PIGB p.Val78=
c.234G>A · rs781403925 · VCV3007061
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00334%, amr)
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 -1.2 | GERP -7 |
| Overall | ||
| CADD | 1.901 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.00334%
Admixed American · 2/59,960 alleles
Filtering AF
0.000553%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.000207%
Overall
0.000186%
3/1,612,836 alleles · very rare
exomes 2/1,460,690 · genomes 1/152,146 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Admixed Americangrpmax | 0.00334% | 29,980 |
| South Asian | 0.0011% | 91,052 |
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
- PIGB
- Protein
- p.Val78=
- Coding
- c.234G>A
- MANE Select
- NM_004855
- dbSNP
- rs781403925
- Type
- single nucleotide variant
- Location
- chr15:55320345 (GRCh38)
- Gene constraint
- LOEUF 1.098 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 88.48
Similar variants
- PIGB p.Val78Ala Uncertain significance ★ ⚠ same residue
- PIGB c.795-1G>C Likely pathogenic ★★ same type
- PIGB c.795-2A>G Likely pathogenic ★★ same type
- PIGB c.847-10A>G Pathogenic ★★ same type
- PIGB p.Asp155His Likely pathogenic ★★ same type
- PIGB p.Leu131Ter Pathogenic ★★ same type
- PIGB p.Lys31Ter Pathogenic ★★ same type
- PIGB p.Ala400Thr 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/pigb-p-val78 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown