ClinVar Miner

List of variants in gene FAT4 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_001291303.3(FAT4):c.6219A>G (p.Gln2073=) rs35355603 0.00545
NM_001291303.3(FAT4):c.10853C>T (p.Thr3618Met) rs111423173 0.00407
NM_001291303.3(FAT4):c.12855T>C (p.Asp4285=) rs78040862 0.00362
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.7358G>T (p.Ser2453Ile) rs72914988 0.00327
NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val) rs142747281 0.00288
NM_001291303.3(FAT4):c.13554G>A (p.Leu4518=) rs78235204 0.00273
NM_001291303.3(FAT4):c.7935C>T (p.Asp2645=) rs146157250 0.00244
NM_001291303.3(FAT4):c.5987A>G (p.Lys1996Arg) rs140055438 0.00242
NM_001291303.3(FAT4):c.10390A>G (p.Ile3464Val) rs147872710 0.00237
NM_001291303.3(FAT4):c.1128G>A (p.Val376=) rs202216461 0.00236
NM_001291303.3(FAT4):c.524G>T (p.Arg175Leu) rs143534324 0.00217
NM_001291303.3(FAT4):c.7787T>C (p.Leu2596Ser) rs111501860 0.00205
NM_001291303.3(FAT4):c.13404G>A (p.Val4468=) rs149993049 0.00181
NM_001291303.3(FAT4):c.4839G>A (p.Ser1613=) rs180866934 0.00164
NM_001291303.3(FAT4):c.3294T>A (p.Pro1098=) rs200300207 0.00140
NM_001291303.3(FAT4):c.3192C>T (p.Asp1064=) rs140899478 0.00127
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.14940A>G (p.Glu4980=) rs149073729 0.00088
NM_001291303.3(FAT4):c.12713C>T (p.Ala4238Val) rs183396105 0.00087
NM_001291303.3(FAT4):c.11619C>T (p.Cys3873=) rs141328606 0.00084
NM_001291303.3(FAT4):c.9810G>A (p.Val3270=) rs139518045 0.00062
NM_001291303.3(FAT4):c.12769G>A (p.Glu4257Lys) rs143513466 0.00056
NM_001291303.3(FAT4):c.11693C>T (p.Ala3898Val) rs138275098 0.00054
NM_001291303.3(FAT4):c.131A>C (p.Glu44Ala) rs200221425 0.00052
NM_001291303.3(FAT4):c.185G>C (p.Gly62Ala) rs201009019 0.00045
NM_001291303.3(FAT4):c.1419T>C (p.Pro473=) rs199637020 0.00034
NM_001291303.3(FAT4):c.8055C>T (p.Ser2685=) rs139033158 0.00032
NM_001291303.3(FAT4):c.10392C>A (p.Ile3464=) rs140494092 0.00029
NM_001291303.3(FAT4):c.9627C>T (p.Ala3209=) rs148558216 0.00029
NM_001291303.3(FAT4):c.12321T>C (p.Asn4107=) rs200344963 0.00024
NM_001291303.3(FAT4):c.13029T>C (p.Leu4343=) rs146822665 0.00024
NM_001291303.3(FAT4):c.9141C>T (p.Ser3047=) rs146492311 0.00024
NM_001291303.3(FAT4):c.1296T>C (p.Pro432=) rs372007282 0.00023
NM_001291303.3(FAT4):c.14388G>A (p.Arg4796=) rs149584153 0.00023
NM_001291303.3(FAT4):c.14877A>G (p.Ala4959=) rs376402724 0.00021
NM_001291303.3(FAT4):c.829G>A (p.Ala277Thr) rs183191959 0.00021
NM_001291303.3(FAT4):c.6732G>A (p.Thr2244=) rs138078089 0.00013
NM_001291303.3(FAT4):c.7326G>A (p.Ala2442=) rs201829586 0.00012
NM_001291303.3(FAT4):c.12716T>C (p.Met4239Thr) rs137954725 0.00011
NM_001291303.3(FAT4):c.2985G>A (p.Val995=) rs201226727 0.00011
