ClinVar Miner

List of variants in gene ANKRD11 reported as likely benign for not specified

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_013275.6(ANKRD11):c.744+18C>G rs147328392 0.00441
NM_013275.6(ANKRD11):c.6323G>A (p.Gly2108Asp) rs201509886 0.00152
NM_013275.6(ANKRD11):c.2240C>T (p.Ser747Leu) rs138898373 0.00057
NM_013275.6(ANKRD11):c.6797C>T (p.Ala2266Val) rs748996527 0.00035
NM_013275.6(ANKRD11):c.2373G>A (p.Lys791=) rs138267414 0.00024
NM_013275.6(ANKRD11):c.3282C>G (p.Ile1094Met) rs139384857 0.00019
NM_013275.6(ANKRD11):c.6712A>G (p.Ser2238Gly) rs770209899 0.00016
NM_013275.6(ANKRD11):c.1577A>T (p.His526Leu) rs374369335 0.00012
NM_013275.6(ANKRD11):c.2505C>T (p.Asp835=) rs544199816 0.00008
NM_013275.6(ANKRD11):c.6024C>T (p.Phe2008=) rs375589721 0.00006
NM_013275.6(ANKRD11):c.3097A>T (p.Ser1033Cys) rs201929972 0.00003
NM_013275.6(ANKRD11):c.541G>A (p.Ala181Thr) rs777123332 0.00003
NM_013275.6(ANKRD11):c.5898C>T (p.Thr1966=) rs140586593 0.00002
NM_013275.6(ANKRD11):c.5823C>T (p.Ala1941=) rs775856441 0.00001
NM_013275.6(ANKRD11):c.4244A>G (p.Glu1415Gly) rs756014125
NM_013275.6(ANKRD11):c.5646C>G (p.Val1882=)
NM_013275.6(ANKRD11):c.6072G>C (p.Pro2024=) rs542077760
NM_013275.6(ANKRD11):c.6218C>T (p.Pro2073Leu) rs770387752

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