ClinVar Miner

List of variants in gene FAT4 reported as uncertain significance for not specified

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Gene type:
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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_001291303.3(FAT4):c.2811G>T (p.Lys937Asn) rs112454576 0.00367
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.7052A>G (p.Asn2351Ser) rs145105421 0.00096
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.13417G>A (p.Val4473Ile) rs145835705 0.00048
NM_001291303.3(FAT4):c.9602A>G (p.Tyr3201Cys) rs115895451 0.00044
NM_001291303.3(FAT4):c.8078C>T (p.Ser2693Leu) rs148918820 0.00025
NM_001291303.3(FAT4):c.6094A>G (p.Thr2032Ala) rs147314754 0.00015
NM_001291303.3(FAT4):c.9597T>A (p.Asp3199Glu) rs568003396 0.00010
NM_001291303.3(FAT4):c.7813A>G (p.Ile2605Val) rs745697037 0.00009
NM_001291303.3(FAT4):c.7848T>G (p.Ile2616Met) rs766719947 0.00005
NM_001291303.3(FAT4):c.14311C>T (p.Arg4771Cys) rs144845192 0.00004
NM_001291303.3(FAT4):c.10940A>G (p.Asp3647Gly) rs780015426 0.00003
NM_001291303.3(FAT4):c.3328G>A (p.Glu1110Lys) rs377275274 0.00003
NM_001291303.3(FAT4):c.1163C>T (p.Pro388Leu) rs991371776 0.00002
NM_001291303.3(FAT4):c.9156C>A (p.Asp3052Glu) rs761372826 0.00002
NM_001291303.3(FAT4):c.9800A>G (p.His3267Arg) rs773545119 0.00002
NM_001291303.3(FAT4):c.11482G>A (p.Val3828Ile) rs773534151 0.00001
NM_001291303.3(FAT4):c.14726C>T (p.Ala4909Val) rs373253210 0.00001
NM_001291303.3(FAT4):c.8332A>C (p.Ile2778Leu) rs773858750 0.00001
NM_001291303.3(FAT4):c.12017C>T (p.Thr4006Met)
NM_001291303.3(FAT4):c.4726A>C (p.Ile1576Leu)
NM_001291303.3(FAT4):c.5420G>A (p.Arg1807His)
NM_001291303.3(FAT4):c.7267G>A (p.Ala2423Thr) rs776977766

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