ClinVar Miner

List of variants in gene FAT4 reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP
NM_001291303.3(FAT4):c.12479+8G>A rs150505878
NM_001291303.3(FAT4):c.13029T>C (p.Leu4343=) rs146822665
NM_001291303.3(FAT4):c.13088G>T (p.Gly4363Val)
NM_001291303.3(FAT4):c.13111A>G (p.Met4371Val) rs139260545
NM_001291303.3(FAT4):c.14940A>G (p.Glu4980=) rs149073729
NM_001291303.3(FAT4):c.2216A>G (p.Asn739Ser)
NM_001291303.3(FAT4):c.2450C>T (p.Ala817Val)
NM_001291303.3(FAT4):c.3192C>T (p.Asp1064=) rs140899478
NM_001291303.3(FAT4):c.3658T>A (p.Ser1220Thr) rs181368820
NM_001291303.3(FAT4):c.5883T>C (p.Ser1961=) rs117016099
NM_001291303.3(FAT4):c.7326G>A (p.Ala2442=) rs201829586
NM_001291303.3(FAT4):c.7452T>C (p.Gly2484=)
NM_001291303.3(FAT4):c.7466C>T (p.Ala2489Val)
NM_001291303.3(FAT4):c.8055C>T (p.Ser2685=) rs139033158
NM_001291303.3(FAT4):c.9141C>T (p.Ser3047=) rs146492311
NM_001291303.3(FAT4):c.9451G>A (p.Ala3151Thr)
NM_001291303.3(FAT4):c.9627C>T (p.Ala3209=) rs148558216
NM_024582.4(FAT4):c.10101A>G (p.Glu3367=) rs147646369
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.10847C>T (p.Thr3616Met) rs111423173
NM_024582.4(FAT4):c.1101A>G (p.Val367=) rs57692448
NM_024582.4(FAT4):c.1128G>A (p.Val376=) rs202216461
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.11664C>T (p.Cys3888=) rs150894545
NM_024582.4(FAT4):c.11687C>T (p.Ala3896Val) rs138275098
NM_024582.4(FAT4):c.11814A>G (p.Ser3938=) rs17009721
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.12208-5C>T rs17009761
NM_024582.4(FAT4):c.12500C>T (p.Thr4167Ile) rs115822434
NM_024582.4(FAT4):c.12813G>A (p.Val4271=) rs6824160
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.12980A>G (p.Asp4327Gly) rs114234553
NM_024582.4(FAT4):c.13398G>A (p.Val4466=) rs149993049
NM_024582.4(FAT4):c.13548G>A (p.Leu4516=) rs78235204
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.14660G>A (p.Arg4887Lys) rs35845544
NM_024582.4(FAT4):c.14682C>T (p.His4894=) rs35862879
NM_024582.4(FAT4):c.14914C>T (p.Pro4972Ser) rs1014867
NM_024582.4(FAT4):c.2316A>G (p.Gln772=) rs187427286
NM_024582.4(FAT4):c.2322C>T (p.Pro774=) rs200593370
NM_024582.4(FAT4):c.2420C>T (p.Ala807Val) rs1039808
NM_024582.4(FAT4):c.2811G>T (p.Lys937Asn) rs112454576
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.3402A>T (p.Glu1134Asp) rs144768563
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.4154T>C (p.Leu1385Ser) rs139883132
NM_024582.4(FAT4):c.4219G>A (p.Val1407Ile) rs114227532
NM_024582.4(FAT4):c.4303A>G (p.Ile1435Val) rs142747281
NM_024582.4(FAT4):c.4305C>T (p.Ile1435=) rs2710555
NM_024582.4(FAT4):c.5760T>C (p.Asp1920=) rs958415
NM_024582.4(FAT4):c.5921-14C>T rs190218898
NM_024582.4(FAT4):c.6219A>G (p.Gln2073=) rs35355603
NM_024582.4(FAT4):c.6478A>G (p.Lys2160Glu) rs75942329
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.739C>A (p.Pro247Thr) rs191329848
NM_024582.4(FAT4):c.7701G>C (p.Val2567=) rs988863
NM_024582.4(FAT4):c.7781T>C (p.Leu2594Ser) rs111501860
NM_024582.4(FAT4):c.7929C>T (p.Asp2643=) rs146157250
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.9822C>T (p.Pro3274=) rs73849226
NM_024582.4(FAT4):c.9870G>A (p.Gly3290=) rs115219562
NM_024582.4(FAT4):c.9885G>A (p.Val3295=) rs139704889

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