MSH2-OT1

Chr 2

MSH2 overlapping transcript 1

Also known as: HCG2040054

I cannot provide a clinical summary for MSH2-OT1 as no information about this gene's protein function, associated diseases, or inheritance pattern was provided in the data below the prompt. To write an accurate clinical summary following the strict rules specified, I would need details about what the protein does, what conditions result from mutations, and the inheritance pattern.

0
Active trials
0
Pubs (1 yr)
16
P/LP submissions
P/LP missense
LOEUF
Mechanism
Clinical SummaryMSH2-OT1
📋
ClinVar Variants
16 unique Pathogenic / Likely Pathogenic· 10 VUS of 27 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

27 submitted variants in ClinVar

Classification Summary

Pathogenic14
Likely Pathogenic2
VUS10
Benign1
14
Pathogenic
2
Likely Pathogenic
10
VUS
1
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
14
Likely Pathogenic
2
VUS
10
Likely Benign
0
Benign
1
Total27

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

MSH2-OT1 · 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.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found