HAR1A

Chr 20

highly accelerated region 1A

Also known as: HAR1F, LINC00064, NCRNA00064

NCBI Gene: 768096ENSG00000225978
60
ClinVar variants
36
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— HAR1A
📋
ClinVar Variants
36 Pathogenic / Likely Pathogenic· 21 VUS of 60 total submissions

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

60 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic30
Likely Pathogenic6
VUS21
Likely Benign3
30
Pathogenic
6
Likely Pathogenic
21
VUS
3
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————30
Likely Pathogenic
————6
VUS
————21
Likely Benign
————3
Benign
————0
Total—60

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

HAR1A · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype Relationships

1 OMIM entry

OMIM
Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
PubMed
Top 10 resultsSearch PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC
Top 5 resultsSearch Europe PMC ↗

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →

External Resources

Links to major genomics databases and tools