Is SETD2 p.Val2022= (c.6066A>G) pathogenic?

SETD2 p.Val2022= (c.6066A>G) is classified Likely benign in SETD2 (ClinVar, Multiple submitters, 3 submitters; last evaluated 2025-03-13). Rare (popmax 0.127%, afr); Associated with Luscan-Lumish syndrome.

What condition is associated with SETD2 p.Val2022= (c.6066A>G)?

SETD2 p.Val2022= (c.6066A>G) is associated with Luscan-Lumish syndrome (ClinVar).

How common is SETD2 p.Val2022= (c.6066A>G) in the general population?

SETD2 p.Val2022= (c.6066A>G) is rare (popmax 0.127%, afr) (gnomAD).

SETD2 p.Val2022=

c.6066A>G · rs149499141 · VCV721750

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 3 submitters

gnomAD v4.1

Rare

rare (popmax 0.127%, afr)

Conditions

Luscan-Lumish syndrome

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 -3.7	GERP -3.2
Overall
CADD	0.592	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.127% African / African-American · 95/74,858 alleles

Filtering AF 0.106% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0985%

Overall 0.00801% 129/1,610,850 alleles · rare exomes 67/1,458,656 · genomes 62/152,194 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.127%	788
Middle Eastern	0.0331%	3,019
Admixed American	0.0183%	5,451
Ashkenazi Jewishnot grpmax-eligible	0.0135%	7,390
Remaining individualsnot grpmax-eligible	0.00641%	15,591
European (non-Finnish)	0.0011%	90,565

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: SETD2
Protein: p.Val2022=
Coding: c.6066A>G
MANE Select: NM_014159
dbSNP: rs149499141
Type: single nucleotide variant
Location: chr3:47067113 (GRCh38)
Gene constraint: LOEUF 0.176 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 43.81 · 43 PDB
Residue 2022: a UniProt-annotated variant site (in aml; uncertain significance; somatic mutation); a UniProt-annotated variant site (in all; uncertain significance; somatic mutation); the 'disordered' region; an α-helix

Full SETD2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Luscan-Lumish syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

SETD2 p.Arg1598Ter Pathogenic/Likely pathogenic ★★ same condition
SETD2 p.Arg1740Gln Pathogenic ★★ ⚠ same condition
SETD2 p.Arg1740Trp Pathogenic/Likely pathogenic ★★ same condition
SETD2 p.Ala1121Thr Uncertain significance ★★ ⚠ same condition
SETD2 p.Ala679Val Uncertain significance ★★ ⚠ same condition
SETD2 p.Arg1065Cys Uncertain significance ★★ same condition
SETD2 p.Arg329Gln Uncertain significance ★★ ⚠ same condition
SETD2 p.Arg368Gln 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/setd2-p-val2022 (accessed [today's date]).

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