FAM230F

Chr 22

family with sequence similarity 230 member F

Also known as: LINC01663

NCBI Gene: 100996432ENSG00000276095
163
ClinVar variants
150
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— FAM230F
📋
ClinVar Variants
150 Pathogenic / Likely Pathogenic· 8 VUS of 163 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

163 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic150
VUS8
Likely Benign4
150
Pathogenic
8
VUS
4
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————150
Likely Pathogenic
————0
VUS
————8
Likely Benign
————4
Benign
————0
Total—162

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

FAM230F · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype

OMIM

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence

No publications found for FAM230F

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →

External Resources

Links to major genomics databases and tools