A>G (p.Gln2073=) rs35355603
NM_024582.4(FAT4):c.6585T>C (p.Asn2195=) rs17009618
NM_024582.4(FAT4):c.6733G>A (p.Val2245Ile) rs112971995
NM_024582.4(FAT4):c.6844-276C>G rs74829391
NM_024582.4(FAT4):c.7019-230T>G rs17009654
NM_024582.4(FAT4):c.7199+264T>A rs7656590
NM_024582.4(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_024582.4(FAT4):c.7444+288C>T rs10084892
NM_024582.4(FAT4):c.7445-62C>T rs115240175
NM_024582.4(FAT4):c.7701G>C (p.Val2567=) rs988863
NM_024582.4(FAT4):c.831G>A (p.Ala277=) rs142490028
NM_024582.4(FAT4):c.8476G>A (p.Asp2826Asn) rs12508222
NM_024582.4(FAT4):c.8538C>T (p.Ser2846=) rs139132509
NM_024582.4(FAT4):c.8586G>A (p.Val2862=) rs111758803
NM_024582.4(FAT4):c.8836A>G (p.Ile2946Val) rs76048257
NM_024582.4(FAT4):c.9643C>T (p.His3215Tyr) rs73849225
NM_024582.4(FAT4):c.9870G>A (p.Gly3290=) rs115219562

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