PKHD1 p.Pro4067=
c.12201G>T · rs750988521 · VCV1121031
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 -7.1 | GERP -5.1 |
| Overall | ||
| CADD | 0.033 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Admixed Americangrpmax | 0.005% | 20,005 |
| Remaining individualsnot grpmax-eligible | 0.0032% | 31,241 |
| African / African-American | 0.00133% | 74,956 |
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
- PKHD1
- Protein
- p.Pro4067=
- Coding
- c.12201G>T
- MANE Select
- NM_138694
- dbSNP
- rs750988521
- Type
- single nucleotide variant
- Location
- chr6:51619105 (GRCh38)
- Gene constraint
- LOEUF 0.783 · pLI <0.01 (gnomAD)
- Residue 4067
- a UniProt-annotated variant site (found in a patient affected by polycystic liver disease; uncertain significance); a UniProt-annotated variant site (found in a patient affected by polycystic liver disease; likely pathogenic)
Disease context
autosomal recessive polycystic kidney disease — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatmentsFor Autosomal recessive polycystic kidney disease (Orphanet):
- Inheritance
- Autosomal recessive
- Onset
- All ages
- Prevalence
- 1-9 / 100 000 (Germany)
Similar variants
- PKHD1 p.Pro4067Leu Uncertain significance ★★ ⚠ same residue
- PKHD1 p.Pro4067Gln Uncertain significance ★ ⚠ same residue
- PKHD1 p.Pro4067Thr Uncertain significance ★ ⚠ same residue
- PKHD1 c.11174+2T>C Likely pathogenic ★★ same condition
- PKHD1 c.11310+1G>C Pathogenic/Likely pathogenic ★★ same condition
- PKHD1 c.11398+2T>C Pathogenic/Likely pathogenic ★★ same condition
- PKHD1 c.11507-1G>A Likely pathogenic ★★ same condition
- PKHD1 c.11665+1G>A Pathogenic/Likely 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/pkhd1-p-pro4067 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown