Is CEL p.Gly611= (c.1833G>C) pathogenic?

CEL p.Gly611= (c.1833G>C) is classified Benign/Likely benign in CEL (ClinVar, Multiple submitters, 4 submitters; last evaluated 2024-11-26). Low-frequency (popmax 1.96%, sas); Associated with maturity-onset diabetes of the young type 8.

What condition is associated with CEL p.Gly611= (c.1833G>C)?

CEL p.Gly611= (c.1833G>C) is associated with maturity-onset diabetes of the young type 8 (ClinVar).

How common is CEL p.Gly611= (c.1833G>C) in the general population?

CEL p.Gly611= (c.1833G>C) is low-frequency (popmax 1.96%, sas) (gnomAD).

How is MODY inherited?

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

CEL p.Gly611=

c.1833G>C · rs1211933243 · VCV1202347

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 4 submitters

gnomAD v4.1

Rare

low-frequency (popmax 1.96%, sas)

Conditions

maturity-onset diabetes of the young type 8

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 -0.96	GERP 0.59
Overall
CADD	1.478	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 1.96% South Asian · 808/41,196 alleles

Filtering AF 1.85% ClinGen BA1/BS1 input FAF95, joint · FAF99 1.8%

Overall 0.72% 2,569/356,854 alleles · low-frequency

Ancestry group	Frequency	1 in
South Asiangrpmax	1.96%	51
Middle Eastern	1.79%	56
African / African-American	1.78%	56
Ashkenazi Jewishnot grpmax-eligible	1.32%	76
Remaining individualsnot grpmax-eligible	0.633%	158
Finnishnot grpmax-eligible	0.559%	179
European (non-Finnish)	0.506%	198
Admixed American	0.499%	200
East Asian	0.142%	706

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: CEL
Protein: p.Gly611=
Coding: c.1833G>C
MANE Select: NM_001807
dbSNP: rs1211933243
Type: single nucleotide variant
Location: chr9:133071335 (GRCh38)
Gene constraint: LOEUF 0.972 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 84.10 · 7 PDB
Residue 611: the 'disordered' region; the '17 x 11 aa tandem repeats, glycodomain, o-linked (mucin type)' region

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

Disease context

maturity-onset diabetes of the young type 8 — 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

CEL p.Gly611Arg Uncertain significance ★ same residue
CEL p.Gly611Glu Likely benign ★ same residue
CEL c.67-3C>A Uncertain significance ★★ same condition
CEL p.Ala295Ser Uncertain significance ★★ same condition
CEL p.Ala548Glu Uncertain significance ★★ same condition
CEL p.Ala722Val Uncertain significance ★★ same condition
CEL p.Arg116Gln Uncertain significance ★★ same condition
CEL p.Arg185Trp 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/cel-p-gly611 (accessed [today's date]).

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