ClinVar Miner

List of variants in gene FAT4 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 108
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HGVS dbSNP gnomAD frequency
NM_001291303.3(FAT4):c.7707G>C (p.Val2569=) rs988863 0.99289
NM_001291303.3(FAT4):c.11624G>A (p.Ser3875Asn) rs12650153 0.99272
NM_001291303.3(FAT4):c.5760T>C (p.Asp1920=) rs958415 0.99029
NM_001291303.3(FAT4):c.2944T>C (p.Leu982=) rs2940779 0.74871
NM_001291303.3(FAT4):c.14604A>G (p.Arg4868=) rs1014866 0.74715
NM_001291303.3(FAT4):c.4305C>T (p.Ile1435=) rs2710555 0.73896
NM_001291303.3(FAT4):c.2420C>T (p.Ala807Val) rs1039808 0.46652
NM_001291303.3(FAT4):c.12214-5C>T rs17009761 0.38645
NM_001291303.3(FAT4):c.10577G>A (p.Gly3526Asp) rs1567047 0.21721
NM_001291303.3(FAT4):c.13623G>A (p.Glu4541=) rs62312781 0.19007
NM_001291303.3(FAT4):c.405C>T (p.Phe135=) rs72928772 0.17506
NM_001291303.3(FAT4):c.6585T>C (p.Asn2195=) rs17009618 0.14565
NM_001291303.3(FAT4):c.9649C>T (p.His3217Tyr) rs73849225 0.12573
NM_001291303.3(FAT4):c.3687G>C (p.Val1229=) rs7657251 0.09845
NM_001291303.3(FAT4):c.12819G>A (p.Val4273=) rs6824160 0.09773
NM_001291303.3(FAT4):c.12909C>T (p.Asp4303=) rs17009825 0.08824
NM_001291303.3(FAT4):c.3769C>G (p.Gln1257Glu) rs36052762 0.05186
NM_001291303.3(FAT4):c.14920C>T (p.Pro4974Ser) rs1014867 0.04974
NM_001291303.3(FAT4):c.11405C>T (p.Ser3802Phe) rs75380987 0.03221
NM_001291303.3(FAT4):c.11820A>G (p.Ser3940=) rs17009721 0.02714
NM_001291303.3(FAT4):c.12852C>T (p.Ser4284=) rs17009819 0.02466
NM_001291303.3(FAT4):c.11488A>G (p.Lys3830Glu) rs17009684 0.02342
NM_001291303.3(FAT4):c.8482G>A (p.Asp2828Asn) rs12508222 0.02049
NM_001291303.3(FAT4):c.14361C>T (p.Val4787=) rs1014865 0.01862
NM_001291303.3(FAT4):c.14183G>A (p.Arg4728Lys) rs72675395 0.01656
NM_001291303.3(FAT4):c.8592G>A (p.Val2864=) rs111758803 0.01583
NM_001291303.3(FAT4):c.1101A>G (p.Val367=) rs57692448 0.01498
NM_001291303.3(FAT4):c.14135C>G (p.Ser4712Cys) rs147662558 0.01304
NM_001291303.3(FAT4):c.9876G>A (p.Gly3292=) rs115219562 0.01168
NM_001291303.3(FAT4):c.8842A>G (p.Ile2948Val) rs76048257 0.01112
NM_001291303.3(FAT4):c.13605G>A (p.Lys4535=) rs75469760 0.01048
NM_001291303.3(FAT4):c.10810A>C (p.Ile3604Leu) rs76491994 0.00978
NM_001291303.3(FAT4):c.3096A>G (p.Ala1032=) rs57537930 0.00811
NM_001291303.3(FAT4):c.8544C>T (p.Ser2848=) rs139132509 0.00802
NM_001291303.3(FAT4):c.11429A>G (p.His3810Arg) rs114637892 0.00732
NM_001291303.3(FAT4):c.12071G>A (p.Arg4024Gln) rs28515675 0.00726
NM_001291303.3(FAT4):c.12506C>T (p.Thr4169Ile) rs115822434 0.00726
NM_001291303.3(FAT4):c.4154T>C (p.Leu1385Ser) rs139883132 0.00597
NM_001291303.3(FAT4):c.14663C>G (p.Ala4888Gly) rs35340865 0.00551
NM_001291303.3(FAT4):c.6219A>G (p.Gln2073=) rs35355603 0.00545
NM_001291303.3(FAT4):c.6478A>G (p.Lys2160Glu) rs75942329 0.00540
NM_001291303.3(FAT4):c.12986A>G (p.Asp4329Gly) rs114234553 0.00519
NM_001291303.3(FAT4):c.10158A>G (p.Ala3386=) rs144585931 0.00489
NM_001291303.3(FAT4):c.14688C>T (p.His4896=) rs35862879 0.00460
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.9891G>A (p.Val3297=) rs139704889 0.00375
NM_001291303.3(FAT4):c.2811G>T (p.Lys937Asn) rs112454576 0.00367
NM_001291303.3(FAT4):c.12855T>C (p.Asp4285=) rs78040862 0.00365
NM_001291303.3(FAT4):c.3658T>A (p.Ser1220Thr) rs181368820 0.00342
NM_001291303.3(FAT4):c.12070C>T (p.Arg4024Trp) rs138019311 0.00333
NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val) rs142747281 0.00288
NM_001291303.3(FAT4):c.13554G>A (p.Leu4518=) rs78235204 0.00277
NM_001291303.3(FAT4):c.14666G>A (p.Arg4889Lys) rs35845544 0.00261
NM_001291303.3(FAT4):c.7935C>T (p.Asp2645=) rs146157250 0.00244
NM_001291303.3(FAT4):c.1128G>A (p.Val376=) rs202216461 0.00236
NM_001291303.3(FAT4):c.7787T>C (p.Leu2596Ser) rs111501860 0.00216
NM_001291303.3(FAT4):c.13404G>A (p.Val4468=) rs149993049 0.00181
NM_001291303.3(FAT4):c.831G>A (p.Ala277=) rs142490028 0.00175
NM_001291303.3(FAT4):c.4839G>A (p.Ser1613=) rs180866934 0.00164
NM_001291303.3(FAT4):c.5921-14C>T rs190218898 0.00151
NM_001291303.3(FAT4):c.10107A>G (p.Glu3369=) rs147646369 0.00140
NM_001291303.3(FAT4):c.4219G>A (p.Val1407Ile) rs114227532 0.00133
NM_001291303.3(FAT4):c.3192C>T (p.Asp1064=) rs140899478 0.00132
NM_001291303.3(FAT4):c.12479+8G>A rs150505878 0.00121
NM_001291303.3(FAT4):c.3402A>T (p.Glu1134Asp) rs144768563 0.00113
NM_001291303.3(FAT4):c.9828C>T (p.Pro3276=) rs73849226 0.00106
NM_001291303.3(FAT4):c.7052A>G (p.Asn2351Ser) rs145105421 0.00096
NM_001291303.3(FAT4):c.14940A>G (p.Glu4980=) rs149073729 0.00088
NM_001291303.3(FAT4):c.10635C>G (p.Pro3545=) rs181032092 0.00087
NM_001291303.3(FAT4):c.11670C>T (p.Cys3890=) rs150894545 0.00086
NM_001291303.3(FAT4):c.2919C>T (p.Val973=) rs144356360 0.00083
NM_001291303.3(FAT4):c.11693C>T (p.Ala3898Val) rs138275098 0.00069
NM_001291303.3(FAT4):c.13111A>G (p.Met4371Val) rs139260545 0.00056
NM_001291303.3(FAT4):c.8055C>T (p.Ser2685=) rs139033158 0.00032
NM_001291303.3(FAT4):c.10461A>T (p.Ser3487=) rs79482316 0.00028
NM_001291303.3(FAT4):c.13029T>C (p.Leu4343=) rs146822665 0.00025
NM_001291303.3(FAT4):c.5883T>C (p.Ser1961=) rs117016099 0.00025
NM_001291303.3(FAT4):c.9141C>T (p.Ser3047=) rs146492311 0.00024
NM_001291303.3(FAT4):c.12108A>G (p.Arg4036=) rs199730809 0.00021
NM_001291303.3(FAT4):c.7452T>C (p.Gly2484=) rs200513521 0.00019
NM_001291303.3(FAT4):c.9627C>T (p.Ala3209=) rs148558216 0.00017
NM_001291303.3(FAT4):c.2322C>T (p.Pro774=) rs200593370 0.00016
NM_001291303.3(FAT4):c.9083A>G (p.Asp3028Gly) rs765151671 0.00014
NM_001291303.3(FAT4):c.7326G>A (p.Ala2442=) rs201829586 0.00012
NM_001291303.3(FAT4):c.8313T>C (p.Asn2771=) rs148344513 0.00012
NM_001291303.3(FAT4):c.9451G>A (p.Ala3151Thr) rs200702071 0.00011
NM_001291303.3(FAT4):c.13088G>T (p.Gly4363Val) rs199797338 0.00010
NM_001291303.3(FAT4):c.6985C>T (p.Arg2329Cys) rs148293496 0.00009
NM_001291303.3(FAT4):c.14678G>A (p.Arg4893Gln) rs151139631 0.00006
NM_001291303.3(FAT4):c.9290G>A (p.Ser3097Asn) rs766108453 0.00004
NM_001291303.3(FAT4):c.14738G>A (p.Gly4913Asp) rs765666547 0.00002
NM_001291303.3(FAT4):c.11034T>C (p.Asp3678=) rs553335263 0.00001
NM_001291303.3(FAT4):c.13807A>G (p.Asn4603Asp) rs780176625 0.00001
NM_001291303.3(FAT4):c.2450C>T (p.Ala817Val) rs539442232 0.00001
NM_001291303.3(FAT4):c.5423C>G (p.Ser1808Cys) rs570452440 0.00001
NM_001291303.3(FAT4):c.5924T>C (p.Ile1975Thr) rs200276252 0.00001
NM_001291303.3(FAT4):c.842C>T (p.Thr281Ile) rs564305264 0.00001
NM_001291303.3(FAT4):c.11495G>A (p.Arg3832His)
NM_001291303.3(FAT4):c.1358A>T (p.Gln453Leu) rs6847454
NM_001291303.3(FAT4):c.1449C>T (p.Asn483=)
NM_001291303.3(FAT4):c.2216A>G (p.Asn739Ser) rs200512777
NM_001291303.3(FAT4):c.2316A>G (p.Gln772=) rs187427286
NM_001291303.3(FAT4):c.2574G>A (p.Glu858=)
NM_001291303.3(FAT4):c.3515C>T (p.Thr1172Ile) rs535333070
NM_001291303.3(FAT4):c.5308-15G>A
NM_001291303.3(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_001291303.3(FAT4):c.7466C>T (p.Ala2489Val) rs144853732

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