ERG p.Asn463fs
c.1388del · rs2516996865 · VCV2637893
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 | escapes | premature termination codon in the last exon (10 of 10) — the truncated protein is likely expressed. PVS1 input, not an applied code |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP 5.1 | GERP 1.3, phastCons 1 |
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
- ERG
- Protein
- p.Asn463fs
- Coding
- c.1388del
- MANE Select
- NM_182918
- dbSNP
- rs2516996865
- Type
- Deletion
- Location
- chr21:38383455 (GRCh38)
- Gene constraint
- LOEUF 0.234 · pLI 1.00 (gnomAD)
- Structure
- AlphaFold pLDDT 60.25 · 8 PDB
- Residue 463
- a functional site (breakpoint for translocation to form elf4-erg oncogene)
Similar variants
- ERG p.Ser182fs Pathogenic same condition
- ERG p.Thr224fs Pathogenic same condition
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/erg-p-asn463fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown