ClinVar Miner

List of variants in gene FAT4 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001291303.3(FAT4):c.10810A>C (p.Ile3604Leu) rs76491994 0.00978
NM_001291303.3(FAT4):c.12986A>G (p.Asp4329Gly) rs114234553 0.00519
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.7358G>T (p.Ser2453Ile) rs72914988 0.00327
NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val) rs142747281 0.00288
NM_001291303.3(FAT4):c.14666G>A (p.Arg4889Lys) rs35845544 0.00261
NM_001291303.3(FAT4):c.7935C>T (p.Asp2645=) rs146157250 0.00244
NM_001291303.3(FAT4):c.524G>T (p.Arg175Leu) rs143534324 0.00217
NM_001291303.3(FAT4):c.5921-14C>T rs190218898 0.00151
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.3768A>G (p.Arg1256=) rs114652326 0.00042
NM_001291303.3(FAT4):c.1698C>T (p.Ala566=) rs370653820 0.00033
NM_001291303.3(FAT4):c.14718C>T (p.Gly4906=) rs147617723 0.00030
NM_001291303.3(FAT4):c.1959C>T (p.Ala653=) rs191491571 0.00021
NM_001291303.3(FAT4):c.7131A>G (p.Ala2377=) rs138403046 0.00014
NM_001291303.3(FAT4):c.11358A>G (p.Glu3786=) rs369625076 0.00007
NM_001291303.3(FAT4):c.12381G>A (p.Val4127=) rs377051363 0.00007
NM_001291303.3(FAT4):c.3351G>A (p.Ser1117=) rs769768427 0.00004
NM_001291303.3(FAT4):c.12870G>C (p.Gly4290=) rs779040505 0.00003
NM_001291303.3(FAT4):c.4530T>C (p.Tyr1510=) rs368207419 0.00003
NM_001291303.3(FAT4):c.4542C>T (p.Asn1514=) rs199793434 0.00003
NM_001291303.3(FAT4):c.9696G>A (p.Ala3232=) rs142877205 0.00002
NM_001291303.3(FAT4):c.10395C>T (p.Thr3465=) rs768300702 0.00001
NM_001291303.3(FAT4):c.12299+6G>C rs541775780 0.00001
NM_001291303.3(FAT4):c.5308-19G>A rs1369164587 0.00001
NM_001291303.3(FAT4):c.5424C>G (p.Ser1808=) rs200354953 0.00001
NM_001291303.3(FAT4):c.960G>A (p.Ser320=) rs1057523940 0.00001
NM_001291303.3(FAT4):c.10155T>A (p.Gly3385=) rs780130895
NM_001291303.3(FAT4):c.12927T>C (p.Phe4309=) rs146058039
NM_001291303.3(FAT4):c.4944G>A (p.Val1648=)
NM_001291303.3(FAT4):c.5322C>T (p.Leu1774=)
NM_001291303.3(FAT4):c.5921-18dup rs535120107
NM_001291303.3(FAT4):c.738C>T (p.Asn246=)
NM_001291303.3(FAT4):c.7466C>T (p.Ala2489Val) rs144853732
NM_001291303.3(FAT4):c.7593C>T (p.Asn2531=) rs367971071
NM_001291303.3(FAT4):c.8985C>T (p.Thr2995=) rs1057521481

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