NHS p.Asp433Glu
c.1299C>A · rs200022378 · VCV3234630
Uncertain significance
Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.000448%, nfe)
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| REVEL | 0.078 | moderately benign-leaning |
|---|---|---|
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP 0.88 | GERP 0.99, phastCons 1 |
| Regional constraint | o/e 0.79 | unconstrained · MANE · 357 kb · p 1.3e-14 · regional, not allelic |
| Overall | ||
| CADD | 17.4 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.000448%
European (non-Finnish) · 4/892,800 alleles
Filtering AF
0.000105%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 7.1e-05%
Overall
0.000331%
4/1,208,324 alleles · very rare
exomes 4/1,095,063 · genomes 0/113,261 · joint denominator
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
- NHS
- Protein
- p.Asp433Glu
- Coding
- c.1299C>A
- MANE Select
- NM_001291867
- dbSNP
- rs200022378
- Type
- single nucleotide variant
- Location
- chrX:17725405 (GRCh38)
- Structure
- AlphaFold pLDDT 43.65
Similar variants
- NHS p.Arg248Ter Pathogenic ★★ same type
- NHS p.Arg394Ter Pathogenic ★★ same type
- NHS p.Arg900Ter Pathogenic ★★ same type
- NHS p.Gln411Ter Pathogenic ★★ same type
- NHS p.Gln80Ter Pathogenic/Likely pathogenic ★★ same type
- NHS p.Ala564Val Uncertain significance ★★ same type
- NHS p.Ala745Val Uncertain significance ★★ same type
- NHS p.Arg162Cys Uncertain significance ★★ 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/nhs-p-asp433glu (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown