Is FLG p.Ala3426Val (c.10277C>T) pathogenic?

FLG p.Ala3426Val (c.10277C>T) is classified Uncertain significance in FLG (ClinVar, Single submitter, 1 submitter; last evaluated 2024-06-19). AlphaMissense: likely benign (0.1467); Rare (popmax 0.2%, eas); Associated with Inborn genetic diseases.

What condition is associated with FLG p.Ala3426Val (c.10277C>T)?

FLG p.Ala3426Val (c.10277C>T) is associated with Inborn genetic diseases (ClinVar).

How common is FLG p.Ala3426Val (c.10277C>T) in the general population?

FLG p.Ala3426Val (c.10277C>T) is rare (popmax 0.2%, eas) (gnomAD).

What do computational predictors say about FLG p.Ala3426Val (c.10277C>T)?

AlphaMissense predicts likely benign (score 0.1467) — an in-silico prediction, not a clinical call.

FLG p.Ala3426Val

c.10277C>T · VCV3279049

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.1467 · ACMG-weighted

gnomAD v4.1

Rare

rare (popmax 0.2%, eas)

Missense predictors

0/2 damaging

AlphaMissense, REVEL · SaProt no call

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.1467	likely benign
REVEL	0.04	moderately benign-leaning
SaProt	—	not scored · why
⇒ AlphaMissense and REVEL both call this tolerated; SaProt makes no call.
Splicing
SpliceAI	—	not looked up on this page · why
Constraint at this position
Conservation	phyloP -20	GERP -3.2
Regional constraint	o/e 1.38	unconstrained · MANE · 2,903 bp · p 2.8e-40 · regional, not allelic
Overall
CADD	0.027	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification

AlphaMissense carries the ACMG weight for missense; REVEL is an independent agreement signal.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.2% East Asian · 89/44,506 alleles

Filtering AF 0.166% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.154%

Overall 0.00832% 134/1,610,294 alleles · rare

Ancestry group	Frequency	1 in
East Asiangrpmax	0.2%	500
Admixed American	0.0235%	4,261
Remaining individualsnot grpmax-eligible	0.0128%	7,798
European (non-Finnish)	0.00187%	53,554
Finnishnot grpmax-eligible	0.00156%	63,962

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: FLG
Protein: p.Ala3426Val
Coding: c.10277C>T
MANE Select: NM_002016
Type: single nucleotide variant
Location: chr1:152304609 (GRCh38)

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

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

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/flg-p-ala3426val (accessed [today's date]).

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