RAB30-DT

Chr 11

RAB30 divergent transcript

Also known as: RAB30-AS1

I cannot provide a clinical summary for RAB30-DT as no functional, phenotypic, or inheritance information was provided in the data. RAB30-DT appears to be a long non-coding RNA or transcript variant, but without supporting clinical or molecular data, I cannot make any claims about associated diseases or inheritance patterns.

Clinical SummaryRAB30-DT
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ClinVar Variants
4 unique Pathogenic / Likely Pathogenic· 1 VUS of 5 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

5 submitted variants in ClinVar

Classification Summary

Pathogenic4
VUS1
4
Pathogenic
1
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
4
Likely Pathogenic
0
VUS
1
Likely Benign
0
Benign
0
Total5

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

RAB30-DT · 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
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