CIC p.Glu1013fs
c.3036_3037insC · rs1555765151 · VCV451627
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 haploinsufficient gene (ClinGen); NMD-escape possible for C-terminal truncations |
|---|---|---|
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP -0.03 | GERP -0.96, phastCons 0.85 |
Predicted loss-of-function is descriptive, not an applied PVS1 code.
Population frequency
No gnomAD frequency available for this variant. This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.
Variant & gene context
- Gene
- CIC
- Protein
- p.Glu1013fs
- Coding
- c.3036_3037insC
- MANE Select
- NM_001386298
- dbSNP
- rs1555765151
- Type
- Insertion
- Location
- chr19:42287097 (GRCh38)
- Structure
- AlphaFold pLDDT 75.09
Similar variants
- CIC p.Glu1391fs Pathogenic ★ same type
- SLC25A1 c.*247_*248insCACTTGTCCATGTGCTTACTGTGAACCCTGTGCC Benign ★ same type
- SLC25A1 c.*65_*66insAT Benign ★ same type
- SLC25A1 c.*66_*67insTG 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/cic-p-glu1013fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown