ANKRD35-DT

Chr 1

ANKRD35 divergent transcript

76
ClinVar variants
61
Pathogenic / LP
pLI score
0
Active trials
Clinical SummaryANKRD35-DT
📋
ClinVar Variants
61 Pathogenic / Likely Pathogenic· 10 VUS of 76 total submissions
Some data sources returned errors (2)

ensembl: Error: Ensembl fetch failed: 400 for https://rest.ensembl.org/lookup/symbol/homo_sapiens/ANKRD35-DT?content-type=application/json&expand=1

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

76 submitted variants in ClinVar

Classification Summary

Pathogenic51
Likely Pathogenic10
VUS10
Likely Benign1
Benign2
Conflicting2
51
Pathogenic
10
Likely Pathogenic
10
VUS
1
Likely Benign
2
Benign
2
Conflicting

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
51
Likely Pathogenic
10
VUS
10
Likely Benign
1
Benign
2
Conflicting
2
Total76

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

ANKRD35-DT · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype

No OMIM entries found.