Is CHKB p.Lys27Met (c.80A>T) pathogenic?

CHKB p.Lys27Met (c.80A>T) is classified Uncertain significance in CHKB (ClinVar, Multiple submitters, 2 submitters; last evaluated 2026-02-24). AlphaMissense: likely benign (0.1188); Very rare (popmax 0.00136%, nfe); Associated with Inborn genetic diseases.

What condition is associated with CHKB p.Lys27Met (c.80A>T)?

CHKB p.Lys27Met (c.80A>T) is associated with Inborn genetic diseases (ClinVar).

How common is CHKB p.Lys27Met (c.80A>T) in the general population?

CHKB p.Lys27Met (c.80A>T) is very rare (popmax 0.00136%, nfe) (gnomAD).

What do computational predictors say about CHKB p.Lys27Met (c.80A>T)?

AlphaMissense predicts likely benign (score 0.1188) — an in-silico prediction, not a clinical call.

CHKB p.Lys27Met

c.80A>T · VCV4228150

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

AlphaMissense

likely benign

0.1188 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00136%, nfe)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.1188	likely benign
REVEL	0.016	strongly benign-leaning
SaProt	LLR -6.59	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	<0.2	all four deltas below 0.2 · T>C here scores Δ0.24 · evaluated, not missing
Constraint at this position
Conservation	phyloP 0.14	GERP -0.34
Regional constraint	o/e 1.03	unconstrained · MANE · 3,597 bp · p 0.53 · regional, not allelic
Overall
CADD	17.16	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00136% European (non-Finnish) · 16/1,178,978 alleles

Filtering AF 0.000803% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00065%

Overall 0.0011% 16/1,457,740 alleles · very rare

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: CHKB
Protein: p.Lys27Met
Coding: c.80A>T
MANE Select: NM_005198
Type: single nucleotide variant
Location: chr22:50582702 (GRCh38)
Gene constraint: LOEUF 1.015 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 86.54 · 3 PDB

Full CHKB gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

CHKB p.Lys27Arg Uncertain significance ★★ ⚠ same residue
CHKB p.Lys27= Likely benign ★ same residue
CHKB p.Gln309Glu Uncertain significance ★★ ⚠ same condition
CHKB p.Glu97Asp Uncertain significance ★★ ⚠ same condition
CHKB p.Gly12Glu Uncertain significance ★★ ⚠ same condition
CHKB p.Gly190Glu Uncertain significance ★★ ⚠ same condition
CHKB p.Gly386Glu Uncertain significance ★★ ⚠ same condition
CHKB p.His315Arg Uncertain significance ★★ ⚠ 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/chkb-p-lys27met (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown