PHKG2 p.Asp153=
c.459T>C · rs2543462649 · VCV2828458
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
Conditions
1
glycogen storage disease IXc
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 2.3 | GERP -1.4, phastCons 1 |
| Overall | ||
| CADD | 12.18 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.
Variant & gene context
- Gene
- PHKG2
- Protein
- p.Asp153=
- Coding
- c.459T>C
- MANE Select
- NM_000294
- dbSNP
- rs2543462649
- Type
- single nucleotide variant
- Location
- chr16:30753460 (GRCh38)
- Gene constraint
- LOEUF 0.876 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
- Structure
- AlphaFold pLDDT 83.77 · 1 PDB
- Residue 153
- the protein kinase domain; an active site
Disease context
glycogen storage disease IXc — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatmentsFor Glycogen storage disease due to liver phosphorylase kinase deficiency (Orphanet):
- Inheritance
- Autosomal recessive, X-linked recessive
- Onset
- Childhood
- Prevalence
- 1-9 / 100 000 (Europe)
Similar variants
- PHKG2 p.Asp153Val Conflicting classifications of pathogenicity ★ ⚠ same residue
- PHKG2 c.96-11G>A Pathogenic/Likely pathogenic ★★ same condition
- PHKG2 p.Arg152Ter Pathogenic/Likely pathogenic ★★ same condition
- PHKG2 p.Arg185Ter Pathogenic ★★ same condition
- PHKG2 p.Arg279Cys Pathogenic/Likely pathogenic ★★ same condition
- PHKG2 p.Arg309Trp Likely pathogenic ★★ ⚠ same condition
- PHKG2 p.Arg44Ter Pathogenic ★★ same condition
- PHKG2 p.Arg76Ter 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/phkg2-p-asp153 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown