AMN p.Arg164His
c.491G>A · VCV3293032
Computational evidence
| Protein change | ||
| AlphaMissense | 0.1129 | likely benign |
|---|---|---|
| REVEL | 0.234 | benign-leaning |
| SaProt | LLR -6.70 | tolerated |
| ⇒ AlphaMissense, REVEL and SaProt all call this tolerated. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP 2.3 | GERP -2.2, phastCons 1 |
| Regional constraint | o/e 1.06 | unconstrained · MANE · 7,988 bp · p 0.14 · regional, not allelic |
| Overall | ||
| CADD | 18.33 | PHRED · no single calibrated threshold — expert panels disagree |
ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification
AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.
Population frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Remaining individualsnot grpmax-eligible | 0.0144% | 6,928 |
| European (non-Finnish)grpmax | 0.000593% | 168,510 |
Remaining individuals shows a higher raw frequency than the grpmax group above it. gnomAD excludes bottlenecked groups — Finnish, Ashkenazi Jewish, Amish and “Remaining individuals” — from grpmax, because founder effects make their frequencies unrepresentative for filtering. The table is sorted by frequency, so an excluded group can sit above the grpmax row.
Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.
Variant & gene context
- Gene
- AMN
- Protein
- p.Arg164His
- Coding
- c.491G>A
- MANE Select
- NM_030943
- Type
- single nucleotide variant
- Location
- chr14:102928953 (GRCh38)
- Gene constraint
- LOEUF 1.446 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
- Structure
- AlphaFold pLDDT 80.78 · 1 PDB
- Residue 164
- a disulfide bond; a β-strand
Similar variants
- AMN p.Arg164= Likely benign ★★ same residue
- AMN p.Ala238Thr Uncertain significance ★★ ⚠ same condition
- AMN p.Ala44Thr Uncertain significance ★★ ⚠ same condition
- AMN p.Arg271Trp Uncertain significance ★★ ⚠ same condition
- AMN p.Arg424Gly Uncertain significance ★★ ⚠ same condition
- AMN p.Cys250Trp Uncertain significance ★★ ⚠ same condition
- AMN p.Gln288His Uncertain significance ★★ ⚠ same condition
- AMN p.Pro444Ser Uncertain significance ★★ ⚠ 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/amn-p-arg164his (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown