ClinVar Miner

List of variants in gene ANKRD11 reported as likely benign

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Gene type:
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Total variants: 108
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HGVS dbSNP
NM_001256182.2(ANKRD11):c.2216C>T (p.Ser739Leu) rs146294483
NM_001256182.2(ANKRD11):c.6283C>G (p.Leu2095Val)
NM_001256182.2(ANKRD11):c.7090G>A (p.Ala2364Thr)
NM_001256182.2(ANKRD11):c.7519C>A (p.Gln2507Lys) rs572878194
NM_013275.6(ANKRD11):c.1027G>A (p.Val343Ile)
NM_013275.6(ANKRD11):c.1035C>T (p.Asp345=)
NM_013275.6(ANKRD11):c.136G>A (p.Asp46Asn)
NM_013275.6(ANKRD11):c.1413G>A (p.Lys471=)
NM_013275.6(ANKRD11):c.1725C>T (p.Ser575=)
NM_013275.6(ANKRD11):c.1842C>T (p.Ser614=)
NM_013275.6(ANKRD11):c.1851C>T (p.Gly617=)
NM_013275.6(ANKRD11):c.1852G>A (p.Ala618Thr)
NM_013275.6(ANKRD11):c.1857C>T (p.Val619=)
NM_013275.6(ANKRD11):c.195C>T (p.Gly65=)
NM_013275.6(ANKRD11):c.207G>A (p.Glu69=)
NM_013275.6(ANKRD11):c.2184C>G (p.Ile728Met)
NM_013275.6(ANKRD11):c.2217G>A (p.Ser739=)
NM_013275.6(ANKRD11):c.2373G>A (p.Lys791=) rs138267414
NM_013275.6(ANKRD11):c.2505C>T (p.Asp835=) rs544199816
NM_013275.6(ANKRD11):c.2610C>T (p.Ser870=)
NM_013275.6(ANKRD11):c.2684G>A (p.Arg895Gln) rs199800166
NM_013275.6(ANKRD11):c.2825G>A (p.Arg942Lys) rs1057520729
NM_013275.6(ANKRD11):c.282C>G (p.Ala94=)
NM_013275.6(ANKRD11):c.2841C>T (p.Ala947=)
NM_013275.6(ANKRD11):c.2888_2896del (p.Asp963_Arg965del) rs769651265
NM_013275.6(ANKRD11):c.2889C>T (p.Asp963=)
NM_013275.6(ANKRD11):c.3045C>G (p.Pro1015=)
NM_013275.6(ANKRD11):c.306G>C (p.Leu102=)
NM_013275.6(ANKRD11):c.3097A>T (p.Ser1033Cys) rs201929972
NM_013275.6(ANKRD11):c.3197A>G (p.His1066Arg)
NM_013275.6(ANKRD11):c.3437C>T (p.Thr1146Met)
NM_013275.6(ANKRD11):c.3483C>T (p.Ser1161=)
NM_013275.6(ANKRD11):c.3578C>T (p.Ala1193Val)
NM_013275.6(ANKRD11):c.3584G>A (p.Arg1195Lys)
NM_013275.6(ANKRD11):c.3660G>A (p.Arg1220=)
NM_013275.6(ANKRD11):c.375C>T (p.Ala125=)
NM_013275.6(ANKRD11):c.3826G>A (p.Ala1276Thr)
NM_013275.6(ANKRD11):c.3872A>G (p.Glu1291Gly) rs377605019
NM_013275.6(ANKRD11):c.389A>G (p.Asn130Ser)
NM_013275.6(ANKRD11):c.3969C>T (p.Val1323=)
NM_013275.6(ANKRD11):c.3973T>C (p.Phe1325Leu)
NM_013275.6(ANKRD11):c.3977C>T (p.Thr1326Met) rs144673419
NM_013275.6(ANKRD11):c.4149C>T (p.Gly1383=)
NM_013275.6(ANKRD11):c.4235T>C (p.Ile1412Thr) rs578198369
NM_013275.6(ANKRD11):c.4237G>A (p.Glu1413Lys) rs140373729
NM_013275.6(ANKRD11):c.4297T>C (p.Ser1433Pro) rs1567569593
NM_013275.6(ANKRD11):c.4317G>A (p.Lys1439=)
NM_013275.6(ANKRD11):c.4382A>G (p.Lys1461Arg)
NM_013275.6(ANKRD11):c.4440T>C (p.His1480=)
NM_013275.6(ANKRD11):c.4443G>A (p.Ala1481=)
NM_013275.6(ANKRD11):c.4533C>T (p.Pro1511=)
NM_013275.6(ANKRD11):c.4568C>T (p.Pro1523Leu)
