ClinVar Miner

List of variants in gene FAT4 reported as uncertain significance

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Gene type:
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Total variants: 131
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HGVS dbSNP
NM_001291303.1(FAT4):c.10560G>A (p.Met3520Ile) rs144506470
NM_001291303.1(FAT4):c.8588T>C (p.Phe2863Ser) rs1560614899
NM_001291303.3(FAT4):c.1012G>A (p.Glu338Lys)
NM_001291303.3(FAT4):c.10262T>C (p.Ile3421Thr)
NM_001291303.3(FAT4):c.10451C>G (p.Ala3484Gly)
NM_001291303.3(FAT4):c.10468C>A (p.Pro3490Thr)
NM_001291303.3(FAT4):c.1099G>A (p.Val367Ile)
NM_001291303.3(FAT4):c.11152C>T (p.Arg3718Cys)
NM_001291303.3(FAT4):c.11260A>G (p.Ser3754Gly)
NM_001291303.3(FAT4):c.11706T>G (p.Asp3902Glu)
NM_001291303.3(FAT4):c.11814A>C (p.Glu3938Asp)
NM_001291303.3(FAT4):c.1198G>T (p.Gly400Trp)
NM_001291303.3(FAT4):c.12085G>A (p.Ala4029Thr)
NM_001291303.3(FAT4):c.13193T>C (p.Ile4398Thr) rs200729108
NM_001291303.3(FAT4):c.13385G>A (p.Arg4462Lys)
NM_001291303.3(FAT4):c.13388C>T (p.Thr4463Ile)
NM_001291303.3(FAT4):c.13402G>A (p.Val4468Met)
NM_001291303.3(FAT4):c.13564G>C (p.Val4522Leu)
NM_001291303.3(FAT4):c.13641GAA[2] (p.Lys4551del) rs1560639673
NM_001291303.3(FAT4):c.14105G>A (p.Arg4702Gln)
NM_001291303.3(FAT4):c.14311C>T (p.Arg4771Cys)
NM_001291303.3(FAT4):c.14404C>T (p.Pro4802Ser)
NM_001291303.3(FAT4):c.14743G>A (p.Ala4915Thr)
NM_001291303.3(FAT4):c.14837T>C (p.Val4946Ala)
NM_001291303.3(FAT4):c.14841T>A (p.Asp4947Glu) rs768693221
NM_001291303.3(FAT4):c.1827C>A (p.Asp609Glu)
NM_001291303.3(FAT4):c.2290G>A (p.Val764Ile)
NM_001291303.3(FAT4):c.2324A>G (p.Asn775Ser)
NM_001291303.3(FAT4):c.2705TGG[1] (p.Val903del) rs541157165
NM_001291303.3(FAT4):c.2917G>A (p.Val973Ile)
NM_001291303.3(FAT4):c.3167G>A (p.Ser1056Asn)
NM_001291303.3(FAT4):c.3212T>C (p.Val1071Ala) rs200138872
NM_001291303.3(FAT4):c.3505C>T (p.Arg1169Trp)
NM_001291303.3(FAT4):c.3722A>G (p.Asn1241Ser)
NM_001291303.3(FAT4):c.3726T>G (p.Asn1242Lys)
NM_001291303.3(FAT4):c.3738C>G (p.His1246Gln)
NM_001291303.3(FAT4):c.4169T>C (p.Ile1390Thr)
NM_001291303.3(FAT4):c.418A>G (p.Ile140Val)
NM_001291303.3(FAT4):c.4411A>G (p.Ile1471Val)
NM_001291303.3(FAT4):c.4432A>G (p.Ile1478Val)
NM_001291303.3(FAT4):c.44C>G (p.Pro15Arg)
NM_001291303.3(FAT4):c.4543G>A (p.Val1515Met)
NM_001291303.3(FAT4):c.5161A>G (p.Thr1721Ala)
NM_001291303.3(FAT4):c.5246T>C (p.Val1749Ala)
NM_001291303.3(FAT4):c.5792A>G (p.Tyr1931Cys)
NM_001291303.3(FAT4):c.5889_5890delinsAA (p.Leu1964Ile)
NM_001291303.3(FAT4):c.5944A>G (p.Ser1982Gly)
NM_001291303.3(FAT4):c.6515A>C (p.Asp2172Ala)
NM_001291303.3(FAT4):c.7312G>T (p.Val2438Phe)
NM_001291303.3(FAT4):c.733G>A (p.Asp245Asn)
NM_001291303.3(FAT4):c.739C>T (p.Pro247Ser) rs191329848
NM_001291303.3(FAT4):c.7466C>A (p.Ala2489Glu)
NM_001291303.3(FAT4):c.8162A>G (p.Asn2721Ser) rs1452280145
NM_001291303.3(FAT4):c.8280A>C (p.Lys2760Asn) rs750907829
NM_001291303.3(FAT4):c.8290A>C (p.Asn2764His) rs147281598
NM_001291303.3(FAT4):c.8313T>C (p.Asn2771=)
NM_001291303.3(FAT4):c.8363C>G (p.Pro2788Arg)
NM_001291303.3(FAT4):c.8408T>C (p.Ile2803Thr)
NM_001291303.3(FAT4):c.8417A>C (p.Asn2806Thr)
NM_001291303.3(FAT4):c.8525G>A (p.Arg2842His)
NM_001291303.3(FAT4):c.8753A>G (p.Glu2918Gly)
NM_001291303.3(FAT4):c.9152C>A (p.Ser3051Tyr)
NM_001291303.3(FAT4):c.9279A>C (p.Gln3093His) rs769424345
NM_001291303.3(FAT4):c.9313A>G (p.Ser3105Gly) rs764097811
NM_001291303.3(FAT4):c.9800A>G (p.His3267Arg) rs773545119
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.10384A>G (p.Ile3462Val) rs147872710
NM_024582.4(FAT4):c.10787C>G (p.Ser3596Cys) rs558897707
NM_024582.4(FAT4):c.11034G>A (p.Thr3678=) rs147998041
NM_024582.4(FAT4):c.11147G>A (p.Arg3716His) rs139635339
NM_024582.4(FAT4):c.1128G>A (p.Val376=) rs202216461
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.12064C>T (p.Arg4022Trp) rs138019311
NM_024582.4(FAT4):c.12125G>A (p.Gly4042Asp) rs760328375
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.12845C>T (p.Ser4282Phe) rs199682210
NM_024582.4(FAT4):c.13174C>T (p.Pro4392Ser) rs772779154
NM_024582.4(FAT4):c.13286A>T (p.Asp4429Val) rs774943740
NM_024582.4(FAT4):c.13393G>A (p.Val4465Met) rs1215405311
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.13519G>C (p.Ala4507Pro) rs1553931010
NM_024582.4(FAT4):c.14435G>A (p.Arg4812Lys) rs756452113
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.3842A>G (p.Tyr1281Cys) rs1317645126
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.4526G>A (p.Arg1509Gln) rs776836295
NM_024582.4(FAT4):c.4745G>A (p.Gly1582Glu) rs1553959187
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.5317G>T (p.Ala1773Ser) rs750458935
NM_024582.4(FAT4):c.5347G>A (p.Ala1783Thr) rs571447839
NM_024582.4(FAT4):c.5367C>T (p.Ile1789=) rs144922340
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.5884A>T (p.Thr1962Ser) rs749792331
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.6554C>A (p.Thr2185Lys) rs1553968839
NM_024582.4(FAT4):c.6719C>T (p.Thr2240Ile) rs774192877
NM_024582.4(FAT4):c.6977C>T (p.Thr2326Ile) rs200344386
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.7225A>T (p.Thr2409Ser) rs147297895
NM_024582.4(FAT4):c.7261G>A (p.Ala2421Thr) rs776977766
NM_024582.4(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_024582.4(FAT4):c.7510T>G (p.Ser2504Ala) rs148603730
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.913A>T (p.Ile305Phe) rs1553958385
NM_024582.4(FAT4):c.9150C>A (p.Asp3050Glu) rs761372826
NM_024582.4(FAT4):c.9157C>A (p.Gln3053Lys) rs199778782
NM_024582.4(FAT4):c.9229A>G (p.Ile3077Val) rs138817920
NM_024582.4(FAT4):c.9359T>C (p.Met3120Thr) rs371686578
NM_024582.4(FAT4):c.9596A>G (p.Tyr3199Cys) rs115895451

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