ClinVar Miner

Variants in gene ANK2 with conflicting interpretations

Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
985 111 0 49 33 1 8 81

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign association
pathogenic 0 1 3 2 1 0
likely pathogenic 1 0 3 1 0 0
uncertain significance 4 4 0 28 9 1
likely benign 2 1 28 0 48 0
benign 1 0 9 48 0 0

All variants with conflicting interpretations #

Total variants: 81
Download table as spreadsheet
NM_001148.6(ANK2):c.10118C>T (p.Ala3373Val) rs371358639
NM_001148.6(ANK2):c.10362G>C (p.Arg3454Ser) rs55726422
NM_001148.6(ANK2):c.10371G>A (p.Thr3457=) rs142908806
NM_001148.6(ANK2):c.10395G>A (p.Glu3465=) rs147423696
NM_001148.6(ANK2):c.10861C>G (p.Leu3621Val) rs45570339
NM_001148.6(ANK2):c.10901T>A (p.Val3634Asp) rs66785829
NM_001148.6(ANK2):c.11032+17G>A rs587780853
NM_001148.6(ANK2):c.11032+19A>G rs200769962
NM_001148.6(ANK2):c.11198_11200del (p.Gly3733del) rs730880049
NM_001148.6(ANK2):c.11218C>A (p.Leu3740Ile) rs35530544
NM_001148.6(ANK2):c.11231C>A (p.Thr3744Asn) rs121912705
NM_001148.6(ANK2):c.1135C>T (p.Arg379Cys) rs143043717
NM_001148.6(ANK2):c.11538C>T (p.Leu3846=) rs45602336
NM_001148.6(ANK2):c.11594A>G (p.Asp3865Gly) rs140606121
NM_001148.6(ANK2):c.11716C>T (p.Arg3906Trp) rs121912706
NM_001148.6(ANK2):c.11718G>A (p.Arg3906=) rs35724152
NM_001148.6(ANK2):c.1177G>A (p.Ala393Thr) rs147458476
NM_001148.6(ANK2):c.11791G>A (p.Glu3931Lys) rs45454496
NM_001148.6(ANK2):c.130C>G (p.Leu44Val) rs145272651
NM_001148.6(ANK2):c.1401A>G (p.Ala467=) rs142159132
NM_001148.6(ANK2):c.1773T>C (p.Ser591=) rs374775005
NM_001148.6(ANK2):c.1783-4A>G rs755543636
NM_001148.6(ANK2):c.1899A>G (p.Leu633=) rs377608305
NM_001148.6(ANK2):c.2060A>G (p.Asn687Ser) rs29372
NM_001148.6(ANK2):c.2127T>C (p.Asn709=) rs113454484
NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg) rs371787039
NM_001148.6(ANK2):c.2278-11G>A rs146312675
NM_001148.6(ANK2):c.231G>A (p.Val77=) rs149699185
NM_001148.6(ANK2):c.2377-8C>T rs139893914
NM_001148.6(ANK2):c.2592T>C (p.Pro864=) rs138641014
NM_001148.6(ANK2):c.261G>A (p.Gly87=) rs145502481
NM_001148.6(ANK2):c.2679A>G (p.Gly893=) rs766183219
NM_001148.6(ANK2):c.2712C>T (p.Ser904=) rs149310669
NM_001148.6(ANK2):c.2727T>A (p.Thr909=) rs144548535
NM_001148.6(ANK2):c.2970A>C (p.Arg990=) rs35956627
NM_001148.6(ANK2):c.3074G>C (p.Gly1025Ala) rs773532854
NM_001148.6(ANK2):c.3136C>T (p.Leu1046=) rs149840991
NM_001148.6(ANK2):c.3255G>A (p.Ala1085=) rs56173868
NM_001148.6(ANK2):c.3543C>T (p.Ala1181=) rs76685232
NM_001148.6(ANK2):c.3931G>A (p.Val1311Ile) rs34065266
NM_001148.6(ANK2):c.4152T>C (p.Asp1384=) rs116128106
NM_001148.6(ANK2):c.4310C>T (p.Thr1437Met) rs142534126
NM_001148.6(ANK2):c.4315G>T (p.Gly1439Cys) rs34591340
NM_001148.6(ANK2):c.4373A>G (p.Glu1458Gly) rs72544141
NM_001148.6(ANK2):c.4456G>C (p.Val1486Leu) rs149678604
NM_001148.6(ANK2):c.4744C>T (p.Arg1582Trp) rs35249198
NM_001148.6(ANK2):c.4745G>A (p.Arg1582Gln) rs138842207
NM_001148.6(ANK2):c.4782T>G (p.Ile1594Met) rs775386505
NM_001148.6(ANK2):c.5231C>A (p.Ala1744Asp) rs147706514
NM_001148.6(ANK2):c.5313G>A (p.Lys1771=) rs140992864
NM_001148.6(ANK2):c.5715G>A (p.Ser1905=) rs143404578
NM_001148.6(ANK2):c.5985G>A (p.Lys1995=) rs116652427
NM_001148.6(ANK2):c.615C>T (p.Thr205=) rs587780852
NM_001148.6(ANK2):c.6228G>T (p.Lys2076Asn) rs144848998
NM_001148.6(ANK2):c.6648C>G (p.Gly2216=) rs140926982
NM_001148.6(ANK2):c.669+3A>G rs370475820
NM_001148.6(ANK2):c.6854T>C (p.Ile2285Thr) rs150684838
NM_001148.6(ANK2):c.7117A>G (p.Thr2373Ala) rs184514058
NM_001148.6(ANK2):c.7132G>A (p.Glu2378Lys) rs141191319
NM_001148.6(ANK2):c.7236A>T (p.Ala2412=) rs1394535709
NM_001148.6(ANK2):c.7255G>A (p.Glu2419Lys) rs752704424
NM_001148.6(ANK2):c.7267G>A (p.Ala2423Thr) rs3733616
NM_001148.6(ANK2):c.7436A>G (p.Lys2479Arg) rs201619005
NM_001148.6(ANK2):c.7488A>G (p.Thr2496=) rs143161930
NM_001148.6(ANK2):c.7831T>C (p.Tyr2611His) rs35338364
NM_001148.6(ANK2):c.7902G>A (p.Val2634=) rs150878494
NM_001148.6(ANK2):c.8324A>G (p.His2775Arg) rs534934297
NM_001148.6(ANK2):c.8388G>A (p.Pro2796=) rs369684289
NM_001148.6(ANK2):c.8673C>T (p.Pro2891=) rs374884110
NM_001148.6(ANK2):c.8843C>G (p.Ala2948Gly) rs138438183
NM_001148.6(ANK2):c.9061G>A (p.Ala3021Thr) rs74348333
NM_001148.6(ANK2):c.9286A>G (p.Ser3096Gly) rs144158934
NM_001148.6(ANK2):c.9454A>G (p.Thr3152Ala) rs61741040
NM_001148.6(ANK2):c.9526G>T (p.Asp3176Tyr) rs138928206
NM_001148.6(ANK2):c.962G>A (p.Arg321Gln) rs150226540
NM_001148.6(ANK2):c.9825T>G (p.Asp3275Glu) rs149043752
NM_001148.6(ANK2):c.9854T>C (p.Ile3285Thr) rs36210417
NM_001148.6(ANK2):c.9900C>A (p.Ser3300Arg) rs34270799
NM_001148.6(ANK2):c.9936C>T (p.Ser3312=) rs758162927
NM_001148.6(ANK2):c.997C>T (p.Leu333=) rs201024064
Single allele

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