NSD1 p.Arg74=
c.222A>G · rs201780407 · VCV1618913
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.0039%, nfe)
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP 9.4 | GERP 2.8, phastCons 1 |
| Overall | ||
| CADD | 13.78 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.0039%
European (non-Finnish) · 46/1,178,808 alleles
Filtering AF
0.00299%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.00267%
Overall
0.00316%
51/1,612,632 alleles · very rare
exomes 48/1,460,518 · genomes 3/152,114 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| European (non-Finnish)grpmax | 0.0039% | 25,626 |
| Remaining individualsnot grpmax-eligible | 0.0032% | 31,221 |
| African / African-American | 0.00267% | 37,433 |
| Admixed American | 0.00167% | 59,982 |
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
- NSD1
- Protein
- p.Arg74=
- Coding
- c.222A>G
- MANE Select
- NM_022455
- dbSNP
- rs201780407
- Type
- single nucleotide variant
- Location
- chr5:177135325 (GRCh38)
- Gene constraint
- LOEUF 0.144 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
- Structure
- AlphaFold pLDDT 45.26 · 4 PDB
Similar variants
- NSD1 c.1064-2A>G Pathogenic/Likely pathogenic ★★ same type
- NSD1 c.3921+1G>A Likely pathogenic ★★ same type
- NSD1 c.4192+2T>G Pathogenic ★★ same type
- NSD1 c.4303-1G>C Likely pathogenic ★★ same type
- NSD1 c.4378+1G>A Pathogenic/Likely pathogenic ★★ same type
- NSD1 c.4766-2A>G Pathogenic/Likely pathogenic ★★ same type
- NSD1 c.4966+1G>A Pathogenic ★★ same type
- NSD1 c.4966+1G>C 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/nsd1-p-arg74 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown