ClinVar Miner

List of variants in gene USP9X reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_001039591.3(USP9X):c.6105T>C (p.Pro2035=) rs374464442 0.00073
NM_001039591.3(USP9X):c.4668C>T (p.Phe1556=) rs377596178 0.00047
NM_001039591.3(USP9X):c.7470G>A (p.Ser2490=) rs200344642 0.00037
NM_001039591.3(USP9X):c.6360A>G (p.Ile2120Met) rs201128029 0.00013
NM_001039591.3(USP9X):c.5340C>T (p.Thr1780=) rs371672710 0.00010
NM_001039591.3(USP9X):c.3103C>T (p.Pro1035Ser) rs372177157 0.00003
NM_001039591.3(USP9X):c.3892T>C (p.Leu1298=) rs1361298317 0.00002
NM_001039591.3(USP9X):c.5920A>G (p.Ile1974Val) rs760867179 0.00002
NM_001039591.3(USP9X):c.1778G>C (p.Ser593Thr) rs368381992 0.00001
NM_001039591.3(USP9X):c.2779G>A (p.Val927Ile) rs1156545933 0.00001
NM_001039591.3(USP9X):c.3503G>A (p.Arg1168Gln) rs1271252455 0.00001
NM_001039591.3(USP9X):c.558C>T (p.Ile186=) rs1188501864 0.00001
NM_001039591.3(USP9X):c.6799C>T (p.Pro2267Ser) rs763353056 0.00001
NM_001039591.3(USP9X):c.1053G>A (p.Lys351=)
NM_001039591.3(USP9X):c.1527C>T (p.Asn509=)
NM_001039591.3(USP9X):c.2087C>G (p.Ala696Gly) rs2147113785
NM_001039591.3(USP9X):c.2133A>G (p.Leu711=)
NM_001039591.3(USP9X):c.2308G>T (p.Gly770Ter)
NM_001039591.3(USP9X):c.2415A>G (p.Gln805=)
NM_001039591.3(USP9X):c.2637-2A>G
NM_001039591.3(USP9X):c.2883T>C (p.Ile961=)
NM_001039591.3(USP9X):c.2915T>G (p.Met972Arg)
NM_001039591.3(USP9X):c.3050A>G (p.Tyr1017Cys) rs2062729211
NM_001039591.3(USP9X):c.307G>A (p.Asp103Asn)
NM_001039591.3(USP9X):c.3144G>A (p.Pro1048=) rs200527638
NM_001039591.3(USP9X):c.3245G>A (p.Gly1082Asp)
NM_001039591.3(USP9X):c.3410C>T (p.Pro1137Leu)
NM_001039591.3(USP9X):c.343G>A (p.Ala115Thr)
NM_001039591.3(USP9X):c.3511G>T (p.Ala1171Ser) rs2147158960
NM_001039591.3(USP9X):c.3654A>C (p.Ser1218=)
NM_001039591.3(USP9X):c.3696T>C (p.Tyr1232=)
NM_001039591.3(USP9X):c.3870A>G (p.Glu1290=)
NM_001039591.3(USP9X):c.3958C>A (p.Leu1320Ile)
NM_001039591.3(USP9X):c.3960A>G (p.Leu1320=)
NM_001039591.3(USP9X):c.4118del (p.Gly1373fs) rs2062986710
NM_001039591.3(USP9X):c.4156G>A (p.Ala1386Thr)
NM_001039591.3(USP9X):c.420G>T (p.Trp140Cys) rs1555919860
NM_001039591.3(USP9X):c.4275G>A (p.Thr1425=)
NM_001039591.3(USP9X):c.438G>A (p.Arg146=)
NM_001039591.3(USP9X):c.4406C>T (p.Pro1469Leu) rs1010165716
NM_001039591.3(USP9X):c.4604-7C>T
NM_001039591.3(USP9X):c.5304A>G (p.Ala1768=)
NM_001039591.3(USP9X):c.5331+4C>A
NM_001039591.3(USP9X):c.5331+4C>T rs375119776
NM_001039591.3(USP9X):c.538C>A (p.Pro180Thr) rs2147035203
NM_001039591.3(USP9X):c.5632G>A (p.Gly1878Arg)
NM_001039591.3(USP9X):c.6138A>G (p.Gln2046=)
NM_001039591.3(USP9X):c.6471A>G (p.Leu2157=)
NM_001039591.3(USP9X):c.6852T>C (p.Ser2284=)
NM_001039591.3(USP9X):c.7211T>C (p.Ile2404Thr) rs2147276690
NM_001039591.3(USP9X):c.7215G>T (p.Leu2405=)
NM_001039591.3(USP9X):c.7452T>C (p.Ala2484=)
NM_001039591.3(USP9X):c.7592_7593del (p.Arg2531fs)
NM_001039591.3(USP9X):c.7607C>T (p.Ala2536Val)
NM_001039591.3(USP9X):c.7620T>C (p.Tyr2540=)
NM_001039591.3(USP9X):c.802C>T (p.Leu268Phe) rs2062417635
NM_001039591.3(USP9X):c.993A>G (p.Leu331=) rs1601965887

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