ClinVar Miner

List of variants in gene ANK2 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.11673T>C (p.His3891=) rs2293324 0.30277
NM_001148.6(ANK2):c.3579C>T (p.Arg1193=) rs3736575 0.23645
NM_001148.6(ANK2):c.3893+14G>T rs2272231 0.21141
NM_001148.6(ANK2):c.8503C>T (p.Pro2835Ser) rs3733617 0.14405
NM_001148.6(ANK2):c.9648A>G (p.Glu3216=) rs10013743 0.12780
NM_001148.6(ANK2):c.10888+20C>T rs35728190 0.10852
NM_001148.4(ANK2):c.*7C>T rs35446871 0.03095
NM_001148.6(ANK2):c.9900C>A (p.Ser3300Arg) rs34270799 0.01986
NM_001148.6(ANK2):c.2377-8C>T rs139893914 0.00682
NM_001148.6(ANK2):c.9454A>G (p.Thr3152Ala) rs61741040 0.00340
NM_001148.6(ANK2):c.10395G>A (p.Glu3465=) rs147423696 0.00282
NM_001148.6(ANK2):c.9286A>G (p.Ser3096Gly) rs144158934 0.00238
NM_001148.6(ANK2):c.11791G>A (p.Glu3931Lys) rs45454496 0.00235
NM_001148.6(ANK2):c.2277+9C>T rs141965666 0.00205
NM_001148.6(ANK2):c.10371G>A (p.Thr3457=) rs142908806 0.00203
NM_001148.6(ANK2):c.10901T>A (p.Val3634Asp) rs66785829 0.00200
NM_001148.6(ANK2):c.8354C>T (p.Ser2785Leu) rs145895389 0.00170
NM_001148.6(ANK2):c.3255G>T (p.Ala1085=) rs56173868 0.00156
NM_001148.6(ANK2):c.8658A>G (p.Leu2886=) rs149433267 0.00133
NM_001148.6(ANK2):c.11718G>A (p.Arg3906=) rs35724152 0.00128
NM_001148.6(ANK2):c.11725T>C (p.Ser3909Pro) rs141124755 0.00100
NM_001148.6(ANK2):c.11716C>T (p.Arg3906Trp) rs121912706 0.00094
NM_001148.6(ANK2):c.4745G>A (p.Arg1582Gln) rs138842207 0.00090
NM_001148.6(ANK2):c.11524C>T (p.Arg3842Trp) rs139797180 0.00088
NM_001148.6(ANK2):c.11538C>T (p.Leu3846=) rs45602336 0.00084
NM_001148.6(ANK2):c.11493G>T (p.Glu3831Asp) rs144046572 0.00070
NM_001148.6(ANK2):c.2900+5135G>A rs139641776 0.00054
NM_001148.6(ANK2):c.130C>G (p.Leu44Val) rs145272651 0.00051
NM_001148.6(ANK2):c.231G>A (p.Val77=) rs149699185 0.00049
NM_001148.6(ANK2):c.2727T>A (p.Thr909=) rs144548535 0.00036
NM_001148.6(ANK2):c.10531C>T (p.Leu3511=) rs148462839 0.00022
NM_001148.6(ANK2):c.997C>T (p.Leu333=) rs201024064 0.00021
NM_001148.6(ANK2):c.1638A>G (p.Ala546=) rs372133055 0.00019
NM_001148.6(ANK2):c.6633C>T (p.Ala2211=) rs143516811 0.00018
NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg) rs371787039 0.00014
NM_001148.6(ANK2):c.4372-7C>T rs370720661 0.00014
NM_001148.6(ANK2):c.11119G>A (p.Asp3707Asn) rs199549660 0.00013
NM_001148.6(ANK2):c.8673C>T (p.Pro2891=) rs374884110 0.00010
NM_001148.6(ANK2):c.2127T>C (p.Asn709=) rs113454484 0.00009
