DKFZP434A062

Chr 9

uncharacterized LOC26102

I cannot provide a clinical summary for DKFZP434A062 as no information about this gene's protein function, associated diseases, or inheritance pattern was provided in the data you referenced. To write an accurate clinical summary following the specified guidelines, I would need details about the protein's function, phenotypes associated with mutations, and genetic inheritance information.

Clinical SummaryDKFZP434A062
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ClinVar Variants
48 unique Pathogenic / Likely Pathogenic· 1 VUS of 49 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

49 submitted variants in ClinVar

Classification Summary

Pathogenic47
Likely Pathogenic1
VUS1
47
Pathogenic
1
Likely Pathogenic
1
VUS

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
47
Likely Pathogenic
1
VUS
1
Likely Benign
0
Benign
0
Total49

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

DKFZP434A062 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

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Clinical Literature
Open Research Assistant →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found