Is GABBR2 p.Val601= (c.1803G>T) pathogenic?

GABBR2 p.Val601= (c.1803G>T) is classified Likely benign in GABBR2 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-10-26). Very rare (popmax 0.00459%, eas); Associated with Epileptic encephalopathy.

What condition is associated with GABBR2 p.Val601= (c.1803G>T)?

GABBR2 p.Val601= (c.1803G>T) is associated with Epileptic encephalopathy (ClinVar).

How common is GABBR2 p.Val601= (c.1803G>T) in the general population?

GABBR2 p.Val601= (c.1803G>T) is very rare (popmax 0.00459%, eas) (gnomAD).

GABBR2 p.Val601=

c.1803G>T · rs780693472 · VCV1084776

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00459%, eas)

Conditions

Epileptic encephalopathy

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 -2.6	GERP -5
Overall
CADD	3.978	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00459% East Asian · 2/43,540 alleles

Filtering AF 0.00104% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000835%

Overall 0.00156% 25/1,597,514 alleles · very rare exomes 23/1,445,338 · genomes 2/152,176 · joint denominator

Ancestry group	Frequency	1 in
East Asiangrpmax	0.00459%	21,770
African / African-American	0.0027%	37,068
South Asian	0.00226%	44,181
European (non-Finnish)	0.00162%	61,718

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: GABBR2
Protein: p.Val601=
Coding: c.1803G>T
MANE Select: NM_005458
dbSNP: rs780693472
Type: single nucleotide variant
Location: chr9:98362805 (GRCh38)
Gene constraint: LOEUF 0.394 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 78.00 · 26 PDB
Residue 601: an α-helix

Full GABBR2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Epileptic encephalopathy — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

GABBR2 p.Val601Met Uncertain significance ★ ⚠ same residue
GABBR2 p.Gly693Trp Pathogenic ★★ same condition
GABBR2 p.Ala444Thr Uncertain significance ★★ ⚠ same condition
GABBR2 p.Ala580Ser Uncertain significance ★★ ⚠ same condition
GABBR2 p.Ala69Pro Uncertain significance ★★ ⚠ same condition
GABBR2 p.Ala708Ser Uncertain significance ★★ ⚠ same condition
GABBR2 p.Arg301His Uncertain significance ★★ ⚠ same condition
GABBR2 p.Arg48Trp 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/gabbr2-p-val601 (accessed [today's date]).

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