CTR9 p.Ala198fs
c.593del · VCV3693658
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 in a LoF-intolerant gene |
|---|---|---|
| NMD | predicted | premature termination codon in exon 6 of 25 |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP 12 | GERP 2.2, phastCons 1 |
Predicted loss-of-function is descriptive, not an applied PVS1 code.
Variant & gene context
- Gene
- CTR9
- Protein
- p.Ala198fs
- Coding
- c.593del
- MANE Select
- NM_014633
- Type
- Deletion
- Location
- chr11:10760173 (GRCh38)
- Gene constraint
- LOEUF 0.368 · pLI 1.00 (gnomAD)
- Structure
- AlphaFold pLDDT 76.62 · 21 PDB
- Residue 198
- an α-helix
Similar variants
- CTR9 p.Ala198= Uncertain significance ★★ same residue
- CTR9 p.Asp771fs Uncertain significance ★ same type
- CTR9 p.Ile6fs Uncertain significance ★ same type
- CTR9 p.Leu733del Uncertain significance ★ same type
- CTR9 p.Lys958_Lys959del Uncertain significance ★ same type
- CTR9 c.1194+15del Likely benign ★ same type
- CTR9 c.1687-137del Likely benign ★ same type
- CTR9 c.2373-23_2373-19del Likely 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/ctr9-p-ala198fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown