ClinVar Miner

List of variants in gene FAT4 reported as likely benign by GeneDx

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Total variants: 61
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HGVS dbSNP
NM_024582.4(FAT4):c.10101A>G (p.Glu3367=) rs147646369
NM_024582.4(FAT4):c.10384A>G (p.Ile3462Val) rs147872710
NM_024582.4(FAT4):c.10847C>T (p.Thr3616Met) rs111423173
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.11613C>T (p.Cys3871=) rs141328606
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.12293+6G>C rs541775780
NM_024582.4(FAT4):c.12375G>A (p.Val4125=) rs377051363
NM_024582.4(FAT4):c.12864G>C (p.Gly4288=) rs779040505
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.1299C>G (p.Ser433=) rs764678411
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.14319G>A (p.Pro4773=) rs758537642
NM_024582.4(FAT4):c.14382G>A (p.Arg4794=) rs149584153
NM_024582.4(FAT4):c.14571G>A (p.Arg4857=) rs144832106
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.14929G>A (p.Ala4977Thr) rs17009858
NM_024582.4(FAT4):c.1698C>T (p.Ala566=) rs370653820
NM_024582.4(FAT4):c.185G>C (p.Gly62Ala) rs201009019
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.2322C>T (p.Pro774=) rs200593370
NM_024582.4(FAT4):c.2811G>T (p.Lys937Asn) rs112454576
NM_024582.4(FAT4):c.3294T>A (p.Pro1098=) rs200300207
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.3768A>G (p.Arg1256=) rs114652326
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.4530T>C (p.Tyr1510=) rs368207419
NM_024582.4(FAT4):c.4542C>T (p.Asn1514=) rs199793434
NM_024582.4(FAT4):c.4941C>T (p.Asn1647=) rs184884584
NM_024582.4(FAT4):c.524G>T (p.Arg175Leu) rs143534324
NM_024582.4(FAT4):c.5307+40T>C rs569179408
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.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.6478A>G (p.Lys2160Glu) rs75942329
NM_024582.4(FAT4):c.7131A>G (p.Ala2377=) rs138403046
NM_024582.4(FAT4):c.7352G>T (p.Ser2451Ile) rs72914988
NM_024582.4(FAT4):c.7587C>T (p.Asn2529=) rs367971071
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.8979C>T (p.Thr2993=) rs1057521481
NM_024582.4(FAT4):c.9077A>G (p.Asp3026Gly) rs765151671
NM_024582.4(FAT4):c.960G>A (p.Ser320=) rs1057523940
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.9885G>A (p.Val3295=) rs139704889

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