CASC17

Chr 17

cancer susceptibility 17

Also known as: LINC00600

0
Active trials
5
Pathogenic / LP
7
ClinVar variants
1
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummaryCASC17
📋
ClinVar Variants
5 Pathogenic / Likely Pathogenic· 1 VUS of 7 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

7 submitted variants in ClinVar

Classification Summary

Pathogenic5
VUS1
Likely Benign1
5
Pathogenic
1
VUS
1
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
5
Likely Pathogenic
0
VUS
1
Likely Benign
1
Benign
0
Total7

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

CASC17 · protein map & ClinVar variants

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

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
PubMed
Top 1 results · since 2015Search PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found