ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 63
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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 0.00365
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 0.00277
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 0.00216
NM_001291303.3(FAT4):c.13404G>A (p.Val4468=) rs149993049 0.00181
NM_001291303.3(FAT4):c.3294T>A (p.Pro1098=) rs200300207 0.00140
NM_001291303.3(FAT4):c.3192C>T (p.Asp1064=) rs140899478 0.00132
NM_001291303.3(FAT4):c.3402A>T (p.Glu1134Asp) rs144768563 0.00113
NM_001291303.3(FAT4):c.11619C>T (p.Cys3873=) rs141328606 0.00092
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.9810G>A (p.Val3270=) rs139518045 0.00062
NM_001291303.3(FAT4):c.12769G>A (p.Glu4257Lys) rs143513466 0.00056
NM_001291303.3(FAT4):c.131A>C (p.Glu44Ala) rs200221425 0.00049
NM_001291303.3(FAT4):c.1419T>C (p.Pro473=) rs199637020 0.00034
NM_001291303.3(FAT4):c.10392C>A (p.Ile3464=) rs140494092 0.00032
NM_001291303.3(FAT4):c.13029T>C (p.Leu4343=) rs146822665 0.00025
NM_001291303.3(FAT4):c.9141C>T (p.Ser3047=) rs146492311 0.00024
NM_001291303.3(FAT4):c.1296T>C (p.Pro432=) rs372007282 0.00022
NM_001291303.3(FAT4):c.14877A>G (p.Ala4959=) rs376402724 0.00021
NM_001291303.3(FAT4):c.2985G>A (p.Val995=) rs201226727 0.00012
NM_001291303.3(FAT4):c.12716T>C (p.Met4239Thr) rs137954725 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.6597T>C (p.Asn2199=) rs377502295 0.00006
NM_001291303.3(FAT4):c.4599C>T (p.Asn1533=) rs371858685 0.00005
NM_001291303.3(FAT4):c.11943A>T (p.Gly3981=) rs754755525 0.00004
NM_001291303.3(FAT4):c.3978A>G (p.Glu1326=) rs201916729 0.00003
NM_001291303.3(FAT4):c.13011C>T (p.Phe4337=) rs778396214 0.00001
NM_001291303.3(FAT4):c.13416C>T (p.Gly4472=) rs141983394 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.6408A>G (p.Ser2136=) rs760022203 0.00001
NM_001291303.3(FAT4):c.7578C>T (p.Ala2526=) rs748125780 0.00001
NM_001291303.3(FAT4):c.12045C>T (p.Tyr4015=)
NM_001291303.3(FAT4):c.13248G>A (p.Leu4416=)
NM_001291303.3(FAT4):c.13827C>T (p.Ser4609=) rs767553555
NM_001291303.3(FAT4):c.1479T>C (p.Tyr493=)
NM_001291303.3(FAT4):c.1545C>T (p.Val515=)
NM_001291303.3(FAT4):c.2316A>G (p.Gln772=) rs187427286
NM_001291303.3(FAT4):c.3228A>G (p.Ala1076=) rs777609137
NM_001291303.3(FAT4):c.3822C>T (p.Asp1274=)
NM_001291303.3(FAT4):c.6171A>C (p.Thr2057=)
NM_001291303.3(FAT4):c.6174C>T (p.Tyr2058=)
NM_001291303.3(FAT4):c.6303C>T (p.Thr2101=)
NM_001291303.3(FAT4):c.7251A>G (p.Gly2417=)
NM_001291303.3(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_001291303.3(FAT4):c.7725G>C (p.Thr2575=)
NM_001291303.3(FAT4):c.780T>G (p.Pro260=)
NM_001291303.3(FAT4):c.7815C>T (p.Ile2605=) rs201257189
NM_001291303.3(FAT4):c.8826C>T (p.Gly2942=)
NM_001291303.3(FAT4):c.9084T>C (p.Asp3028=) rs2126058982
NM_001291303.3(FAT4):c.9606C>T (p.Phe3202=) rs758295187

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