ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 92
Download table as spreadsheet
HGVS dbSNP
NM_001291303.3(FAT4):c.10262T>C (p.Ile3421Thr)
NM_001291303.3(FAT4):c.10451C>G (p.Ala3484Gly)
NM_001291303.3(FAT4):c.10468C>A (p.Pro3490Thr)
NM_001291303.3(FAT4):c.11152C>T (p.Arg3718Cys)
NM_001291303.3(FAT4):c.11260A>G (p.Ser3754Gly)
NM_001291303.3(FAT4):c.11814A>C (p.Glu3938Asp)
NM_001291303.3(FAT4):c.1198G>T (p.Gly400Trp)
NM_001291303.3(FAT4):c.13193T>C (p.Ile4398Thr) rs200729108
NM_001291303.3(FAT4):c.13388C>T (p.Thr4463Ile)
NM_001291303.3(FAT4):c.13564G>C (p.Val4522Leu)
NM_001291303.3(FAT4):c.13641GAA[2] (p.Lys4551del) rs1560639673
NM_001291303.3(FAT4):c.14105G>A (p.Arg4702Gln)
NM_001291303.3(FAT4):c.14743G>A (p.Ala4915Thr)
NM_001291303.3(FAT4):c.14837T>C (p.Val4946Ala)
NM_001291303.3(FAT4):c.14841T>A (p.Asp4947Glu) rs768693221
NM_001291303.3(FAT4):c.1827C>A (p.Asp609Glu)
NM_001291303.3(FAT4):c.2324A>G (p.Asn775Ser)
NM_001291303.3(FAT4):c.2705TGG[1] (p.Val903del) rs541157165
NM_001291303.3(FAT4):c.2917G>A (p.Val973Ile)
NM_001291303.3(FAT4):c.3167G>A (p.Ser1056Asn)
NM_001291303.3(FAT4):c.3505C>T (p.Arg1169Trp)
NM_001291303.3(FAT4):c.3722A>G (p.Asn1241Ser)
NM_001291303.3(FAT4):c.3726T>G (p.Asn1242Lys)
NM_001291303.3(FAT4):c.4169T>C (p.Ile1390Thr)
NM_001291303.3(FAT4):c.418A>G (p.Ile140Val)
NM_001291303.3(FAT4):c.4411A>G (p.Ile1471Val)
NM_001291303.3(FAT4):c.44C>G (p.Pro15Arg)
NM_001291303.3(FAT4):c.4543G>A (p.Val1515Met)
NM_001291303.3(FAT4):c.5246T>C (p.Val1749Ala)
NM_001291303.3(FAT4):c.5792A>G (p.Tyr1931Cys)
NM_001291303.3(FAT4):c.5889_5890delinsAA (p.Leu1964Ile)
NM_001291303.3(FAT4):c.7312G>T (p.Val2438Phe)
NM_001291303.3(FAT4):c.733G>A (p.Asp245Asn)
NM_001291303.3(FAT4):c.739C>T (p.Pro247Ser) rs191329848
NM_001291303.3(FAT4):c.7466C>A (p.Ala2489Glu)
NM_001291303.3(FAT4):c.8162A>G (p.Asn2721Ser) rs1452280145
NM_001291303.3(FAT4):c.8280A>C (p.Lys2760Asn) rs750907829
NM_001291303.3(FAT4):c.8290A>C (p.Asn2764His) rs147281598
NM_001291303.3(FAT4):c.8363C>G (p.Pro2788Arg)
NM_001291303.3(FAT4):c.8408T>C (p.Ile2803Thr)
NM_001291303.3(FAT4):c.8417A>C (p.Asn2806Thr)
NM_001291303.3(FAT4):c.8525G>A (p.Arg2842His)
NM_024582.4(FAT4):c.10055C>A (p.Thr3352Asn) rs145285004
NM_024582.4(FAT4):c.10193C>T (p.Ala3398Val) rs1553927211
NM_024582.4(FAT4):c.10384A>G (p.Ile3462Val) rs147872710
NM_024582.4(FAT4):c.10787C>G (p.Ser3596Cys) rs558897707
NM_024582.4(FAT4):c.11034G>A (p.Thr3678=) rs147998041
NM_024582.4(FAT4):c.11147G>A (p.Arg3716His) rs139635339
NM_024582.4(FAT4):c.1128G>A (p.Val376=) rs202216461
NM_024582.4(FAT4):c.12060C>T (p.Gly4020=) rs144476127
NM_024582.4(FAT4):c.1237A>G (p.Lys413Glu) rs1471306819
NM_024582.4(FAT4):c.12605C>T (p.Thr4202Ile) rs1173461199
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.12845C>T (p.Ser4282Phe) rs199682210
NM_024582.4(FAT4):c.13174C>T (p.Pro4392Ser) rs772779154
NM_024582.4(FAT4):c.13286A>T (p.Asp4429Val) rs774943740
NM_024582.4(FAT4):c.13411G>A (p.Val4471Ile) rs145835705
NM_024582.4(FAT4):c.13454C>T (p.Ala4485Val) rs141234678
NM_024582.4(FAT4):c.14671C>G (p.Arg4891Gly) rs765997899
NM_024582.4(FAT4):c.2896A>G (p.Ile966Val) rs778631726
NM_024582.4(FAT4):c.3065A>G (p.Asp1022Gly) rs372060616
NM_024582.4(FAT4):c.3842A>G (p.Tyr1281Cys) rs1317645126
NM_024582.4(FAT4):c.4250C>A (p.Pro1417His) rs201515596
NM_024582.4(FAT4):c.4257C>G (p.Ser1419Arg) rs377613970
NM_024582.4(FAT4):c.4526G>A (p.Arg1509Gln) rs776836295
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.5317G>T (p.Ala1773Ser) rs750458935
NM_024582.4(FAT4):c.5347G>A (p.Ala1783Thr) rs571447839
NM_024582.4(FAT4):c.5367C>T (p.Ile1789=) rs144922340
NM_024582.4(FAT4):c.5401C>T (p.Arg1801Trp) rs201887525
NM_024582.4(FAT4):c.5597C>T (p.Thr1866Met) rs141773516
NM_024582.4(FAT4):c.6554C>A (p.Thr2185Lys) rs1553968839
NM_024582.4(FAT4):c.6719C>T (p.Thr2240Ile) rs774192877
NM_024582.4(FAT4):c.6977C>T (p.Thr2326Ile) rs200344386
NM_024582.4(FAT4):c.6991G>A (p.Val2331Ile) rs752320782
NM_024582.4(FAT4):c.7103C>A (p.Ala2368Glu) rs116568645
NM_024582.4(FAT4):c.7196T>C (p.Ile2399Thr) rs140285782
NM_024582.4(FAT4):c.7225A>T (p.Thr2409Ser) rs147297895
NM_024582.4(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_024582.4(FAT4):c.7510T>G (p.Ser2504Ala) rs148603730
NM_024582.4(FAT4):c.8015A>T (p.Asp2672Val) rs138655269
NM_024582.4(FAT4):c.8072C>T (p.Ser2691Leu) rs148918820
NM_024582.4(FAT4):c.8326A>G (p.Ile2776Val) rs773858750
NM_024582.4(FAT4):c.8725T>C (p.Tyr2909His) rs148655455
NM_024582.4(FAT4):c.8855T>G (p.Ile2952Arg) rs762222146
NM_024582.4(FAT4):c.9150C>A (p.Asp3050Glu) rs761372826
NM_024582.4(FAT4):c.9157C>A (p.Gln3053Lys) rs199778782
NM_024582.4(FAT4):c.9229A>G (p.Ile3077Val) rs138817920
NM_024582.4(FAT4):c.9359T>C (p.Met3120Thr) rs371686578
NM_024582.4(FAT4):c.9596A>G (p.Tyr3199Cys) rs115895451

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.