Is KLF11 p.Pro162= (c.486A>G) pathogenic?

KLF11 p.Pro162= (c.486A>G) is classified Benign/Likely benign in KLF11 (ClinVar, Multiple submitters, 5 submitters; last evaluated 2025-09-08). Rare (popmax 0.253%, afr); Associated with maturity-onset diabetes of the young type 7.

What condition is associated with KLF11 p.Pro162= (c.486A>G)?

KLF11 p.Pro162= (c.486A>G) is associated with maturity-onset diabetes of the young type 7 (ClinVar).

How common is KLF11 p.Pro162= (c.486A>G) in the general population?

KLF11 p.Pro162= (c.486A>G) is rare (popmax 0.253%, afr) (gnomAD).

How is MODY inherited?

Typically Autosomal dominant, Not applicable (Orphanet). A genetic counselor can assess individual risk for a family.

KLF11 p.Pro162=

c.486A>G · rs146462049 · VCV330628

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 5 submitters

gnomAD v4.1

Rare

rare (popmax 0.253%, afr)

Conditions

maturity-onset diabetes of the young type 7

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 -0.92	GERP -3.6
Overall
CADD	1.674	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.253% African / African-American · 190/75,046 alleles

Filtering AF 0.224% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.212%

Overall 0.0123% 198/1,613,804 alleles · rare

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.253%	395
Admixed American	0.00666%	15,006
Remaining individualsnot grpmax-eligible	0.0064%	15,626

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: KLF11
Protein: p.Pro162=
Coding: c.486A>G
MANE Select: NM_003597
dbSNP: rs146462049
Type: single nucleotide variant
Location: chr2:10047823 (GRCh38)
Gene constraint: LOEUF 1.07 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 49.73

Full KLF11 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

maturity-onset diabetes of the young type 7 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For MODY (Orphanet):

Inheritance: Autosomal dominant, Not applicable
Onset: Adolescent, Adult, Childhood
Prevalence: 1-5 / 10 000 (Europe)

Similar variants

KLF11 c.-104C>T Uncertain significance ★★ same condition
KLF11 p.Ala146Val Uncertain significance ★★ ⚠ same condition
KLF11 p.Ala321Pro Uncertain significance ★★ ⚠ same condition
KLF11 p.Ala89Val Uncertain significance ★★ ⚠ same condition
KLF11 p.Arg120Gly Uncertain significance ★★ ⚠ same condition
KLF11 p.Arg390Gln Uncertain significance ★★ same condition
KLF11 p.Gln215Lys Uncertain significance ★★ ⚠ same condition
KLF11 p.Gly331Val 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/klf11-p-pro162 (accessed [today's date]).

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