FAM197Y9
Chr Yfamily with sequence similarity 197 Y-linked member 9
I don't have sufficient information about the FAM197Y9 gene to write a clinical summary. The gene symbol suggests it may be part of the FAM197 family, but without specific data about the protein function, associated diseases, inheritance patterns, or clinical phenotypes, I cannot provide the requested 2-3 sentence clinical summary that meets your strict requirements for accuracy and evidence-based content.
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
64 submitted variants in ClinVar
Classification Summary
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 55 |
Likely Pathogenic | — | — | — | — | 2 |
VUS | — | — | — | — | 3 |
Likely Benign | — | — | — | — | 3 |
Benign | — | — | — | — | 0 |
| Total | — | 63 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
FAM197Y9 · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
3D Protein StructureAlphaFold
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →No open access results found
External Resources
Links to major genomics databases and tools