Is IRF6 p.Phe276Ser (c.827T>C) pathogenic?

IRF6 p.Phe276Ser (c.827T>C) is classified Likely pathogenic in IRF6 (ClinVar, Single submitter, 1 submitter). AlphaMissense: likely pathogenic (0.9997); Absent from gnomAD v4.1; Associated with orofacial cleft 6, susceptibility to.

What condition is associated with IRF6 p.Phe276Ser (c.827T>C)?

IRF6 p.Phe276Ser (c.827T>C) is associated with orofacial cleft 6, susceptibility to, van der Woude syndrome 1, autosomal dominant popliteal pterygium syndrome (ClinVar).

How common is IRF6 p.Phe276Ser (c.827T>C) in the general population?

IRF6 p.Phe276Ser (c.827T>C) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about IRF6 p.Phe276Ser (c.827T>C)?

AlphaMissense predicts likely pathogenic (score 0.9997) — an in-silico prediction, not a clinical call.

IRF6 p.Phe276Ser

c.827T>C · VCV3383146

Likely pathogenic Single submitter

Classification

Likely pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.9997 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

3/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

orofacial cleft 6, susceptibility to

Computational evidence

Protein change
AlphaMissense	0.9997	likely pathogenic ✓ concordant with ClinVar · top 4% in IRF6
REVEL	0.95	strongly pathogenic-leaning
SaProt	LLR -13.90	damaging
⇒ AlphaMissense, REVEL and SaProt all call this damaging.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 11	GERP 2.9, phastCons 1
Regional constraint	o/e 0.56	unconstrained · MANE · 3,658 bp · p 7.6e-11 · regional, not allelic
Overall
CADD	32.0	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: IRF6
Protein: p.Phe276Ser
Coding: c.827T>C
MANE Select: NM_006147
Type: single nucleotide variant
Location: chr1:209790728 (GRCh38)
Gene constraint: LOEUF 0.214 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 74.19

Full IRF6 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

orofacial cleft 6, susceptibility to — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: van der Woude syndrome 1 autosomal dominant popliteal pterygium syndrome

Similar variants

IRF6 c.1060+1G>A Pathogenic/Likely pathogenic ★★ same condition
IRF6 p.Arg250Gln Pathogenic/Likely pathogenic ★★ same condition
IRF6 p.Arg250Ter Pathogenic ★★ same condition
IRF6 p.Arg400Trp Pathogenic ★★ same condition
IRF6 p.Arg412Ter Pathogenic ★★ same condition
IRF6 p.Arg6Cys Pathogenic/Likely pathogenic ★★ same condition
IRF6 p.Arg84Cys Pathogenic/Likely pathogenic ★★ same condition
IRF6 p.Arg84His 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/irf6-p-phe276ser (accessed [today's date]).

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