NM_013275.6(ANKRD11):c.4609G>A (p.Gly1537Ser) rs1347006212
NM_013275.6(ANKRD11):c.4667C>G (p.Ala1556Gly) rs781186923
NM_013275.6(ANKRD11):c.4831C>T (p.Leu1611=) rs1567567396
NM_013275.6(ANKRD11):c.4872G>A (p.Ala1624=) rs143426579
NM_013275.6(ANKRD11):c.5061G>A (p.Glu1687=)
NM_013275.6(ANKRD11):c.5088C>G (p.Asp1696Glu) rs146205997
NM_013275.6(ANKRD11):c.5112C>A (p.Pro1704=)
NM_013275.6(ANKRD11):c.5178C>T (p.Ser1726=)
NM_013275.6(ANKRD11):c.5241C>T (p.Pro1747=)
NM_013275.6(ANKRD11):c.5250C>T (p.Thr1750=)
NM_013275.6(ANKRD11):c.541G>A (p.Ala181Thr) rs777123332
NM_013275.6(ANKRD11):c.543C>T (p.Ala181=)
NM_013275.6(ANKRD11):c.5484G>A (p.Ser1828=)
NM_013275.6(ANKRD11):c.5509C>T (p.Pro1837Ser)
NM_013275.6(ANKRD11):c.5578C>T (p.Pro1860Ser)
NM_013275.6(ANKRD11):c.5625C>T (p.Val1875=)
NM_013275.6(ANKRD11):c.5629C>T (p.Pro1877Ser)
NM_013275.6(ANKRD11):c.5632T>C (p.Ser1878Pro)
NM_013275.6(ANKRD11):c.5889C>T (p.Ile1963=)
NM_013275.6(ANKRD11):c.5916C>T (p.Ser1972=)
NM_013275.6(ANKRD11):c.5998C>T (p.Leu2000Phe)
NM_013275.6(ANKRD11):c.6020C>T (p.Pro2007Leu) rs200531141
NM_013275.6(ANKRD11):c.6065C>T (p.Pro2022Leu)
NM_013275.6(ANKRD11):c.6106G>A (p.Asp2036Asn) rs201636725
NM_013275.6(ANKRD11):c.6112A>G (p.Lys2038Glu) rs200724087
NM_013275.6(ANKRD11):c.6125A>G (p.Asp2042Gly)
NM_013275.6(ANKRD11):c.6140C>G (p.Ala2047Gly)
NM_013275.6(ANKRD11):c.6153A>G (p.Ser2051=)
NM_013275.6(ANKRD11):c.6312C>T (p.Asp2104=)
NM_013275.6(ANKRD11):c.6323G>A (p.Gly2108Asp) rs201509886
NM_013275.6(ANKRD11):c.6362C>T (p.Ala2121Val) rs747992186
NM_013275.6(ANKRD11):c.6366C>T (p.Asp2122=)
NM_013275.6(ANKRD11):c.6580C>G (p.Gln2194Glu)
NM_013275.6(ANKRD11):c.6597C>T (p.Leu2199=)
NM_013275.6(ANKRD11):c.6621C>T (p.Pro2207=)
NM_013275.6(ANKRD11):c.6628G>C (p.Glu2210Gln) rs1350625482
NM_013275.6(ANKRD11):c.6698G>A (p.Gly2233Glu)
NM_013275.6(ANKRD11):c.6712A>G (p.Ser2238Gly)
NM_013275.6(ANKRD11):c.6725C>T (p.Ala2242Val)
NM_013275.6(ANKRD11):c.6745C>T (p.Arg2249Cys) rs202081612
NM_013275.6(ANKRD11):c.6746G>A (p.Arg2249His)
NM_013275.6(ANKRD11):c.6792C>T (p.Pro2264=)
NM_013275.6(ANKRD11):c.6797C>T (p.Ala2266Val) rs748996527
NM_013275.6(ANKRD11):c.6810C>T (p.Ala2270=) rs1210625952
NM_013275.6(ANKRD11):c.6826C>T (p.Pro2276Ser)
NM_013275.6(ANKRD11):c.6919C>T (p.Pro2307Ser) rs575642464
NM_013275.6(ANKRD11):c.7296C>T (p.Ser2432=)
NM_013275.6(ANKRD11):c.7324C>T (p.Leu2442=)
NM_013275.6(ANKRD11):c.744+18C>G rs147328392
NM_013275.6(ANKRD11):c.7677G>A (p.Leu2559=)
NM_013275.6(ANKRD11):c.7731A>C (p.Ser2577=)
NM_013275.6(ANKRD11):c.7806+4G>A rs373180876
NM_013275.6(ANKRD11):c.7839C>G (p.Ala2613=)
NM_013275.6(ANKRD11):c.843C>T (p.Asn281=)
NM_013275.6(ANKRD11):c.888G>A (p.Ser296=)
NM_013275.6(ANKRD11):c.890C>T (p.Thr297Met)

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