ClinVar Miner

List of variants in gene ANKRD11 reported by Fulgent Genetics, Fulgent Genetics

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Gene type:
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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_013275.6(ANKRD11):c.744+18C>G rs147328392 0.00441
NM_013275.6(ANKRD11):c.5088C>G (p.Asp1696Glu) rs146205997 0.00150
NM_013275.6(ANKRD11):c.6868C>T (p.Pro2290Ser) rs374668457 0.00140
NM_013275.6(ANKRD11):c.1852G>A (p.Ala618Thr) rs140370885 0.00042
NM_013275.6(ANKRD11):c.1577A>T (p.His526Leu) rs374369335 0.00012
NM_013275.6(ANKRD11):c.6085G>A (p.Val2029Ile) rs199785661 0.00003
NM_013275.6(ANKRD11):c.3340T>A (p.Tyr1114Asn) rs1461435321 0.00001
NM_013275.6(ANKRD11):c.4561G>A (p.Glu1521Lys) rs1332875546 0.00001
NM_013275.6(ANKRD11):c.4925C>T (p.Pro1642Leu) rs753598147 0.00001
NM_013275.6(ANKRD11):c.1844C>G (p.Ala615Gly) rs115797011
NM_013275.6(ANKRD11):c.1977C>G (p.Tyr659Ter) rs749201074
NM_013275.6(ANKRD11):c.2408_2412del (p.Lys803fs) rs886039902
NM_013275.6(ANKRD11):c.3431C>T (p.Pro1144Leu) rs137894790
NM_013275.6(ANKRD11):c.4206C>G (p.Tyr1402Ter) rs749632782
NM_013275.6(ANKRD11):c.4475_4498del (p.1484_1491LLRHHRDE[1]) rs534329317
NM_013275.6(ANKRD11):c.6262G>A (p.Ala2088Thr) rs753691962
NM_013275.6(ANKRD11):c.7618C>T (p.Arg2540Trp) rs1555523386

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