NM_001291303.3(FAT4):c.12381G>A (p.Val4127=) rs377051363 0.00007
NM_001291303.3(FAT4):c.1802A>G (p.Glu601Gly) rs377156485 0.00007
NM_001291303.3(FAT4):c.4599C>T (p.Asn1533=) rs371858685 0.00005
NM_001291303.3(FAT4):c.6597T>C (p.Asn2199=) rs377502295 0.00005
NM_001291303.3(FAT4):c.11943A>T (p.Gly3981=) rs754755525 0.00004
NM_001291303.3(FAT4):c.3351G>A (p.Ser1117=) rs769768427 0.00004
NM_001291303.3(FAT4):c.7962C>T (p.Tyr2654=) rs546465658 0.00004
NM_001291303.3(FAT4):c.3978A>G (p.Glu1326=) rs201916729 0.00003
NM_001291303.3(FAT4):c.4542C>T (p.Asn1514=) rs199793434 0.00003
NM_001291303.3(FAT4):c.13011C>T (p.Phe4337=) rs778396214 0.00002
NM_001291303.3(FAT4):c.13416C>T (p.Gly4472=) rs141983394 0.00002
NM_001291303.3(FAT4):c.12045C>T (p.Tyr4015=) rs962551463 0.00001
NM_001291303.3(FAT4):c.1485T>C (p.Ser495=) rs370574664 0.00001
NM_001291303.3(FAT4):c.1980G>A (p.Leu660=) rs1355988118 0.00001
NM_001291303.3(FAT4):c.3154T>C (p.Leu1052=) rs867529121 0.00001
NM_001291303.3(FAT4):c.3822C>T (p.Asp1274=) rs1730875855 0.00001
NM_001291303.3(FAT4):c.4815C>T (p.Asp1605=) rs763330003 0.00001
NM_001291303.3(FAT4):c.6174C>T (p.Tyr2058=) rs756809322 0.00001
NM_001291303.3(FAT4):c.6408A>G (p.Ser2136=) rs760022203 0.00001
NM_001291303.3(FAT4):c.7251A>G (p.Gly2417=) rs763936792 0.00001
NM_001291303.3(FAT4):c.7578C>T (p.Ala2526=) rs748125780 0.00001
NM_001291303.3(FAT4):c.8826C>T (p.Gly2942=) rs1355664497 0.00001
NM_001291303.3(FAT4):c.9360A>G (p.Ala3120=) rs957324299 0.00001
NM_001291303.3(FAT4):c.9450A>G (p.Leu3150=) rs771111719 0.00001
NM_001291303.3(FAT4):c.9606C>T (p.Phe3202=) rs758295187 0.00001
NM_001291303.3(FAT4):c.1092C>T (p.Tyr364=) rs1730667393
NM_001291303.3(FAT4):c.11088G>A (p.Thr3696=) rs368928868
NM_001291303.3(FAT4):c.13065A>G (p.Ala4355=) rs150038254
NM_001291303.3(FAT4):c.13248G>A (p.Leu4416=) rs1727561767
NM_001291303.3(FAT4):c.13827C>T (p.Ser4609=) rs767553555
NM_001291303.3(FAT4):c.1479T>C (p.Tyr493=) rs2530428255
NM_001291303.3(FAT4):c.1545C>T (p.Val515=) rs1456788389
NM_001291303.3(FAT4):c.2316A>G (p.Gln772=) rs187427286
NM_001291303.3(FAT4):c.2511T>C (p.Gly837=) rs1316972214
NM_001291303.3(FAT4):c.3228A>G (p.Ala1076=) rs777609137
NM_001291303.3(FAT4):c.3606T>C (p.Asp1202=)
NM_001291303.3(FAT4):c.5889T>A (p.Val1963=)
NM_001291303.3(FAT4):c.6171A>C (p.Thr2057=) rs748908321
NM_001291303.3(FAT4):c.6303C>T (p.Thr2101=) rs1735000392
NM_001291303.3(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_001291303.3(FAT4):c.7725G>C (p.Thr2575=) rs140288688
NM_001291303.3(FAT4):c.780T>G (p.Pro260=) rs756940330
NM_001291303.3(FAT4):c.7815C>T (p.Ile2605=) rs201257189
NM_001291303.3(FAT4):c.9084T>C (p.Asp3028=) rs2126058982

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