ClinVar Miner

Variants with conflicting interpretations studied for Developmental cataract

Coded as:
Minimum review status of the submission for Developmental cataract: Collection method of the submission for Developmental cataract:
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
87 5 0 11 8 0 6 23

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
Developmental cataract pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 0 3 1 1 0
likely pathogenic 6 0 3 1 0
uncertain significance 0 1 0 5 4
likely benign 1 0 1 0 1
benign 0 0 1 3 0

Condition to condition summary #

Total conditions: 15
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 3 0 8 5 0 4 17
not specified 0 1 0 1 4 0 0 5
Developmental cataract 111 1 0 2 0 0 1 3
Abnormality of the eye 0 0 0 1 0 0 0 1
CRYAB-related disorder 0 0 0 0 1 0 0 1
CRYBB2-related disorder 0 0 0 1 0 0 0 1
CRYGA-related disorder 0 0 0 0 1 0 1 1
Cardiovascular phenotype 0 0 0 0 1 0 0 1
Cataract 9, multiple types, with microcornea 0 1 0 1 0 0 0 1
EYA1-related disorder 0 0 0 0 1 0 0 1
Myofibrillar Myopathy, Dominant 0 0 0 0 1 0 0 1
NECTIN3-related disorder 0 0 0 0 0 0 1 1
Nephrolithiasis/nephrocalcinosis 0 0 0 0 1 0 0 1
Zonular Pulverulent Cataract 0 0 0 1 0 0 0 1
acorea-microphthalmia-cataract syndrome 0 0 0 1 0 0 0 1

All variants with conflicting interpretations #

Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_018238.3(AGK):c.-100G>A rs552726046 0.00401
NM_001886.3(CRYBA4):c.40-1G>C rs142090709 0.00358
NM_000276.4(OCRL):c.439+3A>G rs61752971 0.00248
NM_005267.5(GJA8):c.658A>G (p.Asn220Asp) rs138140155 0.00229
NM_014617.4(CRYGA):c.239G>A (p.Arg80His) rs139353014 0.00221
NM_015480.3(NECTIN3):c.886A>C (p.Asn296His) rs79006549 0.00178
NM_012293.3(PXDN):c.3190G>A (p.Ala1064Thr) rs202132697 0.00162
NM_001289808.2(CRYAB):c.460G>A (p.Gly154Ser) rs150516929 0.00086
NM_000503.6(EYA1):c.1460C>T (p.Ser487Leu) rs139717960 0.00069
NM_000138.5(FBN1):c.3422C>T (p.Pro1141Leu) rs2228241 0.00057
NM_001123385.2(BCOR):c.3277G>A (p.Glu1093Lys) rs144736705 0.00014
NM_000496.3(CRYBB2):c.583T>G (p.Trp195Gly) rs147344332 0.00007
NM_000496.3(CRYBB2):c.463C>T (p.Gln155Ter) rs74315489 0.00001
NM_000394.4(CRYAA):c.34C>T (p.Arg12Cys) rs397515624
NM_000394.4(CRYAA):c.440del (p.Gln147fs) rs1114167311
NM_001289808.2(CRYAB):c.320G>T (p.Arg107Leu) rs144451841
NM_005267.5(GJA8):c.151G>A (p.Asp51Asn) rs864309703
NM_005267.5(GJA8):c.565C>T (p.Pro189Ser) rs2149015924
NM_005267.5(GJA8):c.64G>A (p.Gly22Ser) rs2149015335
NM_006891.4(CRYGD):c.70C>A (p.Pro24Thr) rs28931605
NM_021954.4(GJA3):c.176C>T (p.Pro59Leu) rs864309691
NM_021954.4(GJA3):c.56C>T (p.Thr19Met) rs1114167307
NM_024513.4(FYCO1):c.3001_3003delinsGAA (p.Asn1001Glu) rs71622515

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