ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_001291303.3(FAT4):c.7199+91C>T rs80234380 0.02324
NM_001291303.3(FAT4):c.5920+118A>C rs12510547 0.02290
NM_001291303.3(FAT4):c.5921-122C>T rs72914914 0.00999
NM_001291303.3(FAT4):c.11801-332T>C rs80253507 0.00828
NM_001291303.3(FAT4):c.6844-291T>C rs115421593 0.00797
NM_001291303.3(FAT4):c.12213+130A>G rs77364073 0.00783
NM_001291303.3(FAT4):c.12299+52T>C rs115877455 0.00727
NM_001291303.3(FAT4):c.11801-128T>C rs147095064 0.00487
NM_001291303.3(FAT4):c.11801-285T>C rs192334885 0.00483
NM_001291303.3(FAT4):c.5921-23T>A rs374890941 0.00458
NM_001291303.3(FAT4):c.12605-165A>G rs140903503 0.00430
NM_001291303.3(FAT4):c.7200-312T>A rs191546349 0.00397
NM_001291303.3(FAT4):c.5920+260G>A rs116805434 0.00385
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.14666G>A (p.Arg4889Lys) rs35845544 0.00261
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.5176-31C>T rs10033970 0.00199
NM_001291303.3(FAT4):c.13404G>A (p.Val4468=) rs149993049 0.00181
NM_001291303.3(FAT4):c.12479+8G>A rs150505878 0.00165
NM_001291303.3(FAT4):c.5921-14C>T rs190218898 0.00151
NM_001291303.3(FAT4):c.3294T>A (p.Pro1098=) rs200300207 0.00140
NM_001291303.3(FAT4):c.10107A>G (p.Glu3369=) rs147646369 0.00127
NM_001291303.3(FAT4):c.3192C>T (p.Asp1064=) rs140899478 0.00127
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.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.12713C>T (p.Ala4238Val) rs183396105 0.00087
NM_001291303.3(FAT4):c.11670C>T (p.Cys3890=) rs150894545 0.00086
NM_001291303.3(FAT4):c.3682C>G (p.Gln1228Glu) rs200227715 0.00086
NM_001291303.3(FAT4):c.11619C>T (p.Cys3873=) rs141328606 0.00084
NM_001291303.3(FAT4):c.13111A>G (p.Met4371Val) rs139260545 0.00064
NM_001291303.3(FAT4):c.9810G>A (p.Val3270=) rs139518045 0.00062
NM_001291303.3(FAT4):c.11693C>T (p.Ala3898Val) rs138275098 0.00054
NM_001291303.3(FAT4):c.8290A>C (p.Asn2764His) rs147281598 0.00051
NM_001291303.3(FAT4):c.10560G>A (p.Met3520Ile) rs144506470 0.00047
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.13206C>A (p.Gly4402=) rs200101519 0.00032
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.9451G>A (p.Ala3151Thr) rs200702071 0.00027
NM_001291303.3(FAT4):c.3417T>C (p.Phe1139=) rs367935912 0.00025
NM_001291303.3(FAT4):c.9141C>T (p.Ser3047=) rs146492311 0.00024
NM_001291303.3(FAT4):c.1296T>C (p.Pro432=) rs372007282 0.00023
NM_001291303.3(FAT4):c.14388G>A (p.Arg4796=) rs149584153 0.00023
NM_001291303.3(FAT4):c.1959C>T (p.Ala653=) rs191491571 0.00021
NM_001291303.3(FAT4):c.4941C>T (p.Asn1647=) rs184884584 0.00021
NM_001291303.3(FAT4):c.2322C>T (p.Pro774=) rs200593370 0.00016
NM_001291303.3(FAT4):c.7131A>G (p.Ala2377=) rs138403046 0.00014
NM_001291303.3(FAT4):c.14325G>A (p.Pro4775=) rs758537642 0.00013
NM_001291303.3(FAT4):c.9083A>G (p.Asp3028Gly) rs765151671 0.00013
NM_001291303.3(FAT4):c.14935G>A (p.Ala4979Thr) rs17009858 0.00011
NM_001291303.3(FAT4):c.14577G>A (p.Arg4859=) rs144832106 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.11358A>G (p.Glu3786=) rs369625076 0.00006
NM_001291303.3(FAT4):c.4530T>C (p.Tyr1510=) rs368207419 0.00005
NM_001291303.3(FAT4):c.5307+40T>C rs569179408 0.00005
NM_001291303.3(FAT4):c.1299C>G (p.Ser433=) rs764678411 0.00004
NM_001291303.3(FAT4):c.3351G>A (p.Ser1117=) rs769768427 0.00004
NM_001291303.3(FAT4):c.5598G>A (p.Thr1866=) rs370130221 0.00004
NM_001291303.3(FAT4):c.12299+6G>C rs541775780 0.00003
NM_001291303.3(FAT4):c.12870G>C (p.Gly4290=) rs779040505 0.00003
NM_001291303.3(FAT4):c.4542C>T (p.Asn1514=) rs199793434 0.00003
NM_001291303.3(FAT4):c.2057G>A (p.Ser686Asn) rs374104309 0.00001
NM_001291303.3(FAT4):c.5308-19G>A rs1369164587 0.00001
NM_001291303.3(FAT4):c.5424C>G (p.Ser1808=) rs200354953 0.00001
NM_001291303.3(FAT4):c.842C>T (p.Thr281Ile) rs564305264 0.00001
NM_001291303.3(FAT4):c.960G>A (p.Ser320=) rs1057523940 0.00001
NM_001291303.3(FAT4):c.11906-282C>T rs115018218
NM_001291303.3(FAT4):c.12214-42G>C rs180692127
NM_001291303.3(FAT4):c.12927T>C (p.Phe4309=) rs146058039
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.5553T>G (p.Pro1851=) rs2126019880
NM_001291303.3(FAT4):c.5920+314del rs147990721
NM_001291303.3(FAT4):c.5921-18dup rs535120107
NM_001291303.3(FAT4):c.7466C>T (p.Ala2489Val) rs144853732
NM_001291303.3(FAT4):c.7593C>T (p.Asn2531=) rs367971071
NM_001291303.3(FAT4):c.7707G>T (p.Val2569=) rs988863
NM_001291303.3(FAT4):c.8985C>T (p.Thr2995=) rs1057521481

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