ClinVar Miner

List of variants in gene WDR62 reported by Mayo Clinic Laboratories, Mayo Clinic

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001083961.2(WDR62):c.253G>A (p.Val85Met) rs146274964 0.00161
NM_001083961.2(WDR62):c.1228G>T (p.Val410Leu) rs139460397 0.00077
NM_001083961.2(WDR62):c.82C>T (p.Arg28Trp) rs200283315 0.00038
NM_001083961.2(WDR62):c.4549C>T (p.Arg1517Trp) rs373621531 0.00025
NM_001083961.2(WDR62):c.1576G>A (p.Glu526Lys) rs147875659 0.00022
NM_001083961.2(WDR62):c.1480G>A (p.Gly494Arg) rs587784543 0.00006
NM_001083961.2(WDR62):c.2972A>T (p.Asp991Val) rs749528768 0.00006
NM_001083961.2(WDR62):c.3857G>A (p.Arg1286His) rs371385084 0.00004
NM_001083961.2(WDR62):c.4144C>T (p.Pro1382Ser) rs772768990 0.00004
NM_001083961.2(WDR62):c.2887G>A (p.Val963Met) rs113046428 0.00002
NM_001083961.2(WDR62):c.3878C>A (p.Ala1293Asp) rs868263026 0.00002
NM_001083961.2(WDR62):c.2335C>G (p.Gln779Glu) rs751933719 0.00001
NM_001083961.2(WDR62):c.4499A>G (p.Asp1500Gly) rs771866189 0.00001
NM_001083961.2(WDR62):c.979T>C (p.Tyr327His) rs781278130 0.00001
NM_001083961.2(WDR62):c.1516C>T (p.His506Tyr)
NM_001083961.2(WDR62):c.1701GAA[1] (p.Lys568del) rs768262786
NM_001083961.2(WDR62):c.2315A>G (p.Lys772Arg) rs2145796413
NM_001083961.2(WDR62):c.2396_2397del (p.Glu799fs) rs747870811
NM_001083961.2(WDR62):c.2764C>T (p.Arg922Cys)
NM_001083961.2(WDR62):c.3088G>A (p.Ala1030Thr)
NM_001083961.2(WDR62):c.3761C>G (p.Ser1254Cys)

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