FAM197Y7

Chr Y

family with sequence similarity 197 Y-linked member 7

Also known as: FAM197Y7P

I cannot provide a clinical summary for FAM197Y7 as no information about this gene's protein function, associated diseases, or inheritance pattern was provided in the data below the instructions.

Clinical SummaryFAM197Y7
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ClinVar Variants
21 unique Pathogenic / Likely Pathogenic of 22 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

22 submitted variants in ClinVar

Classification Summary

Pathogenic19
Likely Pathogenic2
Likely Benign1
19
Pathogenic
2
Likely Pathogenic
1
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
19
Likely Pathogenic
2
VUS
0
Likely Benign
1
Benign
0
Total22

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

FAM197Y7 · 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 →
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