ClinVar Miner

List of variants in gene combination ANK2, LOC126807137 reported by Fulgent Genetics, Fulgent Genetics

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.7831T>C (p.Tyr2611His) rs35338364 0.00539
NM_001148.6(ANK2):c.7971C>T (p.Ser2657=) rs146085234 0.00051
NM_001148.6(ANK2):c.7265G>A (p.Ser2422Asn) rs140341680 0.00019
NM_001148.6(ANK2):c.7148C>T (p.Pro2383Leu) rs35960628 0.00017
NM_001148.6(ANK2):c.7868C>G (p.Ser2623Cys) rs116253689 0.00010
NM_001148.6(ANK2):c.7412G>A (p.Ser2471Asn) rs375139170 0.00006
NM_001148.6(ANK2):c.7105G>T (p.Val2369Phe) rs758054052 0.00004
NM_001148.6(ANK2):c.7149G>A (p.Pro2383=) rs200877971 0.00004
NM_001148.6(ANK2):c.7396C>T (p.Arg2466Cys) rs562115547 0.00004
NM_001148.6(ANK2):c.6977A>G (p.Asp2326Gly) rs777618921 0.00003
NM_001148.6(ANK2):c.7136C>A (p.Thr2379Lys) rs753351853 0.00003
NM_001148.6(ANK2):c.7142C>A (p.Ala2381Asp) rs764841248 0.00002
NM_001148.6(ANK2):c.7244G>A (p.Ser2415Asn) rs749832637 0.00002
NM_001148.6(ANK2):c.6820C>T (p.Arg2274Cys) rs140258681 0.00001
NM_001148.6(ANK2):c.7082A>G (p.His2361Arg) rs745718831 0.00001
NM_001148.6(ANK2):c.7120G>T (p.Ala2374Ser) rs763277342 0.00001
NM_001148.6(ANK2):c.7169A>T (p.Lys2390Met) rs769894397 0.00001
NM_001148.6(ANK2):c.7307C>T (p.Ser2436Phe) rs761246790 0.00001
NM_001148.6(ANK2):c.7528C>T (p.Leu2510Phe) rs1293101023 0.00001
NM_001148.6(ANK2):c.7742G>A (p.Arg2581Lys) rs369041815 0.00001
NM_001148.6(ANK2):c.7054_7059del (p.Gly2352_Gln2353del) rs774514148
NM_001148.6(ANK2):c.7106T>G (p.Val2369Gly) rs28377576
NM_001148.6(ANK2):c.7388C>T (p.Ser2463Phe) rs2095742714
NM_001148.6(ANK2):c.7553A>G (p.Glu2518Gly) rs926379811
NM_001148.6(ANK2):c.7860TTC[1] (p.Ser2624del) rs772341643
NM_001148.6(ANK2):c.7971C>G (p.Ser2657Arg) rs146085234

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