CFHR1 p.Asp35=
c.105T>C · VCV4683958
Benign/Likely benign
Multiple submitters
Classification
Benign/Likely benign
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 2 submitters
gnomAD v4.1
Rare
low-frequency (popmax 4.3%, afr)
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 -4.2 | GERP -3.6 |
| Overall | ||
| CADD | 2.83 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
4.3%
African / African-American · 2,508/58,302 alleles
Filtering AF
4.16%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 4.1%
Overall
0.199%
3,021/1,519,846 alleles · low-frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| African / African-Americangrpmax | 4.3% | 23 |
| Middle Eastern | 0.561% | 178 |
| Remaining individualsnot grpmax-eligible | 0.278% | 360 |
| Admixed American | 0.259% | 386 |
| European (non-Finnish) | 0.0145% | 6,900 |
| South Asian | 0.00876% | 11,421 |
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
- CFHR1
- Protein
- p.Asp35=
- Coding
- c.105T>C
- MANE Select
- NM_002113
- Type
- single nucleotide variant
- Location
- chr1:196825523 (GRCh38)
- Gene constraint
- LOEUF 1.208 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 89.21 · 2 PDB
- Residue 35
- the sushi 1 domain; a disulfide bond
Similar variants
- CFHR1 p.Asp35fs Uncertain significance ★ same residue
- CFHR1 p.Asp218Asn Uncertain significance ★★ ⚠ same type
- CFHR1 p.Gln44Ter Uncertain significance ★★ same type
- CFHR1 p.Ile214Asn Uncertain significance ★★ ⚠ same type
- CFHR1 p.Ile70Val Uncertain significance ★★ ⚠ same type
- CFHR1 p.Pro223Leu Uncertain significance ★★ ⚠ same type
- CFHR1 p.Tyr304Cys Uncertain significance ★★ ⚠ same type
- CFHR1 c.253+108G>C Benign ★★ 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/cfhr1-p-asp35 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown