SLC52A2 p.Pro192=
c.576C>T · rs782333547 · VCV702235
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
ultra-rare (popmax 0.033%, mid)
Conditions
1
Brown-Vialetto-van Laere syndrome 2
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 -12 | GERP -3 |
| Overall | ||
| CADD | 0.081 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.033%
Middle Eastern · 2/6,062 alleles
Filtering AF
0.0154%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.0129%
Overall
0.00254%
41/1,613,016 alleles · ultra-rare
exomes 41/1,460,670 · genomes 0/152,346 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Middle Easterngrpmax | 0.033% | 3,031 |
| South Asian | 0.0231% | 4,338 |
| East Asian | 0.00446% | 22,444 |
| African / African-American | 0.00266% | 37,527 |
| European (non-Finnish) | 0.00119% | 84,288 |
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
- SLC52A2
- Protein
- p.Pro192=
- Coding
- c.576C>T
- MANE Select
- NM_001363118
- dbSNP
- rs782333547
- Type
- single nucleotide variant
- Location
- chr8:144360068 (GRCh38)
- Gene constraint
- LOEUF 0.955 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 84.50 · 1 PDB
Similar variants
- SLC52A2 c.131-1G>C Likely pathogenic ★★ same condition
- SLC52A2 p.Ala420Thr Pathogenic/Likely pathogenic ★★ ⚠ same condition
- SLC52A2 p.Cys325Gly Likely pathogenic ★★ ⚠ same condition
- SLC52A2 p.Gln270Ter Pathogenic/Likely pathogenic ★★ same condition
- SLC52A2 p.Gly306Arg Pathogenic ★★ same condition
- SLC52A2 p.Gly306Glu Likely pathogenic ★★ same condition
- SLC52A2 p.Leu312Pro Pathogenic/Likely pathogenic ★★ same condition
- SLC52A2 p.Leu339Pro Pathogenic ★★ same condition
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/slc52a2-p-pro192 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown