ClinVar Miner

List of variants in gene FAT4 reported as likely benign for FAT4-related disorder

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Gene type:
ClinVar version:
Total variants: 108
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HGVS dbSNP gnomAD frequency
NM_001291303.3(FAT4):c.6733G>A (p.Val2245Ile) rs112971995 0.00426
NM_001291303.3(FAT4):c.10853C>T (p.Thr3618Met) rs111423173 0.00407
NM_001291303.3(FAT4):c.7358G>T (p.Ser2453Ile) rs72914988 0.00327
NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val) rs142747281 0.00288
NM_001291303.3(FAT4):c.13554G>A (p.Leu4518=) rs78235204 0.00273
NM_001291303.3(FAT4):c.7935C>T (p.Asp2645=) rs146157250 0.00244
NM_001291303.3(FAT4):c.5987A>G (p.Lys1996Arg) rs140055438 0.00242
NM_001291303.3(FAT4):c.10390A>G (p.Ile3464Val) rs147872710 0.00237
NM_001291303.3(FAT4):c.14159C>G (p.Ala4720Gly) rs76607227 0.00206
NM_001291303.3(FAT4):c.7787T>C (p.Leu2596Ser) rs111501860 0.00205
NM_001291303.3(FAT4):c.13404G>A (p.Val4468=) rs149993049 0.00181
NM_001291303.3(FAT4):c.3294T>A (p.Pro1098=) rs200300207 0.00140
NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val) rs145639192 0.00135
NM_001291303.3(FAT4):c.3424G>A (p.Val1142Met) rs202188213 0.00127
NM_001291303.3(FAT4):c.1855C>T (p.Arg619Cys) rs202125547 0.00121
NM_001291303.3(FAT4):c.8021A>T (p.Asp2674Val) rs138655269 0.00121
NM_001291303.3(FAT4):c.3402A>T (p.Glu1134Asp) rs144768563 0.00113
NM_001291303.3(FAT4):c.7052A>G (p.Asn2351Ser) rs145105421 0.00096
NM_001291303.3(FAT4):c.7231A>T (p.Thr2411Ser) rs147297895 0.00084
NM_001291303.3(FAT4):c.7103C>A (p.Ala2368Glu) rs116568645 0.00074
NM_001291303.3(FAT4):c.13111A>G (p.Met4371Val) rs139260545 0.00064
NM_001291303.3(FAT4):c.11260A>G (p.Ser3754Gly) rs79909102 0.00058
NM_001291303.3(FAT4):c.11693C>T (p.Ala3898Val) rs138275098 0.00054
NM_001291303.3(FAT4):c.13417G>A (p.Val4473Ile) rs145835705 0.00048
NM_001291303.3(FAT4):c.185G>C (p.Gly62Ala) rs201009019 0.00045
NM_001291303.3(FAT4):c.3768A>G (p.Arg1256=) rs114652326 0.00042
NM_001291303.3(FAT4):c.2917G>A (p.Val973Ile) rs199497561 0.00041
NM_001291303.3(FAT4):c.12066C>T (p.Gly4022=) rs144476127 0.00036
NM_001291303.3(FAT4):c.14718C>T (p.Gly4906=) rs147617723 0.00030
NM_001291303.3(FAT4):c.1698C>T (p.Ala566=) rs370653820 0.00030
NM_001291303.3(FAT4):c.10392C>A (p.Ile3464=) rs140494092 0.00029
NM_001291303.3(FAT4):c.8580C>T (p.Val2860=) rs144031841 0.00026
NM_001291303.3(FAT4):c.14877A>G (p.Ala4959=) rs376402724 0.00021
NM_001291303.3(FAT4):c.4941C>T (p.Asn1647=) rs184884584 0.00021
NM_001291303.3(FAT4):c.13088G>T (p.Gly4363Val) rs199797338 0.00020
NM_001291303.3(FAT4):c.5924T>C (p.Ile1975Thr) rs200276252 0.00019
NM_001291303.3(FAT4):c.7452T>C (p.Gly2484=) rs200513521 0.00019
NM_001291303.3(FAT4):c.11906-10C>T rs370757220 0.00015
NM_001291303.3(FAT4):c.13878C>T (p.Asn4626=) rs369989432 0.00013
NM_001291303.3(FAT4):c.14325G>A (p.Pro4775=) rs758537642 0.00013
NM_001291303.3(FAT4):c.390C>T (p.Asp130=) rs373639016 0.00013
NM_001291303.3(FAT4):c.8313T>C (p.Asn2771=) rs148344513 0.00012
NM_001291303.3(FAT4):c.7266C>T (p.Ser2422=) rs147010455 0.00010
NM_001291303.3(FAT4):c.12085G>A (p.Ala4029Thr) rs140544054 0.00009
NM_001291303.3(FAT4):c.6729C>T (p.Ser2243=) rs368872163 0.00009
NM_001291303.3(FAT4):c.7813A>G (p.Ile2605Val) rs745697037 0.00009
NM_001291303.3(FAT4):c.12381G>A (p.Val4127=) rs377051363 0.00007
NM_001291303.3(FAT4):c.4797C>A (p.Leu1599=) rs746466001 0.00007
NM_001291303.3(FAT4):c.14678G>A (p.Arg4893Gln) rs151139631 0.00006
NM_001291303.3(FAT4):c.2450C>T (p.Ala817Val) rs539442232 0.00006
NM_001291303.3(FAT4):c.5308-5T>C rs373654898 0.00006
NM_001291303.3(FAT4):c.5404T>C (p.Leu1802=) rs191940938 0.00005
NM_001291303.3(FAT4):c.6324C>G (p.Leu2108=) rs140302868 0.00005
NM_001291303.3(FAT4):c.8854A>C (p.Ser2952Arg) rs538489921 0.00005
NM_001291303.3(FAT4):c.11943A>T (p.Gly3981=) rs754755525 0.00004
NM_001291303.3(FAT4):c.12768C>T (p.Ser4256=) rs1006074076 0.00004
NM_001291303.3(FAT4):c.1299C>G (p.Ser433=) rs764678411 0.00004
NM_001291303.3(FAT4):c.14472A>G (p.Pro4824=) rs201832398 0.00004
NM_001291303.3(FAT4):c.5532C>T (p.Pro1844=) rs374897074 0.00004
NM_001291303.3(FAT4):c.7962C>T (p.Tyr2654=) rs546465658 0.00004
NM_001291303.3(FAT4):c.9006G>A (p.Thr3002=) rs142357260 0.00004
NM_001291303.3(FAT4):c.91C>T (p.Leu31=) rs756659900 0.00004
NM_001291303.3(FAT4):c.10188C>T (p.Thr3396=) rs771506746 0.00003
NM_001291303.3(FAT4):c.12486T>C (p.Pro4162=) rs569666845 0.00003
NM_001291303.3(FAT4):c.12870G>C (p.Gly4290=) rs779040505 0.00003
NM_001291303.3(FAT4):c.2574G>A (p.Glu858=) rs371041455 0.00003
NM_001291303.3(FAT4):c.2646A>T (p.Thr882=) rs187912140 0.00003
NM_001291303.3(FAT4):c.3999C>T (p.Leu1333=) rs761822656 0.00003
NM_001291303.3(FAT4):c.5943T>C (p.Tyr1981=) rs149373164 0.00003
NM_001291303.3(FAT4):c.13209G>A (p.Pro4403=) rs763983959 0.00002
NM_001291303.3(FAT4):c.14738G>A (p.Gly4913Asp) rs765666547 0.00002
NM_001291303.3(FAT4):c.1845C>T (p.Asn615=) rs548524386 0.00002
NM_001291303.3(FAT4):c.2376A>G (p.Val792=) rs779400775 0.00002
NM_001291303.3(FAT4):c.3327C>T (p.Phe1109=) rs763960674 0.00002
NM_001291303.3(FAT4):c.6444T>C (p.Asn2148=) rs779420772 0.00002
NM_001291303.3(FAT4):c.6531C>T (p.Phe2177=) rs775866114 0.00002
NM_001291303.3(FAT4):c.9981T>C (p.Arg3327=) rs752677813 0.00002
NM_001291303.3(FAT4):c.10407A>G (p.Glu3469=) rs747627861 0.00001
NM_001291303.3(FAT4):c.11022A>G (p.Pro3674=) rs771392259 0.00001
NM_001291303.3(FAT4):c.12465A>G (p.Gln4155=) rs1727063661 0.00001
NM_001291303.3(FAT4):c.235G>T (p.Ala79Ser) rs767730943 0.00001
NM_001291303.3(FAT4):c.3012C>A (p.Thr1004=) rs550025709 0.00001
NM_001291303.3(FAT4):c.4365A>G (p.Leu1455=) rs757401187 0.00001
NM_001291303.3(FAT4):c.5308-9T>C rs199866344 0.00001
NM_001291303.3(FAT4):c.6618T>C (p.Ser2206=) rs1735020530 0.00001
NM_001291303.3(FAT4):c.842C>T (p.Thr281Ile) rs564305264 0.00001
NM_001291303.3(FAT4):c.9222A>G (p.Gln3074=) rs541662297 0.00001
NM_001291303.3(FAT4):c.9282C>T (p.Ser3094=) rs773285768 0.00001
NM_001291303.3(FAT4):c.9306G>A (p.Glu3102=) rs752903305 0.00001
NM_001291303.3(FAT4):c.10116T>G (p.Ser3372=) rs2530908375
NM_001291303.3(FAT4):c.10578C>A (p.Gly3526=) rs770783630
NM_001291303.3(FAT4):c.11991C>T (p.Asn3997=)
NM_001291303.3(FAT4):c.12430A>C (p.Arg4144=) rs777578313
NM_001291303.3(FAT4):c.13548C>T (p.Thr4516=) rs138057366
NM_001291303.3(FAT4):c.2316A>G (p.Gln772=) rs187427286
NM_001291303.3(FAT4):c.2705TGG[1] (p.Val903del) rs541157165
NM_001291303.3(FAT4):c.2994A>G (p.Gln998=) rs1034387310
NM_001291303.3(FAT4):c.4425A>G (p.Lys1475=) rs2530451461
NM_001291303.3(FAT4):c.4803T>G (p.Val1601=)
NM_001291303.3(FAT4):c.5920+9T>C rs2530757339
NM_001291303.3(FAT4):c.6192T>C (p.Pro2064=)
NM_001291303.3(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_001291303.3(FAT4):c.7466C>T (p.Ala2489Val) rs144853732
NM_001291303.3(FAT4):c.7725G>T (p.Thr2575=) rs140288688
NM_001291303.3(FAT4):c.7815C>T (p.Ile2605=) rs201257189
NM_001291303.3(FAT4):c.876G>A (p.Glu292=) rs1560752487
NM_001291303.3(FAT4):c.9057A>G (p.Ser3019=) rs763659763
NM_001291303.3(FAT4):c.9474A>G (p.Leu3158=) rs780508167

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