ClinVar Miner

List of variants in gene FAT4 reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

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Gene type:
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Total variants: 18
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NM_001291303.3(FAT4):c.13193T>C (p.Ile4398Thr) rs200729108
NM_001291303.3(FAT4):c.14841T>A (p.Asp4947Glu) rs768693221
NM_001291303.3(FAT4):c.4543G>A (p.Val1515Met)
NM_001291303.3(FAT4):c.5792A>G (p.Tyr1931Cys)
NM_001291303.3(FAT4):c.739C>T (p.Pro247Ser) rs191329848
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.8417A>C (p.Asn2806Thr)
NM_024582.4(FAT4):c.10384A>G (p.Ile3462Val) rs147872710
NM_024582.4(FAT4):c.1128G>A (p.Val376=) rs202216461
NM_024582.4(FAT4):c.13286A>T (p.Asp4429Val) rs774943740
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.5401C>T (p.Arg1801Trp) rs201887525
NM_024582.4(FAT4):c.6977C>T (p.Thr2326Ile) rs200344386
NM_024582.4(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_024582.4(FAT4):c.9150C>A (p.Asp3050Glu) rs761372826

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