DKFZP434A062

Chr 9

uncharacterized LOC26102

0
Active trials
48
Pathogenic / LP
49
ClinVar variants
1
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummaryDKFZP434A062
📋
ClinVar Variants
48 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.

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Landmark / reviewRecent case evidence
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found