ESR2 p.Ser157=
c.471G>A · VCV4751346
Benign
Single submitter
Classification
Benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
rare (popmax 0.301%, eas)
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 -6 | GERP -4.9 |
| Overall | ||
| CADD | 1.26 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.301%
East Asian · 135/44,888 alleles
Filtering AF
0.259%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.244%
Overall
0.0112%
181/1,614,138 alleles · rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| East Asiangrpmax | 0.301% | 333 |
| African / African-American | 0.0147% | 6,823 |
| Admixed American | 0.00333% | 30,011 |
| Remaining individualsnot grpmax-eligible | 0.0032% | 31,255 |
| European (non-Finnish) | 0.00246% | 40,688 |
| South Asian | 0.0022% | 45,541 |
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
- ESR2
- Protein
- p.Ser157=
- Coding
- c.471G>A
- MANE Select
- NM_001437
- Type
- single nucleotide variant
- Location
- chr14:64280045 (GRCh38)
- Gene constraint
- LOEUF 1.002 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 69.76 · 39 PDB
- Residue 157
- a DNA-binding region
Similar variants
- ESR2 p.Ala432Thr Uncertain significance ★★ ⚠ same type
- ESR2 p.Arg230Gln Uncertain significance ★★ ⚠ same type
- ESR2 p.Arg346Cys Uncertain significance ★★ ⚠ same type
- ESR2 p.Arg388Gln Uncertain significance ★★ ⚠ same type
- ESR2 p.Asn407Ser Uncertain significance ★★ ⚠ same type
- ESR2 p.Asp154Asn Uncertain significance ★★ ⚠ same type
- ESR2 p.Cys169Phe Uncertain significance ★★ ⚠ same type
- ESR2 p.Gly243Asp 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/esr2-p-ser157 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown