ADGRL2 p.Ser759=
c.2277A>G · rs151060845 · VCV2638901
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
rare (popmax 0.172%, nfe)
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| REVEL | 0.036 | moderately benign-leaning |
|---|---|---|
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP -1.3 | GERP -7.1 |
| Overall | ||
| CADD | 2.7 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.172%
European (non-Finnish) · 2,031/1,179,984 alleles
Filtering AF
0.166%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.163%
Overall
0.134%
2,170/1,614,082 alleles · rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| European (non-Finnish)grpmax | 0.172% | 581 |
| Finnishnot grpmax-eligible | 0.108% | 928 |
| Remaining individualsnot grpmax-eligible | 0.0704% | 1,421 |
| African / African-American | 0.028% | 3,573 |
| Middle Eastern | 0.0165% | 6,062 |
| Admixed American | 0.00667% | 15,004 |
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
- ADGRL2
- Protein
- p.Ser759=
- Coding
- c.2277A>G
- MANE Select
- NM_001366006
- dbSNP
- rs151060845
- Type
- single nucleotide variant
- Location
- chr1:81966537 (GRCh38)
- Gene constraint
- LOEUF 0.301 · pLI 1.00 (gnomAD)
- Structure
- AlphaFold pLDDT 69.66 · 1 PDB
- Residue 759
- the gain-b domain
Similar variants
- ADGRL2 p.Lys555Arg Likely benign ★★ same type
- ADGRL2 p.Thr1294= Benign ★★ same type
- ADGRL2 p.Ala1070Thr Uncertain significance ★ ⚠ same type
- ADGRL2 p.Ala1090Val Uncertain significance ★ ⚠ same type
- ADGRL2 p.Ala160Val Uncertain significance ★ ⚠ same type
- ADGRL2 p.Ala170Val Uncertain significance ★ ⚠ same type
- ADGRL2 p.Ala191Ser Uncertain significance ★ ⚠ same type
- ADGRL2 p.Ala29Val 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/adgrl2-p-ser759 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown