ClinVar Miner

Variants with conflicting interpretations studied for ANKRD26-related condition

Minimum review status of the submission for ANKRD26-related condition: Collection method of the submission for ANKRD26-related condition:
Minimum review status of the other submission: Collection method of the other submission:
Minimum conflict level:
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
31 18 0 20 16 0 0 32

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.

All conditions
ANKRD26-related condition uncertain significance likely benign benign
uncertain significance 0 1 0
likely benign 15 0 14
benign 0 6 0

Condition to condition summary #

Total conditions: 2
Download table as spreadsheet
Condition 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
not provided 0 20 0 18 14 0 0 30
not specified 0 9 0 5 9 0 0 14

All variants with conflicting interpretations #

Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_014915.3(ANKRD26):c.1269+11_1269+12del rs375101238 0.01366
NM_014915.3(ANKRD26):c.4445T>C (p.Ile1482Thr) rs80097260 0.00437
NM_014915.3(ANKRD26):c.2559+3A>G rs192827581 0.00257
NM_014915.3(ANKRD26):c.92G>C (p.Gly31Ala) rs199849785 0.00202
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.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.679C>T (p.Pro227Ser) rs201638257 0.00039
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.1970A>T (p.Asp657Val) rs193178384 0.00027
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.153C>G (p.His51Gln) rs139049098 0.00021
NM_014915.3(ANKRD26):c.110A>G (p.Gln37Arg) rs543170486 0.00013
NM_014915.3(ANKRD26):c.-117G>A rs560384691 0.00011
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.1565-4dup
NM_014915.3(ANKRD26):c.1867C>T (p.Arg623Trp)
NM_014915.3(ANKRD26):c.2053G>A (p.Asp685Asn)
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.937G>T (p.Asp313Tyr) rs61730102
NM_014915.3(ANKRD26):c.948T>C (p.Asp316=) rs569751156

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