PCNT p.His2829fs
c.8484dup · rs2519011808 · VCV2700638
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 38 of 47 |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP -2 | GERP -3.8 |
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
- PCNT
- Protein
- p.His2829fs
- Coding
- c.8484dup
- MANE Select
- NM_006031
- dbSNP
- rs2519011808
- Type
- Duplication
- Location
- chr21:46431947 (GRCh38)
- Gene constraint
- LOEUF 0.943 · pLI <0.01 (gnomAD)
Similar variants
- PCNT p.His2829= Likely benign ★ same residue
- PCNT p.Ala2957fs Pathogenic ★★ same type
- PCNT p.Gln783fs Pathogenic ★★ same type
- PCNT p.Glu998fs Pathogenic/Likely pathogenic ★★ same type
- PCNT p.His2484fs Pathogenic/Likely pathogenic ★★ same type
- PCNT p.Leu1200fs Pathogenic/Likely pathogenic ★★ same type
- PCNT p.Val2138fs Pathogenic/Likely pathogenic ★★ same type
- PCNT p.Val3179fs Pathogenic/Likely pathogenic ★★ 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/pcnt-p-his2829fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown