ClinVar Miner

List of variants in gene FAT1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_005245.4(FAT1):c.4754C>T (p.Thr1585Met) rs111886222 0.00784
NM_005245.4(FAT1):c.3803G>A (p.Arg1268Gln) rs113970444 0.00774
NM_005245.4(FAT1):c.883G>A (p.Val295Met) rs61733573 0.00490
NM_005245.4(FAT1):c.7698C>T (p.Val2566=) rs192818736 0.00479
NM_005245.4(FAT1):c.2163G>A (p.Pro721=) rs140935307 0.00461
NM_005245.4(FAT1):c.12330C>T (p.Gly4110=) rs116628547 0.00411
NM_005245.4(FAT1):c.3446T>C (p.Met1149Thr) rs77280820 0.00389
NM_005245.4(FAT1):c.3503C>T (p.Ser1168Leu) rs200633985 0.00375
NM_005245.4(FAT1):c.12522G>A (p.Pro4174=) rs72716245 0.00217
NM_005245.4(FAT1):c.2563G>A (p.Gly855Arg) rs180820128 0.00216
NM_005245.4(FAT1):c.9440T>G (p.Val3147Gly) rs188733415 0.00208
NM_005245.4(FAT1):c.5646A>G (p.Pro1882=) rs116471329 0.00138
NM_005245.4(FAT1):c.2641C>T (p.Arg881Cys) rs201450896 0.00089
NM_005245.4(FAT1):c.2955C>T (p.Ile985=) rs200907501 0.00086
NM_005245.4(FAT1):c.2734G>A (p.Val912Ile) rs200097846 0.00076
NM_005245.4(FAT1):c.1146C>A (p.Pro382=) rs371822287 0.00057
NM_005245.4(FAT1):c.2236A>G (p.Thr746Ala) rs372906523 0.00026
NM_005245.4(FAT1):c.1335G>A (p.Ala445=) rs200594788 0.00017
NM_005245.4(FAT1):c.2832C>T (p.Thr944=) rs551051361 0.00010
NM_005245.4(FAT1):c.56G>C (p.Gly19Ala) rs200192750 0.00009
NM_005245.4(FAT1):c.843C>T (p.Cys281=) rs376291103 0.00009
NM_005245.4(FAT1):c.9399C>T (p.Thr3133=) rs368175543 0.00006
NM_005245.4(FAT1):c.12303C>T (p.Gly4101=) rs755127492 0.00004
NM_005245.4(FAT1):c.2836A>G (p.Ile946Val) rs778221022 0.00002
NM_005245.4(FAT1):c.10227G>A (p.Thr3409=)
NM_005245.4(FAT1):c.10271C>T (p.Thr3424Met)
NM_005245.4(FAT1):c.10416C>T (p.Asn3472=)
NM_005245.4(FAT1):c.10424C>G (p.Pro3475Arg)
NM_005245.4(FAT1):c.11796T>C (p.Thr3932=)
NM_005245.4(FAT1):c.12104-7G>A
NM_005245.4(FAT1):c.13074C>T (p.Ala4358=)
NM_005245.4(FAT1):c.1906G>A (p.Ala636Thr)
NM_005245.4(FAT1):c.2426A>G (p.His809Arg)
NM_005245.4(FAT1):c.2610T>C (p.Ile870=)
NM_005245.4(FAT1):c.315A>G (p.Thr105=)
NM_005245.4(FAT1):c.3363G>A (p.Ser1121=)
NM_005245.4(FAT1):c.3785G>A (p.Arg1262Gln)
NM_005245.4(FAT1):c.4675G>A (p.Ala1559Thr)
NM_005245.4(FAT1):c.4959G>A (p.Val1653=)
NM_005245.4(FAT1):c.5628C>G (p.Pro1876=)
NM_005245.4(FAT1):c.6234G>A (p.Ala2078=)
NM_005245.4(FAT1):c.6312T>A (p.Thr2104=)
NM_005245.4(FAT1):c.7113C>T (p.Ser2371=)
NM_005245.4(FAT1):c.9448A>G (p.Thr3150Ala)

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