ClinVar Miner

Variants in gene ANK3 with conflicting interpretations

See also:
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
979 116 0 52 34 0 2 85

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 2 0 0
likely pathogenic 1 0 1 0 0
uncertain significance 2 1 0 31 5
likely benign 0 0 31 0 51
benign 0 0 5 51 0

All variants with conflicting interpretations #

Total variants: 85
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020987.5(ANK3):c.8895T>C (p.Ala2965=) rs10740006 0.18901
NM_020987.5(ANK3):c.9368A>G (p.Lys3123Arg) rs10821668 0.18742
NM_020987.5(ANK3):c.1218T>C (p.Ile406=) rs2297979 0.17447
NM_020987.5(ANK3):c.4201-3T>C rs2393595 0.12356
NM_020987.5(ANK3):c.6066C>T (p.Ala2022=) rs17208576 0.07406
NM_020987.5(ANK3):c.8655C>A (p.His2885Gln) rs11599164 0.07405
NM_020987.5(ANK3):c.9349A>G (p.Ile3117Val) rs28932171 0.07385
NM_020987.5(ANK3):c.9137C>G (p.Thr3046Ser) rs74153183 0.06794
NM_020987.5(ANK3):c.8013C>T (p.Ser2671=) rs41274674 0.04537
NM_020987.5(ANK3):c.2565T>C (p.Asn855=) rs10994234 0.03800
NM_020987.5(ANK3):c.909A>C (p.Thr303=) rs73269474 0.03053
NM_020987.5(ANK3):c.12769A>G (p.Ile4257Val) rs12261793 0.03012
NM_020987.5(ANK3):c.2124T>C (p.Asp708=) rs34552044 0.02906
NM_020987.5(ANK3):c.402T>C (p.Asn134=) rs1031688 0.02324
NM_020987.5(ANK3):c.11685C>T (p.Ser3895=) rs7923682 0.02183
NM_020987.5(ANK3):c.1491+6C>T rs76733192 0.02170
NM_020987.5(ANK3):c.8988G>C (p.Gln2996His) rs41274672 0.01542
NM_020987.5(ANK3):c.7140C>T (p.His2380=) rs3802696 0.01444
NM_020987.5(ANK3):c.10953A>C (p.Lys3651Asn) rs115903343 0.01085
NM_020987.5(ANK3):c.382A>G (p.Thr128Ala) rs114937210 0.01080
NM_020987.5(ANK3):c.7715T>C (p.Ile2572Thr) rs61732398 0.01022
NM_020987.5(ANK3):c.2615-6882A>G rs41283526 0.00832
NM_020987.5(ANK3):c.1047C>T (p.Cys349=) rs117138204 0.00580
NM_020987.5(ANK3):c.2544T>C (p.Asp848=) rs60764245 0.00564
NM_020987.5(ANK3):c.6953A>G (p.Lys2318Arg) rs59021407 0.00532
NM_020987.5(ANK3):c.13106G>A (p.Arg4369Gln) rs141939315 0.00503
NM_020987.5(ANK3):c.13065+20G>A rs142778119 0.00477
NM_020987.5(ANK3):c.7225T>C (p.Ser2409Pro) rs148904927 0.00459
NM_020987.5(ANK3):c.8508T>C (p.His2836=) rs11815168 0.00416
NM_020987.5(ANK3):c.3984G>A (p.Leu1328=) rs149052618 0.00393
NM_020987.5(ANK3):c.2322G>C (p.Gly774=) rs138823660 0.00344
NM_020987.5(ANK3):c.6955G>A (p.Asp2319Asn) rs140463162 0.00330
NM_020987.5(ANK3):c.10055A>G (p.Glu3352Gly) rs61845768 0.00329
NM_020987.5(ANK3):c.2889C>T (p.Tyr963=) rs149682716 0.00309
NM_020987.5(ANK3):c.5582C>T (p.Thr1861Met) rs117475706 0.00292
NM_020987.5(ANK3):c.2103C>T (p.Leu701=) rs142415903 0.00280
NM_020987.5(ANK3):c.756G>A (p.Thr252=) rs117266082 0.00280
NM_020987.5(ANK3):c.2674T>C (p.Leu892=) rs61732401 0.00273
NM_020987.5(ANK3):c.2316G>A (p.Gln772=) rs143430852 0.00240
NM_020987.5(ANK3):c.2523T>C (p.Asn841=) rs144773457 0.00222
NM_020987.5(ANK3):c.9997A>T (p.Thr3333Ser) rs140183285 0.00178
NM_020987.5(ANK3):c.10688A>G (p.Glu3563Gly) rs147527383 0.00177
NM_020987.5(ANK3):c.4465C>T (p.Pro1489Ser) rs41274676 0.00152
NM_020987.5(ANK3):c.1492-12C>A rs41283530 0.00138
NM_020987.5(ANK3):c.5137G>A (p.Val1713Ile) rs544357242 0.00134
NM_020987.5(ANK3):c.8534G>A (p.Gly2845Glu) rs139022925 0.00126
NM_020987.5(ANK3):c.2200C>T (p.Leu734=) rs144696256 0.00120
NM_020987.5(ANK3):c.11825A>G (p.Lys3942Arg) rs148549519 0.00116
NM_020987.5(ANK3):c.4029G>A (p.Glu1343=) rs116757606 0.00114
NM_020987.5(ANK3):c.9935C>T (p.Ala3312Val) rs201625904 0.00101
NM_020987.5(ANK3):c.10761G>A (p.Thr3587=) rs138986388 0.00087
NM_020987.5(ANK3):c.7305T>C (p.Tyr2435=) rs115257011 0.00079
NM_020987.5(ANK3):c.7469C>T (p.Pro2490Leu) rs140741466 0.00073
NM_020987.5(ANK3):c.4826C>T (p.Thr1609Met) rs148024054 0.00058
NM_020987.5(ANK3):c.315+10A>G rs202079424 0.00050
NM_020987.5(ANK3):c.11678G>C (p.Ser3893Thr) rs12260663 0.00044
NM_020987.5(ANK3):c.11366A>G (p.Asn3789Ser) rs144123544 0.00043
NM_020987.5(ANK3):c.6555G>T (p.Gln2185His) rs144465058 0.00036
NM_020987.5(ANK3):c.2173G>A (p.Ala725Thr) rs144051466 0.00030
NM_020987.5(ANK3):c.11090C>G (p.Ser3697Cys) rs148109897 0.00024
NM_020987.5(ANK3):c.5981C>T (p.Ser1994Leu) rs141251507 0.00024
NM_001204403.2(ANK3):c.86G>A (p.Ser29Asn) rs758576419 0.00019
NM_020987.5(ANK3):c.4085G>C (p.Gly1362Ala) rs200556767 0.00019
NM_020987.5(ANK3):c.4907G>A (p.Arg1636Lys) rs188159332 0.00017
NM_020987.5(ANK3):c.11159C>T (p.Thr3720Met) rs201547988 0.00014
NM_020987.5(ANK3):c.11251A>G (p.Ser3751Gly) rs200489439 0.00014
NM_020987.5(ANK3):c.2385T>C (p.Asn795=) rs372094828 0.00014
NM_020987.5(ANK3):c.1789-10G>A rs200791367 0.00013
NM_020987.5(ANK3):c.6945T>G (p.His2315Gln) rs375411220 0.00010
NM_020987.5(ANK3):c.4314A>G (p.Ala1438=) rs199845615 0.00009
NM_020987.5(ANK3):c.2976G>A (p.Ala992=) rs747475542 0.00006
NM_020987.5(ANK3):c.4699G>A (p.Val1567Met) rs180798231 0.00006
NM_020987.5(ANK3):c.6072C>T (p.Ser2024=) rs532643979 0.00004
NM_020987.5(ANK3):c.8174G>A (p.Gly2725Asp) rs993289778 0.00001
NM_020987.5(ANK3):c.11007C>A (p.Thr3669=) rs2131966858
NM_020987.5(ANK3):c.12596-355G>T
NM_020987.5(ANK3):c.12672T>A (p.Asp4224Glu)
NM_020987.5(ANK3):c.1290C>G (p.Thr430=) rs374761322
NM_020987.5(ANK3):c.2502G>A (p.Met834Ile) rs2132296500
NM_020987.5(ANK3):c.2614+6del rs370950407
NM_020987.5(ANK3):c.2902G>C (p.Asp968His) rs730882195
NM_020987.5(ANK3):c.3045G>T (p.Thr1015=) rs3750800
NM_020987.5(ANK3):c.3105C>G (p.Pro1035=) rs55680239
NM_020987.5(ANK3):c.4365_4368del (p.Arg1456fs) rs2084966849
NM_020987.5(ANK3):c.468C>G (p.Val156=) rs71495633

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.