ClinVar Miner

List of variants in gene FAT4 studied for not specified

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Gene type:
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Total variants: 110
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HGVS dbSNP
NM_001291303.3(FAT4):c.14311C>T (p.Arg4771Cys)
NM_001291303.3(FAT4):c.9800A>G (p.His3267Arg) rs773545119
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.11352A>G (p.Glu3784=) rs369625076
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.11613C>T (p.Cys3871=) rs141328606
NM_024582.4(FAT4):c.11618G>A (p.Ser3873Asn) rs12650153
NM_024582.4(FAT4):c.1163C>T (p.Pro388Leu) rs991371776
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.12293+6G>C rs541775780
NM_024582.4(FAT4):c.12375G>A (p.Val4125=) rs377051363
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.12864G>C (p.Gly4288=) rs779040505
NM_024582.4(FAT4):c.12903C>T (p.Asp4301=) rs17009825
NM_024582.4(FAT4):c.12921T>C (p.Phe4307=) rs146058039
NM_024582.4(FAT4):c.1296T>C (p.Pro432=) rs372007282
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.13411G>A (p.Val4471Ile) rs145835705
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.14319G>A (p.Pro4773=) rs758537642
NM_024582.4(FAT4):c.14355C>T (p.Val4785=) rs1014865
NM_024582.4(FAT4):c.14382G>A (p.Arg4794=) rs149584153
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.14712C>T (p.Gly4904=) rs147617723
NM_024582.4(FAT4):c.14914C>T (p.Pro4972Ser) rs1014867
NM_024582.4(FAT4):c.1698C>T (p.Ala566=) rs370653820
NM_024582.4(FAT4):c.1959C>T (p.Ala653=) rs191491571
NM_024582.4(FAT4):c.2316A>G (p.Gln772=) rs187427286
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.2944T>C (p.Leu982=) rs2940779
NM_024582.4(FAT4):c.3096A>G (p.Ala1032=) rs57537930
NM_024582.4(FAT4):c.3294T>A (p.Pro1098=) rs200300207
NM_024582.4(FAT4):c.3328G>A (p.Glu1110Lys) rs377275274
NM_024582.4(FAT4):c.3351G>A (p.Ser1117=) rs769768427
NM_024582.4(FAT4):c.3402A>T (p.Glu1134Asp) rs144768563
NM_024582.4(FAT4):c.3417T>C (p.Phe1139=) rs367935912
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.3687G>C (p.Val1229=) rs7657251
NM_024582.4(FAT4):c.3768A>G (p.Arg1256=) rs114652326
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.4530T>C (p.Tyr1510=) rs368207419
NM_024582.4(FAT4):c.4542C>T (p.Asn1514=) rs199793434
NM_024582.4(FAT4):c.524G>T (p.Arg175Leu) rs143534324
NM_024582.4(FAT4):c.5275A>G (p.Ile1759Val) rs145639192
NM_024582.4(FAT4):c.5308-19G>A rs1369164587
NM_024582.4(FAT4):c.5424C>G (p.Ser1808=) rs200354953
NM_024582.4(FAT4):c.5598G>A (p.Thr1866=) rs370130221
NM_024582.4(FAT4):c.5760T>C (p.Asp1920=) rs958415
NM_024582.4(FAT4):c.5921-14C>T rs190218898
NM_024582.4(FAT4):c.5921-18dup rs535120107
NM_024582.4(FAT4):c.5987A>G (p.Lys1996Arg) rs140055438
NM_024582.4(FAT4):c.6094A>G (p.Thr2032Ala) rs147314754
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.7131A>G (p.Ala2377=) rs138403046
NM_024582.4(FAT4):c.7261G>A (p.Ala2421Thr) rs776977766
NM_024582.4(FAT4):c.7352G>T (p.Ser2451Ile) rs72914988
NM_024582.4(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_024582.4(FAT4):c.7587C>T (p.Asn2529=) rs367971071
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.7807A>G (p.Ile2603Val) rs745697037
NM_024582.4(FAT4):c.7929C>T (p.Asp2643=) rs146157250
NM_024582.4(FAT4):c.8072C>T (p.Ser2691Leu) rs148918820
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.8979C>T (p.Thr2993=) rs1057521481
NM_024582.4(FAT4):c.9596A>G (p.Tyr3199Cys) rs115895451
NM_024582.4(FAT4):c.960G>A (p.Ser320=) rs1057523940
NM_024582.4(FAT4):c.9643C>T (p.His3215Tyr) rs73849225
NM_024582.4(FAT4):c.9690G>A (p.Ala3230=) rs142877205
NM_024582.4(FAT4):c.9804G>A (p.Val3268=) rs139518045
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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