ClinVar Miner

Variants in gene ANK3 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
268 15 0 22 16 0 1 39

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 1 0 0 0
likely pathogenic 1 0 1 0 0
uncertain significance 0 1 0 14 2
likely benign 0 0 14 0 21
benign 0 0 2 21 0

All variants with conflicting interpretations #

Total variants: 39
Download table as spreadsheet
NM_020987.5(ANK3):c.10055A>G (p.Glu3352Gly) rs61845768
NM_020987.5(ANK3):c.10688A>G (p.Glu3563Gly) rs147527383
NM_020987.5(ANK3):c.10761G>A (p.Thr3587=) rs138986388
NM_020987.5(ANK3):c.10953A>C (p.Lys3651Asn) rs115903343
NM_020987.5(ANK3):c.11366A>G (p.Asn3789Ser) rs144123544
NM_020987.5(ANK3):c.11678G>C (p.Ser3893Thr) rs12260663
NM_020987.5(ANK3):c.12769A>G (p.Ile4257Val) rs12261793
NM_020987.5(ANK3):c.1290C>G (p.Thr430=) rs374761322
NM_020987.5(ANK3):c.13106G>A (p.Arg4369Gln) rs141939315
NM_020987.5(ANK3):c.1491+6C>T rs76733192
NM_020987.5(ANK3):c.1789-10G>A rs200791367
NM_020987.5(ANK3):c.2103C>T (p.Leu701=) rs142415903
NM_020987.5(ANK3):c.2316G>A (p.Gln772=) rs143430852
NM_020987.5(ANK3):c.2614+6del rs370950407
NM_020987.5(ANK3):c.2902G>C (p.Asp968His) rs730882195
NM_020987.5(ANK3):c.3105C>G (p.Pro1035=) rs55680239
NM_020987.5(ANK3):c.315+10A>G rs202079424
NM_020987.5(ANK3):c.3822C>G (p.Ser1274=) rs184515022
NM_020987.5(ANK3):c.382A>G (p.Thr128Ala) rs114937210
NM_020987.5(ANK3):c.4029G>A (p.Glu1343=) rs116757606
NM_020987.5(ANK3):c.4085G>C (p.Gly1362Ala) rs200556767
NM_020987.5(ANK3):c.4365_4368del (p.Arg1456fs)
NM_020987.5(ANK3):c.4465C>T (p.Pro1489Ser) rs41274676
NM_020987.5(ANK3):c.4699G>A (p.Val1567Met) rs180798231
NM_020987.5(ANK3):c.4907G>A (p.Arg1636Lys) rs188159332
NM_020987.5(ANK3):c.5137G>A (p.Val1713Ile) rs544357242
NM_020987.5(ANK3):c.5582C>T (p.Thr1861Met) rs117475706
NM_020987.5(ANK3):c.6072C>T (p.Ser2024=) rs532643979
NM_020987.5(ANK3):c.6953A>G (p.Lys2318Arg) rs59021407
NM_020987.5(ANK3):c.6955G>A (p.Asp2319Asn) rs140463162
NM_020987.5(ANK3):c.7225T>C (p.Ser2409Pro) rs148904927
NM_020987.5(ANK3):c.7305T>C (p.Tyr2435=) rs115257011
NM_020987.5(ANK3):c.7469C>T (p.Pro2490Leu) rs140741466
NM_020987.5(ANK3):c.756G>A (p.Thr252=) rs117266082
NM_020987.5(ANK3):c.7715T>C (p.Ile2572Thr) rs61732398
NM_020987.5(ANK3):c.8508T>C (p.His2836=) rs11815168
NM_020987.5(ANK3):c.8988G>C (p.Gln2996His) rs41274672
NM_020987.5(ANK3):c.909A>C (p.Thr303=) rs73269474
NM_020987.5(ANK3):c.9997A>T (p.Thr3333Ser) rs140183285

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