Is IL2RA p.Phe36Ser (c.107T>C) pathogenic?

IL2RA p.Phe36Ser (c.107T>C) is classified Uncertain significance in IL2RA (ClinVar, Multiple submitters, 2 submitters; last evaluated 2023-12-20). AlphaMissense: likely pathogenic (0.7102); Absent from gnomAD v4.1; Associated with immunodeficiency due to CD25 deficiency.

What condition is associated with IL2RA p.Phe36Ser (c.107T>C)?

IL2RA p.Phe36Ser (c.107T>C) is associated with immunodeficiency due to CD25 deficiency (ClinVar).

How common is IL2RA p.Phe36Ser (c.107T>C) in the general population?

IL2RA p.Phe36Ser (c.107T>C) is absent from gnomAD v4.1 (gnomAD).

How is Immunodeficiency due to CD25 deficiency inherited?

Typically Autosomal recessive (Orphanet). A genetic counselor can assess individual risk for a family.

What do computational predictors say about IL2RA p.Phe36Ser (c.107T>C)?

AlphaMissense predicts likely pathogenic (score 0.7102) — an in-silico prediction, not a clinical call.

IL2RA p.Phe36Ser

c.107T>C · rs1839477553 · VCV1374040

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

AlphaMissense

likely pathogenic

0.7102 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

2/2 damaging

AlphaMissense, SaProt · REVEL no call

Conditions

immunodeficiency due to CD25 deficiency

Computational evidence

Protein change
AlphaMissense	0.7102	likely pathogenic
REVEL	0.294	indeterminate
SaProt	LLR -10.31	damaging
⇒ AlphaMissense and SaProt both call this damaging; REVEL makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 2.1	GERP -2.2, phastCons 1
Regional constraint	o/e 0.92	unconstrained · MANE · 49 kb · p 0.11 · regional, not allelic
Overall
CADD	17.75	PHRED · no single calibrated threshold — expert panels disagree

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

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: IL2RA
Protein: p.Phe36Ser
Coding: c.107T>C
MANE Select: NM_000417
dbSNP: rs1839477553
Type: single nucleotide variant
Location: chr10:6025983 (GRCh38)
Gene constraint: LOEUF 0.906 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 72.72 · 10 PDB
Residue 36: a disulfide bond; a β-strand; the sushi 1 domain

Full IL2RA gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

immunodeficiency due to CD25 deficiency — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Immunodeficiency due to CD25 deficiency (Orphanet):

Inheritance: Autosomal recessive
Onset: Infancy

Similar variants

IL2RA p.Gln101Ter Pathogenic ★★ same condition
IL2RA c.655+4C>T Uncertain significance ★★ same condition
IL2RA c.*1026G>T Uncertain significance ★★ same condition
IL2RA p.Arg206Cys Uncertain significance ★★ ⚠ same condition
IL2RA p.Arg206His Uncertain significance ★★ ⚠ same condition
IL2RA p.Arg263Trp Uncertain significance ★★ ⚠ same condition
IL2RA p.Arg56His Uncertain significance ★★ ⚠ same condition
IL2RA p.Arg88Gln 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/il2ra-p-phe36ser (accessed [today's date]).

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