Wikidata:Database reports/Constraint violations/P3331
Constraint violations report for HGVS nomenclature (Discussion, uses, items, changes, related properties): Sequence Variant Nomenclature from the Human Genome Variation Society (HGVS)
Data time stamp: (UTC) — Items processed: 986
The report is generated based on the settings on Property:P3331#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.
Data time stamp: (UTC) — Items processed: 986
The report is generated based on the settings on Property:P3331#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.
"Scope" violations
editViolations count: 0
"Format" violations
editViolations count: 0
"Format" violations
editViolations count: 14 (+ 1 exceptions)
- EGFR G719D (Q32964822): ENSP00000275493.2:p.Gly719Asp
- EGFR L838P (Q32964852): ENSP00000275493.2:p.Leu838Pro
- EGFR L747_S752delinsQ (Q32965225): ENSP00000275493.2:p.Leu747_Ser752delinsGln
- VHL L158fs (c.471dupT) (Q32965860): ENSP00000256474.2:p.Leu158SerfsTer16
- VHL L101G (c.301_302delinsGG) (Q32966039): ENSP00000256474.2:p.Leu101Gly
- chrX:g.153762634G>A (G6PD:p.S218F) (Q38153319): >A chrX:g.153762634G>A
- VHL K159fs (c.473dup) (Q42786630): ENSP00000256474.2:p.Lys159GlufsTer15
- VHL *214L (c.641G>T) (Q42786716): >T NM_000551:c.641G>T
- VHL C77fs (c.228dup) (Q42786813): ENSP00000256474.2:p.Cys77LeufsTer?
- ABL1 BCR::ABL F317C (Q56241017): >G ENST00000318560:c.950T>G
- NM_000277.2(PAH):c.1A>G (p.Met1Val) (Q64401263): >G NST00000307000.7:c.-147A>G
- KIT F506_F508DUP (Q66084576): p.Phe506_Phe508dup
- KIT F506_F508DUP (Q66084576): c.55592192_55592200dup
- VHL F76del (c.224_226delTCT) (Q96007079): ENSP00000256474.2:p.Phe76del
"Entity types" violations
editViolations count: 0