Wikidata

Wikidata:Database reports/Constraint violations/P3329

< Wikidata:Database reports‎ | Constraint violations
Constraint violations report for CIViC variant ID (Discussion, uses, items, changes, related properties): identifier used in the CIViC database to identify specific variant
Data time stamp: (UTC) — Items processed: 2,012
The report is generated based on the settings on Property:P3329#P2302.
Updates overwrite this page. Some may already be fixed since the last update: check RecentChangesLinked.
When incremental dumps and the bot work as planned, items fixed before 07:00 UTC disappear in the next update. The report is not updated if only the item count changes.
The report can include false positives. There is no need to "fix" them.

"Format" violations

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Violations count: 0

"Item instance of (P31)" violations

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Violations count: 310

"Entity types" violations

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Violations count: 0

"Scope" violations

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Violations count: 0

"Type sequence variant (Q15304597)" violations

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Violations count: 423

Types statistics

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Accepted Type Usage
Yes sequence variant (Q15304597) 585
Yes missense mutation (Q2656896) 563
Yes transcript fusion (Q28419128) 219
Yes Frameshift Truncation (Q28371705) 67
Yes Loss Of Function Variant (Q27907094) 50
Yes Stop Gained (Q28371788) 45
No Transcript Amplification (Q27907091) 34
Yes Protein Altering Variant (Q27907087) 33
Yes Inframe Deletion (Q28371783) 25
Yes Inframe Insertion (Q27908066) 22
Yes Frameshift Variant (Q28419131) 22
Yes Gain Of Function Variant (Q28371786) 20
Yes transcript variant (Q28371782) 19
Yes exon variant (Q27908063) 13
Yes gene variant (Q28381983) 12
Yes Polymorphic Sequence Variant (Q28419136) 9
No Synonymous Variant (Q28419125) 9
No Transcript Ablation (Q28381986) 7
Yes Exon Loss Variant (Q28419122) 7
No Splice Donor Variant (Q29937349) 7
No splice acceptor variant (Q42866965) 6
No Stop Lost (Q28419141) 6
No wild type (Q128723) 6
Yes single-nucleotide polymorphism (Q501128) 4
No 3 Prime UTR Variant (Q28419124) 4
Yes Intron Variant (Q28419129) 3
No Start Lost (Q29938065) 3
No Frameshift Elongation (Q28381989) 3
No Regulatory Region Variant (Q28381988) 3
No disruptive inframe deletion (Q42866969) 3
No Plus 1 Frameshift Variant (Q28381736) 3
Yes loss of heterozygosity (Q2617554) 3
No Short Tandem Repeat Variation (Q28419126) 2
Yes Coding Sequence Variant (Q28371787) 2
No Coding Transcript Intron Variant (Q28419134) 2
No Minus 1 Frameshift Variant (Q28419135) 2
No Indel (Q32949508) 2
No microsatellite (Q265193) 2
Yes Coding Transcript Variant (Q29907183) 2
No inframe indel (Q42866966) 1
Yes deleterious mutation (Q120878399) 1
No feature truncation (Q42805784) 1
No DNA binding site (Q5205743) 1
No Insertion (Q32937968) 1
No 3 Prime UTR Truncation (Q28419139) 1
No 5 Prime UTR Exon Variant (Q28419138) 1
Yes inframe variant (Q28419132) 1
No Transcription Variant (Q28419121) 1
No Copy Number Change (Q28381984) 1
No 5 Prime UTR Variant (Q27919343) 1
No Nonsynonymous Variant (Q27905684) 1
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