FGF8 p.Phe112fs
c.332_333dup · VCV4909325
Uncertain significance
Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
Consequence
frameshift
predicted LoF
gnomAD v4.1
Rare
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Consequence | frameshift | predicted loss-of-function |
|---|---|---|
| NMD | predicted | premature termination codon in exon 4 of 6 |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP 11 | GERP 2.2, phastCons 1 |
Predicted loss-of-function is descriptive, not an applied PVS1 code.
Variant & gene context
- Gene
- FGF8
- Protein
- p.Phe112fs
- Coding
- c.332_333dup
- MANE Select
- NM_033163
- Type
- Duplication
- Location
- chr10:101774735 (GRCh38)
- Gene constraint
- LOEUF 0.765 · pLI 0.06 (gnomAD)
- Structure
- AlphaFold pLDDT 81.34 · 1 PDB
- Residue 112
- a turn
Similar variants
- FGF8 p.His211fs Likely pathogenic ★ same type
- FGF8 p.Gly29_Arg34dup Conflicting classifications of pathogenicity ★ same type
- FGF8 c.*187dup Benign ★ same type
Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →
Cite Sugi Variant
Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/fgf8-p-phe112fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown