MVP-DT
Chr 16MVP divergent transcript
935
ClinVar variants
78
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— MVP-DT
📋
ClinVar Variants
78 Pathogenic / Likely Pathogenic· 221 VUS of 935 total submissions
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
935 submitted variants in ClinVar
Classification Summary
Pathogenic62
Likely Pathogenic16
VUS221
Likely Benign80
Conflicting6
62
Pathogenic
16
Likely Pathogenic
221
VUS
80
Likely Benign
6
Conflicting
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | 33 | 3 | 26 | 0 | 62 |
Likely Pathogenic | 9 | 6 | 1 | 0 | 16 |
VUS | 7 | 208 | 4 | 2 | 221 |
Likely Benign | 0 | 12 | 5 | 63 | 80 |
Benign | 0 | 0 | 0 | 0 | 0 |
Conflicting | — | 6 | |||
| Total | 49 | 229 | 36 | 65 | 385 |
LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
MVP-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.
External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
SFARI Gene
Autism-gene association scoring (SFARI)
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)
Clinical Literature
Landmark / reviewRecent case evidence
No publications found for MVP-DT
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
SFARI Gene
Autism-gene association scoring (SFARI)
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)