ClinVar Miner

List of variants in gene FAT4 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 225
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HGVS dbSNP gnomAD frequency
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.5987A>G (p.Lys1996Arg) rs140055438 0.00242
NM_001291303.3(FAT4):c.7787T>C (p.Leu2596Ser) rs111501860 0.00216
NM_001291303.3(FAT4):c.3962T>C (p.Phe1321Ser) rs147900577 0.00070
NM_001291303.3(FAT4):c.11260A>G (p.Ser3754Gly) rs79909102 0.00061
NM_001291303.3(FAT4):c.5792A>G (p.Tyr1931Cys) rs139716832 0.00061
NM_001291303.3(FAT4):c.12769G>A (p.Glu4257Lys) rs143513466 0.00056
NM_001291303.3(FAT4):c.13111A>G (p.Met4371Val) rs139260545 0.00056
NM_001291303.3(FAT4):c.8290A>C (p.Asn2764His) rs147281598 0.00051
NM_001291303.3(FAT4):c.4199G>A (p.Arg1400His) rs376791829 0.00047
NM_001291303.3(FAT4):c.2917G>A (p.Val973Ile) rs199497561 0.00044
NM_001291303.3(FAT4):c.12647G>A (p.Arg4216His) rs148170326 0.00041
NM_001291303.3(FAT4):c.13460C>T (p.Ala4487Val) rs141234678 0.00040
NM_001291303.3(FAT4):c.6731C>T (p.Thr2244Met) rs145342353 0.00030
NM_001291303.3(FAT4):c.8854A>C (p.Ser2952Arg) rs538489921 0.00029
NM_001291303.3(FAT4):c.11378T>C (p.Leu3793Pro) rs149757393 0.00023
NM_001291303.3(FAT4):c.11380C>T (p.Arg3794Trp) rs201859188 0.00020
NM_001291303.3(FAT4):c.761A>T (p.His254Leu) rs201036193 0.00019
NM_001291303.3(FAT4):c.8812C>A (p.Gln2938Lys) rs370499753 0.00019
NM_001291303.3(FAT4):c.6977C>T (p.Thr2326Ile) rs200344386 0.00017
NM_001291303.3(FAT4):c.7079A>G (p.Asn2360Ser) rs534302520 0.00017
NM_001291303.3(FAT4):c.10643A>G (p.Tyr3548Cys) rs79726583 0.00015
NM_001291303.3(FAT4):c.5311G>A (p.Ala1771Thr) rs147751409 0.00015
NM_001291303.3(FAT4):c.13802C>T (p.Pro4601Leu) rs200851934 0.00014
NM_001291303.3(FAT4):c.1099G>A (p.Val367Ile) rs747531733 0.00013
NM_001291303.3(FAT4):c.5401C>T (p.Arg1801Trp) rs201887525 0.00013
NM_001291303.3(FAT4):c.13193T>C (p.Ile4398Thr) rs200729108 0.00012
NM_001291303.3(FAT4):c.13388C>T (p.Thr4463Ile) rs199971037 0.00011
NM_001291303.3(FAT4):c.7264A>T (p.Ser2422Cys) rs139924242 0.00011
NM_001291303.3(FAT4):c.13088G>T (p.Gly4363Val) rs199797338 0.00010
NM_001291303.3(FAT4):c.9597T>A (p.Asp3199Glu) rs568003396 0.00010
NM_001291303.3(FAT4):c.13634C>T (p.Pro4545Leu) rs200092854 0.00009
NM_001291303.3(FAT4):c.5429A>T (p.Tyr1810Phe) rs201947859 0.00009
NM_001291303.3(FAT4):c.6976A>G (p.Thr2326Ala) rs757774648 0.00009
NM_001291303.3(FAT4):c.7312G>T (p.Val2438Phe) rs376545643 0.00009
NM_001291303.3(FAT4):c.821C>T (p.Ala274Val) rs199605036 0.00009
NM_001291303.3(FAT4):c.8636A>G (p.Tyr2879Cys) rs781160819 0.00007
NM_001291303.3(FAT4):c.10750C>G (p.Leu3584Val) rs751277769 0.00006
NM_001291303.3(FAT4):c.10780C>T (p.Pro3594Ser) rs374073545 0.00006
NM_001291303.3(FAT4):c.12166G>T (p.Val4056Leu) rs753998777 0.00006
NM_001291303.3(FAT4):c.1222G>A (p.Glu408Lys) rs574924064 0.00006
NM_001291303.3(FAT4):c.1289G>A (p.Arg430His) rs774644392 0.00006
NM_001291303.3(FAT4):c.4706A>G (p.Asn1569Ser) rs768412027 0.00006
NM_001291303.3(FAT4):c.6917A>G (p.Asn2306Ser) rs369144497 0.00006
NM_001291303.3(FAT4):c.8408T>C (p.Ile2803Thr) rs745425307 0.00006
NM_001291303.3(FAT4):c.1811T>G (p.Met604Arg) rs376751408 0.00005
NM_001291303.3(FAT4):c.8525G>A (p.Arg2842His) rs146180798 0.00005
NM_001291303.3(FAT4):c.11725A>G (p.Ser3909Gly) rs531337325 0.00004
NM_001291303.3(FAT4):c.13837G>A (p.Ala4613Thr) rs151087097 0.00004
NM_001291303.3(FAT4):c.14530A>T (p.Ser4844Cys) rs780522985 0.00004
NM_001291303.3(FAT4):c.2021G>A (p.Arg674His) rs759309740 0.00004
NM_001291303.3(FAT4):c.3095C>T (p.Ala1032Val) rs754931963 0.00004
NM_001291303.3(FAT4):c.4081G>A (p.Gly1361Arg) rs200361960 0.00004
NM_001291303.3(FAT4):c.548G>A (p.Gly183Glu) rs771566742 0.00004
NM_001291303.3(FAT4):c.6086C>T (p.Ser2029Phe) rs145573597 0.00004
NM_001291303.3(FAT4):c.1663C>T (p.Arg555Trp) rs756991867 0.00003
NM_001291303.3(FAT4):c.458A>G (p.Gln153Arg) rs745934649 0.00003
NM_001291303.3(FAT4):c.11152C>T (p.Arg3718Cys) rs774217003 0.00002
NM_001291303.3(FAT4):c.13144G>A (p.Gly4382Arg) rs368409720 0.00002
NM_001291303.3(FAT4):c.13594A>G (p.Arg4532Gly) rs373502916 0.00002
NM_001291303.3(FAT4):c.2158A>G (p.Thr720Ala) rs367762836 0.00002
NM_001291303.3(FAT4):c.4060A>G (p.Ile1354Val) rs200273982 0.00002
NM_001291303.3(FAT4):c.4274T>G (p.Ile1425Ser) rs759931847 0.00002
NM_001291303.3(FAT4):c.5645A>G (p.Glu1882Gly) rs757125413 0.00002
NM_001291303.3(FAT4):c.10868T>C (p.Val3623Ala) rs530781443 0.00001
NM_001291303.3(FAT4):c.12107G>C (p.Arg4036Thr) rs897405265 0.00001
NM_001291303.3(FAT4):c.12340A>G (p.Ile4114Val) rs948622582 0.00001
NM_001291303.3(FAT4):c.132G>C (p.Glu44Asp) rs763601689 0.00001
NM_001291303.3(FAT4):c.14441G>A (p.Arg4814Lys) rs756452113 0.00001
NM_001291303.3(FAT4):c.1613G>A (p.Gly538Glu) rs1193758539 0.00001
NM_001291303.3(FAT4):c.176C>T (p.Thr59Ile) rs757284999 0.00001
NM_001291303.3(FAT4):c.2450C>T (p.Ala817Val) rs539442232 0.00001
NM_001291303.3(FAT4):c.2641A>G (p.Ile881Val) rs183643556 0.00001
NM_001291303.3(FAT4):c.2834A>G (p.Lys945Arg) rs1376872414 0.00001
NM_001291303.3(FAT4):c.3236C>T (p.Pro1079Leu) rs185325824 0.00001
NM_001291303.3(FAT4):c.5501T>G (p.Val1834Gly) rs748063320 0.00001
NM_001291303.3(FAT4):c.6109G>A (p.Val2037Ile) rs1192093557 0.00001
NM_001291303.3(FAT4):c.7516T>G (p.Ser2506Ala) rs148603730 0.00001
NM_001291303.3(FAT4):c.8216C>A (p.Ser2739Tyr) rs748854090 0.00001
NM_001291303.3(FAT4):c.10034A>G (p.Lys3345Arg)
NM_001291303.3(FAT4):c.10306A>T (p.Ile3436Phe)
NM_001291303.3(FAT4):c.10338C>G (p.Ile3446Met)
NM_001291303.3(FAT4):c.10379A>C (p.Gln3460Pro)
NM_001291303.3(FAT4):c.10490C>G (p.Ser3497Cys)
NM_001291303.3(FAT4):c.10847C>T (p.Ser3616Phe)
NM_001291303.3(FAT4):c.11219G>C (p.Ser3740Thr)
NM_001291303.3(FAT4):c.11290C>A (p.Leu3764Ile)
NM_001291303.3(FAT4):c.11294T>C (p.Leu3765Ser)
NM_001291303.3(FAT4):c.11296G>T (p.Ala3766Ser)
NM_001291303.3(FAT4):c.11420C>T (p.Ser3807Phe)
NM_001291303.3(FAT4):c.11528A>T (p.Glu3843Val)
NM_001291303.3(FAT4):c.11769C>A (p.Ser3923Arg)
NM_001291303.3(FAT4):c.11831G>A (p.Cys3944Tyr)
NM_001291303.3(FAT4):c.11926G>A (p.Glu3976Lys)
NM_001291303.3(FAT4):c.11945T>G (p.Phe3982Cys)
NM_001291303.3(FAT4):c.11966A>C (p.Glu3989Ala) rs2126076090
NM_001291303.3(FAT4):c.12043T>C (p.Tyr4015His)
NM_001291303.3(FAT4):c.12131G>A (p.Gly4044Asp) rs760328375
NM_001291303.3(FAT4):c.12249C>G (p.Asn4083Lys)
NM_001291303.3(FAT4):c.12271G>C (p.Val4091Leu) rs2126082991
NM_001291303.3(FAT4):c.12301A>T (p.Thr4101Ser)
NM_001291303.3(FAT4):c.12543T>A (p.Asp4181Glu)
NM_001291303.3(FAT4):c.12575A>G (p.Glu4192Gly)
NM_001291303.3(FAT4):c.1262A>C (p.Lys421Thr)
NM_001291303.3(FAT4):c.12676A>C (p.Lys4226Gln)
NM_001291303.3(FAT4):c.12679C>T (p.Arg4227Trp)
NM_001291303.3(FAT4):c.12698A>G (p.Gln4233Arg)
NM_001291303.3(FAT4):c.12812C>T (p.Thr4271Ile)
NM_001291303.3(FAT4):c.13145G>T (p.Gly4382Val)
NM_001291303.3(FAT4):c.13163C>G (p.Ser4388Cys)
NM_001291303.3(FAT4):c.13192A>T (p.Ile4398Phe)
NM_001291303.3(FAT4):c.13606G>A (p.Ala4536Thr) rs1212647138
NM_001291303.3(FAT4):c.13618A>G (p.Lys4540Glu)
NM_001291303.3(FAT4):c.13673T>C (p.Phe4558Ser)
NM_001291303.3(FAT4):c.13762A>G (p.Arg4588Gly)
NM_001291303.3(FAT4):c.1378A>G (p.Ser460Gly)
NM_001291303.3(FAT4):c.13820T>C (p.Ile4607Thr)
NM_001291303.3(FAT4):c.13934G>A (p.Arg4645His)
NM_001291303.3(FAT4):c.13966C>T (p.His4656Tyr)
NM_001291303.3(FAT4):c.14032C>G (p.Pro4678Ala)
NM_001291303.3(FAT4):c.14033C>A (p.Pro4678His)
NM_001291303.3(FAT4):c.14048G>A (p.Gly4683Asp)
NM_001291303.3(FAT4):c.14089C>G (p.Pro4697Ala)
NM_001291303.3(FAT4):c.14384A>G (p.Glu4795Gly)
NM_001291303.3(FAT4):c.14431G>A (p.Asp4811Asn)
NM_001291303.3(FAT4):c.14479A>G (p.Arg4827Gly)
NM_001291303.3(FAT4):c.1462G>A (p.Ala488Thr)
NM_001291303.3(FAT4):c.14708G>C (p.Gly4903Ala)
NM_001291303.3(FAT4):c.14719A>G (p.Thr4907Ala) rs769212397
NM_001291303.3(FAT4):c.14815G>T (p.Gly4939Cys)
NM_001291303.3(FAT4):c.1532G>A (p.Arg511His)
NM_001291303.3(FAT4):c.1654A>G (p.Ile552Val)
NM_001291303.3(FAT4):c.1681C>T (p.Pro561Ser)
NM_001291303.3(FAT4):c.1714C>A (p.Leu572Ile)
NM_001291303.3(FAT4):c.172G>A (p.Gly58Ser)
NM_001291303.3(FAT4):c.1827C>A (p.Asp609Glu) rs370300509
NM_001291303.3(FAT4):c.1855C>A (p.Arg619Ser)
NM_001291303.3(FAT4):c.192C>G (p.Ile64Met)
NM_001291303.3(FAT4):c.1966T>C (p.Ser656Pro) rs1730743959
NM_001291303.3(FAT4):c.2126C>T (p.Thr709Ile)
NM_001291303.3(FAT4):c.2273C>G (p.Ala758Gly)
NM_001291303.3(FAT4):c.2458A>G (p.Met820Val)
NM_001291303.3(FAT4):c.2462A>G (p.Asp821Gly)
NM_001291303.3(FAT4):c.2494A>G (p.Thr832Ala)
NM_001291303.3(FAT4):c.25A>T (p.Thr9Ser)
NM_001291303.3(FAT4):c.2614A>G (p.Thr872Ala)
NM_001291303.3(FAT4):c.2665A>G (p.Asn889Asp)
NM_001291303.3(FAT4):c.2735T>C (p.Ile912Thr)
NM_001291303.3(FAT4):c.2947A>T (p.Thr983Ser)
NM_001291303.3(FAT4):c.2981C>T (p.Pro994Leu)
NM_001291303.3(FAT4):c.3178C>T (p.Arg1060Cys)
NM_001291303.3(FAT4):c.3288C>A (p.Asn1096Lys)
NM_001291303.3(FAT4):c.3317C>T (p.Thr1106Ile)
NM_001291303.3(FAT4):c.3509G>C (p.Arg1170Thr)
NM_001291303.3(FAT4):c.3577C>G (p.Gln1193Glu)
NM_001291303.3(FAT4):c.3580G>A (p.Ala1194Thr)
NM_001291303.3(FAT4):c.3683A>G (p.Gln1228Arg)
NM_001291303.3(FAT4):c.3809T>C (p.Ile1270Thr)
NM_001291303.3(FAT4):c.3877A>G (p.Ile1293Val)
NM_001291303.3(FAT4):c.3908T>A (p.Ile1303Asn)
NM_001291303.3(FAT4):c.4168A>G (p.Ile1390Val)
NM_001291303.3(FAT4):c.4352T>C (p.Ile1451Thr)
NM_001291303.3(FAT4):c.4413A>G (p.Ile1471Met) rs2125945055
NM_001291303.3(FAT4):c.4420G>A (p.Val1474Ile)
NM_001291303.3(FAT4):c.4595A>T (p.Gln1532Leu)
NM_001291303.3(FAT4):c.4745G>A (p.Gly1582Glu) rs1553959187
NM_001291303.3(FAT4):c.4837T>A (p.Ser1613Thr)
NM_001291303.3(FAT4):c.4907C>T (p.Thr1636Ile)
NM_001291303.3(FAT4):c.4937C>T (p.Thr1646Ile)
NM_001291303.3(FAT4):c.5134A>T (p.Ile1712Leu)
NM_001291303.3(FAT4):c.518C>T (p.Ser173Phe)
NM_001291303.3(FAT4):c.5261G>A (p.Gly1754Glu)
NM_001291303.3(FAT4):c.5347G>T (p.Ala1783Ser)
NM_001291303.3(FAT4):c.5419C>T (p.Arg1807Cys)
NM_001291303.3(FAT4):c.5520A>C (p.Lys1840Asn)
NM_001291303.3(FAT4):c.5549T>C (p.Ile1850Thr)
NM_001291303.3(FAT4):c.5884A>T (p.Thr1962Ser) rs749792331
NM_001291303.3(FAT4):c.5962A>G (p.Ser1988Gly)
NM_001291303.3(FAT4):c.6001A>G (p.Lys2001Glu)
NM_001291303.3(FAT4):c.6066C>G (p.Asp2022Glu)
NM_001291303.3(FAT4):c.6170C>T (p.Thr2057Ile)
NM_001291303.3(FAT4):c.617G>A (p.Gly206Asp)
NM_001291303.3(FAT4):c.6223A>G (p.Thr2075Ala)
NM_001291303.3(FAT4):c.6287A>G (p.Lys2096Arg)
NM_001291303.3(FAT4):c.6424G>T (p.Val2142Phe)
NM_001291303.3(FAT4):c.6448A>G (p.Asn2150Asp)
NM_001291303.3(FAT4):c.6517A>T (p.Ile2173Leu)
NM_001291303.3(FAT4):c.6535G>T (p.Ala2179Ser)
NM_001291303.3(FAT4):c.6637G>T (p.Val2213Phe)
NM_001291303.3(FAT4):c.6640G>T (p.Ala2214Ser) rs149686118
NM_001291303.3(FAT4):c.6826C>T (p.Pro2276Ser)
NM_001291303.3(FAT4):c.6905G>C (p.Gly2302Ala) rs143204873
NM_001291303.3(FAT4):c.6946C>G (p.Leu2316Val)
NM_001291303.3(FAT4):c.7018G>C (p.Gly2340Arg)
NM_001291303.3(FAT4):c.7025C>T (p.Pro2342Leu)
NM_001291303.3(FAT4):c.7151T>C (p.Leu2384Ser)
NM_001291303.3(FAT4):c.7163C>T (p.Ala2388Val)
NM_001291303.3(FAT4):c.727A>C (p.Ile243Leu)
NM_001291303.3(FAT4):c.7400G>A (p.Arg2467Lys)
NM_001291303.3(FAT4):c.7444C>A (p.Leu2482Ile)
NM_001291303.3(FAT4):c.7451G>A (p.Gly2484Asp)
NM_001291303.3(FAT4):c.7593C>G (p.Asn2531Lys)
NM_001291303.3(FAT4):c.772G>C (p.Gly258Arg)
NM_001291303.3(FAT4):c.7799C>A (p.Pro2600His)
NM_001291303.3(FAT4):c.785A>G (p.Asp262Gly)
NM_001291303.3(FAT4):c.7979C>G (p.Thr2660Arg) rs761286125
NM_001291303.3(FAT4):c.8067A>G (p.Ile2689Met)
NM_001291303.3(FAT4):c.8147A>T (p.Asn2716Ile)
NM_001291303.3(FAT4):c.8211A>T (p.Lys2737Asn)
NM_001291303.3(FAT4):c.8444A>G (p.Asp2815Gly) rs763149272
NM_001291303.3(FAT4):c.8450G>T (p.Ser2817Ile)
NM_001291303.3(FAT4):c.8470C>A (p.Pro2824Thr)
NM_001291303.3(FAT4):c.8549A>G (p.His2850Arg)
NM_001291303.3(FAT4):c.8566G>A (p.Val2856Ile)
NM_001291303.3(FAT4):c.8723A>G (p.Gln2908Arg)
NM_001291303.3(FAT4):c.8764A>T (p.Ile2922Phe)
NM_001291303.3(FAT4):c.8862A>G (p.Ile2954Met)
NM_001291303.3(FAT4):c.8920A>C (p.Asn2974His) rs1205109272
NM_001291303.3(FAT4):c.8962A>C (p.Ser2988Arg)
NM_001291303.3(FAT4):c.8987A>G (p.Lys2996Arg)
NM_001291303.3(FAT4):c.9112A>G (p.Asn3038Asp)
NM_001291303.3(FAT4):c.9358G>T (p.Ala3120Ser)
NM_001291303.3(FAT4):c.9379A>G (p.Lys3127Glu)
NM_001291303.3(FAT4):c.9487G>C (p.Glu3163Gln)

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