ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 115
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HGVS dbSNP
NM_001291285.1(FAT4):c.131A>C (p.Glu44Ala) rs200221425
NM_001291303.1(FAT4):c.10560G>A (p.Met3520Ile) rs144506470
NM_001291303.3(FAT4):c.10035G>T (p.Lys3345Asn)
NM_001291303.3(FAT4):c.10095A>G (p.Arg3365=) rs1240262001
NM_001291303.3(FAT4):c.10224A>G (p.Leu3408=) rs761771089
NM_001291303.3(FAT4):c.10227C>T (p.Asn3409=) rs368992969
NM_001291303.3(FAT4):c.10392C>A (p.Ile3464=) rs140494092
NM_001291303.3(FAT4):c.10395C>T (p.Thr3465=) rs768300702
NM_001291303.3(FAT4):c.10527G>A (p.Gly3509=)
NM_001291303.3(FAT4):c.10570C>T (p.Arg3524Trp)
NM_001291303.3(FAT4):c.10689C>T (p.Ser3563=) rs200550116
NM_001291303.3(FAT4):c.1092C>T (p.Tyr364=)
NM_001291303.3(FAT4):c.10935G>T (p.Val3645=) rs758367201
NM_001291303.3(FAT4):c.1107G>A (p.Glu369=) rs1578512638
NM_001291303.3(FAT4):c.11256G>A (p.Leu3752=) rs372230232
NM_001291303.3(FAT4):c.11694G>A (p.Ala3898=) rs189735159
NM_001291303.3(FAT4):c.11906-10C>T
NM_001291303.3(FAT4):c.12144T>C (p.Tyr4048=) rs1475901716
NM_001291303.3(FAT4):c.12300-10A>G rs779397693
NM_001291303.3(FAT4):c.12321T>C (p.Asn4107=) rs200344963
NM_001291303.3(FAT4):c.1244C>G (p.Pro415Arg)
NM_001291303.3(FAT4):c.12499G>A (p.Ala4167Thr)
NM_001291303.3(FAT4):c.1254C>T (p.Ser418=) rs781465335
NM_001291303.3(FAT4):c.12713C>T (p.Ala4238Val) rs183396105
NM_001291303.3(FAT4):c.12777C>T (p.Gly4259=) rs558612271
NM_001291303.3(FAT4):c.12822+7T>C rs372948727
NM_001291303.3(FAT4):c.12853G>A (p.Asp4285Asn)
NM_001291303.3(FAT4):c.129C>G (p.Ala43=) rs769721255
NM_001291303.3(FAT4):c.13179T>C (p.Asp4393=) rs376657630
NM_001291303.3(FAT4):c.13305C>T (p.His4435=) rs1357034003
NM_001291303.3(FAT4):c.13347C>T (p.Ser4449=) rs758589643
NM_001291303.3(FAT4):c.13461G>C (p.Ala4487=) rs776669972
NM_001291303.3(FAT4):c.13548C>T (p.Thr4516=) rs138057366
NM_001291303.3(FAT4):c.13634C>T (p.Pro4545Leu)
NM_001291303.3(FAT4):c.13965G>A (p.Arg4655=) rs756243213
NM_001291303.3(FAT4):c.14159C>G (p.Ala4720Gly) rs76607227
NM_001291303.3(FAT4):c.1419T>C (p.Pro473=)
NM_001291303.3(FAT4):c.14304A>G (p.Pro4768=) rs1217156870
NM_001291303.3(FAT4):c.14430A>G (p.Ala4810=)
NM_001291303.3(FAT4):c.14875G>A (p.Ala4959Thr)
NM_001291303.3(FAT4):c.1608C>T (p.Ser536=) rs375970737
NM_001291303.3(FAT4):c.1794A>G (p.Thr598=) rs1578514072
NM_001291303.3(FAT4):c.1845C>T (p.Asn615=) rs548524386
NM_001291303.3(FAT4):c.1855C>T (p.Arg619Cys) rs202125547
NM_001291303.3(FAT4):c.1956A>G (p.Gln652=) rs761128725
NM_001291303.3(FAT4):c.2145C>T (p.Asp715=)
NM_001291303.3(FAT4):c.2286A>G (p.Gln762=) rs771276464
NM_001291303.3(FAT4):c.2316A>C (p.Gln772His)
NM_001291303.3(FAT4):c.2343C>T (p.Ile781=) rs373586010
NM_001291303.3(FAT4):c.2475C>T (p.Asn825=) rs764273048
NM_001291303.3(FAT4):c.2705TGG[1] (p.Val903del) rs541157165
NM_001291303.3(FAT4):c.2883C>T (p.Ser961=) rs756899944
NM_001291303.3(FAT4):c.2886C>T (p.Tyr962=) rs1302137252
NM_001291303.3(FAT4):c.3067A>G (p.Lys1023Glu)
NM_001291303.3(FAT4):c.3120A>G (p.Thr1040=) rs202128638
NM_001291303.3(FAT4):c.3153A>G (p.Gln1051=) rs372689449
NM_001291303.3(FAT4):c.3212T>C (p.Val1071Ala) rs200138872
NM_001291303.3(FAT4):c.3962T>C (p.Phe1321Ser)
NM_001291303.3(FAT4):c.4599C>T (p.Asn1533=) rs371858685
NM_001291303.3(FAT4):c.4773G>A (p.Val1591=) rs779545626
NM_001291303.3(FAT4):c.4953A>G (p.Ile1651Met) rs201688197
NM_001291303.3(FAT4):c.5229C>T (p.Asp1743=) rs777915862
NM_001291303.3(FAT4):c.5308-9T>C rs199866344
NM_001291303.3(FAT4):c.5530C>T (p.Pro1844Ser) rs76963800
NM_001291303.3(FAT4):c.5751A>C (p.Arg1917=)
NM_001291303.3(FAT4):c.5808T>C (p.Asp1936=) rs770131334
NM_001291303.3(FAT4):c.6210C>T (p.Phe2070=) rs771989829
NM_001291303.3(FAT4):c.6234T>C (p.Asp2078=) rs1578616858
NM_001291303.3(FAT4):c.6597T>C (p.Asn2199=)
NM_001291303.3(FAT4):c.6957A>G (p.Thr2319=) rs201407156
NM_001291303.3(FAT4):c.7018+9A>G
NM_001291303.3(FAT4):c.7053C>T (p.Asn2351=) rs199682494
NM_001291303.3(FAT4):c.7080T>C (p.Asn2360=) rs552658366
NM_001291303.3(FAT4):c.7266C>T (p.Ser2422=) rs147010455
NM_001291303.3(FAT4):c.7578C>T (p.Ala2526=) rs748125780
NM_001291303.3(FAT4):c.7582G>A (p.Gly2528Arg)
NM_001291303.3(FAT4):c.761A>T (p.His254Leu) rs201036193
NM_001291303.3(FAT4):c.7947T>G (p.Pro2649=) rs375259992
NM_001291303.3(FAT4):c.81G>A (p.Val27=)
NM_001291303.3(FAT4):c.8205G>A (p.Arg2735=) rs769526903
NM_001291303.3(FAT4):c.8227C>T (p.Leu2743=)
NM_001291303.3(FAT4):c.8231C>T (p.Thr2744Ile)
NM_001291303.3(FAT4):c.8290A>C (p.Asn2764His) rs147281598
NM_001291303.3(FAT4):c.829G>A (p.Ala277Thr)
NM_001291303.3(FAT4):c.9896G>A (p.Arg3299His)
NM_001291303.3(FAT4):c.9975C>T (p.Ser3325=) rs374971295
NM_024582.4(FAT4):c.10384A>G (p.Ile3462Val) rs147872710
NM_024582.4(FAT4):c.11613C>T (p.Cys3871=) rs141328606
NM_024582.4(FAT4):c.12060C>T (p.Gly4020=) rs144476127
NM_024582.4(FAT4):c.12641G>A (p.Arg4214His) rs148170326
NM_024582.4(FAT4):c.12763G>A (p.Glu4255Lys) rs143513466
NM_024582.4(FAT4):c.1296T>C (p.Pro432=) rs372007282
NM_024582.4(FAT4):c.1299C>G (p.Ser433=) rs764678411
NM_024582.4(FAT4):c.13411G>A (p.Val4471Ile) rs145835705
NM_024582.4(FAT4):c.14319G>A (p.Pro4773=) rs758537642
NM_024582.4(FAT4):c.14382G>A (p.Arg4794=) rs149584153
NM_024582.4(FAT4):c.14929G>A (p.Ala4977Thr) rs17009858
NM_024582.4(FAT4):c.185G>C (p.Gly62Ala) rs201009019
NM_024582.4(FAT4):c.2896A>G (p.Ile966Val) rs778631726
NM_024582.4(FAT4):c.3294T>A (p.Pro1098=) rs200300207
NM_024582.4(FAT4):c.3417T>C (p.Phe1139=) rs367935912
NM_024582.4(FAT4):c.3424G>A (p.Val1142Met) rs202188213
NM_024582.4(FAT4):c.3682C>G (p.Gln1228Glu) rs200227715
NM_024582.4(FAT4):c.524G>T (p.Arg175Leu) rs143534324
NM_024582.4(FAT4):c.5275A>G (p.Ile1759Val) rs145639192
NM_024582.4(FAT4):c.5367C>T (p.Ile1789=) rs144922340
NM_024582.4(FAT4):c.5424C>G (p.Ser1808=) rs200354953
NM_024582.4(FAT4):c.5987A>G (p.Lys1996Arg) rs140055438
NM_024582.4(FAT4):c.6977C>T (p.Thr2326Ile) rs200344386
NM_024582.4(FAT4):c.7103C>A (p.Ala2368Glu) rs116568645
NM_024582.4(FAT4):c.7225A>T (p.Thr2409Ser) rs147297895
NM_024582.4(FAT4):c.7352G>T (p.Ser2451Ile) rs72914988
NM_024582.4(FAT4):c.7807A>G (p.Ile2603Val) rs745697037
NM_024582.4(FAT4):c.8015A>T (p.Asp2672Val) rs138655269
NM_024582.4(FAT4):c.9804G>A (p.Val3268=) rs139518045

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