ClinVar Miner

List of variants in gene FAT4 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val) rs145639192 0.00145
NM_001291303.3(FAT4):c.5792A>G (p.Tyr1931Cys) rs139716832 0.00061
NM_001291303.3(FAT4):c.8290A>C (p.Asn2764His) rs147281598 0.00051
NM_001291303.3(FAT4):c.6977C>T (p.Thr2326Ile) rs200344386 0.00017
NM_001291303.3(FAT4):c.6970C>T (p.Arg2324Trp) rs559079176 0.00014
NM_001291303.3(FAT4):c.5401C>T (p.Arg1801Trp) rs201887525 0.00013
NM_001291303.3(FAT4):c.13193T>C (p.Ile4398Thr) rs200729108 0.00012
NM_001291303.3(FAT4):c.6050T>C (p.Val2017Ala) rs188126059 0.00011
NM_001291303.3(FAT4):c.6985C>T (p.Arg2329Cys) rs148293496 0.00009
NM_001291303.3(FAT4):c.2273C>T (p.Ala758Val) rs570502199 0.00006
NM_001291303.3(FAT4):c.4543G>A (p.Val1515Met) rs773912269 0.00006
NM_001291303.3(FAT4):c.2689A>G (p.Ile897Val) rs112101185 0.00004
NM_001291303.3(FAT4):c.247A>G (p.Ile83Val) rs375241448 0.00003
NM_001291303.3(FAT4):c.10357G>A (p.Gly3453Ser) rs369887674 0.00002
NM_001291303.3(FAT4):c.9156C>A (p.Asp3052Glu) rs761372826 0.00002
NM_001291303.3(FAT4):c.173G>T (p.Gly58Val) rs749929736 0.00001
NM_001291303.3(FAT4):c.2057G>A (p.Ser686Asn) rs374104309 0.00001
NM_001291303.3(FAT4):c.2824A>G (p.Ile942Val) rs368138514 0.00001
NM_001291303.3(FAT4):c.4526G>A (p.Arg1509Gln) rs776836295 0.00001
NM_001291303.3(FAT4):c.8162A>G (p.Asn2721Ser) rs1452280145 0.00001
NM_001291303.3(FAT4):c.8280A>C (p.Lys2760Asn) rs750907829 0.00001
NM_001291303.3(FAT4):c.11347A>G (p.Thr3783Ala)
NM_001291303.3(FAT4):c.12431G>A (p.Arg4144Lys)
NM_001291303.3(FAT4):c.13292A>T (p.Asp4431Val) rs774943740
NM_001291303.3(FAT4):c.14644G>A (p.Asp4882Asn)
NM_001291303.3(FAT4):c.14841T>A (p.Asp4947Glu) rs768693221
NM_001291303.3(FAT4):c.2072C>T (p.Pro691Leu)
NM_001291303.3(FAT4):c.3483T>G (p.Phe1161Leu)
NM_001291303.3(FAT4):c.4567A>G (p.Asn1523Asp)
NM_001291303.3(FAT4):c.7382T>A (p.Val2461Asp)
NM_001291303.3(FAT4):c.739C>T (p.Pro247Ser) rs191329848
NM_001291303.3(FAT4):c.8315C>A (p.Ala2772Asp)
NM_001291303.3(FAT4):c.8417A>C (p.Asn2806Thr) rs1725960134
NM_001291303.3(FAT4):c.9583G>A (p.Val3195Ile)

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