Is EHMT1 p.Val211= (c.633C>T) pathogenic?

EHMT1 p.Val211= (c.633C>T) is classified Benign in EHMT1 (ClinVar, Single submitter, 1 submitter; last evaluated 2024-01-02). Rare (popmax 0.158%, eas); Associated with Kleefstra syndrome 1.

What condition is associated with EHMT1 p.Val211= (c.633C>T)?

EHMT1 p.Val211= (c.633C>T) is associated with Kleefstra syndrome 1 (ClinVar).

How common is EHMT1 p.Val211= (c.633C>T) in the general population?

EHMT1 p.Val211= (c.633C>T) is rare (popmax 0.158%, eas) (gnomAD).

EHMT1 p.Val211=

c.633C>T · rs751159756 · VCV1549825

Benign Single submitter

Classification

Benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

rare (popmax 0.158%, eas)

Conditions

Kleefstra syndrome 1

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 0.19	GERP -0.25, phastCons 0.007
Overall
CADD	9.298	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.158% East Asian · 71/44,888 alleles

Filtering AF 0.129% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.118%

Overall 0.00565% 91/1,611,886 alleles · rare

Ancestry group	Frequency	1 in
East Asiangrpmax	0.158%	632
Admixed American	0.00167%	59,988
Remaining individualsnot grpmax-eligible	0.0016%	62,440
European (non-Finnish)	0.00144%	69,411
South Asian	0.0011%	91,060

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: EHMT1
Protein: p.Val211=
Coding: c.633C>T
MANE Select: NM_024757
dbSNP: rs751159756
Type: single nucleotide variant
Location: chr9:137717173 (GRCh38)
Gene constraint: LOEUF 0.159 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 64.89 · 22 PDB
Residue 211: the 'disordered' region

Full EHMT1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Kleefstra syndrome 1 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

EHMT1 p.Val211Ile Benign/Likely benign ★★ same residue
EHMT1 p.Val211Ala Conflicting classifications of pathogenicity ★ ⚠ same residue
EHMT1 c.1370-1G>C Likely pathogenic ★★ same condition
EHMT1 c.1647+2T>C Pathogenic/Likely pathogenic ★★ same condition
EHMT1 c.2193-1G>C Pathogenic ★★ same condition
EHMT1 c.2276-2A>G Pathogenic ★★ same condition
EHMT1 c.2712+1G>A Pathogenic ★★ same condition
EHMT1 c.2867+2T>C 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/ehmt1-p-val211 (accessed [today's date]).

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