ClinVar Miner

Variants in gene FAT4 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 62
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HGVS dbSNP gnomAD frequency
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.5987A>G (p.Lys1996Arg) rs140055438 0.00242
NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val) rs145639192 0.00145
NM_001291303.3(FAT4):c.3424G>A (p.Val1142Met) rs202188213 0.00140
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.11619C>T (p.Cys3873=) rs141328606 0.00092
NM_001291303.3(FAT4):c.7231A>T (p.Thr2411Ser) rs147297895 0.00091
NM_001291303.3(FAT4):c.3682C>G (p.Gln1228Glu) rs200227715 0.00087
NM_001291303.3(FAT4):c.7103C>A (p.Ala2368Glu) rs116568645 0.00066
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.13555G>A (p.Ala4519Thr) rs202148971 0.00055
NM_001291303.3(FAT4):c.8290A>C (p.Asn2764His) rs147281598 0.00051
NM_001291303.3(FAT4):c.131A>C (p.Glu44Ala) rs200221425 0.00049
NM_001291303.3(FAT4):c.12342C>G (p.Ile4114Met) rs150804471 0.00048
NM_001291303.3(FAT4):c.13417G>A (p.Val4473Ile) rs145835705 0.00048
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.12066C>T (p.Gly4022=) rs144476127 0.00036
NM_001291303.3(FAT4):c.5367C>T (p.Ile1789=) rs144922340 0.00035
NM_001291303.3(FAT4):c.5552C>T (p.Pro1851Leu) rs138655912 0.00035
NM_001291303.3(FAT4):c.10570C>T (p.Arg3524Trp) rs145569482 0.00034
NM_001291303.3(FAT4):c.5054G>A (p.Arg1685Gln) rs376422522 0.00034
NM_001291303.3(FAT4):c.4432A>C (p.Ile1478Leu) rs200565115 0.00033
NM_001291303.3(FAT4):c.5597C>T (p.Thr1866Met) rs141773516 0.00033
NM_001291303.3(FAT4):c.6731C>T (p.Thr2244Met) rs145342353 0.00030
NM_001291303.3(FAT4):c.11040G>A (p.Thr3680=) rs147998041 0.00026
NM_001291303.3(FAT4):c.7196T>C (p.Ile2399Thr) rs140285782 0.00023
NM_001291303.3(FAT4):c.829G>A (p.Ala277Thr) rs183191959 0.00021
NM_001291303.3(FAT4):c.11380C>T (p.Arg3794Trp) rs201859188 0.00020
NM_001291303.3(FAT4):c.6977C>T (p.Thr2326Ile) rs200344386 0.00017
NM_001291303.3(FAT4):c.6094A>G (p.Thr2032Ala) rs147314754 0.00015
NM_001291303.3(FAT4):c.11153G>A (p.Arg3718His) rs139635339 0.00014
NM_001291303.3(FAT4):c.11822T>C (p.Val3941Ala) rs578140620 0.00014
NM_001291303.3(FAT4):c.1099G>A (p.Val367Ile) rs747531733 0.00013
NM_001291303.3(FAT4):c.4549A>C (p.Ile1517Leu) rs374899663 0.00013
NM_001291303.3(FAT4):c.13193T>C (p.Ile4398Thr) rs200729108 0.00012
NM_001291303.3(FAT4):c.12716T>C (p.Met4239Thr) rs137954725 0.00011
NM_001291303.3(FAT4):c.6050T>C (p.Val2017Ala) rs188126059 0.00011
NM_001291303.3(FAT4):c.12778G>A (p.Val4260Ile) rs369024765 0.00010
NM_001291303.3(FAT4):c.9597T>A (p.Asp3199Glu) rs568003396 0.00010
NM_001291303.3(FAT4):c.14362G>A (p.Gly4788Arg) rs138173652 0.00009
NM_001291303.3(FAT4):c.7813A>G (p.Ile2605Val) rs745697037 0.00009
NM_001291303.3(FAT4):c.8537G>A (p.Arg2846Gln) rs373393333 0.00009
NM_001291303.3(FAT4):c.1802A>G (p.Glu601Gly) rs377156485 0.00007
NM_001291303.3(FAT4):c.12499G>A (p.Ala4167Thr) rs369432764 0.00006
NM_001291303.3(FAT4):c.2273C>T (p.Ala758Val) rs570502199 0.00006
NM_001291303.3(FAT4):c.9163C>A (p.Gln3055Lys) rs199778782 0.00005
NM_001291303.3(FAT4):c.12768C>T (p.Ser4256=) rs1006074076 0.00004
NM_001291303.3(FAT4):c.14169G>T (p.Leu4723Phe) rs760377475 0.00002
NM_001291303.3(FAT4):c.4964G>A (p.Ser1655Asn) rs572010193 0.00002
NM_001291303.3(FAT4):c.7966A>C (p.Lys2656Gln) rs760398912 0.00002
NM_001291303.3(FAT4):c.2057G>A (p.Ser686Asn) rs374104309 0.00001
NM_001291303.3(FAT4):c.2896A>G (p.Ile966Val) rs778631726 0.00001
NM_001291303.3(FAT4):c.2214C>A (p.Val738=)
NM_001291303.3(FAT4):c.2705TGG[1] (p.Val903del) rs541157165

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