ClinVar Miner

Variants in gene ANKRD26 with conflicting interpretations

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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
827 120 0 44 31 0 2 69

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
pathogenic 0 3 0 0 0
likely pathogenic 3 0 2 0 0
uncertain significance 0 2 0 26 13
likely benign 0 0 26 0 41
benign 0 0 13 41 0

All variants with conflicting interpretations #

Total variants: 69
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014915.3(ANKRD26):c.1207+15A>G rs115864032 0.03406
NM_014915.3(ANKRD26):c.3384G>A (p.Lys1128=) rs41299210 0.01449
NM_014915.3(ANKRD26):c.1269+11_1269+12del rs375101238 0.01366
NM_014915.3(ANKRD26):c.576G>A (p.Gln192=) rs41279942 0.01351
NM_014915.3(ANKRD26):c.2071T>C (p.Ser691Pro) rs73596345 0.01174
NM_014915.3(ANKRD26):c.3655G>A (p.Val1219Ile) rs146819984 0.00781
NM_014915.2(ANKRD26):c.-184G>T rs527666933 0.00525
NM_014915.3(ANKRD26):c.4445T>C (p.Ile1482Thr) rs80097260 0.00437
NM_014915.3(ANKRD26):c.1747C>G (p.Gln583Glu) rs56151272 0.00260
NM_014915.3(ANKRD26):c.2584C>G (p.Gln862Glu) rs74128547 0.00260
NM_014915.3(ANKRD26):c.2559+3A>G rs192827581 0.00257
NM_014915.3(ANKRD26):c.2332G>C (p.Glu778Gln) rs139949439 0.00251
NM_014915.3(ANKRD26):c.2679A>G (p.Gln893=) rs61730098 0.00215
NM_014915.3(ANKRD26):c.1133A>G (p.Glu378Gly) rs186243874 0.00188
NM_014915.3(ANKRD26):c.3007G>A (p.Glu1003Lys) rs41304587 0.00141
NM_014915.3(ANKRD26):c.4259G>A (p.Cys1420Tyr) rs146159734 0.00138
NM_014915.3(ANKRD26):c.2170A>C (p.Ser724Arg) rs141748831 0.00136
NM_014915.3(ANKRD26):c.542C>T (p.Thr181Ile) rs191015656 0.00093
NM_014915.3(ANKRD26):c.1806G>A (p.Glu602=) rs187923892 0.00086
NM_014915.3(ANKRD26):c.1451T>C (p.Val484Ala) rs201461870 0.00085
NM_014915.3(ANKRD26):c.3735G>A (p.Thr1245=) rs199716344 0.00079
NM_014915.3(ANKRD26):c.1998A>G (p.Lys666=) rs372489280 0.00052
NM_014915.3(ANKRD26):c.945A>G (p.Gln315=) rs200199151 0.00052
NM_014915.3(ANKRD26):c.4188T>C (p.Asp1396=) rs199589035 0.00046
NM_014915.3(ANKRD26):c.4916G>A (p.Arg1639Gln) rs184369322 0.00042
NM_014915.3(ANKRD26):c.679C>T (p.Pro227Ser) rs201638257 0.00039
NM_014915.3(ANKRD26):c.4490T>A (p.Val1497Asp) rs149647444 0.00037
NM_014915.3(ANKRD26):c.2855A>C (p.Lys952Thr) rs564448342 0.00035
NM_014915.3(ANKRD26):c.1728T>C (p.Asp576=) rs200379534 0.00031
NM_014915.3(ANKRD26):c.599A>G (p.Lys200Arg) rs150623081 0.00031
NM_014915.3(ANKRD26):c.2697+9A>G rs370796881 0.00029
NM_014915.3(ANKRD26):c.1970A>T (p.Asp657Val) rs193178384 0.00027
NM_014915.3(ANKRD26):c.2232T>A (p.Asn744Lys) rs368921201 0.00024
NM_014915.3(ANKRD26):c.3761A>G (p.Asp1254Gly) rs368705077 0.00024
NM_014915.3(ANKRD26):c.874+8G>T rs377114195 0.00023
NM_014915.3(ANKRD26):c.1635+9T>C rs199590440 0.00016
NM_014915.3(ANKRD26):c.-117G>A rs560384691 0.00011
NM_014915.3(ANKRD26):c.678A>T (p.Ile226=) rs143421550 0.00011
NM_014915.3(ANKRD26):c.2005A>G (p.Asn669Asp) rs368602859 0.00010
NM_014915.3(ANKRD26):c.2559+10T>A rs768668962 0.00009
NM_014915.3(ANKRD26):c.301G>A (p.Asp101Asn) rs199753643 0.00007
NM_014915.3(ANKRD26):c.3286C>T (p.Arg1096Trp) rs367849518 0.00007
NM_014915.3(ANKRD26):c.4636G>C (p.Asp1546His) rs753924410 0.00006
NM_014915.3(ANKRD26):c.756G>A (p.Pro252=) rs201128867 0.00005
NM_014915.3(ANKRD26):c.1565-4T>C rs747570982 0.00004
NM_014915.3(ANKRD26):c.1035_1036insT (p.Lys346Ter) rs780613456 0.00002
NM_014915.3(ANKRD26):c.501G>T (p.Leu167Phe) rs183398279 0.00002
NM_014915.3(ANKRD26):c.-126T>C rs1589393792 0.00001
NM_014915.3(ANKRD26):c.2151G>A (p.Met717Ile) rs188446159 0.00001
NM_014915.3(ANKRD26):c.513T>C (p.Asn171=) rs745670666 0.00001
NM_001256053.2(ANKRD26):c.1815-2_1815del rs564681878
NM_014915.3(ANKRD26):c.-118C>T rs1589393759
NM_014915.3(ANKRD26):c.-134G>A rs863223318
NM_014915.3(ANKRD26):c.1269+7_1269+9del rs200015812
NM_014915.3(ANKRD26):c.1565-4dup
NM_014915.3(ANKRD26):c.1867C>T (p.Arg623Trp)
NM_014915.3(ANKRD26):c.1986-3dup rs113123391
NM_014915.3(ANKRD26):c.2053G>A (p.Asp685Asn)
NM_014915.3(ANKRD26):c.228A>C (p.Arg76Ser)
NM_014915.3(ANKRD26):c.2325A>G (p.Ser775=)
NM_014915.3(ANKRD26):c.240C>T (p.Asn80=)
NM_014915.3(ANKRD26):c.371A>T (p.Gln124Leu) rs200100926
NM_014915.3(ANKRD26):c.4564A>G (p.Met1522Val)
NM_014915.3(ANKRD26):c.4651G>A (p.Glu1551Lys)
NM_014915.3(ANKRD26):c.521C>G (p.Ala174Gly)
NM_014915.3(ANKRD26):c.710-6T>C
NM_014915.3(ANKRD26):c.937G>A (p.Asp313Asn) rs61730102
NM_014915.3(ANKRD26):c.937G>T (p.Asp313Tyr) rs61730102
NM_014915.3(ANKRD26):c.948T>C (p.Asp316=) rs569751156

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