ClinVar Miner

List of variants in gene ANKRD11 reported as uncertain significance for not provided

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Total variants: 27
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HGVS dbSNP
NM_013275.6(ANKRD11):c.1133A>G (p.Asn378Ser) rs202203523
NM_013275.6(ANKRD11):c.1425G>T (p.Lys475Asn) rs1057523418
NM_013275.6(ANKRD11):c.149A>T (p.Glu50Val) rs1567614253
NM_013275.6(ANKRD11):c.1559C>T (p.Ala520Val) rs1415129056
NM_013275.6(ANKRD11):c.1994A>G (p.Lys665Arg)
NM_013275.6(ANKRD11):c.227-5C>G rs1303795065
NM_013275.6(ANKRD11):c.2535G>T (p.Leu845Phe) rs1555529022
NM_013275.6(ANKRD11):c.2942G>A (p.Cys981Tyr) rs1085307572
NM_013275.6(ANKRD11):c.3343A>G (p.Ile1115Val)
NM_013275.6(ANKRD11):c.3625A>G (p.Lys1209Glu) rs866638426
NM_013275.6(ANKRD11):c.4667C>G (p.Ala1556Gly) rs781186923
NM_013275.6(ANKRD11):c.5552A>G (p.Tyr1851Cys) rs376366933
NM_013275.6(ANKRD11):c.5651C>T (p.Ser1884Leu) rs1555526636
NM_013275.6(ANKRD11):c.6046C>T (p.Pro2016Ser) rs1449729767
NM_013275.6(ANKRD11):c.6127G>A (p.Ala2043Thr) rs1322632964
NM_013275.6(ANKRD11):c.6377G>A (p.Gly2126Asp)
NM_013275.6(ANKRD11):c.6580C>G (p.Gln2194Glu)
NM_013275.6(ANKRD11):c.6704C>T (p.Pro2235Leu) rs1394383095
NM_013275.6(ANKRD11):c.6712A>G (p.Ser2238Gly)
NM_013275.6(ANKRD11):c.6923G>T (p.Gly2308Val) rs1057522245
NM_013275.6(ANKRD11):c.6982C>G (p.Arg2328Gly) rs1567553783
NM_013275.6(ANKRD11):c.7418C>T (p.Thr2473Met) rs765378650
NM_013275.6(ANKRD11):c.7436A>G (p.Asp2479Gly) rs1555524796
NM_013275.6(ANKRD11):c.7470+5G>T rs1555524784
NM_013275.6(ANKRD11):c.7618C>T (p.Arg2540Trp) rs1555523386
NM_013275.6(ANKRD11):c.7753C>T (p.Arg2585Cys) rs1567537304
NM_013275.6(ANKRD11):c.7927G>A (p.Glu2643Lys) rs1064796264

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