NM_001148.6(ANK2):c.11683G>A (p.Val3895Met) rs72556370 0.00007
NM_001148.6(ANK2):c.11354A>G (p.Gln3785Arg) rs150808807 0.00006
NM_001148.6(ANK2):c.1135C>T (p.Arg379Cys) rs143043717 0.00006
NM_001148.6(ANK2):c.8124A>G (p.Val2708=) rs776586126 0.00006
NM_001148.6(ANK2):c.8484T>C (p.Asp2828=) rs371140760 0.00006
NM_001148.6(ANK2):c.85-5C>T rs372560419 0.00006
NM_001148.6(ANK2):c.1881+9C>A rs200659747 0.00003
NM_001148.6(ANK2):c.2384A>C (p.Asn795Thr) rs769106499 0.00002
NM_001148.6(ANK2):c.3927A>G (p.Glu1309=) rs567570285 0.00002
NM_001148.6(ANK2):c.10573G>A (p.Glu3525Lys) rs781552524 0.00001
NM_001148.6(ANK2):c.121G>A (p.Ala41Thr) rs1085307623 0.00001
NM_001148.6(ANK2):c.1803T>C (p.His601=) rs144016063 0.00001
NM_001148.6(ANK2):c.2819C>G (p.Ala940Gly) rs537484483 0.00001
NM_001148.6(ANK2):c.3125+6G>A rs763791737 0.00001
NM_001148.6(ANK2):c.3526G>T (p.Val1176Leu) rs777113752 0.00001
NM_001148.6(ANK2):c.3969C>T (p.Cys1323=) rs756674393 0.00001
NM_001148.6(ANK2):c.10117G>A (p.Ala3373Thr)
NM_001148.6(ANK2):c.10362G>C (p.Arg3454Ser) rs55726422
NM_001148.6(ANK2):c.10976G>T (p.Arg3659Leu) rs556640912
NM_001148.6(ANK2):c.11086G>A (p.Glu3696Lys) rs199473347
NM_001148.6(ANK2):c.11477T>C (p.Ile3826Thr)
NM_001148.6(ANK2):c.11559T>C (p.Asp3853=)
NM_001148.6(ANK2):c.11859+1310A>G
NM_001148.6(ANK2):c.11859+1321T>C
NM_001148.6(ANK2):c.11859+1353A>T
NM_001148.6(ANK2):c.11859+2T>G
NM_001148.6(ANK2):c.1375G>A (p.Val459Ile)
NM_001148.6(ANK2):c.1711G>T (p.Ala571Ser) rs1400057725
NM_001148.6(ANK2):c.1937C>T (p.Ser646Phe) rs786205724
NM_001148.6(ANK2):c.2080-5T>C
NM_001148.6(ANK2):c.2142C>T (p.Leu714=)
NM_001148.6(ANK2):c.2230G>A (p.Val744Ile)
NM_001148.6(ANK2):c.2377-143A>G
NM_001148.6(ANK2):c.2583C>T (p.Tyr861=) rs529426179
NM_001148.6(ANK2):c.2693+2287C>T
NM_001148.6(ANK2):c.2698C>T (p.Arg900Ter)
NM_001148.6(ANK2):c.2991A>G (p.Lys997=)
NM_001148.6(ANK2):c.4567_4575del (p.Thr1523_Val1525del)
NM_001148.6(ANK2):c.6587G>A (p.Gly2196Asp)
NM_001148.6(ANK2):c.85-57017G>A
NM_001148.6(ANK2):c.85-57022A>C
NM_001148.6(ANK2):c.8544C>A (p.Ser2848=)
NM_001148.6(ANK2):c.8601C>T (p.Ala2867=) rs1239213547
NM_001148.6(ANK2):c.863G>A (p.Arg288Gln)
NM_001148.6(ANK2):c.8866T>C (p.Ser2956Pro)
NM_001148.6(ANK2):c.9212T>G (p.Val3071Gly)
NM_001148.6(ANK2):c.9474G>T (p.Pro3158=) rs145111737
NM_001148.6(ANK2):c.9590A>G (p.Asp3197Gly)
NM_001354269.3(ANK2):c.22G>A (p.Ala8Thr)

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